CQV Coordinator Pharmaceuticals F/M/X - Beerse

The candidate will own end-to-end cash & liquidity management for a portfolio of EMEA affiliates.They will act as trusted treasury business partner and drive value-adding projects that optimise capital structure risk exposure and cash processes. · ...

Own end-to-end cash & liquidity management for a portfolio of EMEA affiliates, act as trusted treasury business partner, and drive value-adding projects that optimise capital structure, risk exposure and cash processes. · ...

Job description · Mission description: · We are looking for a CQV manager to provide documented evidence that all equipment and utilities used in IM SC are qualified and remain in a state of control, ensuring processes and products meet regulatory and business specifications. · K ...

This is a challenging role in our Small Molecule Method Development team where you will be responsible for developing and validating analytical methods for drug characterization throughout their lifecycle.We look forward to meeting you · ...

We are seeking a detail-oriented Lifecycle Management Specialist Consultant with 4–6 years of experience in pharmaceutical manufacturing or operations to support Johnson & Johnson Innovative Medicine's Primary Container team within the MSAT (Manufacturing Sciences & Technology) o ...

Amaris Consulting is seeking a detail-oriented Lifecycle Management Specialist Consultant with 4–6 years of experience in pharmaceutical manufacturing or operations to support Johnson & Johnson Innovative Medicine's Primary Container team within the MSAT (Manufacturing Sciences & ...

We are seeking a detail-oriented Lifecycle Management Specialist Consultant with 4–6 years of experience in pharmaceutical manufacturing or operations to support Johnson & Johnson Innovative Medicine's Primary Container team within the MSAT (Manufacturing Sciences & Technology) o ...

Amaris is seeking a Senior Digital Transformation Lead to drive the end-to-end digital rollout of a new state-of-the-art manufacturing facility. · 7–10 years of experience in digital transformation, industrial IT, or automation projects. · Proven track record in leading complex d ...

+Job summary · Amaris Consulting seeks a Senior Digital Transformation Lead for a high-impact role in executing comprehensive digital strategies across various business lines. · + + Main Responsibilities + ...

Amaris is seeking a Senior Digital Transformation Lead to drive the end-to-end digital rollout of a new state-of-the-art manufacturing facility and its his high-impact role is central to executing a comprehensive Digital Strategy for a fully digitalized, connected factory from pr ...

Join Amaris and support one of our key pharmaceutical clients as a Validation Specialist focused on ensuring compliance and operational excellence in Quality Control (QC) and Manufacturing. · Proven experience in qualification of small-scale equipment (e.g., balances, pH meters, ...

Amaris is seeking a Senior Digital Transformation Lead to drive the end-to-end digital rollout of a new state-of-the-art manufacturing facility. · ...

Job Description · Mission Description: · Ensure full regulatory and procedural compliance for all qualification activities across the complete lifecycle of the manufacturing systems from concept through retirement. · Key Responsibilities · Document Review & Approval · Review and ...

Job Description · Mission · Supporting QA Engineering department in ensuring full regulatory and procedural compliance throughout the entire qualification lifecycle (concept → project → operational → retirement) for all manufacturing systems. · Key Responsibilities · Review and a ...

Join Amaris and support one of our key pharmaceutical clients as a Validation Specialist focused on ensuring compliance and operational excellence in Quality Control (QC) and Manufacturing. · This is a hands-on technical role offering direct impact on product quality and regulato ...

We are seeking a skilled and motivated Validation Engineer to join our team supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment. · Minimum 3 years of experience in a pharmaceutical or life sciences environment within a GMP-regulate ...

Join Amaris Consulting and support one of our key pharmaceutical clients as a Validation Specialist focused on ensuring compliance and operational excellence in Quality Control (QC) and Manufacturing. · This is a hands-on technical role offering direct impact on product quality a ...

We are seeking a skilled and motivated Validation Engineer to join our team, · supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment.Develop, implement, and execute User Requirement Specifications (URS), System Impact Assessment (SIA ...

Job Description · Mission Description: · Ensure full regulatory and procedural compliance for all qualification activities across the complete lifecycle of the manufacturing systems from concept through retirement. · Key Responsibilities · Document Review & Approval · Review and ...

Job Description · Mission · Supporting QA Engineering department in ensuring full regulatory and procedural compliance throughout the entire qualification lifecycle (concept → project → operational → retirement) for all manufacturing systems. · Key Responsibilities · Review and a ...