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- Aufgaben: Ensure compliance with pharma standards and lead CSV activities for IT systems.
- Arbeitgeber: Join a leading biopharmaceutical company known for innovation and growth.
- Mitarbeitervorteile: Collaborative work environment with opportunities for professional growth.
- Warum dieser Job: Work on impactful projects that directly support patient outcomes in a dynamic team.
- Gewünschte Qualifikationen: Bachelor’s degree and 7-10 years in pharma/biotech; fluent in English and French.
- Andere Informationen: Swiss residency or valid work permit required; cross-border candidates welcome.
Das voraussichtliche Gehalt liegt zwischen 72000 - 100000 € pro Jahr.
4-6 months contractor – FRENCH Speaking necessary
Our customer is an innovative biopharmaceutical Big Pharma company. For an on site assignment for the brand new commercial manufacturing site we are looking for 2 experts in CSV for Pharma Industry.
As part of their continuous growth, our client is implementing new IT systems at their local manufacturing and packaging units. To support these initiatives, we are seeking an experienced CSV and IT Compliance Engineer/Manager.
You have:
- Bachelor’s degree in Science, Engineering, or a related discipline.
- 7-10 years of experience in the pharmaceutical or biotechnology industry, including expertise in Quality Management Systems and GxP systems such as MES and SAP.
- Proficiency in Computer System Validation (CSV), Data Integrity requirements, and regulatory frameworks (21-CFR Part 11, EudraLex, MHRA).
- Experience with Six Sigma, Lean, or Business Process Change techniques is a plus.
- Strong analytical and structured working style with exceptional attention to detail.
- Excellent communication and collaboration skills to work in multidisciplinary, international teams.
- Fully operational in both English and French.
- Swiss residency or a valid Swiss work permit is mandatory (cross-border candidates welcome)
Your tasks:
- Ensure compliance with pharmaceutical industry standards and regulations, including EU-GMP Annex 11 and 21-CFR part 11.
- Lead Computer System Validation (CSV) activities for site IT systems and infrastructure.
- Act as the local representative for global IT projects with quality implications, such as Digital Modernization initiatives.
- Oversee the qualification of site IT infrastructure in collaboration with global teams.
- Define quality expectations and support the IT department and third parties in implementing GMP-compliant systems.
- Conduct risk-based prioritization of IT activities in support of Quality Assurance.
- Translate compliance requirements into test conditions and acceptance criteria for application functionality (IQ, PQ, FAT).
- Ensure adherence to design and governance standards while contributing to effective communication with stakeholders.
You will:
- Be part of an innovative, dynamic team at a globally recognized biopharmaceutical leader.
- Work on impactful projects that directly support patient outcomes.
- Enjoy a collaborative work environment with opportunities for professional growth.
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CSV and IT Compliance Engineer/Manager Arbeitgeber: gloor & lang Pharma and Biotech Recruiting
Kontaktperson:
gloor & lang Pharma and Biotech Recruiting HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: CSV and IT Compliance Engineer/Manager
✨Tip Number 1
Make sure to highlight your experience with Computer System Validation (CSV) and regulatory frameworks in your conversations. This is crucial for the role, and demonstrating your expertise can set you apart from other candidates.
✨Tip Number 2
Since this position requires strong communication skills in both English and French, practice discussing your previous projects and experiences in both languages. Being able to switch seamlessly between the two will show your fluency and adaptability.
✨Tip Number 3
Familiarize yourself with the specific IT systems mentioned in the job description, such as MES and SAP. Having a solid understanding of these systems will allow you to speak confidently about how you can contribute to their implementation and compliance.
✨Tip Number 4
Network with professionals in the biopharmaceutical industry, especially those who have experience with quality management systems. Engaging with others in the field can provide valuable insights and potentially lead to referrals for the position.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: CSV and IT Compliance Engineer/Manager
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and qualifications required for the CSV and IT Compliance Engineer/Manager position. Tailor your application to highlight relevant experiences.
Highlight Relevant Experience: Emphasize your 7-10 years of experience in the pharmaceutical or biotechnology industry, particularly focusing on your expertise in Computer System Validation (CSV) and Quality Management Systems. Use specific examples to demonstrate your skills.
Showcase Language Proficiency: Since proficiency in both English and French is mandatory, make sure to clearly indicate your language skills in your CV and cover letter. If applicable, provide examples of how you've used these languages in a professional context.
Tailor Your Documents: Customize your CV and cover letter to reflect the specific requirements mentioned in the job description, such as knowledge of regulatory frameworks and experience with IT systems like MES and SAP. This will show that you are a strong fit for the role.
Wie du dich auf ein Vorstellungsgespräch bei gloor & lang Pharma and Biotech Recruiting vorbereitest
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with Computer System Validation (CSV) and regulatory frameworks like 21-CFR Part 11. Highlight specific projects where you ensured compliance and how you navigated challenges in the pharmaceutical industry.
✨Demonstrate Your Analytical Skills
Since the role requires a strong analytical and structured working style, be ready to provide examples of how you've approached problem-solving in past roles. Discuss any methodologies like Six Sigma or Lean that you've applied to improve processes.
✨Communicate Effectively in Both Languages
As the position requires proficiency in both English and French, practice discussing your qualifications and experiences in both languages. This will not only demonstrate your language skills but also your ability to communicate in a multicultural environment.
✨Prepare for Scenario-Based Questions
Expect questions that assess your ability to handle real-world situations related to IT compliance and quality management. Think of scenarios where you had to prioritize IT activities or translate compliance requirements into actionable steps.
