Breda
Full-time
2-5 years experience
On-site

Key Skills

Pharmaceutical operations
Supply chain management
Product lifecycle management
Regulatory affairs
Change management
Data analysis
Stakeholder management
Cross-functional collaboration
Project coordination
Master data management
Serialization
Process improvement
Documentation
Logistics
Communication

Job Description

About the Company Our client is a global biotechnology company with a strong presence in the Netherlands and a major operations site in Breda. The site plays an important role in the supply chain of medicines, supporting the labelling, assembly, storage and distribution of products to markets worldwide.You will join an international environment where Supply Chain, Regulatory, Manufacturing, Commercial and Operations teams work closely together to ensure medicines are delivered to patients safely and efficiently. About the Role We are looking for a Regional Operations Associate to support the management of pharmaceutical products throughout their lifecycle across the EMEA region.You will work at the intersection of Supply Chain, Regulatory Affairs, Manufacturing, Commercial and Operations, helping to coordinate product launches, lifecycle changes, variations and end-of-life activities.This is a role for someone who enjoys working with multiple stakeholders, managing processes and data, and making sure regional requirements are translated correctly into operational execution.As you gain experience, you will take increasing ownership of product lifecycle activities independently. Responsibilities Support the management of products throughout their full lifecycle, from launch through changes and end-of-life. Coordinate and maintain the regional variation plan, working with Regulatory and other key stakeholders. Support new product launches and ensure regional requirements are ready for implementation. Assess labelling requirements and maintain the relevant documentation and systems. Coordinate specialised shipping activities for assigned products. Ensure accurate and complete handovers to manufacturing sites. Coordinate product and SKU discontinuations. Facilitate activities between Supply Chain, Regulatory Affairs, Operations and Commercial/Marketing teams. Support master data and serialization activities. Coordinate registration samples and product demonstration requests. Lead smaller improvement initiatives and identify opportunities to simplify or standardise processes. Collect and analyse data to support customer and business requests. Qualifications Bachelor’s or Master’s degree in Supply Chain, Business, Life Sciences, Pharmacy or a related field. Required Skills 1-3 years of relevant experience in pharmaceutical operations, supply chain or a closely related environment. Strong written and spoken English. Experience working in an international, cross-functional environment. Understanding of pharmaceutical supply chain processes is highly relevant. Experience with product lifecycle management, change management or multidisciplinary projects is an advantage. Strong analytical and data-oriented approach. Comfortable working with multiple stakeholders and coordinating activities across different functions. Action-oriented, organised and customer-focused. Tech-savvy, with the ability to work confidently with systems, data and digital tools. APICS, CPIM, CIRM or similar supply chain certification is a plus.

Core Responsibilities

The Operations Associate will manage pharmaceutical products throughout their lifecycle, coordinating activities between supply chain, regulatory, and commercial teams. They will also support product launches, maintain regional variation plans, and lead process improvement initiatives.

Requirements

Candidates must hold a Bachelor’s or Master’s degree in a relevant field such as Supply Chain, Business, or Life Sciences. A minimum of 1-3 years of experience in pharmaceutical operations or supply chain is required, along with strong analytical skills and English proficiency.

About SIRE® Life Sciences 🧬

Industry: Biotechnology Research

Company size: 201-500 employees

SIREĀ® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIREĀ® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com

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