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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:        
  • Capillary Electrophoresis and/or Empower Data Chromatography software
  • Full understanding of QC operation and GMP/GDP
  • Desire for problem solving/ continuous improvement
Day to Day Responsibilities:        
  • Routine testing and lab upkeep
  • Accountability for achievements each day
  • Team and communication

Summary
Candidate will be working on site
Targeting candidates with 4-6 years of industry/ non academia experience and some Capillary electrophoresis experience
  • Quality Control Separation Sciences lab is searching is for an team member to support testing for routine, in-process, and stability samples.
  • 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.
  • Responsibilities will include, but are not limited to:
  • Performing analytical testing for CE (capillary electrophoresis, SDS-PAGE, polysorbate extraction and other general chemistry testing.
  • 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 in CE or SDS-PAGE
  • 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.

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

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