7203 Quality Document Control Specialist

Onsite with Hybrid option after training The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various *** departments the documentation that is necessary to perform cGxP activities. Other responsibilities include auditing existing documentation, reporting document...

Description We're looking for a Document Control Specialist, working in Pharmaceuticals and Medical Products industry in 300 Bel Marin Keys Boulevard, Novato, California, United States. Receives, reviews, edits, formats, updates, and manages various documents within electronic document system. All work must be completed through workflows established in...

QC Analyst Location: Novato, CA. (On-Site) 12-month assignment (potential to extend or convert) Pay Rate: $28/hr. Schedule: Morning Shift Our pharmaceutical industry client, a global leader in therapeutics for rare and life-threatening genetic diseases, is looking for a QC Analyst that will primarily focus on the centralized program management of reference...

QC Analyst Location: Novato, CA. (On-Site) 12-month assignment (potential to extend or convert) Pay Rate: $28/hr. Schedule: Morning Shift Our pharmaceutical industry client, a global leader in therapeutics for rare and life-threatening genetic diseases, is looking for a QC Analyst that will primarily focus on the centralized program management of reference...

The QC Microbiology department is responsible for performing environmental monitoring and microbiological test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics. RESPONSIBILITIESSchedule (4 days/10 hours):Sunday...

Quality Technical Manager Job ID: 24-01475 Technical Manager, Quality Systems Description * is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom...

Description Client's is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to...

Quality Systems Technical Manager Location: Novato, CA 9-month assignment (potential to extend) Pay Rate: $50-60/hour Our leading pharmaceutical client is looking for a global leader in developing therapeutics for patients with serious and life-threatening rare genetic diseases. Summary Description: The Quality Systems Technical Manager plays a vital role in...

Job DescriptionJob DescriptionBiotechnology company is hiring a Quality Technical Manager to ensure the company's Quality Systems, such as Documentation, Deviation, CAPA, Change Control, Self-Inspection and Risk Management are consistently administered and followed. ResponsibilitiesParticipate in inspection readiness, regulatory inspection support and...

Innova Solutions is immediately hiring for Specialist, QA OperationsPosition type: Full time ContractDuration: 13+ Months Location: Novato, CAAs a Specialist, QA Operations you will: DescriptionPrimary Responsibilities: Provide quality oversight of one or more portions of operations including, but not limited to; Direct observation of manufacturing operation...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

Job Details Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Description Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

DescriptionWho We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and...

Who We Are BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...