Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, he…
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Senior Engineer, IT Laboratory & Quality Systems, Devens Biologics Digital Plant
Devens, Massachusetts, United States · Hybrid
$127k–$134k/yr
Senior$29B raised
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Associate Director, Aseptic & Sterile Process Engineering
Devens, Massachusetts, United States · Hybrid
$171k–$207k/yr
Senior+$29B raised
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Job Purpose As a Machine Service Technician at VulcanForms Inc., you will work in an operations shop floor environment and help to ensure our cutting-edge technology is running effectively. Your role will involve mechani…
Job Purpose As a Machine Service Technician at VulcanForms Inc., Devens, MA, you will work in an operations shop floor environment and help to ensure our cutting edge technology is running effectively. Your role will inv…
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a va…
Senior Specialist, Associate Aseptic Process Validation Engineer
Devens, Massachusetts, United States · On-site
$88k–$106k/yr
Mid level$29B raised
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Skills: Aseptic Process Validation, cGMP, Aseptic Process Simulations, Risk Assessment, Change Control
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$84k–$94k/yr
Full-time
bachelor degree, postgraduate degree
Medical Coverage, Dental Insurance, Vision Insurance, Life Insurance, Disability Insurance, 401(k) With Company Match
Posted 2d ago
~40 hrs/week
Responsibilities
Lead the design and execution of phase-appropriate analytical methods for the development and manufacture of active pharmaceutical ingredients. Responsible for release and stability testing, authoring technical documents, and ensuring compliance with GMP and FDA regulations.
Requirements
Requires a degree in Analytical Chemistry (BS with 5+ years, MS with 3+ years, or PhD) and at least 5 years of experience in method development for small molecule APIs. Proficiency in various chromatography and spectroscopy techniques is essential.
Full job description
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
The Scientist Group Leader is responsible for the development and implementation of analytical procedures and specifications in support of the development and manufacture of active pharmaceutical ingredients (APIs) for traditional synthetic molecules (including potent) and peptides. Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (LC-MS, GC-MS, NMR, ICP-MS, FTIR and UV-Vis), and physical properties (particle size, water content, etc.). Core Responsibilities:
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 forboth 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.
Qualifications
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
Additional Information
The position is full-time, Monday-Friday, 8:00am-5:00pm, with overtime as needed. Candidates living within a commutable range of Devens, MA are encouraged to apply.
Compensation: $84,000-94,000
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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
It’s so much more than a specimen. It's a life.
With over 30 years of specialized expertise in infectious disease, immunology, transplant, and allergy testing for immunocompromised and critical patients, Eurofins Viracor is committed to helping medical professionals, transplant teams, reference labs and biopharmaceutical companies get results faster, when it matters most.
Eurofins Viracor is passionate about providing timely, actionable test results, never losing sight of the connection between the testing we perform and the patients our results ultimately serve.
Find out more by visiting us at www.eurofins-viracor.com/clinical
Eurofins Viracor is an equal opportunity employer.
Offices: 18000 W 99th St, Lenexa, Kansas 66219, US
How many Engineering jobs are open in Devens, MA right now?
There are currently 172 open engineering positions in Devens, MA listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Engineering roles in Devens, MA?
Companies currently hiring include VulcanForms Inc., Bristol Myers Squibb, Commonwealth Fusion Systems, SMC, Veranova, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Engineering jobs in Devens, MA?
Yes — 15 of the 172 open engineering positions offer remote or hybrid work (1 remote, 14 hybrid).
How do I apply for Engineering jobs in Devens, MA?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.