Associate - QA Clinical Trial Packaging

Company : BioSpace, Inc.
Location : Indianapolis, IN, 46204
Posted Date : 15 September 2025
Job Details
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Organization Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Product Research and Development (PRD) Quality Assurance (QA) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA CT Packaging is responsible for oversight of packaging and release of finished goods material within PRD and assures compliance with quality systems and current Good Manufacturing Practices (cGMP).
Responsibilities:
- Ensure appropriate execution of the Quality Systems to sustain cGMP compliance.
- Ensure adequate document control and data integrity for packaging instructions and cGMP standards.
- Review/approve/release batch records.
- Create/verify Certificates of Analysis.
- Provide quality support for packaging operation.
- Investigate, review/approve deviation investigations.
- Review/approve change controls, protocols and master label proofs.
- Review/approve allowable dating, stability justifications and retest dating for clinical trial (CT) Materials.
- Provide Quality oversight for Collaboration Partners as needed.
- Assist with regulatory body audits and site self-inspections to ensure cGMP compliance.
- Provide guidance to counterparts within organization.
- Bachelor of Science degree in STEM related field, or equivalent experience
- Minimum 1 year of experience in pharmaceutical manufacturing (CT packaging experience preferred)
- Strong knowledge of cGMPs, Quality Systems and FDA Regulations
- SAP Power user experience
- Standard Operating Procedure writer experience.
- Ability to work across functional areas with people of all levels of the organization.
- Strong oral and written communication skills.
- Demonstrated interpersonal and networking skills.
- Ability to gather, edit, organize, and summarize information from multiple sources including databases, websites, site interviews and audits.
- Ability to influence team interactions and lead initiatives.
- Must exhibit attention to detail.
- Ability to work under time pressure with proven demonstration of good judgement in making decisions under minimal supervision.
- Excellent teamwork skills
- This position is onsite based in Indianapolis, IN. It will require onsite presence the majority of the time.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$63,000 - $162,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Company
Science has been our calling from the beginning. Colonel Eli Lilly founded the company in 1876 and charged employees to "take what you find here and make it better and better." More than 147 years later, we remain committed to his vision through every aspect of our business and the people we serve, starting with discovering the best treatments for those who take our medicines and extending to health care professionals, employees and the communities in which we live. Moreover, you can also count on the team at Lilly to be incredibly civic-minded, supporting our communities through philanthropy, volunteerism, and a creative and innovative can-do spirit.
Company info
Location 893 S Delaware St
Indianapolis
Indiana
46285
United States
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