Sr. QC Associate (HPLC, Gas Chromatography) / Pharma Industry

at Pioneer Data Systems Inc
Location West Greenwich, Rhode Island
Date Posted June 22, 2022
Category Mining / Oil / Gas
Job Type Not Specified

Description

Our client, a world-leading Pharmaceutical Company in West Greenwich, RI is currently looking for a Sr. QC Associate (HPLC, Gas Chromatography) to join their expanding team.

Position Details:

  • Job Title: Sr. QC Associate (HPLC, Gas Chromatography) / Pharma Industry
  • Duration: 12 months contract, extendable up to 36 months
  • Location: West Greenwich, RI


Note:

  • The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
  • You may participate in the company group medical insurance plan


Job Description:

  • Candidate will be working on site
  • Targeting candidates with 4-6 years of industry/ non academia experience and complex Instrumentation experience, including HPLC and GC
  • Quality Control Raw Materials lab is searching is for an team member to support testing for raw material testing.
  • This person will be responsible for working in the Quality Control laboratory, using GMPs and GDPs to execute analytical testing.
  • The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Job Requirements:
Responsibilities will include, but are not limited to:

  • Performing analytical testing for HPLC, GC and ICP-MS
  • Interacting cross-functionally with a wide variety of people and teams;
  • Troubleshoot, solve problems and communicate with stakeholders.
  • Participate in initiatives and projects that may be departmental or organizational in scope.
  • Evaluate lab practices for compliance and operational excellence on a continuous basis.


Qualifications:

  • 4-6 years of experience with lab instrumentation and/or Empower software
  • Bachelors Degree in any science field
  • Demonstrated experience in investigations and QC processes
  • Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision
  • Strong communication skills (both written and oral), facilitation and presentation skills
  • Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience
  • Understanding of biopharmaceuticals process and related unit operations
  • Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
  • Independent, self-motivated, organized, able to multi-task in time-sensitive environments.


Top 3 Must Have Skill Sets:

  • GMP/QC experience (non-academia)
  • HPLC, GC and/or ICPMS and chromatography data software
  • Quality mindset in team environment


Day to Day Responsibilities:

  • Routine testing and lab operations
  • Maintaining training
  • Problem solving


Employee Value Proposition:

  • Great biotech/pharma to work for


Red Flags:

  • Only academia experience with complex instrumentation
  • Job variability

"Client requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of assignment. In accordance with applicable law, Client will provide reasonable accommodations to staff augmentation external workers who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to client, its operations, or its staff.

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