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Director Drug Product Formulation Development Jobs in Kentucky

Servier

Assoc Director, Oral Solid Drug Product

Boston, KY · On-site

$198K - $207K/yr

The Associate Director, Oral Solid Drug Product serves as the technical subject matter expert for ... drug product formulation and process development and manufacturing support including experience ...

Servier

Assoc Director, Oral Solid Drug Product

Boston, KY · On-site

$198K - $207K/yr

The Associate Director, Oral Solid Drug Product serves as the technical subject matter expert for ... drug product formulation and process development and manufacturing support including experience ...

gpac

Entry-Level Nutritionist

Bowling Green, KY · On-site

... formulation development, and quality initiatives within their pet food manufacturing operations. This role will work cross-functionally with quality, production, and procurement teams to ensure pet ...

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Director Drug Product Formulation Development information

What does a director drug product formulation development do?

A Director of Drug Product Formulation Development leads teams responsible for designing and optimizing pharmaceutical formulations, ensuring that drugs are safe, effective, and manufacturable at scale. This role involves overseeing the development of drug products from early-stage research through to clinical trials and commercial manufacturing. The director collaborates with cross-functional teams, manages regulatory compliance, and ensures that product development aligns with company goals and industry standards.

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

To thrive as a Director of Drug Product Formulation Development, you need an advanced degree in pharmaceutical sciences or a related field, extensive experience in formulation development, and a deep understanding of regulatory requirements. Familiarity with analytical instrumentation, formulation software, and quality management systems, as well as certifications like PMP or Six Sigma, are highly beneficial. Strong leadership, strategic thinking, and cross-functional communication skills set outstanding candidates apart. These competencies ensure the successful development, optimization, and regulatory approval of drug products in a highly competitive and regulated environment.

What are some typical challenges faced by a director drug product formulation development, and how are they addressed within the team?

A Director of Drug Product Formulation Development often encounters challenges such as balancing innovative formulation approaches with regulatory compliance, managing cross-functional timelines, and ensuring scalability from laboratory to commercial manufacturing. Addressing these challenges typically involves close collaboration with analytical, regulatory, and manufacturing teams to align goals and troubleshoot issues early. Open communication, regular project reviews, and fostering a culture of continuous learning help the team adapt quickly to evolving project requirements and industry standards.

What are popular job titles related to Director Drug Product Formulation Development jobs in Kentucky?

For Director Drug Product Formulation Development jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching Director Drug Product Formulation Development jobs in Kentucky look for?

The top searched job categories for Director Drug Product Formulation Development jobs in Kentucky are:

What cities in Kentucky are hiring for Director Drug Product Formulation Development jobs?

Cities in Kentucky with the most Director Drug Product Formulation Development job openings:

Director Drug Product Formulation Development jobs near you
Infographic showing various Director Drug Product Formulation Development job openings in Kentucky as of June 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Assoc Director, Oral Solid Drug Product

Servier

Boston, KY • On-site

$198K - $207K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

About Servier
With commercial stage products and a promising pipeline, we are Servier Group, a unique global organization headquartered in France. Operating in more than 150 countries and governed by a non-profit foundation, we have multiple medicines approved in oncology, cardiology, and other therapeutic areas.
Servier's 2030 Ambition aims to establish the Group as a recognized, innovative, and patient-centered leader in Oncology, Neurology, and Cardiometabolism & Venous Diseases (CMVD). Over half of our research and development efforts are focused on targeted therapies to address unmet patient needs.
Within Servier Industry, the Manufacturing Science and Analytical Technology (MSAT) organization plays a key role in driving technical excellence, industrial transformation, and lifecycle management - enabling manufacturing robustness, quality, and compliance across all product modalities and technologies.
Role Summary
Within MSAT, the Oral Solid Drug Product team is responsible for providing technical stewardship and manufacturing science support across oral solid drug product lifecycle.
The Associate Director, Oral Solid Drug Product serves as the technical subject matter expert for Onco/Neuro Oral Solid products reporting to the MSAT Oral Solid Drug Product Onco/Neuro Lead. This role provides scientific and process expertise to support the manufacturing and lifecycle management of Oncology and Neurology related oral solid drug products across internal and external manufacturing sites.
Primary Responsibilities
Technical Oversight of Internal and External Manufacturing Processes
  • Provide technical oversight of manufacturing processes for assigned oral solid commercial products at Servier internal sites in collaboration with Site MSAT and at external partners (CMOs) as part of Virtual Plant Teams
  • Lead internal cross-functional Technical Teams to facilitate drug product related technical topics in collaboration with other functions
    • Prepare and manage meeting agendas, minutes, and action follow-up
    • Facilitate alignment on technical project timelines, supply impact, and budget considerations.
  • Lead or support deviation investigations, root cause analyses, and CAPA definition for process-related issues, ensuring robust closure and knowledge transfer.
  • Maintain and oversee process monitoring and Continued Process Verification (CPV) for assigned commercial products across manufacturing sites.
  • Build and maintain MSAT knowledge repository for assigned commercial products and processes

