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QA Release Specialist

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At HemoCue, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn idea... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At HemoCue, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
HemoCue is a leading provider of point-of-care diagnostic solutions, enabling healthcare practitioners across clinical settings and geographies to improve patient outcomes and clinical workflows. For more than four decades we’ve been advancing what’s possible at the point of care. HemoCue offers point-of-care testing for hemoglobin, glucose and HbA1c as well as total and differential white blood cell count.
Learn about the Danaher Business System which makes everything possible.


The QA Release Specialist for HemoCue is responsible for release of finished goods and to secure that the finished goods are in compliance with our QMS and regulatory requirements. The QA Release Specialist will also collaborate with Operations regarding Nonconformances and QA Operations is the owner of the Nonconformance process.
This position reports to the Manager QA Operations and is part of the QA Operations within RAQA located in Ängelholm, Sweden and will be an on-site role.
You will be a part of the QA Operations and report to the responsible for that our finished goods are in compliance with our QMS and regulatory requirements. If you thrive in a multifunctional, developing and sometimes challenging role what have close collaboration with multiple functions within the organization and want to work to build a world-class QA Operations organization—read on.


In this role, you will have the opportunity to:
Make sure that our finished goods are in compliance with our QMS and regulatory requirement and release them for shipping


Review and approve investigations, material dispositions and required actions regarding Nonconformances


Drive continuous improvements together with Operations


Cooperate closely with other functions within the organization

The essential requirements of the job include:
Bachelor’s degree within science or technology or equivalent working experience


2 years of Quality Assurance experience within Medical Device or similar industry


Knowledge and experience within IVDR/IVDD, ISO 13485, Quality System Regulations for Medical Devices and risk management for medical devices (ISO 14971)


Communication skills (verbal as well as in writing) in Swedish fluent and English moderate or fluent


Detail-oriented and able to work independently as well as within a team

Don't hesitate to send in your application as interviews are ongoing. We look forward to reviewing your application. Welcome!
HemoCue, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job.
Check out our benefits at Danaher Benefits Info.
Fackliga kontakter:
Unionen: Henrik Pommer, 0431–481244
Akademikerföreningen: Katarina Cooper, 0431–481302 Visa mindre

IMDS and Compliance Engineer

The Koenigsegg R&D team is a small, agile hub of highly talented individuals, where the sum is greater than the parts. Koenigsegg is committed to hiring and developing top talent from across the world for any given discipline. Our world-class team operates with a non-conventional, ‘Lean Development’ philosophy of high inter-disciplinary collaboration, flat organizational structure, and technical contribution at all levels. You will be expected to challenge... Visa mer
The Koenigsegg R&D team is a small, agile hub of highly talented individuals, where the sum is greater than the parts. Koenigsegg is committed to hiring and developing top talent from across the world for any given discipline. Our world-class team operates with a non-conventional, ‘Lean Development’ philosophy of high inter-disciplinary collaboration, flat organizational structure, and technical contribution at all levels. You will be expected to challenge and to be challenged, to create, and to innovate.

For this role we are looking for someone with a genuine passion for engineering the best vehicles in the world. You will be working in a fast-paced, entrepreneurial company, leading the way in the hypercar business. You’ll work alongside accomplished, world-renowned engineers on perhaps the most exciting automotive programs in existence today.

You will have the opportunity to build, lead and manage Koenigsegg Global Compliance Program including creating processes and procedures.

Responsibilities

- This task requires strong knowledge of IMDS. You will be responsible for managing the IMDS in the company.
- This task requires excellent understanding and application of Global Regulatory Compliance laws, directives, and automotive industry-specific safety regulations (e.g., RoHS, REACH, CA Prop 65, SCIP etc.).
- Interdisciplinary work is the key. Collaboration with R&D, Quality, Manufacturing, Purchasing Departments is crucial.
- Your task requires to identify areas of potential regulatory compliance at risk at the plant, product, and departments. You need to develop programs and procedures to relieve potential risk(s).
- Act as a technical expert in the application of existing and new global regulatory compliance laws/directives/regulations.
- Serve as the primary compliance contact.
- Serve as the project manager for regulatory compliance contract activities by working with labs/authorities/agencies to develop pricing and planning.

Need to have

- Minimum BSc. in Chemical/Environmental Engineering or other related engineering disciplines.
- Strong knowledge of IMDS is a must.
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Minimum 3 years of experience with following regulatory frameworks on a global scale.

- REACH
- ROHS
- Recycling
- Product End of Life
- SCIP etc
- Strong understanding of CE certification


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Excellent communication skills (verbal / written)

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Able to work independently and within a team.

- Strong interpersonal and communication to build relationships across the Koenigsegg organization as well as with authorities and test labs.
- Effectively handle multitasking, organize workload, and meet deadlines.
- Be ready to technically challenge and to be challenged while executing above mentioned tasks.

