QC Associate

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Job description

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.

QC Associate

Job Description

• Location: Devens, Massachusetts
• Type: Contract
• Job

Our client, a leading pharmaceutical company, is hiring a QC Associate, on a contract basis.

Job ID #: 80792

Work Location:
Devens, MA - 100% on site

Summary:

• This position will perform routine testing for QC Bioassay.
• Primary responsibilities include media preparation, cell maintenance/passaging, instrument maintenance and calibration, inventory and ordering.
• Other analytical support as needed.
• Strong technical lab skills using pipettes, analytical balances, pH meter, etc. is a must. Experience with electronic notebooks.
• Proficient in common computer software applications, including Empower, and effective communication skills, both oral and written are needed.
• Candidate must have strong general laboratory and organizational skills, attention to detail, flexibility, and the ability to work as part of a team.

Education/Experience:

• BS in a science related field, with 1 year of experience in a GMP QC lab is required (or equivalent experience in a related biopharmaceutical GLP or GMP lab environment). Note the BS is required.

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