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Hourly Formulation Scientist Jobs (NOW HIRING)

Granules

Formulation Scientist (Solid Orals)

Chantilly, VA · On-site

$100K - $110K/yr

... formulation of relevant and scientifically based conclusions * Coordinates studies with other technical groups (i.e., Analytical Sciences, Biopharmaceutics, Legal, Regulatory & Tech Services)

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How much do hourly formulation scientist jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for hourly formulation scientist in the United States is $37.61, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $43.51 per hour, depending on experience, location, and employer.

What does a typical day look like for an Hourly Formulation Scientist, and how do they collaborate with other teams?

A typical day for an Hourly Formulation Scientist involves preparing and testing various formulations, documenting experimental results, and adjusting ingredient ratios based on protocols or supervisor feedback. Collaboration is key, as you’ll often work alongside analytical chemists, quality assurance, and production teams to ensure formulations meet both regulatory and performance standards. Effective communication and attention to detail are essential since you may need to report findings, troubleshoot challenges, and implement suggestions from cross-functional team members.

What are the key skills and qualifications needed to thrive as an Hourly Formulation Scientist, and why are they important?

To excel as an Hourly Formulation Scientist, you need a strong background in chemistry or a related science, laboratory skills, and a relevant degree or coursework. Familiarity with laboratory equipment, analytical instruments (such as HPLC or GC), and standard operating procedures, as well as knowledge of safety protocols, is typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies ensure accurate formulation development, adherence to safety and quality standards, and smooth collaboration within research teams.

What is the difference between Hourly Formulation Scientist vs Laboratory Technician?

AspectHourly Formulation ScientistLaboratory Technician
Required CredentialsBachelor's degree in Chemistry, Pharmacy, or related fieldAssociate's degree or relevant certification
Work EnvironmentResearch labs, formulation development settingsTesting labs, quality control, sample preparation
Employer & Industry UsagePharmaceutical, cosmetics, chemical industriesManufacturing, quality assurance, research facilities

The Hourly Formulation Scientist and Laboratory Technician roles often overlap in work environment and industry but differ mainly in responsibilities and qualifications. The scientist focuses on developing and optimizing formulations, requiring a higher level of education, while technicians support testing and sample preparation. Both roles are essential in research and manufacturing settings, but the formulation scientist typically has more specialized responsibilities.

What does an Hourly Formulation Scientist do?

An Hourly Formulation Scientist is responsible for developing, testing, and optimizing formulations for products, often in industries such as pharmaceuticals, cosmetics, or chemicals. They work in laboratory settings to mix ingredients, conduct experiments, and ensure products meet quality and safety standards. Working on an hourly basis typically means they are paid by the hour, which may offer flexible scheduling but may not include benefits like salaried positions. Their role is crucial in turning raw materials into stable, effective final products that are ready for manufacturing and distribution.
What cities are hiring for Hourly Formulation Scientist jobs? Cities with the most Hourly Formulation Scientist job openings:
What are the most commonly searched types of Formulation Scientist jobs? The most popular types of Formulation Scientist jobs are:
What states have the most Hourly Formulation Scientist jobs? States with the most job openings for Hourly Formulation Scientist jobs include:
Hourly Formulation Scientist jobs near you

Formulation Scientist (Solid Orals)

Granules

Chantilly, VA • On-site

$100K - $110K/yr

Full-time

Posted 12 days ago

Be an early applicant

Job description

Description:

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.


Job Summary

  • Under general direction, manages, plans, and executes projects for product development.
  • Under limited direction and supervision, carries out design and development of solid oral dosage forms using quality by design (QbD concept) through ANDA filing and/or product launch.
  • Under limited direction and supervision, carries out design and development of complex oral dosage forms using QbD concepts through ANDA filing and/or product launch.
  • Develops and executes formulation strategies related to product development (i.e., project planning and timelines, experimental design, data evaluation, formulation of relevant and scientifically based conclusions
  • Coordinates studies with other technical groups (i.e., Analytical Sciences, Biopharmaceutics, Legal, Regulatory & Tech Services).
  • Maintains a high level of expertise within the field and develops new technologies and concepts to be applied in the development of oral controlled release drug products.
  • Participates as a project leader, manager and/or ad hoc member in Product Development efforts, and identifies, analyzes and suggests corrective actions to optimize R&D processes, technology and regulatory compliance issues.


Principal Accountabilities

  • Developing pharmaceutical products, leading to successful ANDA filings and approval in a timely manner.
  • Managing and scheduling multiple projects, setting objectives, prioritizing activities to meet the milestones in a fast-paced environment.
  • Designing, formulation and process development for various drug from project initiation to commercialization by following appropriate GMP regulations and safety requirements.
  • Participate in the set-up and operation of pilot scale equipment and instrumentation for the completion of small production runs in collaboration with the R&D technician.
  • Design and conduct pre-formulation and formulation studies, process development and optimization of prescription dosage form designs and ANDA oral Dosage forms using DOE
  • Perform Literature search and Evaluate patents to develop non-infringing strategies
  • Preparation of product manufacturing, batch records and protocols for different product development stages, including from R&D prototype formulations to process validations following SOPs and procedures, ensuring the detailed record and data keeping.
  • Utilize formulation techniques, processing equipment and unit operations including Wurster Coating, Tablet Coating, Compression, Blending, Encapsulation, HPLC, Spectrophotometry, Dissolution, Viscometer to develop Bio-Equivalent products
  • Review Analytical Data, draft SOP’s, Process Evaluation protocols, IQ, OQ, PQ protocols and GMP Manufacturing Batch records, Packaging Batch Records.
  • Characterization of APIs, excipients and in process products; analysis of in-process samples or in-process products based on protocols and QbD concept, preparing various formulation samples to support cross-functional programs as needs.
  • Completes documentation associated with manufacturing processes (e.g. batch record, protocols, and logbooks) with detail and accuracy.
  • Establishing documentation management systems for CMC development and meeting FDA GMP, regulatory requirement, and FDA onsite inspections.
  • Comprehensive knowledge of IVIVC, QbD and Design of Experiments (DOE).
  • Ensuring all regulatory documents in compliance with SOPs, FDA Regulations, and cGMP policy where applicable.
  • Knowledge of manufacturing regulatory programs and objectives (cGMP, CFR 210 and 211).
  • Maintaining compliance with GMP, SOPs and DEA regulations.
  • Coordinate with Regulatory Affairs, Operations, QC/QA and Supply Departments to ensure that projects are planned and executed in a timely manner.


Management Responsibility

The Senior Scientist leads the assigned projects and guides the operation of the product development ranging from selection of staff, choice of methods, purchase of equipment, quality assurance, quality control, safety, hours of operation, scheduling of staff, and utilization management.


Reports to

Sr. Vice President, R&D

Requirements:

Minimum Requirements


Knowledge & Skills Good communication skills, critical thinking, flexibility, time management, self-motivation.
Minimum Experience & Education

  • Ph.D. in pharmaceutical sciences with minimum of 2 years' experience OR;
  • Masters in pharmaceutical sciences with minimum of 5 year' experience in generic product development, with emphasis in solid/liquid orals or an equivalent combination of education and experience.

Disclaimer: The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.