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Analytical QC Analyst

Job in Norton, Bristol County, Massachusetts, 02766, USA
Listing for: Proclinical Staffing
Full Time position
Listed on 2026-01-24
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Analytical QC Analyst - Contract - Norton, MA

Ensure the accuracy and integrity behind every dose through high-precision analytical testing.

Proclinical is seeking an Analytical QC Analyst to support quality control operations for a pharmaceutical organization in MA. This position plays a key role in ensuring timely and efficient quality control processes.

Primary Responsibilities

The successful candidate will contribute to maintaining high standards of quality and compliance from development through commercialization. You will perform routine and non-routine testing, assist with laboratory operations, and support method transfers and validations.

Skills & Requirements
  • Degree in chemistry, biology, biochemistry, or a related scientific field (Associate s Degree, Biotech Certificate, or equivalent considered).
  • Hands-on experience with HPLC and UPLC.
  • Experience in a regulated laboratory setting within the pharmaceutical or biotech industry.
  • Proficiency in data analysis preferred.
  • Strong attention to detail and ability to adapt to shifting priorities.
  • Effective communication and teamwork skills.
  • Familiarity with LIMS, Excel, Word, and PowerPoint is beneficial.
The Analytical QC Analyst s responsibilities will be:
  • Conduct routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability studies following established SOPs.
  • Maintain training records, adhere to testing schedules, and complete assignments on time to support QC activities and project timelines.
  • Assist with laboratory equipment maintenance, inventory management, and preparation of reagents and samples.
  • Ensure timely submission of data and perform data review as needed.
  • Perform operational tasks such as raw material sampling, environmental monitoring, and product testing.
  • Contribute to the revision and updating of controlled documents, including SOPs and test methods.
  • Adhere to internal policies, SOPs, and regulatory standards (e.g., GMP, GLP, ICH guidelines).
  • Collaborate with QC and cross-functional teams to ensure smooth operations.
  • Participate in ongoing training to enhance expertise in QC techniques and regulatory compliance.
  • Support data verification for regulatory submissions and inspection readiness activities.
  • Assist with onsite audits and inspections as required.
  • Contribute to continuous improvement initiatives to enhance QC processes and laboratory efficiency.

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at

If you are interested in applying to this exciting opportunity, then please click  Apply  or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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