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Brandon Bejuandem

@brandonbejuandem

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I lead cGMP document control and lot release operations for regulated life sciences manufacturing.

United States

Message

At MilliporeSigma, I lead document control and lot release activities for regulated manufacturing, reviewing batch records, Certificates of Analysis, test results, and final release documentation to support compliant product disposition.

I've progressed from Quality Assurance Technician to Quality Compliance Supervisor and Quality Assurance Supervisor, leading teams, supporting FDA and ISO audit readiness, managing deviations and change control, and improving release workflows through KPI and trend analysis.

Experience

Work history, roles, and key accomplishments

Current

Quality Assurance Supervisor

Current

MilliporeSigma

Jun 2022 - Present (4 years 3 months)

Lead document control and lot release activities for regulated manufacturing operations, ensuring controlled records and product disposition decisions meet internal procedures, specifications, and cGMP expectations. Review and approve batch records, Certificates of Analysis, test results, and final release documentation for raw materials, intermediates, and finished products.

Document Control Lot Release Batch Record Review GMP Quality Systems Data Integrity Deviation Management CAPA KPI Analysis Cross functional Leadership

Quality Compliance Supervisor

MilliporeSigma

Aug 2021 - Jun 2022 (10 months)

Supervised the Document Control team responsible for SOPs, forms, specifications, policies, and work instructions across the document lifecycle. Ensured controlled documents were created, reviewed, approved, issued, revised, and archived in accordance with internal procedures and applicable FDA, ISO 13485, ISO 9001, and cGMP requirements.

Document Control SOP Management FDA Regulations ISO 13485 ISO 9001 GMP Change Control Audit Readiness Training and Compliance Continuous Improvement

Quality Assurance Technician

MilliporeSigma

Nov 2020 - Jul 2021 (8 months)

Maintained controlled SOPs, work instructions, forms, specifications, and policies, including revision tracking, approval routing, issuance, archival, and obsolescence. Supported TrackWise-based quality records and document workflows while maintaining accuracy, traceability, and compliance with established procedures.

Document Control Trackwise SOP Management GMP Quality Records Management Training CAPA Deviation Management