QC Scientist II, Analytical Chemistry (3rd shift)

Pharmaron•Coventry, RI

3d•$75,000 - $85,000•Onsite

About The Position

This position supports manufacturing and process chemistry activities through analytical method validation, transfer, sample testing, and ensuring the QC laboratory complies with applicable guidelines. The role is based in Coventry, Rhode Island, and works the third shift from 11:00 p.m. to 7:30 a.m. Pharmaron is a global contract research organization supporting pharmaceutical and biotechnology companies from drug discovery through manufacturing. Its services span small molecules, ADCs, biologics, and gene therapies, and the company operates across the United States, the United Kingdom, and China. The QC Scientist II performs routine quality control testing and documentation, supports analytical method transfer and validation, maintains laboratory compliance, and contributes to investigations, audits, and team training. The position requires the ability to work independently and collaboratively in a cross-functional environment.

Requirements

Bachelor’s or master’s degree in chemistry or a related field.
At least 2 years of pharmaceutical industry experience.
Ability to perform routine QC work independently with minimal guidance.
Proven skills in analytical method verification and validation for small molecules.
Ability to manage multiple competing activities and meet timelines.
Ability to work in a cross-functional environment.
Experience with HPLC, GC, FTIR, UV, and wet chemistry.
Working knowledge of cGMP and applicable FDA, EMA, and ICH guidance.
Excellent verbal and written communication skills.

Responsibilities

Sample raw materials and conduct QC testing of raw materials, intermediates, APIs, in-process control samples, and cleaning verification samples according to established procedures.
Document and report experimental results promptly and in accordance with department practices and governing procedures.
Participate in method transfer and validation activities, including executing protocols and preparing reports.
Review experimental data, notebooks, and instrument qualification protocols and reports.
Write, revise, develop, and evaluate SOPs.
Maintain good laboratory practices and GMP compliance with applicable safety and environmental requirements.
Report laboratory events or deviations and participate in investigations.
Ensure quality in QC and analytical work and accurately document relevant information in accordance with cGMPs.
Train team members on instruments and testing methods.
Participate in, support, and facilitate site audits as directed and required.
Perform other related assignments and duties as required and assigned.
Work effectively both independently and in team or matrix environments.