Proactive participation in the local expansion of the qualification and validation business field
Independent execution of qualification (DQ, IQ, OQ and PQ) and/or validation activities (process, cleaning and computerized system validation) in compliance with current cGMP regulations
Independent execution of GxP risk analyses
Coordination and interface management within qualification and/or validation projects
Creation of GMP documents (e.g. SOPs, DQ-, IQ-, OQ-, PPQ-documents)
Support in consulting tasks in the field of qualification and validation
Participation in project-specific offers and cost estimations
Your Profile
Completed studies in biotechnology, chemical engineering, pharmaceutical or medical technology or equivalent training
2-3 years (senior: 7+ years) of professional experience in planning and executing projects in the pharmaceutical industry
Knowledge and professional experience in qualification and/or validation
Independent, structured and quality-oriented working style
Very good German and English in speech and writing
Willingness to travel for project-specific assignments in Germany and abroad
Additional senior skills:
Experience in managing and leading employees within projects
Experience in customer and supplier/subcontractor management
Proactive engagement in customer care
Very good analytical skills and a team-oriented working style
Benefits
Flat hierarchies
Flexible working hours with core working times
Remote work
Modern office with height-adjustable desks
Employee referral program
Restaurant vouchers
Global travel insurance
Comprehensive expense reimbursement policy
Highest standard for occupational safety
Free cold and hot beverages
Free job ticket
Opportunity for unpaid leave
Part-time work possible
High awareness of company culture
Job-sharing program
Sustainability
At BakerHicks, we are committed to combating climate change and have been actively engaged in environmental efforts for years. Our group aims to become climate-neutral by 2030. We have developed an approach for project execution that focuses on sustainability and efficiency. We live sustainability not only in our customer projects but also within the company, and encourage the use of public transportation within our incentive system.
(Senior) Qualification / Validation Engineer
Tyrol; Vienna
Your Responsibilities
Proactive participation in the local expansion of the qualification and validation business field
Independent execution of qualification (DQ, IQ, OQ and PQ) and/or validation activities (process, cleaning and computerized system validation) in compliance with current cGMP regulations
Independent execution of GxP risk analyses
Coordination and interface management within qualification and/or validation projects
Creation of GMP documents (e.g. SOPs, DQ-, IQ-, OQ-, PPQ-documents)
Support in consulting tasks in the field of qualification and validation
Participation in project-specific offers and cost estimations
Your Profile
Completed studies in biotechnology, chemical engineering, pharmaceutical or medical technology or equivalent training
2-3 years (senior: 7+ years) of professional experience in planning and executing projects in the pharmaceutical industry
Knowledge and professional experience in qualification and/or validation
Independent, structured and quality-oriented working style
Very good German and English in speech and writing
Willingness to travel for project-specific assignments in Germany and abroad
Additional senior skills:
Experience in managing and leading employees within projects
Experience in customer and supplier/subcontractor management
Proactive engagement in customer care
Very good analytical skills and a team-oriented working style
Benefits
Flat hierarchies
Flexible working hours with core working times
Remote work
Modern office with height-adjustable desks
Employee referral program
Restaurant vouchers
Global travel insurance
Comprehensive expense reimbursement policy
Highest standard for occupational safety
Free cold and hot beverages
Free job ticket
Opportunity for unpaid leave
Part-time work possible
High awareness of company culture
Job-sharing program
Sustainability
At BakerHicks, we are committed to combating climate change and have been actively engaged in environmental efforts for years. Our group aims to become climate-neutral by 2030. We have developed an approach for project execution that focuses on sustainability and efficiency. We live sustainability not only in our customer projects but also within the company, and encourage the use of public transportation within our incentive system.
What You'll Do
Proactive participation in the local expansion of the qualification and validation business field
Independent execution of qualification (DQ, IQ, OQ and PQ) and/or validation activities (process, cleaning and computerized system validation) in compliance with current cGMP regulations
Independent execution of GxP risk analyses
Coordination and interface management within qualification and/or validation projects
Creation of GMP documents (e.g. SOPs, DQ-, IQ-, OQ-, PPQ-documents)
Support in consulting tasks in the field of qualification and validation
