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Pharmaceutical Product Development Jobs (NOW HIRING)

Colorcon

Product Development Engineer

Belen, NM · On-site

Our focus on market issues and technology development has earned Colorcon an international reputation as a pharmaceutical supplier of choice. That reputation is based on superior product quality ...

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How much do pharmaceutical product development jobs pay per year?

As of Jun 1, 2026, the average yearly pay for pharmaceutical product development in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What is a Pharmaceutical Product Development job?

A Pharmaceutical Product Development job involves researching, designing, and testing new drugs to ensure safety, efficacy, and regulatory compliance. Professionals in this role collaborate with scientists, regulatory agencies, and manufacturing teams to bring medications from concept to market. Responsibilities may include preclinical and clinical trials, formulation development, and quality assurance. This role requires expertise in chemistry, biology, pharmacology, and regulatory affairs to meet industry standards.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Product Development position, and why are they important?

Pharmaceutical Product Development professionals require a background in chemistry, pharmacology, or a related scientific field, typically with a bachelor's or advanced degree. Familiarity with industry-standard tools such as laboratory information management systems (LIMS), statistical analysis software, and regulatory documentation systems is essential, as well as certifications like Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP). Strong project management, problem-solving abilities, and effective communication skills help individuals excel in cross-functional teams and fast-paced environments. These competencies ensure successful product formulation, regulatory compliance, and timely advancement of pharmaceutical projects.

What are the typical career growth opportunities for someone in Pharmaceutical Product Development?

Pharmaceutical Product Development offers a variety of career advancement paths, including progression to senior scientist, project manager, or leadership roles within research and development teams. With experience, professionals can also specialize in areas such as regulatory affairs, quality assurance, or clinical trial coordination. Many organizations encourage ongoing education and certifications, which can open doors to advanced technical or management positions. The collaborative nature of this field also allows you to build a strong professional network and gain exposure to multiple facets of the pharmaceutical industry, supporting long-term career development.

What is product development in the pharmaceutical industry?

Product development in the pharmaceutical industry involves designing, testing, and bringing new drugs or formulations to market. It includes stages such as research, preclinical testing, clinical trials, and regulatory approval, requiring collaboration among scientists, regulatory experts, and quality assurance teams.
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Pharmaceutical Product Development jobs near you
Infographic showing various Pharmaceutical Product Development job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 22% Physical, 11% Hybrid, and 67% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.
Director, Pharmaceutical Development

Director, Pharmaceutical Development

Fulcrum Therapeutics

Cambridge, MA • On-site

$240K/yr

Full-time

Posted 23 days ago

Job description

Company Overview
Fulcrum Therapeutics, Inc. ("Fulcrum") [NASDAQ: FULC] is a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases. Fulcrum is deeply committed to bringing hope and new options to patients suffering from rare hematologic disorders and is developing a pipeline of clinical and preclinical assets. Fulcrum's lead clinical asset is pociredir, a first-in-class small molecule designed to increase the expression of fetal hemoglobin for the treatment of sickle cell disease and other hemoglobinopathies. We are working to expand our portfolio of clinical-stage assets and seek a driven and strategic leader to head our Pharmaceutical Development function.
Description
Reporting to the Head of Technical Operations, the Director of Pharmaceutical Development will lead all drug product development activities including technical, managerial, and budgetary aspects. This includes formulation development, manufacture of clinical trial material, process optimization, scale-up, and validation. The successful candidate will lead, plan and manage the technical and business-related activities associated with drug product development and manufacturing at contract development and manufacturing vendors for all dosage form programs.
Key Responsibilities
  • Lead all strategic and tactical aspects of drug product development at Fulcrum
  • Design and execute pharmaceutical product development plans for all development programs in accordance with corporate goals
  • Collaborate with colleagues in Drug Substance, Analytical, ClinOps, QA, and Reg CMC to ensure plans are cross-functional, phase-appropriate, and on time
  • Lead pharmaceutical development for the pociredir program, including CTM for pivotal clinical studies, pre-validation studies, validation plans, and commercial launch supply
  • Lead and manage product development, technology transfer, and clinical manufacturing activities at contract manufacturing organizations (CMOs), assuring compliance with Regulatory and Quality requirements
  • Lead pediatric formulation development efforts, as required
  • Review and approve a broad spectrum of documents (MBRs, Specifications, Protocols, Reports, etc.) at CMOs
  • Generate, review and approve documents related to Drug Product (formulation, process development, manufacturing, etc.) for Regulatory submissions (IND/IMPD and NDA/MAA)

Qualifications
  • D with 10 years or MS with equivalent years of experience. Professional background in Pharmaceutical Sciences (preferred) or Chemical Engineering
  • Proven track record and leadership in phase-appropriate drug development through pivotal studies (required) and approval (preferred)
  • SME in material science aspects of dosage forms and drug delivery, with emphasis on solid oral dosage forms; strong knowledge in Dissolution, Biopharmaceutics and PK
  • Well versed in Regulatory CMC and ICH guidance, including exposure to FDA interactions (e.g. via EOP2 or preNDA meetings)
  • Strong written and oral communication skills; highly effective collaborator with "customers" in ClinOps and Commercial
  • Ability to hire and recruit staff, including key contractors and consultants
  • Positive work presence; responds to stress and ambiguity with humor

Base Salary Pay Range
$240,000-$240,000 USD

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