Associate Process Expert (2nd shift/Wed-Sat)

Are you motivated by solving complex manufacturing challenges where quality, compliance, and patients come first? As an Associate Process Expert, you will play a critical role on the shopfloor, acting as a trusted partner to manufacturing and quality teams to resolve unexpected events and ensure processes remain compliant, robust, and inspection‑ready. Your work will directly support safe, reliable production of our cutting-edge Radioligand Therapy (RLT) treatments by leading investigations, driving effective corrective and preventive actions, and strengthening a culture of continuous improvement in a fast‑paced Good Manufacturing Practice (GMP) environment.Location: Millburn, NJ, United StatesRelocation Support: This role is based in Millburn, NJ, United States. Novartis is unable to offer relocation support: please only apply if accessible.NOTE: This is a 2nd shift role, hours are expected to be 1:00 pm – 11:30 pm, Wednesday – Sunday.Key ResponsibilitiesProvide on‑the‑floor support by triaging unexpected manufacturing events with Production and Quality teams.Open, author, and drive deviations and investigations to timely, compliant closure.Apply process knowledge and root cause analysis tools to identify and resolve product or process issues.Develop, document, and implement effective corrective and preventive actions to prevent recurrence.Ensure investigations are complete, accurate, defensible, and inspection‑ready for critical and major events.Execute or support experimental plans and manufacturing runs required to support investigations.Partner cross‑functionally to maintain compliant manufacturing operations during and after deviations.Essential RequirementsBachelor of Science degree in Engineering, Pharmacy, Pharmaceutical Technology, Chemistry, or equivalent scientific discipline.Minimum one year of experience in a process support role on the shopfloor of Good Manufacturing Practice manufacturing and/or Quality Assurance or Quality Control.Proven understanding of pharmaceutical manufacturing processes and regulatory requirements.Strong technical writing skills with the ability to produce clear, complete, and inspection‑ready documentation.Demonstrated quality mindset with the ability to work effectively on the shopfloor with cross‑functional teams.Desirable RequirementsHands‑on experience authoring and managing deviations, investigations, and corrective and preventive actions.The salary for this position is expected to range between $33.65 and $62.50 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.To learn more about the culture, rewards and benefits we offer our people click Thrive Together.