CrawlJobs Logo
Baxter Logo Baxter · IT - Administration

Sr. Engineer, Manufacturing Engineering

Malta, Marsa Employment contract 32000.00 EUR / Year · Job Posted May 30, 2026
Apply Position
Job Link Share

Job Description

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride. We are currently looking for a Senior Manufacturing Process Engineer to join our team in Malta. In this role, you will play a key part in ensuring that manufacturing processes run smoothly, efficiently, and in full compliance with regulatory and quality standards. You will drive process engineering activities across production areas, helping to deliver products to customers on time while improving quality, yield, and overall performance. Working closely with cross-functional teams and external partners, you will support continuous improvement initiatives and help create a reliable, high-performing manufacturing environment.

Job Responsibility

  • Perform routine and non-routine calibration and maintenance activities for analytical laboratory instruments in accordance with approved procedures and schedules
  • Plan, schedule, and manage calibration and maintenance activities performed by external service providers or equipment manufacturers, including supplier-calibrated instruments
  • Review service reports and calibration certificates to ensure completeness, accuracy, and compliance with internal procedures and regulatory expectations
  • Provide technical support in the event of instrument malfunctions or failures, including troubleshooting, root cause identification, and coordination with equipment manufacturers or service providers to resolve issues
  • Collaborate closely with Quality team members to ensure calibration and maintenance activities are aligned with quality system requirements, including data integrity, documentation standards, and change management processes
  • Ensure adherence to applicable Quality Systems, GLP principles, and regulatory requirements
  • actively participate in audit preparation, inspections, and responses to audit findings related to calibration and maintenance activities

Requirements

  • Bachelor's degree in Engineering (Mechanical, Electrical, Manufacturing, or related field)
  • Minimum 3+ years of experience in a manufacturing environment
  • Strong ability to analyze statistical and process data and translate insights into actionable improvements
  • Experience with process improvement methodologies and tools (e.g., FMEA, SPC, Lean principles)
  • Ability to manage multiple priorities in a fast-paced manufacturing environment
  • Ability to work in a regulated environment and ensure compliance with quality and safety standards
  • Strong problem-solving skills with a proactive and resourceful mindset
  • Effective communication and collaboration skills to work with cross-functional teams and external partners

What we offer

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Baxter - All Job Offers

Looking for more opportunities?

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

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Sr. Engineer, Manufacturing Engineering

8 matching positions

New

Sr. Engineer, Manufacturing Engineering

Being an Engineer at Baxter means you play a critical role in helping us achieve...
Location
Location
Malta , Marsa
Salary
Salary:
32000.00 EUR / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in Manufacturing industry 3+ years is required for Senior Bachelors Degree in Engineering field (Mechanical, Electrical or Manufacturing)
  • Ability to interpret and analyze statistical data and information and financial reports, understand, and resolve technical difficulties, interface with internal engineering/technical experts and external technical representatives, manage multiple priorities in a manufacturing plant setting, and be resourceful to a large manufacturing department.
Job Responsibility
Job Responsibility
  • Ensure products are provided to customers on time so that product quality, yield, operating costs and process efficiencies are met
  • Responsible for assuring compliances to all regulatory requirements – FDA, OSHA, OFCCP, EPA, etc
  • Adheres to all environmental, health and safety SOPs, equipment, policies and procedures, including any process specific requirements
  • Perform analytical review, recommend, and implement corrective action for any exception condition
  • Identify/Execute/Implement process specific improvements within all production areas arising from both quality and performance issues
  • Areas of focus include: DPM, Conversion loss, SPC, CIPM, FMEA, EPC, Digitization and iCare
  • Support Maintenance Activities and upkeep of respective documentation
  • Maintain and update departmental Standard Local Operating Procedures
  • Support plant-wide strategic plan programs and activities
  • Reporting directly to the Maintenance Area Principal Engineer
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Sr. Engineer, Manufacturing Engineering

