Associate Scientist Biopharm

The main aim of the role is to carry out quality control testing of pharmaceutical and biopharmaceutical products to ensure compliance with predefined quality and safety standards.
Perform routine and non-routine analysis with accuracy and efficiency.
Complete test records on time, ensuring compliance with SOPs and regulatory standards.
Identify opportunities for quality and service improvement; contribute to continuous improvement projects.
Adhere to GMP guidelines and internal quality standards; ensure all activities are documented and traceable.
Participate in Root Cause Analysis and prepare Exception reports.
Gain proficiency in assigned tests/areas of testing; maintain training records.
Provide training to colleagues in techniques/tests where competency is proven.
Provide cover for colleagues as required.
Participate in weekend rota, overtime, and On-Call/Call-out schedules.
Ensure customer requirements
1 to 3 years of GMP experience
Strong attention to detail
HPLC experience and exposure to biologics testing
Organized, accurate, and strong documentation skills
Good understanding of GMP
Ability to work independently and in a team
Professionalism, quality consciousness, and willingness to learn
Proactive, flexible, and customer-focused
Excellent communication skills

Employment type
Full-time

Work arrangement
No