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Pharmaceutical Developer Jobs (NOW HIRING)

Actalent

Pharmaceutical Operator

Stratford, CT

$25 - $30/hr

We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing ® winner for both client and talent service. The ...

Jubilant Pharma, LLC

Join a Leader in Pharmaceutical Manufacturing -- And Build What's Next As Spokane's Largest ... The engineer will also contribute technical direction for complex projects and exhibit clear ...

Jubilant Pharma, LLC

Join a Leader in Pharmaceutical Manufacturing -- And Build What's Next As Spokane's Largest ... The Project Engineer III provides pharmaceutical engineering expertise primarily in the area of ...

Jubilant Pharma, LLC

Engineer I, Project

Spokane, WA · On-site

Join a Leader in Pharmaceutical Manufacturing -- And Build What's Next As Spokane's Largest ... The engineer will also contribute technical direction for complex projects and exhibit clear ...

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How much do pharmaceutical developer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for pharmaceutical developer in the United States is $52.84, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $64.66 per hour, depending on experience, location, and employer.

What is a pharmaceutical developer?

Pharmaceutical developers are professionals who design, create, and test new medications and drug therapies. They work on the research and development of pharmaceuticals, ensuring that new drugs are safe, effective, and meet regulatory standards. Their work involves a combination of biology, chemistry, and clinical trials to bring new treatments from the laboratory to the market. Pharmaceutical developers often collaborate with scientists, regulatory agencies, and manufacturers throughout the drug development process.

What are the main challenges a pharmaceutical developer faces during the drug development process?

Pharmaceutical Developers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing lengthy development timelines. Balancing innovation with compliance is crucial, as each stage— from research and formulation to clinical trials— involves rigorous testing and documentation. Collaboration with cross-functional teams like regulatory affairs, quality assurance, and clinical researchers is essential to successfully advance a drug candidate through each development phase.

What are the key skills and qualifications needed to thrive as a pharmaceutical developer, and why are they important?

To thrive as a Pharmaceutical Developer, you need a solid background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree. Familiarity with analytical instruments, Good Laboratory Practice (GLP), regulatory compliance systems, and data analysis software is crucial. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills help set outstanding professionals apart. These competencies ensure the safe, efficient, and compliant development of new medications in a highly regulated industry.

What is the difference between Pharmaceutical Developer vs Pharmaceutical Scientist?

AspectPharmaceutical DeveloperPharmaceutical Scientist
Required CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fieldBachelor's, Master's, or PhD in Pharmaceutical Sciences, Chemistry, or related field
Work EnvironmentLaboratories, R&D departments, manufacturing settingsResearch labs, academic institutions, pharmaceutical companies
Employer & Industry UsagePharmaceutical companies, biotech firms, R&D centersResearch institutions, pharmaceutical companies, academia
Common Search & ComparisonYesYes

Pharmaceutical Developers focus on designing, developing, and optimizing new drug formulations and delivery methods, often working closely with manufacturing. Pharmaceutical Scientists conduct research to understand drug properties, mechanisms, and efficacy, primarily in laboratory or academic settings. While both roles require similar educational backgrounds and work within the pharmaceutical industry, their core responsibilities differ: development versus scientific research.

How do you become a pharmaceutical developer?

To become a pharmaceutical developer, individuals typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, followed by relevant experience or advanced degrees such as a master's or Ph.D. in pharmaceutical sciences or medicinal chemistry. Skills in laboratory research, knowledge of drug development processes, and familiarity with regulatory requirements are essential for success in this role.

How much do pharmaceutical developers make?

Pharmaceutical developers typically earn a median annual salary of around $80,000 to $120,000, depending on experience, education, and location. Senior roles or those with specialized skills in drug formulation or regulatory affairs can earn higher salaries, often exceeding $150,000 annually.

What cities are hiring for Pharmaceutical Developer jobs?

Cities with the most Pharmaceutical Developer job openings:

What states have the most Pharmaceutical Developer jobs?

States with the most job openings for Pharmaceutical Developer jobs include:

What are popular job titles related to Pharmaceutical Developer jobs?

For Pharmaceutical Developer jobs, the most frequently searched job titles are:

Pharmaceutical Developer jobs near you
Infographic showing various Pharmaceutical Developer job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 2% Part Time, and 14% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.

Senior Pharmaceutical CQV Engineer / Lead (Citizen or Residents only / Anywhere from US - Multiple L

Thousand Oaks, CA • On-site

JSB Staffing Solutions, Pvt. Ltd.
See more jobs at JSB Staffing Solutions, Pvt. Ltd.external

Other

Posted 20 days ago

Key responsibilities

  • Lead and execute CQV activities for pharmaceutical and biotech capital projects.

  • Develop and execute commissioning plans, IQ/OQ/PQ protocols, validation test scripts, traceability matrices, and summary reports.

  • Coordinate field execution activities, perform system walkdowns, review turnover packages, and support validation documentation to ensure compliance with cGMP, FDA, ISPE, and GAMP guidelines.

Job description

Pharmaceutical Senior CQV Engineer position is a direct hire which is expected to be on-site in Thousand Oaks, CA (Onsite).

Summary

We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations.

This role requires hands-on technical expertise, strong project coordination skills, and a thorough understanding of FDA and cGMP compliance requirements. The Senior CQV Engineer will work cross-functionally with Engineering, Quality, Manufacturing, Automation, and external vendors to ensure successful project execution and operational readiness within fast-paced life sciences environments.

Key Responsibilities

  • Lead and execute CQV activities for pharmaceutical and biotech capital projects.
  • Develop and execute:
    • Commissioning plans
    • IQ/OQ/PQ protocols
    • Validation test scripts
    • Traceability matrices
    • Summary reports
  • Support startup and qualification of:
    • Process equipment
    • Clean utilities
    • HVAC systems
    • Manufacturing suites
    • Automation and control systems
  • Coordinate field execution activities with engineering, construction, vendors, and operations teams.
  • Perform system walkdowns and turnover package reviews.
  • Support deviation investigations, CAPAs, and change control activities.
  • Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines.
  • Participate in FAT/SAT execution and acceptance activities.
  • Support project schedule development and milestone tracking.
  • Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and successful system release.
  • Mentor junior CQV engineers and validation specialists as needed.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related technical discipline.
  • 5-10+ years of CQV, validation, or pharmaceutical engineering experience within GMP-regulated environments.
  • Strong knowledge of:
    • cGMP regulations
    • FDA validation requirements
    • ISPE Baseline Guides
    • GAMP 5 principles
  • Experience executing commissioning and qualification for:
    • Process equipment
    • Utilities
    • HVAC systems
    • Cleanrooms
    • Automation systems
  • Experience authoring and reviewing validation lifecycle documentation.
  • Strong technical writing and documentation skills.
  • Ability to work independently within fast-paced project environments.

Preferred Qualifications

  • Experience in biologics, sterile manufacturing, fill-finish, or aseptic processing environments.
  • Previous consulting experience within life sciences industries preferred.
  • Familiarity with:
    • DeltaV
    • MES systems
    • SCADA platforms
    • Kneat or electronic validation systems
  • PMP certification or equivalent project leadership experience is a plus.
  • Strong client-facing communication and leadership skills.

Additional Skills & Competencies

  • Excellent organizational and multitasking abilities
  • Strong problem-solving and analytical skills
  • Ability to manage multiple priorities and deadlines
  • Comfortable working in both office and field environments
  • Ability to travel to client sites as required

Apply