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Formulation Manager Jobs (NOW HIRING)

Director of Formulation

Boca Raton, FL · On-site

$110K - $145K/yr

... manage and influence decision-making to ensure supply and achieve the company's goals. * Work ... Deep passion for hands-on formulation development work in our innovation lab. * Formulate products ...

... manage and influence decision-making to ensure supply and achieve the company's goals. * Work ... Deep passion for hands-on formulation development work in our innovation lab. * Formulate products ...

Formulation Chemist The Chemist II is responsible for product development and testing activities ... Strong organizational and time management skills. * Ability to research and write scientific ...

New

Formulation Chemist Mativ is a global leader in specialty materials headquartered in Alpharetta ... When applicable, manage internal process improvement projects, including but not limited to raw ...

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Formulation Manager information

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How much do formulation manager jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for formulation manager 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 is a formulation manager?

Formulation Managers are professionals responsible for overseeing the development and optimization of product formulations, particularly in industries like pharmaceuticals, cosmetics, food, and chemicals. They lead teams to design, test, and refine product mixtures to meet quality, safety, and regulatory standards. Their role often involves coordinating with research, production, and quality assurance departments to ensure that product formulations are effective, stable, and cost-efficient. Formulation Managers also stay updated on industry trends and regulatory changes to keep their company's products competitive. Effective communication, project management, and technical expertise are key skills for this role.

What are some common challenges faced by a formulation manager in coordinating cross-functional teams?

Formulation Managers often work closely with R&D, quality assurance, regulatory, and production teams to bring new products from concept to launch. A common challenge is ensuring clear communication and alignment across departments, especially when dealing with tight timelines or shifting project priorities. Balancing technical requirements, regulatory compliance, and manufacturing feasibility can also be demanding. Successful Formulation Managers are proactive in problem-solving and skilled at fostering strong collaboration to keep projects on track.

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

To thrive as a Formulation Manager, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by an advanced degree and experience in product formulation. Familiarity with laboratory equipment, formulation development software, and regulatory compliance systems is typically required. Strong leadership, problem-solving, and project management skills help you effectively lead teams and navigate complex product development cycles. These competencies are crucial for ensuring product quality, regulatory adherence, and timely delivery of innovative formulations.

What is the difference between Formulation Manager vs Formulation Scientist?

AspectFormulation ManagerFormulation Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmacy, or related field; often requires experience in project managementBachelor's or Master's in Chemistry, Pharmacy, or related field; focus on research skills
Work EnvironmentOversees teams in R&D or manufacturing settings, manages projects, and coordinates formulation developmentConducts laboratory research, experiments, and formulation testing
Industry UsageCommonly used in pharmaceutical, cosmetics, and chemical industries for leadership rolesPrimarily used in research and development departments for formulation development

The Formulation Manager typically oversees formulation projects, manages teams, and ensures product development aligns with business goals. In contrast, the Formulation Scientist focuses on conducting experiments and developing formulations in the lab. Both roles require similar educational backgrounds but differ in responsibilities and scope within the formulation process.

What cities are hiring for Formulation Manager jobs? Cities with the most Formulation Manager job openings:
What are the most commonly searched types of Formulation jobs? The most popular types of Formulation jobs are:
What states have the most Formulation Manager jobs? States with the most job openings for Formulation Manager jobs include:
What job categories do people searching Formulation Manager jobs look for? The top searched job categories for Formulation Manager jobs are:
Infographic showing various Formulation Manager job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $47,488 per year, or $22.8 per hour.

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 16 days ago


University Of Iowa Health Care rating

7.4

Company rating: 7.4 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

265th of 887 rated healthcare providers


Job description

Description
The Formulation Scientist I will report to the Director of Preformulation and Formulation Development and provide support by conducting experiments, investigations, or evaluations. The incumbent will participate in the formulation and process development for small molecule and biotherapeutic agents. This is a laboratory-based position performing formulation and process development activities specifically for therapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. This position performs all assigned formulation and analytical chemistry techniques with minimal supervision after the training period. This position will demonstrate a strong desire and ability to learn scientific principles and their cause and effect on scientific outcomes. This position will review other scientist's protocols, reports, specifications and test methods and will be responsible to efficiently learn to present interpretations. This position will be responsible for preparing data summary presentations, compiling data, and authoring technical reports and regulatory filings associated with their work. Effective communication skills are desirable for interactions with laboratory scientists, project managers and colleagues performing various functions, serving on multi-disciplinary project teams within UI Pharmaceuticals.
About the University of Iowa Pharmaceuticals
UI Pharmaceuticals is a Contract Development and Manufacturing Organization (CDMO) within the College of Pharmacy at the University of Iowa. Our mission is to improve quality of life by applying our pharmaceutical expertise to advance innovative products into clinical trials. Our vision is to be the premier partner for biotech, government, and research institutions.
We are located on the main campus in Iowa City, which offers a great place to live, top rated schools, a vibrant night life, and world class health care facilities. As a University of Iowa employee, you will have access to an excellent benefits package.
Key Areas of Responsibility
Research, Experiments, Investigations and Evaluations
  • Coordinate and implement multiple research projects/programs under the direction of departmental Director.
  • Perform basic and complex techniques as outlined in research plans, assure fidelity to scientific protocols, assist in design of research plans/protocols.
  • Experience in lab scale process of drug product formulation and scale-up of formulations through pilot scale.

