MSAT Process Engineer Job at Randstad (Woluwé-Saint-Lambert)

Bio Process Engineer

The Bio Process Engineer main responsibilities are : - Be accountable for overse...

Location

Belgium , Strombeek-Bever

Salary:

Not provided

Randstad

Expiration Date

August 24, 2026

Requirements

Medior profile required – Min 3-5 years of experience with exposure in 2 or more departments: Engineering, Automation, Operation, MSAT or similar
In-depth technical knowledge of biomanufacturing processes
Advanced project management skills, including creation of automated reporting, adaptation of sequencing, planning, risk management, and stakeholder engagement
Experience with Operational Excellence methodologies (Yellow to Green Belt certification)
Strong knowledge of automation systems, including Siemens PCS7
Good understanding of Critical Process Parameters (CPPs), Key Performance Parameters (KPPs), and Process Parameters (PPs)
Proficiency in Process and Instrumentation Diagrams (P&IDs) and Functional Design Specifications (FDS)
Troubleshooting experience (root causes, CAPAs) with problem-solving abilities. Capacity to tackle major technical challenges and to drive innovative solutions
A good understanding backed up by experience of current Good Manufacturing Practices (cGMP)
Good leadership abilities, with a collaborative and inclusive approach to team management

Job Responsibility

Be accountable for overseeing process-oriented projects related to equipment and systems, integrating product, engineering, Digitalization and automation components
Address minor and major investigations across product, engineering, and automation domains
Execute process and equipment-oriented projects, integrating product, engineering, digitalization and automation components
Facilitate comprehensive project plans, including budgets, timelines, and resource allocations
Facilitate project kick-off meetings and provide ongoing guidance to project teams
Monitor project progress, identify risks, and implement mitigation strategies as needed
Serve as the primary liaison with internal teams and external suppliers
Ensuring effective communication and collaboration
Challenge existing proposals and solutions, leveraging expertise to drive innovation and optimization

Fulltime

Process Engineer, Manufacturing Science & Technology

As we move our cell therapy programs through late-stage development toward BLA s...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

B.S. with 3 + years or M.S. with 2-3 years' experience within biologics process development, MSAT or manufacturing under cGMP processes or PhD degree
Previous experience and working knowledge of T-cells or immunological cell therapies
Experience with cell therapy manufacturing scale up, technology transfer, and process development and optimization is required
Experience supporting late-stage MSAT activities, including process characterization, PPQ planning/execution, scale-up/scale-out strategies, and continued process verification
Direct involvement in BLA-enabling MSAT deliverables such as Module 3 process descriptions, validation packages, tech transfer documentation, and inspection readiness strongly preferred
Good working knowledge in cGMP manufacturing of biological process and ICH regulations
Strong written and verbal communication skills
Highly organized and efficient
Able to work independently
Strong problem-solving skills

Job Responsibility

Support technology transfer of mature, optimized processes to CMOs for clinical and late-phase cGMP manufacturing, ensuring readiness for PPQ and commercial-scale operations
Provide manufacturing oversight at CMOs, including person-in-plant support, review of manufacturing performance, and real-time issue escalation to maintain phase-appropriate control strategies
Execute process development and characterization studies, generate high-quality protocols and reports, and present data to cross-functional teams to inform PPQ planning and BLA Module 3 content
Ensure timely and accurate data capture, supporting data integrity requirements for late-stage filings, validation packages, and regulatory inspections
Maintain all training requirements in a compliant state, aligning with expectations for late-stage manufacturing and inspection readiness
Support phase-appropriate cell therapy processes using QbD principles, including identification of CPPs/CMAs and contributing to control strategy refinement for BLA submission
Identify and evaluate new technologies that enhance scalability, robustness, cost efficiency, and process consistency in preparation for commercial readiness
Provide ongoing oversight of CMO operations, including batch record and testing documentation review, data trending, and deviation/CAPA support consistent with PPQ and late-stage expectations
Coordinate internal and external activities related to patient material and product logistics, ensuring compliant chain-of-identity/chain-of-custody processes critical for pivotal trial operations
Support MSAT planning for development and validation materials, maintaining inventory and coordinating procurement to enable process characterization and PPQ readiness

What we offer

health and retirement, PTO, and stock option plans

Fulltime

Associate MSAT Engineer

We are looking for a highly motivated and dynamic Associate MSAT Engineer to joi...

