ZS

Zosano Pharma

- NASDAQ:ZSAN
Last Updated 2019-09-13

Job Listings

Track Zosano Pharma hiring and firing trends, filtered by title, location, type, date, category and date of posting.

Records

Open dataset
Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Date Added Date Updated GICS Sector GICS Industry
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 22nd, 2019 12:00AM Validation Engineer Open Process Development Full-Time Fremont California USA Apr 23rd, 2019 12:00AM <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Purpose of Position &amp; Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b></p> <p>Zosano Pharma has an exciting opportunity for a Validation Engineer II position responsible for process and equipment validation to support the commercialization of a novel microneedle medical product.<span>  </span>The Validation Engineer will be responsible for activities related to validating the equipment and process for a new commercial line and the associated support equipment.<span>  </span>Validation will include confirming that mechanical, electrical, and automation systems as well as process validation work meet the defined user requirements.<span>  </span>The candidate will be responsible for strategic planning, generating and approving validation protocols, overseeing and executing validation protocols and writing validation summary reports.<span>  </span>The candidate will also manage validation efforts with equipment manufacturers and commercial manufacturing organizations from FAT to Process Validation.<span>  </span>The position will require 20-30% travel.</p> <p><b><span style="font-family: 'Arial',sans-serif"> </span></b></p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b><b><span style="font-family: 'Arial',sans-serif"></span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop and manage the Validation Program at Zosano. </p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Strategic development and design of Validation Master Plans.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Draft or review qualification documents including IQ, OQ, PQ and PV.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Support Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT) for new equipment.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Execute, manage and support validation activities at CMO’s.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop strategies for Process Qualification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Review validation documents executed by CMO’s (Protocols, executed documents, and Reports).</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Assess validation deviations.</p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Position Requirements:</span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Bachelor’s Degree in Engineering (Mechanical or Electrical Preferred) with 5-8 years of experience in Biotechnology or Medical Devices with an emphasis on validation.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Have experience with writing and execution IQ/OQ/PQ’s and process validation activities.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of design control and Quality Risk Management principles.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of statistics used to support validation justification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of cGMP and Good Documentation Practices.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Possess good communication skills and be capable of managing complex programs and be knowledgeable of cGMP manufacturing and validation concepts.</p> Aug 22nd, 2019 12:34PM Aug 22nd, 2019 12:34PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 22nd, 2019 12:00AM Equipment Engineer Open Equipment Engineering Full-Time Fremont California USA Jul 3rd, 2019 12:00AM <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">POSITION SUMMARY</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">We are looking for an experienced, motivated individual to provide equipment maintenance support and tooling design of complex automated custom manufacturing equipment. The position involves working with tooling mechanical systems electrical, pneumatic and vacuum systems in a clean room environment. He/she should have good analytical thinking skills and very detail oriented with excellent mechanical design aptitude.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">RESPONSIBILITIES</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to design, perform modifications on mechanical tooling to improve equipment performance.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He/she will manage vendors and take ownership of the project from concept to final implementation.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with Process and Manufacturing engineering and other cross functional groups to improve equipment reliability and minimize equipment downtime.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He /she must be able to understand and work with control automation for equipment upgrade and repairs.</span></p> <p><span style="font-size: 12px;font-family: Helvetica, sans-serif">-</span><span style="font-size: 12px;font-family: Helvetica, sans-serif"> </span><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Perform root cause analysis and implement improvements using change control procedures.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with cross functional groups in developing equipment user requirement specifications.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Functions with other support department in during manufacturing operations.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Supervise contractors and vendors on equipment upgrades.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to work in a clean room environment.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Manage and mentor technicians to help improve technicians workmanship</span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></b></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">QUALIFICATIONS</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Minimum 8 years working as an equipment engineer in the biotechnology or pharmaceutical industry.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- BS in Mechanical/Electrical Engineering or equivalent</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Well experienced in tooling design using Solidworks or equivalent is a must.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- The ability to read and interpret electrical drawings is a plus.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Be a self-starter and willing to tackle difficult technical issues.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Sound knowledge of pharmaceutical industry standards and guidelines, cGMP, GAMP, ICH, ASTM E2500</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Experienced with manufacturing equipment software, which includes Allen Bradley PLCs, programmable HMIs, vision inspection systems, Siemens PLCs, and ELAU Motion PLCs is a plus</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be willing and able to work flexible hours, nights and weekends, in support of manufacturing production.