Senior Consultant

📋 Description

• You will assist clients in establishing objectives and strategies for manufacturing IT.

• You will contribute to the design, documentation, and maintenance of pharmaceutical manufacturing processes.

• You will convert customer requirements into software applications.

• You will organize and conduct best practice product workshops at client locations.

• You will choose and implement appropriate technology to enhance all manufacturing-related operations and optimize their strategic advantages.

• You will provide guidance to clients in the planning, monitoring, and execution of program rollouts.

• You will lead and coordinate the implementation of MES systems for clients.

• You will keep track of changes or advancements in technology to identify ways the company can achieve a competitive edge.

• You will oversee business development in alignment with company objectives and prepare reports for upper management.

• You will develop, monitor, and execute the client's deployment plan.

• You will manage the client's implementation approach and pinpoint areas for improvement.

• You will create and establish IT policies and systems to support the strategies defined by upper management.

• You will cultivate relationships with clients and identify potential new business opportunities.

• You will oversee IT initiatives and collaborate with internal technical staff.

• You will recognize the need for enhancements, changes, or new personnel and report these to upper management.

⛳️ Requirements

• You hold a degree in IT/Computer Science or a related field.

• You possess experience in integrating MES with other Level 4/3/2 systems (e.g., ERP, LIMS, SCADA, etc.), with a strong preference for Level 2 integration.

• You have experience with Automation/Level 2 integration (e.g., MES to Level 2 such as Delta-V, PLCs, etc.).

• You bring 10 years of experience in the life sciences industry working on large-scale applications.

• You have five (5) years of experience in the life sciences industry utilizing PAS-X.

• You are willing to travel at least 25% of the time.

• You possess an excellent understanding of GMP/GAMP principles.

• You have extensive knowledge of the life sciences sector.

• You have a solid understanding of the PAS-X application.

• You have demonstrated experience in gathering requirements and executing test specifications.

• You have significant experience in Computer System Validation (CSV) for manufacturing systems.

• You are capable of effectively communicating and presenting to various leadership levels.

• You exhibit excellent organizational skills.

• You possess superior analytical and problem-solving abilities.

• You have a solid understanding of data analysis, budgeting, and business operations.

• You have relevant project management experience; a certification (PMP/IPMA) is a plus.

🏝️ Benefits

• You will work in a modern environment that fosters an open culture for improvements and new ideas.

• You will be part of a globally operating company with a diverse customer base and a growing business.

• You will benefit from international collaboration within a group-expert network to implement company-wide concepts.

• You will be part of a team that focuses on customer requirements.

• You will receive an attractive compensation package that includes health, dental, vision insurance, and a retirement plan.