Basic Qualifications Bachelor's degree. 4+ years plus direct people leadership experience. 8+ years ... biotech manufacturing environments. Deep understanding of GxP, Good Manufacturing Practices (GMP ...
Basic Qualifications Bachelor's degree. 4+ years plus direct people leadership experience. 8+ years ... biotech manufacturing environments. Deep understanding of GxP, Good Manufacturing Practices (GMP ...
The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ... the pharmaceutical, biotech, or medical device industry. * Strong knowledge of applicable ...
The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ... the pharmaceutical, biotech, or medical device industry. * Strong knowledge of applicable ...
Associate Director, Global Regulatory Advertising and Promotion
Indianapolis, IN · On-site
$103K - $288K/yr
The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ... the pharmaceutical, biotech, or medical device industry. * Strong knowledge of applicable ...
Associate Director, Global Regulatory Advertising and Promotion
Indianapolis, IN · On-site
$103K - $288K/yr
The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ... the pharmaceutical, biotech, or medical device industry. * Strong knowledge of applicable ...
Statistics Leader / Associate Director of Statistics
$150K - $250K/yr
Experience supporting clinical development in pharmaceutical, biotech, or CRO settings ... Highly organized, self-directed, and able to manage multiple priorities across projects #LI-GSK ...
Statistics Leader / Associate Director of Statistics
$150K - $250K/yr
Experience supporting clinical development in pharmaceutical, biotech, or CRO settings ... Highly organized, self-directed, and able to manage multiple priorities across projects #LI-GSK ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$257K/yr
Direct inspection readiness activities and represent Quality Control during regulatory inspections ... pharmaceutical, biotechnology, or related regulated industry including at least 5 years of ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$257K/yr
Direct inspection readiness activities and represent Quality Control during regulatory inspections ... pharmaceutical, biotechnology, or related regulated industry including at least 5 years of ...
Associate Director - Technical Services/Manufacturing Science (TSMS) - API External Manufacturing...
Indianapolis, IN · On-site
$123K - $180K/yr
Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our ... or biotechnology industry * Proven leadership experience, including direct supervision and ...
Associate Director - Technical Services/Manufacturing Science (TSMS) - API External Manufacturing...
Indianapolis, IN · On-site
$123K - $180K/yr
Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our ... or biotechnology industry * Proven leadership experience, including direct supervision and ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$138K - $257K/yr
... of experience within the pharmaceutical, biotechnology, or related regulated ... Direct experience with investigations and root cause analysis in pharmaceutical or medical device ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$138K - $257K/yr
... of experience within the pharmaceutical, biotechnology, or related regulated ... Direct experience with investigations and root cause analysis in pharmaceutical or medical device ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$138K - $257K/yr
... of experience within the pharmaceutical, biotechnology, or related regulated ... Direct experience with investigations and root cause analysis in pharmaceutical or medical device ...
Site QC Head (Associate Director)
Indianapolis, IN · On-site
$138K - $257K/yr
... of experience within the pharmaceutical, biotechnology, or related regulated ... Direct experience with investigations and root cause analysis in pharmaceutical or medical device ...
Associate Director - Technical Services/Manufacturing Science (TSMS) - API External Manufacturing (P
Indianapolis, IN · On-site
$123K - $180K/yr
Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our ... or biotechnology industry * Proven leadership experience, including direct supervision and ...
Associate Director - Technical Services/Manufacturing Science (TSMS) - API External Manufacturing (P
Indianapolis, IN · On-site
$123K - $180K/yr
Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our ... or biotechnology industry * Proven leadership experience, including direct supervision and ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
Director, Patient Services
Jeffersonville, IN · On-site
$120 - $190/hr
Train and develop internal staff, serving as a leader and mentor to the team and associates; ensure ... Knowledge of the specialty pharmaceutical and biotech marketplace and product commercialization.
New
Director, Patient Services
Jeffersonville, IN · On-site
$120 - $190/hr
Train and develop internal staff, serving as a leader and mentor to the team and associates; ensure ... Knowledge of the specialty pharmaceutical and biotech marketplace and product commercialization.
New
Senior Director, Business Development Communication
Indianapolis, IN · On-site
$154.50 - $226.60/hr
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... Established relationships with business and biotech reporters covering deals and dealmakers across ...
New
Senior Director, Business Development Communication
Indianapolis, IN · On-site
$154.50 - $226.60/hr
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... Established relationships with business and biotech reporters covering deals and dealmakers across ...
New
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... biotech podcasters, deal-focused newsletters and Substacks, and biotech and life-sciences ...
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... biotech podcasters, deal-focused newsletters and Substacks, and biotech and life-sciences ...
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... Established relationships with business and biotech reporters covering deals and dealmakers across ...
Reporting to the Associate Vice President, Enterprise Communications, the Senior Director, Business ... Established relationships with business and biotech reporters covering deals and dealmakers across ...
Director, Production
$190K - $231K/yr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... associate(s). * Collaborate with other functional areas for the triage of deviations ...
Director, Production
$190K - $231K/yr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... associate(s). * Collaborate with other functional areas for the triage of deviations ...
Director, Production
Indianapolis, IN · On-site
$190K - $231K/yr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... associate(s). * Collaborate with other functional areas for the triage of deviations ...
Director, Production
Indianapolis, IN · On-site
$190K - $231K/yr
... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... associate(s). * Collaborate with other functional areas for the triage of deviations ...
Associate Veterinarian
Syracuse, IN · On-site
Associate Veterinarian eGenesis is a clinical-stage biotechnology company developing human ... Provide direct clinical and surgical care * Execute surveillance programs (SAF & DPF) * Review ...