Availability

- According to agreement
- Full time


Koenigsegg is most known for building some of the fastest cars in the world; with almost all of our megacar technologies that are patented and made in-house by our almost 500 world-class technicians, engineers, sourcing experts, production craftsmen, and communicators.

What we’ve created is a unique proving ground of engineering creativity that makes use of our breakthrough megacar development and legacy to push the boundaries of sustainable mobility technology.

So, what’s next?

We are on a universe-denting mission to develop the next generation of breakthrough tech and products. We are looking for outstanding, impactful, and authentic individuals to grow with us. Our ambitions are inspiring but will push the limits of what is possible – requiring one to work efficiently amid our cross-functional teams to execute at high-quality levels.

The goal is clear: innovate and transform. Visa mindre

Quality Assurance Design Specialist to HemoCue AB

Do you want to make a difference by developing key lifesaving medical device products? Are you an energetic and organized person who looks for new challenges? Do you want to work for a truly global business who refuse to compromise when it comes to caring for people? If your answer is yes, you may be the candidate we are looking for!   About the company HemoCue, part of the Radiometer Group since April 2013, is a global leader in point-of-care testing. ... Visa mer
Do you want to make a difference by developing key lifesaving medical device products? Are you an energetic and organized person who looks for new challenges? Do you want to work for a truly global business who refuse to compromise when it comes to caring for people? If your answer is yes, you may be the candidate we are looking for!

 

About the company
HemoCue, part of the Radiometer Group since April 2013, is a global leader in point-of-care testing.

HemoCue AB (Ängelholm, Sweden), introduced in 1982 the first accurate, near-patient hemoglobin test. The company also sells point-of-care tests for glucose, urine albumin, HbA1c, total and differential white blood cell count. Further information, visit www.hemocue.com

 

The QA team
You will be part of a QA team that today consists of seven people with different background and experience. The team is responsible for quality assurance and quality development activities within the core processes Supply Chain Management and Product Lifecycle Management. This includes QA expertise during product development, production and further development of the already released products and manufacturing processes, handling of non-conformities as well as the qualification, auditing and monitoring of suppliers.

 

As a QA Design Specialist you will be working in cross functional team with R&D, Operations and Marketing and provide QA expertise and guidance to ensure safe, reliable and compliant products during new product development and maintenance of existing products.

 

The Job
To be successful, you must cooperate cross-functionally and provide your QA expertise by supporting, guiding, training and communicating towards the best result with your partners. Your responsibilities and tasks will include

 

- Act as QA Core team member in Development Project performing activities according to HemoCue Product Life Cycle Management process
- Ensure that procedures and activities related to Design Control are in compliance with requirements in ISO 13485 and QSR as well as with industry best practice
- Assessing overall product risk by facilitating the use of risk management tools and contributing to the risk management evaluations



Qualifications
You have a University degree in science or technology (Master or Bachelor)

Experience from the following areas is required

 

- Minimum three years of experience from QA or R&D in medical device industry or a QA role with focus on supporting R&D with QA expertise in a regulated industry  
- Ensure that Design Changes (to product and manufacturing process) are planned and implemented according to the Engineering Change Control Procedure and relevant considerations are taken regarding quality and regulatory requirements
- Knowledge and trained in relevant standards and regulations, QSR and specifically Design Control (QSR 820.30), ISO 13485, ISO 14971
- You have strong communication skills and can motivate and inspire your colleagues, even when there are conflicting demands

Good knowledge of Swedish and English in speech and writing are essential.



Personality
As a person you are a team player, efficient, structured and solution-oriented and who likes a fast pace. You find it easy to communicate with other people and enjoy working in a company that is driven by continuous improvement, both in terms of equipment and processes.



We offer you
A unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combine to make it both fun and meaningful to go to work. Both in Sweden and abroad you will meet enthusiastic colleagues who take pride in making a difference in a company whose products can truly impact other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.

 

How do I apply for this position?
This recruitment is handled by Macavoy, and you apply with an updated CV and personal letter via www.macavoy.se or www.hemocue.se. We will work with a continuous selection. So, please send your application without delay. If you have any questions regarding this position, please do not hesitate to call, Markus Holmgren 010-330 54 81.

 

We look forward to your application!

 

Who´s Macavoy?
Macavoy is the small recruiting agency working with the big competencies. Macavoy are specialized in recruiting managers, project managers and specialist within Engineering. Read more about the company at www.macavoy.se and follow us at LinkedIn to find out what´s happening.

 

 

And finally, about Danaher…
Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries. A globally diverse team of 71,000 associates, we are united by our culture and operating system, the Danaher Business System, which is our competitive advantage. In 2014, we generated $19.9B in revenue and our market cap exceeded $60B. We are #149 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 2,000% over 20yrs.

At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team. Visa mindre