About this role
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As part of our IT Quality Services business unit at the headquarters in Frankenthal (Palatinate), you support our customers from pharmaceuticals, biotechnology, medical technology and chemistry in the introduction, optimization and validation of modern LIMS solutions. In varied projects, you will accompany the entire system lifecycle and ensure that digital laboratory processes are designed efficiently, compliant and future-proof. Tasks Advising our customers on the introduction, optimization and validation of LIMS solutions in regulated environments Coordinating and carrying out LIMS lifecycle activities taking into account regulatory
Requirements
(e.g. GAMP 5, EU GMP, GLP and FDA) Supporting system selection as well as
Requirements
engineering, risk management and test management Planning, coordinating and carrying out (re-)validation activities as part of Computer System Validation (CSV) Supporting the integration of laboratory equipment as well as checking audit trails and Data integrity Collaboration with customers, departments and system providers to successfully implement projects Active participation in the expansion and further development of our consulting area for LIMS and Lab Informatics Qualification Experience with LIMS systems, laboratory processes and computer-aided system validation (CSV) in regulated environments Knowledge of relevant regulatory
Requirements
, e.g. B. GAMP 5, GMP, GLP or FDA 21 CFR Part 11 Structured, analytical and solution-oriented way of working Strong communication skills as well as empathy and tact in dealing with different stakeholders Very good knowledge of German (at least C1) and good knowledge of English Willingness to undertake project-related trips as part of customer assignments Practical experience in a laboratory environment as well as knowledge of LIMS, ELN or LES systems is desirable
Benefits
Flexible working hours: You can choose your working hours Freely allocate flexitime within the framework. Hybrid working: We offer you a modern workplace and also give you the opportunity to work mobile. Getting started with an onboarding program: A personal mentor will accompany you as you get started and will help you arrive at EXCO quickly.
Family-friendly company: We support you and your family with, among other things, kindergarten subsidies and additional
Benefits
for children's sick days. Attractive remuneration models: In addition to an attractive annual salary, you benefit from additional vacation days, special leave for certain occasions and fair compensation for overtime. Individual further development: We invest in your professional and personal development with individually tailored training and further education.
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 - even for private use. Employee
Benefits
and company social
Benefits
: Benefit from company pension schemes, accident insurance, corporate
Benefits
, health offers and discounts from our cooperation partners. Why you should start at EXCO EXCO is an owner-managed 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 implement 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-proof industry. You can find further information about EXCO as an employer and your entry and development opportunities on our careers page. We look forward to getting to know you!
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