Associate Veterinarian
Syracuse, IN · On-site
Associate Veterinarian eGenesis is a clinical-stage biotechnology company developing human ... Provide direct clinical and surgical care * Execute surveillance programs (SAF & DPF) * Review ...
About eGenesis eGenesis is a clinical-stage biotechnology company developing human-compatible ... The Associate Veterinarian reports to the Director of Veterinary Services and serves primarily a ...
Quick apply
Environmental Manager
Bloomington, IN · On-site
$108K - $111K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... This position reports to the Associate Director of Environmental, Health, Safety, & Sustainability ...
Environmental Manager
Bloomington, IN · On-site
$108K - $111K/yr
... biotech companies to bring their sterile injectable products to market. With facilities in ... This position reports to the Associate Director of Environmental, Health, Safety, & Sustainability ...
Biotechnology Associate Director information
What is the difference between Biotechnology Associate Director vs Biotechnology Scientist?
| Aspect | Biotechnology Associate Director | Biotechnology Scientist |
|---|---|---|
| Required Credentials | Master's or PhD in Biotechnology, Life Sciences, or related field; extensive industry experience | Master's or PhD; focus on research and development |
| Work Environment | Leadership roles in R&D teams, project management, strategic planning | Laboratory research, experimental design, data analysis |
| Employer & Industry Usage | Biotech companies, pharmaceutical firms, biotech divisions | Research institutions, biotech companies, academia |
| Common Search & Comparison | Often compared for leadership and strategic roles | Focused on scientific research and experimentation |
The Biotechnology Associate Director typically holds a leadership position overseeing research teams and strategic projects, requiring extensive experience and advanced degrees. In contrast, a Biotechnology Scientist primarily conducts laboratory research and experiments. Both roles are vital in biotech companies, but they differ in responsibilities, focus, and career level.
What are the key skills and qualifications needed to thrive as a biotechnology associate director?
What does a biotechnology associate director do?
What are some common challenges biotechnology associate directors face when leading cross-functional teams?

Full-time
Posted 4 days ago
Job description
Company Overview At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Job Position Overview The Global Manufacturing and Quality Learning and Development (GMQLD) organization is dedicated to delivering learning solutions and strategies that empower Lilly's Manufacturing and Quality organizations to achieve our mission: making medicine with safety first and quality always. The Functions Learning Leader is the recognized internal expert in learning and capability development for site and central functions — driving excellence through a team of L&D professionals and serving as the critical connector between platform execution and the global Center of Excellence (CoE). This role operates at the intersection of global strategy and platform and site-specific needs — ensuring that learning priorities, governance frameworks, and compliance standards are consistently and effectively delivered across every site the platform serves. Responsibilities Leadership & High-Performance Team Development Build and lead a high-performing global functions team by setting a clear standard of excellence, holding accountability to outcomes with directness and care, and addressing performance gaps and talent gaps. Bring high emotional intelligence to team leadership — reading individual motivators, team dynamics, and organizational pressure accurately to coach effectively, sustain cohesion through change, and create an environment where strong performers thrive. Translate strategic priorities into clear team direction and execution rhythm — removing blockers, maintaining momentum, and closing the gap between what leadership asks for and what the team delivers. Develop team members across craft, partner influence, and leadership capacity — coaching individuals to frame problems well, bring solutions, and operate with increasing independence and confidence. Operate as a skilled problem-solver and credible cross-functional partner — navigating sophisticated, matrixed relationships across platforms, sites, and senior leadership with substance, influence, and a clear line of sight to business outcomes. Strategic Leadership & Governance Serve as the primary L&D Leader across site and central functions, ensuring alignment with global L&D strategies, policies, and procedures while meeting local operational needs. Partner with the global CoE, LA and LEPs to implement future-facing learning solutions that drive performance, compliance, and operational excellence. Ensure global governance frameworks are driven for site and central functions, in partnership with Platform Lead, maintaining inspection and audit readiness in real time. Act as a champion for a modern learning culture, shifting away from site-based traditional document-based training toward interactive, digital, and experiential global, network and platform-based learning solutions. Learning Strategy & Execution Support the team by providing function-specific L&D initiatives that enable compliance, manufacturing excellence and employee development. Drive learning effectiveness measurement using real-time data and analytics to ensure programs deliver measurable business impact. Partner cross-functionally with customers to embed a learning culture across functions and sites. Ensure audit and inspection readiness, proactively addressing training gaps and regulatory expectations. Advocate for technology-enabled learning, including AI, immersive simulations, digital academies, and just-in-time learning solutions. Learning Effectiveness & Performance Measurement Ensure implementation of the GMQLD strategy for measuring learning program effectiveness across functions — including evaluation frameworks, assessment design, and business impact methodologies. Stakeholder Engagement & Cross-Functional Influence Operate as a strategic partner to Senior Director, CoE, CoE, LAs, Site LEPs, Quality, Operations, HR, and Tech@Lilly — influencing decisions and driving alignment across a sophisticated, matrixed global organization. Lead without authority across a global network, driving results through collaboration, influence, and a clear line of sight to business outcomes. Basic Qualifications Bachelor's degree. 4+ years plus direct people leadership experience. 8+ years of experience in Learning & Development, Talent Development or Manufacturing Training, with a focus on regulated pharmaceutical or biotech manufacturing environments. Deep understanding of GxP, Good Manufacturing Practices (GMP), regulatory requirements, and compliance training across global manufacturing networks. Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN #J-18808-Ljbffr