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Pharmaceutical Engineering Jobs in Virginia (NOW HIRING)

TekWissen

Engineering Manager

Manassas, VA

S. in Engineering discipline (Chemical /Biochemical strongly preferred) * 7 to 10 years' experience in cGMP, 21CFR Part 820, 21CFR Part 210 and 211, and/or Pharmaceutical manufacturing. Specific ...

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Pharmaceutical Engineering information

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How much do pharmaceutical engineering jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for pharmaceutical engineering in Virginia is $38.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.20 and $40.05 per hour, depending on experience, location, and employer.

What is pharmaceutical engineering?

Pharmaceutical engineering is a branch of engineering focused on the design, development, and manufacturing of medications and pharmaceutical products. It combines principles from chemical engineering, biomedical engineering, and pharmaceutical sciences to ensure the safe, effective, and efficient production of drugs. Professionals in this field work on process development, quality control, scaling up laboratory processes to industrial levels, and adhering to regulatory standards. Pharmaceutical engineers play a crucial role in bringing new medicines to market and maintaining the quality of existing products.

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

To thrive as a Pharmaceutical Engineer, you typically need a strong background in chemical engineering, biology, or pharmaceutical sciences, supported by at least a bachelor's degree in a related field. Familiarity with industry-standard tools such as GMP (Good Manufacturing Practice) systems, process simulation software, and regulatory compliance certifications is crucial. Exceptional problem-solving abilities, attention to detail, and effective teamwork make professionals stand out in this role. These skills ensure the safe, efficient, and compliant development and manufacturing of pharmaceutical products, directly impacting patient safety and product quality.

What are some common challenges faced by pharmaceutical engineers when working on cross-functional project teams?

Pharmaceutical engineers often collaborate with professionals from research, quality assurance, regulatory, and manufacturing teams. One common challenge is aligning technical requirements with strict regulatory standards while meeting project timelines. Communication can also become complex due to the diverse expertise and priorities of each group. Successful pharmaceutical engineers proactively facilitate information sharing and adapt to feedback, ensuring that project goals are achieved without compromising quality or compliance.

What is the difference between Pharmaceutical Engineering vs Chemical Engineering?

AspectPharmaceutical EngineeringChemical Engineering
Required CredentialsBachelor's in Pharmaceutical Engineering or related field, certifications in GMPBachelor's in Chemical Engineering, professional engineering license
Work EnvironmentPharmaceutical manufacturing facilities, labsChemical plants, refineries, research labs
Industry UsagePharmaceutical companies, biotech firmsChemical, energy, and manufacturing industries

Pharmaceutical Engineering focuses on designing and optimizing processes for drug manufacturing, ensuring compliance with health regulations. Chemical Engineering has a broader scope, involving the development of chemical processes across various industries. While both roles require similar educational backgrounds, Pharmaceutical Engineers specialize in pharmaceuticals, whereas Chemical Engineers work in diverse chemical sectors.

Are pharmaceutical engineers in demand?

Pharmaceutical engineers are in demand due to the ongoing need for drug development, manufacturing, and quality assurance in the pharmaceutical industry. They often require knowledge of process engineering, regulatory standards, and specialized tools, making their skills valuable in both research and production environments.

What do pharmaceutical engineers do?

Pharmaceutical engineers design and develop processes for manufacturing drugs and medical products, ensuring they are safe, effective, and produced efficiently. They work with equipment, chemical processes, and quality control standards, often using tools like process simulation software and adhering to regulatory requirements.

What are popular job titles related to Pharmaceutical Engineering jobs in Virginia?

For Pharmaceutical Engineering jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Engineering jobs in Virginia look for?

The top searched job categories for Pharmaceutical Engineering jobs in Virginia are:

Pharmaceutical Engineering jobs near you
Infographic showing various Pharmaceutical Engineering job openings in Virginia as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 2% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $79,313 per year, or $38.1 per hour.

Senior Manager, Engineering (Oral Solid Dosage)

Granules Pharmaceuticals

Chantilly, VA • On-site

$120K - $140K/yr

Full-time

Re-posted 4 days ago

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.


We are seeking an experienced and highly motivated Senior Manager of Engineering to lead all engineering and facility operations within our Oral Solid Dosage (OSD) manufacturing site. This role oversees equipment reliability, facility systems, utilities, capital projects, and continuous improvement initiatives while ensuring full compliance with cGMP, safety, and regulatory standards. The ideal candidate brings deep technical expertise in OSD processes and strong knowledge of facility engineering, including HVAC, clean utilities, building systems, and environmental controls. 


Key Responsibilities:

Engineering Leadership


  • Lead and manage engineering teams supporting OSD manufacturing, packaging, utilities, and facility systems.
  • Provide technical direction for troubleshooting, equipment optimization, and process improvements.
  • Develop long-term engineering strategies that support operational excellence and asset reliability.


OSD Equipment & Process Support


  • Oversee installation, qualification, and maintenance of OSD equipment such as granulators, fluid bed dryers, tablet presses, capsule fillers, coaters, blenders, and packaging lines.
  • Ensure equipment operates at peak performance with minimal downtime.
  • Lead root-cause investigations and implement CAPA for equipment and process issues.
  • Experience in PM and Calibration of the equipment. 


Facility Engineering & Utilities Management


  • Oversee operation and maintenance of HVAC systems, cleanrooms, compressed air, chilled water, boilers, vacuum systems, and other critical utilities.
  • Ensure environmental controls meet cGMP requirements for temperature, humidity, pressure differentials, and air quality.
  • Manage facility maintenance programs, preventive maintenance schedules, and reliability initiatives.
  • Support facility expansions, renovations, and infrastructure upgrades.
  • Ensure compliance with OSHA, environmental regulations, and internal safety standards.


Compliance & Quality


  • Ensure all engineering and facility operations comply with cGMP, FDA, EU, and internal quality standards.
  • Support audits, inspections, and documentation requirements.
  • Maintain engineering documentation, change controls, and validation protocols.


Safety & Risk Management


  • Champion a strong safety culture across engineering and operations.
  • Conduct risk assessments (FMEA, HAZOP) and implement engineering controls to ensure safe operations.
  • Ensure facility systems meet safety, environmental, and regulatory requirements.


Continuous Improvement


  • Drive initiatives to improve equipment reliability, reduce downtime, and enhance process efficiency.
  • Implement Lean, Six Sigma, and reliability engineering methodologies.
  • Identify opportunities for automation, modernization, and energy efficiency.


Team Development


  • Mentor and develop engineering and facility staff, fostering technical growth and leadership capability.
  • Build a collaborative, high-performance engineering organization.

Requirements


Qualification Required: 


  • Bachelor's degree in mechanical, Chemical, Electrical Engineering, or related field.
  • 12+ years of engineering experience in pharmaceutical OSD manufacturing.
  • Strong knowledge of facility engineering, including HVAC, clean utilities, building systems, and environmental controls.
  • Proven leadership experience managing engineering and facility teams.
  • Deep understanding of cGMP, validation, and regulatory requirements.


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

Apply