PAS-X Author

PAS-X Author/Client-X Author / Manufacturing Systems Specialist

We are looking for experienced professionals to support pharmaceutical manufacturing operations in highly regulated environments. The ideal candidate will bring hands-on experience with Werum Client-X, along with strong knowledge of pharmaceutical manufacturing processes and authoring activities. This role will support onsite work across manufacturing locations and requires candidates who can operate effectively in GxP-regulated environments.

Required Skills &

Qualifications:

• Hands-on experience with Werum Client-X
• Experience in Client-X authoring
• Strong understanding of life sciences / pharmaceutical manufacturing
• Experience working in regulated / GxP environments
• Strong knowledge of Drug Product (DP) processes
• Ability to work onsite in manufacturing environments
• Strong communication and stakeholder-facing skills
• Prior work experience at client or in client's Industry

Preferred Skills &

Qualifications:

• Experience with Drug Substance (DS) processes
• Experience supporting multiple pharmaceutical manufacturing sites
• Ability to travel as needed, up to 50%

Day-to-Day Responsibilities:

• Support Client-X-related manufacturing systems activities in a pharmaceutical production environment
• Participate in Client-X authoring and related system support duties
• Work closely with plant and site stakeholders to support manufacturing execution activities
• Contribute to batch process execution and manufacturing systems alignment
• Support regulated manufacturing operations in accordance with GxP requirements
• Collaborate with cross-functional teams across manufacturing and systems environments