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Quality Control Senior Associate

West Greenwich, RI
“This Company 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 at this company. In accordance with applicable law, this company 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 this company, its operations, or its staff.”

Top 3 Must Have Skill Sets:            
Must Have:
  • HPLC, GC, GC-MS or ICPMS experience, pertaining to routine use and troubleshooting
  • GMP laboratory experience
  • Teamwork and motivation to problem solve and improve self, operations, and processes
Day to Day Responsibilities:            
  • Quality Control Raw Materials is searching is for an analytical scientist to support testing for Raw Materials of routine samples for use within our network manufacturing operations.
  • This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
  • The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
  • Responsibilities will include, but are not limited to:
  • Performing analytical testing for HPLC, UPLC, Gas Chromatography, GC-MS and/or IC-PMS
  • 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.
Summary
**Targeting candidates with 4-6 years of industry/ non academia experienc

Qualifications
4-6 years of experience in HPLC, GC, GC-MS and/or ICP/MS
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
Compendial 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.

"This posting is for Contingent Worker, not an FTE"

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