Validation Engineer to Nolato MediTech in Hörby

Technogarden / Kemiingenjörsjobb / Hörby
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Nolato MediTech develops and manufactures polymer products and systems in close cooperation with leading customers within medical technology and pharmaceuticals. We are a world leader in injection molding of silicone and have extensive knowledge in injection molding thermoplastic medical technology products, with special competence in 2K and 3K molding. Medical Excellence is our way of exceeding our clients' very high standards and expectations. By adapting the principles within Lean to good manufacturing and documentation practices (GMP & GDP), we are increasing value for our clients. Nolato MediTech has two production sites in Lomma and Hörby with cleanroom production class 8 and hygiene production according to ISO 14644-1.

Nolato MediTech is expanding and looking for an experienced Validation Engineer to our quality department.

Main responsibilities
As a validation engineer your responsibility will be divided into two areas:

• planning and executing of clean room validation and the periodic review of
existingcleanrooms
• equipment qualification including data integrity and software validation.

Your main responsibilities are to plan, document and lead qualifications and validation in conformance to current regulations.

Furthermore you will:

• Lead and conduct risk analysis (p-FMEA) to develop various validation tests
• Issue validation plans, protocols and reports
• Lead the URS work and qualification tests
• Conduct deviation investigations
• Lead improvements projects

As a validation engineer, you have a continuous and close contact with project managers, production, technical engineers and the purchasing department. The position is a permanent full time employment and placed in Hörby. You should be a non-smoker/snuff user.

Qualifications
We expect you to have a bachelor degree or similar level in experience and have worked as a validation engineer in the pharmaceutical and/or medical device industry for at least 3 years. You should have good knowledge of:

• GAMP5/Part 11
• ISO 14644-1/ISO14644-2
• Report writing (IQ, OQ, PQ)
• Production and manufacturing processes

As a person you should be quality minded, driven, proactive, structured and analytical. You will work in a customer-oriented, international environment so you must be fluent in both English and Swedish

We offer
We offer you an important role in a world leading medical technology company where you will work with products that add great value to the end user. Nolato MediTech is a fast growing and profitable company in an industry of the future that offers great development opportunities.

Application
For further information about the position please contact Recruitment Consultant Jörgen Björkman at Technogarden, 0739-80 83 95.

Varaktighet, arbetstid
Heltid Anställningstid enligt överenskommelse

Publiceringsdatum
2018-09-25

Ersättning
Lön enligt överenskommelse

Så ansöker du
Sista dag att ansöka är 2018-10-21
Klicka på denna länk för att göra din ansökan

Kontakt
Jörgen Björkman jorgen.bjorkman@technogarden.se +46 739 80 83 95

Företag
Technogarden

Adress
Technogarden
Scheelevägen 2
22381 Lund

Kontorsadress
Scheelevägen 2 , Lund

Jobbnummer
4367485

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