Career
Technical Sales Manager International (m/w)
Responsibilities:
Acquisition of new customers in target markets and technical sales activities
Working on the Gerber and Dxf files to prepare the projects before transferring them to technical team in order to establish the feasibility and design for manufacturing
Manage existing customers and ensure/sustain running business
Act as a vector between customers and technical support staffs and production engineers to meet customer needs.
Proactive, forecast sales in order to ensure expectations achievement of objectives
Identification of new opportunities fitting within Swissflex Microcircuits market
Concentration with technical management on developing new services, products, and technologies.
Attend industry events, prospection and trade fairs
General requirements.
Degree in electronics and physics engineer
Experience with photolithography in microelectronics, desirable 5 years
Global sales experience preferred 5 years with B2B experience, ability to understand microelectronics circuits technology and applications in industry network
Experience with sales and customer acquisition and ability to contracts with customers
Capable to work independently but supported with technical and production teams.
Ability and willing to travel up to 80% of time
Experiences with customers technical files and understanding
Excellent knowledge of production of microelectronics, perfect overview of various production processes, manufacturing equipment, materials and finishes.
Excellent experience with thin film deposition technology
Transfer the customers CAD Design file which will be assisted with engineering team
Coordination customers design projects with engineering team to evaluation of feasibility and manufacturing possibilities
Excellent knowledge of the IPC standards for microelectronics technology, ceramics and aluminium based circuits
Language skills:
English & German fluent.
Working knowledge of French would be desirable
Design Engineer & Production Processes
Job Description:
Provide design & process engineering instructions to produce a diverse range of custom thin film flexible circuits & devices.
Daily work includes CAD design & layout, detailing & documentation of manufacturing process instructions, test, and characterization of completed thin film flexible circuits & devices.
Key Responsibilities:
Create manufacturing specifications; generate production sequences, routings, and technical work instructions.
Use CAD to design and layout Photomasks and production tooling which supports production requirements.
Work closely with production planning to support released products and work orders.
Support production issues by assisting process engineers with analyses.
Manage manufacturing documentation required for product manufacturing revise drawings, work instructions, and process routings.
Identify ways to streamline design tasks, reduce lead times, and reduce manufacturing costs.
Work with other relevant Sales and Production departments to determine estimated costs, run times, cost reductions, yield improvements.
Work with internal and external suppliers on manufacturing process details.
Qualifications:
MS degree in Physics, Materials Science, Engineering
5+ Years of experience in mechanical design, thermal design, or process engineering.
Design Engineer with 5+ years of industry experience in supporting semiconductor or thin film production processes such as sputtering, plating, photolithography, dry and wet etching, etc.
Working experience in a semiconductor fabrication facility is highly desirable.
Strong developing and implementing innovative solutions to complex problems in a timely manner.
Experience in supporting Clean-room production.
Proficient in creating/updating mechanical design files in CAD mechanical drawings.
Additional Qualifications:
Experience in ERP and programming.
Ability to work collaboratively with cross-functional teams.
Excellent verbal and technical writing skills in (FR, DE, EN)
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
Head of Product Development Engineer
Dynamic high-tech company in the field of microelectronics, specializing in next generation of thin-film flexible and rigid electronics with exciting opportunities. The company has made remarkable progress in developing the production technologies and high-performance thin film technology and is now expanding to increase production volume.
Responsibilities
Head of Product Development Engineer will be responsible for leading the team in developing a product portfolio strategy and in the long-term product planning process.
The candidate will be required to conceptualize and execute innovative product ideas and applications.
This position requires perform key responsibilities, including:
– Designing and Engineering of product development roadmap to ensure successful execution of the company’s strategy.
– Product development, production and commercial functions and meeting key business outcomes across those areas.
– Establishing Product Development Roadmap
– Applications and system engineering for defined products
– Bringing the customers into product portfolio and individual product development plan
– Development of processes for new product development, from the idea to release stage including user research, testing and roll-out
– Functioning as point of contact for product design and management, product and quality assurance.
