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Lead Bioprocess Engineer Jobs (NOW HIRING)

Begell House Inc.

Site Process Engineer

Bend, OR · On-site

In this role, you will monitor and optimize unit operations, lead investigations and root-cause ... This role offers exposure to advanced bioprocess technologies, global projects, and a collaborative ...

Emergent Biosolutions

BioProcess Specialist

Canton, MA · On-site

... Engineering, and external stakeholders to ensure robust, compliant, and efficient bioprocess ... Lead and support complex investigations (process- and product-impacting deviations), author high ...

Prolific Machines

Optical Engineer

Emeryville, CA · On-site

$149K - $193K/yr

You will work closely with the Lead Optical Engineer to enable optical simulations, modeling ... This individual will collaborate with Hardware, Data, Biology, and Bioprocess Engineering teams on ...

DutchTechX

Optical Engineer

Emeryville, CA · On-site

$149K - $193K/yr

You will work closely with the Lead Optical Engineer to enable optical simulations, modeling ... This individual will collaborate with Hardware, Data, Biology, and Bioprocess Engineering teams on ...

Prolific Machines

Optical Engineer

Emeryville, CA · On-site

$115K - $175K/yr

You will work closely with the Lead Optical Engineer to enable optical simulations, modeling ... This individual will collaborate with Hardware, Data, Biology, and Bioprocess Engineering teams on ...

Prolific Machines

Optical Engineer

Emeryville, CA · On-site

$149K - $193K/yr

You will work closely with the Lead Optical Engineer to enable optical simulations, modeling ... This individual will collaborate with Hardware, Data, Biology, and Bioprocess Engineering teams on ...

Prolific Machines

Optical Engineer

Emeryville, CA · On-site

$115K - $175K/yr

You will work closely with the Lead Optical Engineer to enable optical simulations, modeling ... This individual will collaborate with Hardware, Data, Biology, and Bioprocess Engineering teams on ...

PM Group

Lead Process Engineer

Boston, MA · On-site

$120K - $160K/yr

Overview The Lead Process Engineer position is an exciting opportunity to join PM Group's quickly ... Bachelor's degree in Chemical Engineering, Mechanical Engineering, Bioprocess Engineering, or a ...

Merck Group

Bioprocess Applications Engineer 3

Bedford, MA · On-site

$84K - $127K/yr

Your Role We're seeking a Bioprocess Applications Engineer 3 to join the Single Use and Integrated ... Lead development, optimization, and lifecycle management of Raman chemometric models for mAb ...

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Lead Bioprocess Engineer information

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How much do lead bioprocess engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for lead bioprocess engineer in the United States is $123,784.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,500.00 and $135,000.00 per year, depending on experience, location, and employer.

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For Lead Bioprocess Engineer jobs, the most frequently searched job titles are:

Infographic showing various Lead Bioprocess Engineer job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $123,784 per year, or $59.5 per hour.

MSAT Bioprocess Engineer III / IV

Frederick, MD • On-site

Theradaptive
11 - 50 employees
Learn more about Theradaptiveexternal

Full-time

Re-posted 12 days ago

Job description

Theradaptive is revolutionizing the field of therapeutic delivery with a pipeline of best-in-class products that address multiple global markets. Theradaptive is performing cutting edge science in the area of regenerative medicine, working at the interface of biology and tissue repair.
Our lead therapeutics are in the following indications:
  • Spinal Fusion
  • Long Bone Repair
  • Osteochondral Repair
  • Dental and Facial Bone Repair
  • Immuno-Oncology

We are an innovative, fast-paced team that is advancing a diverse array of cutting-edge translational research projects.
POSITION SUMMARY
Theradaptive is seeking a skilled and driven MSAT Process Engineer III/IV to join our Manufacturing Science and Technology team. This role will provide hands-on technical leadership and manufacturing support for GMP operations, lead deviation investigations and CAPA activities, support process validation and continued process verification (CPV), and partner cross-functionally to advance Theradaptive's combination product pipeline. The successful candidate will bring strong technical judgment, a data-driven approach to problem solving, and the ability to translate process knowledge into robust, compliant, and scalable manufacturing solutions.
Travel requirement: Up to 10%, primarily to support CMO/CDMO technology transfer activities.
RESPONSIBILITIES
GMP Manufacturing Support
  • Serve as the primary technical point of contact for day-to-day GMP manufacturing operations.
  • Monitor real-time manufacturing activities, troubleshoot process issues, and drive timely resolution of technical challenges.
  • Ensure manufacturing processes remain continuously aligned with cGMP requirements and applicable regulatory expectations.

