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Bio Manufacturing Jobs in Virginia (NOW HIRING)

Hollister Incorporated

Quality Auditor

Stuarts Draft, VA · On-site

Ability to pull and submit radiation dose, bio-burden, water test and any other special non-routine ... Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on ...

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Alfa Laval

Job Page CTA Left

Richmond, VA · On-site

$120K - $150K/yr

Identify and develop opportunities in underpenetrated and emerging protein markets, including bio ... and manufacturers. * Lead strategic account planning and national partnership discussions.

CRDF Global

Biosecurity Expertise

Arlington, VA

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

CRDF Global

Biosecurity Expertise

Arlington, VA · On-site

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

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All JobsBio Manufacturing JobsBio Manufacturing Jobs in Virginia

Bio Manufacturing information

What is the job of a biotechnician?

A biotechnician assists in laboratory and manufacturing processes related to biotechnology, including preparing samples, operating equipment, and maintaining lab records. They often work under supervision in cleanroom environments and may need certifications in laboratory techniques or safety protocols.

What are the key skills and qualifications needed to thrive in Bio Manufacturing, and why are they important?

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 jobs pay 10,000 a month without a degree?

In bio manufacturing, high-paying roles such as senior process technicians or manufacturing managers can reach or exceed $10,000 per month with extensive experience and specialized skills. These positions often require technical knowledge, certifications, and hands-on expertise but may not always require a formal degree. Advancement depends on industry experience, technical proficiency, and leadership abilities.

What is bio manufacturing?

Bio manufacturing involves producing biological products such as pharmaceuticals, vaccines, and biochemicals using living organisms, cells, or enzymes. It requires knowledge of cell culture, bioprocessing techniques, and often involves working in controlled environments like cleanrooms. Bio manufacturing roles may also require familiarity with GMP standards and specialized equipment.

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.

Is biotech a high paying job?

Bio manufacturing jobs in the biotech industry tend to offer competitive salaries, especially for roles requiring specialized skills such as quality control, process engineering, or laboratory work. Salaries can vary based on experience, education, location, and certifications, with many positions offering above-average pay compared to other manufacturing roles.
What are popular job titles related to Bio Manufacturing jobs in Virginia? For Bio Manufacturing jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Bio Manufacturing jobs in Virginia look for? The top searched job categories for Bio Manufacturing jobs in Virginia are:
Bio Manufacturing jobs near you
Infographic showing various Bio Manufacturing job openings in Virginia as of June 2026, with employment types broken down into 2% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Analytical Chemist II /Bio-Chemist (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

Full-time

Posted 22 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.
**Multiple positions available in QC **
Job Summary:
The role of QC Biochemist/Analytical Chemist II is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing raw materials, in-process, finished formulations, stability samples, method development and/or transfers, and cleaning validations. Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity, and timing. Responsible for the safe and efficient execution of job duties.
JOB DUTIES & RESPONSIBILITIES:
  • Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished product release and stability using approved methods and various instrumentation while adhering to cGMP and established policies.
  • Conduct analytical USP method verifications, validations, and method transfer activities for raw materials and finished dosage forms.
  • Perform the Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, UV spectrophotometer, Dissolution apparatus, KF Auto titrator, FT-IRS spectrophotometer, Polarimeter and Refractometer.
  • Compile laboratory test data and perform appropriate analyses that include physical (solubility, viscosity),chemical (titration) and analytical (FTIR, HPLC, ICP-MS, UV-Vis, KF, IC) testing etc.
  • Complete documentation needed to support testing procedures including test forms and logbooks.
  • Interpret test results, compare them to established specifications and control limits, and ensure appropriateness of data for release. Treats data with a high level of integrity and ethics.
  • Participate in out-of-specification and failure investigations. Support all aspects of laboratory investigations.
  • Prepare, review and approve analytical data, technical reports and analytical methods.
  • Coordinate Microbiological, preservative efficacy/ antimicrobial effectiveness testing requirement as per USP/USP-NF for Active pharmaceutical ingredients, Inactive and Finished products and stability samples for regulatory filings.

Physical Requirements/Working Environment:
  • Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.
  • Commitment to long hours of work when necessary to achieve goals.
  • Respirator, lab coat and safety glasses required. Ability to work with potent substances using a glove-box.

Job Type : Full-time
This Job Is Ideal for Someone Who Is:
  • Dependable - more reliable than spontaneous
  • People-oriented - enjoys interacting with people and working on group projects
  • Adaptable/flexible - enjoys doing work that requires frequent shifts in direction
  • Detail-oriented - would rather focus on the details of work than the bigger picture
  • Achievement-oriented - enjoys taking on challenges, even if they might fail
  • Autonomous/Independent - enjoys working with little direction
  • Innovative - prefers working in unconventional ways or on tasks that require creativity
  • High stress tolerance - thrives in a high-pressure environment

Requirements
Preferred Knowledge & Skills:
  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.

Required Experience & Education:
  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
  • Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.

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