– Building and leading a team of Product, Applications and Reliability Engineers to develop new products
– Working Knowledge of Electronics, Mechanical and Quality management systems would be preferred.
Experience required.
The candidate should have a relevant university degree in electronics and physics engineer.
The candidate’s experience should include at least 3-5 years in a leadership position in product development, and at least 5 years of
experience in in developing innovative products (product development experience in microelectronics would be preferable).
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
R&D engineering ultra-thin flexible wearable and bendable electronics
We are looking for a scientific or a R&D engineering ultra-thin flexible wearable and bendable electronics and applications.
Your profile
Diploma or master degree in Electronics Engineering or Physics
Photolithography and Multilayer electronics
Highly motivated with good experimental and experiences
Experience in semiconductor technology and in one or more of the following fields would be an advantage: RF and integrated circuit design
Flexible electronics Materials (Glass panel, PET film, PI film, PEN film, Metal (Alu, Cu))
Processing (Photolithography, Vacuum deposition, wet/dry etch processing, coating single and double side)
Application (Sensors “Biometric”, Medical “Catheter technology, Implantable and Diagnostic”, Solar cells, Display, RFID, Gas sensors, Heaters, etc.)
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
Principal Engineer in Advanced Electrophysiological Catheters
Job Title: Principal Engineer
Department: Research and Development in Advanced Electrophysiological Catheters
Reporting To: Chief Technical Officer (CTO)
This position will report directly to the CTO. SWISSFLEX MICROCIRCUITS AG specific duties will be determined and coordinated in conjunction with the corporate needs and strategic plans and will be subject to change given ongoing business and product development needs.
Job Summary
SWISSFLEX MICROCIRCUITS AG is a leading research and development innovative catheters in treatment of cardiac arrhythmias by developing catheter mapping and ablation technologies.
The principal engineering position at SWISSFLEX MICROCIRCUITS AG is an engineering professional with 5+ years of experience in the medical device industry or other regulated industry. The qualified candidate will be responsible for providing guidance and oversight to multiple teams or individuals working on numerous products or developing various forms of medical device technologies. This individual is a leader who thinks strategically and has long-range company goals in mind and will manage all phases of technical projects.
They will oversee the products or project’s conception, product design, product design documentation and manage scheduling, estimating, and securing materials and vendors. The principal engineer will also conduct engineering studies and investigations and prepare reports for company leadership. They also provide engineering guidance to other departments, help to train new engineers, and keep abreast of industry trends and issues.
Key Job Responsibilities:
- Provide technical leadership for the design and development of medical devices.
- Assist in the transfer of new products from R&D to production.
- Establish processes and manufacturing documentation for new catheter products.
- Identify processes to fabricate new products.
- Use CAD software for part and assembly design and detail drawings.
- Perform experiments to determine validity of designs.
- Provide technical leadership for development projects.
- Define product requirements.
- Design and development of tooling
- Perform or manage design verification, equipment qualification and product and process validations.
- Prepare and maintain product documentation including DXF, drawings, BOM, test protocols and reports, etc.
- Supervise and advise team members as necessary.
- Comply with applicable FDA and international regulatory laws/standards.
- Other duties as assigned or required.
Additional Requirements:
- Master’s Degree in mechanical or biomedical engineering or equivalent experience.
- Five (5) years industry experience with a medical device, pharmaceutical, biotechnology company
- Two (2) years supervisory experience
- Knowledge FDA/MDD regulations as they relate to Class III medical devices.
- Demonstration of excellent communication (written and oral) skills
- Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment.
- Prior experience with non-invasive medical devices in advanced catheters.
- Prior experience with a start-up medical device company
- Ability to present and teach detailed technical information, to all levels of company personnel and customers.
Personal and Experiences Qualifications:
- MS. in Biomedical Engineering and MBA, or equivalent combination of 4-year and graduate degrees in Engineering, Natural and Life Sciences and Business
- 5 years of experience in Medical Devices, Diagnostic or Life Science industries with at least 3 years of Upstream Product Marketing and/or Product Management
- Solid understanding of human cardiovascular anatomy, physiology, clinical practice, and clinical science; the understanding of cardiac electrophysiology and electrophysiology devices is highly required.
