Production Technician I

Novartis; Millburn (NJ); On-site; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Production Technician I to join their Millburn, NJ facility. The role involves executing production for Radioligand Therapies while adhering to stringent regulatory standards. Candidates should have a background in engineering or science, with experience in cGMP environments preferred. This position requires flexibility with shifts and may involve mandatory overtime. Join a diverse team committed to excellence and innovation in healthcare.

Benefits

Potential bonuses

Benefits

Qualifications

• 1+ year experience in cGMP or aseptic environment preferred.
• Ability to gown aseptically and work in a Grade C clean room.

Responsibilities

• Executes all activities related to the manufacturing of RLT products.
• Completes required training on SOPs and aseptic techniques.
• Prepares documentation like batch records and shipping documents.

Skills

cGMP

Aseptic Techniques

Teamwork

Education

Bachelor’s degree in Engineering or Science

Job description

Join to apply for the Production Technician I role at Novartis

Summary
This role is located on-site in Millburn, NJ. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment.
The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner.

About The Role

Key Responsibilities:

1. Executes all activities related to the manufacturing of RLT products, including operating and maintaining grade A isolators, focusing on KPI goals, and ensuring all safety guidelines are followed.
2. Completes required training on SOPs, aseptic techniques, gowning, and other relevant areas.
3. Supports production readiness activities such as cleaning, sterilization, and environmental monitoring.
4. Prepares materials maintaining material identity per batch monitoring system.
5. Follows all cGMP compliance activities.
6. Participates in qualification/validation activities and assists with deviations and inspections.
7. Prepares documentation like batch records, shipping documents, and training materials.

Shift:

Sun-Wed or Wed-Sat, AM Shift - 6am-6pm (12-hour rotating shifts). Flexibility preferred. May involve mandatory overtime.

Essential Requirements

1. Bachelor’s degree in Engineering or Science preferred; alternatively, 1+ year experience in cGMP or aseptic environment.
2. Knowledge of cGMP and FDA guidelines related to aseptic manufacturing preferred.
3. Ability to gown aseptically and work in a Grade C clean room environment.
4. Near vision of 20/20 with no color vision impairment; corrective lenses permitted.
5. Ability to lift up to 35 pounds.
6. Radio Pharma experience preferred.

The pay range is $27.79 to $51.59/hour, with potential bonuses and benefits. Final salary depends on various factors including experience and location. The company does not sponsor visas for this position.

We are committed to diversity and inclusion. For accommodations during the application process, contact [email] or call [phone].