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- Aufgaben: Join us as a CQV Engineer to ensure top-notch quality in production equipment.
- Arbeitgeber: Be part of our innovative Techfirm Industrial Services team in Switzerland.
- Mitarbeitervorteile: Enjoy a full-time role with opportunities for professional growth and development.
- Warum dieser Job: Tackle exciting challenges while making a real impact in the pharmaceutical/biotech industry.
- Gewünschte Qualifikationen: Bachelor's degree in Life Sciences or Engineering and 3 years of relevant experience required.
- Andere Informationen: Fluent English is essential; EU/EFTA nationals or valid work permit needed.
Das voraussichtliche Gehalt liegt zwischen 60000 - 84000 € pro Jahr.
For our Techfirm Industrial Services team, we would like to integrate a CQV Engineer ready to join us in Switzerland to take up new challenges together!
As a CQV Engineer, you will provide the necessary expertise and assistance to further improve and maintain the quality standards for their operations and products.
Responsibilities:
- You are in charge of the commissioning and qualification of production equipment .
- You will write protocols and perform acceptance tests at the supplier and at the customer site (FAT/SAT) .
- You will be responsible for the Installation, Operational and Performance Qualification (IQ, OQ, PQ ) and write the reports.
- In collaboration with the Validation Department , you will work on various process validation projects (e.g. cleaning, sterility, freeze-drying ).
- You will draft Validation Plans (VMP) up to Validation reports .
Minimum Requirements:
- Minimum Bachelor’s degree in Life Sciences or Engineering.
- Minimum of 3 years of work experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry.
- Experience with DeltaV (Emerson), COMOS/KNEAT platforms would be a real plus.
- Fluent English language written and verbal communication skills; any further language is a plus.
- cGMP knowledge and knowledge of regulatory requirements.
If you are interested in joining us, please send your CV to .
Please note, that we can only consider Swiss or EU/EFTA nationals or applicants with a valid residence or work permit for Switzerland.
Seniority Level:
Mid-Senior level
Employment Type:
Full-time
Job Function:
Quality Assurance
Industries:
Human Resources
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COMMISSIONNING, QUALIFICATION & VALIDATION ENGINEER (M/W/D) - Arbeitgeber: TechFirm Group
Kontaktperson:
TechFirm Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: COMMISSIONNING, QUALIFICATION & VALIDATION ENGINEER (M/W/D) -
✨Tip Number 1
Make sure to highlight your experience with commissioning and qualification activities in the pharmaceutical or biotech industry during any networking opportunities. This will help you stand out as a candidate who understands the specific challenges and requirements of the role.
✨Tip Number 2
Familiarize yourself with DeltaV and COMOS/KNEAT platforms, as having knowledge of these systems can significantly boost your profile. Consider online courses or tutorials to get a basic understanding if you're not already experienced.
✨Tip Number 3
Engage with professionals in the CQV field through LinkedIn or industry-specific forums. Building connections can provide insights into the company culture and may even lead to referrals, which can be a great advantage in the hiring process.
✨Tip Number 4
Stay updated on cGMP regulations and other relevant compliance standards. Being knowledgeable about current regulatory requirements will demonstrate your commitment to quality assurance and make you a more attractive candidate.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: COMMISSIONNING, QUALIFICATION & VALIDATION ENGINEER (M/W/D) -
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the CQV Engineer position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in commissioning, qualification, and validation activities, particularly in the pharmaceutical or biotech industry. Use specific examples to demonstrate your expertise.
Showcase Technical Skills: Mention any relevant technical skills, such as familiarity with DeltaV or COMOS/KNEAT platforms. Highlight your knowledge of cGMP and regulatory requirements, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are interested in the position and how your background aligns with the company's needs. Be sure to express your enthusiasm for joining the Techfirm Industrial Services team.
Wie du dich auf ein Vorstellungsgespräch bei TechFirm Group vorbereitest
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with commissioning, qualification, and validation processes in detail. Highlight specific projects where you successfully implemented IQ, OQ, and PQ protocols, and be ready to explain the challenges you faced and how you overcame them.
✨Familiarize Yourself with Relevant Tools
If you have experience with DeltaV or COMOS/KNEAT platforms, make sure to mention it during the interview. If not, take some time to research these tools and understand their applications in the pharmaceutical industry, as this knowledge could set you apart from other candidates.
✨Demonstrate Your Understanding of cGMP
Since knowledge of current Good Manufacturing Practices (cGMP) is crucial for this role, be ready to discuss how you have applied these standards in your previous work. Provide examples of how you ensured compliance and maintained quality throughout the validation process.
✨Prepare for Behavioral Questions
Expect questions that assess your problem-solving skills and ability to work collaboratively. Use the STAR method (Situation, Task, Action, Result) to structure your responses, focusing on how you contributed to team success in past projects.