- Demonstrate ability to drive medical product development from concept to product realization in a variety of technical areas, including capital hardware and software, implantable medical devices, disposable interventional devices (such as catheters), or similar; solid understanding of VOC practices and FDA/CE quality management system requirements is a must.
- Practical understanding of commercialization processes in different geographies and is highly desirable; professional experience in customer-facing roles such as Downstream Marketing, Field Clinical Engineering or Sales is a significant plus.
- Strong technical verbal and written communication skills; demonstrated experience in medical writing on both professional and consumer levels is desirable.
- Strong cross-functional leadership in fast-paced environment, comfort under conditions of uncertainty, strong analytical and financial acumen combined with bias for action.
- Demonstrated experience handling multiple cross-functional projects; project management certification is a definite plus.
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
Production Manager in Advanced Electrophysiological Catheters
Job Title: Production Manager
Department: Operations in Advanced Electrophysiological Catheters
Reporting To: Chief Technical Officer (CTO)
This position will report directly to CTO. SWISSFLEX MICROCIRCUITS AG specific duties will be determined and coordinated in conjunction with the corporate needs and strategic plans and will be subject to change given ongoing business and product development needs.
Job Summary
SWISSFLEX MICROCIRCUITS AG is a leading research and development innovative catheters in treatment of cardiac arrhythmias by developing catheter mapping and ablation technologies. The Production Manager at SWISSFLEX MICROCIRCUITS AG is a medical device professional with 5+ years of experience in medical device manufacturing. The qualified candidate will be responsible for production support and personnel supervision during manufacturing. Candidate must have strong leadership skills, adherence to manufacturing controls and QMS documentation requirements. Be able to provide direction as well as supervision and discipline to the manufacturing assembly team.
Key Job Responsibilities:
- Provide technical leadership for the design and development of medical devices.
- Review, update, and ensure team adherence to manufacturing process instruction, production, and manufacturing methods.
- Identify opportunities for improvements to process equipment, fixtures, and workspaces.
- Track production orders, build progress, yield data, and provide clear and accurate updates for management.
- Supports preventive maintenance and calibration of production equipment.
- Maintains product and company reputation by complying with regulations.
- Provides support for new product development and manufacturing.
- Experience with and use of ERP systems
- Support product orders and shipping.
- Comply with applicable FDA and international regulatory laws/standards.
- Other duties as assigned or required.
- Other duties as assigned or required.
Additional Requirements:
- Bachelor’s Degree in mechanical or biomedical engineering or equivalent experience.
- Five (5) years industry experience with a medical device, pharmaceutical, biotechnology company
- Two (2) years supervisory experience
- Knowledge FDA/MDD regulations as they relate to Class III medical devices.
- Demonstration of excellent communication (written and oral) skills
- Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment.
- Work closely with equipment and service vendors.
- Good time and project management skills, good prioritization, and communication skills.
- Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment.
- Prior experience with non-invasive medical devices in advanced catheters.
- Prior experience with a start-up medical device company
- Ability to present and teach detailed technical information, to all levels of company personnel and customers.
Personal and Experiences Qualifications:
- BS. in Biomedical Engineering and MBA, or equivalent combination of 3-year and graduate degrees in Engineering, Natural and Life Sciences and Business
- 5 years of experience in Medical Devices, Diagnostic or Life Science industries with at least 3 years of Upstream Product Marketing and/or Product Management
- Solid understanding of human cardiovascular anatomy, physiology, clinical practice, and clinical science; the understanding of cardiac electrophysiology and electrophysiology devices is highly required.
- Demonstrate ability to drive medical product development from concept to product realization in a variety of technical areas, including capital hardware and software, implantable medical devices, disposable interventional devices (such as catheters), or similar; solid understanding of VOC practices and FDA/CE quality management system requirements is a must.
