Senior PAS-X Solution Consultant

Description

You will be the PAS-X subject matter expert (SME) for a global MES template rollout across several pharmaceutical manufacturing sites.

You will shape PAS-X solution design, integration, process standardisation, testing and deployment in a GxP-regulated environment.

You need deep Werum PAS-X skills, pharmaceutical manufacturing knowledge, SAP integration experience and electronic batch record (EBR) know-how.

The company is a Business and IT consultancy focused on life sciences, working with pharma, healthcare and animal health firms. It has over 450 employees across 25 offices worldwide and works mainly on S4HANA, data and cloud.

Responsibilities

• Act as the go-to PAS-X SME across global manufacturing programmes.
• Help design, build and roll out a global PAS-X template solution.
• Work with business stakeholders, manufacturing teams and technical partners to standardise and improve processes.
• Support process design in ARIS and testing in HP ALM.
• Take part in end-to-end testing, validation, deployment and hypercare.
• Keep all work aligned with global manufacturing standards and governance.

Requirements

• Hands-on PAS-X experience in weighing and dispensing, material flow, label management, master data (including SAP-integrated master data), custom attributes and characteristics, production unit maintenance, exception management, rights and roles, and electronic signatures and workflows.
• Working knowledge of master batch record (MBR) and formula design, generic MBR (gMBR) and PVL concepts, in-process control (IPC), EBR, equipment management, state diagrams, machine integration and batch record review (BRR).
• Strong experience integrating PAS-X with SAP WM and/or SAP EWM.
• Experience with PAS-X MSI and PAS-X APIs.
• Ability to create and manage orders, materials and master data for end-to-end testing.
• Experience with PAS-X reporting and data extraction, and with PAS-X PDA (Product Data Access).
• Experience exporting data to enterprise reporting platforms and data lakes, and familiarity with Power BI.
• Background in pharmaceutical, biotechnology or life sciences, with a solid grasp of ISA-95, GxP and computer system validation (CSV).
• Preferred: experience supporting global template deployments and multi-site rollouts.
• Preferred: strong communication and stakeholder management skills.
• Preferred: ability to work effectively with global cross-functional teams.
• Preferred: experience in large-scale digital manufacturing transformation programmes.
• Preferred: exposure to manufacturing operations across multiple international sites.
• Highly desirable: experience with Crystal Reports and/or Jaspersoft.

Conditions

Remote work is possible, up to 25 days per year from any global location.

Selection starts with a profile review by the talent acquisition team, which takes about 2 weeks.

A 15 to 30 minute introductory call, by Teams or phone, covers the company, the role and your expectations.

A 30-minute technical interview with one of the company's experts follows.

For some roles, a 30 to 60 minute online client interview may be added.

The company aims to give timely feedback and move quickly to the next step.

The company is an equal opportunity employer and is committed to an inclusive workplace.

Benefits

• Flexible time off beyond the standard holiday allowance.
• Up to 25 days per year of remote work from any global location.
• A team integration budget for meeting and bonding with colleagues.
• A special gift from the company on your birthday.
• CHF 1,500 per year for professional development.
• Regular workshops and training to build technical and soft skills.
• A competitive salary and benefits package that reflects your impact.
• A referral reward for recommending new hires.
• Loyalty-based benefits from your third year through the Unity Scheme.
• Financial help when relocating for work.
• Help with visas, permits and international assignments.
• Perks tailored to your country of residence.