Employee Responsibilities:
- Executes drug product development and commercialization studies, new product introduction and process validation at the commercial site.
- Designs and executers process characterization activities. Ensures appropriate design principles including DOE are used where applicable.
- Authors protocols for studies, ensures appropriate design of experiment and sample size selections.
- Responsible for sample submissions and tracking. Employs statistical tools and methods to analyze results.
- Authors technical reports that can be used as a source of documentation for regulatory filing. Also writes or performs second-person review for high-quality CMC sections for regulatory submissions.
The Ideal Candidate would possess:
- Experience with operation and maintenance of pilot-scale pharmaceutical processing equipment
- Ability to manage laboratory inventory for experimental execution and facility/equipment maintenance
- Strong scientific, computer, organizational, and documentation skills
- Excellent interpersonal, communication (oral and written), and collaboration skills and attention to detail
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- Ability to perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
- Knowledgeable of GMPs as applied to manufacturing of biologics and vaccines
Qualifications
- Bachelor’s/Master’s degree in engineering, biomedical engineering, chemistry, biology, or related field
- Previous liquid formulation experience, including aseptic technique skills
- Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.
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
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.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
