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Drug Development Engineer Jobs (NOW HIRING)

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Drug Development Engineer information

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$49K

$96.2K

$153.5K

How much do drug development engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for drug development engineer in the United States is $96,155.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,500.00 and $106,500.00 per year, depending on experience, location, and employer.

What does a drug development engineer do?

A Drug Development Engineer is responsible for designing, testing, and optimizing processes to develop new pharmaceutical drugs. They work closely with scientists, chemists, and regulatory teams to ensure that medications are both effective and safe. Their work involves scaling up laboratory findings to commercial production, troubleshooting manufacturing issues, and complying with regulatory standards. Drug Development Engineers play a crucial role in bringing new medicines from the research phase to the market.

What are some common challenges faced by drug development engineers during the early stages of a project?

Drug Development Engineers often encounter challenges such as balancing stringent regulatory requirements with innovative design, ensuring scalability of laboratory processes for mass production, and managing cross-functional communication between research, manufacturing, and quality assurance teams. Additionally, adapting to frequent changes in project scope as new data emerges and addressing unforeseen technical issues can require flexibility and strong problem-solving skills. Building effective collaboration with chemists, biologists, and clinical teams is essential for overcoming these obstacles and driving the project forward.

What are the key skills and qualifications needed to thrive as a drug development engineer, and why are they important?

To thrive as a Drug Development Engineer, you need a strong background in pharmaceutical sciences, chemical engineering, or related fields, often supported by a relevant degree. Familiarity with laboratory instrumentation, drug formulation software, and regulatory compliance systems like Good Manufacturing Practice (GMP) is vital. Strong problem-solving, project management, and collaboration abilities distinguish top performers in this role. These skills are essential to ensure the safe, efficient, and compliant development of new pharmaceutical products.

What is the difference between Drug Development Engineer vs Pharmaceutical Process Engineer?

AspectDrug Development EngineerPharmaceutical Process Engineer
CredentialsBachelor's or Master's in Chemical, Pharmaceutical, or Biomedical EngineeringBachelor's or Master's in Chemical, Pharmaceutical, or Process Engineering
Work EnvironmentResearch labs, R&D departments, early-stage developmentManufacturing facilities, production lines, process optimization
Industry UsageDrug discovery, formulation, preclinical testingScale-up, process improvement, manufacturing efficiency

While both roles focus on pharmaceutical products, Drug Development Engineers primarily work on creating and testing new drug formulations in research settings. In contrast, Pharmaceutical Process Engineers focus on scaling up production processes and optimizing manufacturing operations. Both roles require similar educational backgrounds and collaborate closely in the drug development lifecycle.

Are pharmaceutical development engineers in demand?

Pharmaceutical development engineers are in demand due to ongoing innovation in drug discovery and manufacturing. They are essential for developing new medications, and demand is expected to grow with advancements in biotechnology and regulatory requirements, often requiring skills in process optimization and regulatory compliance.

Is drug development a good career?

A career as a drug development engineer involves designing and testing new pharmaceuticals, often requiring a strong background in chemistry, biology, or engineering. It offers opportunities for innovation, research, and contributing to healthcare, with roles typically requiring advanced degrees and adherence to regulatory standards. The field can be rewarding for those interested in science and problem-solving, with steady demand in the pharmaceutical industry.

What degree do I need to be a drug development engineer?

A drug development engineer typically needs at least a bachelor's degree in chemical engineering, biomedical engineering, pharmaceutical sciences, or a related field. Advanced roles may require a master's or doctoral degree, along with knowledge of laboratory techniques, regulatory standards, and experience with drug formulation and testing.

What are popular job titles related to Drug Development Engineer jobs?

For Drug Development Engineer jobs, the most frequently searched job titles are:

Infographic showing various Drug Development Engineer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $96,155 per year, or $46.2 per hour.

Director, Drug Development AI Nexus Decision Integration Lead

Brisbane, CA • On-site

Bristol Myers Squibb
Scientific Research and Development Services • 10K+ employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz


Job description

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.