Being an Engineer at Baxter means you play a critical role in helping us achieve...
Location
Location
Malta , Marsa
Salary
Salary:
32000.00 EUR / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Engineering (Mechanical, Electrical, Manufacturing, or related field)
  • Minimum 3+ years of experience in a manufacturing environment
  • Strong ability to analyze statistical and process data and translate insights into actionable improvements
  • Experience with process improvement methodologies and tools (e.g., FMEA, SPC, Lean principles)
  • Ability to manage multiple priorities in a fast-paced manufacturing environment
  • Ability to work in a regulated environment and ensure compliance with quality and safety standards
  • Strong problem-solving skills with a proactive and resourceful mindset
  • Effective communication and collaboration skills to work with cross-functional teams and external partners.
Job Responsibility
Job Responsibility
  • Perform routine and non-routine calibration and maintenance activities for analytical laboratory instruments in accordance with approved procedures and schedules
  • Plan, schedule, and manage calibration and maintenance activities performed by external service providers or equipment manufacturers, including supplier-calibrated instruments
  • Review service reports and calibration certificates to ensure completeness, accuracy, and compliance with internal procedures and regulatory expectations
  • Provide technical support in the event of instrument malfunctions or failures, including troubleshooting, root cause identification, and coordination with equipment manufacturers or service providers to resolve issues
  • Collaborate closely with Quality team members to ensure calibration and maintenance activities are aligned with quality system requirements, including data integrity, documentation standards, and change management processes
  • Ensure adherence to applicable Quality Systems, GLP principles, and regulatory requirements
  • actively participate in audit preparation, inspections, and responses to audit findings related to calibration and maintenance activities.
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • competitive benefits
  • discretionary bonuses
  • long-term incentive
  • Fulltime
Read More
Arrow Right

Sr. Engineer, Manufacturing Engineering

Being an Engineer at Baxter means you play a critical role in helping us achieve...
Location
Location
Malta , Marsa
Salary
Salary:
32000.00 EUR / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Engineering (Mechanical, Electrical, Manufacturing, or related field)
  • Minimum 3+ years of experience in a manufacturing environment
  • Strong ability to analyze statistical and process data and translate insights into actionable improvements
  • Experience with process improvement methodologies and tools (e.g., FMEA, SPC, Lean principles)
  • Ability to manage multiple priorities in a fast-paced manufacturing environment
  • Ability to work in a regulated environment and ensure compliance with quality and safety standards
  • Strong problem-solving skills with a proactive and resourceful mindset
  • Effective communication and collaboration skills to work with cross-functional teams and external partners.
Job Responsibility
Job Responsibility
  • Perform routine and non-routine calibration and maintenance activities for analytical laboratory instruments in accordance with approved procedures and schedules
  • Plan, schedule, and manage calibration and maintenance activities performed by external service providers or equipment manufacturers, including supplier-calibrated instruments
  • Review service reports and calibration certificates to ensure completeness, accuracy, and compliance with internal procedures and regulatory expectations
  • Provide technical support in the event of instrument malfunctions or failures, including troubleshooting, root cause identification, and coordination with equipment manufacturers or service providers to resolve issues
  • Collaborate closely with Quality team members to ensure calibration and maintenance activities are aligned with quality system requirements, including data integrity, documentation standards, and change management processes
  • Ensure adherence to applicable Quality Systems, GLP principles, and regulatory requirements
  • actively participate in audit preparation, inspections, and responses to audit findings related to calibration and maintenance activities.
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Engineer / Sr Engineer, Manufacturing Sciences & Technology (mRNA/LNP)

Beam is looking for a highly motivated Engineer/Senior Engineer to join our grow...
Location
Location
United States , Cambridge, MA
Salary
Salary:
100000.00 - 135000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Ph.D. in Chemical Engineering, Bioengineering, Biochemistry, or equivalent with minimum 6 years of relevant work experience
  • M.S. degree with a minimum of 8 years of relevant work experience
  • B.S. degree with a minimum 10 years of relevant work experience
  • Demonstrated experience in technology transfer, scale-up, and implementation of downstream unit operations, such as tangential flow filtration, normal flow filtration, and chromatography
  • Experience in executing Process Validation lifecycle approach
  • i.e. process design, PPQ, and CPV
  • Experience in leading cross-functional teams for non-conformance event investigations, Root Cause Analyses (RCAs), and CAPAs
  • Outstanding written, verbal, and presentation skills
  • ability to communicate strategies, plans, and results to a diverse audience
  • Ability to simultaneously manage multiple projects and priorities and adjust quickly to dynamic situations
Job Responsibility
Job Responsibility
  • Supports MS&T activities related to mRNA and LNP programs
  • Supports the technology transfer and implementation of mRNA and LNP GMP manufacturing processes, collaborates with sending and receiving site cross-functional team members
  • Supports bulk drug substance and bulk drug product manufacturing across the full product lifecycle, including process design, process performance qualification (PPQ), commercial production, and continued process verification (CPV)
  • Authors technical documentation, including technology transfer plans, facility fit and gap analysis reports, manufacturing study protocols and reports, and risk assessments
  • Supports equipment design to meet process needs and compliance/regulatory expectations
  • supports Engineering and Validation departments with subsequent procurement, qualification, and GMP readiness
  • Supports regulatory submissions, responses, on-site audits, and inspections
  • Represents MS&T in cross-functional teams related to mRNA/LNP programs and manufacturing operations
  • Provides person-in-plant (PIP) support in manufacturing at Beam Durham
  • Supports MS&T lab and non-GMP analytical testing of in-process intermediates, as needed
  • Fulltime
Read More
Arrow Right