Deviation Management & Investigations
  • Lead and independently author deviation investigations, applying structured root cause analysis (RCA) methodologies (e.g., 5-Why, Fishbone, FTA).
  • Develop and track robust CAPA plans; assess effectiveness and drive closure in a compliant and timely manner.
  • Manage change control activities, evaluating technical impact and ensuring thorough documentation.

Process Validation & Continued Process Verification (CPV)
  • Own and execute process validation activities including Process Performance Qualification (PPQ) protocols and reports.
  • Apply Design of Experiments (DOE) principles to support process characterization, parameter optimization, validation strategy, and establishment of robust process control ranges.
  • Analyze CPV metrics and process datasets to proactively identify trends, risks, and opportunities for improvement.
  • Support product lifecycle management and post-approval change activities.

Technology Transfer
  • Lead or support technology transfer activities between process development, internal GMP manufacturing, and external contract manufacturing organizations (CMOs/CDMOs).
  • Author and review technology transfer plans, batch records, and technical reports to ensure manufacturing readiness.
  • Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations.

GMP Documentation
  • Author, review, and approve GMP documentation including deviations, technical reports, validation protocols/reports, change controls, and SOPs.
  • Maintain high documentation standards consistent with regulatory expectations and internal quality systems.

Cross-Functional Collaboration & Continuous Improvement
  • Partner cross-functionally with Manufacturing, QC, QA, Supply Chain, and Regulatory teams to drive compliant, efficient operations.
  • Champion continuous improvement initiatives and apply process excellence principles to manufacturing performance.
  • Participate in audit and inspection readiness activities, including preparation of technical summaries and subject-matter expert support.

QUALIFICATIONS
  • Bachelor's or master's degree in engineering, Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
  • Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP manufacturing support in biologics or medical devices,
  • Demonstrated ability to independently lead deviation investigations, CAPA development, and change control activities.
  • Hands-on experience with process validation (PV), Process Performance Qualification (PPQ) and CPV programs.
  • Prior involvement in technology transfer activities, including transfers to or from CMO/CDMO partners, preferred.
  • Working knowledge of biologics unit operations, including one or more of the following:
    • Cell culture (mammalian, microbial, or primary cell systems)
    • Downstream purification (chromatography, filtration, centrifugation)
    • Formulation and fill-finish operations
  • Experience with statistical data analysis, SPC charting, and process trending tools.
  • Familiarity with regulatory frameworks including FDA 21 CFR Part 211/600, ICH Q8/Q9/Q10, and ISO standards.
  • Proficiency with GMP documentation systems (electronic or paper-based) and quality management systems (e.g., Track Wise, Master Control).
  • Data-driven problem solver with strong scientific judgment.
  • Clear technical communicator and cross-functional collaborator.
  • Detail-oriented, accountable, adaptable, and improvement-minded.

PHYSICAL DEMANDS
  • Ability to work in classified cleanroom environments and meet all applicable gowning and PPE requirements.
  • Capacity to stand for extended periods and perform repetitive technical tasks in a GMP setting.
  • Ability to lift and handle laboratory equipment and supplies as required.

COMPENSATION RANGE:
$108,000-$139,000 annually, based on qualifications and level.
POSITION LOCATION:
On-site at Theradaptive's corporate headquarters in Frederick, MD.
https://www.theradaptive.com
Theradaptive is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, ethnic or national origin, ancestry, pregnancy (including childbirth or related condition), citizenship, familial status, mental or

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