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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.

Clinical Labeling Specialist

Job Description

  • Location: Summit, NJ
  • Type: Contract
  • Job #77969

Our client, a leading pharmaceutical company, is hiring a Clinical Labeling Specialist on a contract basis.

Work Location:
Summit, NJ – 100% on-site


  • Individual contributor to packaging and labeling materials project management, strategic and tactical change planning and forecasting of new product markets and indications launches to ensure the Cell Therapy Operations organization meets its performance objectives.
  • The position will support local site in-process labeling materials artwork strategy, as well as network shared packaging and labeling materials artwork strategy across the product lifecycle.
  • Responsibility to deliver in cross functional teams and drive alignment for packaging and labeling materials projects including manufacturing, engineering, regulatory and supply chain to achieve internal and regulatory requirements.
  • Ensures assurance of supply and compliance to content for new product markets and indications launches, safety updates and other core packaging and labeling materials programs.

Knowledge/Skills Required/Education:

  • Bachelor’s Degree in Science, Engineering, Business or Supply Chain with 3 years’ experience in Operations, Regulatory or Quality environment.
  • Proficiency in English (both written and oral).
  • Experience working effectively across different cultures, multiple functional areas and in complex matrix environments.
  • Excellent written and oral communication skills with all levels of management and personnel.
  • Demonstrated success in problem-solving skills.
  • Strong interpersonal and organizational skills.
  • Understands Regulatory, Quality and Supply Chain aspects of labeling and impact of non-compliance.
  • Knowledge of applicable regulations and standards affecting Cell Therapy products, specifically regulations and standards affecting Packaging and Labeling Control.


  • Individual contributor to strategic and tactical planning for label change projects.
  • Responsibility for the creation, accuracy, and completeness of label change projects within the Manufacturing Execution System.
  • Participate in change projects and associated deliverables for launches, site transfers, country/area specific changes, issue resolution and other labeling focused projects.
  • Ownership role within the packaging and labeling materials artwork strategy.
  • Support network shared packaging and labeling materials strategy development and maintenance over the product life cycle.
  • Change Plan contributor for labeling operations.
  • Act as owner for specific packaging and labeling materials business processes and assume role of documentation subject matter expert.
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