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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.

QA Incoming Inspection and Material Disposition Associate

Job Description

  • Location: Devens, Massachusetts
  • Type: Contract
  • Job #79853

Our client, a leading pharmaceutical company, is hiring a QA Incoming Inspection and Material Disposition Associate, on a contract basis.

Job ID #: 79853

Work Location:
Devens, MA – 100% on site

Summary:
The Quality Assurance Incoming Material Disposition Specialist is responsible for supporting the incoming inspection and disposition of incoming materials such as consumables and raw materials at the Devens Cell Therapy Facility. Perform incoming inspection and review of the disposition deliverables to support disposition of materials and batches within the inventory management systems. Assure materials comply with all company policies, standards, Network & Global Standard Operating Procedures.

Knowledge/Skills:

  • Experience in a laboratory, manufacturing, quality, or warehouse environment desired.
  • Prior evidence of successful participation on work/study teams where combined contribution, collaboration, and time bound results are expected.
  • Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web-based applications, as well as ERP solutions such as SAP.
  • Previous work/academic experience where attention to detail and personal accountability were critical to success.
  • Strong communication skills and the ability to follow written and verbal instructions.

Education/Experience:

  • B.S., in science, engineering, biochemistry, related discipline, or its equivalent
  • 1 year of directly relevant experience in a regulated cGMP environment.
  • Any combination of education, experience, and military service in line with recommendations above will be considered.

Responsibilities:

  • Works closely with Supply Chain and Manufacturing with regards to discrepancy with nonconforming material as well as the incoming material process.
  • Inspects incoming materials such as consumables, packaging and raw materials per Standard Operating Procedures and material specifications.
  • Performs review of the disposition deliverables to support disposition of materials and batches within the inventory management systems.
  • Assures materials comply with all company policies, standards, Network & Global Standard Operating Procedures.
  • Reviews documentation to support disposition of incoming materials.
  • Works in electronic systems such as SAP, Learning Management, and Document management systems.
  • May contribute to drafting, reviewing, or approving procedural documents.
  • Works on assignments of simple to moderate complexity where some judgment is required in resolving problems and making routine recommendations.
  • Other duties as required.

Working Conditions:

  • Work is generally performed seated in a Warehouse condition but may require standing and walking for up to 10% of the time. Lighting and temperature are adequate and there are no abnormal conditions caused by noise, dust, etc.
  • Work in a cGMP laboratory and/or manufacturing environment following techniques which require one to maintain a high attention to detail. Properly use Personal Protective Equipment (PPE), gowning for restricted areas, aseptic processing, handling chemicals, and work in a general office environment.
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