Job Description
Responsibilities
- Review deviations, investigations, and CAPA as part of daily functions, and ensure the integrity and traceability of all data generated and reported.
- Provide support to other departments such as Production, Quality Control, Validation, and Engineering.
- Develop and report quality metrics for deviations and other systems, as assigned.
- Assume additional responsibilities under the quality system program, as trained and assigned.
Qualifications
- Bachelor's degree in Science required (preferably in Microbiology, Chemistry, or Biology).
- Minimum 2–3 years of Quality Assurance experience in the biopharmaceutical or pharmaceutical manufacturing industry.
- Specialist-level expertise with advanced knowledge of quality systems (change control, deviations, investigations, root cause analysis, CAPA, and risk assessments).
- Demonstrated judgment, technical competence, and subject-matter ...