- Practical understanding of commercialization processes in different geographies and is highly desirable; professional experience in customer-facing roles such as Downstream Marketing, Field Clinical Engineering or Sales is a significant plus.
- Strong technical verbal and written communication skills; demonstrated experience in medical writing on both professional and consumer levels is desirable.
- Strong cross-functional leadership in fast-paced environment, comfort under conditions of uncertainty, strong analytical and financial acumen combined with bias for action.
- Demonstrated experience handling multiple cross-functional projects; project management certification is a definite plus.
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
Principal Process Development Engineer in Advanced Electrophysiological Catheters
Job Title: Principal Process Development Engineer
Department: Operations Engineering in Advanced Electrophysiological Catheters
Reporting To: Chief Technical Officer (CTO)
This position will report directly to the CTO. SWISSFLEX MICROCIRCUITS AG specific duties will be determined and coordinated in conjunction with the corporate needs and strategic plans and will be subject to change given ongoing business and product development needs.
Job Summary
SWISSFLEX MICROCIRCUITS AG is a leading research and development innovative catheters in treatment of cardiac arrhythmias by developing catheter mapping and ablation technologies.
The Principal Process Development Engineer position at SWISSFLEX MICROCIRCUITS AG is an engineering professional with 5+ years of experience in the medical device industry or other regulated industry. The qualified candidate will be responsible for providing guidance and oversight to multiple teams or individuals working on numerous products or developing various forms of medical device technologies. This individual is a leader who thinks strategically and has long-range company goals in mind and will manage all phases of technical projects. They will oversee the product or project conception, product design, product design documentation and manage scheduling, estimating and securing materials and vendors. The Principal Process Development Engineer will also conduct engineering studies and investigations and prepare reports for company leadership. They also provide engineering guidance to other departments, help to train new engineers and keep abreast of industry trends and issues.
Key Job Duties and Responsibilities:
- Provide technical leadership for the design and development of medical devices
- Assist in the transfer of new products from R&D to production
- Establish processes and manufacturing documentation for new catheter products.
- Identify processes to fabricate new products.
- Use CAD software for part and assembly design and detail drawings.
- Perform experiments to determine validity of designs.
- Provide technical leadership for development projects.
- Define product requirements.
- Design and development of tooling
- Perform or manage design verification, equipment qualification and product and process validations.
- Prepare and maintain product documentation including DXF, drawings, BOM, test protocols and reports, etc.
- Supervise and advise team members as necessary.
- Comply with applicable FDA and international regulatory laws/standards.
- Other duties as assigned or required.
Additional Requirements:
- Master’s Degree in mechanical or biomedical engineering or equivalent experience.
- Five (5) years industry experience with a medical device, pharmaceutical, biotechnology company
- Two (2) years supervisory experience
- Knowledge FDA/MDD regulations as they relate to Class III medical devices.
- Demonstration of excellent communication (written and oral) skills
- Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment.
- Prior experience with non-invasive medical devices in advanced catheters.
- Prior experience with a start-up medical device company
- Ability to present and teach detailed technical information, to all levels of company personnel and customers.
Personal and Experiences Qualifications:
- MS. in Biomedical Engineering and MBA, or equivalent combination of 4-year and graduate degrees in Engineering, Natural and Life Sciences and Business
- 5 years of experience in Medical Devices, Diagnostic or Life Science industries with at least 3 years of Upstream Product Marketing and/or Product Management
- Solid understanding of human cardiovascular anatomy, physiology, clinical practice, and clinical science; the understanding of cardiac electrophysiology and electrophysiology devices is highly required.
- Demonstrate ability to drive medical product development from concept to product realization in a variety of technical areas, including capital hardware and software, implantable medical devices, disposable interventional devices (such as catheters), or similar; solid understanding of VOC practices and FDA/CE quality management system requirements is a must.
- Practical understanding of commercialization processes in different geographies and is highly desirable; professional experience in customer-facing roles such as Downstream Marketing, Field Clinical Engineering or Sales is a significant plus.
