CrawlJobs Logo

Lead Bioprocess Engineer

United Kingdom, Bath · Job Posted May 20, 2026
Apply Position
Job Link Share

Job Description

Lead Bioprocess Engineer - Scale-Up & Pilot Operations Location: Somerset, UK (site-based) Type: Full-time We are seeking an experienced Lead Bioprocess Engineer to lead the scale-up and industrialisation of an innovative bioprocess platform. This role combines technical leadership with hands-on delivery, focusing on translating early-stage science into pilot-scale and commercially viable processes. The Role You will take ownership of bioprocess development and scale-up activities, working closely with R&D, engineering, and operations teams to move processes from lab through to pilot and beyond. A strong on-site presence is essential, and you will be actively involved in running experiments, troubleshooting processes, and optimising performance. Key responsibilities include: Leading end-to-end scale-up activities, from bench through pilot-scale demonstration Translating cell culture and tissue engineering processes into scalable manufacturing solutions Taking a hands-on role in process optimisation, troubleshooting, and system improvements across both unit operations and the wider platform Designing and overseeing scale-down models and experimental plans to support robust scaling strategies Driving improvements in process efficiency, cost of goods, and environmental performance Ensuring appropriate process documentation, validation, and technical standards are maintained Collaborating with internal teams and external partners to support technology development and delivery Managing and developing a team of engineers and scientists (3-5 direct reports) About You You will bring a strong combination of technical depth, practical experience, and leadership capability, with a clear track record in bioprocess scale-up and industrial biotechnology. Key requirements: Advanced qualification in bioprocess, biochemical, or chemical engineering Extensive industry experience in bioprocess development and scaling Proven track record working with bioreactors and associated unit operations from bench to pilot scale Strong understanding of upstream and/or downstream processing, including troubleshooting and optimisation Experience with CIP/SIP, contamination control, and operational challenges in bioprocess environments Demonstrated experience in leading teams and delivering complex technical programmes A practical, hands-on mindset, comfortable working directly with equipment and processes on-site A proactive, can-do attitude, with the ability to solve complex problems and adapt in a fast-paced environment Why Apply? This is an opportunity to play a central role in scaling a novel bioprocess technology, combining technical leadership with hands-on engineering and science. You will work in a collaborative, innovation-driven environment where your experience will directly influence the transition from R&D to real-world production. If you are a technically strong bioprocess expert who enjoys being close to the process, leading teams, and delivering scale-up in practice, this role offers a highly impactful next step. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Job Responsibility

  • Leading end-to-end scale-up activities, from bench through pilot-scale demonstration
  • Translating cell culture and tissue engineering processes into scalable manufacturing solutions
  • Taking a hands-on role in process optimisation, troubleshooting, and system improvements across both unit operations and the wider platform
  • Designing and overseeing scale-down models and experimental plans to support robust scaling strategies
  • Driving improvements in process efficiency, cost of goods, and environmental performance
  • Ensuring appropriate process documentation, validation, and technical standards are maintained
  • Collaborating with internal teams and external partners to support technology development and delivery
  • Managing and developing a team of engineers and scientists (3-5 direct reports)

Requirements

  • Advanced qualification in bioprocess, biochemical, or chemical engineering
  • Extensive industry experience in bioprocess development and scaling
  • Proven track record working with bioreactors and associated unit operations from bench to pilot scale
  • Strong understanding of upstream and/or downstream processing, including troubleshooting and optimisation
  • Experience with CIP/SIP, contamination control, and operational challenges in bioprocess environments
  • Demonstrated experience in leading teams and delivering complex technical programmes
  • A practical, hands-on mindset, comfortable working directly with equipment and processes on-site
  • A proactive, can-do attitude, with the ability to solve complex problems and adapt in a fast-paced environment

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Lead Bioprocess Engineer

8 matching positions

New

Specialist Manufacturing: Manufacturing Execution System (MES)

