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

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 - 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 - Bulk Drug Substance Downstream - Nights

Location

United States , Holly Springs

Salary:

Not provided

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

Job Responsibility

Completes work in accordance with established cGMP procedures and policies
Initiate quality non-conformance (NC) reports
Interact with regulatory agencies as needed and guided
Assure proper gowning and aseptic techniques are always followed
Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)
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

What we offer

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 and bi-annual company-wide shutdowns
Flexible work models, including remote work arrangements, where possible

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

New

Account Executive

You’ll own the full sales cycle: finding prospects, building relationships, runn...

Location

United States , Denver

Salary:

Not provided

Blue Margin

Expiration Date

Until further notice

Requirements

3+ years of B2B sales experience in technology professional services
Demonstrated track record of self-sourcing pipeline
Comfortable running own outbound motion including cold outreach, networking, and multi-touch email campaigns
Fluent with modern sales tools and AI-assisted workflows
Collaborative by nature and effective at orchestrating internal resources to move deals forward
Consultative selling style with strong discovery and listening skills
Organized, self-directed, and accountable to pipeline metrics and revenue targets
Denver-based preferred
Some travel to Fort Collins headquarters expected

Job Responsibility

Build and manage own pipeline through outbound prospecting, networking, cold outreach, email sequences, and partner relationships
Sell into mid-market companies and PE-backed portfolio companies
Own the full sales cycle while leveraging a team-based approach
Develop fluency in Blue Margin's solutions and the broader Microsoft Fabric, Snowflake, Power BI, and AI landscape
Leverage AI-assisted tools for prospecting, outreach, pipeline management, and call review
Maintain accurate pipeline data and activity in HubSpot
Collaborate with delivery and customer success teams to ensure deals are set up for long-term client success

What we offer

Licenses to all major frontier LLMs and a full modern AI toolset for your work
Opportunity to grow with an established, expanding company in a high-demand market
Collaborative team of four AEs with strong internal support at every stage of the deal
Hybrid work flexibility
Health, dental, vision, disability, and life insurance
401(k) with 4% company match
PTO, sick leave, and paid holidays

Fulltime

New

Upper School English Teacher

Buckingham Browne & Nichols School is seeking a part-time (80%), dynamic, studen...

Location

United States , Cambridge

Salary:

69500.00 - 115754.00 USD / Year

Buckingham Browne & Nichols School

Expiration Date

Until further notice

Requirements

Hold an undergraduate degree in literature or a related field
Create a dynamic and engaging classroom experience for students
Offer a wide range of opportunities for learning in the classroom (small group work, full-class discussion, debates, presentations, etc.)
Demonstrate agility in adjusting teaching approaches to best support the critical thinking, writing, and creativity of all students
Build students’ confidence in their independent ability to read, write, and think critically and creatively
Work effectively with students, parents, faculty, and staff
Seek collaboration with a team of colleagues within the English Department and with teachers in other disciplines
Value advancing students’ knowledge and affirmation of themselves and others
Integrate our School’s mission, values, and DEIG commitments into their teaching practices
Commit to working in and fostering an inclusive community by advancing the efforts of anti-racism and equity in their classes and the broader community

Job Responsibility

Plans and develops an engaging, age-appropriate course of study in the classroom, adhering to educational best practices and curriculum guidelines
Prepares materials for lessons, assignments, and tests
evaluates, corrects, and grades student performance
Supervises the behavior of students in the classroom, school grounds, and educational trips and discusses academic difficulties or behavioral problems with students as they arise
Communicates progress and concerns with tact and professionalism to parents and, as appropriate, other faculty, staff, and/or campus Director
Builds and maintains positive relationships with parents, students, and colleagues
Enforces safety and security standards for students, staff, and visitors
Maintains required paperwork for individual student files, attendance and incident reports, and other necessary records
Monitors halls, study periods, and lunchrooms with other faculty and staff
Participates in faculty meetings, educational conferences, in-service opportunities, workshops, and other training seminars

Parttime

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Production Engineer for Space Electronics Manufacturing Process Optimization

Job Description

Job Responsibility

Requirements

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