| Job alert | Jobs 31 - 40 of 291 |
Validation Engineer
VTI Life Sciences
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Fremont, CA, 94555
... Desired Skills and Experience: 3+ Years GMP experience qualifying QC Instruments and manufacturing equipment and validating associated software Bachelors Degree in a related field. Prior experience in the biotech or pharmaceutical industry Ambitious ... - May 15
Research Development Laboratory Technician
Kelly Science, Engineering, Technology & Telecom
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Sunnyvale, CA, 94087
... Experience in a CAP/ CLIA/ GMP/ ISO regulated environment. - May 19
Scientist II
Joulé
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Pleasanton, CA, 94588
... sequencing library preparation •Follow protocols precisely, and with extreme care under design control regulations and GMP laboratory conditions •Be comfortable with and able to adapt to regular protocol changes as protocols are being developed ... - May 17
Manufacturing Engineer II
QAPEL MEDICAL INC
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Fremont, CA, 94538
... Knowledge of international regulations, standards, and guidelines (current MOD, ISO 13485, CMDR, J-GMP, Risk Management, Usability) Effective/ Excellent verbal and written communications Project management experience and detailed project planning is ... - May 10
Logistics Associate
Fladger Associates
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Fremont, CA
... Consults internal customers in areas of Inventory Management Experience: High School diploma or GED 2 years GMP warehouse experience Required: Ability to learn and apply all relevant WIs, SOPs, and other regulatory requirements. Ability to read ... - May 22
Maintenance Manager
Jobot
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San Leandro, CA, 94579
... Implement and uphold Good Manufacturing Practices (GMP) and Lean Manufacturing principles to improve efficiency and productivity. Train and supervise maintenance department staff. Coordinate with vendors and suppliers as needed. Qualifications: A ... - Apr 23
Documentation Specialist III Hybrid Remote
Kaztronix
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Fremont, CA
... Skills: Expert knowledge in AutoCAD and design Site facility knowledge Experience in GMP manufacturing facilities An ability to read, understand and modify Engineering drawings, including P&ID s Required Skills: BIOPHARMACEUTICAL DOCUMENT MANAGEMENT ... - May 10
Scientist II (Onsite, Pleasanton, CA) (DNA, Library, NGS)
Maxis Clinical Sciences
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Pleasanton, CA, 94566
... •Follow protocols precisely, and with extreme care under design control regulations and GMP laboratory conditions. •Be comfortable with and able to adapt to regular protocol changes as protocols are being developed and improved. •Regularly work with ... - May 18
Sr. Director, Regulatory Affairs Strategy
Taiho Oncology
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Pleasanton, CA, 94566
... Together with Quality Assurance, manage regulatory compliance for sponsor activities for drug supply, documentation, GMP and GCP requirements. Prepare project and/or status reports. This position requires travel. Education/Certification Requirements ... - May 23
Scientist II
Joulé
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Pleasanton, CA, 94588
... sequencing library preparation •Follow protocols precisely, and with extreme care under design control regulations and GMP laboratory conditions •Be comfortable with and able to adapt to regular protocol changes as protocols are being developed ... - May 17