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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 -Data Analyst

Job Description

  • Location: Summit, NJ
  • Type: Contract
  • Job #77386

Our client, a leading pharmaceutical company, is hiring a Quality Data Analyst on a contract basis.

Role: DM Analyst

Work Location:
Summit, NJ – 50% on-site


  • The DM analyst is responsible for evaluating Deviations to identify patterns and trends, monitor trend investigations E2E including CAPAS and EC to eliminate trends, perform analysis of deviation data and summarize information for Annual Product Quality Review and other required reports. Notification to management of identified trends.

Knowledge/Skills Required/Education:

  • Must have knowledge and experience with cGMP manufacturing, Quality, and compliance.
  • Must have experience with Deviations, Root Cause Analysis, and CAPAs.
  • Must have knowledge of data trending and tracking, including use of statistical analysis software a plus.
  • Proficient in Excel data mining and report creation.
  • Ability to use electronic Quality systems such as Infinity.
  • Junior to intermediate ability to interpret results and situations and articulate recommendations for resolution.
  • Knowledge of US and global cGMP requirements.
  • Excellent verbal and written communication skills.
  • Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision.
  • Work is self-directed.
  • Confident in making decisions for non-routine issues.
  • Able to prepare written communications and communicate problems to management with clarity and accuracy.
  • Able to effectively multi-task.
  • Associate degree or higher required, three years of experience in the pharmaceutical or related industry. Equivalent combination of education and experience acceptable.


  • Responsible for trending of deviations at S12.
  • Facilitates Trending Governance meetings. Issues minutes and notifies senior leadership of any risks or delays.
  • Reviews all deviations and notifies management of any trends.
  • Must have ability to author reports, interpret results, and generate conclusions consistent with Quality risk management principles.
  • Knowledge of quality processes, including investigations, and CAPA management.
  • Able to effectively multi-task.
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