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

Job Description Summary

Internal Title: Associate Expert Science & Technology
Location: East Hanover, NJ, United States (On-Site)

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.

 

Job Description

Key Responsibilities:

• This position requires strong organizational and scientific technical skills and experience with the routine handling of cells in culture.
• 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

Essential Requirements:

• Education: BA/BS or MS in biology, chemistry, biochemistry, microbiology or other related science, plus a 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 ork 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

Desirable Requirements:

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

The salary for this position is expected to range between $73,1500-$136,500/year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

 

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. 

 

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

 

Salary Range

$73,500.00 - $136,500.00

 

Skills Desired

Environment, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure)