About this role:
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.
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.
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation.
Key Responsibilities:
• Ownership for the processing of the assigned Patient starting material in the clean room environment.
• Ability to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) areas for extended periods of time. Cell washing with the ability to work with automated equipment such as the CS5
• Verification of intermediate process days which include expertise with the wave bioreactor, NC-200 and in process environmental monitoring
• Maintains and prepares equipment/environment for use, proficient in the use of production related IT systems such as SAP, LIMS and MES, documents all steps in the assigned Batch record in line with GMP requirements
• Conduct all necessary processing/verification steps for the assigned lot with highest skill level of aseptic technique.
• Conduct all necessary processing/verification steps for assigned lots of media with the highest skill level of aseptic technique
• Conducts routine and dynamic environmental monitoring as required
• Assist on Deviation Investigations and Inspections, Participation in assigned qualification/ validation activities
• Responsible for Successful on time completion of required training curriculum comprising of the necessary Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role.
• Perform other duties as assigned; ie. batch record review, process streamline improvements, safety walk-throughs
Additional Specifications:
• This position is a Sunday-Thursday PM shift role
• Ability to work different shift, weekends and overtime will be required. Your shift will be fixed according to business need.
• Ability to work with magnetic field equipment.
• Ability to lift 50 lbs unassisted.
• Ability to stand for an extended period of time
• Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials.
• Ability to adapt and learn new and complex equipment and systems and detailed scientific content.
• Ability to collaborate with other groups, teams and departments in addressing process related issues in a highly diverse environment.
Minimum requirements
• HS diploma or GED required. A minimum of 1 year experience in cGMP or academic or lab setting with aseptic experience
• Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline may be considered in lieu of industry experience
• Ability to perform complex calculations and an understanding of scientific notations required
Desirable Requirements (not mandatory but are used to prioritize candidates who have described preferred qualifications but does not eliminate candidates from being considered)
• Experience in cell therapy manufacturing preferred.
• Experience desired in: Aseptic processing in ISO 5 biosafety cabinets.
• Universal precautions for handling human derived materials in BSL-2 containment areas. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.
Other Qualifications:
• Ability to work different shift, weekends and overtime will be required. Your shift will be fixed according to business need.
• Ability to work with magnetic field equipment.
• Ability to stand for an extended period of time
• Ability to lift 50 lbs unassisted.
• Requires handling of chemicals such as corrosives, solvents & bio-hazardous materials.
• Ability to adapt and learn new and complex equipment and systems and detailed scientific content.
• Ability to collaborate with other groups, teams and departments in addressing process related issues in a highly diverse
The pay range for this position at commencement of employment is expected to be between $59,900 and $89,900 per year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
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: https://www.novartis.com/about/strategy/people-and-culture
You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook: https://www.novartis.com/careers/benefits-rewards
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 in order to perform the essential functions of a position, please send an e-mail to [email protected] 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.
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: https://talentnetwork.novartis.com/network
About the Department At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide....
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