In this vital role you will communicate and interface between the GMP manufactur...
Location
Location
United States , Holly Springs
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree OR Master's degree in chemistry, biology, or engineering & 3 years of biotechnology operations experience or Bachelor's degree and 5 years of biotechnology operations experience or Associate's degree & 10 years of biotechnology operations experience or High school diploma / GED & 12 years of biotechnology operations experience
  • Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry
  • Excellent cross-functional project management, meeting facilitation, and technical writing skills
  • Experience in GMP manufacturing operations
  • Strong technical knowledge of drug substance processing (Inoculation, Bioreactors, Harvest, chromatography, filtration, buffer preparation) and a broad understanding of related disciplinary areas in bioprocessing
  • Extensive experience with electronic batch record design in Koerber PAS|X or comparable software for electronic batch records with some understanding of editing and validation
  • Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms
  • Ability to coach, mentor and/or cross train colleagues within core technical areas
Job Responsibility
Job Responsibility
  • Communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups
  • Ensure all Electronic Batch Records accurately document the manufacturing process
  • Drive batch record optimization between the manufacturing floor and the global MES team
  • Propose, participate, and lead team improvement initiatives to drive improved productivity on manufacturing floor
  • Coordinate with Global MES Team, Manufacturing, Process Development, Process Owner, and Quality to create and modify electronic batch records to support implementation of new products and/or technologies into the plant
  • Lead and/or participate in projects, ensuring electronic batch records accurately and effectively record all necessary process data for unit operations in Koerber PAS|X
  • Support Manufacturing in troubleshooting, problem solving and RCAs
  • Support CAPA development to prevent error recurrence
  • Own Generic Master Batch Record (GMBR) optimizations and function as primary liaison between site MES and global MES team to drive on time deliveries of GMBRs
  • Respond to regulatory questions and/or audit findings
What we offer
What we offer
  • Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • Discretionary annual bonus program or sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans and bi-annual company-wide shutdowns
  • Flexible work models including remote work arrangements where possible
  • Fulltime
Read More
Arrow Right

Senior Director Research & Development

The Single-Use Technologies Division (SUD) is a global leader in the design and ...
Location
Location
United States , Plainville
Salary
Salary:
212000.00 - 317000.00 USD / Year
mygwork.com Logo
myGwork - LGBTQ+ Business Community
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in engineering, physical sciences, or chemistry required
  • Master's degree or Ph.D. preferred
  • 10+ years of progressive R&D leadership experience, preferably within bioprocessing, bioproduction, or regulated medical device environments
  • Demonstrated success leading global, multi-site teams and delivering complex products from concept through commercialization
  • Strong background in bioprocess systems and equipment
  • experience with single-use technologies strongly preferred
  • Experience with digital and data-enabled systems (automation, control systems, MES, ERP, historians, analytics) preferred
  • Ability to influence across functions and operate effectively in a matrixed, fast-paced environment
  • Ability to travel up to 25% domestically and internationally
Job Responsibility
Job Responsibility
  • Serve as an integral member of the SUD leadership team, representing R&D in strategic planning (STRAP), portfolio prioritization, and Annual Operating Plan (AOP) processes
  • Own and execute the global R&D and product development strategy aligned with the business and market needs
  • Partner closely with Product Management, Market Development, Manufacturing Engineering, Operations, Quality, and Commercial teams to drive end-to-end lifecycle execution
  • Engage directly with customers and commercial teams on complex technical programs
  • Partner with the Bioproduction Group Innovation team, other business groups, and the Corporate Innovation Council to develop next-generation products, platforms, and differentiated intellectual property
  • Drive technology collaboration across divisions and business units to accelerate innovation and leverage enterprise capabilities
  • Translate customer and market requirements into differentiated products that meet cost, quality, performance, regulatory, and time-to-market expectations
  • Lead the advancement of digitalization, automation, and data-enabled technologies within single-use and bioprocessing systems
  • Champion all aspects of regulated product development, ensuring compliance with design control and quality system requirements
  • Serve as process owner for New Product Introduction (NPI), Engineer-to-Order (ETO/customization), and product improvement processes
What we offer
What we offer
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
  • Variable annual bonus based on company, team, and/or individual performance results
  • Fulltime
Read More
Arrow Right