Technology Transfer and Lifecycle Management
  • Lead or support tech transfers, scale changes, PPQ, and launch readiness activities across global sites.
  • Conduct and document process fit assessments, risk evaluations, and FMEA as part of the lifecycle management strategy.
  • Participate in process optimization efforts, including yield, throughput, and quality performance improvements across the network.

CMC and Regulatory Support
  • Author or review CMC-related sections of regulatory submissions (e.g., post-approval changes, variations, new market filings as needed).
  • Support Regulatory CMC in responding to health authority questions related to commercial manufacturing processes and controls.
  • Ensure manufacturing and validation strategies are aligned with GMP, ICH, and global regulatory expectations.

Subject Matter Expertise and Continuous Improvement
  • Support implementation and optimization of manufacturing processes and related control/sampling strategies (e.g., granulations, compression, coating, pellet layering, capsule filling, segregation control measures).
  • Specify and support qualification/optimization of tooling and equipment such as: tablet presses, precision capsule fillers for pellets, fluid-bed coaters, high-shear granulators, roller compactors, and containment/segregation equipment.
  • Anticipate scale-dependent challenges (e.g., compression dwell time effects, layer adhesion, segregation during handling) and define scale-up acceptance criteria, equivalence studies and narrative for regulatory dossiers.
  • Recommend and deploy PAT tools where beneficial (NIR, weight/force monitoring, in-line content estimation) for real-time or near-real-time assurance of processes
  • Perform risk and criticality assessments to identify gaps and define improvements in line with quality, regulatory, and business expectations.
  • Stay current with industry trends, scientific literature, and evolving technologies related to OSD manufacturing and MSAT best practices.

Education and Required Skills
  • Bachelor's Degree in Pharmaceutical Sciences, Chemical Engineering or related technical field with minimum of 8 years relevant experience, or preferably a Masters or PhD in Pharmaceutical Sciences, Chemical Engineering or related technical field with a minimum of 6 years of relevant experience in drug product formulation and process development and manufacturing support including experience with regulatory submissions
  • In-depth knowledge of formulation concepts/techniques across immediate-release and extended-release oral solid dosage forms and relevant manufacturing processes, e.g., blending, granulation including dry/roller compaction and wet/high-shear/fluid bed technologies, tablet compression, tablet coating, capsule filling
  • In-depth knowledge of primary container closure components used for oral solid dosage forms
  • Expertise in use/application of basic statistical methodologies and software (e.g., Minitab, JMP or equivalent)
  • Expertise in use/application of variety of problem-solving tools e.g. Ishikawa, Kepner-Tregoe (KT), five-whys, etc.
  • Experience leading or supporting tech transfers, deviation investigations, change controls, and regulatory documentation.
  • Strong knowledge of GMP, ICH guidelines, and regulatory submission expectations for commercial products.
  • Comfortable working in a global matrixed team with cross-functional collaboration across Quality, Manufacturing, Supply Chain, and Regulatory.
  • Strong ability to strategically plan, organize, and manage multiple projects simultaneously
  • Excellent written/oral communication and presentation skills
  • Excellent communication and documentation skills; able to interface effectively with internal stakeholders and external partners.
  • A continuous improvement and learning mindset, aligned with Servier's strategic direction and patient-first values.

Travel and Location
  • Domestic and international travel up to 20%
  • If based in Massachusetts, hybrid (2-3 days in our Boston office) preferred. Open to remote candidates.

Job Description
Candidate Profile
Servier's Commitment
Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Salary Range
The salary range for this role is $162,000 - $185,000. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Employees in this position are also eligible for Short-Term and Long-Term incentive programs. Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements). For more information on our benefits, please visit this link.

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