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Sterile Validation – Healthcare / Efficacy Specialist - Biocides

Workscope: Research Associate
We have been an independent service provider for the agrochemical and industrial chemical industry since 1996, with currently over 530 employees at sites in Europe, Asia and the USA. As a leading service provider with an international focus, we offer comprehensive advice on the registration of agrochemicals, biocides, industrial chemicals, veterinary pharmaceuticals, medical devices and biotechnological pharmaceuticals.


To support our team we are currently seeking a:

Sterile Validation - Healthcare / Efficacy Specialist - Biocides 

Ref. No. 2017-05/JV


Role and Responsibilities
  • Support of the compliance team with regard to assisting our clients with the validation of their manufacture of sterile products (sterilization, packaging, transport)
  • Evaluation of methods for determining the microbiological and particulate cleanliness of air, surfaces etc.
  • Evaluation and establishment of hygiene concepts
  • Support in the validation of reprocessing procedures of reusable medical devices
  • Development of authorization strategy for biocidal products regarding the efficacy of the product
  • Evaluation of efficacy studies and publications regarding their validity
  • Preparation of study summaries including evaluation of the study reports and potentially planning and monitoring of efficacy studies
  • Compilation of scientific expert statements and position papers
  • Preparation and coordination of biocidal active substance dossiers and biocidal product dossiers
  • Communication and close co-operation with our clients and authorities throughout Europe and on a global scale

Profile and Qualifications
  • University degree in environmental or natural science, engineering or equivalent
  • Solid background in Microbiology
  • At least 2 years' experience in the authorization of biocides in the international regulatory field (EU and worldwide), particularly with the Biocidal Products Regulation (EU) No. 528/2012 and or respective activity in the certification and authorization of Medical Devices according to 93/42 EEC
  • Very good interpersonal skills
  • Excellent communication and presentation skills
  • Excellent language skills in English and German (spoken and written); additional language skills would be an asset
  • Self-motivated with the ability to work in a team

Benefits
  • You will be working in a modern, professional, fast-growing, internationally active organisation with a high degree of responsibility and independence
  • Intensive on-the-job training will be provided in a competent multidisciplinary team
  • We support the compatibility of work and family by offering flexible working hours as well as childcare subvention
  • Our knoell academy offers various training opportunities
  • We offer the opportunity to participate in the company pension scheme
  • Under specific conditions you have the chance to participate in the employee participation program

Contact detail


How to apply:
Bewerbungen bitte nur online über unsere Homepage: www.knoell.com
Send application to
Dr. Knoell Consult GmbH
Human Resources
Dynamostr. 19
D-68165 Mannheim
Tel. 0621 - 718858 - 0
 

Job profile


Working hours
Can be Full-Time or Part-Time
Contract duration
Permanent
Type of job
Specialist
Work experience
jobexperience is required
Region
France, Spain, United Kingdom, Germany (Baden-Württemberg, Berlin, Nordrhein-Westfalen), Switzerland (Basel-Stadt)
Working place
68165 Mannheim
Area of expertise
Healthcare & Public Health, Agricultural Sciences, Biology & Life Sciences, Chemistry, Veterinary Medicine, Geo Sciences, Pharmaceutics, Medical Engineering