Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.
QA Technical and Validation Supervisor
Cikarang, Indonesia, 17530
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.
Advantage to Have:
- Understanding of ISO related and GSDP standard (CDOB) are advantageous
- Ability to manage and update SOPs and Work Instructions in alignment with regulatory changes
Why join APL:
- We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
- We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
- As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
- Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
- Our Total Rewards program is designed to support your overall well-being in every aspect
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