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Tech Operations - Manufacturing Science & Tech

GMP
Shop Floor
Writing Skills
Documentation
Continuous Improvement
Operations
Description:

~~~Please note: This is a temporary contractor opportunity at Novartis ~~~
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!

Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com

Ready to work with/through Magnit at Novartis? Please read on...
Tech Operations - Manufacturing Science & Technology - Onsite Millburn, NJ

Step into a role where your expertise supports the cutting edge of Radioligand Therapy manufacturing. As a Process Expert, you’ll be the go-to partner on the shop floor—ensuring each batch is produced safely, efficiently, and in full compliance. You’ll lead investigations, drive continuous improvement, and support seamless technology transfers, all while mentoring others and maintaining inspection readiness. This is your opportunity to make a meaningful impact in a dynamic, purpose-driven environment where innovation and quality go hand in hand.
 

Key Responsibilities:
• Lead investigations for deviations, including Out Of Specification and Out Of Expectation results
• Collaborate cross-functionally to assess deviation impact and identify root causes
• Initiate and track CAPAs, ensuring timely resolution and effectiveness verification
• Act as change manager for manufacturing change control working cross-functionally to implement process improvements
• Escalate deviations according to guidelines and present details clearly, including root cause and CAPAs.
• Draft manufacturing documentation

Essential Requirements:
• Bachelor’s degree required, preferably in a scientific discipline
• Minimum 1 year’s of previous GMP experience is required
• Proven background in the pharmaceutical industry with hands-on manufacturing exposure
• Strong understanding of deviation management, CAPA processes, and regulatory compliance
• Excellent communication and collaboration skills across cross-functional teams
• Technical writing skills
Shift: Monday – Friday (onsite)

Location: Millburn, NJ (Onsite)
Shift: Monday - Thursday, 8:00am - 6:30pm
Pay Rate: $35.71 - $39.29/hr based on experience and qualifications (W2 Only)
Contract: 5-month 
Health, dental, vision, 401k

Why Novartis: 
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

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.

Accommodation: 
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.
 

QUALIFICATION/ LICENSURE :
  • Work Authorization : Green Card, US Citizen, Other valid work visa
  • Preferred years of experience : 1+ Years
  • Travel Required : No travel required
  • Shift timings: Onsite: Millburn, NJ
Job Location Millburn, New Jersey
Pay USD 35.71 - USD 39.29 Per Hour
Contract Duration 5 month(s)