GMP Operational Quality Senior Manager

BioPharma Consulting JAD Group; Boston (MA); On-site; USD 140,000 - 190,000; Full time

Job summary

BioPharma Consulting JAD Group seeks an experienced GMP Operational Quality Senior Manager in Boston to drive QA/compliance for biologics and devices. You will lead complex projects, ensure GMP disposition, and coordinate with CMOs and internal teams to sustain compliant solutions.

The ideal candidate brings deep cGMP knowledge, risk management, RCA and CAPA leadership, and hands-on experience with QDocs/TrackWise/Veeva. This 1-year contract offers impactful quality-system improvements.

Qualifications

• In-depth knowledge of cGMPs in a biologics + devices pharmaceutical setting and global GMP requirements.
• Experience managing complex projects with CMOs and continuous improvement within stated objectives and timelines.
• Experience identifying, assessing and mitigating potential risks utilizing quality risk management best practices.
• Experience leading event investigations, RCA, and CAPA.
• Experience with electronic document management systems (e.g., QDocs, TrackWise, Veeva).

Responsibilities

• Collaborate with internally and external business partners to resolve complex quality issues to ensure compliant solutions
• Participates in cross-functional teams as an experienced Quality technical resource
• Drafts and enforces Quality Agreements between CMOs/Suppliers and Vertex, as needed
• Assists Change Control owners with ensuring compliance to change procedure requirements
• Initiates and assesses change controls
• Conducts quality investigations /deviations and reviews corrective action plans for adequacy and compliance. This includes root cause analysis and product impact assessments for investigations resulting from deviations and OOS.
• Ensures appropriate CAPA actions are identified and addressed.
• Approves investigations/CAPAs.
• Performs review and approval of master and executed batch records to support drug substance (DS), drug product (DP) and finished goods (FG) disposition activities
• Provides tactics to address compliance gaps or recommends enhancements to cross-functional quality systems
• Conducts GMP document review, including procedures, work instructions, specifications, methods, protocols, and method reports
• Identify and communicate risks and assist with risk mitigation plans as necessary
• Supports internal audit or external audit programs

Skills

GMP compliance

QA/QC

Risk management

Root cause analysis

CAPA

Cross-functional collaboration

Education

Bachelor's degree in a scientific or allied health field

Tools

QDocs

TrackWise

Veeva

Job description

The GMP Operational Quality Senior Manager is an advanced technical resource in the principles and application of quality assurance and compliance. This role coordinates or executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products and devices.

Responsibilities:

• Collaborate with internally and external business partners to resolve complex quality issues to ensure compliant solutions
• Participates in cross-functional teams as an experienced Quality technical resource
• Drafts and enforces Quality Agreements between CMOs/Suppliers and Vertex, as needed
• Assists Change Control owners with ensuring compliance to change procedure requirements
• Initiates and assesses change controls
• Conducts quality investigations /deviations and reviews corrective action plans for adequacy and compliance. This includes root cause analysis and product impact assessments for investigations resulting from deviations and OOS.
• Ensures appropriate CAPA actions are identified and addressed.
• Approves investigations/CAPAs.
• Performs review and approval of master and executed batch records to support drug substance (DS), drug product (DP) and finished goods (FG) disposition activities
• Provides tactics to address compliance gaps or recommends enhancements to cross-functional quality systems
• Conducts GMP document review, including procedures, work instructions, specifications, methods, protocols, and method reports
• Identify and communicate risks and assist with risk mitigation plans as necessary
• Supports internal audit or external audit programs

• Bachelor's degree in a scientific or allied health field.
• 8 years of experience.

Must have:

• In- depth knowledge of both the conceptual and practical application of cGMPs in a biologics + devices pharmaceutical setting; in-depth knowledge of global GMP requirements in support of GMP Drug Product manufacturing
• Experience managing complex projects with contract manufacturing organizations and continuous improvement within stated objectives and timelines
• Experience in identifying, assessing and mitigating potential risks utilizing quality risk management best practices
• Experience successfully leading event investigations, Root Cause Analysis (RCA), and CAPA
• Experience with electronic document management systems (e.g., QDocs, Trackwise, Veeva)

1 year contract with possible extension

Administrative shift