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Biotech Process Development Jobs (NOW HIRING)

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role OverviewThe Scientist I, Process Development (PD) will be responsible for developing ...

Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies. Our leading CDMO client is eager to hire an Aseptic Downstream Process Development ...

Engineer II, Process Development

Norwood, MA ยท On-site

$74K - $118K/yr

Experience/education in biotechnology process/product development. * Preferred: Hands on experience with AKTA FPLC, Hamilton, Tangential flow filtration (TFF), HPLC/UPLC instrumentation and pump ...

We are seeking a highly motivated Process Development Scientist with expertise in ... Experience working in a pharmaceutical/biotech setting * Excellent written and verbal communication ...

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Direct the development and optimization of upstream processes including but not limited to: seed ...

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Biotech Process Development information

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How much do biotech process development jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for biotech process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

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

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
More about Biotech Process Development jobs
What cities are hiring for Biotech Process Development jobs? Cities with the most Biotech Process Development job openings:
What states have the most Biotech Process Development jobs? States with the most job openings for Biotech Process Development jobs include:
Infographic showing various Biotech Process Development job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 2% As Needed, 89% Full Time, 1% Part Time, 6% Contract, and 1% Summer. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Downstream Process Development Scientist I

Wheeler Bio, Inc.

Oklahoma City, OK โ€ข On-site

Full-time

Re-posted 14 days ago


Job description

Location: Oklahoma City, OK
Department: Process Development
Job Type: Full-Time

Position Overview:

We are seeking an experienced and highly motivated Biotech Process Development Scientist I to join our innovative team. This role will focus on advanced process development, optimization, and scale-up of bioprocesses for the production of biologics and therapeutic products. As a Downstream Process Development Scientist I, you will work independently and as part of a multidisciplinary team to drive the development of robust, scalable processes while collaborating with other departments to ensure project success.

Key Responsibilities:

ยทย ย ย ย ย ย ย ย  Independently design, optimize, and execute experiments to advance bioprocesses for downstream operations, including monoclonal antibodies, Fc-fusion proteins, bispecific antibodies, and cytokines.

ยทย ย ย ย ย ย ย ย  Lead the development and scale-up of bioprocesses from laboratory-scale through to pilot-scale and provide technical expertise for technology transfer to commercial manufacturing for clarification, chromatography (including affinity, ion exchange, hydrophobic interaction and mixed-mode), viral inactivation and viral filtration, ultra-filtration/diafiltration and filtration unit operations and process steps.

ยทย ย ย ย ย ย ย ย  Manage and execute viral clearance studies.

ยทย ย ย ย ย ย ย ย  Assist in the optimization of downstream bioprocess parameters for yield, purity, and product quality attributes, collaborating with upstream, analytical and formulation teams.

ยทย ย ย ย ย ย ย ย  Troubleshoot and resolve complex technical challenges by analyzing process data, performing root cause analysis, and implementing corrective actions.

ยทย ย ย ย ย ย ย ย  Collaborate with cross-functional teams, including Upstream and Analytical Development, Quality Assurance, MSAT, and Manufacturing to ensure the successful progression of projects.

ยทย ย ย ย ย ย ย ย  Lead the preparation and review of detailed technical documentation, including experimental protocols, reports, standard operating procedures (SOPs), and regulatory filings.

ยทย ย ย ย ย ย ย ย  Monitor and ensure compliance with industry regulations, including Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and FDA guidelines throughout the process development lifecycle.

ยทย ย ย ย ย ย ย ย  Provide mentorship and guidance to junior team members, helping to develop their skills and knowledge in bioprocess development.

ยทย ย ย ย ย ย ย ย  Plan and execute experiments in a timely manner, ensuring all milestones and timelines are met.

ยทย ย ย ย ย ย ย ย  Prepare presentations for internal stakeholders and regulatory authorities to communicate process development progress, challenges, and solutions.

ยทย ย ย ย ย ย ย ย  Contribute to the preparation of process development budgets and timelines, and track project deliverables against established goals.

Qualifications:

  • Bachelorโ€™s degree in Biological Sciences, Chemical Engineering, Biotechnology, or a related field. A Masterโ€™s degree or Ph.D. is a plus.
  • Minimum of 4-6 years of experience in bioprocess development, preferably within a biotech, pharmaceutical, or biologics manufacturing environment.
  • Strong hands-on experience with purification techniques, viral clearance, and process characterization.
  • Expertise in process development strategies for scaling up from laboratory to pilot scale and facilitating technology transfer to manufacturing.
  • Proficiency with process analytical technologies (PAT), and experience with downstream purification equipment, and chromatography techniques.
  • Strong understanding of regulatory requirements, including GMP, GLP, FDA, and ICH guidelines.
  • Experience in AKTA purification systems and UNICORN software and liquid handling platforms is preferred.
  • Proficiency in data analysis and process modeling using software tools such as Excel, JMP, GraphPad, or similar platforms.
  • Strong problem-solving, troubleshooting, and critical-thinking skills with the ability to manage multiple projects simultaneously.
  • Excellent written and verbal communication skills, with the ability to convey complex technical concepts to both technical and non-technical stakeholders.
  • Proven ability to work effectively both independently and in a team-oriented, collaborative environment.

Physical Requirements:

ยทย ย ย ย ย ย ย ย  Ability to perform lab-based tasks, including standing for long periods, working with various laboratory equipment, and handling biological samples.

ยทย ย ย ย ย ย ย ย  Must be able to lift and carry equipment, reagents, and materials weighing up to 25 pounds.

Working Conditions:

  • This position requires flexibility in working hours, including potential shift work, weekends, and on-call duties as necessary.
  • Work involves the handling of biological materials.