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Origin Biologics Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Project Manager - Downstream Biologics Description: Leads capital projects within downstream ... origin, veteran status, or disability status.

Validation & Engineering Group, Inc

PR

Project Manager - Downstream Biologics Description: Leads capital projects within downstream ... origin, veteran status, or disability status.

Validation & Engineering Group, Inc

PR

Project Manager - Downstream Biologics Description: Leads capital projects within downstream ... origin, veteran status, or disability status.

Validation & Engineering Group, Inc

PR

Project Manager - Downstream Biologics Description: Leads capital projects within downstream ... origin, veteran status, or disability status.

WuXi Biologics

QA Specialist I

Cranbury, NJ · On-site

WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have ... origin, or protected veteran status and will not be discriminated against on the basis of ...

WuXi Biologics

Warehouse Technician

Cranbury, NJ · On-site

$24 - $27/hr

WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have ... origin, or protected veteran status and will not be discriminated against on the basis of ...

System One

Biologist

Boston, MA · On-site

$74.83 - $88.04/hr

Job Title: Biologist (7+ years) Location: Boston, MA Type: Contract Compensation: $74.83 - 88.04 ... origin, disability, family care or medical leave status, genetic information, veteran status ...

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Origin Biologics information

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$29.5K

$100.5K

$117.5K

How much do origin biologics jobs pay per year?

As of Jul 24, 2026, the average yearly pay for origin biologics in the United States is $100,501.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What jobs can I get with bioscience?

With a background in bioscience, you can pursue roles such as research scientist, laboratory technician, quality control analyst, or bioprocess engineer. These positions often require knowledge of laboratory techniques, data analysis, and sometimes specialized certifications or advanced degrees.

What does a typical workday look like at Origin Biologics?

A typical workday at Origin Biologics may involve conducting laboratory experiments, analyzing samples, documenting results, and collaborating closely with research scientists and quality assurance teams. The role often requires adherence to strict protocols and good laboratory practices to ensure safety and product reliability. You may also participate in team meetings to discuss project progress or troubleshoot technical issues. This dynamic environment encourages ongoing learning and teamwork, providing opportunities to develop new skills and contribute to innovative biologic products.

What is an Origin Biologics job?

An Origin Biologics job typically involves working with biological materials, such as human or animal-derived cells, tissues, or proteins, for medical and research applications. Employees in this field may engage in roles related to manufacturing, quality control, regulatory compliance, or research and development. These jobs require knowledge of biotechnology, laboratory procedures, and industry regulations to ensure the safety and efficacy of biological products.

What is a bioscience job?

A bioscience job involves working in the field of biological sciences, often focusing on research, development, or manufacturing related to health, medicine, or biotechnology. These roles typically require knowledge of laboratory techniques, scientific analysis, and sometimes specialized certifications or degrees in biology, biochemistry, or related fields.

What are the key skills and qualifications needed to thrive in the Origin Biologics position, and why are they important?

To thrive at Origin Biologics, you generally need a background in life sciences such as biology, biochemistry, or biotechnology, along with relevant laboratory experience. Familiarity with lab equipment, aseptic techniques, Good Manufacturing Practice (GMP), and industry-specific software or certifications like ISO 13485 is highly valued. Attention to detail, strong problem-solving abilities, and effective teamwork and communication skills are also essential. These competencies ensure accuracy, compliance, and efficiency while contributing to high-quality biologics research, development, or production.

More about Origin Biologics jobs
What cities are hiring for Origin Biologics jobs? Cities with the most Origin Biologics job openings:
What are the most commonly searched types of Origin Biologics jobs? The most popular types of Origin Biologics jobs are:
What states have the most Origin Biologics jobs? States with the most job openings for Origin Biologics jobs include:
What job categories do people searching Origin Biologics jobs look for? The top searched job categories for Origin Biologics jobs are:
Origin Biologics jobs near you
Infographic showing various Origin Biologics job openings in the United States as of July 2026, with employment types broken down into 33% Full Time, 17% Part Time, 17% Temporary, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $100,501 per year, or $48.3 per hour.

Project Manager - Downstream Biologics

Validation & Engineering Group, Inc

PR

Full-time

Posted 15 days ago

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.