Job Introduction
Position: Senior Analytical Chemist, Quality Control
Location: Rushden
Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We’re proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules to biologics and gene therapies, and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.
About the Role
Pharmaron is currently looking to recruit a Senior Analytical Chemist to join the Chemistry Quality Control Department at their Rushden facility. In this role, you will be responsible for performing GLP/GMP quality control (QC) analysis of materials manufactured by custom synthesis teams.
You will have an excellent working knowledge and experience of a range of analytical techniques, primarily spectroscopic and chromatographic, gained within industry and be able to manage your own workload and assist in the scheduling / co-ordination of activities for specific QC process or projects.
Key Responsibilities
-
Have proven sustained expertise in analytical procedures and skills relevant to the team, and will demonstrate continuing competence in analytical techniques and processes
-
Co-ordinate stability studies, approving stability protocols/reports and liaising with clients as required
-
Carry out quality control (QC) analysis of materials manufactured by custom synthesis teams as required
-
Perform QC analysis of materials on stability as required
-
Be able to interpret analytical results and describe and explain them to a wider audience
-
Maintain accurate and clear laboratory records
-
Ensure that QC instruments are maintained in a calibrated/validated state, organising external service support promptly as required
-
Participate in verification/validation of analytical methods, drafting method verification protocols/reports, and controlled analysis documents
-
Prepare out-of-specification (OOS) and deviation documentation when necessary
-
Participate in the validation/qualification of laboratory equipment as required
-
QC release raw materials from Quarantine for use in GMP manufacture
-
Carry out QC review of analytical data
Candidate Profile
-
Degree in Chemistry, or relevant experience
-
Experience as a practicing analyst particularly with chromatographic and spectroscopic techniques
-
A working knowledge and practical experience of Stability testing
-
Good theoretical grounding of chromatographic and spectroscopic techniques
-
Knowledge of quality/regulatory standards and quality systems
-
Good written and verbal communication skills
-
Radiation protection awareness
-
Ability to work with minimum supervision and as part of a team
-
Conscientious and meticulous in laboratory and written work
-
Good time management skills and ability to work to tight deadlines
-
Proven ability to problem solve
-
Willing to get involved with new ideas and initiatives
Why Pharmaron?
Collaborative Culture: Thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
