Data Reviewer, Biosafety – GMP

🔥 0 minutes ago

🧀 Wisconsin – Remote

🧀 Wisconsin – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🎁 Product Marketing

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This company has sponsored H1B visas in the past.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Review routine and complex analytical analysis experiments involving pharmaceutical and biopharmaceutical compounds • Evaluate laboratory data for compliance with analytical methods, client directives, SOPs, GLP, GMP, and acceptance criteria • Review sample results for scientific soundness, completeness, accurate data representation, and final reported results • Review data entered into databases and reports and monitor laboratory data quality • Communicate with laboratory staff to maintain the quality of laboratory documentation • Deliver clear and concise review findings identifying deficiencies in analytical data or reports • Escalate significant deficiencies to the project leader or supervisor • Facilitate discussions with laboratory staff on documentation practices and quality findings • Advocate for quality and review process changes • Identify and support process improvement initiatives • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree or equivalent and relevant formal academic / vocational qualification • 2+ years of comparable experience, or equivalent combination of education, training, and experience • Previous experience with formal data review in a GMP Lab strongly preferred • Thorough knowledge of SOPs and Federal Regulations, including GLP and GMP • Thorough knowledge of chromatography may be required • Strong technical knowledge of laboratory procedures, methodology, and standards • Strong verbal and written communication skills • Strong attention to detail • Ability to train staff on basic review techniques • Ability to independently review laboratory reports and analytical methods • Ability to work efficiently in a remote capacity • Must be legally authorized to work in the United States without sponsorship • Must be able to pass a comprehensive background check, including drug screening • Ability to lift and move objects up to 25 pounds • Ability to use and learn standard office equipment and technology proficiently • Ability to work upright and stationary and/or standing for typical working hours • Ability to work in non-traditional work environments • Ability to perform successfully under pressure while prioritizing and handling multiple projects or activities

🏖️ Benefits

• Fully remote work arrangement • Full-time employment • Career development resources and support • Accessibility assistance or accommodations during the application process • Equal employment opportunity and affirmative action protections

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