Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry!
Have a look below and apply or send me your CV directly.
Join the team and be part of an innovative company that values inclusion, growth, and impact. Our dynamic work environment offers brilliant opportunities for advancement. We're seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Key responsibilities:
- The Technical Lead supports the CAPEX Project Manager by taking the lead in technical coordination activities across cross-functional teams. The role involves ensuring that all technical deliverables are designed, written, reviewed, approved and executed in accordance with internal engineering standards and regulatory expectations. The candidate acts as the key technical contact point for all involved stakeholders and external partners, contributing to the successful and compliant execution of engineering and qualification projects in GMP-regulated environments.
- Where prescribed and required, wear protective equipment consistently and replace when defective.
- Eliminating hazards and risks immediately where possible, otherwise report them to supervisor immediately.
- Conduct and lead risk assessments, including FMEA and design reviews.
- Support Annex 1 related projects and contribute to ensuring compliance of manufacturing systems with GMP and internal standards.
- Drive the technical development of solutions to ensure process and equipment compliance.
- Author and review project related documents including URS, URB, and project descriptions.
- Review and align external supplier deliverables with internal engineering and quality standards.
- Serve as the technical point of contact between departments including Sterility Assurance (SA), Quality Assurance (QA), Production (PRO), Process Engineering (PE), and Project Delivery (PD).
- Lead and participate in project meetings, ensuring technical topics are clarified, documented, and followed up.
- Represent the technical function in cross - functional workshops and ensure alignment on technical decisions.
- Provide technical support during plant shutdown periods, including preparation, execution, and post - shutdown evaluations.
- Preferably on - site presence for coordination, with up to 40% flexibility for home office.
- Act as a technical liaison and support contact for operators.
- Support training sessions and information briefings for shopfloor personnel.
Requirements:
- Bachelor's or master's degree in engineering (Mechanical, Electrical, Process, Chemical, or equivalent).
- Fluent in English (written and spoken) & German language skills are necessary
- Minimum 5 years of experience in technical project execution within GMP-regulated environments (pharmaceutical, biotech, or life sciences).
- Solid understanding of cGMP, EU Annex 1, and engineering documentation.
- Proven experience in FMEA, technical troubleshooting, and interfacing with multiple departments.
- Strong communication and organizational skills, with the ability to proactively drive tasks and deliverables.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
Apply Now:
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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