Senior Systems Specialist - Controls Engineering Automation

The Senior Systems Specialist - Controls Engineering is responsible for independ...
Location
Location
India , Bangalore
Salary
Salary:
Not provided
danaher.com Logo
Danaher Corporation
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Electrical, Electronics, or Instrumentation & Controls Engineering required
  • A minimum of 8 years of industrial experience in the design and development of industrial automation and control software, including participation in the complete software development lifecycle
  • Experienced in designing Automation HMI/SCADA solutions, as well as diagnosing and programming programmable logic controllers (PLCs) on at least two platforms such as Aveva System Platform, Rockwell Automation FactoryTalk, DeltaV, Siemens, or similar
  • Strong experience with hardware interfaces, communication protocols, and PID control loops
  • Familiarity with Engineering Change Orders (ECO) & Engineering Change Requests (ECR), comprehensive knowledge of PLM tools such as MAGIC, ALM, Azure DevOps, Jira, or equivalent, and practical expertise in defect management, software verification, and testing
Job Responsibility
Job Responsibility
  • Oversee and actively contribute to all phases of the automation software development lifecycle, including conceptual design, detailed engineering, simulation/modeling, verification, and validation, ensuring alignment with project objectives and compliance requirements
  • Support the design, development, and lifecycle management of bioprocessing systems, aiding in the delivery of project milestones and advancing continuous improvement efforts
  • Lead and implement change management processes, including Engineering Change Requests (ECR) and Engineering Change Orders (ECO), in accordance with established quality and regulatory standards
  • Identify, assess, and resolve technical challenges, delivering effective solutions and promoting ongoing process enhancements
  • Provide technical leadership and mentorship to new team members, fostering a collaborative and high-performing work environment
What we offer
What we offer
  • health care program
  • paid time off
  • Fulltime
Read More
Arrow Right

Business Development Manager Gene Therapy

The Business Development Manager Gene Therapy is responsible for driving commerc...
Location
Location
Spain , Barcelona
Salary
Salary:
Not provided
danaher.com Logo
Danaher Corporation
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree or higher in Life Sciences, Biotechnology, Biochemistry, Chemical Engineering, or a related scientific discipline
  • Strong Experience in bioprocessing, cell and gene therapy, vaccines, or advanced therapy commercialization, application support, or technical sales
  • Demonstrated experience working with advanced therapy modalities such as viral vectors, nucleic acids, or cell‑based manufacturing processes
  • Proficiency using CRM systems (e.g., SFDC) for opportunity, funnel, and project tracking
  • Experience supporting Design‑In programs, technical evaluations, or customer adoption of complex bioprocessing technologies
  • Ability to travel up to 40%-50%, including overnight travel, within the assigned territory
  • Must have a valid driver's license with an acceptable driving record
Job Responsibility
Job Responsibility
  • Own advanced therapy workflows including Viral Vectors, Vaccines based on Viral Vectors, pDNA, exosomes, Synthetic DNA, mRNA, and Oligonucleotides, with a deep understanding of biological activity, development, and manufacturing processes
  • Drive order growth within the assigned territory by expanding Cytiva technologies with existing customers and introducing Cytiva solutions into gene therapy programs through Design‑In initiatives
  • Partner with Field Application Specialists (FAS) to test, demonstrate, and deliver technical training on Cytiva technologies at customer sites, clearly differentiating Cytiva's value proposition
  • Support marketing and lead generation activities by collaborating with Field Event Marketing, identifying and supporting key regional events, congresses, and customer engagements to generate and convert MQLs
  • Manage CRM and funnel execution by maintaining MQLs, Design‑In projects, and Opportunities in SFDC in alignment with the MQL, Design‑In, and Funnel Management Playbooks
What we offer
What we offer
  • Remote work arrangement
  • health care program
  • paid time off
  • Fulltime
Read More
Arrow Right

Sr Engineer, PD Process Validation & Business Strategy

In this vital role you will be a part of the Process Development Drug Substance ...
Location
Location
United States , Holly Springs
Salary
Salary:
115494.60 - 156257.40 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school diploma / GED and 10 years of biologics process development, process engineering, or process validation experience OR
  • Associate's degree and 8 years of biologics process development, process engineering, or process validation experience OR
  • Bachelor's degree and 4 years of biologics process development, process engineering, or process validation experience OR
  • Master's degree and 2 years of biologics process development, process engineering, or process validation experience OR
  • Doctorate degree
Job Responsibility
Job Responsibility
  • Lead the development of Process Validation/Process Performance Qualification strategy for New Products, ensuring alignment with regulatory guidelines and industry standards
  • Apply a fundamental understanding of Upstream (Cell Culture) and Downstream (Purification) bioprocessing to support process validation, technology transfer support, and plant start-up
  • Lead the execution of validation projects and/or protocols and the collection of data to ensure completion of process validation activities
  • Provide cross-functional process monitoring support as needed
  • Provide guidance for the generation, resolution and closure of deviations
  • Lead ANC PD business strategy activities to improve network practice, develop digital tools, and optimize the ANC PD business operations
  • Ensure safety and compliance of process development activities
  • Provide process validation floor process support as required
  • Lead process validation support for regulatory filing, inspection, and other CMC activities
What we offer
What we offer
  • Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • Discretionary annual bonus program
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible
  • Fulltime
Read More
Arrow Right

