Pharmaceutical Data Review Scientist

Eurofins Scientific

Portage, MIOn-siteFull time
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Location
Portage, MI
Work style
On-site
Job type
Full time
Posted
Oct 16
3 days ago
Career path

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About the company

Eurofins Scientific

Biotechnology · 10,001+ employees

Eurofins Scientific on LinkedIn

What you'll do

  • Review laboratory data for accuracy, clarity, and compliance with GMP/GLP, departmental, corporate, and client SOPs.
  • Analyze proteins and related impurities or raw materials, troubleshoot methods and instruments, and produce written reports.

What you need

  • <p><strong>The Ideal Candidate would possess:</strong></p><ul><li>Strong computer, scientific, and organizational skills</li><li>Excellent communication (oral and written) and attention to detail</li><li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li><li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li></ul><p><strong>Minimum Qualifications:</strong></p><ul><li>Bachelor's degree in chemistry or other related degree concentration, or&#xa0;equivalent directly-related experience</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li></ul>
  • Education: a bachelor's degree

Key skills

GMPGLPanalytical techniquesorganizational skillsExcellent communicationattention to detailcomplex calculationsTroubleshoot methodinstrumentation problems

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Perks

  • Comprehensive medical coverage
  • dental
  • vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation
  • holidays

See full description on company page, apply now

Read the full posting here
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 non-routine 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 Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques Determine if data is compliant and defendable based on industry regulations and methodology Verify data is of sound quality following all method, industry, and client requirements where applicable Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area; perform complex calculations Troubleshoot method and instrumentation problems Use office and instrumentation specific computer software Produce written reports (e.g., SOP, OMC, client reports The Ideal Candidate would possess: Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, 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: Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, first shift position Monday - Friday, 8:00am - 5:00pm. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply. Excellent full time benefits including Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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