Are you detail-oriented and enjoy working with the latest technology and state-of-the-art equipment in a versatile project team? If so, Aptio Group wants to meet you! 

This is an opportunity to work on high-impact projects in the pharmaceutical industry and contribute to world-class manufacturing facilities.

As a Process Specialist, you will be a cornerstone of the process engineering team, responsible for designing, installing, and supporting process equipment across Cell Culture (Upstream), Purification (Downstream), Clean Utility/CIP, and Solution Preparation systems. You will collaborate with multidisciplinary teams, vendors, and user groups to ensure projects are executed efficiently, safely, and in compliance with GMP standards.

Key Responsibilities:

• Design, specify, and install new process equipment, providing technical support and troubleshooting at a specialist level.
• Manage and coordinate activities with engineering providers, vendors, project teams, and user groups.
• Review URSs, technical documents, and validation materials; challenge technical changes and ensure optimal solutions are approved and implemented.
• Support design supervision, guidance, and technical reviews.
• Supervise installation activities and collaborate closely with the commissioning team.
• Scope and implement equipment modifications as required.
• Drive process and equipment changes, including risk assessments and technical troubleshooting for purification equipment.
• Review validation protocols, support commissioning and validation testing, and provide training to production teams.

About You:

• Bachelor’s degree in Engineering or a related discipline.
• 10–15 years of experience in GMP manufacturing, engineering, or pharmaceutical facilities.
• Strong team player but comfortable working independently.
• Experience with project management and risk management in complex projects.
• Self-driven, curious, and proactive with a “can-do” attitude.
• Hands-on experience with commercial GMP equipment.
• Fluent in spoken and written English.

Why Join Aptio Group

• Opportunity to work on high-impact projects within the pharma and biotech sectors.
• Collaborative, inclusive, and growth-oriented culture.
• Competitive compensation and benefits package.
• Ongoing professional development and career progression support.
• Flexible working arrangements and a commitment to work–life balance.

How to Apply

• Please submit your CV and a brief motivational text (no longer than 10 lines) via the link below. Try to also include something personal about what makes you, you.
• If you have any questions about the position, feel free to contact us
• We encourage all qualified candidates - regardless of gender, age, background, or orientation -to apply for the position. We look forward to hearing from you!