Position: Associate 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.
About the Role
We’re looking for a proactive and detail‑oriented Associate Analytical Chemist to join our Chemistry Quality Control team at our Rushden site. In this role you will support laboratory operations through routine and specialised analytical tasks including carrying out scheduled calibration and verification of instruments, documenting all activities in line with GMP and internal SOPs. You’ll troubleshoot minor equipment issues, coordinate on‑site work by service engineers, and ensure maintenance activities meet safety and compliance standards.
This position is ideal for someone who is detail‑focused, organised, and and able to work effectively within a regulated laboratory setting.
Key Responsibilities
1. Perform scheduled calibration and verification of analytical instruments (e.g., pipettes, balances).
2. Document calibration activities in accordance with GMP and internal SOPs.
3. Troubleshoot minor instrument issues and escalate complex problems as needed.
4. Coordinate and oversee on-site work performed by service engineers during instrument installation, maintenance, and repair.
5. Ensure adherence to safety and compliance requirements during engineering activities.
6. Review and approve service reports and maintenance documentation.
7. Conduct routine radiation monitoring in designated laboratory areas.
8. Maintain accurate records of radiation levels and ensure compliance with regulatory limits.
Candidate Profile
9. BSc Chemistry, Analytical Chemistry or closely related discipline
10. Practical laboratory skills with experience within an Analytical laboratory desirable
11. Conscientious and meticulous in laboratory and written work with the ability to keep accurate records (e.g. logbooks, calibration certificates)
12. Knowledge of quality/regulatory standards and quality systems and / or radiation protection is advantageous
13. Good written and verbal communication skills
14. Ability to propose pragmatic improvements to SOPs and workflows
15. Good interpersonal skills with the ability to work as part of a team
16. Good time management skills and ability to work to tight deadlines
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.