Deviation Writing/CAPA Backlog Support - Madison, WI (REF7623Y)

Company: ProPharma Group MIS Limited
Location: Madison
Posted on: February 25, 2021

Job Description:

• 1 E Main St, Madison, WI 53703, USA
• Contract Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Job Description Client is looking for QA Consultant to provide QC lab-based support. Project duration is estimated at 12 weeks with the potential for extension. Initial 2 weeks would be on-site, then remaining duration would be remote. Resource would carry out the following duties and responsibilities:--
  • Handling overdue Deviations
  • Writing required deviations
  • Writing required CAPA's Qualifications Qualified candidates must have:
    • Previous experience in a GMP/FDA regulated work environment.
    • Possess an Analytical/Quality Control laboratory background.
    • Have prior experience in deviation writing, expeirence with tools and techniques for root cause analysis Additional Information All candidates must be legally eligible to work in the United States. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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