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Salary
≈ $47k – $119k per year (Estimated)
Location
In office (Livingston)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 31, 2026. First seen by Alion on Oct 30, 2026. EMD Group scores A on the Alion truth index.

Overview
Company
Impact
Profile match
EMD Group is the name used in the United States and Canada by Merck KGaA, the science and technology group headquartered in Darmstadt, Germany, whose businesses cover healthcare, life science and electronics. Founded in 1668 and still majority-owned by the Merck family, the group operates in North America through EMD Serono, MilliporeSigma and EMD Electronics, with major sites in Burlington and Billerica in Massachusetts and Saint Louis in Missouri. Its board lists manufacturing technicians, process and quality engineers, data engineers and scientists, finance analysts and shared-service roles in Bengaluru, Manila and Tokyo.

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:

Working as an R&D Scientist at our Livingston site, you will perform laboratory operations supporting reagent development and manufacturing in compliance with quality and regulatory requirements. Responsibilities include protein expression, fermentation, purification, filtration, and immunoassay development; developing protocols and manufacturing procedures; analyzing and reviewing methods; meeting deadlines; and maintaining documentation in accordance with applicable cGMP, FDA, ISO, and Quality System requirements.

Essential Job Functions:

  • Perform laboratory operations such as fermentation, protein expression, protein purification, and immunoassays (eg, ELISA, SDS-PAGE, liquid chromatography)
  • Develop and control method design with respect to new products and contract manufacturing projects, and ensure smooth transition to routine manufacture
  • Collect, analyze, and interpret data from verification testing to ensure that products meet all specifications
  • Develop, write, and update documents pertaining to lab procedures and product manufacturing to maintain cGMP and ISO compliance; write lab reports or project summaries as requested
  • Contribute ideas and suggestions to improve standard laboratory techniques, improve protocols, processes, and equipment.
  • Provide customer support and direct customer communication as part of business development and ongoing customer interaction.
  • Support the Quality Management System to meet applicable Regulatory requirements (US FDA CFRs, IVD 98/79/EC, and any other applicable regulations) and International Quality Standards (ISO9001, ISO13485 and any other applicable standards).
  • Assist in the timely closure of all non-conformances, failure investigation reports and corrective/preventative actions, and help develop strategies for continuous improvement.

Who you Are:

  • BSc in a Life Sciences discipline (Biology, Biotechnology, Chemistry, etc.) with 2+ years of post graduate relevant laboratory experience - OR - MSc in a Life Science discipline with 1+ year of post graduate relevant laboratory experience - OR - PhD in a Life Science Discipline.
  • Experience in any of the following areas, with a preference of protein experience: protein expression systems (bacterial and/or mammalian), protein purification (eg, HPLC, FPLC), immunoassays (eg, ELISA, Western, SDS-PAGE), molecular biology techniques (eg, cloning, PCR, nucleic acid isolation); serological and biochemistry techniques
  • Excellent oral and written communication skills
  • Can work independently, but also works well in group setting/team mentality

Preferred Additional Qualifications:

  • Experience working in regulated environments (eg, GMP, ISO13485 and/or FDA-filings).
  • Good organizational, time management, and project management skills.
  • Multi-tasker who can handle multiple projects at one time.
  • Ability to troubleshoot problems in experimental design.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

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