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Last Name*

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First Name*

Last Name*

Email*

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Job type: Permanent

Discipline: Senior/Director & VP, Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP)

Location: United States

VP Quality - Permanent - Onsite

Proclinical Staffing is seeking a VP Quality to join a cutting-edge biotech company. This is a permanent role located in Mountain View, CA.

Skills & Requirements:

Extensive experience with PMA submissions for class 3 combination devices.
Proven track record in navigating the dynamic landscape of startup environments.
Demonstrated capability in assembling and leading a quality team from the ground up.
Proficiency in working with Vascular Devices.
Expertise in drug delivery.

The VP Quality will:

Drive the evolution of our Quality Management System (QMS) to meet global quality objectives and regulatory requirements.
Lead core quality system activities to uphold compliance with international medical device regulations and certifications.
Craft, refine, and uphold procedures, specifications, and standards for product quality control in adherence to ISO 13485, MDR, and 21 CFR 820.
Ensure adherence to FDA, ISO, and industry-specific standards, maintaining impeccable regulatory compliance.
Proactively identify and address quality risks, overseeing training, supplier management, and complaint processes.
Establish and implement robust quality control processes, orchestrating investigations and corrective actions as necessary.
Cultivate a high-performing quality team through strategic recruitment, comprehensive training, and ongoing mentorship.

Compensation:

$220,000 - $250,000 annually

If you are having difficulty in applying or if you have any questions, please contact Ollie Archer at (+1) 347-410-8645 or o.archer@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDCQA

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