
QC Chemist II
23 hours ago
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
This role will be responsible for method transfer/verification/validation, and project work supporting the manufacture and release of pharmaceutical raw materials, intermediates, and products. The role contributes to building and maintaining QC lab cGMP systems, delivering analytical solutions to clients through expertise in method qualification and validation strategies, ensuring timely delivery of projects.
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
Minimum Requirements / Qualifications:
Degree in Chemistry or closely related scientific discipline
At least 3 years relevant industry experience
Knowledge and application of GMP regulations and international guidelines
Ability to work independently and meet critical timelines
Effective communication skills at all levels
Excellent attention to detail
Excellent organisational skills
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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