FULLTIME
Specialist- QA (Pharma, Biological Products and Medical Devices)

Celogen Pharma
Not specified · onsite · Posted 12d ago
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Undisclosed3–7 yrsfulltimeNot specified
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Section · 01
About this role
- Develop and implement comprehensive quality assurance plans to ensure compliance with regulatory requirements.
- Conduct regular audits and inspections to identify areas for improvement in quality management systems.
- Collaborate with cross-functional teams to resolve quality-related issues and improve overall product quality.
- Analyze data and trends to identify opportunities for process improvements and implement changes as needed.
- Ensure all quality control processes are documented and maintained according to regulatory standards.
- Provide training and guidance to employees on quality management systems and procedures.
Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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Section · 02
Skills
AuditingProduct qualityISO 9001biologyauditsChemistryBiotechnologyQuality AssuranceQuality ControlMedical DevicescompliancePharmaPharmaceuticalquality managementCommunication And Interpersonal Skills