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About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

Quality Control Technician

Job Description

  • Location: Devens, MA
  • Type: Contract
  • Job #75413

Our client, a leading pharmaceutical company is hiring a Quality Control Technician on a contract basis.

Work Location:
Devens, MA – on site

Knowledge/Skills Required/Education:

  • Required BS or Associate Degree – knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, 0-3 years of experience.
  • Knowledge of basic laboratory techniques such as pH, volumetric measurement, pipetting, analytical weighing and basic laboratory safety practices preferred.
  • Attention to detail and demonstrated organizational skills.
  • Demonstrated manual dexterity.
  • Knowledge of basic electronic systems (email, MS Office, etc.)


  • Performs routine testing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment.
  • Executes routine procedures based on methodologies/responsibilities of the specific QC sub-team. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).
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