Novartis Farmacéutica
Supervisor, Cell Processing Team (x2) - PM Shift
Novartis Farmacéutica, Morris Plains, New Jersey, us, 07950
Supervisor, Cell Processing Team (x2) - PM Shift
Job ID REQ-10028650USASummary
#Onsite
This role is located on-site in Morris Plains, NJ. Novartis is unable to offer relocation support for this role. Please only apply if the location is accessible for you.
As a Cell Processing Supervisor, you will manage the day-to-day operations on the 2nd shift related to the Manufacturing Unit to produce and deliver the highest quality product in a compliant, efficient, safe, and cost-effective manner, with minimal direction.
The ideal candidate for this role is a self-starter and has exceptional communication and follow-through with the ability to lead and positively influence others.About the Role
Key Responsibilities:Lead and facilitate Shop Floor meetings. Ensure the Shop Floor achieves targets for Quality, Safety, and Productivity (Production throughout times and batch record review). Compile area metrics, reports, and performance levels as required, including reporting to higher-level management.Craft Module schedule to ensure business needs are achieved while balancing personnel scheduling adjustments.Maintain a daily physical presence with direct reports in the module on and off the shop floor to supervise, coach, and support. Responsible for training all direct reports.Ability to gown aseptically and work in a clean room environment (ISO 8, 7, and ISO 5) areas for extended periods of time.Provide support to all employees in the area to ensure they are equipped with all tools, training, and documentation to perform their tasks. Ensure associates are demonstrating the proper aseptic techniques and behaviors.Maintain an "audit read" shop floor. Assist with internal pre-audit walkthroughs, cGMP housekeeping, and general organization and upkeep of manufacturing spaces.Adhere to all SOPs, cGMPs, and safety rules and regulations and ensure associates are executing tasks per approved policies and applicable procedures.Work with the team to resolve tactical issues and facilitate Corrective Actions and Preventive Actions (CAPAs).Shift:
This role is on-site in Morris Plains, NJ. We are hiring for both shifts - Sun-Wed (1x) & Wed-Sat (1x). Flexibility on shift is preferred when applying. Shift hours are from 12pm-10pm.Minimum Requirements
Bachelor’s Degree is required. BS/BA degree in Biotechnology, Biopharmaceutical, Pharmaceutical Technology, Chemistry, Microbiology, Pharmacy, or other Life Science-related scientific degree is preferred.A minimum of 3 years’ experience in cGMP.Minimum 1 year of lead/supervisor experience preferred.Proven process understanding (Pharma, GMP, Regulatory aspects).Cell therapy manufacturing highly desirable.Project management, Operational Excellence, Product/Process Development, or Regulatory experience is desired.Company will not sponsor visas for this position.Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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Job ID REQ-10028650USASummary
#Onsite
This role is located on-site in Morris Plains, NJ. Novartis is unable to offer relocation support for this role. Please only apply if the location is accessible for you.
As a Cell Processing Supervisor, you will manage the day-to-day operations on the 2nd shift related to the Manufacturing Unit to produce and deliver the highest quality product in a compliant, efficient, safe, and cost-effective manner, with minimal direction.
The ideal candidate for this role is a self-starter and has exceptional communication and follow-through with the ability to lead and positively influence others.About the Role
Key Responsibilities:Lead and facilitate Shop Floor meetings. Ensure the Shop Floor achieves targets for Quality, Safety, and Productivity (Production throughout times and batch record review). Compile area metrics, reports, and performance levels as required, including reporting to higher-level management.Craft Module schedule to ensure business needs are achieved while balancing personnel scheduling adjustments.Maintain a daily physical presence with direct reports in the module on and off the shop floor to supervise, coach, and support. Responsible for training all direct reports.Ability to gown aseptically and work in a clean room environment (ISO 8, 7, and ISO 5) areas for extended periods of time.Provide support to all employees in the area to ensure they are equipped with all tools, training, and documentation to perform their tasks. Ensure associates are demonstrating the proper aseptic techniques and behaviors.Maintain an "audit read" shop floor. Assist with internal pre-audit walkthroughs, cGMP housekeeping, and general organization and upkeep of manufacturing spaces.Adhere to all SOPs, cGMPs, and safety rules and regulations and ensure associates are executing tasks per approved policies and applicable procedures.Work with the team to resolve tactical issues and facilitate Corrective Actions and Preventive Actions (CAPAs).Shift:
This role is on-site in Morris Plains, NJ. We are hiring for both shifts - Sun-Wed (1x) & Wed-Sat (1x). Flexibility on shift is preferred when applying. Shift hours are from 12pm-10pm.Minimum Requirements
Bachelor’s Degree is required. BS/BA degree in Biotechnology, Biopharmaceutical, Pharmaceutical Technology, Chemistry, Microbiology, Pharmacy, or other Life Science-related scientific degree is preferred.A minimum of 3 years’ experience in cGMP.Minimum 1 year of lead/supervisor experience preferred.Proven process understanding (Pharma, GMP, Regulatory aspects).Cell therapy manufacturing highly desirable.Project management, Operational Excellence, Product/Process Development, or Regulatory experience is desired.Company will not sponsor visas for this position.Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
#J-18808-Ljbffr