SUMMARY

Onsite

This role is located on-site in Millburn, NJ. Novartis is unable to offer relocation support for this role. Please only apply if the location is accessible for you.
The Production Lead is responsible for the daily operations, specifically to direct, manage operations related to the Production Unit to produce and deliver product with high quality, in a compliant, efficient, and cost-effective manner while safety is maintained.

ESSENTIAL REQUIREMENTS:

• Bachelor’s degree in a STEM field (Science, Technology, Engineering & Math) is preferred; If the applicant does not have a degree, 2 additional years of experience in pharmaceutical cGMP or aseptic environment is required beyond the below years
• 3+ years of relevant pharmaceutical experience
• 1+ years of experience on shop floor

OR:

• Bachelor’s degree in a STEM field (Science, Technology, Engineering & Math) is preferred; If the applicant does not have a degree, 2 additional years of experience in pharmaceutical cGMP or aseptic environment is required beyond the below years
• 2+ years of Novartis RLT manufacturing experience

DESIRABLE REQUIREMENTS:

• Previous Radio pharma experience a plus
  Shift: This role is 12-Hour Shifts, alternating Wednesday’s.

NOVARTIS COMPENSATION AND BENEFIT SUMMARY:

The salary for this position is expected to range between $37.02 and $68.75 per hour.
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.

KEY RESPONSIBILITIES:

• Ensure batches are executed and records all applicable data in compliance with cGMP expectations.
• Author and review Standard Operating Procedures that pertain to Production-related activities.
• Engage with Production Management and Process Experts to identify and implement process improvements within areas of expertise.
• Maintain an “audit ready” module. Assist with internal pre-audits walkthroughs, cGMP housekeeping and general organization and upkeep of manufacturing spaces.
• Assist Production Manager with communication of job-related information during daily meetings and organize the team for daily activities.
• Supervise training to ensure new hires have necessary technical skills and knowledge.
• Adhere to all SOPs, cGMPs, and safety rules and regulations.
• Ensure associate are demonstrating proper aseptic behaviors and Good Documentation Practices on the Shop Floor. Provides innovative solutions to complex or process improvement issues.
• Support investigations and impact assessments for deviations.
• A self-motivated individual with a strong sense of ownership and discipline.