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Biologics Process Operator Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Manage projects related to downstream biologics processes, including fill/finish, cell culture ... Experience supporting manufacturing capacity expansion projects within existing operating ...

Validation & Engineering Group, Inc

PR

Manage projects related to downstream biologics processes, including fill/finish, cell culture ... Experience supporting manufacturing capacity expansion projects within existing operating ...

Validation & Engineering Group, Inc

PR

Manage projects related to downstream biologics processes, including fill/finish, cell culture ... Experience supporting manufacturing capacity expansion projects within existing operating ...

Validation & Engineering Group, Inc

PR

Manage projects related to downstream biologics processes, including fill/finish, cell culture ... Experience supporting manufacturing capacity expansion projects within existing operating ...

Validation & Engineering Group, Inc

PR

Manage projects related to downstream biologics processes, including fill/finish, cell culture ... Experience supporting manufacturing capacity expansion projects within existing operating ...

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Biologics Process Operator information

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$21

$31

How much do biologics process operator jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for biologics process operator in the United States is $21.15, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $23.08 per hour, depending on experience, location, and employer.

What does a process operator work?

A biologics process operator is responsible for operating and monitoring equipment used in the production of biological products, such as vaccines or therapies. They follow standard operating procedures, ensure quality control, and maintain a clean, safe environment, often working in shifts and requiring knowledge of GMP regulations and equipment handling.

What jobs can I get with bioscience?

A biologics process operator is a job in the bioscience field that involves managing the production of biological products such as vaccines and therapies. Other related roles include research scientist, quality control analyst, manufacturing technician, and regulatory affairs specialist. These jobs often require knowledge of laboratory techniques, Good Manufacturing Practices (GMP), and sometimes certifications or training in bioscience or biotechnology.

What is the difference between Biologics Process Operator vs Bioprocess Technician?

AspectBiologics Process OperatorBioprocess Technician
CredentialsTypically requires a high school diploma or associate degree, with on-the-job trainingOften requires an associate degree or relevant technical certification
Work EnvironmentManufacturing facilities, cleanrooms, labsBiotech manufacturing plants, laboratories
Industry UsageCommonly employed in biologics productionUsed in biopharmaceutical manufacturing and research
Job FocusOperating bioprocess equipment, monitoring productionSupporting bioprocessing activities, data recording

The main difference between a Biologics Process Operator and a Bioprocess Technician lies in their specific roles and responsibilities. While both work in biologics manufacturing environments and may require similar certifications, the operator primarily focuses on running and monitoring bioprocess equipment, whereas the technician supports broader bioprocess activities and data management. Both roles are essential in ensuring efficient biologics production.

Where do process operators make the most money?

Process operators in the biologics industry tend to earn higher salaries in regions with a strong pharmaceutical or biotech presence, such as major biotech hubs or regions with high living costs. Factors like experience, certifications, and working in large manufacturing facilities can also influence earning potential.

Do you need a degree to be a process operator?

Biologics process operators typically do not require a college degree but need relevant technical training, certifications, or experience in manufacturing or laboratory environments. Employers often value hands-on skills, knowledge of GMP regulations, and familiarity with process equipment. Some positions may prefer or require an associate's or bachelor's degree depending on complexity and company standards.
More about Biologics Process Operator jobs
What cities are hiring for Biologics Process Operator jobs? Cities with the most Biologics Process Operator job openings:
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What job categories do people searching Biologics Process Operator jobs look for? The top searched job categories for Biologics Process Operator jobs are:
Biologics Process Operator jobs near you
Infographic showing various Biologics Process Operator job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, and 33% Temporary. Highlights an 100% In-person job distribution, with an average salary of $43,984 per year, or $21.1 per hour.

Project Manager - Downstream Biologics

Validation & Engineering Group, Inc

Cincinnati, OH

Full-time

Posted 17 days ago

Key responsibilities

  • Lead capital projects from initiation through design, construction, and CQV completion within downstream biologics manufacturing.

  • Coordinate cross-functional teams including Engineering, Site Operations, and CQV stakeholders to achieve project objectives.

  • Present project updates, project status, and key decisions to Global Engineering leadership and site executives.

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Project Manager – Downstream Biologics

Description:

Leads capital projects within downstream biologics manufacturing, supporting capacity expansion and facility enhancements within existing operations. Manages projects through the full project lifecycle from concept through engineering, construction, and CQV, ensuring alignment with business and site objectives.

Responsibilities:

  • Lead capital projects from initiation through design, construction, and CQV completion.
  • Manage projects related to downstream biologics processes, including fill/finish, cell culture, reactors, and related systems.
  • Drive capacity expansion initiatives within existing manufacturing facilities.
  • Coordinate cross-functional teams including Engineering, Site Operations, and CQV stakeholders.
  • Present project updates, project status, and key decisions to Global Engineering leadership and site executives.
  • Ensure adherence to scope, schedule, cost, and quality objectives.
  • Manage project execution to support business goals and site operational requirements.
  • Facilitate communication and collaboration across project teams and stakeholders.
  • Support project planning, risk management, and decision-making throughout the project lifecycle.

Qualifications:

  • Experience leading capital projects within pharmaceutical, biotechnology, or biologics manufacturing environments.
  • Strong knowledge of downstream biologics manufacturing processes, including fill/finish, cell culture, reactors, and associated process systems.
  • Experience managing projects through engineering, construction, commissioning, qualification, and validation (CQV) phases.
  • Experience supporting manufacturing capacity expansion projects within existing operating facilities.
  • Strong project management skills with demonstrated ability to manage scope, schedule, cost, and quality objectives.
  • Experience leading cross-functional teams and coordinating multiple stakeholders.
  • Strong leadership, communication, and presentation skills.
  • Ability to present project updates and strategic recommendations to senior leadership and executive stakeholders.
  • Strong organizational, analytical, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced project environment.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.