Scientist Group Leader

🕒 July 25

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $84k - $94k / year

⏰ Full Time

🟠 Senior

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👻 Ghost score 30%

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Eurofins

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🍽️ Food & Beverage

🏥 Healthcare

📦 Logistics

💰 $30M Grant on 2021-10

Food & Beverage • Healthcare • Logistics

Eurofins is a global leader in testing and laboratory services. With approximately 62,000 employees and over 900 laboratories across 62 countries, the company provides a wide range of testing services across various industries. Eurofins offers services such as food and feed testing, consumer product testing, genomic services, clinical diagnostics, forensic services, environment testing, and pharmaceutical testing. The company is committed to scientific innovation and sustainability, and it plays a critical role in testing for health, safety, and environmental impacts worldwide.

📋 Description

• Lead the design, development, and execution of phase-appropriate analytical methods in compliance with ICH and Health Authority guidelines. • Perform release and stability testing on starting materials, intermediates and API for both development and GMP samples. • Author and review technical documents including method qualification/validation/transfer protocols and reports for analytical procedures. • Maintain and troubleshoot analytical instrumentation. • Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed. • Ensures work in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.

🎯 Requirements

• BS in Analytical chemistry or equivalent with 5+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • MS in Analytical chemistry or equivalent with 3+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • PhD in Analytical chemistry or equivalent with related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • Experience with common analytical techniques such as: HPLC/UPLC, GC, NMR, UV, KF, FTIR, XRPD, LC-MS, GC-MS and ICP-MS. • Minimum of 5 years’ experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs). • Experience with Process Development of APIs. • Previous leadership experience preferred

🏖️ Benefits

• 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

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