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A global player in the pharmaceutical industry with more than 100.000 employees is looking for a new CVQ Head in Switzerland. If you have a proven record of several years of experience in Verification and Qualification in the pharma industry and want to lead the CVQ team please apply here.
JOB:
-Leading and managing the CVQ team, taking ownership for all functions within CVQ
-Motivates and guides the CVQ team and addresses personnel issues as they arise immediately
-Ensures adequate resources for an efficient and reliable CVQ procedure and operation in alignment with the company strategy
-Ensure the sustainable technical operation for all new facilities, a cost-effective CVQ approach for different projects across the entire site
-Supports the management as well as team leaders from other departments in relation to CVQ subject matter
-Represents CVQ during GMP audits and inspections
-Encourages a culture of continuous improvement and development of technologies and procedures within CVQ
-Responsible for all CVQ activities at site for all the different projects
-Responsible for the development and continuous improvement in regards of compliance topics, establish work standards with current GMP and regulatory requirements in collaboration with the quality department
-Ensures the compliance with health, safety and environmental requirements within CVQ
-Exchange of information between the various departments and sites with qualification strategies and regarding all CVQ tasks and duties
-Continuous improvement of GMP compliant requalification and calibration systems based on current industrial principles and regulatory requirements
-Develop commissioning strategies to ensure GxP compliance of manufacturing and infrastructure systems in an efficient way
-Adheres to general safety rules, policies, procedures and instructions as rolled out by the EHSS functions and endorsed by the site management.
-Adheres to general cGMP rules, Quality policies, procedures and instruction as rolled out by the Quality function and endorsed by the site management
Requirements:
Education:
-Bachelor's degree or equivalent experience; educational concentration in pharmaceutical engineering, chemical engineering or equivalent
Experience:
-Profound experience working in the pharmaceutical sector in a GMP environment
-Relevant qualification in a Quality field or relevant working experience within the are
-Experience of positively dealing with distractions or barriers to progress
-Ability to plan and prioritize with drive and determination - results orientated and able to meet deadlines
-Willingness to learn new skills and embrace procedures
-Effectively liaise with Engineering and QA at all staff levels
Knowledge, Skills, Abilities:
-Excellent verbal and written communication skills in English and German
-Very good understanding of GMP guidelines
-Proven track record of dealing with Commissioning, Verification and Qualification
-Good understanding of technical installations and pharmaceutical processes
-Familiar with innovative quality management tools and systems
What we offer:
-Employment with an innovative, future-oriented organisation
-Outstanding career and development prospects
-Company pension scheme and other fringe benefits
-Exciting company culture which stands for integrity, intensity, involvement and innovation
Head of CQV
- Location Switzerland
- Job type Permanent
- Salary Negotiable
- Discipline Bioengineering & Medical Engineering
- Reference PR/353152_1649945968
JOB:
-Leading and managing the CVQ team, taking ownership for all functions within CVQ
-Motivates and guides the CVQ team and addresses personnel issues as they arise immediately
-Ensures adequate resources for an efficient and reliable CVQ procedure and operation in alignment with the company strategy
-Ensure the sustainable technical operation for all new facilities, a cost-effective CVQ approach for different projects across the entire site
-Supports the management as well as team leaders from other departments in relation to CVQ subject matter
-Represents CVQ during GMP audits and inspections
-Encourages a culture of continuous improvement and development of technologies and procedures within CVQ
-Responsible for all CVQ activities at site for all the different projects
-Responsible for the development and continuous improvement in regards of compliance topics, establish work standards with current GMP and regulatory requirements in collaboration with the quality department
-Ensures the compliance with health, safety and environmental requirements within CVQ
-Exchange of information between the various departments and sites with qualification strategies and regarding all CVQ tasks and duties
-Continuous improvement of GMP compliant requalification and calibration systems based on current industrial principles and regulatory requirements
-Develop commissioning strategies to ensure GxP compliance of manufacturing and infrastructure systems in an efficient way
-Adheres to general safety rules, policies, procedures and instructions as rolled out by the EHSS functions and endorsed by the site management.
-Adheres to general cGMP rules, Quality policies, procedures and instruction as rolled out by the Quality function and endorsed by the site management
Requirements:
Education:
-Bachelor's degree or equivalent experience; educational concentration in pharmaceutical engineering, chemical engineering or equivalent
Experience:
-Profound experience working in the pharmaceutical sector in a GMP environment
-Relevant qualification in a Quality field or relevant working experience within the are
-Experience of positively dealing with distractions or barriers to progress
-Ability to plan and prioritize with drive and determination - results orientated and able to meet deadlines
-Willingness to learn new skills and embrace procedures
-Effectively liaise with Engineering and QA at all staff levels
Knowledge, Skills, Abilities:
-Excellent verbal and written communication skills in English and German
-Very good understanding of GMP guidelines
-Proven track record of dealing with Commissioning, Verification and Qualification
-Good understanding of technical installations and pharmaceutical processes
-Familiar with innovative quality management tools and systems
What we offer:
-Employment with an innovative, future-oriented organisation
-Outstanding career and development prospects
-Company pension scheme and other fringe benefits
-Exciting company culture which stands for integrity, intensity, involvement and innovation