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- Aufgaben: Lead CQV activities for a High Bay GMP Warehouse, ensuring compliance and coordination.
- Arbeitgeber: Join a dynamic team in Stein, Switzerland, focused on innovative warehouse solutions.
- Mitarbeitervorteile: Enjoy a 12-month contract with opportunities for growth and collaboration.
- Warum dieser Job: Be a key player in a cutting-edge environment, impacting healthcare logistics.
- Gewünschte Qualifikationen: Experience in CQV within GMP settings and expertise in cold/ambient systems required.
- Andere Informationen: Collaborate with diverse teams and lead exciting commissioning projects.
Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.
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CQV Lead Engineer – GMP Warehouse (m/w/d), Basel-Stadt
Client:
Location:
Job Category:
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Job Reference:
38b8fa70ed0b
Job Views:
4
Posted:
03.03.2025
Expiry Date:
17.04.2025
Job Description:
We are seeking a skilled and experienced CQV Lead Engineer to support the commissioning, qualification, and validation (CQV) activities for a High Bay GMP Warehouse. The role will involve both cold and ambient temperature environments and will include responsibility for driving and coordinating all CQ activities. The position is based at a client site in Stein, Switzerland, with an initial contract duration of 12 months.
Key Responsibilities:
- Ensure CQV activities are carried out in compliance with internal guidelines, C&Q Plans, and supporting Validation Plans.
- Serve as the CQV Subject Matter Expert (SME) for the High Bay warehouse scope, including both cold and ambient temperature systems (high preference).
- Support CQV execution for key equipment, including semi-automated and fully automated visual inspection machines, as well as other small support equipment (e.g., LAF, thawing units, fridges, freezers, cold/freezer rooms) while aligning with the execution approach for equivalent systems in the QC building.
- Lead and execute commissioning activities for allocated areas or systems.
- Coordinate execution activities with the supporting CSV team and global IT teams.
- Lead C&Q testing activities, supported by vendors and contractors.
- Develop any supporting validation plans related to the scope of execution.
- Support the updates of the Master C&Q Plan and other supporting plans throughout the project lifecycle.
- Collaborate with various disciplines, including HSE, Automation, Electrical, Instrumentation, Operations, and Engineering.
Qualifications:
- Proven experience in CQV activities, particularly within GMP environments.
- Expertise in cold and ambient temperature systems.
- Strong background in commissioning and qualification of complex equipment and systems.
- Ability to work with cross-functional teams, including IT and CSV groups.
- Excellent communication and leadership skills.
If you are interested in this challenging and rewarding opportunity, we would be pleased to receive your application.
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CQV Lead Engineer - GMP Warehouse (m/w/d) Arbeitgeber: TN Switzerland
Kontaktperson:
TN Switzerland HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: CQV Lead Engineer - GMP Warehouse (m/w/d)
✨Tip Number 1
Make sure to highlight your experience with CQV activities in GMP environments during the interview. Be prepared to discuss specific projects where you successfully led commissioning and qualification efforts.
✨Tip Number 2
Familiarize yourself with the specific cold and ambient temperature systems mentioned in the job description. Showing that you understand these systems will demonstrate your expertise and readiness for the role.
✨Tip Number 3
Network with professionals in the CQV field, especially those who have experience in GMP warehouses. This can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 4
Prepare to discuss your leadership and communication skills, as these are crucial for coordinating with cross-functional teams. Think of examples where you successfully led a team or project.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: CQV Lead Engineer - GMP Warehouse (m/w/d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the CQV Lead Engineer position. Understand the key responsibilities and qualifications required, especially the focus on GMP environments and cold/ambient temperature systems.
Tailor Your CV: Customize your CV to highlight your relevant experience in CQV activities, particularly in GMP settings. Emphasize your expertise in commissioning and qualification of complex equipment, as well as your ability to work with cross-functional teams.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and your understanding of the responsibilities. Mention specific experiences that align with the job requirements, such as leading CQV activities or collaborating with various disciplines.
Proofread Your Application: Before submitting your application, carefully proofread all documents for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a role in CQV activities.
Wie du dich auf ein Vorstellungsgespräch bei TN Switzerland vorbereitest
✨Showcase Your CQV Expertise
Be prepared to discuss your previous experience with commissioning, qualification, and validation activities in GMP environments. Highlight specific projects where you led CQV efforts, especially those involving cold and ambient temperature systems.
✨Demonstrate Leadership Skills
Since the role requires leading and coordinating CQ activities, share examples of how you've successfully managed teams or projects. Emphasize your ability to collaborate with cross-functional teams, including IT and CSV groups.
✨Understand the Technical Details
Familiarize yourself with the specific equipment and systems mentioned in the job description, such as semi-automated visual inspection machines and cold storage units. Being able to discuss these technologies will show your technical competence.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in past CQV roles and how you overcame them, particularly in relation to compliance with internal guidelines and validation plans.
