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Quality Control Scientist; 3rd shift

Job in Coventry, Kent County, Rhode Island, 02816, USA
Listing for: Pharmaron Beijing Co. Ltd.
Full Time position
Listed on 2026-03-13
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Salary/Wage Range or Industry Benchmark: 80000 - 90000 USD Yearly USD 80000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Quality Control Scientist (3rd shift)

Position
:
Quality Control Scientist

Salary Range
: $80k - $90k

Work Schedule
: (3rd shift, working hours: 11 pm- 7am)

Location
:
Coventry, RI

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) 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, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers
. To learn more, visit

Job Overview

The Quality Control Scientist will support quality control testing for API manufacturing and development activities at Pharmaron's Coventry, RI facility. This role performs analytical testing of raw materials, intermediates, and active pharmaceutical ingredients using a variety of analytical techniques in a cGMP-regulated laboratory environment.

This role offers an excellent opportunity to build expertise in GMP pharmaceutical manufacturing while working with advanced analytical instrumentation in a fast-paced CDMO environment.

Key Responsibilities
  • Perform QC testing of raw materials, intermediates, APIs, IPC samples, and cleaning verification samples following established procedures.
  • Document and report analytical results in compliance with cGMP and laboratory procedures.
  • Participate in analytical method transfer and validation activities, including executing protocols and preparing reports.
  • Review analytical data, laboratory notebooks, and instrument qualification documentation.
  • Investigate laboratory deviations and support root cause analysis and corrective actions.
  • Maintain laboratory equipment and support instrument qualification and maintenance activities.
  • Prepare and revise standard operating procedures (SOPs) and technical documentation.
  • Provide training to laboratory personnel on analytical instrumentation and testing methods.
  • Support internal and external regulatory and client audits.
  • Collaborate with cross-functional teams including Manufacturing, Process Chemistry, and Quality Assurance.
  • Perform other related assignments and duties as required and assigned.
What We're Looking For
  • BS or MS degree in Chemistry or related scientific discipline
  • 2+ years of pharmaceutical or biotechnology industry experience in a GMP laboratory environment
  • Hands-on experience with chromatography and analytical instrumentation including:
    • HPLC
    • GC
    • FTIR
    • UV spectroscopy
    • wet chemistry techniques
  • Experience performing QC testing of APIs, intermediates, or raw materials preferred
  • Working knowledge of cGMP and applicable FDA, EMA, and ICH regulatory guidelines
  • Strong attention to detail and ability to maintain accurate laboratory documentation
  • Ability to work both independently and within cross-functional scientific teams
  • Strong written and verbal communication skills
  • Ability to manage multiple priorities in a fast-paced laboratory environment
Why Pharmaron?

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.

Collaborative Culture

You will 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  culture, which sets Pharmaron apart from other organizations, has evolved from our deep…

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