Location

Canada , Vancouver

Salary:

57000.00 - 71154.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

2+ years of related work experience in bioprocess development within a GMP manufacturing setting
BSc in Engineering (Mechanical, Biomedical, Chemical, or Industrial) or Life Sciences (Biotech, Pharmaceutical Sciences)
Strongly self-motivated and able to identify project needs and follow that up with building and implementing solutions
Strong interpersonal skills with the ability to work collaboratively as a member of cross-functional team
Excellent documentation and communication skills, as well as strong attention to detail
Able to learn new technologies and platforms quickly, accurately, and efficiently
Enthusiastic about applying expertise to biopharmaceutical manufacturing

Job Responsibility

Performing data collection, analysis, and trending for manufacturing batches (e.g., bioreactor, chromatography, and filtration steps)
Supporting execution and documentation of process characterization, scale-up, or troubleshooting studies
Participating in deviation investigations and supporting root cause analysis
Maintaining and organizing process monitoring databases and dashboards
Collaborating with Manufacturing, QA, and Process Development teams to transfer knowledge and support batch readiness activities
Contributing to continuous improvement initiatives (e.g., process robustness, yield improvement, or documentation efficiency)

What we offer

Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Teams and social groups to build community and connections

Fulltime

MSAT Network Service Assurance Engineer

We are seeking an MSAT Network Service Assurance Engineer to support Vodafone’s ...

Location

India , Bangalore

Salary:

Not provided

Vodafone

Expiration Date

Until further notice

Requirements

Analytical and detail-oriented individual with a solid understanding of mobile network operations
Experienced in telecommunications technologies such as GSM, LTE, and 5G, with awareness across RAN and Core domains
Comfortable interpreting end-to-end service flows for voice, data, and messaging services
Familiar with signalling protocols and interfaces (including Diameter, GTP, SIP, SS7, HTTP/2, PFCP, and 4G/5G core interfaces) to support effective troubleshooting
Confident working in ticket-driven, reactive environments while managing multiple incidents simultaneously
A collaborative team contributor with clear and effective communication skills in English
Self-motivated, organised, and able to deliver results under pressure

Job Responsibility

Investigate, triage, and progress mobile network faults raised through Customer Operations and internal ticketing systems
Manage incidents end-to-end, including diagnosis, impact assessment, prioritisation, escalation, and resolution tracking
Maintain ownership of assigned faults and ensure alignment with SLAs and operational expectations
Collaborate with second-line support teams, engineering functions, and external partners to resolve complex network issues
Escalate incidents appropriately where resolution is outside MSAT scope, ensuring clear accountability and follow-through
Provide accurate, timely, and high-quality updates in ticketing and operational reporting tools
Support service recovery activities to restore customer services at pace and with minimal disruption
Identify recurring fault trends and contribute to continuous improvement of fault handling processes
Maintain documentation and actively support knowledge sharing within the team

What we offer

Exposure to complex, customer-impacting incidents within a global mobile network environment
Opportunities to collaborate with diverse technical teams across Vodafone markets
A role at the forefront of network integration and transformation activities
Continuous learning through hands-on incident management and service assurance operations

Fulltime

MSAT Network Service Assurance Engineer

We are seeking an MSAT Network Service Assurance Engineer to support Vodafone’s ...

Location

India , Bangalore

Salary:

Not provided

Vodafone

Expiration Date

Until further notice

Requirements

Analytical and detail-oriented individual with a solid understanding of mobile network operations
Experienced in telecommunications technologies such as GSM, LTE, and 5G, with awareness across RAN and Core domains
Comfortable interpreting end-to-end service flows for voice, data, and messaging services
Familiar with signalling protocols and interfaces (including Diameter, GTP, SIP, SS7, HTTP/2, PFCP, and 4G/5G core interfaces) to support effective troubleshooting
Confident working in ticket-driven, reactive environments while managing multiple incidents simultaneously
A collaborative team contributor with clear and effective communication skills in English
Self-motivated, organised, and able to deliver results under pressure

