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Drug Product Jobs (NOW HIRING)

FUJIFILM Biotechnologies

As Associate Director, Drug Product Manufacturing, you will build and lead a new organization to achieve GMP readiness, onboard customers, and drive operational excellence across formulation, aseptic ...

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Drug Product information

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$51.5K

$159.4K

$197K

How much do drug product jobs pay per year?

As of Jul 28, 2026, the average yearly pay for drug product in the United States is $159,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,000.00 and $197,000.00 per year, depending on experience, location, and employer.

What is a Drug Product?

A drug product refers to a finished dosage form that contains an active pharmaceutical ingredient (API) along with other inactive ingredients, known as excipients. It is manufactured to be administered to patients for the diagnosis, cure, mitigation, treatment, or prevention of diseases. Examples include tablets, capsules, injections, and ointments. Drug products must meet regulatory standards for safety, efficacy, and quality before they can be marketed and used by the public.

What are the key skills and qualifications needed to thrive as a Drug Product Specialist, and why are they important?

To thrive as a Drug Product Specialist, a strong background in pharmaceutical sciences, formulation development, and regulatory compliance—often supported by a relevant degree—is essential. Familiarity with laboratory equipment, quality management systems (QMS), and regulatory submission tools such as eCTD is typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills in this role. These competencies ensure safe, effective product development and regulatory approval, which are critical to patient safety and business success.

What are the typical challenges faced when working in a Drug Product development role?

Professionals in Drug Product development often encounter challenges such as balancing strict regulatory requirements with tight project timelines, managing cross-functional collaboration with formulation scientists, analytical chemists, and manufacturing teams, and adapting to evolving technologies and methodologies. It's common to work in a fast-paced environment where priorities can shift quickly, requiring strong organizational and communication skills. Additionally, troubleshooting formulation or stability issues and ensuring scalability from lab to manufacturing are frequent aspects of the role.

What is the difference between Drug Product vs Drug Development Specialist?

AspectDrug ProductDrug Development Specialist
CredentialsPharmacy, pharmaceutical sciences, or related degreePharmacy, chemistry, or pharmaceutical sciences
Work EnvironmentManufacturing facilities, quality control labsResearch labs, clinical trial settings
Industry UsageManufacturing, quality assurance, regulatory complianceResearch, formulation, clinical development

Drug Product professionals focus on the manufacturing, quality, and regulatory aspects of finished pharmaceutical products. In contrast, Drug Development Specialists are involved in the research, formulation, and clinical testing phases of new drugs. Both roles require similar educational backgrounds but differ in their focus within the drug lifecycle and work environments.

More about Drug Product jobs
What cities are hiring for Drug Product jobs? Cities with the most Drug Product job openings:
What states have the most Drug Product jobs? States with the most job openings for Drug Product jobs include:
What job categories do people searching Drug Product jobs look for? The top searched job categories for Drug Product jobs are:
Drug Product jobs near you
Infographic showing various Drug Product job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $159,405 per year, or $76.6 per hour.

Director Drug Product Development

Clinical Dynamix, Inc.

Jersey City, NJ • On-site

$195K - $230K/yr

Full-time

Posted 21 days ago

Job description

Client is seeking an experienced Director, Drug Product Development, to be based in their Northern NJ Office. This role will lead drug product strategy and execution across our clinical-stage portfolio, supporting the advancement of innovative therapies for patients with serious rare diseases.

Position Summary:

The Director, Drug Product Development will lead formulation, manufacturing, and lifecycle activities for drug product candidates from development through clinical-stage execution. This role partners across CMC, Quality, Regulatory, Supply Chain, and external manufacturers to ensure drug products are robust, scalable, and aligned with program timelines and regulatory requirements.

Responsibilities:

· Drug Product Development Strategy: Lead drug product development strategy across the clinical-stage portfolio, including formulation design, process development, manufacturability, and lifecycle planning.

  • Formulation & Clinical Supply Execution: Develop and optimize scalable dosage forms and manufacturing processes to support clinical studies, technical transfers, and reliable product supply. Conduct drug product risk assessment and develop risk mitigation plans.
  • External Manufacturing Leadership: Select, oversee, and manage CDMOs, CMOs, and other external partners to ensure timely execution, quality performance, and alignment with program objectives.
  • CMC Regulatory Support: Contribute to CMC strategy and author, review, or support regulatory submissions and responses, amendments, briefing documents, and other health authority interactions as needed.
  • Cross-Functional Program Leadership: Partner closely with Analytical Development, Drug Substance, Quality, Regulatory, Clinical Operations, and Supply Chain to align technical plans with development timelines, budgets, and program priorities.
  • Technical Representation & Governance: Represent drug product development in internal governance forums and external meetings with manufacturers, auditors, consultants, and development partners, serving as a key technical leader for product-related decisions.

Requirements and Preferred Skills:

· Ph.D. in Pharmaceutical Sciences, Chemical Engineering, or related Physical Sciences with at least 12 years of experience, or M.S. with 15 years of experience working in drug product development in the pharmaceutical or biotechnology industry.

  • In-depth knowledge and hands-on experience leading drug product development and CMC activities for small molecule programs in a clinical-stage biotechnology or pharmaceutical environment.
  • Demonstrated success advancing programs through key development milestones, including clinical trial supply, process scale-up, technology transfer, and regulatory submissions.
  • Strong working knowledge of CMC regulatory requirements and development expectations for IND-enabling and clinical-stage programs. Proven experience writing CMC drug product sections in regulatory submissions.
  • Experience managing CDMOs, CMOs, and other external development and manufacturing partners, with the ability to drive accountability, timelines, and quality outcomes.
  • Broad cross-functional CMC expertise, with the ability to work effectively across Drug Substance, Analytical, Quality, Regulatory, Supply Chain, and Clinical teams.
  • Excellent written and verbal communication skills, including the ability to communicate complex technical issues clearly to internal and external stakeholders.
  • Strong leadership, judgment, and problem-solving skills, with the ability to operate effectively in a fast-paced, resource-conscious, entrepreneurial environment.
  • Proven ability to build productive relationships with external partners, consultants, and scientific advisors.
  • Experience mentoring team members and contributing to a collaborative, high-accountability culture is preferred.