LIMS Consultant & Validation Expert (m/w/d)

As part of our Business Unit IT Quality Services at our headquarters in Frankenthal (Pfalz), you will support our customers from the pharmaceutical, biotechnology, medical technology, and chemical industries in introducing, optimizing, and validating modern LIMS solutions.

In varied projects, you will accompany the entire system lifecycle and ensure that digital laboratory processes are designed to be efficient, compliant, and future-proof.

Aufgaben

• Consultation of our customers on the introduction, optimization, and validation of LIMS solutions in regulated environments
• Coordination and implementation of LIMS lifecycle activities taking into account regulatory requirements (e.g. GAMP 5, EU GMP, GLP, and FDA)
• Support in system selection as well as requirements engineering, risk management, and test management
• Planning, coordination, and implementation of (re-)validation activities within the scope of Computer System Validation (CSV)
• Support in integrating laboratory equipment and testing audit trails and data integrity
• Collaboration with customers, departments, and system providers to successfully implement projects
• Active participation in expanding and further developing our consulting department for LIMS and Lab Informatics

Qualifikation

• Experience with LIMS systems, laboratory processes, and computer-supported system validation (CSV) in regulated environments
• Knowledge of relevant regulatory requirements, e.g. GAMP 5, GMP, GLP, or FDA 21 CFR Part 11
• Structured, analytical, and solution-oriented working style
• Excellent communication skills as well as empathy and intuition in dealing with different stakeholders
• Very good German language skills (at least C1) and good English language skills
• Willingness to project-related travel within the scope of customer assignments
• Prior experience in a laboratory environment and knowledge of LIMS, ELN, or LES systems are desirable

Benefits

Flexible Working Hours: You can schedule your working hours freely within the scope of flexible working hours.

Hybrid Work: We offer you a modern equipped workplace and give you the opportunity to work mobile as well.

Onboarding Program: A personal mentor will accompany you during your onboarding process and support you in getting started quickly at EXCO.

Family-Friendly Company: We support you and your family, for example, with kindergarten allowance and additional benefits for child sick leave.

Attractive Remuneration Models: In addition to an attractive annual salary, you will benefit from additional vacation days, special leave at certain occasions, and a fair compensation for overtime work.

Individual Professional Development: We invest in your professional and personal development with individually tailored training and further education opportunities.

Company Events: Look forward to regular events and joint activities with your colleagues.

Bike Leasing Offers: Take advantage of attractive leasing offers for bicycles and e-bikes – also for private use.

Employee Benefits and Corporate Social Benefits: Benefit from corporate pension, accident insurance, corporate benefits, health offers, and discounts at our cooperation partners.

Why you should start with EXCO

EXCO is a family-owned technical service provider for development and quality assurance with a 30-year history of success and growth. With over 150 employees at 8 locations, we realize innovative projects for our global customers from the medical technology, pharmaceutical, biotechnology, and chemical industries. We offer our employees long-term career prospects and the opportunity to grow together with us in a crisis-resistant industry.

You can find more information about EXCO as an employer and your entry and development opportunities on our career website.

We look forward to getting to know you!

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