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Stellen zum Suchbegriff Biotechnologie finden sich auch in folgenden Orten:

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Compliance Manager (w/m)

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DSM Bright Science. Brighter Living.

Royal DSM is a purpose led global science-based company in Nutrition, Health and Sustainable Living.
DSM is driving economic prosperity, environmental progress and social advances to create sustainable value for all stakeholders. DSM delivers innovative business solutions for human nutrition, animal nutrition, personal care and aroma, medical devices, green products and applications, and new mobility and connectivity.
DSM and its associated companies deliver annual net sales of about Euro 10 billion with approximately 23000 employees. The company is listed on Euronext Amsterdam. More information can be found at www.dsm.com.

This position is responsible for managing and coordinating the quality/regulatory/scientific compliance activities at each manufacturing area. This position will assist the Head of Manufacturing and Head of Quality with assuring timely investigations, resolution of issues and implementation of corrective measures by using scientific principles, root cause analysis and compliance minded corrective and preventative actions related to manufacturing.
Compliance Manager (w/m)
-Maintains awareness of current GMP-trends and manufacture processes and supports continuous improvement within the manufacturing area
-Prepare SOPs and investigation documents as well as tracking- and trending-analysis and KPIs relevant to business process
-Resolve production discrepancies and customer complaints as related to product release, which must take into account all manufacturing processes, quality testing and customer requirements
-Provide support for regulatory agency inspections / customer audits / internal audits
-Maintain facility good quality standard
-Function as the document control and record management administrator for the respective manufacturing groups
-Recommends changes in established processes to quality
-Report and take any necessary action to prevent quality problems from occurring
-Provide support to QA department for special projects
-Stay current with key regulatory and certifying agency guidelines and regulations
-Provide support to the regulatory team (Pharma and IVD)
-MSc in Biotechnology, Biology, Microbiology, Chemistry, Pharmacy or Food science related fields
-Minimum of 5+ years' experience with proven track record in a GMP production site
-1-3 years of experience in RA in IN-vitro Diagnostic/Technology field
-Ideally knowledge of IVD
-Product classification; Definition of applicable standards; Conformity assessment procedures
-Fluent in English & German



Einleitung :



Referenz Tochtergesellschaften : 400-BASEL CITY

Name der Advisor : Beck Matthias
Name des Unternehmens : Bâle Office

Name der Tochtergesellschaft : Basel City

Anschrift :
Barfüsserplatz 3
Basel
4051
Firmenbeschreibung :
DSM Bright Science. Brighter Living.

Royal DSM is a purpose led global science-based company in Nutrition, Health and Sustainable Living.
DSM is driving economic prosperity, environmental progress and social advances to create sustainable value for all stakeholders. DSM delivers innovative business solutions for human nutrition, animal nutrition, personal care and aroma, medical devices, green products and applications, and new mobility and connectivity.
DSM and its associated companies deliver annual net sales of about Euro 10 billion with approximately 23000 employees. The company is listed on Euronext Amsterdam. More information can be found at www.dsm.com.

This position is responsible for managing and coordinating the quality/regulatory/scientific compliance activities at each manufacturing area. This position will assist the Head of Manufacturing and Head of Quality with assuring timely investigations, resolution of issues and implementation of corrective measures by using scientific principles, root cause analysis and compliance minded corrective and preventative actions related to manufacturing.


Stellenbeschreibung :
-Maintains awareness of current GMP-trends and manufacture processes and supports continuous improvement within the manufacturing area
-Prepare SOPs and investigation documents as well as tracking- and trending-analysis and KPIs relevant to business process
-Resolve production discrepancies and customer complaints as related to product release, which must take into account all manufacturing processes, quality testing and customer requirements
-Provide support for regulatory agency inspections / customer audits / internal audits
-Maintain facility good quality standard
-Function as the document control and record management administrator for the respective manufacturing groups
-Recommends changes in established processes to quality
-Report and take any necessary action to prevent quality problems from occurring
-Provide support to QA department for special projects
-Stay current with key regulatory and certifying agency guidelines and regulations
-Provide support to the regulatory team (Pharma and IVD)


Datum : 2020-02-23
Art des Unternehmens : Pharmaindustrie


Kontakt Advisor :
Name : Beck
Vorname : Matthias

Email : matthias.beck@manpower.ch
Telefonieren : 058 307 3100


Jobboard kontakt email : contact7055@manpch.contactrh.com
Identifizierung tochtergesellschaft :
400-BASEL CITY
Referenz : 201825-87-1

Datum der Veröffentlichung : 2020-02-21 13:55:31


Gesuchtes Profil :
-MSc in Biotechnology, Biology, Microbiology, Chemistry, Pharmacy or Food science related fields
-Minimum of 5+ years' experience with proven track record in a GMP production site
-1-3 years of experience in RA in IN-vitro Diagnostic/Technology field
-Ideally knowledge of IVD
-Product classification; Definition of applicable standards; Conformity assessment procedures
-Fluent in English & German

Land : Schweiz
Stadt : Aesch
Postleitzahl : 4147

Unternehmenssektor : Chemie & Life Sciences

Kategorien : None

Schlussteil :
Interested?
Do you have interest in this challenge? To apply for this vacancy, please apply on https://www.manpower.ch and complete application documents (cv, job references and proof of qualification) with your notice period and salary expectations. Please note that only online applications will be processed.

Reference check procedures are part of the DSM Recruitment & Selection Process. You will be contacted when these references checks are required.

Royal DSM is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, or any other characteristic protected by law.

Gesamtbewertung

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