Contributes as part of a small team of scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.
~100% testing, as well as associated protocol/report documentation and presentations; may include technology transfer activities, regulatory support, and possible project team participation.
2-5 years industry experience working with plate based and gel methods. Preferably experience with one or more of following methods, ELISA, SDS-PAGE, Western blot, receptor binding.
Experience in high throughput technologies and automated liquid handling systems (Tecan, Janus, etc.) a plus
Background in qualification and validation activities for regulatory support a plus.
Demonstrated hands-on trouble-shooting capabilities for plate-based method is a must.
Independently executes method for quantitation of product-related impurities.
Computer competency is essential with emphasis on spreadsheet-based software
Understands and applies advanced scientific principles, theories, concepts, practices and standards for product development.
Conducts work in compliance with cGMP/GLP, safety and regulatory requirements.
Demonstrates 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.
The Ideal Candidate would possess:
Technical expertise in one or more bioanalytical and bioassay technologies, including experience with ELISA, gel-based methods, cell-based assays and demonstrated experience of working with cell culture.
Experience working with one or more of following methods: ELISA, MSD, SDS-PAGE, Western Blot, Octet protein binding assays, Host Cell Protein assays and, qPCR will be preferred.
Experience working with plate washers, plate readers, automated instruments like Janus, Tecan and softwares like SoftMax Pro is preferred.
Knowledge of theories, principles and techniques of relevant scientific areas and basic understanding of industry practices and standards.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Minimum Qualifications:
Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full time year of college in related major)
Minimum of 2 years of ELISA experience is required.
Authorization to work in the United States indefinitely without restriction or sponsorship .
What we offer:
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
Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lexington, Massachusetts are encouraged to apply.
Eurofins Lancaster Laboratories Professional Scientific Services ® (PSS) is a global, award-winning insourcing solution that places our people at our clients' site 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 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.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