Sr Manufacturing Engineer

The Senior Manufacturing Engineer is a key site operations representative. The M...
Location
Location
United States , Hayward
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Science of Mechanical, Biomedical or Electrical Engineering
  • 3-5 years of experience in the Maintenance/Engineering field in a Pharmaceutical or Medical device manufacturing industry, preferred
  • Experience with statistical analysis with tools as Minitab or SAS, preferred
  • Experience with Microsoft Office Suite
  • Green Belt, Black Belt or PMP certification preferred
  • Ability to identify, define, and solve complex problems using a data-driven problem solving approach (i.e. DMAIC)
  • Technical writing ability for protocol generation, execution, and reporting to qualify processes and equipment
  • Strong technical skillset in the area of manufacturing engineering: design for manufacturability (DFM), EH&S guidelines, GMP/GDP guidelines, and process validation
  • Excellent problem-solving, organizational, analytical and critical thinking skills
  • Effective communication and interpersonal skills at all levels of employees, suppliers, and consultants
Job Responsibility
Job Responsibility
  • Drive continuous improvement in production performance, quality, and reliability through data-driven analysis, RCFA, FMECA, and statistical tools (SPC, SQC, DOE, Minitab, InfinityQS)
  • Provide hands-on technical support for manufacturing equipment and automation, ensuring optimal performance, maintenance, and compliance with regulatory and safety requirements
  • Lead nonconformance investigations (CAPA/NCR), including root cause analysis, corrective/preventive actions, effectiveness checks, and timely reporting to review boards and management
  • Partner with Manufacturing to implement lean principles and process improvements, supporting process validation (IQ/OQ/PQ), PFMEA, and overall product assembly optimization
  • Maintain accurate, compliant engineering and quality documentation (e.g., validation plans, protocols, reports) and prepare failure analysis reports to prevent recurring issues
  • Manage and support projects within budget and operational constraints, including capital planning, while delivering on Safety, Quality, Service, Cost, and Schedule objectives
  • Monitor and improve key production metrics (labor, yield, lead time, capability) through daily engagement with manufacturing and proactive data analysis
  • Ensure compliance with safety, GMP, and environmental regulations, including EHS standards, required training, and oversight of regulated systems and operations
  • Complete all required project updates, training, and administrative deliverables in a timely and accurate manner
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • medical and dental coverage that start on day one
  • insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Sr Manufacturing Engineer

The Senior Manufacturing Engineer is a key site operations representative. The M...
Location
Location
United States , Hayward
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Science of Mechanical, Biomedical or Electrical Engineering
  • 3-5 years of experience in the Maintenance/Engineering field in a Pharmaceutical or Medical device manufacturing industry, preferred
  • Experience with statistical analysis as Minitab or SAS, preferred
  • Experience with Microsoft Office Suite
  • Green Belt, Black Belt or PMP certification preferred
  • Ability to identify, define, and solve complex problems using a data-driven problem solving approach (i.e. DMAIC)
  • Technical writing ability for protocol generation, execution, and reporting to qualify processes and equipment
  • Strong technical skillset in design for manufacturability (DFM), EH&S guidelines, GMP/GDP guidelines, and process validation
  • Excellent problem-solving, organizational, analytical and critical thinking skills
  • Effective communication and interpersonal skills at all levels
Job Responsibility
Job Responsibility
  • Drive continuous improvement in production performance, quality, and reliability through data-driven analysis, RCFA, FMECA, and statistical tools
  • Provide hands-on technical support for manufacturing equipment and automation, ensuring optimal performance, maintenance, and compliance
  • Lead nonconformance investigations (CAPA/NCR), including root cause analysis, corrective/preventive actions, effectiveness checks, and timely reporting
  • Partner with Manufacturing to implement lean principles and process improvements, supporting process validation (IQ/OQ/PQ), PFMEA, and overall product assembly optimization
  • Maintain accurate, compliant engineering and quality documentation and prepare failure analysis reports
  • Manage and support projects within budget and operational constraints, including capital planning
  • Monitor and improve key production metrics through daily engagement with manufacturing
  • Ensure compliance with safety, GMP, and environmental regulations
  • Complete all required project updates, training, and administrative deliverables in a timely and accurate manner
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Sr Manufacturing Engineer

