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Associate Director/Director, External Quality Control
3 months ago
Our clinical stage pharmaceutical client HQ in Boston, MA is growing and looking to add an
Associate Director/Director of External QC (Analytical) (REMOTE).
This role will provide oversight of all external cGMP analytical testing. They will work in partnership with Technical Operations, Quality Assurance and external laboratories to assure that QC analytical testing is performed in compliance with applicable regulations, company quality standards and current industry practices. The responsibilities also include providing leadership for all QC testing to support vaccine manufacturing, identifying and mitigating product quality, safety, and regulatory compliance risks, as well as working to establish internal Quality Control processes.
Oversees the overall Quality Control analytical testing strategy
Ensures QC testing at external GMP laboratories meet applicable regulatory requirements
Ensures proper investigation into the root cause of product and/or process failures
Leads OOS investigations, deviations, CAPA and change controls
Provides support for all testing, tasks, and documentation in support of Validation Studies including Process Validation, Media Fills, Method Validation, and development of analytical methods
Drafts and reviews appropriate sections of Regulatory submissions
Interacts with agents from Regulatory agencies and participates in Audits and Inspections
Supports the preparation of dossiers and data packages for interactions between the Company and Regulatory agencies
Writes and proposes revisions to Standard Operating Procedures, Analytical Methods, Technical Reports, and related Forms.
Reviews and assesses proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate
Liaises with other departments to ensure business continuity including Quality, Manufacturing, MS&T, Supply Chain, and Regulatory
Requirements:
Minimum of a bachelor’s degree in biological sciences; advanced degree in biological sciences desirable
A minimum of 8 years’ experience in a QC analytical testing laboratory
A minimum of 4 years’ experience in a management role
Experience with coordinating QC testing at external contract laboratories
Experience with aseptic manufacturing and biologics/vaccines
Expertise in microbiology, virology and environmental monitoring testing
Strong understanding of Quality Control testing requirements for pre-clinical, clinical, and commercial stage work.
Comprehensive knowledge of compliance with cGMP regulations
Highly skilled in root cause investigations, change control, and regulatory inspections
Able to handle multiple projects and exercise good judgment in prioritizing tasks
Excellent verbal, written and organization skills
Ability to establish and maintain good working relationships with other functions and levels within the company and with external groups and organizations (vendors, investigators, regulatory authorities, and other stakeholders)
Other:
Willingness to travel (20-25%) to various meetings or third-party sites, including overnight trips.
Some international travel may be required.
Location Remote-US East Coast preferred
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