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Biopharmaceutical Manufacturing Associate Jobs in Virginia

MSD

Quality Drug Substance Design Lead

Elkton, VA · On-site

At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the ... Quality Design Lead, Drug Substance Manufacturing (Associate Director) Purpose The Quality Design ...

MSD

Quality Drug Product Design Lead

Elkton, VA · On-site

At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the ... Quality Design Lead, Drug Product Manufacturing (Associate Director) Purpose The Quality Design ...

Merck

Quality Drug Product Design Lead

Elkton, VA · On-site

At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the ... Quality Design Lead, Drug Product Manufacturing (Associate Director) Purpose The Quality Design ...

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How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Virginia is $26.89, according to ZipRecruiter salary data. Most workers in this role earn between $22.88 and $31.44 per hour, depending on experience, location, and employer.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

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Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, and 17% Hybrid job distribution, with an average salary of $55,928 per year, or $26.9 per hour.

Temporary Manufacturing Associate I, Lab Operations

Sterling, VA • On-site

Maravai LifeSciences
Biotechnology Research and Development • 51 - 200 employees
Learn more about Maravai LifeSciencesexternal

Temporary

Medical, Retirement, PTO

Posted 21 days ago

Job description

Who we are: 

Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.  

At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitableculture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. 

Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team as a Temporary Manufactruring Associate I, Lab Operations. The primary role of Manufacturing Associate I is to formulate reagents, package supports, phosphoramidites, and other non-hazardous materials needed for the synthesis and purification of oligonucleotides as well as working with Hazardous materials and knowledge of general chemistry techniques.

How you will make an impact: 

  • Prepare catalog products using manufacturing instructions, procedures and protocols
  • Associated tasks include packaging, labeling, and storing of product
  • Maintaining inventory of catalog products and raw materials
  • General laboratory maintenance and equipment maintenance
  • Evaluation and cleaning of necessary production glassware
  • Evaluation and assembly of support columns
  • Distribution of products with correct documentation, using good documentation practices.
  • Inspection of finished goods.
  • Fulfill products from stock for customer orders
  • Inspection of completed orders prior to shipment
  • Assist with general shipping and receiving of products and materials
  • Proper storage, handling, and disposal of organic solvents, hazardous chemicals, and waste
  • Perform other functions and duties as required.
  • Work with hazardous materials on Daily basis that will require wearing proper PPE at all time
  • Able to life 50lbs.
  • Making 40-70 liter batches at a time
  • Perform other functions and duties as required

 The skills and experience that you will bring: 

  • High School diploma required.
  • Must have good communication skills, written and verbal. 
  • Must be able to follow written Standard Operating Procedures (SOPs)/Work Instructions (WIs) 
  • as well as personalized instruction from leaders. 
  • Must be self-motivated and able to work both in a team setting as well as individually. 
  • Must be able to work in a fact paced environment without getting overwhelmed. 
  • Must be able to perform repetitious activities while maintaining accuracy. 
  • Must have excellent attention to detail and be able to perform detail-oriented work requiring fine motor skills. 
  • Must be a good timekeeper and ensure prompt arrival to work for each scheduled shift. 
  • Must have functional knowledge of Microsoft Office Suite. 
  • Experience with FileMaker database and NetSuite ERP software a plus. 
  • This is a manufacturing and production based job. No real research is involved.  

#LI-Onsite

The benefits of being a #MiracleMaker: 

  • You have the potential to change, improve, and save lives around the world. 
  • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. 
  • We offer comprehensive medical plans and HSA/FSA options. 
  • Fertility & family planning assistance. 
  • A variety of additional optional benefits and insurance options, including pet insurance. 
  • Retirement contributions. 
  • Holidays & Paid Time Off. 

Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/ 

To view more opportunities to become a #MiracleMaker, visit our career site at  https://www.maravai.com/careers/  

Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

Click here to view Maravai LifeSciences Privacy Notice 

HIRING SCAM ALERT 

Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: 

  • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) 
  • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. 
  • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. 

 If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov. 

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