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Bio Manufacturing Jobs in Virginia (NOW HIRING)

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options. Responsibilities: * Analyze bio-availability and ...

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options. Responsibilities: * Analyze bio-availability and ...

Biochemist

Chantilly, VA · On-site

$69K - $73K/yr

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options. Responsibilities: * Analyze bio-availability and ...

About Krystal Bio At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines ...

Senior IT Analyst

Danville, VA · On-site

$110K - $120K/yr

The Company develops, manufactures, and supplies tailored formulations and intermediates that ... bio-based formulations. Ascent's products are used as critical ingredients and process aids in ...

New

... Science Manufacturing Projects is preferred. • Experience using MS Office tools, including ... Bio/Pharma, #EPCMV, #globallifescience, #Construction #LI-SH1 Jacobs is an Equal Opportunity ...

S. biotechnologies and bio-pharmaceutical supply chains by denying adversaries access to genomic data, biotechnology intellectual property, and manufacturing capacity This portfolio supports partner ...

Chief Technology Officer

Ashburn, VA · On-site

$180K - $200K/yr

... manufacturer relationships, and BOM-cost discipline from first prototype through scale-up. • ... systems, or bio-inspired mechanisms. • Experience with high-performance, dynamic robotic ...

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Bio Manufacturing information

What is bio manufacturing?

Bio manufacturing, also known as biomanufacturing, is the process of using biological systems like cells or enzymes to produce commercial products such as medicines, vaccines, biofuels, and food ingredients. This field combines biology, engineering, and technology to create products in a controlled and scalable way, often using fermentation or cell culture techniques. Biomanufacturing plays a critical role in the pharmaceutical, biotechnology, and food industries, enabling the production of complex molecules that are difficult to synthesize chemically. Professionals in this field work on developing, optimizing, and scaling up these biological processes to ensure high-quality and cost-effective product output.

What are the key skills and qualifications needed to thrive in bio manufacturing?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

Infographic showing various Bio Manufacturing job openings in Virginia as of August 2026, with employment types broken down into 54% Full Time, 28% Part Time, and 18% Contract. Highlights an 100% In-person job distribution.

Biochemist

Chantilly, VA • On-site

$69K - $73K/yr

Full-time

Re-posted 13 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.


Responsibilities: 


  •  Analyze bio-availability and bioequivalency of pharmaceutical products using HPLC, UV-Vis, GC, FTIR
  • Perform routine release tests of  raw materials and finished products using OOS/OOT and LIMS
  • Perform in-vivo dissolution test related to the biopharmaceutic characteristics of the drug substance and bioequivalence studies using cGMP/cGLP, Empower, Titration, HPLC, dissolution 
  • Perform solubility studies of drug substances as per Bio-Pharmaceutics classification system (BCS) in accordance with FDA regulations
  • Conduct and coordinate elemental impurities study for Pharmaceutical Products as per ICH guidance;
  • Interpret test results and established specifications and control limits to ensure appropriateness of data for release; Analyze biochemical results 


Submit resume referencing job code ASY001 to HR, Granules Pharmaceuticals, Inc., 3701 Concorde Parkway, Chantilly, VA  20151 


Requirements

Educational Requirements:

Must have a Bachelor's degree in Biochemistry, Chemistry, or Biotechnology plus 2 years experience in Quality Control within a Pharmaceutical Manufacturing company.  


Skills Requirements: 

Skills and knowledge in HPLC, UV-Vis, FTIR, OOS/OOT, Dissolution, Titration, cGMP, LIMS