- Strong technical verbal and written communication skills; demonstrated experience in medical writing on both professional and consumer levels is desirable.
- Strong cross-functional leadership in fast-paced environment, comfort under conditions of uncertainty, strong analytical and financial acumen combined with bias for action.
- Demonstrated experience handling multiple cross-functional projects; project management certification is a definite plus.
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
R&D Product Development Engineer in Advanced Electrophysiological Catheters
Job Title: R&D Product Development Engineer
Department: R&D Product Development Engineer in Advanced Electrophysiological Catheters
Reporting To: Chief Technical Officer (CTO)
This position will report directly to the CTO. SWISSFLEX MICROCIRCUITS AG specific duties will be determined and coordinated in conjunction with the corporate needs and strategic plans and will be subject to change given ongoing business and product development needs.
Job Summary
SWISSFLEX MICROCIRCUITS AG is a leading research and development innovative catheters in treatment of cardiac arrhythmias by developing catheter mapping and ablation technologies.
The primary role of the R&D Product Development Engineer is to provide catheter prototyping and device assembly support to the engineering team. The R&D Product Development Engineer periodically conducts verification testing to assess the functionality of catheter prototypes. The R&D Product Development Engineer trains production assembly team members for production of new catheter designs. The ideal candidate is a seasoned expert production assembler ready to move from the medical device production environment into the R&D department.
The R&D Product Development Engineer position at SWISSFLEX MICROCIRCUITS AG is an engineering professional with 5+ years of experience in the medical device industry or other regulated industry. The qualified candidate will be responsible for providing guidance and oversight to multiple teams or individuals working on numerous products or developing various forms of medical device technologies. This individual is a leader who thinks strategically and has long-range company goals in mind and will manage all phases of technical projects. They will oversee the product or project conception, product design, product design documentation and manage scheduling, estimating, and securing materials and vendors. The R&D Product Development Engineer will also conduct engineering studies and investigations and prepare reports for company leadership. They also provide engineering guidance to other departments, help to train new engineers, and keep abreast of industry trends and issues.
Key Job Duties and Responsibilities:
- Provide technical leadership for the design and development of medical devices.
- Proficient with catheter manufacturing tools and practices (hot torches, adhesives, shrink tubing, tubing cutters etc.)
- Strong problem-solving skills, independent thinker, and attention to detail
- Comfortable working with small parts and sub-assemblies by using templates or measurements.
- Assemble/fabricate components, examine/evaluate connections for fit.
- Verify specifications by measuring completed components.
- Resolve assembly problems and communicate all problems with R&D engineering.
- Keeps equipment operational by ensuring all have the proper asset and calibration labels.
- Maintain a safe and clean working environment by complying with company procedures, rules, and regulations.
- Maintain lab supply inventory by checking stock periodically to determine inventory level; anticipating needed supplies; communicates need to appropriate personnel.
- Documents all actions by completing R&D production and quality forms.
- Build prototypes for feasibility testing, animal studies and pilot manufacturing builds.
- Assist in the transfer of new products from R&D to production.
- Establish processes and manufacturing documentation for new catheter products.
- Identify processes to fabricate new products.
- Use CAD software for part and assembly design and detail drawings.
- Perform experiments to determine validity of designs.
- Provide technical leadership for development projects.
- Define product requirements.
- Design and development of tooling
- Perform or manage design verification, equipment qualification and product and process validations.
- Prepare and maintain product documentation including DXF, drawings, BOM, test protocols and reports, etc.
- Supervise and advise team members as necessary.
- Comply with applicable FDA and international regulatory laws/standards.
- Other duties as assigned or required.
Additional Requirements:
- Master’s Degree in mechanical or biomedical engineering or equivalent experience.
- Five (5) years industry experience with a medical device, pharmaceutical, biotechnology company
- Two (2) years supervisory experience
- Knowledge FDA/MDD regulations as they relate to Class III medical devices.
- Demonstration of excellent communication (written and oral) skills
- Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environment.
- Prior experience with non-invasive medical devices in advanced catheters.
