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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 #78034

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

Work Location:
Devens, MA – 100% on site

Summary:

  • The QC Analyst is responsible for supporting Quality Control analytical testing of Incoming Raw Materials. This includes in-house testing and sending out samples to contract testing labs. Some of the testing methods performed in house are HPLC/UPLC, Conductivity, OSMO, Titration, Melting Point and various other techniques.

Knowledge/Skills Required/Education:

  • Bachelor’s degree required, preferably in Science.
  • 1 year of relevant work experience, preferably in a regulated environment.
  • An equivalent combination of education and experience may substitute.
  • Hands-on experience with various bioanalytical techniques including ELISA, qPCR and FACS.
  • Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Problem-solving ability/mentality, technically adept and logical.
  • Ability to set priorities and manage timelines.
  • Ability to work with management.
  • Ability to communicate effectively with peers, department management and cross-functional peers.

Responsibilities:

  • Perform testing of incoming Raw Materials.
  • Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
  • Anticipate and troubleshoot problems.
  • Complete all work in a timely manner.
  • Work and communicate effectively within the team to ensure timelines are met.
  • Perform peer review of testing data.
  • Review all data in accordance with applicable procedures and cGMP requirements.
  • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
  • Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required.
  • Document training per procedural and cGMP requirements.
  • Support document revision, project, CAPA, and investigation/deviation related tasks.
  • Communicate effectively with management regarding task completion, roadblocks, and needs.
  • Performs other tasks as assigned.
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