
Analytical Expert
6 days ago
Join a pharmaceutical manufacturing and biotechnology research company as a Senior Analytical Specialist. We are seeking an experienced professional to support the manufacture and release of pharmaceutical raw materials, intermediates, and products.
">- We are looking for a highly skilled individual with expertise in method qualification and validation strategies, ensuring timely delivery of projects. The successful candidate will contribute to building and maintaining QC lab cGMP systems, delivering analytical solutions to clients through their knowledge of pharmacopoeia and regulations.
Key responsibilities include:
Key Responsibilities- Support new equipment qualification, lab computerized systems, and chemistry lab setup
- Perform transfer/verification/validation of laboratory procedures within the team
- Prepare technical documentation (protocols, analytical write-ups, SOPs, specifications, reports)
- Conduct cGMP-compliant analysis of incoming goods, intermediates, and finished products
- Review analytical and laboratory data for accuracy, completeness, and procedural compliance
- Stay updated with new pharmacopoeia and regulations; identify and close compliance gaps
- Perform investigation write-ups and deviations, ensuring timely closure under QMS procedures
- Manage QC chemical, reference standards, and consumable stock levels
- Maintain personal training records and assist in training team members
- Communicate effectively locally and internationally and engage in problem solving
- Participate in Practical Process Improvement (PPI) and continuous improvement initiatives
- Promote a Quality Culture and the company's 4i values
- Ensure compliance with cGMP, HSE, and 5S in all areas of work
- Undertake ad-hoc activities as required by the business
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