- Prior experience with a start-up medical device company
- Ability to present and teach detailed technical information, to all levels of company personnel and customers.
Personal and Experiences Qualifications:
- MS. in Biomedical Engineering and MBA, or equivalent combination of 4-year and graduate degrees in Engineering, Natural and Life Sciences and Business
- 5 years of experience in Medical Devices, Diagnostic or Life Science industries with at least 3 years of Upstream Product Marketing and/or Product Management
- Solid understanding of human cardiovascular anatomy, physiology, clinical practice, and clinical science; the understanding of cardiac electrophysiology and electrophysiology devices is highly required.
- Demonstrate ability to drive medical product development from concept to product realization in a variety of technical areas, including capital hardware and software, implantable medical devices, disposable interventional devices (such as catheters), or similar; solid understanding of VOC practices and FDA/CE quality management system requirements is a must.
- Practical understanding of commercialization processes in different geographies and is highly desirable; professional experience in customer-facing roles such as Downstream Marketing, Field Clinical Engineering or Sales is a significant plus.
- Strong technical verbal and written communication skills; demonstrated experience in medical writing on both professional and consumer levels is desirable.
- Strong cross-functional leadership in fast-paced environment, comfort under conditions of uncertainty, strong analytical and financial acumen combined with bias for action.
- Demonstrated experience handling multiple cross-functional projects; project management certification is a definite plus.
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch
Catheter Assembler
Job Title: Catheter Assembler
Department: Operations in Advanced Electrophysiological Catheters Assembling
Reporting To: Production Manager
This position will report directly to the Production Manager.
Job Summary
SWISSFLEX MICROCIRCUITS AG is a leading research and development innovative catheters in treatment of cardiac arrhythmias by developing catheter mapping and ablation technologies.
The primary responsibility of the Catheter Assembler is to perform assembly line tasks as well as identify areas of improvement to increase efficiency.
Key Job Duties and Responsibilities:
- Proficient with catheter manufacturing tools and practices (hot torches, adhesives, shrink tubing, tubing cutters etc.)
- Strong problem-solving skills, independent thinker, and attention to detail
- Comfortable working with small parts and sub-assemblies by using templates or measurements.
- Assemble/fabricate components, examine/evaluate connections for fit.
- Verify specifications by measuring completed components.
- Resolve assembly problems and communicate all problems with R&D engineering.
- Keeps equipment operational by ensuring all have the proper asset and calibration labels.
- Maintain a safe and clean working environment by complying with company procedures, rules, and regulations.
- Maintain lab supply inventory by checking stock periodically to determine inventory level; anticipating needed supplies; communicates need to appropriate personnel.
- Assembles, repairs, inspect and/or test products following written instructions.
- Work with a team to assemble entire products or components.
- Rotate through tasks for specific production processes
- Conduct quality inspections on products and parts.
- Prepare finished products for shipment.
- Maintain a clean and orderly work area.
- Set up and operates a variety of machines following written instructions.
- Record information on approved documents.
- Train other employees when necessary
- Reads and interprets documents associated with the completion of assembly assignments. Utilizes knowledge of basic math, drawings.
Personal and Experiences Qualifications Requirements:
- H.S. diploma or equivalent plus 2-5 years of related work experience or equivalent combination of education and work experience
- Previous experience in manufacturing, assembly, or other related fields
- Familiarity with assembly tools and equipment
- Ability to handle physical workload.
- Ability to work well in teams.
- Ability to thrive in a fast-paced environment.
- Clean room experience and application of environmental procedures experience
- Working knowledge of QSR and GMP
The candidate should have good communication skills in French, English and German and should be able to work within an international team.
The candidate should not hesitate to travel if required.
Please send your complete application:
– Motivation letter
– Curriculum vitae
and addresses of at least two referees to
SWISSFLEX MICROCIRCUITS AG
Erlenstrasse 44,
2555 Brügg, Switzerland
info@swissflexmicrocircuits.ch
www.swissflexmicrocircuits.ch