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Biotech Manufacturing Jobs in Virginia (NOW HIRING)

Manufacturing Engineer

Middletown, VA · On-site

$64K - $82K/yr

Pharma, Biotech, Medical Device, or Life Sciences experience * Fill-Finish manufacturing * Filling, Capping, and Labeling equipment * CQV support experience Interested candidates can apply with an ...

Demonstrated ability to successfully gown into aseptic manufacturing areas * Excellent organization ... The Biotechnician II position will work in a cleanroom environment and follow cGMP batch records ...

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

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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Showing results 1-20

Biotech Manufacturing information

See Virginia salary details

$12

$20

$33

How much do biotech manufacturing jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for biotech manufacturing in Virginia is $20.66, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $23.12 per hour, depending on experience, location, and employer.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.
What are popular job titles related to Biotech Manufacturing jobs in Virginia? For Biotech Manufacturing jobs in Virginia, the most frequently searched job titles are:
Infographic showing various Biotech Manufacturing job openings in Virginia as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $42,970 per year, or $20.7 per hour.
Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) GOFP

Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) GOFP

Afton Scientific, LLC

Charlottesville, VA • On-site

$30 - $34/hr

Full-time

Re-posted 11 days ago


Job description

About the job
At Afton Scientific, every role contributes to advancing the quality and reliability of sterile pharmaceutical manufacturing. Our team is driven by innovation, collaboration, and a commitment to excellence. We support employees at every stage of their career by fostering an environment where development, learning, and meaningful impact are possible.
We invite you to explore opportunities to join our organization and contribute to our mission. We are currently seeking a Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) to support our growing biopharmaceutical operations at our on-site facility in Charlottesville, Virginia. (Relocation + Sign On Bonus )
Overview of this Position:
The Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) plays a critical role in sterile pharmaceutical manufacturing by operating and maintaining isolator systems for aseptic filling processes. This position ensures compliance with Good Manufacturing Practices (GMP) and supports the production of high-quality injectable drug products in a controlled environment.
Pay Details: Non-exempt position, range of $30 - $34 per hour, depending on level of experience.
Non-Negotiable Requirements:
• At least two (2) years of experience operating isolators in a sterile/aseptic manufacturing facility
• At least two (2) years of experience in a GMP manufacturing facility
• At least one (1) year of experience with routine cleaning, decontamination, and setup of isolators according to SOPs.
• High School Diploma or GED
Preferred Requirements:
• Experience working with Master Control, and/or SAP.
• Experience with cleanroom operations and environmental monitoring
• Experience with automated filling equipment and troubleshooting isolator
• Previous experience in pharmaceutical or biotech manufacturing
• Exceptional attention to detail and communication skills
• Bachelor's degree in biology and /or Life Sciences
Responsibilities Include:
• Operate isolator systems for aseptic filling of sterile injectable products
• Perform routine cleaning, decontamination, and setup of isolators according to SOPs
• Handle sterile components and materials in compliance with aseptic techniques
• Complete batch records and controlled documentation accurately and timely
• Monitor and document environmental conditions and equipment performance
• Collaborate with Quality Assurance and Engineering teams to resolve issues and maintain compliance
• Participating in training and continuous improvement initiatives
• Maintain a clean and organized work environment in accordance with GMP standards
Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this job. This role may require sitting, standing, or walking for extended periods; using a computer; and working in a standard office environment. Specific physical or environmental requirements will be addressed through the reasonable accommodation process. We do not discriminate based on disability and will provide reasonable accommodation as required by law.