whose primary responsibility will be the issuance and reconciliation of Batch Production Records (BPRs) in compliance with GMP and company SOPs. This role plays a critical part in ensuring documentation integrity and production readiness in a regulated manufacturing environment.
Responsibilities
Prepare and issue Master Batch Records (MBRs) and Batch Production Records (BPRs) to Production in accordance with approved templates and schedules.
Ensure all components, packaging materials, and documents are reconciled and accounted for before issuance.
Verify that issued BPRs are complete, accurate, and compliant with regulatory and internal requirements.
Coordinate with Production Planning, Warehousing, and Manufacturing to ensure timely issuance of batch records.
Maintain controlled copies of all issued documents and ensure proper archiving of unused or voided records.
Track issuance logs and maintain records for traceability and audits.
Support batch record revisions and assist in implementing changes through the change control process.
Assist in training staff on documentation practices related to batch records.
Participate in internal audits and support external inspections as required.
Skills
Diploma or Bachelor's degree in Life Sciences, Chemistry, or related field.
1-3 years of experience in a QA role within a GMP-regulated environment (nutraceuticals, pharmaceuticals, or food manufacturing preferred).
Strong understanding of Good Manufacturing Practices (GMP) and document control principles.
Excellent attention to detail and organizational skills.
Proficient in Microsoft Office (Word, Excel, Outlook).
Ability to work independently and collaborate cross-functionally.
Join us as a Quality Assurance Associate where your expertise will contribute significantly to maintaining our commitment to excellence in product quality.
Job Types: Full-time, Permanent
Pay: $23.00-$25.00 per hour
Benefits:
Dental care
Extended health care
Schedule:
8 hour shift
Monday to Friday
Work Location: In person
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