Quality Control Manager
McGuff Companies
Newport Beach, CA (In Person)
Full-Time
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Job Description
Type:
full-timeJob Description:
Organization Overview MPI is an FDA-reviewed manufacturer of NDA and ANDA products, operating as:- A sterile fill/finish pharmaceutical manufacturer
A CMO/CDMO
partner- A registered 503B outsourcing facility MPI operates two facilities totaling approximately 100,000 square feet of manufacturing space and continues to expand sterile production capacity.
- Production quality monitoring
- Incoming materials oversight and disposition
- Analytical chemistry laboratory operations
- Microbiology laboratory operations
- Enterprise document control administration (MasterControl or equivalent) This leader will ensure inspection readiness, regulatory compliance, scientific rigor, and robust data integrity governance across the organization.
- Lead and develop multidisciplinary QC teams
- Oversee incoming material receipt, quarantine, sampling coordination, testing, and release
- Direct analytical and microbiological testing in support of batch release
- Review and approve laboratory investigations (OOS, OOT, deviations, CAPA, change controls)
- Administer and optimize the enterprise EDMS (MasterControl preferred)
- Ensure compliance with 21 CFR Parts 210, 211, and 11
- Maintain full ALCOA+ data integrity compliance
- Serve as QC SME during FDA inspections and client audits
- Drive process improvement initiatives aligned with growth objectives This is not a maintenance role - it is a leadership position intended to strengthen systems, elevate performance standards, and support continued sterile manufacturing expansion.
- Bachelor's degree in chemistry, microbiology, pharmacy, or related discipline (advanced degree preferred)
- 7+ years of progressive experience in sterile drug manufacturing within FDA-regulated cGMP environments
- Demonstrated leadership over analytical chemistry and/or microbiology laboratories
- Direct experience with enterprise EDMS platforms (MasterControl strongly preferred)
- Strong working knowledge of 21 CFR Parts 210, 211, and 11
- Proven track record supporting FDA inspections
- Established expertise in data integrity and ALCOA+ principles Highly Valued Experience
- Sterile fill/finish or aseptic processing environments
- 503B outsourcing operations
- CMO/CDMO or client-facing manufacturing
- LIMS integration with EDMS platforms Compensation & Benefits MPI offers a competitive compensation package commensurate with experience and leadership scope, including:
- Competitive base salary (structured for senior-level talent)
- Performance-based incentive opportunity
- Comprehensive medical, dental, and vision coverage
- 401(k) with company contribution
- Paid time off and company holidays Compensation will align with the candidate's regulatory experience, inspection history, and leadership background. Why This Role Appeals to Leaders from Larger Organizations
- Greater operational autonomy
- Direct executive visibility
- Broader systems ownership (materials, labs, document control)
- Meaningful impact on inspection readiness and quality infrastructure
- Growth trajectory within an expanding sterile manufacturing operation This opportunity is well-suited for a quality professional seeking to transition from a highly matrixed corporate structure into a leadership role with tangible influence and accountability.
MPI@mcguff.com
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