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For our client Merck in Aubonne, we are looking for a Cleaning Validation Expert (m/f/d) for a period of 12 months.
Your Role :
Coordinate cleaning validation and monitoring activities in line with the life cycle of a manufacturing process for biotech manufacturing equipment
Establish and execute validation protocols and reports for cleaning validation
Ensure reliability and conformity of validation and control activities in line with internal and regulatory procedures and guidelines
Provide technical support to cleaning activities associated with the manufacturing process.
Perform successful and on time resolution of incidents and deviations related to cleaning validation exercises (Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results)
Support the periodic process review and etablish documentation relation to control of the process (PCS, sampling plans and commercial panel testing )
Lead the enhancement of cleaning practices
Share best practices and train teams
Be cleaning Expert during audits and inspections
Who You Are:
Bachelor's or Master's Degree in Science, Pharmacy or Engineering.
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries.
Fluent in english and french
Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes.
Proficient time management skills, planning and organization capabilities.
Proven leadership & teamwork skills, self starter, results oriented and build and maintain strong relationships with multiple groups.
Proficient in Risk Assessment/Management Proven assessment, analytical and problem-solving skills.
Proficient presentation skills and Technical Writing/Oral communication skills (English) Proficient in cGMP's, and FDA Regulations as it applies to pharmaceutical industry.
For our client Merck in Aubonne, we are looking for a Cleaning Validation Expert (m/f/d) for a period of 12 months.
Your Role :
Coordinate cleaning validation and monitoring activities in line with the life cycle of a manufacturing process for biotech manufacturing equipment
Establish and execute validation protocols and reports for cleaning validation
Ensure reliability and conformity of validation and control activities in line with internal and regulatory procedures and guidelines
Provide technical support to cleaning activities associated with the manufacturing process.
Perform successful and on time resolution of incidents and deviations related to cleaning validation exercises (Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results)
Support the periodic process review and etablish documentation relation to control of the process (PCS, sampling plans and commercial panel testing )
Lead the enhancement of cleaning practices
Share best practices and train teams
Be cleaning Expert during audits and inspections
Who You Are:
Bachelor's or Master's Degree in Science, Pharmacy or Engineering.
Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries.
Fluent in english and french
Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes.
Proficient time management skills, planning and organization capabilities.
Proven leadership & teamwork skills, self starter, results oriented and build and maintain strong relationships with multiple groups.
Proficient in Risk Assessment/Management Proven assessment, analytical and problem-solving skills.
Proficient presentation skills and Technical Writing/Oral communication skills (English) Proficient in cGMP's, and FDA Regulations as it applies to pharmaceutical industry.
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wir sind da um deine Fragen zu beantworten.
KK
Kata Kulcsár
Lausanne Professionals Life Sciences
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For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.Your role : As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:Documentation and archiving:Manage the distribution and life cycle of GxP documentation.Administration of operational activ
For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.Your role : As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:Documentation and archiving:Manage the distribution and life cycle of GxP documentation.Administration of operational activ
For our client Merck in Aubonne, we are currently looking for a ‘Cleaning Validation Expert’ until the end of 2025.The Cleaning validation within the Fill & Finish Department leads and manages all the cleaning validation activities within our site to ensure new production equipment and product implementation, the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requir
For our client Merck in Aubonne, we are currently looking for a ‘Cleaning Validation Expert’ until the end of 2025.The Cleaning validation within the Fill & Finish Department leads and manages all the cleaning validation activities within our site to ensure new production equipment and product implementation, the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requir
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