</span></p> Aug 22nd, 2019 12:34PM Aug 22nd, 2019 12:34PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 30th, 2019 12:00AM Validation Engineer Open Process Development Full-Time Fremont California USA Apr 23rd, 2019 12:00AM <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Purpose of Position &amp; Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b></p> <p>Zosano Pharma has an exciting opportunity for a Validation Engineer II position responsible for process and equipment validation to support the commercialization of a novel microneedle medical product.<span>  </span>The Validation Engineer will be responsible for activities related to validating the equipment and process for a new commercial line and the associated support equipment.<span>  </span>Validation will include confirming that mechanical, electrical, and automation systems as well as process validation work meet the defined user requirements.<span>  </span>The candidate will be responsible for strategic planning, generating and approving validation protocols, overseeing and executing validation protocols and writing validation summary reports.<span>  </span>The candidate will also manage validation efforts with equipment manufacturers and commercial manufacturing organizations from FAT to Process Validation.<span>  </span>The position will require 20-30% travel.</p> <p><b><span style="font-family: 'Arial',sans-serif"> </span></b></p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b><b><span style="font-family: 'Arial',sans-serif"></span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop and manage the Validation Program at Zosano. </p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Strategic development and design of Validation Master Plans.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Draft or review qualification documents including IQ, OQ, PQ and PV.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Support Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT) for new equipment.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Execute, manage and support validation activities at CMO’s.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop strategies for Process Qualification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Review validation documents executed by CMO’s (Protocols, executed documents, and Reports).</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Assess validation deviations.</p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Position Requirements:</span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Bachelor’s Degree in Engineering (Mechanical or Electrical Preferred) with 5-8 years of experience in Biotechnology or Medical Devices with an emphasis on validation.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Have experience with writing and execution IQ/OQ/PQ’s and process validation activities.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of design control and Quality Risk Management principles.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of statistics used to support validation justification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of cGMP and Good Documentation Practices.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Possess good communication skills and be capable of managing complex programs and be knowledgeable of cGMP manufacturing and validation concepts.</p> Aug 30th, 2019 10:37AM Aug 30th, 2019 10:37AM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 30th, 2019 12:00AM Equipment Engineer Open Equipment Engineering Full-Time Fremont California USA Jul 3rd, 2019 12:00AM <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">POSITION SUMMARY</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">We are looking for an experienced, motivated individual to provide equipment maintenance support and tooling design of complex automated custom manufacturing equipment. The position involves working with tooling mechanical systems electrical, pneumatic and vacuum systems in a clean room environment. He/she should have good analytical thinking skills and very detail oriented with excellent mechanical design aptitude.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">RESPONSIBILITIES</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to design, perform modifications on mechanical tooling to improve equipment performance.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He/she will manage vendors and take ownership of the project from concept to final implementation.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with Process and Manufacturing engineering and other cross functional groups to improve equipment reliability and minimize equipment downtime.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He /she must be able to understand and work with control automation for equipment upgrade and repairs.</span></p> <p><span style="font-size: 12px;font-family: Helvetica, sans-serif">-</span><span style="font-size: 12px;font-family: Helvetica, sans-serif"> </span><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Perform root cause analysis and implement improvements using change control procedures.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with cross functional groups in developing equipment user requirement specifications.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Functions with other support department in during manufacturing operations.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Supervise contractors and vendors on equipment upgrades.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to work in a clean room environment.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Manage and mentor technicians to help improve technicians workmanship</span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></b></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">QUALIFICATIONS</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Minimum 8 years working as an equipment engineer in the biotechnology or pharmaceutical industry.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- BS in Mechanical/Electrical Engineering or equivalent</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Well experienced in tooling design using Solidworks or equivalent is a must.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- The ability to read and interpret electrical drawings is a plus.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Be a self-starter and willing to tackle difficult technical issues.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Sound knowledge of pharmaceutical industry standards and guidelines, cGMP, GAMP, ICH, ASTM E2500</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Experienced with manufacturing equipment software, which includes Allen Bradley PLCs, programmable HMIs, vision inspection systems, Siemens PLCs, and ELAU Motion PLCs is a plus</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be willing and able to work flexible hours, nights and weekends, in support of manufacturing production.</span></p> Aug 30th, 2019 10:37AM Aug 30th, 2019 10:37AM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Sep 3rd, 2019 12:00AM Validation Engineer Open Process Development Full-Time Fremont California USA Apr 23rd, 2019 12:00AM <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Purpose of Position &amp; Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b></p> <p>Zosano Pharma has an exciting opportunity for a Validation Engineer II position responsible for process and equipment validation to support the commercialization of a novel microneedle medical product.