Bioprocess Engineer

Virtue America

New Jersey, United States0–2 yrs1h agovia LinkedIn

This job at a glance

Who can apply
New grads and up to 2 years · Bachelor's degree or Master's degree
Must know
OperationsTroubleshootingData analysisBusiness analysisExcelMicrosoft Office
Work
On-site in New Jersey
Pay
Not stated by the employer.
Skill demand
Operations72%Troubleshooting51%Business analysis33%Data analysis13%of 99 similar entry-level jobs posted in the US this week
Listed
Oct 28, 2026 · still open

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About the Role

We are seeking a motivated and detail-oriented Bioprocess Engineer to support the development, optimization, monitoring, and documentation of biological manufacturing processes within the pharmaceutical and biotechnology industries. This entry-level opportunity is suitable for candidates with an academic background in Biotechnology, Bioprocess Engineering, Biochemical Engineering, Microbiology, Biochemistry, or related Life Sciences disciplines.

Key Responsibilities

  • Bioprocess Development: Assist in developing and evaluating biological processes used in the production of therapeutic proteins, vaccines, enzymes, and other biopharmaceutical products.
  • Upstream Processing: Support process activities involving cell culture, microbial fermentation, media preparation, inoculum development, and bioreactor operations.
  • Downstream Processing: Assist with documentation and evaluation of purification processes, including filtration, centrifugation, chromatography, and product recovery.
  • Bioreactor Monitoring: Help monitor process parameters such as temperature, pH, dissolved oxygen, agitation speed, pressure, and nutrient levels.
  • Process Optimization: Analyze process data to identify variations, trends, and opportunities to improve yield, productivity, consistency, and process efficiency.
  • Technical Documentation: Prepare and maintain batch records, process flow diagrams, laboratory notebooks, experimental reports, and technical procedures.
  • GMP Compliance: Support adherence to applicable GMP requirements, laboratory safety practices, data integrity principles, and established operating procedures.
  • Process Troubleshooting: Assist in identifying process deviations and investigating unexpected results in fermentation, cell culture, and purification activities.
  • Quality and Data Analysis: Collect, organize, and interpret experimental data to support process evaluation, reproducibility, and product quality.
  • Equipment and Process Support: Assist with documentation related to bioreactors, pumps, filtration systems, and other bioprocess equipment.
  • Cross-Functional Collaboration: Coordinate with Quality Assurance, Quality Control, Manufacturing, Process Development, and Validation teams to support biomanufacturing activities.
  • Continuous Improvement: Participate in process improvement initiatives, technical reviews, and activities supporting process consistency and operational efficiency.

Requirements & Tech Stack

  • Bachelor's or Master's degree in Biotechnology, Bioprocess Engineering, Biochemical Engineering, Biochemistry, Microbiology, Chemical Engineering, Biological Sciences, or a related field.
  • Basic understanding of upstream and downstream bioprocessing principles.
  • Familiarity with cell culture, fermentation, bioreactors, and biological product manufacturing concepts.
  • Fundamental knowledge of filtration, chromatography, purification, and separation techniques.
  • Understanding of process parameters, experimental design, data interpretation, and process optimization.
  • Basic knowledge of GMP, SOPs, laboratory safety, and data integrity practices.
  • Proficiency in Microsoft Excel, Word, and PowerPoint for data analysis and technical documentation.

Qualifications

  • Strong analytical thinking, attention to detail, and problem-solving abilities.
  • Good written and verbal communication skills.
  • Ability to maintain accurate experimental records and follow established procedures.
  • Willingness to learn biopharmaceutical manufacturing technologies and regulated industry practices.
  • Ability to collaborate effectively with technical and cross-functional teams.

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