- job summary: The QC Critical Reagents Analyst is responsible for maintaining the Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks ajob summary: The QC Critical Reagents Analyst is responsible for maintaining the Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks a
- job summary: One of the world's leading companies in the fields of health and nutrition, delivering breakthrough innovations in healthcare and agriculture. Contribute to a world in which diseases are not only treated but effectively prevented or cured, in which people can take better care of their own health needs, Join this team which is Guided by the purpose "Science for a better life" This role requires employees to be fully vaccinated against COVID-19job summary: One of the world's leading companies in the fields of health and nutrition, delivering breakthrough innovations in healthcare and agriculture. Contribute to a world in which diseases are not only treated but effectively prevented or cured, in which people can take better care of their own health needs, Join this team which is Guided by the purpose "Science for a better life" This role requires employees to be fully vaccinated against COVID-19
- job summary: Regulatory Medical Writer - Protocols/Immunology We are seeking an experienced Regulatory Medical Writer to support a small biotech on a part-time contract basis. This role will focus on developing and revising protocols and amendments for three Phase III immunology studies. Contract: Through 12/31/25 Hours: PT~10-20 hours per week Rate: $110-120 per hour w2 only Therapeutic Area: Immunology Focus: Phase III protocols & amendments locjob summary: Regulatory Medical Writer - Protocols/Immunology We are seeking an experienced Regulatory Medical Writer to support a small biotech on a part-time contract basis. This role will focus on developing and revising protocols and amendments for three Phase III immunology studies. Contract: Through 12/31/25 Hours: PT~10-20 hours per week Rate: $110-120 per hour w2 only Therapeutic Area: Immunology Focus: Phase III protocols & amendments loc
- job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversightjob summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight
- job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncojob summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
- job summary: Immediate openings for 15-20+ Bioprocess / Biomanufacturing Associates with a leading, global company focused on gene therapy innovation, located in the North Bay region of the Bay area. Shifts: All shifts/days available: Manufacturing operations are 24/7 5 x 8 hour shift4 x 10 hour shift3 x 12 and 4x12 hour shifts Shift pay rates are as follows: 1st shift: 7am-3pm2nd shift: 3pm-11pm (10% shift differential added to the pay rate)3rd sjob summary: Immediate openings for 15-20+ Bioprocess / Biomanufacturing Associates with a leading, global company focused on gene therapy innovation, located in the North Bay region of the Bay area. Shifts: All shifts/days available: Manufacturing operations are 24/7 5 x 8 hour shift4 x 10 hour shift3 x 12 and 4x12 hour shifts Shift pay rates are as follows: 1st shift: 7am-3pm2nd shift: 3pm-11pm (10% shift differential added to the pay rate)3rd s
