Production Support Supervisor, Nights

Location: Carlsbad, CaliforniaRelocation Support: This role is based in Carlsbad, California. Novartis is unable to offer relocation support: please only apply if accessible.You will help deliver life-changing radioligand therapies to patients while leading critical overnight manufacturing operations. As a Production Support Supervisor, you will combine hands-on expertise with frontline leadership-overseeing the setup and preparation of instruments and equipment, and ensuring every batch is produced safely, efficiently, and to the highest quality standards.NOTE: Two positions are available working 12-hour rotating shifts. One position will work Sunday - Wednesday and the second will work Wednesday - Saturday. Shift hours are expected to be 6 pm - 7 am. Periodic mandatory overtime may be necessary to ensure process continuity and completion.Key ResponsibilitiesExecute all activities supporting the manufacturing of radioligand drug products, including operating and maintaining Grade C isolators, manually cleaning the cell, and performing sterilization of the isolatorsEnsure adherence to Standard Operating Procedures and batch records throughout all production activitiesPrepare and verify materials, maintaining material identity in accordance with defined proceduresConduct routine and dynamic environmental monitoring to support compliant manufacturing conditionsComplete and review production documentation, including batch records, shipping documents, and training recordsParticipate in assigned qualification/validation activities and support packaging of finished product, as necessary.Ensure technician training completion and support ongoing development to build a capable and compliant teamPromote a culture of quality, safety, and compliance, encouraging accountability and continuous improvement across the teamEssential RequirementsBachelor's degree with 3 years of pharmaceutical manufacturing experience or 5 years of pharmaceutical manufacturing experience required without degree. Strong knowledge of cGMP regulations and FDA guidance including solid understanding of manufacturing operations, validation processes, and production documentation requirementsAbility to work in cleanroom environments, wearing full personal protective equipment for extended periodsFlexibility to work night shifts and support extended hours to maintain continuous manufacturing operationsNear vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.Makeup, jewelry, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas.Ability to lift or carry up to 35 pounds.Desirable RequirementsTraining in radiochemistry or radio pharmacyPrior experience with low bioburden manufacturingThe salary for this position is expected to range between $85,400 and $158,600 per year. 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 here.