HPLC Development Specialist at Eurofins

Cambridge, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Mar, 26

Salary

44.0

Posted On

13 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Techniques, Method Development, Validation, Problem-Solving Skills, Communication Skills, Organizational Skills, Team Collaboration, Technical Expertise, Data Interpretation, cGMP Compliance, GLP Compliance, Safety Standards, Experiment Planning, Troubleshooting, Record Keeping, Cross-Functional Collaboration

Industry

Medical and Diagnostic Laboratories

Description

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 We are seeking a highly motivated Analytical Development Scientist to join a collaborative team focused on supporting synthetic molecule development. This role involves designing, optimizing, and qualifying analytical methods to enable process and formulation development. The ideal candidate will bring strong technical expertise, problem-solving skills, and a proactive mindset to contribute meaningfully to project execution and innovation. The position is scheduled to start in January 2026. Key Responsibilities: Develop, optimize, and qualify analytical methods for synthetic molecules. Provide analytical support for process and formulation development activities. Independently plan and execute experiments; interpret and communicate complex data. Troubleshoot technical issues and implement effective solutions. Ensure compliance with cGMP/GLP, safety, and regulatory standards. Write clear, concise technical reports and maintain accurate records. Collaborate with cross-functional teams to meet project goals. Coordinate lab work and contribute to team-based problem solving. Learn and apply new techniques while managing multiple tasks efficiently. 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.

Responsibilities

The role involves developing, optimizing, and qualifying analytical methods for synthetic molecules while providing analytical support for process and formulation development activities. The candidate will also troubleshoot technical issues and ensure compliance with regulatory standards.