Associate Expert Science & Technology, Analytical Development, Potency & Flow

Novartis • East Hanover, NJ

234d • $73,500 - $136,500

About The Position

This position will be located at East Hanover site and will not have the ability to be located remotely. Please note that this role would not provide relocation and only local candidates will be considered. Bench to bedside! This exciting role serves as an Associate Expert Science & Technology to develop, optimize, and implement novel analytical methodologies for our CAR-T cell therapy products. The successful candidate will work with a talented and experienced team in our Technical Research and Development organization at East Hanover, New Jersey. The successful candidate will be an important part of the potency and flow team, participating in analytical method development, qualification, and method transfer activities within the department. In addition, this role may also execute analytical assays to understand/characterize the function of our cell therapy products. He/ She will interface regularly and build relationships with other functions such as Process Development, Quality Control and Manufacturing Sciences & Technology to collaboratively drive projects to meet the established timelines while maintaining the highest quality and data integrity standards. This individual will uphold Novartis Values & Beliefs and Code of Ethics to successfully support our bold mission of delivering effective CAR-T cell products for patients in need.

Requirements

• BA/BS or MS in biology, chemistry, biochemistry, microbiology or other related science.
• Minimum of 1 year of prior experience in industry or academia.
• Understanding of the scientific principles underpinning of cellular based analytical methods including ELISA and Cell-based assays.
• Expertise with aseptic technique and mammalian cell culture including suspension cells.
• Scientific curiosity.
• Ability to communicate clearly with a variety of cross-functional teams.
• Detail-oriented with expertise in problem solving and solid decision-making abilities.
• Established ability to work in a regulated environment.
• Good presentation skills and scientific/technical writing skills.
• Must have good work ethic and demonstrated ability to work collaboratively within a large team and individually.

Nice To Haves

• Human T-cell culture experience is preferred.
• Experience writing laboratory SOPs and technical instructions is preferred.
• Experience with GMP is preferred.

Responsibilities

• Plan, organize, perform and document scientific experiments under moderate supervision.
• Perform analytical testing including flow cytometry, and cell based bioassays including cytokine release, cytolytic activity and proliferation following appropriate SOPs and procedures.
• Review and approve data generated by other team members.
• Record and maintain meticulous records in electronic laboratory notebook in compliance with Quality standards.
• Identify opportunities for method improvement and execute optimization of analytical methods.
• Drive project timelines and deliverables while meeting internal quality and data integrity requirements.
• Communicate effectively and present complex data within the department and cross-functionally.
• Author and review method related technical documents to ensure completeness, accuracy, consistency and clarity.
• Support lab management including inventorying, clinical sample cryopreservation, sample management.

Benefits

• Salary range: $73,500 - $136,500/year.
• Sign-on bonus.
• Restricted stock units.
• Discretionary awards.
• Full range of medical benefits.
• 401(k) eligibility.
• Various paid time off benefits, such as vacation, sick time, and parental leave.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree