- Novo Nordisk (Bloomington, IN)
- …systems + Collaborate significantly with cross functional groups including Validation , Quality Control, Manufacturing, Process Development, and Facilities ... is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product… more
- Lilly (Indianapolis, IN)
- …experience mentoring and training technical teams. + Previous experience as a process engineer within the Pharmaceutical Industry. + Strong equipment/ process ... and volunteerism. **Position Brand Description:** Principal Engineer - Secondary Loop Process Engineer will be responsible for ensuring the reliable operation and… more
- Novo Nordisk (Bloomington, IN)
- … Engineering Schedule: regular business hours You will work closely with process engineering, operations, manufacturing science & technology, validation , and IT ... is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product… more
- Novo Nordisk (Bloomington, IN)
- …systems + Collaborate significantly with cross functional groups including Validation , Quality Control, Manufacturing, Process Development, and Facilities ... is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product… more
- PDS Tech Commercial, Inc. (Indianapolis, IN)
- …capability, through data trending and statistical analysis of critical variables, ensuring process (es) are robust, in continued state of validation and ... for the product(s) assigned:** * Responsible for ensuring the continued state of validation ( process , cleaning, ongoing verification etc.). * Ensure that the… more
- Lilly (Indianapolis, IN)
- …This role will provide quality assurance expertise in the implementation, validation , ongoing maintenance, and lifecycle management of electronic laboratory and ... coupled with proven experience supporting cGMP electronic systems within pharmaceutical manufacturing, particularly those related to APIs. **Responsibilities:** The… more
- Lilly (Lebanon, IN)
- …technical reports supporting process control strategies, technology transfers, process validation , deviation/adverse event reporting, process ... lead, or assist in the planning and execution of process validation activities. + As required, may...of experience in a cGMP small molecule/API manufacturing. + Process and equipment knowledge of active pharmaceutical … more
- Novo Nordisk (Bloomington, IN)
- …team + Collaborate significantly with cross functional groups including Validation , Quality Control, Manufacturing, Process Development, and Facilities ... validated systems + Collaborate significantly with cross functional groups including Validation , Quality Control, Process Engineering, Manufacturing, Process … more
- Lilly (Indianapolis, IN)
- …of documentation preparation, review and approval. + Understand the electronic batch record, process flow document (PFD) and validation of the process ... documentation preparation and review; monitoring of the processes through start-up/ validation and on-going manufacture and establishing strong deviation investigation… more
- Lilly (Indianapolis, IN)
- … variability and capability. + Understand, justify and document the state of validation ( process and cleaning) with data that evaluate the capability of ... to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials,… more