<span>  </span>The Validation Engineer will be responsible for activities related to validating the equipment and process for a new commercial line and the associated support equipment.<span>  </span>Validation will include confirming that mechanical, electrical, and automation systems as well as process validation work meet the defined user requirements.<span>  </span>The candidate will be responsible for strategic planning, generating and approving validation protocols, overseeing and executing validation protocols and writing validation summary reports.<span>  </span>The candidate will also manage validation efforts with equipment manufacturers and commercial manufacturing organizations from FAT to Process Validation.<span>  </span>The position will require 20-30% travel.</p> <p><b><span style="font-family: 'Arial',sans-serif"> </span></b></p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b><b><span style="font-family: 'Arial',sans-serif"></span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop and manage the Validation Program at Zosano. </p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Strategic development and design of Validation Master Plans.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Draft or review qualification documents including IQ, OQ, PQ and PV.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Support Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT) for new equipment.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Execute, manage and support validation activities at CMO’s.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop strategies for Process Qualification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Review validation documents executed by CMO’s (Protocols, executed documents, and Reports).</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Assess validation deviations.</p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Position Requirements:</span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Bachelor’s Degree in Engineering (Mechanical or Electrical Preferred) with 5-8 years of experience in Biotechnology or Medical Devices with an emphasis on validation.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Have experience with writing and execution IQ/OQ/PQ’s and process validation activities.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of design control and Quality Risk Management principles.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of statistics used to support validation justification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of cGMP and Good Documentation Practices.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Possess good communication skills and be capable of managing complex programs and be knowledgeable of cGMP manufacturing and validation concepts.</p> Sep 3rd, 2019 12:40PM Sep 3rd, 2019 12:40PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Sep 3rd, 2019 12:00AM Equipment Engineer Open Equipment Engineering Full-Time Fremont California USA Jul 3rd, 2019 12:00AM <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">POSITION SUMMARY</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">We are looking for an experienced, motivated individual to provide equipment maintenance support and tooling design of complex automated custom manufacturing equipment. The position involves working with tooling mechanical systems electrical, pneumatic and vacuum systems in a clean room environment. He/she should have good analytical thinking skills and very detail oriented with excellent mechanical design aptitude.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">RESPONSIBILITIES</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to design, perform modifications on mechanical tooling to improve equipment performance.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He/she will manage vendors and take ownership of the project from concept to final implementation.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with Process and Manufacturing engineering and other cross functional groups to improve equipment reliability and minimize equipment downtime.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He /she must be able to understand and work with control automation for equipment upgrade and repairs.</span></p> <p><span style="font-size: 12px;font-family: Helvetica, sans-serif">-</span><span style="font-size: 12px;font-family: Helvetica, sans-serif"> </span><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Perform root cause analysis and implement improvements using change control procedures.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with cross functional groups in developing equipment user requirement specifications.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Functions with other support department in during manufacturing operations.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Supervise contractors and vendors on equipment upgrades.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to work in a clean room environment.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Manage and mentor technicians to help improve technicians workmanship</span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></b></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">QUALIFICATIONS</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Minimum 8 years working as an equipment engineer in the biotechnology or pharmaceutical industry.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- BS in Mechanical/Electrical Engineering or equivalent</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Well experienced in tooling design using Solidworks or equivalent is a must.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- The ability to read and interpret electrical drawings is a plus.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Be a self-starter and willing to tackle difficult technical issues.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Sound knowledge of pharmaceutical industry standards and guidelines, cGMP, GAMP, ICH, ASTM E2500</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Experienced with manufacturing equipment software, which includes Allen Bradley PLCs, programmable HMIs, vision inspection systems, Siemens PLCs, and ELAU Motion PLCs is a plus</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be willing and able to work flexible hours, nights and weekends, in support of manufacturing production.</span></p> Sep 3rd, 2019 12:40PM Sep 3rd, 2019 12:40PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 24th, 2019 12:00AM Validation Engineer Open Process Development Full-Time Fremont California USA Apr 23rd, 2019 12:00AM <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Purpose of Position &amp; Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b></p> <p>Zosano Pharma has an exciting opportunity for a Validation Engineer II position responsible for process and equipment validation to support the commercialization of a novel microneedle medical product.<span>  </span>The Validation Engineer will be responsible for activities related to validating the equipment and process for a new commercial line and the associated support equipment.