Auf einen Blick
- 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 making a real impact in the pharmaceutical sector.
- Gewünschte Qualifikationen: Must have CSV expertise, knowledge of ISPE GAMP5, and experience in regulated environments.
- Andere Informationen: Ideal for those passionate about compliance and data integrity in pharma.
Das voraussichtliche Gehalt liegt zwischen 72000 - 100000 € pro Jahr.
Get AI-powered advice on this job and more exclusive features. 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 #J-18808-Ljbffr
Validation Engineer Arbeitgeber: Whatjobs

Kontaktperson:
Whatjobs 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 reaching out directly to the job poster or hiring manager at Hamlyn Williams. A direct message expressing your interest and relevant experience can set you apart from other candidates.
✨Tip Number 4
Join online forums or groups focused on CSV and validation engineering in the pharmaceutical sector. Engaging with these communities can provide valuable insights and potentially lead to job referrals.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Validation Engineer
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly understand the responsibilities and requirements of a Validation Engineer in the pharmaceutical industry. Familiarize yourself with ISPE GAMP5 and ASTM guidelines, as well as Data Integrity Principles.
Tailor Your CV: Customize your CV to highlight your experience in CSV and the pharmaceutical sector. Emphasize any hands-on tasks you've completed and your familiarity with regulatory requirements and compliance in GxP environments.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the industry. Mention specific experiences that align with the job description, particularly your knowledge of automation and data flow.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors or typos, and that all information is clear and concise. A polished application reflects your attention to detail.
Wie du dich auf ein Vorstellungsgespräch bei Whatjobs vorbereitest
✨Showcase Your CSV Expertise
Be prepared to discuss your hands-on experience with Computer System Validation (CSV) in detail. Highlight specific projects where you applied ISPE GAMP5 and ASTM guidelines, as this will demonstrate your expertise and relevance to the role.
✨Understand Regulatory Requirements
Familiarize yourself with the regulatory requirements applicable to GxP environments. During the interview, express your awareness of these regulations and how you ensure compliance in your previous roles.
✨Discuss Data Integrity Principles
Make sure to articulate your understanding of Data Integrity Principles, particularly ALCOA+. Provide examples of how you've implemented these principles in past projects to ensure compliance and data quality.
✨Demonstrate Automation Knowledge
Since automation is a key aspect of the role, be ready to discuss your experience with automation processes and vertical integration. Explain how you have managed data flow in automated systems to enhance efficiency and compliance.