- Lilly (Indianapolis, IN)
- …and Development (PRD) Quality Assurance ( QA ) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA CT ... stability justifications and retest dating for clinical trial (CT) Materials. + Provide Quality oversight for Collaboration Partners as needed. + Assist with… more
- Lilly (Indianapolis, IN)
- …for people around the world. **Main Purpose and Objectives of Position:** The Quality Assurance Principal Associate has the responsibility for providing ... Trial activities manufactured at Collaboration Partners (CPs). The Quality Assurance Representative provides assistance within CP parenteral and dry… more
- Bristol Myers Squibb (Indianapolis, IN)
- …the following. Other duties may be assigned. + Member of CMC Development Teams providing Quality ( QA ) input from pre- clinical to end of product life cycle ... Director of Chemistry, Manufacturing & Controls (CMC) - Quality Assurance develops and drives Quality...and implementation. Also, as appropriate and compound/product specific, responsible Quality member for oversight and QA approver… more
- Lilly (Indianapolis, IN)
- …product batches for Indianapolis Parenteral products, including commercial and clinical trial materials to ensure high quality medicine (GMP Compliance) is ... better for people around the world. **Organization Overview:** The mission of Quality Assurance is to provide independent oversight for manufacturing operations… more
- Medtronic (IN)
- …RESPONSIBILITIES:** The following responsibilities are to be performed as appropriate in clinical trial case support and/or case support following commercial ... wave forms, and ancillary procedural solutions + Knowledge of Clinical trial protocols, and Congenital Therapies and...+ Report and device complaints to proper departments within quality assurance within Medtronic + Help drive… more
- Ascension Health (Carmel, IN)
- …A LICENSED RN IN THE STATE OF INDIANA.** **PREFER AT LEAST 2 YRS CLINICAL TRIAL RESEARCH EXPERIENCE.** **Benefits** Paid time off (PTO) Various health insurance ... results on an on-going basis to research team. + Participate in quality assurance /improvement initiatives. Ensure compliance with applicable standards of care… more
- Lilly (Indianapolis, IN)
- …finalization of CMC documents for global regulatory submissions, including Clinical Trial Applications, Market Authorization Applications, post-approval ... are defined based on approved submissions for products and communicated to Manufacturing and Quality Assurance . + Accountable to approve use of CMC content to… more