Panda International Vacatures in België

As a Quality Auditor at Panda International, you will ensure compliance with Good Clinical Practice (GCP) across global clinical activities. · Plan and execute risk-based GCP audits of investigator sites, CROs, vendors, laboratories, and internal systems. · Support regulatory ins ...

Role Summary: · In this pivotal role as QA Lab Supervisor at Panda International, you will be responsible for ensuring the highest standards of quality control and assurance across our laboratory operations. With a strong focus on compliance, innovation, and teamwork, your expert ...

Immunoassays Development Senior Scientist · We are supporting a diagnostics company in the search for an R&D Senior Scientist with strong hands-on expertise in immunoassay development, particularly on automated ELISA-based platforms, combined with a solid background in protein ch ...

Research And Development Scientist · We are seeking a skilled Research And Development Scientist to support our diagnostics company. · This role requires a scientist with hands-on expertise in immunoassay development. · The successful candidate will lead immunoassay development a ...

The Global Quality Auditor GCP is responsible for ensuring compliance with Good Clinical Practice (GCP) across global clinical activities. · 7+ years of experience in GCP auditing · Key responsibilities include: · Responsibilities · Planning and executing risk-based GCP audits of ...

Process Validation Engineer · This role involves ensuring timely revalidation of manufacturing and sterilization processes. · The ideal candidate will have experience introducing pharmaceutical products into manufacturing sites. · Additionally, they should be familiar with curren ...

Scientist Role Overview · We are recruiting a Scientist to join an advanced analytical development environment focused on molecular and materials characterization of pharmaceutical products. This role sits within a specialized analytical team supporting research, development, and ...

A specialised organisation active in nuclear medicine and radiopharmaceutical manufacturing is strengthening its Quality function to support ongoing production and scale-up activities. · The company operates in a highly regulated environment and plays a critical role in supplying ...

The QA CSV Engineer ensures regulatory compliance of computerized systems throughout their full lifecycle within a CAR-T manufacturing environment. · ...

The position plays a critical role at the intersection of procurement, quality compliance, and supply chain operations. · ...

Project Manager · About the Role · We seek an experienced project manager to lead automation and process equipment projects within a highly regulated CAR-T manufacturing environment. This role combines technical depth in GxP-compliant automation systems with strong project leader ...

C&Q SME (Commissioning & Qualification Subject Matter Expert) · Objectives and Responsibilities · The function holder: · Supports the C&Q group in providing documented evidence that all equipment and utilities used within the organization are qualified and remain in a state of co ...

Immunoassays Development Senior Scientist · We are supporting a diagnostics company in the search for an R&D Senior Scientist with strong hands-on expertise in immunoassay development, particularly on automated ELISA-based platforms, combined with a solid background in protein ch ...

This role supports the start-up and expansion of CAR-T manufacturing operations in Europe contributing to the delivery of innovative cell therapies for cancer treatment. · We support technology transfer equipment introduction system implementation activities contribute to process ...

You will operate within a GMP analytical and MSAT environment as a senior Subject Matter Expert leading analytical validation and qualification activities across MSAT PAD and QC laboratories. · ...

This role is essential for ensuring the quality and compliance of computerized systems within a brand-new biological drug substance manufacturing facility helping to shape a reliable and efficient validation environment · The CSV specialist will own and manage the end-to-end CSV ...

Location: On-site · Contract: Until 31 December 2026 · Function: Engineering · About the Role · We are seeking an experienced Project Manager - Engineering & Automation to lead automation and process equipment projects within a highly regulated CAR-T manufacturing environment. · ...

Location: · On-site · Contract: · Until 31 December 2026 · Function: · Engineering · About the Role · We are seeking an experienced · Project Manager - Engineering & Automation · to lead automation and process equipment projects within a highly regulated CAR-T manufacturing envir ...

We are hiring a Cleaning Validation Engineer to join the Manufacturing Science & Technology (MSAT) team with a dedicated focus on cleaning validation in a GMP-regulated API manufacturing environment. · ...

This role supports the start-up and expansion of CAR-T manufacturing operations in Europe contributing to the delivery of innovative cell therapies for cancer treatment. · ...