Pharmaceutical Operations Manager
5 days ago
This is an excellent opportunity for a motivated individual to join our team as a Quality Specialist.
Responsibilities:
- Administer event management systems, ensuring compliance with regulatory requirements.
- Design and approve batch records.
- Coordinate site change control systems, minimizing disruptions to operations.
- Develop and implement validation protocols and reports.
- Collaborate with cross-functional teams to review and approve SOPs.
- Prepare for regulatory and customer GMP inspections, ensuring a smooth process.
Requirements
To be successful in this role, you will need a degree in a scientific/technical field and relevant experience in quality assurance within the pharmaceutical or biotech industry.
Familiarity with FDA/EMEA regulations and the ability to apply GMP principles to daily tasks is essential.
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