Job Openings - Mersifarma

Quality Control Staff

Perform sampling, testing, and inspection of raw materials, packaging materials, intermediate products, bulk products, and finished products in accordance with approved procedures.
Ensure all quality control activities comply with Standard Operating Procedures (SOPs), product specifications, and Good Manufacturing Practices (GMP/cGMP).
Conduct physical, chemical, and/or microbiological analyses (as applicable) using validated analytical methods.
Operate, maintain, and verify laboratory equipment to ensure proper functionality, and report any abnormalities or equipment issues.
Record and document testing results accurately, completely, and in a timely manner in accordance with Good Documentation Practices (GDP).
Identify, report, and support investigations related to Out of Specification (OOS) results, deviations, and other quality-related issues.
Collaborate with the Production, Quality Assurance, and other cross-functional teams to resolve quality concerns and maintain product quality standards.
Ensure laboratory activities comply with GMP/cGMP requirements, regulatory standards, and the company's Quality Management System.
Participate in analytical method validation, method transfer, equipment qualification, calibration, and continuous quality improvement initiatives, as required.
Maintain laboratory cleanliness, safety, and organization in compliance with EHS (Environment, Health & Safety) policies and company regulations.

Bachelor's Degree in Chemistry or a Professional Pharmacy Degree (Licensed Pharmacist/Apothecary).
Minimum 1 year of experience in Quality Control within the pharmaceutical industry is preferred; fresh graduates are welcome to apply.
Strong understanding of Good Manufacturing Practices (GMP/cGMP) and Good Documentation Practices (GDP).
Familiarity with laboratory analytical techniques and instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Tester, or other analytical equipment is an advantage.
Proficient in Microsoft Office applications, particularly Microsoft Excel and Word.
Strong analytical thinking, attention to detail, and problem-solving skills.
Excellent communication and teamwork abilities.
Willing to work in shifts when required.
Demonstrates high integrity and a strong commitment to quality, compliance, and regulatory standards within the pharmaceutical industry.