The Director, Drug Development AI Nexus Decision Integration Lead is a newly created leadership role at the intersection of drug development, artificial intelligence, and operating model transformation. This individual will serve as the primary bridge between Drug Development, Research and the AI Nexus team, translating strategic priorities, business requirements, and decision-making needs into AI-enabled workflows, governance processes, data requirements, and platform capabilities that improve the quality, speed, and consistency of development decisions.

Positioned within Drug Development Excellence (DDE), this role has broad cross-functional reach across Drug Development and plays a critical role in advancing BMS's vision for AI-enabled decision-making. The scope extends beyond the integration of AI Nexus into Global Program Teams (GPTs) to encompass portfolio-level decision workflows, governance cadences, and the broader agentic intelligence ecosystem being established across R&D. Working in close partnership with BI&T, Research, and functional leaders, the role will drive strategic prioritization, workflow redesign, AI-data readiness, adoption, and organizational change to enable new ways of working.

The ideal candidate is a credible drug development leader who can bridge the worlds of science, operations, and technology. They possess a deep understanding of how development decisions are made and can translate complex business needs into scalable, AI-enabled solutions by partnering effectively with business, data, and technology teams. They are equally comfortable discussing portfolio strategy, development planning, phase transitions, governance processes, data architecture, and emerging AI capabilities, and they can connect these domains to deliver measurable business impact. Success in this role requires strategic thinking, creativity, influence without authority, and the ability to inspire and mobilize cross-functional teams toward AI-native ways of working.
AI Nexus Integration & Embedded Workflow Redesign
  • Translate Drug Development strategic priorities, business requirements, and decision-making needs into scalable business capabilities, AI-enabled workflows, data requirements, and AI Nexus roadmap priorities.
  • Serve as the Drug Development anchor for the AI Nexus platform, translating the AI Nexus vision into executable workflows embedded directly in Global Program Teams (GPTs) and governance forums
  • Map, prioritize, and redesign key Drug Development decision points - from Phase transition and regulatory milestone reviews to portfolio-level governance - to leverage AI Nexus-enabled evidence, agentic analysis, and learning loops
  • Partner with AI Nexus Product Leadership (BI&T) and Platform Engineering teams to communicate Drug Development decision needs and ensure the platform is built and iterated to serve them
  • Operate as an "embedded translator" between Drug Development operational and clinical needs and AI Nexus technical capabilities - converting ambiguous decision problems into structured, AI-ready workflow requirements with defined data requirements
Change Leadership & Adoption
  • Drive AI Nexus adoption across Drug Development through demonstrated value in live GPTs and culture-driven change management - not through mandates or training-first approaches
  • Build and sustain a network of Drug Development champions, GPT leads, and functional stakeholders who actively use and shape Nexus workflows
  • Develop and execute adoption strategies tailored to Drug Development archetypes - study teams, clinicians, program leaders, and executive leaders - recognizing that each group engages with agentic systems and data differently
  • Serve as a visible change agent for the broader evolution of Drug Development toward an agentic operating model, demonstrating what AI-augmented ways of working look like in practice
  • Actively contribute to the AI Nexus SteerCo and cross-functional working groups, ensuring Drug Development priorities are reflected in platform roadmap and investment decisions
Operating Model & Continuous Improvement
  • Help define and operationalize an AI-native Drug Development operating model, embedding AI-enabled decision support, governance integration, learning systems, and workflow standards across development processes.
  • Design scalable frameworks that can extend from GPT-level integration to broader Drug Development governance and cross-TA portfolio processes
  • Track and report on AI Nexus adoption, impact, and return across Drug Development functions; ensure metrics align to decision quality, speed and portfolio outcomes, and use data to drive prioritization and course correction
  • Contribute to the broader DD vision of operational excellence - where quality, speed, and efficiency are produced as outcomes of an integrated, intelligence-driven system

We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Brisbane - CA - US: $251,570 - $304,839 Cambridge Crossing: $251,570 - $304,839 Madison - Giralda - NJ - US: $224,610 - $272,178 Princeton - NJ - US: $224,610 - $272,178

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.


Benefits:


Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).


U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.


Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.


Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.


U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits


How We Work

Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/


Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself athttps://careers.bms.com/fraud-protection.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


If this posting is missing required information required by local law or incorrect, contact BMS atTAEnablement@bms.comwith the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.


R1605823 : Director, Drug Development AI Nexus Decision Integration Lead

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US