We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.

Responsibilities Include: 

• Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment
• 90% Method development, qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
  • May include technology transfer activities, regulatory support, and possible project team participation
• 10% Analytical testing
• Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities

The Ideal Candidate will Have: 

• Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.
• Experience working in a GMP/GLP environment
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives
• Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development

Minimum Qualifications: 

• BS in Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
  • 2 years of demonstrated work experience with cell-based assays
• Or MS in Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
  • 6 months of Demonstrated experience with cell-based assays
• Experience with experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays
• Excellent communication (oral and written) and attention to detail
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Authorization to work in the United States indefinitely without restriction or sponsorship

What to Expect in the Hiring Process: 

• 10-15 Minute Phone Interview with the Region Recruiter
• 45-60 Minute Virtual Interview with the Manager and/or Group Leader
• 30 Minute Virtual Meeting with the Site Director

Additional Details: 

The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holiday

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.