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Adept Source
Redwood City
Title: Director, Quality Assurance, Pharma Location: Redwood City, CA (hybrid model) Type of role: FTE, Full time Salary: plus bonus and equity Our start-up Biotech client is seeking an Associate Director / Director Quality Assurance to join the...
Job Source: Adept SourceInnova Solutions Inc.
San Mateo, CA, United States
Associate Director* - Biotech/R&D/Science Job ID: 973330 San Mateo , California Job Type: Contract Added - 06/07/24 Job Description Innova Solutions is immediately hiring for a Associate Director Position type: Full time Contract. Duration: 12 months Location: Foster City, CA (Hybrid) As a Associate Director , yo
Job Source: Innova Solutions Inc.Cornerstone Search Group
San Francisco, CA, United States
Head of Device Engineering | Next Gen Bioengineering Start-Up | Report to Founder/CEO | South San Francisco-based | RETAINED SEARCH SUMMARY: Cornerstone Search Group has been retained by a next-generation engineering company, driven by a small team of exceptional engineers and chemists focused on building solid-state biosensors using principles tha
Job Source: Cornerstone Search GroupCornerstone Search Group
San Francisco, CA, United States
San Francisco, CA, United States of America Head of Device Engineering | Next Gen Bioengineering Start-Up | Report to Founder/CEO | South San Francisco-based | RETAINED SEARCH Cornerstone Search Group has been retained by a next-generation engineering company, driven by a small team of exceptional engineers and chemists focused on building solid-st
Job Source: Cornerstone Search GroupComforcehealth
San Mateo, CA, United States
Associate Director* - Biotech/R&D/Science Job ID: 973330 San Mateo , California Job Type: Contract Added - 06/07/24 Job Description Innova Solutions is immediately hiring for a Associate Director Position type: Full time Contract. Duration: 12 months Location: Foster City, CA (Hybrid) As a Associate Director , yo
Job Source: ComforcehealthMeet
Redwood City, CA, United States
Associate Director, Clinical Program Management Hybrid Role - Redwood City, CA Meet has partnered with an exciting biotech that is focused in the chronic illness space! Theyre very well-funded and have a strong mid-stage pipeline (multiple P1/2 trials). They are seeking an Associate Director of Clinical Program Management to join their team! Key Re
Job Source: MeetMeet Recruitment Limited
Redwood City, CA, United States
Associate Director, Clinical Program Management *Hybrid Role - Redwood City, CA* Meet has partnered with an exciting biotech that is focused in the chronic illness space! They're very well-funded and have a strong mid-stage pipeline (multiple P1/2 trials). They are seeking an Associate Director of Clinical Program Management to join their team! Key
Job Source: Meet Recruitment LimitedScorpion Therapeutics
San Francisco, CA, United States
Scorpion is a pioneering clinical-stage oncology company redefining the frontier of precision medicine to deliver optimized and transformational therapies for larger populations of patients with cancer. Scorpion has built a proprietary and fully integrated platform of the most advanced technologies across cancer biology, medicinal chemistry, and da
Job Source: Scorpion TherapeuticsFoster City, CA, United States
No H1B and/or C2C please!!
Required Industry Experience: Pharma/Biotech
Job Title: Associate Director (Business Partner - R&D Quality)
W2 Contract & Hybrid role
Work Location: Foster City, CA
One of our leading Pharmaceutical client is looking for an Associate Director (Business Partner - R&D Quality), act as a R&D Quality Business Partner to client’s R&D functions or vendors supporting Client R&D. will provide strategic, expert advice and consultation on R&D quality, risk and continuous improvement with impact across cross-functional Good Clinical Practices (GCP).
Required Experience:
Significant experience advising business functions in the Biopharma Industry on GCP quality and compliance requirement s, evolving regulations, risk minimization and mitigation, and continuous improvement.
Previous GCP quality experience at a Sponsor or CRO .
Experience working across a broad spectrum of quality and/or compliance activities , including authoring and reviewing SOPs, conducting internal auditing, supporting regulatory inspections, developing and managing CAPAs and deviations, and training others on quality and/or compliance requirements.
Responsibilities:
You will educate assigned groups on Client quality policy and procedural standards, GCP regulations and other requirements.
Responsible for providing expert advice on GCP risk minimization and mitigation.
Helping the business understand potential impacts of risk and alternatives to best address risk.
You will participate in Quality forums, cross-functional teams and/or projects.
Act as the central point of contact for QMS-related communications to assigned groups.
Collaborate with other R&D Quality groups to ensure just-in-time support and resources to assigned groups, including - data, reporting, training, audit, inspection, risk assessment and deviation/ CAPA management support.
If you are a right fit then please apply quick!!
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Email Alert for Quality Director (R&D) - Pharma/Biotech - HYBRID!! jobs in Foster City, CA, United States
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