Quality Assurance Officer Job in Mediwell
- mgm eye institute
- 3 to 7 Yrs
- Baddi
- 10 months ago
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Job Description
- Job Responsibilities: Ensure compliance with GMP, GDP, GLP, and regulatory guidelines. Prepare, review, and update Standard Operating Procedures (SOPs). Maintain and verify Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Manage deviations, CAPA, change controls, and OOS investigations. Conduct internal audits and assist in regulatory inspections (USFDA, WHO-GMP, MHRA, etc.). Perform supplier and vendor audits to ensure material quality standards. Participate in process validation, cleaning validation, and equipment qualification (IQ, OQ, PQ). Ensure water, air, and environmental monitoring in production areas. Coordinate with the QC department for testing and material release. Investigate customer complaints and implement corrective actions. Support product recall procedures and compliance with regulatory requirements. Conduct GMP and quality training for production and warehouse staff. Identify and implement process improvements for quality compliance. Ensure proper storage conditions, temperature monitoring, and good distribution practices (GDP). Work Environment: Office-based role with frequent interaction with production, QC, and warehouse teams. Requires on-site presence in manufacturing areas for process validation and audits Involves regulatory inspections, documentation work, and occasional extended hours during audits or compliance reporting. Job Types: Full-time, Permanent Work Location: In person,
Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: Not SpecifiedFunctional Area: Not SpecifiedRole/Responsibilies: Quality Assurance Officer Job in MediwellContact Details:
Company: Mediwell BiotechLocation(s): Baddi+ View Contact
Keyskills: GMP GLP SOPs deviations CAPA supplier audits process validation cleaning validation equipment qualification air monitoring environmental monitoring customer complaints internal audits
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