Does Granules Pharmaceuticals Inc. sponsor H-1B visas?

Granules Pharmaceuticals Inc. has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the Production Engineer role. Confirm with the employer before applying if visa support is required.

Where is the Production Engineer role at Granules Pharmaceuticals Inc. based?

This role is based in Chantilly, VA.

How many years of experience does this Production Engineer role require?

The posting calls for 3–5 years of relevant experience.

One of 4,529 polymer and materials roles on Crosslinked, each read for materials, degree, visa and salary. See roles like this

H-1B history

Production Engineer

Granules Pharmaceuticals Inc. · Chantilly, VA1mo agoverified 20 h ago

BS-level Process Engineering roles on Crosslinked list a median of $112k (561 that show pay). This posting does not list pay.

Engineer pharmaceutical packaging and manufacturing systems, specs, and material selection for generic drugs

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Worth knowing

Generalist Realistic requirements

The materials angleEvaluate manufacturing and packaging materials and components for bottle packaging; knowledge of pharmaceutical manufacturing materials and container closure systems

H-1B filings

Granules Pharmaceuticals Inc. filed 10 H-1B labor applications for scientist and engineer roles from Jan to Dec 2025.

Most common titles: Process Engineer, Senior Director, Quality Control, Director, Analytical R&D. Median filed pay: $120K a year.

From U.S. Department of Labor disclosure data. A filing is a record of past hiring, not a promise about this role, so confirm sponsorship with the employer. Titles and filed pay ·Every employer's filings

Seniority: Mid-level
Work: On-site
Type: Full-time
Degree: BS
Experience: 3–5 yrs
Industry: Chemicals
Role: Process Engineering

Benefits

pension

Role details

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 4th largest generic pharmaceutical company of controlled substances 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.

The Manufacturing Engineer is responsible for the design, development, qualification, implementation, and continuous improvement of manufacturing systems pharmaceutical products including packaging design. The role supports new product launches, manufacturing line commercialization, manufacturing material selection, artwork execution, supplier management, cost optimization, and regulatory compliance.

Working cross-functionally with Operations, Quality, Regulatory Affairs, Marketing, Supply Chain, Procurement, and external suppliers, the Manufacturing Engineer ensures manufacturing solutions meet FDA requirements, customer expectations, operational efficiencies, and business objectives while maintaining product quality and compliance.

Evaluate manufacturing and packaging materials and components for bottle packaging
Develop manufacturing solutions that improve product protection, manufacturability, consumer usability, and sustainability.
Create, review, approve, and maintain manufacturing specifications for finished goods and manufacturing components.
Ensure SAP material numbers, component numbers, UPCs, GTINs, NDCs, lot coding requirements, and customer-specific information are accurately reflected on manufacturing materials.
Maintain manufacturing documentation in compliance with FDA regulations, cGMP requirements, and company quality systems.
Initiate and support Change Controls, Deviations, CAPAs, and manufacturing qualification activities.
Prepare manufacturing cost analyses and cost estimates to support commercial bids and business development opportunities.

Requirements

Minimum Educational Requrements

Bachelor's Degree In One Of The Following

Manufacturing Engineering
Manufacturing Science
Mechanical Engineering
Industrial Engineering
Materials Science
Chemical Engineering
Related Engineering Discipline

Required

3 to 5+ years of manufacturing engineering experience within a regulated manufacturing environment.
Experience supporting manufacturing operations, manufacturing development, and manufacturing specifications.
Experience working with manufacturing suppliers and contract manufacturing organizations.

Preferred

OTC pharmaceutical, pharmaceutical, nutraceutical, or consumer healthcare industry experiencehighly preferred
Experience with FDA-regulated products and cGMP environments.
Experience supporting manufacturing validation and equipment qualification activities.
Experience with major retail customers such as Walmart, CVS, Walgreens, Target, Costco, and Amazon.

Knowledge, Skills, And Abilities

Strong knowledge of pharmaceutical manufacturing materials and container closure systems.
Advancd Microsoft Excel proficiency.
Experience with TOPS palletization software or equivalent manufacturing design software.
Working knowledge of SAP or ERP systems.
Knowledge of FDA regulations, cGMP requirements, and manufacturing compliance standards.
Understanding of manufacturing line operations, serialization, labeling, coding, and inspection systems.
Familiarity with package testing and transportation validation methodologies.