<span>  </span>Validation will include confirming that mechanical, electrical, and automation systems as well as process validation work meet the defined user requirements.<span>  </span>The candidate will be responsible for strategic planning, generating and approving validation protocols, overseeing and executing validation protocols and writing validation summary reports.<span>  </span>The candidate will also manage validation efforts with equipment manufacturers and commercial manufacturing organizations from FAT to Process Validation.<span>  </span>The position will require 20-30% travel.</p> <p><b><span style="font-family: 'Arial',sans-serif"> </span></b></p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b><b><span style="font-family: 'Arial',sans-serif"></span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop and manage the Validation Program at Zosano. </p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Strategic development and design of Validation Master Plans.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Draft or review qualification documents including IQ, OQ, PQ and PV.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Support Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT) for new equipment.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Execute, manage and support validation activities at CMO’s.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop strategies for Process Qualification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Review validation documents executed by CMO’s (Protocols, executed documents, and Reports).</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Assess validation deviations.</p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Position Requirements:</span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Bachelor’s Degree in Engineering (Mechanical or Electrical Preferred) with 5-8 years of experience in Biotechnology or Medical Devices with an emphasis on validation.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Have experience with writing and execution IQ/OQ/PQ’s and process validation activities.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of design control and Quality Risk Management principles.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of statistics used to support validation justification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of cGMP and Good Documentation Practices.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Possess good communication skills and be capable of managing complex programs and be knowledgeable of cGMP manufacturing and validation concepts.</p> Aug 24th, 2019 12:52PM Aug 24th, 2019 12:52PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 24th, 2019 12:00AM Equipment Engineer Open Equipment Engineering Full-Time Fremont California USA Jul 3rd, 2019 12:00AM <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">POSITION SUMMARY</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">We are looking for an experienced, motivated individual to provide equipment maintenance support and tooling design of complex automated custom manufacturing equipment. The position involves working with tooling mechanical systems electrical, pneumatic and vacuum systems in a clean room environment. He/she should have good analytical thinking skills and very detail oriented with excellent mechanical design aptitude.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">RESPONSIBILITIES</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to design, perform modifications on mechanical tooling to improve equipment performance.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He/she will manage vendors and take ownership of the project from concept to final implementation.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with Process and Manufacturing engineering and other cross functional groups to improve equipment reliability and minimize equipment downtime.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He /she must be able to understand and work with control automation for equipment upgrade and repairs.</span></p> <p><span style="font-size: 12px;font-family: Helvetica, sans-serif">-</span><span style="font-size: 12px;font-family: Helvetica, sans-serif"> </span><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Perform root cause analysis and implement improvements using change control procedures.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with cross functional groups in developing equipment user requirement specifications.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Functions with other support department in during manufacturing operations.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Supervise contractors and vendors on equipment upgrades.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to work in a clean room environment.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Manage and mentor technicians to help improve technicians workmanship</span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></b></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">QUALIFICATIONS</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Minimum 8 years working as an equipment engineer in the biotechnology or pharmaceutical industry.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- BS in Mechanical/Electrical Engineering or equivalent</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Well experienced in tooling design using Solidworks or equivalent is a must.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- The ability to read and interpret electrical drawings is a plus.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Be a self-starter and willing to tackle difficult technical issues.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Sound knowledge of pharmaceutical industry standards and guidelines, cGMP, GAMP, ICH, ASTM E2500</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Experienced with manufacturing equipment software, which includes Allen Bradley PLCs, programmable HMIs, vision inspection systems, Siemens PLCs, and ELAU Motion PLCs is a plus</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be willing and able to work flexible hours, nights and weekends, in support of manufacturing production.</span></p> Aug 24th, 2019 12:52PM Aug 24th, 2019 12:52PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 26th, 2019 12:00AM Validation Engineer Open Process Development Full-Time Fremont California USA Apr 23rd, 2019 12:00AM <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Purpose of Position &amp; Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b></p> <p>Zosano Pharma has an exciting opportunity for a Validation Engineer II position responsible for process and equipment validation to support the commercialization of a novel microneedle medical product.<span>  </span>The Validation Engineer will be responsible for activities related to validating the equipment and process for a new commercial line and the associated support equipment.<span>  </span>Validation will include confirming that mechanical, electrical, and automation systems as well as process validation work meet the defined user requirements.