Similar posts
Scientist
- Permanent
- Biochemistry, Biological Sciences, Laboratory Technician
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for an Upstream Process Development Scientist with a pharmaceutical company located in Philadelphia, PA.
Job Responsibilities:
- Design, plan, set up, execute and monitor experiments related to adherent monolayer and 3D cell culture as well as suspension processes for Cell and Gene therapies.
- Communicates status of operations, safety concerns and maintenance issues, in a timely manner to the Area Management.
- Contributes on training of new employees or colleagues on areas of technical expertise and compliance relevant to the lab setting.
- Effectively communicates with clients and vendors.
- Ability to work in a team environment and independently as required.
- Support media formulation, bioreactor operation and control, scale-up and full scale processing on various cellular types, focus on Cell and Gene therapies.
- Support Technology Transfer activities to Pilot Process Development and GMP manufacturing.
- Set up, execute and monitor experiments to trouble shoot deviation investigation and to assess product impact for projects employing developed technology/processes. Serves as an internal subject matter expert (SME).
- Record experimental results according to GDP standards.
- Ensure and promote safe environmental and laboratory practices.
- Stay current on new technologies as well as relevant scientific literature to help maintain the organization's long-term competitive position and profitability.
- Monitors and communicates inventory needs to the within the department as well as Materials Management group.
- Coordinate material request, bioreactor set up, monitoring, recording.
- Availability to travel approximately 10% of the time.
- Other duties as assigned.
- May be required to assist in other departments.
Skills and Requirements:
- Bachelor's degree with major in Biological or Chemical Engineering, Biological Sciences or other science-related major.
- Experience in upstream bioprocess unit operations such as aseptic processing techniques, culture of adherent and/or anchorage dependent cells and suspension cell culture are required.
- Demonstrated ability to write technical protocols and reports as well as technology transfer protocols as needed.
- Experience in cell banking and cell line development is desired.
- Demonstrated ability for critical thinking, innovation and problem solving.
- Proficient in Oral and Written communication as well as excellent organization and planning skills.
- Ability to work in a team environment and independently as required.
- Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices.
- Able to understand and efficiently communicate risks, and to develop and execute contingency plans.
- Proficient in Microsoft (Excel, Word, Outlook).
- Proficient in Oral & Written communication skills.
- Need to be able to read, write and understand English.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at 267-428-7770.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-112573361_MR2
Related jobs
US$30.00 - US$33.00 per hour
Cambridge, USA
Proclinical is seeking an Associate QC Chemist to join our client's team in Cambridge, MA.
Highly Competitive
Newark, USA
Proclinical is seeking a Principal Scientist - Upstream Development to our client's team.