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How much do director pharmaceutical formulation jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for director pharmaceutical formulation in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $22.84 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Pharmaceutical Formulation, and why are they important?

To thrive as a Director of Pharmaceutical Formulation, you need advanced expertise in pharmaceutical sciences, formulation development, and regulatory knowledge, typically supported by a PhD or MS in pharmacy, chemistry, or related fields. Familiarity with analytical instrumentation, formulation software, and regulatory submission systems (like CTD/eCTD) is crucial. Leadership, strategic thinking, and strong project management abilities help drive innovation and coordinate multidisciplinary teams. These skills ensure the successful development of safe, effective drug products while meeting compliance and business objectives.

What does a Director of Pharmaceutical Formulation do?

A Director of Pharmaceutical Formulation oversees the development and optimization of drug formulations, ensuring products meet quality, safety, and regulatory standards. They lead teams of scientists and coordinate cross-functional efforts to bring new pharmaceutical products from concept to market. This role involves managing formulation strategies, troubleshooting technical issues, and collaborating with regulatory, manufacturing, and quality assurance departments. Additionally, they are responsible for staying updated on industry trends and advancing innovative formulation technologies.

What are the main challenges a Director of Pharmaceutical Formulation faces when leading cross-functional teams?

A Director of Pharmaceutical Formulation often encounters challenges related to coordinating efforts between R&D, quality assurance, regulatory affairs, and manufacturing departments. Balancing innovative formulation development with strict compliance requirements and tight project timelines requires strong communication and project management skills. Additionally, adapting to evolving regulatory guidelines and ensuring seamless technology transfer can add complexity to the role. Success in this position depends on fostering collaboration, maintaining clear documentation, and aligning team objectives with the organization's strategic goals.
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Director Pharmaceutical Formulation jobs near you
Infographic showing various Director Pharmaceutical Formulation job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Temporary. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $47,488 per year, or $22.8 per hour.
Pharmaceutical Formulation Technician

Pharmaceutical Formulation Technician

TriOptus LLC

Wilson, NC • On-site

Other

Posted 13 days ago

Job description

Pharmaceutical Formulation Technician
Wilson, NC - Onsite
Duration - 6-months assignment with possibility for extension
Onsite - 2nd shift (4pm- 2:30am, M-Th)
Manufacturing Pharmaceutical Technician
(Granulation/Blend/Bead Coating)
Job Summary
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.
Primary Responsibilities
  • Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
  • Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
  • Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
  • Identify, report, and resolve quality issues.
  • Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
  • Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
  • Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
  • Report accidents and unsafe conditions or unusual circumstances to supervisor.
  • Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
  • Actively participate in Production team and Site communication meetings.
  • Maintain regular and punctual attendance; work overtime as required.
  • Support GMP investigations and events.
  • Identify and report potential GMP impacting situations.
  • Contribute to Standard Operating Procedure (SOP) writing in your technical area.

Education and Experience Requirements
  • High School Diploma or equivalent.
  • Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.

Necessary Knowledge, Skills, and Abilities
  • General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
  • Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.

Supervisor Responsibilities (if applicable)
  • The Pharmaceutical Technician has no direct reports.

Additional Information/General/Organizational
  • Quality/Compliance: Achieve a standard of excellence with work processes and outcomes while maintaining compliance with policies and all regulatory requirements.
  • Communication: Clear, accurate, effective and timely written and verbal communication. Strong attention to detail and ability to write and record data legibly and accurately in accordance to cGMP regulations.
  • Teamwork/Collaboration: Work effectively with others to achieve goals, build strong working relationships and a positive work environment.
  • Critical thinking/problem solving: general ability to collect, organize and analyze data. Ability to recognize, analyze and solve a variety of problems.
  • Initiative: Ability to take ownership of work, doing what is needed without being asked and appropriate follow-through.
  • Adaptability: Being receptive to feedback, willingness to learn, and open to continuous improvement.
  • Operational Excellence: Embrace and support Operational Excellence Culture and Initiatives.
  • Accountability: Demonstrate ambition and discipline to achieve organizational and career goals
  • Availability: To work site schedule of 10.5 hours a day, Monday-Thursday and overtime as needed.

Physical and Environmental Requirements
  • Occasionally move/traverse, ascend/descend step ladders, stairs, and/or platforms.
  • Wear appropriate Personal Protective Equipment including PAPR (Powered Air Purifying Respirator).
  • Occasionally, transport materials using manual and power assisted vehicles including manually pushing and pulling drums, totes, boxes, and pallets.
  • Lift and maneuver empty drums weighing up to 40 pounds up to five times per day; push and maneuver drums containing product weighing up to 275 pounds up to five times per day.
  • Perform cleaning and assembly/disassembly on production equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts may weigh up to 50 pounds.
  • Ability to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.

Additional Information
  • Relocation is not offered for this position.

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