Overview
Operation QA Supervisor Jobs in Daejeon, South Korea at Robert Walters
Title: Operation QA Supervisor
Company: Robert Walters
Location: Daejeon, South Korea
Job Title: Operation QA Supervisor (QA Operation)
Location: Daejeon, South Korea
Perm/Contract/ Full-time/Part-time: Permanent
On-site/Hybrid/Remote: On-site
Who We Are
Robert Walters is the world’s most trusted talent solutions business. Across the globe, we deliver recruitment, outsourcing, and talent advisory services for businesses of all sizes, opening doors for people with diverse skills, ambitions, and backgrounds.
The Role
Our client is seeking an Operation QA Supervisor (QA Operation) in the Pharmaceutical or Biotechnology division.
Job Description:
Your Role:
- Collaborate with Operations teams to support production activities related to company products within a GMP-compliant manufacturing environment.
- Review production documentation and provide guidance to resolve quality-related manufacturing issues and documentation discrepancies.
- Ensure thorough investigation of all non-conformances and timely implementation of effective corrective and preventive actions.
- Lead change control processes by evaluating proposed changes, assessing their impact, and providing quality input on implementation plans.
- Review and approve controlled documents, including Standard Operating Procedures (SOPs), Master Batch Records, work instructions, protocols, reports, and technical studies.
- Conduct final reviews of batch records and authorize batch release.
- Participate in continuous improvement initiatives to enhance operational efficiency and product quality.
- Oversee regular QA monitoring of manufacturing activities, including aseptic processes within a controlled cleanroom environment.
- Ensure that Operation QA personnel are recruited, trained, and qualified to support project execution and daily operational activities.
- Support site inspections and readiness activities, ensuring the site is audit-ready at all times.
- Lead the site integrity data and contamination control strategy.
- Perform other duties as assigned as necessary.
Who You Are:
- Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, Biology, Biotechnology, Chemistry, or a related discipline.
- Minimum of 10 years of experience in an international pharmaceutical or biotechnology environment, with a strong focus on GMP/ISO 9001 compliance.
- At least 3 years of supervisory experience in a quality assurance or related role.
- Experience in aseptic QA oversight and contamination control strategy establishment is highly preferred.
- High level of accuracy and attention to detail, with excellent interpersonal, verbal, and written communication skills.
- Strong problem-solving and organizational skills, with a meticulous and proactive approach to teamwork.
- Proficient communication skills in English.
This position is being recruited on behalf of our client through our Outsourcing service line. Resource Solutions Limited, trading as Robert Walters, acts as an employment business and agency, partnering with top organisations to help them find the best talent. We welcome applications from all candidates and are committed to providing equal opportunities.
Client promotes collaboration and aims to provide a supportive and inclusive environment where all individuals can maximize their full potential.
As we are continuously hiring for all our clients in the region, we will retain your CV in our database for any other positions that may fit your profile. Therefore, please let us know if you are not agreeable to that.
