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HPLC Development Specialist

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.

Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!

Job Description

  • Contributes as part of a small team of scientists towards the development/optimization, and qualification/verification of analytical methods to support synthetic molecules analytical development.
  • Applies in-depth knowledge of concepts and applications to fit-for-purpose methods development.
  • Provided analytical support for process and formulation development related works.
  • Reviews and interprets data then communicates results to relevant members.
  • Identifies, troubleshoots, and implements resolutions to technical problems/issues. 
  • Conducts work in compliance with cGMP/GLP, safety and regulatory requirements.
  • Writing technical reports for functional area
  • Independently plans and designs experiments and operations within expertise. 
  • Able to clarify requests and provide suggestions and put data into context. 
  • Works with departmental and/or other function members to execute on assignments, under limited supervision.
  • Learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
  • Effectively communicates complex data/decisions within department.
  • Contributes significantly to project related lab works within functional area.
  • Coordinates work with members in the team

Qualifications

  • Working knowledge of analytical techniques with experience using multiple techniques (LC, GC, Dissolution, Karl Fisher, spectroscopic instruments, etc.) for synthetic molecules.
  • Basic understanding of industry practices and standards.
  • Experiences on method development and validation for synthetic molecule products
  • Strong computer, scientific, and organizational skills.
  • Analytical and Problem-Solving Skills - Able to troubleshoot critical issues or problems and determine causes and possible solutions using appropriate information
  • Ability to work well in a team environment 
  • Communication and Organizational skills 
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Education and Experience

  • Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 4+ years relevant industry experience  
  • Master’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 2+ years relevant industry experience

Additional Information

What to Expect in the Hiring Process: 

  • 10-15 Minute Phone Interview with Region Recruiter
  • 45-60 Minute Virtual Interview with Manager and/or Group Leader
  • 45-60 Minute In-Person Meeting to Meet the Team and Discuss the Role 

Additional Details: 

This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to Cambridge, Massachusetts, are strongly encouraged to apply. 

Excellent full-time benefits include:

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Hourly rate is between $39-$44, depending on education and experience 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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Average salary estimate

$86320 / YEARLY (est.)
min
max
$81120K
$91520K

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Full-time, onsite
DATE POSTED
October 30, 2025
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