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Vendor Quality Manager Jobs

Company

Global Technical Talent, an Inc. 5000 Company

Address United States
Employment type CONTRACTOR
Salary
Category Research Services,Biotechnology Research,Pharmaceutical Manufacturing
Expires 2023-09-02
Posted at 8 months ago
Job Description

Vendor Quality Manager

  • Contract Duration 6+ months
  • Pay rate up to $50- $85/hr

The Role:

  • You will work with internal business partners and alignment with business expectations, GxP standards, and other applicable regulatory requirements.
  • The Manager will also partner with R&D to create a quality culture within our client.
  • Reporting to the Director of R&D Vendor Quality within Research & Development Quality (RDQ), located at the Headquarters in Cambridge, MA, the contingent Manager will (i) Work with the RDQ and stakeholders to provide Quality support for our client's R&D Quality vendor program and drive continuous improvement of clinical, non-clinical and pharmacovigilance services to the R&D organization.

Here's What You'll Do:

  • Support in developing and establishing metrics and KPIs for R&D vendor issues
  • May participate in GCP, GLP, or GVP audits
  • Quality checks of vendor quality documents
  • Define and develop a quality agreement process with R&D vendors
  • The Vendor Quality Manager will support strategic initiatives by leading projects to design and deploy process and technology-related improvements and monitoring R&D vendor issues for trends across the operational areas
  • Process vendor requests
  • Develop and write vendor issue procedures

Here's What You'll Bring to the Table:

  • Auditing experience in GCP, GLP, or GVP preferred
  • Strong interpersonal skills and ability to effectively interact with all levels of the organization
  • Ability to collaborate effectively in a dynamic, cross-functional matrix environment
  • Ability to manage multiple projects in a fast-paced environment
  • Ability to work independently and within a team environment
  • Working knowledge of relevant FDA, EU, ICH GCP guidelines, and applicable international GCP regulations, guidelines, and local legislation
  • BS/BA in life sciences and a minimum of 6-8 experience in the Biotech, Pharma, or Vaccine Industry
  • Excellent communication skills

Notes:

  • Location: Cambridge, MA, or Remote


Benefits:

  • 401k Retirement Fund
  • Medical, Vision, and Dental Insurance Plans

About The Company:

  • Come with us as we pursue the uncharted reaches of possibility and make your mark on the future of medicine.
  • Our client operates as a developer of messenger RNA therapeutics. The company develops and discovers drugs that produce proteins or antibodies inside patient cells. Its pipeline includes various drug modalities such as prophylactic vaccines, therapeutic vaccines, intratumoral immuno-oncology, localized therapeutics, and liver intracellular. Through its mRNA therapeutics platform, they develop and produce human proteins, antibodies, and novel proteins, which help in preventing, treating, and curing diseases. It also develops therapeutics in the areas of infectious disease, rare liver disease, immuno-oncology, and cardiovascular disease.