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Role Overview:
We are seeking a Quality Analyst to ensure product quality throughout the manufacturing process in compliance with GMP and SOPs. This role involves in-process testing equipment and environment checks inspection of samples documentation and reporting.
Key Responsibilities:
Perform in-process testing (weight thickness hardness friability etc.) per batch instructions
Conduct room and equipment checks before each manufacturing stage
Execute AQL sampling and inspections as required
Inspect samples and maintain documentation for QC lab
Verify equipment functionality and monitor environmental conditions
Maintain records perform daily balance verifications and ensure isolation of rejected materials
Identify and report non-conformances or discrepancies
Support batch record review and assist with customer complaint reports
Qualifications:
Bachelors degree in Chemistry Pharmaceutical Sciences or related field preferred
Minimum 3 years of quality assurance experience in a GMP pharmaceutical manufacturing environment
Experience with MDI or parenteral products preferred
Strong knowledge of cGMP attention to detail and organizational skills
Proficiency with MS Office and ability to work independently and in teams
Full-time