nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Nov 25th, 2018 12:00AM
|
Senior Mechanical Engineer
|
Open
|
Equip Engineering
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Apr 12th, 2018 12:00AM
|
|
|
|
|
|
|
Nov 25th, 2018 05:23PM
|
Nov 25th, 2018 05:23PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Nov 28th, 2018 12:00AM
|
Senior Mechanical Engineer
|
Open
|
Equip Engineering
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Apr 12th, 2018 12:00AM
|
|
|
|
|
|
|
Nov 28th, 2018 12:10AM
|
Nov 28th, 2018 12:10AM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 8th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 8th, 2019 02:10PM
|
Feb 8th, 2019 02:10PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 9th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 9th, 2019 02:03PM
|
Feb 9th, 2019 02:03PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 10th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 10th, 2019 02:30PM
|
Feb 10th, 2019 02:30PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 17th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 17th, 2019 02:00PM
|
Feb 17th, 2019 02:00PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 18th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 18th, 2019 01:22PM
|
Feb 18th, 2019 01:22PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 19th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 19th, 2019 02:00PM
|
Feb 19th, 2019 02:00PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 20th, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 20th, 2019 01:44PM
|
Feb 20th, 2019 01:44PM
|
Zosano Pharma
|
|
|
nasdaq:zsan
|
zosanopharma.bamboohr.com
|
zosanopharma.bamboohr.com
|
Feb 21st, 2019 12:00AM
|
Senior Materials & Supply Chain Associate
|
Open
|
Mfg Operations
|
Full-Time
|
|
Fremont
|
California
|
USA
|
Feb 4th, 2019 12:00AM
|
|
<p></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">POSITION SUMMARY: </span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">The Materials Handler III in the Supply Chain Group are primarily responsible for the proper warehousing and inventory maintenance of cGMP raw materials, components, intermediates and GMP Manufactured Final Drug Product inventory. Materials Specialists will perform cGMP warehousing duties, maintain accurate inventory records, dispense and transfer cGMP raw materials, components and intermediates from the central warehouse to the appropriate Manufacturing areas, and dispense/distribute Final Drug Product material as required.</span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></b></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Receive, inspect, label, and warehouse cGMP raw materials, components, intermediates, and final drug product material per established SOP’s and Controlled Material Specifications.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Transport and distribute approved cGMP raw materials, components, and final drug product material.<b> </b></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain accurate inventory records of raw material, component, intermediate and final drug product inventory.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain (receipt, stocking) the gowning inventory for GMP Manufacturing. Monitor Vendor performance, resolve issues.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain all Controlled Document Binders (SOP’s, Material Specifications) issued by QA Documentation for use in the Supply Chain Group. </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain and keep current all Material Safety Data Sheets (MSDS) for use in the Supply Chain Group.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform cycle counts of cGMP inventory as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Monitor temperature and humidity chart recorders for all equipment/storage areas within the cGMP warehouse per established SOP’s.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all general Shipping/Receiving functions for Zosano.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Perform all Shipping/Receiving functions related to Final Drug Product and Process Intermediate material. Generate and maintain all associated documentation.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in day to day facilities activities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist in monitoring building systems as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Start and/or shut down facility systems as required.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Assist monitoring facility operations/perform daily walk-throughs as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Respond to Building System Alarms during and between normal work shifts as assigned.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Alert manager of general maintenance, alarms, and equipment issues in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Compliance with Safety Guidelines</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use safety eyewear while inside a manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Use temperature resistant gloves when necessary.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know appropriate emergency response procedures.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know locations of first aid kits, safety showers, and spill kits.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Know evacuation route and assembly area to be used in case of fire or earthquake.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe safe chemical handling practices</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all required gowning procedures throughout the manufacturing area.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Observe all safety guidelines related to warehousing and material movement equipment (forklifts, pallet jacks, hand trucks).</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Maintain personal Training Record </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"></span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow cGMP and Zosano Good Documentation Practices:</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Record information accurately.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Make corrections in a timely manner.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Check all necessary calculations.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review pre-recorded data for accuracy and completion.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ensure all entries are neat and legible</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Understand operator and verifier responsibilities</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Review labels and calibration stickers for accuracy</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Follow up on documentation errors.</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif"> </span></p>
<p><b><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">QUALIFICATIONS & REQUIREMENTS:</span></b></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">High School Diploma</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">3-5 years working experience in a Pharmaceutical, Medical Device, or Biotechnology warehouse environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to maintain accurate inventory records of cGMP materials</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience in completing cGMP documentations, for example, production batch record, inventory record & material request forms</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Hands-on experience with document change orders, deviations or non-conformance reporting</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Working knowledge of desktop computers and commonly used software packages</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Strong work ethics, customer service and communication skills </span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to work within a team oriented environment</span></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Ability to lift 50 pounds.</span></p>
<p></p>
<p><span style="font-size: 9.0pt;font-family: 'Arial',sans-serif">Valid California Driver’s License</span></p>
<p></p>
|
|
|
|
|
Feb 21st, 2019 01:42PM
|
Feb 21st, 2019 01:42PM
|
Zosano Pharma
|
|
|