Production Lead, Weekend Days job opportunity at Novartis.

Home Jobs In United States Of America Tag: Weekend Days Production Lead, Weekend Days position at Novartis


DateMore Than 30 Days Ago bot
Novartis Production Lead, Weekend Days
Experience: 2-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Weekend Days

Copy Link Report
degreeBachelor's (B.A.)
loacation Indianapolis, United States Of America
loacation Indianapolis....United States Of America

Job Description Summary Production Leads play an active role in daily production of isotope manufacturing as well as setup and preparation of instruments and equipment. The Production Lead 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 Lead works closely with the Production Manager to ensure production is executed in a safe and timely manner.   Job Description Major accountabilities: Executes all activities related to the manufacturing of RLT isotope products. Responsibilities include operating and maintaining grade C isolators, focusing on KPI goals as well as ensuring all state, federal and Novartis radiation safety guidelines are adhered to. Responsible for successful on time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Techniques, Gowning Qualifications and other relevant training including HSE for the specific role. Supports all technical aspects related to production readiness including manually cleaning the cell and performing sterilization of the isolators. Conducts routine and dynamic environmental monitoring as required. Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure. Participation in assigned qualification/validation activities, as necessary. Facilitates a culture of “speaking up” and ensuring all cGMP compliance activities are followed. Prepares applicable documents and records such as batch records, shipping documents, and training materials. Participates in periodic mandatory overtime to ensure process continuity and completion. Ensures technicians complete all required training in accordance with published curriculum. Participate in technician professional development counselling to foster a growth culture. Other duties may be assigned, as necessary. Minimum Requirements: Bachelor of Science strongly preferred. If the applicant does not have a degree, a minimum of 2 years of experience in a cGMP or aseptic environment can be substituted. Training in radiochemistry or radio pharmacy is preferred. 4+ years of experience in pharmaceutical manufacturing, with low bioburden manufacturing preferred. Good understanding of manufacturing and validation requirements and activities. Exploitation of new technology and techniques to eliminate non-value adding activities and improve productivity / performance through new processes. Knowledge of cGMP regulations and FDA guidance applicable to isotope manufacturing. Flexibility to don clean room garments and personal protective equipment (PPE). Near 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. Shift : Weekend days, 12 hours   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.    Accessibility and reasonable accommodations The 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 to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or 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.   Salary Range $85,400.00 - $158,600.00   Skills Desired Change Control, Chemical Engineering, Continual Improvement Process, Efficiency, Employment Discrimination, Flexibility, General Hse Knowledge, Good Documentation Practice, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Physics, Process Control, Production Line, Productivity, Risk Management, Root Cause Analysis (RCA), Scheduler, Technology Transfer, Well-Being

Other Ai Matches

Supply & Demand Analyst ( backfill for Demand Manager during LDC project ) Applicants are expected to have a solid experience in handling Job related tasks
Radio Protection Expert Applicants are expected to have a solid experience in handling Job related tasks
Global Monitoring Functional Excellence Lead Applicants are expected to have a solid experience in handling Job related tasks
Medical Lead Oncology Applicants are expected to have a solid experience in handling Job related tasks
Head Product, Project Management & International Lead, RLT Applicants are expected to have a solid experience in handling Project Management & International Lead, RLT related tasks
Manager - Competitive & Social Intelligence Applicants are expected to have a solid experience in handling Job related tasks
Associate Director Pharmacometrics (PhD/PharmD) Applicants are expected to have a solid experience in handling Job related tasks
Associate Director, Case Management Applicants are expected to have a solid experience in handling Case Management related tasks
QA Officer Applicants are expected to have a solid experience in handling Job related tasks
【契約社員】Associate, General Affairs Applicants are expected to have a solid experience in handling General Affairs related tasks
LDC Solution Design Manager, Direct Procurement Applicants are expected to have a solid experience in handling Direct Procurement related tasks
Tehnik v proizvodnji farmacevtskih učinkovin (m/ž/d) Applicants are expected to have a solid experience in handling Job related tasks
Stellvertretender Schichtführer (m/w/d) - Kundl, Tirol Applicants are expected to have a solid experience in handling Tirol related tasks
remote-jobserver Remote
ED, Evidence Generation TA Head - Oncology Applicants are expected to have a solid experience in handling Evidence Generation TA Head - Oncology related tasks
Value & Access Manager Applicants are expected to have a solid experience in handling Job related tasks
Procurement Manager Capital Projects CH Applicants are expected to have a solid experience in handling Job related tasks
Associate Director, Manufacturing Science & Technology – Drug Product Applicants are expected to have a solid experience in handling Manufacturing Science & Technology – Drug Product related tasks
Sol. Design Expert Data & Analytics Manufacturing Applicants are expected to have a solid experience in handling Job related tasks
Director - Genetic Toxicology Expert Applicants are expected to have a solid experience in handling Job related tasks
Director Evidence Generation Applicants are expected to have a solid experience in handling Job related tasks
Quality Assurance Manager Applicants are expected to have a solid experience in handling Job related tasks
Assoc. Director, DDIT Dev, Clinical Enablement, IT Business Analyst Applicants are expected to have a solid experience in handling DDIT Dev, Clinical Enablement, IT Business Analyst related tasks
Process Expert Applicants are expected to have a solid experience in handling Job related tasks