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Ppd 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 ...

Zentalis

Director Product Development

San Diego, CA · On-site

DIRECTOR PRODUCT DEVELOPMENT Zentalis is a clinical oncology innovator developing a treatment ... Master's degree in pharmaceutical sciences, chemistry, chemical engineering or relevant area. * 8+ ...

inteplast

PRODUCT DEVELOPMENT TECHNICIAN

Hollywood, FL · On-site

Product Development Technician A POSITION OBJECTIVE: Responsible for assisting the Product ... Working knowledge of pharmaceutical or nutraceutical formulation and PD processes and techniques ...

Arclin

Product Development Chemist

Moncure, NC

... pharmaceuticals. These vital, everyday products can't fail, and we're here to give the world an ... Product Development Chemist, Moncure, NC Arclin, Inc. is currently seeking talent for a Product ...

Arclin

Product Development Chemist

Moncure, NC · On-site

... pharmaceuticals. These vital, everyday products can't fail, and we're here to give the world an ... Product Development Chemist, Moncure, NC Arclin, Inc. is currently seeking talent for a Product ...

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Ppd Pharmaceutical Product Development information

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How much do ppd pharmaceutical product development jobs pay per year?

As of Aug 7, 2026, the average yearly pay for ppd 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 kind of jobs are PPD Pharmaceutical Product Development careers?

PPD Pharmaceutical Product Development careers include roles such as clinical research associates, project managers, data managers, regulatory affairs specialists, and laboratory scientists. These jobs typically require knowledge of drug development processes, regulatory standards, and proficiency with industry tools and software, often involving teamwork in a regulated environment.

What are the key skills and qualifications needed to thrive in the PPD Pharmaceutical Product Development position?

To thrive in Pharmaceutical Product Development at PPD, you need a solid background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant degree. Experience with laboratory information management systems (LIMS), good manufacturing practices (GMP), and regulatory compliance certifications such as ICH or FDA guidelines is commonly required. Strong attention to detail, problem-solving abilities, and effective teamwork and communication skills set top candidates apart. These competencies ensure accurate development of pharmaceutical products, adherence to regulations, and productive collaboration across multidisciplinary teams.

What is a PPD Pharmaceutical Product Development?

A PPD Pharmaceutical Product Development job typically involves working in clinical research, drug development, or laboratory services to support pharmaceutical and biotech companies. Employees in these roles may conduct clinical trials, analyze data, ensure regulatory compliance, or develop new drug formulations. Positions can range from clinical research associates and project managers to scientists and data analysts. PPD professionals play a critical role in bringing safe and effective drugs to market.

What does a typical day look like for someone working in PPD Pharmaceutical Product Development?

A typical day in Pharmaceutical Product Development at PPD involves designing and executing experiments, analyzing data, and collaborating closely with cross-functional teams such as regulatory affairs, quality assurance, and manufacturing. You'll often participate in project meetings to discuss timelines, troubleshoot technical issues, and ensure alignment with client and regulatory requirements. Documentation of findings, preparation of reports, and contributing to submissions for regulatory approvals are also common tasks. The fast-paced environment requires flexibility and proactive communication to drive projects forward and adapt to evolving priorities.

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Ppd Pharmaceutical Product Development jobs near you
Infographic showing various Ppd Pharmaceutical Product Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.

Director Drug Product Development

Clinical Dynamix, Inc.

Jersey City, NJ

$195K - $230K/yr

Full-time

Re-posted yesterday

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.