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Scientist II Quality Assurance

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1 Vacancy
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Job Location drjobs

Lancaster - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

*THIS IS NOT A DATA SCIENCE POSITION*

Job Summary: Eurofins BPT Small Molecule Method Development and Validation is seeking a Data Review Scientist II to join their team in reviewing batch records and ensuring cGMP quality standards are met.

  • Determine if data is compliant and defendable based on industry regulations and methodology
  • Verify scientific data is of sound quality following all method industry and client requirements where applicable
  • Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulations
  • Review simple and complex routine and nonroutine data (for three or more areas) according to departmental corporate and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
  • Diagnose problems solve simple problems and suggest solutions to complex problems in professional area
  • Review methods to ensure procedures are followed
  • Authorize written reports (e.g. SOP OMC client reports)
  • Other job duties as required

Qualifications :

The Ideal Candidate would possess:

  • Strong scientific and organizational skills
  • Strong attention to detail
  • Previous experience with LIMS preferred 
  • Previous experience with Excel
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team selfmotivation adaptability and a positive attitude
  • Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies

Minimum Qualifications:

  • Bachelors degree in chemistry mathematics physics or other related degree concentration or equivalent directlyrelated experience
  • 3 years of experience in a cGMP environment
  • Authorization to work in the United States indefinitely without restriction or sponsorship


Remote Work :

No


Employment Type :

Fulltime

Employment Type

Full-time

Company Industry

About Company

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