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- Aufgaben: Join our team to ensure top-notch pharmaceutical equipment is qualified and validated.
- Arbeitgeber: Be part of a leading pharmaceutical manufacturing company dedicated to quality and compliance.
- Mitarbeitervorteile: Enjoy a collaborative work environment with opportunities for professional growth and development.
- Warum dieser Job: Make a real impact in healthcare by ensuring the safety and efficacy of pharmaceutical products.
- Gewünschte Qualifikationen: Bachelor's degree in Engineering or Life Sciences; experience in equipment qualification is a must.
- Andere Informationen: Work closely with cross-functional teams and tackle exciting challenges in a regulated industry.
Das voraussichtliche Gehalt liegt zwischen 48000 - 72000 € pro Jahr.
We are seeking a highly motivated Performance Qualification (PQ) Engineer to join our pharmaceutical manufacturing team. The successful candidate will be responsible for the qualification and validation of critical equipment such as parts washers, autoclaves, and thermal mapping systems. This role ensures compliance with industry regulations and supports the delivery of high-quality pharmaceutical products. Key Responsibilities: Perform Performance Qualification (PQ) activities for pharmaceutical manufacturing equipment, including parts washers, autoclaves, and thermal mapping systems. Develop, execute, and review qualification protocols (IQ, OQ, PQ) in accordance with cGMP and regulatory standards. Analyze and interpret validation data, ensuring compliance with industry best practices. Support thermal mapping studies for controlled storage environments, ensuring temperature and humidity consistency. Collaborate with cross-functional teams including Quality Assurance, Engineering, and Manufacturing to optimize equipment performance. Maintain detailed documentation and reports for audits and regulatory inspections. Troubleshoot and resolve validation issues as they arise. Requirements: Bachelor\’s degree in Engineering, Life Sciences, or a related field. Previous experience in equipment qualification and validation within a pharmaceutical or regulated manufacturing environment. Strong understanding of cGMP, FDA, and EU regulatory requirements. Hands-on experience with parts washers, autoclaves, and thermal mapping. Excellent analytical, problem-solving, and documentation skills. Strong communication and teamwork abilities. #J-18808-Ljbffr
Performance Qualification (PQ) Engineer, Visp Arbeitgeber: Whatjobs
Kontaktperson:
Whatjobs HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Performance Qualification (PQ) Engineer, Visp
✨Tip Number 1
Familiarize yourself with the specific equipment mentioned in the job description, such as parts washers and autoclaves. Having hands-on experience or knowledge about these systems will give you an edge during interviews.
✨Tip Number 2
Brush up on your understanding of cGMP and regulatory standards. Being able to discuss how these regulations impact performance qualification will demonstrate your expertise and commitment to compliance.
✨Tip Number 3
Network with professionals in the pharmaceutical manufacturing field. Attend industry events or join relevant online forums to connect with others who can provide insights or even referrals for the PQ Engineer position.
✨Tip Number 4
Prepare to discuss specific examples of past experiences where you successfully executed qualification protocols or resolved validation issues. This will showcase your problem-solving skills and ability to work collaboratively with cross-functional teams.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Performance Qualification (PQ) Engineer, Visp
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Performance Qualification (PQ) Engineer position. Understand the key responsibilities and requirements, especially the importance of cGMP and regulatory standards in your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize any previous experience you have with equipment qualification and validation in a pharmaceutical or regulated manufacturing environment. Be specific about your hands-on experience with parts washers, autoclaves, and thermal mapping systems.
Showcase Analytical Skills: Demonstrate your analytical and problem-solving skills in your application. Provide examples of how you've successfully analyzed validation data or resolved validation issues in past roles.
Tailor Your Documents: Customize your CV and cover letter to reflect the language and requirements mentioned in the job description. Use keywords related to performance qualification, compliance, and teamwork to make your application stand out.
Wie du dich auf ein Vorstellungsgespräch bei Whatjobs vorbereitest
✨Know Your Equipment
Make sure you have a solid understanding of the critical equipment you'll be working with, such as parts washers and autoclaves. Be prepared to discuss your hands-on experience and how you've applied your knowledge in previous roles.
✨Understand cGMP and Regulatory Standards
Familiarize yourself with current Good Manufacturing Practices (cGMP) and relevant FDA and EU regulations. Be ready to explain how these standards impact your work and how you've ensured compliance in past projects.
✨Showcase Your Analytical Skills
Prepare to discuss specific examples where you've analyzed validation data or resolved validation issues. Highlight your problem-solving approach and how it contributed to maintaining high-quality standards.
✨Emphasize Team Collaboration
Since this role involves working with cross-functional teams, be ready to share experiences where you've successfully collaborated with Quality Assurance, Engineering, or Manufacturing teams. Communication is key, so demonstrate your teamwork abilities.
