Associate Analytical Chemist, Quality Control
Position: Associate Analytical Chemist, Quality Control
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.
Key Responsibilities
* Perform scheduled calibration and verification of analytical instruments (e.g., pipettes, balances).
* Document calibration activities in accordance with GMP and internal SOPs.
* Troubleshoot minor instrument issues and escalate complex problems as needed.
* Coordinate and oversee on‑site work performed by service engineers during instrument installation, maintenance, and repair.
* Ensure adherence to safety and compliance requirements during engineering activities.
* Review and approve service reports and maintenance documentation.
* Conduct routine radiation monitoring in designated laboratory areas.
* Maintain accurate records of radiation levels and ensure compliance with regulatory limits.
Candidate Profile
* BSc Chemistry, Analytical Chemistry or closely related discipline.
* Practical laboratory skills with experience within an Analytical laboratory desirable.
* Conscientious and meticulous in laboratory and written work with the ability to keep accurate records (e.g., logbooks, calibration certificates).
* Knowledge of quality/regulatory standards and quality systems and/or radiation protection is advantageous.
* Good written and verbal communication skills.
* Ability to propose pragmatic improvements to SOPs and workflows.
* Good interpersonal skills with the ability to work as part of a team.
* Good time management skills and ability to work to tight deadlines.
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