- Management of overall quality operations for Santen in Korea to ensure its compliance with applicable local regulatory authority and Santens global requirements for importation local testing repackaging storage and distribution of Santen products.
- Responsible as the Quality Management Representative Role for Santen in Korea and ensure the local QA operation/activities and the development implementation and maintenance of a systematic effective and efficient local Quality Management System (QMS) as per applicable local regulatory authority and Santens global requirements.
- Perform quality activities and resolve quality issues for Santen in Korea to support the continuous supply of Santen products in these countries in compliance to applicable local regulatory authority and Santens global/release requirements. Act as responsible pharmacist/importing manager if required.
- Responsible to ensure all vendors including suppliers/service providers used by Santen in Korea is compliant with all corporate/regional and regulatory cGMP/cGDP guidelines and SOPs.
- Maintain a quality compliance program for all vendors including an effective change management system.
- Management all relevant regulatory inspections or certification audits in Korea (GDP/GDPMD by regulators or certification body) to ensure successful maintenance / renewal of license and certification.
- Responsible to ensure Santen products produced by CMOs in Korea/Asia is compliant to applicable established and registered product specifications and requirements.
Qualifications :
Bachelors degree in Pharmacy (Licensed Pharmacist in Korea)
Minimum 15 years of experience in the pharmaceutical and/or medical device industry focused on quality functions
At least 5 years in a GMP manufacturing plant environment
Around 10 years in a commercial quality environment
Approximately 5 years in a quality supervisory or leadership role
Minimum 5 years of people management experience (highly preferred)
Strong knowledge and hands-on experience in developing implementing and maintaining Quality Management Systems (QMS) in compliance with Good Distribution Practice (GDP) or Good Distribution Practice for Medical Devices (GDPMD) experience within the Korean market is essential
Proven expertise in GDP GMP and GIP (must-have)
Demonstrated experience in CMO management (highly preferred)
Fluency in both English and Korean with excellent stakeholder management and communication skills
Additional Information :
Grow your career at Santen
A career at Santen is an opportunity to make a difference. We aspire to contribute to the realization of Happiness with Vision by providing eye health products and services to patients consumers and medical professionals around the world. Guided by our CORE PRINCIPLE Tenki ni sanyo suru Santen is engaged in the global research & development manufacturing and sales and marketing of pharmaceutical products in ophthalmology. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes education and treatment. At Santen we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.
The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs role requirements and individual qualifications regardless of race color ethnicity national origin/ancestry religion sexual orientation gender gender identity/ expression age disability medical condition marital status veteran status or any other characteristic protected by law.
If you require any kind of accommodation during our recruitment process please let the recruiter from our team know.
*Please note that team assignments may be subject to future changes
Remote Work :
No
Employment Type :
Full-time
Management of overall quality operations for Santen in Korea to ensure its compliance with applicable local regulatory authority and Santens global requirements for importation local testing repackaging storage and distribution of Santen products. Responsible as the Quality Management Representative...
- Management of overall quality operations for Santen in Korea to ensure its compliance with applicable local regulatory authority and Santens global requirements for importation local testing repackaging storage and distribution of Santen products.
- Responsible as the Quality Management Representative Role for Santen in Korea and ensure the local QA operation/activities and the development implementation and maintenance of a systematic effective and efficient local Quality Management System (QMS) as per applicable local regulatory authority and Santens global requirements.
- Perform quality activities and resolve quality issues for Santen in Korea to support the continuous supply of Santen products in these countries in compliance to applicable local regulatory authority and Santens global/release requirements. Act as responsible pharmacist/importing manager if required.
- Responsible to ensure all vendors including suppliers/service providers used by Santen in Korea is compliant with all corporate/regional and regulatory cGMP/cGDP guidelines and SOPs.
- Maintain a quality compliance program for all vendors including an effective change management system.
- Management all relevant regulatory inspections or certification audits in Korea (GDP/GDPMD by regulators or certification body) to ensure successful maintenance / renewal of license and certification.
- Responsible to ensure Santen products produced by CMOs in Korea/Asia is compliant to applicable established and registered product specifications and requirements.
Qualifications :
Bachelors degree in Pharmacy (Licensed Pharmacist in Korea)
Minimum 15 years of experience in the pharmaceutical and/or medical device industry focused on quality functions
At least 5 years in a GMP manufacturing plant environment
Around 10 years in a commercial quality environment
Approximately 5 years in a quality supervisory or leadership role
Minimum 5 years of people management experience (highly preferred)
Strong knowledge and hands-on experience in developing implementing and maintaining Quality Management Systems (QMS) in compliance with Good Distribution Practice (GDP) or Good Distribution Practice for Medical Devices (GDPMD) experience within the Korean market is essential
Proven expertise in GDP GMP and GIP (must-have)
Demonstrated experience in CMO management (highly preferred)
Fluency in both English and Korean with excellent stakeholder management and communication skills
Additional Information :
Grow your career at Santen
A career at Santen is an opportunity to make a difference. We aspire to contribute to the realization of Happiness with Vision by providing eye health products and services to patients consumers and medical professionals around the world. Guided by our CORE PRINCIPLE Tenki ni sanyo suru Santen is engaged in the global research & development manufacturing and sales and marketing of pharmaceutical products in ophthalmology. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes education and treatment. At Santen we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.
The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs role requirements and individual qualifications regardless of race color ethnicity national origin/ancestry religion sexual orientation gender gender identity/ expression age disability medical condition marital status veteran status or any other characteristic protected by law.
If you require any kind of accommodation during our recruitment process please let the recruiter from our team know.
*Please note that team assignments may be subject to future changes
Remote Work :
No
Employment Type :
Full-time
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