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Pharmaceutical Formulation Jobs in Virginia (NOW HIRING)

Granules

Formulation Scientist (Solid Orals)

Chantilly, VA · On-site

$100K - $110K/yr

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years ... Develops and executes formulation strategies related to product development (i.e., project planning ...

TekWissen LLC

Formulation Chemist

Middletown, VA · On-site

$30 - $35/hr

... pharmaceutical services under their industry-leading brands. Position: Scientist II - Chemistry ... Strong knowledge of electrochemistry, formulation science, chemical processes, and process ...

TekWissen

Engineering Manager

Manassas, VA

... Pharmaceutical manufacturing. Specific process expertise includes: * Validation, CIP/SIP processes, milling and blending, formulation, aseptic filling, and overall physical control processes

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

$120K - $145K/yr

... formulation and processing suites, with Clean In Place (CIP) and Sanitize In Place (SIP ... Experience authoring, approving, and executing validation protocols for major pharmaceutical ...

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

$120K - $145K/yr

... formulation and processing suites, with Clean In Place (CIP) and Sanitize In Place (SIP ... Experience authoring, approving, and executing validation protocols for major pharmaceutical ...

Air Liquide

Chemical Operator

Richmond, VA

$22 - $27/hr

... formulation, green chemistry, extraction and biotechnologies. Combining the dynamism of an ... The plant specializes in producing ingredients for cosmetic and pharmaceutical products. It has ...

Air Liquide

Chemical Operator

Richmond, VA · On-site

$22 - $27/hr

... formulation, green chemistry, extraction and biotechnologies. Combining the dynamism of an ... The plant specializes in producing ingredients for cosmetic and pharmaceutical products. It has ...

Air Liquide

Chemical Operator

Richmond, VA · On-site

$22 - $27/hr

... formulation, green chemistry, extraction and biotechnologies. Combining the dynamism of an ... The plant specializes in producing ingredients for cosmetic and pharmaceutical products. It has ...

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Pharmaceutical Formulation information

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How much do pharmaceutical formulation jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for pharmaceutical formulation in Virginia is $22.64, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $22.64 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Formulation position, and why are they important?

To excel in Pharmaceutical Formulation, a candidate typically holds a degree in pharmacy, chemistry, or a related field and demonstrates expertise in drug delivery systems, analytical techniques, and formulation development. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and regulatory guidelines is also crucial. Strong analytical thinking, attention to detail, and effective teamwork and communication skills are highly valued. These qualifications ensure that formulations are developed efficiently, compliantly, and with a focus on safety and efficacy.

What are the typical daily responsibilities of someone working in Pharmaceutical Formulation?

Professionals in Pharmaceutical Formulation are responsible for designing and developing dosage forms and ensuring their stability, safety, and efficacy. Daily tasks often include conducting experiments, analyzing raw materials, preparing prototypes, and documenting results according to regulatory standards. Collaboration with analytical scientists, quality assurance, and process engineering teams is common to address formulation challenges and optimize product development. The role frequently involves troubleshooting formulation issues and supporting scale-up activities for manufacturing. A detail-oriented and systematic approach is key to success in this fast-paced, research-driven environment.

What is the highest paying job in pharmaceuticals?

In pharmaceutical formulation, senior roles such as Director of Formulation Development or Vice President of R&D typically have the highest salaries, often exceeding six figures. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee complex projects and strategic decision-making within pharmaceutical companies.

How to become a formulation scientist?

To become a formulation scientist, typically a bachelor's degree in pharmacy, chemistry, chemical engineering, or a related field is required, often followed by a master's or Ph.D. for advanced roles. Gaining experience through internships or entry-level positions in pharmaceutical development, along with knowledge of Good Manufacturing Practices (GMP) and formulation techniques, is essential. Skills in analytical methods, laboratory work, and familiarity with formulation tools are also important for career progression.

What is a pharmaceutical formulator?

A pharmaceutical formulator is a professional responsible for developing and designing the composition of medicines, including selecting appropriate ingredients and creating formulations such as tablets, capsules, or liquids. They work in laboratories, often using specialized tools and adhering to regulatory standards to ensure drug stability, efficacy, and safety.

How much do Pfizer formulation scientists make?

Pfizer formulation scientists typically earn an average salary ranging from $80,000 to $120,000 annually, depending on experience, education, and location. They often work in laboratory settings, utilizing skills in pharmaceutical development and formulation techniques.

What is a Pharmaceutical Formulation job?

A Pharmaceutical Formulation job involves the development of drug products by combining active pharmaceutical ingredients (APIs) with excipients to create a stable, effective, and safe dosage form. Professionals in this role work on designing tablets, capsules, injections, or other drug delivery systems, ensuring proper bioavailability and stability. They also conduct laboratory testing, optimize formulations for large-scale manufacturing, and comply with regulatory guidelines. Their work is essential in bringing new medications to market and improving existing drug formulations.

What are the most commonly searched types of Pharmaceutical Formulation jobs in Virginia? The most popular types of Pharmaceutical Formulation jobs in Virginia are:
What cities in Virginia are hiring for Pharmaceutical Formulation jobs? Cities in Virginia with the most Pharmaceutical Formulation job openings:
Pharmaceutical Formulation jobs near you
Infographic showing various Pharmaceutical Formulation job openings in Virginia as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, and 3% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $47,081 per year, or $22.6 per hour.

Formulation Scientist (Solid Orals)

Granules Pharmaceuticals

Chantilly, VA • On-site

$100K - $110K/yr

Full-time

Posted 14 days ago

Job description

Job Type
Full-time
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.
Salary Description
$100,000 - $110,000 per year

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