Associate Scientist
2 weeks ago
**About the Role**:
Location: Onsite - Morris Plains, NJ
Shift: Wednesday - Saturday 7am - 5:30pm
365 days a year, we aspire to be the best manufacturer of Cell & Gene therapies to ensure our patients have the treatments they need to live longer, healthier lives.
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate).
- Perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, qPCR as well as perform micro/EM testing such as environmental monitoring, gram stain, sterility, endotoxin, and mycoplasma.
- Perform raw material testing such as HPLC, GC, FTIR, osmolarity, UV/VIS, polarimeter, refractometer, and viscometer.
- Maintain controls and reference standards to support testing. Maintenance of Cell Lines and cell banks.
- Review/approve data generated by other team members.
- Perform method qualification/optimization of methods as per appropriate protocols.
- Contribute to OOS/OOE investigations and deviation investigations.
- Knowledge of LabWare LIMS and/or other QC data systems.
- Maintain GMP/GLP quality systems and follows quality policies
**Diversity & Inclusion / EEO**:
- We are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential._
**Role Requirements**:
- BA or MS in chemistry, biochemistry, microbiology, or other related science AND 0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry.
- Knowledge of cGMP and an understanding of the concepts of GLP, good clinical practices and FDA guidelines, applicable state and foreign regulations, and standards routinely used in the industry (i.e., ANSI, ISO, etc.).
- Knowledge of microbiological and environmental monitoring, bioassay, and/or raw material test methods, as appropriate.
- Knowledge of LIMS systems.
- Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.
- Detail-oriented with expertise in problem solving and solid decision-making abilities.
- Strong written and verbal communication skills are essential.
Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Learn more here:
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: Novartis Talent Pool.
Division
Operations
Business Unit
QUALITY
Location
USA
Site
Morris Plains, NJ
Company / Legal Entity
Novartis Pharmaceuticals
Functional Area
Quality
Job Type
Full Time
Employment Type
Regular
Shift Work
Yes
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