Lead Microalgae Scientist

We are seeking a Lead Microalgae Scientist to drive and expand our biology R&D e...
Location
Location
Denmark , Taastrup
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in biotechnology, microbiology, biochemistry, biology or a related field
  • 5+ years of experience working with microalgae or photosynthetic systems
  • Strong expertise in algal physiology, cultivation systems, and experimental design
  • Proven experience translating lab-scale biology into pilot or industrial settings
  • Scientific leadership experience
  • Hands-on, pragmatic approach, and eager to learn
  • Proficient in English (we are 7 different nationalities in Algiecel) and able to communicate and collaborate across disciplines and cultural backgrounds
  • EU work permit and willingness to relocate to CPH area
Job Responsibility
Job Responsibility
  • Define and drive the biology R&D roadmap aligned with company and scale-up goals
  • Act as the internal expert on microalgae biology, cultivation, and performance optimization
  • Translate scientific results into scalable solutions, product-relevant outcomes, and IP
  • Develop a data-driven biology strategy integrating experimental and omics data
  • Lead strain screening, characterization, and optimization for productivity, robustness, and target composition
  • Design and execute experiments in algal physiology, photosynthesis, and cultivation systems
  • Drive improvements in growth rates, photosynthetic efficiency, and biomass quality
  • Work closely with engineering and operations teams in scale-up and process integration
  • Support downstream processing, product development, and quality control of biomass
  • Contribute to translating biology into customer value propositions
What we offer
What we offer
  • Competitive salary package
  • Health insurance
  • Annual collective team-based bonus plan
  • Fulltime
Read More
Arrow Right

Lead Microalgae Scientist

We are seeking a Lead Microalgae Scientist to drive and expand our biology R&D e...
Location
Location
Denmark , Taastrup
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in biotechnology, microbiology, biochemistry, biology or a related field
  • 5+ years of experience working with microalgae or photosynthetic systems
  • Strong expertise in algal physiology, cultivation systems, and experimental design
  • Proven experience translating lab-scale biology into pilot or industrial settings
  • Scientific leadership experience
  • Hands-on, pragmatic approach, and eager to learn
  • Proficient in English (we are 7 different nationalities in Algiecel) and able to communicate and collaborate across disciplines and cultural backgrounds
  • EU work permit and willingness to relocate to CPH area
Job Responsibility
Job Responsibility
  • Define and drive the biology R&D roadmap aligned with company and scale-up goals
  • Act as the internal expert on microalgae biology, cultivation, and performance optimization
  • Translate scientific results into scalable solutions, product-relevant outcomes, and IP
  • Develop a data-driven biology strategy integrating experimental and omics data
  • Lead strain screening, characterization, and optimization for productivity, robustness, and target composition (e.g. protein, omega-3)
  • Design and execute experiments in algal physiology, photosynthesis, and cultivation systems
  • Drive improvements in growth rates, photosynthetic efficiency, and biomass quality
  • Work closely with engineering and operations teams in scale-up and process integration
  • Support downstream processing, product development, and quality control of biomass
  • Contribute to translating biology into customer value propositions
What we offer
What we offer
  • Competitive salary package
  • Health insurance
  • Annual collective team-based bonus plan
  • Fulltime
Read More
Arrow Right

MSAT Bioprocess Specialist

We are working with a leading biopharmaceutical manufacturer who are seeking an ...
Location
Location
United Kingdom , Falkirk
Salary
Salary:
Not provided
srgtalent.com Logo
SRG
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BSc (Hons) or equivalent in a Science or Engineering discipline
  • Proven GMP biologics manufacturing or process development experience
  • Strong organisational and stakeholder influencing skills
  • Demonstrated project management capability and ability to meet deadlines
  • Experience in process scale-up/transfer and providing manufacturing support
  • Effective communication across all levels
  • Experience evaluating materials for process suitability and writing GMP batch records
Job Responsibility
Job Responsibility
  • Lead the technology transfer of new and existing biologics processes into GMP manufacturing
  • Prepare, review, approve and issue GMP manufacturing documentation, including batch records
  • Define scale-up criteria and develop process mass balances and flow diagrams
  • Specify large-scale equipment and assess material suitability for GMP use
  • Generate quality documentation for raw materials and equipment
  • Work within the site Quality Management System, raising and managing change controls
  • Conduct and close investigations, deviations and CAPAs
  • Project manage the introduction of processes into manufacturing from end to end
  • Perform risk assessments aligned with ICH Q9 principles
  • Collaborate cross-functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners
  • Fulltime
Read More
Arrow Right