Senior QC Scientist

Main Responsibilities: • Manage QC test samples, including in-process, release, environmental monitoring, drug substance, and excipient samples. • Oversee stability sample management to ensure proper storage, tracking, and testing schedules. • Maintain regulatory retention samples and reference samples in compliance with applicable requirements. • Ensure accurate documentation and traceability of all sample management activities. • Support laboratory operations by coordinating sample receipt, storage, distribution, and disposal. • Ensure all QC activities are conducted in compliance with cGMP, data integrity, and EHS requirements. About You: • Bachelor's Degree or higher in Pharmacy, Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline. • 3–5 years of experience in the biotechnology, biopharmaceutical, or pharmaceutical industry. • Strong understanding of the drug development lifecycle and quality control processes. • Solid knowledge of cGMP requirements and a strong quality and compliance mindset. • Familiarity with global regulatory requirements and guidelines, including FDA, EMA, NMPA, ICH, WHO, USP, Eur. Ph., and ChP. • Good understanding of regulatory submissions, including IND/IMPD, NDA, and ANDA filings. • Strong organizational, documentation, and communication skills. • Ability to work effectively in a fast-paced and regulated environment. Contract Duration: 12 months