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Director Analytical Research and Development

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Germer International - Pharmaceutical Recruiting
Full Time position
Listed on 2026-09-13
Job specializations:
  • Research/Development
    Research Scientist, Regulatory Compliance Specialist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 190000 - 230000 USD Yearly USD 190000.00 230000.00 YEAR
Job Description & How to Apply Below

#2675 Director Analytical Research and Development

Transformational Position Alert

Global pharmaceutical company seeks technical subject matter expert in drug substance development who also can lead a team from clinical to commercial capabilities

Director of Analytical Research and Development. Direct supervision of the Analytical Associate Directors, plus full-time high level analytical scientists, as applicable. Responsible for organizing the workload of Analytical group personnel by coordinating with Analytical Associate Directors and Analytical project managers/leaders. Prepare and review proposals for new and existing projects and manage projects as needed. Experimental skills related to Analytical development and technologies are a must.

Serve as a principal subject matter expert to the company.

Responsibilities
  • Works closely with the Site Head, the Senior Director of Chemical Development, the Senior Director Quality, and other site leadership to ensure successful completion of ongoing work.
  • Aggressive and diligent leadership and management of programs according to established and adjusted timelines.
  • Direct management responsibility for all Analytical resources.
  • Direct point of contact with customers for project-related communications and coordination.
  • Work closely with other R&D groups, Project Management and other staff to coordinate project progress and resource usage.
  • Project quoting, budgeting, invoicing, and reconciliation.
  • Customer interactions including project discussions and updates, customer visits, contract negotiations, and dispute negotiations.
  • Actively promote the results of the scientific projects within the group and to the customers.
  • Maintain current knowledge of state-of-the-art of chemistry, analytical chemistry, technology, and cGMP regulations. Apply this knowledge to daily problems and ongoing work activities.
  • Maintain current knowledge of regulations and guidances as applicable to Analytical testing and characterization of pharmaceutical products (FDA, ICH, USP, EP, JP etc.)
  • Work to ensure that a spirit of teamwork, cooperation, and can-do attitude always exists within the department.
  • Possess expert knowledge of laboratory PPE expectations.
  • Possess expert knowledge of Analytical Chemistry and be a knowledge resource for the company and for customers.
  • Project management and ensuring timelines are met
  • Works closely with other site management to provide long-range business planning and guidance
  • Thorough knowledge of and experience working under cGMP regulations
  • Excellent publication/patent record
Qualifications/Skills
  • Deep technical expertise in Analytical Chemistry, with extensive application to active pharmaceutical ingredients (APIs) in a regulated environment
  • Exceptional communication and interpersonal skills, with the ability to influence, collaborate, and build strong relationships across diverse teams and leadership levels
  • Strong organizational and problem-solving capabilities, with a focus on delivering results
  • Demonstrated ability to operate independently while aligning to organizational priorities and achieving key business objectives
  • Strong commitment to talent development, including coaching, mentoring, and building high-performing teams through effective knowledge transfer
Experience Requirements
  • Ph.D. in Analytical Chemistry or a related discipline with a minimum of 10 years of relevant experience; alternatively, an M.S. with 15+ years or a B.S. with 20+ years of experience in pharmaceutical chemical process development
  • Demonstrated management experience within a pharmaceutical chemical process development or manufacturing environment
  • Proven expertise in quality control, regulatory compliance, scheduling, and organizational execution, with the ability to apply sound judgment and insight
  • Extensive experience with common analytical techniques and instrumentation (e.g., HPLC, GC, LC/GC-MS, IR)
  • In-depth knowledge of compendial methods (USP, EP, JP), technical application testing, and out-of-specification (OOS) investigations
  • Strong proficiency in developing, interpreting, and implementing standard operating procedures (SOPs)
  • Ability to serve as a technical expert and consultant, providing guidance across cross-functional teams
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