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- Aufgaben: Join our team to support early-phase clinical manufacturing and ensure smooth operations.
- Arbeitgeber: CK QLS is a dynamic player in the pharmaceutical industry, focused on innovation.
- Mitarbeitervorteile: Gain hands-on experience in a fast-paced environment with opportunities for continuous improvement.
- Warum dieser Job: Be part of groundbreaking therapies and contribute to meaningful advancements in healthcare.
- Gewünschte Qualifikationen: Degree in science or engineering; 0-2 years experience in pharma/biotech preferred.
- Andere Informationen: Must be eligible to work in Switzerland; weekend work may be required.
Das voraussichtliche Gehalt liegt zwischen 60000 - 84000 € pro Jahr.
Process Engineer (Contract) Early-Phase Clinical Manufacturing
Location: Lucern, Switzerland
Company: CK QLS (on behalf of our client)
CK QLS are seeking a Process Engineer, to join a dynamic and growing manufacturing team within the pharmaceutical industry. This contract-based role offers the opportunity to support the implementation and GMP manufacturing of early-phase clinical therapies. The successful candidate will be responsible for ensuring the smooth execution of key manufacturing processes and contributing to continuous improvement efforts, in a fast-paced and highly regulated environment.
Key Responsibilities:
- Set up, execute, and troubleshoot upstream, downstream, and support operations in continuous manufacturing and fed-batch processes under GMP guidelines.
- Ensure compliance with GMP principles, Environmental Health and Safety (EHS) standards, and company policies.
- Document and manage process execution, deviations, changes, and Corrective and Preventive Actions (CAPAs).
- Contribute to continuous improvement initiatives and the integration of new technologies in the manufacturing process.
- Create, update, and maintain Standard Operating Procedures (SOPs) and master batch records.
- Manage materials and inventory using ERP systems such as SAP.
- Participate in sampling activities and on-call duties, which may include weekend work.
Requirements:
- Degree in a relevant scientific or engineering discipline.
- 0-2 years of experience in the pharmaceutical or biotech industry.
- Strong knowledge of upstream or downstream processes and GMP requirements.
- Solid problem-solving abilities and adaptability in a GMP-compliant environment.
- Proficiency in English (C1 level) and German (B2 level).
Preferred Qualifications:
- A Bachelor’s or Master’s degree in a relevant field.
- Experience working in a GMP-regulated environment.
- Familiarity with quality management systems and automated manufacturing systems.
- Ability to work collaboratively within a team as well as independently.
Apply:
It is essential that applicants hold entitlement to work in Switzerland. Please quote job reference in all correspondence.
Process Engineer Arbeitgeber: CK Group
Kontaktperson:
CK Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Process Engineer
✨Tip Number 1
Familiarize yourself with GMP guidelines and the specific processes used in early-phase clinical manufacturing. Understanding these concepts will not only help you during the interview but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in process engineering. Engaging with them can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Stay updated on the latest technologies and trends in the biotech field. Being knowledgeable about innovations can set you apart from other candidates and show your enthusiasm for continuous improvement.
✨Tip Number 4
Prepare to discuss specific examples of how you've contributed to process improvements or problem-solving in previous roles or projects. This will highlight your practical experience and adaptability in a GMP-compliant environment.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Process Engineer
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Process Engineer position. Understand the key responsibilities and requirements, especially the importance of GMP compliance and continuous improvement in a manufacturing environment.
Tailor Your CV: Customize your CV to highlight relevant experience in the pharmaceutical or biotech industry. Emphasize any knowledge of upstream or downstream processes, as well as your problem-solving skills and adaptability in a GMP-compliant setting.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the specific needs of the role. Mention your educational qualifications, any relevant experience, and your proficiency in English and German, as these are crucial for the position.
Double-Check Your Application: Before submitting your application, review all documents for accuracy and completeness. Ensure that you have included all required information and that your application reflects your best self.
Wie du dich auf ein Vorstellungsgespräch bei CK Group vorbereitest
✨Understand GMP Guidelines
Make sure you have a solid understanding of Good Manufacturing Practices (GMP) and how they apply to the pharmaceutical industry. Be prepared to discuss specific examples of how you've adhered to these guidelines in past experiences.
✨Showcase Problem-Solving Skills
Prepare to share instances where you've successfully identified and resolved issues in a manufacturing or engineering context. Highlight your adaptability and how you approach troubleshooting in a regulated environment.
✨Familiarize Yourself with ERP Systems
Since managing materials and inventory using ERP systems like SAP is part of the role, brush up on your knowledge of these systems. If you have experience with them, be ready to discuss how you've used them effectively in previous roles.
✨Demonstrate Team Collaboration
This position requires working both independently and as part of a team. Prepare examples that illustrate your ability to collaborate effectively with others, especially in high-pressure situations typical in clinical manufacturing.
