Bachelor's degree in science or chemical engineering
1-3 years qa/qc experience in pharmaceutical industry
Strong knowledge of gmp compliance regulations
The role involves reviewing and approving master batch records, cleaning records, and procedures to ensure strict compliance with set standards
Job Summary
The role involves reviewing and approving master batch records, cleaning records, and procedures to ensure strict compliance with set standards.
Candidates will handle product complaints, conduct thorough investigations, and implement effective Corrective and Preventive Actions (CAPAs) to prevent recurrence.
The position requires applying Six Sigma and lean principles to drive continuous improvement in quality operations and support regulatory inspections.
Matching Summary
Match Score: 85
The role involves reviewing and approving master batch records, cleaning records, and procedures to ensure strict compliance with set standards.
Skills & Requirements
Must-have
Bachelor's Degree in Science or Chemical Engineering
1-3 years QA/QC experience in pharmaceutical industry
Strong knowledge of GMP compliance regulations
Familiarity with ICH Q7a Guidelines and GDP
Experience with Six Sigma and lean principles
Nice-to-have
Proven track record of driving continuous improvement
Excellent attention to detail and problem-solving skills
Ability to work collaboratively in cross-functional teams
Key Requirements
Bachelor's Degree in Science, Chemical Engineering, or related field
1-3 years relevant experience in QA/QC within pharmaceutical industry
Strong knowledge of GMP compliance regulations and ICH Q7a Guidelines