QA Technical and Validation Supervisor
A quality assurance supervisor at Zuellig Pharma's Indonesian operation who oversees validation and qualification of storage, transportation, and passive packaging, maintains SOPs in line with ISO and CDOB standards, and verifies product/material registrations in SAP. Requires a licensed pharmacist with at least 1 year of QA/validation supervisory experience, based in Cikarang.
- Compensation
- Not disclosed
- Location
- Not listed
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 1+ years
- Category
- Qa
- Posted
Skills
Must have
- Bachelor's degree in pharmacy or a related field and licensed pharmacist
- Minimum 1 year experience as a QA/Validation Supervisor in the pharmaceutical or related industry
- Strong communication and interpersonal skills, with ability to influence and build relationships with stakeholders at all levels
Nice to have
- Understanding of ISO related and GSDP standard (CDOB)
- Ability to manage and update SOPs and Work Instructions in alignment with regulatory changes
Full description
About Us:
PT Anugerah Pharmindo Lestari (APL) a Zuellig Pharma company, is a leading healthcare solutions in Indonesia, and our purpose is to make healthcare more accessible to the communities we serve.
We provide world-class distribution, commercialization, and clinical trial support to support the growing healthcare needs in this region. The company was started forty years ago and has grown to become a billion-dollar business covering 514 cities with over 2,500 employees.
Our people serve more than 60,000 direct and indirect medical facilities and work with over 50 clients, including the top 20 pharmaceutical companies in the world.
Purpose of the Role:
To ensure the integrity and compliance of validation and qualification processes across operations and transportation by maintaining up-to-date SOPs and WIs in line with regulatory standards. The Quality Assurance and Validation Supervisor is responsible for overseeing validation activities related to storage, transportation, and passive packaging, while verifying product and material registration in SAP. This role plays a key part in supporting operational efficiency and ensuring adherence to ISO and CDOB standards within the pharmaceutical quality system.
What You’ll do:
- Ensure all validation and qualification activities are executed in accordance with current regulatory requirements, including ISO and CDOB standards.
- Maintain and regularly update Standard Operating Procedures (SOPs) and Work Instructions (WIs) related to validation processes.
- Effectively conduct and document validation for operations and transportation to ensure compliance and product integrity.
- Supervise and review the validation of branch storage facilities, transportation methods, and passive packaging, ensuring timely and accurate completion.
- Continuously assess and develop passive packaging solutions to support operational efficiency and compliance.
- Accurately verify and manage registered materials and products in the SAP system to support traceability and quality control.
- Demonstrate strong leadership in guiding validation teams and collaborate cross-functionally to support quality assurance goals.
- Proactively identify areas for improvement within validation processes and implement corrective actions as needed.
What Will Make You Successful :Must Have:
- Bachelor’s degree in pharmacy or a related field and licensed pharmacist.
- Minimum 1 year experience as a QA/Validation Supervisor in the pharmaceutical or related industry.
- Strong communication and interpersonal skills, with the ability to influence and build relationships with stakeholders at all levels.