Production Support Technician (Nights)
Key ResponsibilitiesExecute manufacturing activities for radioligand drug products following batch records and procedures.Operate and maintain grade C isolators, ensuring compliance with radiation and safety standards.Prepare equipment and materials, maintaining accurate material identity and traceability.Perform cleaning and sterilization of isolators to ensure production readiness.Conduct environmental monitoring activities in line with regulatory and procedural requirements.Support qualification and validation activities as required.Prepare and maintain accurate production documentation, including batch records and training materials.Essential RequirementsAssociate degree or equivalent technical training in science or related field preferred.Minimum two years of experience in pharmaceutical manufacturing or regulated production environment.Knowledge of low bioburden manufacturing practices and aseptic techniques preferred.Ability to follow Standard Operating Procedures and execute tasks with high attention to detail.Willingness to work night shifts and support periodic overtime as required.Shift: Sunday- Tuesday 6 pm- 7 am and then Thursday - Saturday 6pm-7 am. Alternate WednesdayThe salary for this position is expected to range between $16.00 and $30.00 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 hereCompany will not sponsor visas for this position.EEO StatementThe 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, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openingsMinimum RequirementsWork ExperienceOperations Execution (Pharmaceutical Manufacturing)Skills DesiredChange Control, Continual Improvement Process, Efficiency, Flexibility, General HSE Knowledge, Good Documentation Practice, Knowledge of CAPA, Knowledge of GMP, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Process Control, Production Line, Productivity, Risk Management, Root Cause Analysis (RCA), SchedulingLanguagesEnglish