Being an Engineer at Baxter means you play a critical role in helping us achieve...
Location
Location
United States , Hayward
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Science of Mechanical, Biomedical or Electrical Engineering
  • 3-5 years of experience in the Maintenance/Engineering field in a Pharmaceutical or Medical device manufacturing industry, preferred
  • Experience with statistical analysis with tools as Minitab or SAS, preferred
  • Experience with Microsoft Office Suite
  • Green Belt, Black Belt or PMP certification preferred
  • Ability to identify, define, and solve complex problems using a data-driven problem solving approach (i.e. DMAIC)
  • Technical writing ability for protocol generation, execution, and reporting to qualify processes and equipment
  • Strong technical skillset in the area of manufacturing engineering: design for manufacturability (DFM), EH&S guidelines, GMP/GDP guidelines, and process validation
  • Excellent problem-solving, organizational, analytical and critical thinking skills
  • Effective communication and interpersonal skills at all levels of employees, suppliers, and consultants
Job Responsibility
Job Responsibility
  • Drive continuous improvement in production performance, quality, and reliability through data-driven analysis, RCFA, FMECA, and statistical tools (SPC, SQC, DOE, Minitab, InfinityQS)
  • Provide hands-on technical support for manufacturing equipment and automation, ensuring optimal performance, maintenance, and compliance with regulatory and safety requirements
  • Lead nonconformance investigations (CAPA/NCR), including root cause analysis, corrective/preventive actions, effectiveness checks, and timely reporting to review boards and management
  • Partner with Manufacturing to implement lean principles and process improvements, supporting process validation (IQ/OQ/PQ), PFMEA, and overall product assembly optimization
  • Maintain accurate, compliant engineering and quality documentation (e.g., validation plans, protocols, reports) and prepare failure analysis reports to prevent recurring issues
  • Manage and support projects within budget and operational constraints, including capital planning, while delivering on Safety, Quality, Service, Cost, and Schedule objectives
  • Monitor and improve key production metrics (labor, yield, lead time, capability) through daily engagement with manufacturing and proactive data analysis
  • Ensure compliance with safety, GMP, and environmental regulations, including EHS standards, required training, and oversight of regulated systems and operations
  • Complete all required project updates, training, and administrative deliverables in a timely and accurate manner
What we offer
What we offer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
  • Commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • Fulltime
Read More
Arrow Right

Device Engineering Sr. Engineer

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...
Location
Location
United States , Cambridge
Salary
Salary:
115494.60 - 156257.40 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree
  • OR Master's degree and 2 years of Engineering experience
  • OR Bachelor's degree and 4 years of Engineering experience
  • OR Associate's degree and 8 years Engineering experience
  • OR High school diploma / GED and 10 years of Engineering experience
Job Responsibility
Job Responsibility
  • Independently execute tasks within one or more of the Design for Robustness disciplines
  • Kinematic Design, Tolerance Design, Structural Strength Design, Material Design, DFA, DFM
  • Provide technical recommendations to improve design performance, reduce sensitivity to variation, and enhance overall system robustness
  • Collaborate across robustness disciplines to identify risks and mitigations, opportunities and best trade-off solutions
  • Contribute to continuous improvement of robustness disciplines and tools by identifying gaps, proposing improvements, and supporting implementation under governance frameworks
  • Interface effectively with discipline SMEs and incorporating guidance while maintaining ownership of robustness execution within assigned scope
  • Drive structured problem-solving and root cause analysis for design, test, and field performance issues, ensuring robust corrective solutions
  • Collaborate closely with manufacturing, quality, and suppliers to improve product robustness and reduce variation-driven failures
  • Apply systems-level thinking to anticipate how design decisions impact downstream manufacturability and performance
What we offer
What we offer
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible
  • Fulltime
Read More
Arrow Right