Production Engineer for Space Electronics Manufacturing Process Optimization Job at Airbus (Tres Cantos, Madrid Area)

New

Head of digital payload production

The Head of Digital Payload Production (TSEDP) is responsible for leading all ac...

Location

United Kingdom , Portsmouth

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Master’s or Bachelor’s degree in Electrical Engineering, Aerospace Engineering, Industrial Engineering, or related field
10+ years of experience in electronics manufacturing, preferably in aerospace or other high-reliability sectors
Strong knowledge of environmental and functional testing for space-grade hardware
Demonstrated experience managing multidisciplinary engineering and production teams
Experience with Lean/Continuous Improvement methodologies
Familiarity with ECSS standards, space qualification processes, and cleanroom production
Strong leadership, communication, and problem-solving skills
Ability to manage/apprehend complex projects in a fast-paced, mission-critical environment

Job Responsibility

Provide strong and visible leadership to a multidisciplinary team including production technicians, manufacturing engineers, test engineers, and operators
Oversee daily operations of the production line for space-grade electronic units (PCB assembly, integration, harnessing, mechanical assembly)
Ensure compliance with applicable space industry standards (ECSS, NASA, IPC, etc.)
Drive planning, scheduling, and resource allocation to meet project milestones and delivery commitments
Support the HO Manufacturing Engineering team in defining, optimising, and maintaining production processes, work instructions, and tooling
Develop and improve manufacturing flows to increase efficiency, reliability, and repeatability
Accountable for the deliveries of the test engineering teams responsible for developing test procedures, test software, and test sites
Accountable for the successful preparation and execution of Functional testing and Environmental testing (Vibration, Thermal Vacuum (TVAC), Electromagnetic Compatibility (EMC))
Ensure full adherence to quality, safety, and space-level reliability standards
Lead initiatives focused on Lean manufacturing, process optimization, and digitalization

What we offer

Competitive salary
annual profit share
contributory pension
share options
car leasing scheme
free onsite parking
season ticket loan
tax-free technology scheme
discounted shopping
37 hour week

Fulltime

Senior Manufacturing Engineer

Responsible for providing DFM feedback to design engineering, aligning and/or ex...

Location

United States , Longmont

Salary:

100000.00 - 130000.00 USD / Year

Redwire Space

Expiration Date

Until further notice

Requirements

B.S. degree in Manufacturing Engineering or related engineering discipline
Minimum of 5 years of experience in Manufacturing Engineering of electronics, RF antennas, and/or space-flight hardware
Proficient in one or more of the following CAD Software: SolidWorks, Inventor, Catia, Draftsight, AutoCAD

Job Responsibility

GSE & fixture design, review, and timely release
Write activity and project reports, develop action plans, generate build process instructions, and other documentation to support production operations
Design optimized manufacturing processes and maintain associated documentation for training, internal protocol, and industry standard alignment
Data capture and optimization of MES & ERP systems
Develop, evaluate, and improve manufacturing methods to drive: quality improvements, cost reduction, and quality improvements
Monitor and optimize production layout & capacity
Generate technical reporting, and presentations to internal and external stakeholders
Drive non-conformance issues to root cause and timely closure
Lead manufacturing planning updates for the organization
Model exemplary professional conduct as a representative of Redwire

What we offer

Highly competitive benefits package
Commitment to core values of Integrity, Innovation, Impact, Inclusion, and Excellence

Fulltime

Senior Associate Manufacturing - Downstream - Nights

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

92002.00 - 108605.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience
Associate’s Degree + 2 years manufacturing and/or other regulated environment experience
Bachelor’s Degree + 6 months manufacturing and/or other regulated environment experience
Master's Degree
Completion of NC BioWorks Certification Program
Experience in biotechnology or pharmaceutical plant start up
Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment
Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)
Excellent verbal and written communication (technical) skills
Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

Job Responsibility

Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
Initiate quality non-conformance (NC) reports
Interact with regulatory agencies as needed and guided
Assure proper gowning and aseptic techniques are always followed
Perform hands-on downstream biotech operations (Column Chromatography, Tangential Flow Filtration, Viral Filtration, Viral Inactivation, Column Packing among others) including set-up, operation, cleaning, sanitization, monitoring of equipment and assigned area
Run and monitor critical process tasks per assigned procedures
Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBR])
Complete washroom activities: cleaning equipment, small to large scale, used in production activities
Initiate and own manufacturing related process deviations
Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Senior Associate Manufacturing, Upstream - Days

Join Amgen’s Mission of Serving Patients. Be part of Amgen's newest and most adv...

Location

United States , Holly Springs

Salary:

92002.00 - 108605.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience
Associate’s Degree + 2 years manufacturing and/or other regulated environment experience
Bachelor’s Degree + 6 months manufacturing and/or other regulated environment experience
Master's Degree
Completion of NC BioWork Certificate Program
Experience in biotechnology or pharmaceutical plant start up
Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment
Basic understanding of Upstream operation (Vial Thaw, Inoculation/Cell Expansion, Single Use Bioreactor, Production Bioreactor, ATF, Harvest Centrifuge, Depth Filtration)
Excellent verbal and written communication (technical) skills
Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

Job Responsibility

Execute on-the-floor operations within manufacturing in accordance with cGMP practices
Work assigned 12-hour shift, including during inclement weather, some holidays and requested overtime
Complete work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
Initiate Quality observations (Discrepancies, Deviations, Testing Results Analysis (TRA), etc.) as well as support or lead evaluations and investigations into quality observations
Interact with regulatory agencies as needed and guided
Assure proper gowning and aseptic techniques are always followed
Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment of assigned area
Run and monitor critical process tasks per assigned procedures
Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBR])
Complete washroom activities: cleaning equipment, small to large scale, used in production activities

