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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.


Job Description

  • Location: Devens, MA
  • Type: Contract
  • Job #77172

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

Work Location:
Devens, MA – 50% on-site

To provide operations with the appropriate service and advice to assure that site quality systems are in place for regulatory compliance. Incumbent must assure that quality systems and programs such as internal audits, annual product reviews, stability, procedures, change controls, gap analysis, complaints, and other are in compliance with GMP regulations.


  • Assures the site quality systems are in place to avoid any possible regulatory compliance situation at the Site.
  • Manages the different quality systems and programs established at the site such as but not limited to Change Control, Packaging change controls, Stability, Policies and Directives, Gap Analysis, Customer Complaints, TrackWise System, Site Gatekeeper, Regulatory CMC, Internal Audits, Document Control, External Audits, Annual Product Quality Review, and others handled by the Compliance areas as assigned.
  • Prepares Annual Product Quality Reviews report for each pharmaceutical finished packaged and bulk drug products manufactured at the Site as per established timelines.
  • Reviews and prepares regulatory documentation intended for government regulatory agencies (e.g. FDA), such as master files, new and existing product registrations, regulatory submissions, foreign countries registrations, certificates, etc.
  • Reviews, evaluates and approves plant operating documents such as SOPs, change control, qualification reports, CAPA, and process deviations and maintains documents in an organized and traceable manner.
  • Evaluates specifications, documents, protocols, registrations and recommends actions to assure regulatory compliance.
  • Provides assistance in managing all aspects of regulatory and corporate inspections and participates actively during inspections and audits including performing readiness exercises before and during inspections/audits.
  • Evaluates and recommends lots to be placed on stability, evaluate trends, and performs investigations when required.
  • Ensures compliance with procedures, policies and directives to avoid regulatory issues performing Gap Analysis on company documents and observational findings from the pharmaceutical industry.
  • Provides advice and service to all operating departments to assure compliance with cGMPs and other regulations.
  • Investigates customer complaints, issues the corresponding reports indicating possible cause and recommending solutions.
  • Conducts and/or prepares training materials on GMP topics.
  • Performs formal internal audits and pre-approval inspections of manufacturing, laboratory and warehouse operations for cGMPs compliance and, reports and follows up on observed deficiencies on a regular basis.
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