SRA Analyst

Zuellig Pharma; Taguig; Hybrid; PHP 480,000 - 720,000; Full time

Job summary

Zuellig Pharma in Taguig, Philippines, is seeking an SRA Analyst to support secondary repackaging operations in compliance with ISO 9001 and GMP standards. The role involves production scheduling, coordination with clients, and ensuring timely production outputs.

The successful candidate will have experience in secondary packaging operations, a GMP background, and be proficient in SAP to manage stocks and billing. This is a full-time on-site role in Taguig.

Qualifications

• Must-have: Secondary Repackaging Operations experience/ or manufacturing set-up.
• Must-have: Background on Regulatory Standards and Good Manufacturing Practice.
• Must-have: Knowledgeable in SAP.

Responsibilities

• Ensures strict implementation and compliance with processes per established procedures and guidelines.
• Acts as production scheduler to achieve lead times in reprocessing products.
• Screens production orders and materials for redressing requirements and unplanned orders.
• Schedules secondary repackaging activities based on materials availability and capacity.
• Supports the Secondary Repackaging Supervisor in cost calculations and client quotations.
• Distributes SRA documents to clients and submits quality reports as required.
• Monitors SRA stocks in SAP and coordinates with clients on materials needed.

Education

Regulatory Standards and Good Manufacturing Practice

Tools

SAP

Job description

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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.

SRA Analyst

Location: Taguig, Philippines

Zuellig Pharmais a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.

The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.

Purpose of The Role: The SRA Analyst assists in the operational and admin requirements of the Secondary Repackaging Area through a systematic monitoring of activities to ensure a fast and quality output in compliance with the established procedures based on ISO 9001: Current version, Regional Quality Standards, and other legal requirements.

What You’ll Do:

Ensures strict implementation and compliance with processes in accordance with the established procedures, work instructions and guidelines.

Acts as production scheduler to achieve lead time of reprocessing products by doing as follows:

Checking/reviewing list of production orders and goods receipt requiring redressing

Initiating unplanned production orders

Scheduling of secondary repackaging activities based on materials availability and capacity utilization.

Acts as a back-up of Secondary Repackaging Supervisor in the following activities:

Computes for repackaging activity costing and prepares and sends assignment addendum (quotation) to Client.

Acts as a back-up of SRA Associate in the following activities:

Sending SRA documents such as RWI, RPRS and PMRS to Client.

Submit Quality Near Miss Report and Hazard Report.

Confirms SRA stocks on a SAP system basis.

Performs inventory control to ensure a timely execution of production activities by coordinating with Client regarding additional materials (if needed) and any production concerns.

Facilitates sending of Repackaging Batch Records, Item Discrepancy Reports and other pre-requisite documents on stocks release to commercial.

Reviews and timely monitoring of pending and rejected SRA stocks.

Monitors close production orders for the claims of Client and Third-Party Service Provider charges.

Prepares billing to Clients based on the approved rates per activity.

What Will Make You Successful:

Pursue personal growth and learning. Embrace learning and drive own development. The quality of being responsive; able to react quickly.

Must-Have:

• Secondary Repackaging Operations experience/ or manufacturing set-up
• With background on Regulatory Standards and Good Manufacturing Practice
• Knowledgeable in SAP.

Advantage to Have:

• Inventory Control and Management
• Knowledge on GSDP, GMP, GDPMDD, ISO standards
• Knowledge on SAP System
• Knowledge/ experience on Quality and compliance
• Product and Material Handling
• Warehouse Management: Secondary Repackaging Operations
• Proficient in data collection and reporting
• Oral and Written Communication

What We Offer:

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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Zuellig Pharma promotes an inclusive, fair workplace by ensuring equitable employment and compensation based on merit, regardless of background.