Job Responsibility

Investigate, triage, and progress mobile network faults raised through Customer Operations and internal ticketing systems
Manage incidents end-to-end, including diagnosis, impact assessment, prioritisation, escalation, and resolution tracking
Maintain ownership of assigned faults and ensure alignment with SLAs and operational expectations
Collaborate with second-line support teams, engineering functions, and external partners to resolve complex network issues
Escalate incidents appropriately where resolution is outside MSAT scope, ensuring clear accountability and follow-through
Provide accurate, timely, and high-quality updates in ticketing and operational reporting tools
Support service recovery activities to restore customer services at pace and with minimal disruption
Identify recurring fault trends and contribute to continuous improvement of fault handling processes
Maintain documentation and actively support knowledge sharing within the team

What we offer

Exposure to complex, customer-impacting incidents within a global mobile network environment
Opportunities to collaborate with diverse technical teams across Vodafone markets
A role at the forefront of network integration and transformation activities
Continuous learning through hands-on incident management and service assurance operations

Fulltime

MSAT Bioprocess Specialist

We are working with a leading biopharmaceutical manufacturer who are seeking an ...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

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

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

Contamination Control Manager

At SRG, we are excited to be partnering with our client, a biologics Contract De...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Degree in Microbiology, Biology, Biochemistry, Chemical Engineering or related discipline (Master's preferred)
Extensive industry experience in sterile or biologics pharmaceutical manufacturing, ideally within a CDMO
Strong expertise in aseptic processing, cleanroom operations and microbiological contamination control
Proven experience leading FMEA and cross-functional risk assessments
Solid understanding of global regulatory expectations
Ability to influence in matrixed environments with strong communication, coaching and facilitation skills

Job Responsibility

Own and evolve the site Contamination Control Strategy in line with EU/UK GMP Annex 1, FDA and ICH expectations
Embed contamination control principles into facility and equipment design, process flows, cleaning and sterilisation strategies, supplier management and training programmes
Partner with Manufacturing to influence aseptic behaviours, shift routines, operator decision-making and capability development
Collaborate with MSAT across equipment design, tech transfer, scale-up, process characterisation and new product introduction
Ensure full integration of the CCS with Quality systems including deviations, investigations, CAPAs, change control and audit readiness
Lead contamination-focused risk assessments (including FMEA) across client processes, shared equipment, utilities, campaign manufacturing and changeovers
Translate risk into practical, executable operational controls and maintain assessments as living tools informed by data and trends
Design and deploy contamination control training tailored to a CDMO environment, reinforcing learning through hands-on coaching and on-the-floor engagement
Champion a strong site-wide contamination control culture where prevention is everyone's responsibility
Provide governance-level oversight of contamination-related data, driving continuous improvement and reduction of repeat deviations

What we offer

Excellent salary and benefits package including enhanced pension, healthcare and annual bonus scheme
A chance to make a real difference and lead from the front in a key role on site
Working at the forefront of the biologics industry

Fulltime

Process Development Scientist

You will join the Process Development team in Singapore as a Process Development...

Location

Singapore , Tuas

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Degree in chemical engineering, biochemical engineering, life sciences or a related technical discipline
At least 3 years of laboratory or process technician experience, or relevant internships or industrial attachments
Practical skills with common lab tools and equipment (for example pipettes, balances, pH meters, basic chromatography or spectroscopy)
Good written and spoken English with clear communication and record-keeping skills
Comfortable working on-site in Singapore and following safety and hygiene requirements
Commitment to follow documentation, quality and regulatory standards in a manufacturing-support environment

Job Responsibility

Run routine lab and small-scale process experiments under supervision following safety and quality standards
Prepare samples, reagents, buffers and basic solutions, and maintain laboratory and pilot equipment
Collect, record and organise experimental data clearly and accurately in lab notebooks and electronic systems
Support process characterization, scale-up trials and technology transfer activities with production and MSAT colleagues
Support the design, development and implementation of Process Analytical Technology (PAT) tools for real-time process monitoring and control
Apply data analytics, multivariate analysis, and statistical modeling to understand process performance and variability
Develop data-driven process control strategies to improve robustness, yield, and product quality

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

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MSAT Process Engineer

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