<span>  </span>The candidate will be responsible for strategic planning, generating and approving validation protocols, overseeing and executing validation protocols and writing validation summary reports.<span>  </span>The candidate will also manage validation efforts with equipment manufacturers and commercial manufacturing organizations from FAT to Process Validation.<span>  </span>The position will require 20-30% travel.</p> <p><b><span style="font-family: 'Arial',sans-serif"> </span></b></p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Description of Duties</span></b><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">:</span></b><b><span style="font-family: 'Arial',sans-serif"></span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop and manage the Validation Program at Zosano. </p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Strategic development and design of Validation Master Plans.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Draft or review qualification documents including IQ, OQ, PQ and PV.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Support Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT) for new equipment.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Execute, manage and support validation activities at CMO’s.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Develop strategies for Process Qualification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Review validation documents executed by CMO’s (Protocols, executed documents, and Reports).</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Assess validation deviations.</p> <p><b><span style="font-size: 14.0pt;font-family: 'Arial',sans-serif">Position Requirements:</span></b></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Bachelor’s Degree in Engineering (Mechanical or Electrical Preferred) with 5-8 years of experience in Biotechnology or Medical Devices with an emphasis on validation.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Have experience with writing and execution IQ/OQ/PQ’s and process validation activities.<span>  </span></p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of design control and Quality Risk Management principles.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of statistics used to support validation justification.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Working knowledge of cGMP and Good Documentation Practices.</p> <p><span style="font-size: 13.0pt;font-family: 'Arial',sans-serif">• </span>Possess good communication skills and be capable of managing complex programs and be knowledgeable of cGMP manufacturing and validation concepts.</p> Aug 26th, 2019 12:36PM Aug 26th, 2019 12:36PM
nasdaq:zsan zosanopharma.bamboohr.com zosanopharma.bamboohr.com Aug 26th, 2019 12:00AM Equipment Engineer Open Equipment Engineering Full-Time Fremont California USA Jul 3rd, 2019 12:00AM <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">POSITION SUMMARY</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">We are looking for an experienced, motivated individual to provide equipment maintenance support and tooling design of complex automated custom manufacturing equipment. The position involves working with tooling mechanical systems electrical, pneumatic and vacuum systems in a clean room environment. He/she should have good analytical thinking skills and very detail oriented with excellent mechanical design aptitude.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">RESPONSIBILITIES</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to design, perform modifications on mechanical tooling to improve equipment performance.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He/she will manage vendors and take ownership of the project from concept to final implementation.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with Process and Manufacturing engineering and other cross functional groups to improve equipment reliability and minimize equipment downtime.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- He /she must be able to understand and work with control automation for equipment upgrade and repairs.</span></p> <p><span style="font-size: 12px;font-family: Helvetica, sans-serif">-</span><span style="font-size: 12px;font-family: Helvetica, sans-serif"> </span><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Perform root cause analysis and implement improvements using change control procedures.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Participate in equipment capital projects planning and installation, testing, and qualifications of new and existing system.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Work with cross functional groups in developing equipment user requirement specifications.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Functions with other support department in during manufacturing operations.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Supervise contractors and vendors on equipment upgrades.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be able to work in a clean room environment.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Manage and mentor technicians to help improve technicians workmanship</span></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif"> </span></b></p> <p><b><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">QUALIFICATIONS</span></b></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Minimum 8 years working as an equipment engineer in the biotechnology or pharmaceutical industry.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- BS in Mechanical/Electrical Engineering or equivalent</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Well experienced in tooling design using Solidworks or equivalent is a must.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- The ability to read and interpret electrical drawings is a plus.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Be a self-starter and willing to tackle difficult technical issues.</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Sound knowledge of pharmaceutical industry standards and guidelines, cGMP, GAMP, ICH, ASTM E2500</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Experienced with manufacturing equipment software, which includes Allen Bradley PLCs, programmable HMIs, vision inspection systems, Siemens PLCs, and ELAU Motion PLCs is a plus</span></p> <p><span style="color: black;font-size: 9.0pt;font-family: 'Helvetica',sans-serif">- Must be willing and able to work flexible hours, nights and weekends, in support of manufacturing production.</span></p> Aug 26th, 2019 12:36PM Aug 26th, 2019 12:36PM

Request a demo to view additional historical data, and much more.

Make fast
queries

No longer rely on engineers to access data; build and share queries with intuitive tools, and derive insights in real time.

Bookmark queries with your team

Save and share custom queries using a private bookmarking feature, accessible to your whole team.

Be first to know with alerts

Scan data points across millions of companies and receive emails when relevant metrics cross critical thresholds.

Visualize data for quick insights

Create custom keyword-based word clouds, charts, and advanced visualizations to quickly analyze the data.

Map competitor locations

Analyze competitor presence and growth over time by overlaying store locations with the Nearby Competitor feature.