- Lilly (Indianapolis, IN)
- …lesser extent lab projects + Experience in the following areas: GMP manufacturing, LEAN, automation, construction, construction quality, project controls, the ... engineering disciplines, safety, scheduling + The capacity to achieve results and influence through people + Willingness to relocate and/or travel to locations outside of home state/country and have the demonstrated ability to work from long distances with… more
- Novo Nordisk (Bloomington, IN)
- …the client requirements within their operational area. Relationships Reports to Manager , Form/Fill Essential Functions + Supervises the daily activities of business, ... procedures and business plan; receives guidance and oversight from manager + Typically, does not perform the work supervised...manages workload for operational area + Reviews and approves GMP documentation while ensuring safety and GMP … more
- Novo Nordisk (Bloomington, IN)
- …oversight, and continuous improvement of automation systems that support our GMP manufacturing operations. This position focuses on process control systems, with ... emphasis on DeltaV, PLC, and HMI technologies. Relationships Reports to Senior Manager , Process Engineering Schedule: regular business hours You will work closely… more
- Novo Nordisk (Bloomington, IN)
- …the client requirements within their operational area. Relationships Reports to Manager . Essential Functions + Supervises the daily activities of business, technical ... procedures and business plan; receives guidance and oversight from manager + Typically does not perform the work supervised...work load for operational area + Reviews and approves GMP documentations while ensuring safety and GMP … more
- Novo Nordisk (Bloomington, IN)
- …their operational area. Shift: Monday - Friday 3pm-11:30pm Relationships Reports to Manager or above. Essential Functions . Supervises the daily activities of ... procedures and business plan; receives guidance and oversight from manager . Typically, does not perform the work supervised...manages workload for operational area . Reviews and approves GMP documentations while ensuring safety and GMP … more
- Novo Nordisk (Bloomington, IN)
- …Team Novo Nordisk and help us make what matters. Relationships Reports to Manager . Essential Functions + Supplier Management + Provides support for the introduction ... + Review batch documents + Assist with revision of GMP documentation such as Standard Operating Procedures, Master Batch...the floor + Provides dedicated quality floor oversight of GMP operations for the manufacture of master/working cell banks,… more
- FreshRealm (Indianapolis, IN)
- The FSQA Technician role reports to the FSQA Manager and works throughout the Fresh Realm Facility performing all daily and weekly duties in line with the Fresh ... Performs daily audits of the Fresh Realm facility and grounds to monitor GMP compliance + Accountable for making decisions about product disposition. Implements the… more
- Novo Nordisk (Bloomington, IN)
- …systems operate in a safe, and quality-oriented manner. Relationships Reports to: Manager Form/Fill Shift: Weekend PM, 4/3 schedule for SL3 Essential Functions + ... implementation of improvements + Ownership of Corrective Actions, Change Management, GMP document revision, review and approval + Participate and conduct continuous… more
- Novo Nordisk (Bloomington, IN)
- …a lead, coordinating the work of others - but not a people manager + Works autonomously within established procedures and practices + Assist manufacturing personnel ... behavioral or non-conformance to Supervisor + Advance Documentation Skills ( GMP preferred) + Capable of working with minimal supervisor...the job description and will be up to the Manager to be added as required + Review all… more
- Bristol Myers Squibb (Indianapolis, IN)
- …Indianapolis. The Analytical Scientist associate will report directly to the Manager of Analytical Development at the Indianapolis site. **Job Responsibilities:** ... instrument qualification, calibration, and maintenance activities. + Ensure compliance with GMP regulations, safety guidelines, and quality standards. + Work with… more