Location: Innsbruck, Austria
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Job Category:
Employment Type: Full time
Salary: per year
Posted: 01.08.2013
Job Description
Global Pharmaceutical
Company with facilities in Austria seeks a Head of Validation.
This is a permanent position with a competitive salary of up to 100,000 euros (possibly more based on your experience and current salary; we do not want to miss out on good candidates), excellent benefits and bonus scheme. The location is in the Alps and close to Munich.
This role comes with an entirely comprehensive relocation policy that is designed to be as stress-free as possible as well as being entirely cost neutral. It includes international schooling, language classes, temporary accommodation and more (to be discussed upon application).
- Creation and maintenance of the Site Validation Master Plan
- Establish procedures and systems to ensure compliance of validation documents
- Coordination and implementation and monitoring of projects to process validation and equipment qualification
- Create and approve of standard operating procedures and work instructions
- Representation of the validation aspects during inspections and audits
Personal Requirements:
Your science and technology studies (pharmacology, chemistry, microbiology, process engineering) have been successfully completed. You have at least 3 years experience in a GMP regulated production environment and have extensive regulatory knowledge in the field of qualification and validation collected. In addition to your high analytical thinking you have a goal, project-oriented and structured work. They are characterized by excellent social skills and open communication and have already gained some experience with leading teams. We require qualified IT skills and due to the international nature of our business very good English skills.
Please contact Tim Walker to confidentially discuss this position.
SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business
This is a permanent position with a competitive salary of up to 100,000 euros (possibly more based on your experience and current salary; we do not want to miss out on good candidates), excellent benefits and bonus scheme. The location is in the Alps and close to Munich.
This role comes with an entirely comprehensive relocation policy that is designed to be as stress-free as possible as well as being entirely cost neutral. It includes international schooling, language classes, temporary accommodation and more (to be discussed upon application).
- Creation and maintenance of the Site Validation Master Plan
- Establish procedures and systems to ensure compliance of validation documents
- Coordination and implementation and monitoring of projects to process validation and equipment qualification
- Create and approve of standard operating procedures and work instructions
- Representation of the validation aspects during inspections and audits
Personal Requirements:
Your science and technology studies (pharmacology, chemistry, microbiology, process engineering) have been successfully completed. You have at least 3 years experience in a GMP regulated production environment and have extensive regulatory knowledge in the field of qualification and validation collected. In addition to your high analytical thinking you have a goal, project-oriented and structured work. They are characterized by excellent social skills and open communication and have already gained some experience with leading teams. We require qualified IT skills and due to the international nature of our business very good English skills.
Please contact Tim Walker to confidentially discuss this position.
SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business
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