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- Aufgaben: Join a dynamic team as a Validation Engineer, focusing on CSV in the pharma industry.
- Arbeitgeber: Work with a leading pharmaceutical company in Switzerland, known for innovation and quality.
- Mitarbeitervorteile: Enjoy a 12-month contract with opportunities for growth and hands-on experience.
- Warum dieser Job: Be part of an ambitious team and make a real impact in GxP regulated environments.
- Gewünschte Qualifikationen: Must have CSV expertise, knowledge of ISPE GAMP5, and experience in pharma or engineering.
- Andere Informationen: Ideal for those passionate about data integrity and regulatory compliance.
Das voraussichtliche Gehalt liegt zwischen 72000 - 84000 € pro Jahr.
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Direct message the job poster from Hamlyn Williams
Validation and Quality Assurance Consultant – Hamlyn Williams
Are you a CSV expert? Do you have experience in the pharmaceutical industry? Are you looking for a new role?
My client is a large pharmaceutical company in Switzerland and is looking for talented CSV Engineers with strong experience with ISPE GAMP5 and ASTM guidelines to join an ambitious team on a 12-month contract.
Some of the skills the CSV Engineers are required to possess experience with are:
- Experience in the pharma industries and/or engineering companies with proven experience in frontline (hands-on) tasks.
- Knowledge of ISPE GAMP5 and ASTM guidelines, awareness and/or desire to understand all applicable regulatory requirements prior to commencing GxP.
- Experience in automation and vertical integration process and ability to understand data flow.
- Familiar with Data Integrity Principles, ALCOA+ concepts and ensuring compliance in GxP regulated environments.
This is a fantastic opportunity to join a large pharmaceutical organisation in Switzerland– let me know if you are interested!
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Pharmaceutical Manufacturing and Biotechnology Research
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Validation Engineer Arbeitgeber: Hamlyn Williams
Kontaktperson:
Hamlyn Williams HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Validation Engineer
✨Tip Number 1
Make sure to highlight your hands-on experience in the pharmaceutical industry during any networking opportunities. Connect with professionals in the field on platforms like LinkedIn and engage in discussions about ISPE GAMP5 and ASTM guidelines.
✨Tip Number 2
Familiarize yourself with the latest trends and updates in data integrity principles and GxP regulations. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance in regulated environments.
✨Tip Number 3
Consider joining relevant online forums or groups focused on CSV and validation engineering. Engaging with peers can provide insights into the industry and may lead to job referrals or recommendations.
✨Tip Number 4
If you have experience with automation and vertical integration processes, be prepared to discuss specific projects or challenges you've faced. This will showcase your practical skills and problem-solving abilities to potential employers.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Validation Engineer
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Validation Engineer position. Familiarize yourself with the specific skills and experiences required, such as knowledge of ISPE GAMP5 and ASTM guidelines.
Tailor Your CV: Customize your CV to highlight your relevant experience in the pharmaceutical industry and any hands-on tasks you've completed. Emphasize your familiarity with Data Integrity Principles and GxP compliance.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the pharmaceutical industry. Mention your experience with automation and data flow, and how it aligns with the company's needs.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any grammatical errors or typos, and ensure that all information is accurate and clearly presented.
Wie du dich auf ein Vorstellungsgespräch bei Hamlyn Williams vorbereitest
✨Show Your CSV Expertise
Be prepared to discuss your experience with Computer System Validation (CSV) in detail. Highlight specific projects where you applied ISPE GAMP5 and ASTM guidelines, as this will demonstrate your hands-on knowledge and expertise in the field.
✨Understand Regulatory Requirements
Familiarize yourself with the regulatory requirements relevant to GxP before the interview. Showing that you have a proactive approach to understanding compliance will impress the interviewers and show your commitment to quality assurance.
✨Discuss Data Integrity Principles
Be ready to explain your understanding of Data Integrity Principles and ALCOA+ concepts. Provide examples of how you've ensured compliance in previous roles, as this is crucial for working in GxP regulated environments.
✨Demonstrate Automation Knowledge
Talk about your experience with automation and vertical integration processes. Discuss how you understand data flow and how it impacts validation processes, as this will showcase your technical skills and ability to contribute to the team.
