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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.

GxP IT Quality Assurance and Compliance/ CSV

Job Description

  • Location: New Brunswick, NJ
  • Type: Contract
  • Job #73027

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

Work Location

New Brunswick, NJ/Hybrid


Position: GxP IT Quality Assurance and eCompliance

Key Responsibilities and Major Duties


General Activities

• Provide quality assurance oversight across the end-to-end product lifecycle (GPS and R&D) for software development and validation lifecycle activities associated with regulated computerized systems to ensure conformance to cGxPs, guidance documents, applicable industry accepted standards and client requirements.

• Carries out functions of the Global Quality (GQ) GxP-ITQA Quality and eCompliance tower as directed including but not limited to:

• Review and approval of key computer system validation life cycle (VLC) deliverables

• Oversight of key software development life cycle (SDLC) processes such as problem, incident, change, release, deviations, periodic reviews and such.

• QA Review and approval of validation deliverables associated with various client systems such as clinical study databases electronic Case Report Forms (eCRF) and Interactive Response Technologies (IRT), enterprise commercial manufacturing systems such as electronic laboratory notebooks and manufacturing execution systems, local laboratory systems such as FTIR or HPLC systems and others as required.

• Ensure adequate and timely quality assurance / regulatory compliance support

• Report on key metrics across the tower

• Provide support during regulatory agency and third party inspections

• Research new technologies, understand existing processes, and reference recognized standards and frameworks

• Pursue continuous professional development through company paid internal/external training, certifications and/or continuing education.

• Identify opportunities for continuous improvement

• Adherence to client Core Behaviors


Meeting Participation

• Attend GQ ITQA Compliance tower meetings

• Attend GQ ITQA departmental meetings

• Interface meetings with functional areas supported

• Departmental meetings

(Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned)


Key Stakeholders/Contacts

• Lead of the GQ ITQA eCompliance tower

• Other members of GQ GxP-ITQA and department management.

• Staff from the GPS and R&D departments involved in GxP regulated operations

• Information Technology staff at commensurate levels of the organizations including but not limited to:

o Information Security

o Validation Services

o Service and Provider Quality Management

o Hosting Services

o Contracted Enterprise Service Providers

• Management and staff of the associated quality departments



University graduate (science degree preferred)

• University Graduate; BA/BS Life-Sciences degree or diploma preferred.

• Master of Science with 3 years experience or a Bachelor of Science with 5 years experience or Diploma holders with commensurate experience in regulated industry (e.g. 10+ years)



Responsibility and minimum number of years

• Proven experience in the interpretation and understanding of GxPs for the controlled management of electronic records and signatures.

• Minimum 3 years experience in regulated industry required for all candidates.


Key Competencies – knowledge, skills, abilities, other

• Experience in the Biotech/Pharmaceutical Industry or similar, regulated industry required

• Excellent analytical, interpersonal and communication skills, including written and verbal communication.

• Previous experience as a computer system validation / quality assurance / quality control analyst for a life sciences company regulated by the FDA preferred.

• Experience in industry accepted software development and validation life cycle programs and related IT controls. Previous experience in risk-based approach to computerized system validation a plus.

• Understanding of quality risk-management concepts (ICH Q9) preferred.

• Familiarity with the drug development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes.

• Strong sense of ethics, diplomacy, and discretion.

• Commitment to Quality.

• Ability to support various projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team.

• Able to work effectively with multicultural workforce.

• Excellent team player attitude.

• Ability to manage competing priorities.



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