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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.

Associate Specialist, Quality Product Release-Disposition

Job Description

  • Location: Summit, NJ
  • Type: Contract
  • Job #78560

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

Work Location:
Summit, NJ – 100% on site

Summary:
The Associate Specialist is responsible for activities in accordance with corporate policies, standards, procedures, and Global cGMP in support of the QA Disposition group. Functional responsibilities include but are not limited to, ensuring accurate and timely maintenance and review of quality records and manufacturing documentation, inventory management for quality records and manufacturing documentation. Additionally, Associate Specialist supports the receipt of executed batch records and the scanning and uploading of documents and may also support document redaction and document printing.

Knowledge/Skills Required/Education:

  • Must have knowledge and experience with cGMP manufacturing, Quality, and compliance.
  • Must possess an independent mindset.
  • Work is self-directed.
  • Confident in making decisions for non-routine issues.
  • Proposes solutions for issues and works with management to resolve. Follows established procedures and performs work as assigned.
  • Understands continuous improvement and improves efficiency and productivity within the group or project.
  • Builds relationships internally within and with cross functional teams.
  • Able to prepare written communications and communicate problems to Supervisors with clarity and accuracy.
  • Able to effectively multi-task.
  • Knowledge of US and global cGMP requirements.
  • Excellent verbal and written communication skills.
  • B.S degree with 1 year GMP experience in the Pharmaceutical or related industry.
  • Equivalent combination of education and experience acceptable.

Responsibilities:

  • Supports the receiving of executed batch records.
  • Supports the scanning and uploading of quality records.
  • Must be skilled in planning and organizing, decision-making, and building relationships.
  • Contributes to the goals within the work group.
  • Teamwork and ability to work effectively across functional groups and teams to ensure requirements are met.
  • Able to effectively multi-task.
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