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Senior Associate Upstream Manufacturing

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

92002.00 - 108605.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience
Associate’s Degree + 2 years manufacturing and/or other regulated environment experience
Bachelor’s Degree + 6 months manufacturing and/or other regulated environment experience
Master's Degree
Completion of NC BioWork Certificate Program
Experience in biotechnology or pharmaceutical plant start up
Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment
Basic understanding of Upstream operation (Vial Thaw, Inoculation/Cell Expansion, Single Use Bioreactor, Production Bioreactor, ATF, Harvest Centrifuge, Depth Filtration)
Excellent verbal and written communication (technical) skills
Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

Job Responsibility

Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
Initiate quality non-conformance (NC) reports
Interact with regulatory agencies as needed and guided
Assure proper gowning and aseptic techniques are always followed
Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment and assigned area
Run and monitor critical process tasks per assigned procedures
Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBR])
Complete washroom activities: cleaning equipment, small to large scale, used in production activities
Identify, recommend, and implement innovate process improvements and optimizations related to daily routine functions
Assist in the review of documentation for assigned functions (i.e., equipment logs, EBRs, ESPs)

What we offer

competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

New

Project Engineer - Commercial Construction - FIFO

Join a leading Indigenous-led commercial construction company dedicated to deliv...

Location

Australia , Bulimba

Salary:

160000.00 - 190000.00 AUD / Year

Randstad

Expiration Date

February 26, 2026

Requirements

Tertiary or trade Qualification in Construction
Minimum 2 years experience in a site/project Engineer role within the Australian commercial construction industry working for a head contractor

Job Responsibility

Contribute to site meetings and work collaboratively with upper management to ensure
Compile and complete documentation related to your designated workflow
Working within the engineering team managing individual responsibilities, assisting with documentation
Provide leadership in health, safety, quality and environmental management
Review project documents including estimates, design drawing, proposals and contracts per management direction
Stakeholder and resource management - Ensuring relevant labour is on site to deliver key project objectives, and ensuring quality is maintained throughout
Reporting directly to your site based Senior Project Engineer & Project Manager you will have all the support required but also show a capability to work autonomously as required
Manage project schedules, procurement schedules, and subcontractor coordination
Interpret engineering drawings and specifications to ensure site works meet all technical requirements
Implement and maintain rigorous ISO-certified systems for Safety (45001), Quality (9001), and Environment (14001)

What we offer

All flights, site accommodation, uplift and LAFHA are provided
Gain experience in the highly secure Defence sector and specialized government infrastructure
Work within a values-driven organization that balances commercial excellence with community impact

New

HR Project Specialist

We are looking for an HR Project Specialist - (Maternity Leave Cover) to join ou...

Location

Portugal , Lisbon

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Ideally 2 /4 years of experience in HR
Ability to think and act with a project management mindset, structuring initiatives with clear timelines, tasks and deliverables
Proven ability to collaborate with diverse teams and manage multiple projects across departments
Passion for creating a great employee experience and fostering a strong company culture through effective teamwork
Strong stakeholder management, communication and interpersonal skills to work across teams
Continuous Improvement driven mindset to refine HR initiatives
Excellent verbal and written communication skills in English
Ability to act independently by prioritising work, problem-solving and taking ownership of tasks and responsibilities.

Job Responsibility

Onboarding experience - Manage and ensure a seamless onboarding journey that enhances new hire integration and engagement
Employee experience - Develop and implement initiatives that foster a positive, engaging and inclusive work environment
Trainee and internship programmes - Manage and enhance our trainee programs, ensuring alignment with broader business goals
HR project implementation - Lead and support additional HR projects as required, collaborating with other departments to ensure smooth execution and respect for timelines.

What we offer

The chance to work in a multicultural environment
The opportunity to grow your skills and capabilities thanks to our Airbus learning offer (digital solutions, classroom sessions, certified training) and career opportunities across the globe
A hybrid working model, allowing you to combine onsite and offsite work
A modern office, well connected to public transportation
A motivated and fun crew to grow and build and shape the GBS together
An intense and exciting onboarding experience.

Fulltime

New

Staff Pharmacist

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Naples

Salary:

60.00 - 76.00 USD / Hour

CVS Health

Expiration Date

March 28, 2026

Requirements

Active Pharmacy License in the state in which you are employed
Not on the DEA Excluded Parties List
Immunization Certification through an accredited organization (e.g., APhA)
No pending felony charges or convictions for criminal offenses involving controlled substances

Job Responsibility

Patient Safety
Pharmacy Professional Practice
Regulatory Requirements
Quality Assurance
Customer Service
Personnel Management
Inventory Management
Financial Profitability
Loss Prevention
Workflow Management

What we offer

Affordable medical plan options
a 401(k) plan (including matching company contributions)
an employee stock purchase plan
No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching
Benefit solutions that address the different needs and preferences of our colleagues including paid time off, flexible work schedules, family leave, dependent care resources, colleague assistance programs, tuition assistance, retiree medical access and many other benefits depending on eligibility

Fulltime

Production Engineer for Space Electronics Manufacturing Process Optimization

Airbus

Location:
Spain , Tres Cantos, Madrid Area

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 23, 2026

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