Collect, Analyze and Summarize Data
  • Collaborate and interact with scientists, chemists, and manufacturing personnel, and plan and execute the generation, characterization, and analysis of pharmaceutical materials.
  • Collect and interpret experimental data to guide subsequent experiments aimed at pharmaceutical product and process development.
  • Develop formulations and processes suitable for manufacturing clinical trial supplies, in co- operation with internal manufacturing and analytical research groups.

Compliance
  • Assure safety and compliance with required organization and regulatory policies for laboratory activities, respond to compliance and safety violations.
  • Responsible for the appearance, function, maintenance, and compliance of the group's equipment and physical space.
  • Ensure compliance with UI policies and procedures.

Administrative and Project Management
  • Collaborate and interact with collegiate faculty, particularly in the division of Pharmaceutics and Translational Therapeutics (PTT) to advance research and development projects within University of Iowa Development Consortium (UIPDC).
  • Coordinate and manage equipment at facility.
  • Produce written materials in business- and industry-specific technical language related to development of a variety of pharmaceutical products.

Human Resources
  • Assist with Human Resource functions, including interviewing, selection, training, performance review, may provide input in annual staff performance reviews.
  • Design, evaluate, and coordinate training of employees on basic and new laboratory techniques and procedures needed to execute development projects.

To obtain the full job description including key areas of responsibility, technical competencies, and desirable qualifications, please contact Libby Kleppe at libby-kleppe@uiowa.edu.
Qualifications
Required Qualifications
Education
  • MS in Pharmaceutics, Chemistry, or Chemical Engineering; or equivalent combination of relevant education and experience.

Experience
  • Minimum 2 years Industry experience in preformulation/formulation development functions preferred or equivalent postgraduate experience to include:
    • Demonstrated ability to apply scientific principles to preformulation/formulation development of pharmaceutical dosage forms.
    • Hands on experience with basic analytical techniques such as HPLC, UV-Vis, and other routine lab instruments.
    • Demonstrated ability to work independently and collaboratively.
    • Excellent written and oral communication skills.
    • Demonstrated ability to apply good documentation and record practices.
    • Candidate should be knowledgeable with scientific investigation and thinking, proactively identify issues, and develop solutions.

Desirable Qualifications
  • Expertise in the development of freeze-dried formulations for small molecules and biologicals.
  • Expertise in addressing solubility and bioavailability issues in the development for oral or parenteral pharmaceutical products.
  • Expertise in characterization of pharmaceutical materials and an understanding of material properties and their influence on product quality.
  • Working knowledge of cGMPs, including CMC regulatory information required for INDs/NDAs/ANDAs with respect to API, preformulation, formulation, analytical methods, and dosage form manufacturing processes.
  • Working knowledge of statistics relevant to pharmaceutical product development.
  • Knowledge of requirements to safely work with Safebridge 3 compounds.
  • Skillful at authoring and reviewing technical documents including, standard operating procedures, product development reports, batch records etc.

Application and Position Details
  • In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission:
    • Resume
    • Cover Letter
  • Job openings are posted for a minimum of 14 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. 5 professional references will be requested at a later step in the recruitment process. For additional questions, please contact Libby Kleppe at libby-kleppe@uiowa.edu.

Benefits Highlights
  • Regular salaried position. Pay level 4A . Located in Iowa City, Iowa.
  • Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans.
  • For more information about Why Iowa? Click here .

Joining the University of Iowa means becoming a vital part of the Hawkeye community, where your work directly impacts education, research, and student success.
Enjoy exceptional health coverage, university-paid life insurance, robust retirement plans, and generous leave policies. Benefit from 24/7 support services, well-being resources, and access to UI Health Care specialists. Grow professionally with advanced training, leadership development, and tuition assistance.
Iowa City offers a great quality of life with world-class performances at Hancher Auditorium, Big Ten athletics, top-ranked public schools, and outdoor recreation.
Join us in making a difference at a leading Big Ten university and premier public research institution.

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