CQV Engineer / Qualification & Validation Engineer (f/m/d) Jetzt bewerben
CQV Engineer / Qualification & Validation Engineer (f/m/d)

CQV Engineer / Qualification & Validation Engineer (f/m/d)

Visp Vollzeit 48000 - 72000 € / Jahr (geschätzt) No home office possible
Jetzt bewerben
Lonza

Auf einen Blick

  • Aufgaben: Join us as a CQV Engineer to ensure top-notch operations and quality standards.
  • Arbeitgeber: Lonza is a global leader in life sciences, dedicated to improving the world through innovation.
  • Mitarbeitervorteile: Own your career with opportunities for growth and collaboration in a dynamic environment.
  • Warum dieser Job: Make a real impact by qualifying new equipment and driving continuous improvement.
  • Gewünschte Qualifikationen: Technical degree or university degree required; experience in GMP environments is a must.
  • Andere Informationen: Fluency in German and/or English is essential; be ready to tackle challenges creatively.

Das voraussichtliche Gehalt liegt zwischen 48000 - 72000 € pro Jahr.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Join our team at Lonza in Visp, Switzerland as a CQV Engineer / Qualification & Validation Engineer (f/m/d). Work alongside an outstanding team dedicated to maintaining flawless operations and premier standards. This role provides an exciting chance to contribute to our dynamic environment, directly improving the quality and efficiency of our processes. Take part in qualifying and validating brand-new process engineering equipment and facilities, promoting continuous improvement and innovation.

Key responsibilities:

  1. Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems and ongoing SLC support post-implementation.
  2. Supervise and resolve deviations, manage changes (GEP and GMP), and implement CAPAs effectively.
  3. Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution.
  4. Present qualification documents during audits and inspections, showcasing the outstanding standards maintained.

Key requirements:

  1. Graduate from a technical school (HF) / university of applied sciences (FH) or hold a university degree.
  2. Proven experience in a regulated GMP environment, specifically in commissioning, qualification, and validation of systems like refrigerators, freezers, clean media, and process engineering equipment.
  3. Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP is advantageous.
  4. Proficient in both written and spoken German and/or English.
  5. Demonstrate independent, flexible work habits, with excellent communication skills and a structured, focused approach to tasks.
  6. Open to new ideas, agile in thinking, and proactive in problem-solving.

Join us at Lonza AG, where your ideas and skills will help us compete at the highest levels and achieve our ambitious goals. Together, we will successfully implement solutions that make a meaningful difference in the world.

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CQV Engineer / Qualification & Validation Engineer (f/m/d) Arbeitgeber: Lonza

At Lonza in Visp, Switzerland, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through opportunities for professional development and the chance to contribute to groundbreaking projects in life sciences. Join us to be part of a team where your contributions are valued, and together we can make a meaningful impact on the world.
Lonza

Kontaktperson:

Lonza HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: CQV Engineer / Qualification & Validation Engineer (f/m/d)

✨Tip Number 1

Familiarize yourself with the specific regulations and standards in a GMP environment. Understanding these guidelines will not only help you during interviews but also demonstrate your commitment to quality and compliance.

✨Tip Number 2

Network with professionals in the life sciences field, especially those who have experience in commissioning and validation. Engaging with industry experts can provide valuable insights and potentially lead to referrals.

✨Tip Number 3

Stay updated on the latest technologies and tools used in qualification and validation processes. Being knowledgeable about software like COMOS, DMS, or TrackWise can set you apart from other candidates.

✨Tip Number 4

Prepare to discuss specific examples of how you've handled deviations or managed changes in previous roles. Highlighting your problem-solving skills and ability to work under pressure will resonate well with the hiring team.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: CQV Engineer / Qualification & Validation Engineer (f/m/d)

Commissioning and Qualification Expertise
Validation of Systems
GMP Knowledge
Deviation Management
CAPA Implementation
Project Coordination
Technical Documentation Skills
MS Office Proficiency
Familiarity with COMOS, DMS, Kneat, TrackWise, and SAP
Fluent in German and/or English
Independent Work Habits
Excellent Communication Skills
Structured and Focused Approach
Agile Thinking
Proactive Problem-Solving

Tipps für deine Bewerbung 🫡

Understand the Role: Make sure to thoroughly read the job description for the CQV Engineer position at Lonza. Understand the key responsibilities and requirements, and think about how your experience aligns with them.

Tailor Your CV: Customize your CV to highlight relevant experience in commissioning, qualification, and validation within a GMP environment. Emphasize your technical skills and any familiarity with tools like COMOS, DMS, or SAP.

Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the life sciences industry. Mention specific examples of how you've contributed to quality and efficiency in previous positions.

Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, and that your documents are formatted professionally.

Wie du dich auf ein Vorstellungsgespräch bei Lonza vorbereitest

✨Understand the Role

Make sure you have a clear understanding of the CQV Engineer role and its responsibilities. Familiarize yourself with key terms like commissioning, qualification, and validation, as well as the specific systems mentioned in the job description.

✨Showcase Your Experience

Prepare to discuss your previous experience in a regulated GMP environment. Highlight specific projects where you developed commissioning and qualification documents, and be ready to explain how you managed deviations and implemented CAPAs.

✨Demonstrate Communication Skills

Since the role requires coordination between internal teams and external providers, practice articulating your thoughts clearly. Be prepared to give examples of how you've effectively communicated in past roles, especially in challenging situations.

✨Be Proactive and Solution-Oriented

During the interview, showcase your problem-solving skills by discussing how you've approached challenges in the past. Emphasize your ability to think agilely and propose innovative solutions, aligning with Lonza's focus on continuous improvement.

CQV Engineer / Qualification & Validation Engineer (f/m/d)
Lonza Jetzt bewerben
Lonza
  • CQV Engineer / Qualification & Validation Engineer (f/m/d)

    Visp
    Vollzeit
    48000 - 72000 € / Jahr (geschätzt)
    Jetzt bewerben

    Bewerbungsfrist: 2027-01-14

  • Lonza

    Lonza

    5000 - 10000
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