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- Aufgaben: Join our team as a Process Engineer - II, focusing on GMP manufacturing and process optimization.
- Arbeitgeber: Be part of a dynamic Manufacturing Operations team for a leading client in the biotech industry.
- Mitarbeitervorteile: Enjoy a temporary contract with potential extension and opportunities for professional growth.
- Warum dieser Job: Contribute to innovative projects while mentoring junior members in a collaborative environment.
- Gewünschte Qualifikationen: 2-5 years in pharma/biotech with expertise in GMP biologics manufacturing required.
- Andere Informationen: Candidates must be local or willing to relocate to Schachen, Luzern.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
We are looking for a Process Engineer – II – P2 Specialist to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team. Contract: Temporary contract via Randstad Start Date: ASAP End Date: 31/12/2026 (with the possibility of extension) Additional Information: Candidates must either live in the surrounding area or be willing to relocate near Schachen, Luzern. Responsibilities include but are not limited to: Setting up, executing, and troubleshooting upstream, downstream, and support unit operations in continuous and fed-batch manufacturing processes under GMP guidelines. Managing documentation for process execution, deviations, changes, and CAPAs while collaborating with Quality Assurance and other internal stakeholders. Contributing to continuous improvement initiatives and supporting the implementation of new technologies, including non-GMP engineering runs or testing activities. Creating and updating SOPs and electronic master batch records, as well as reviewing technical documentation for process transfer and GMP manufacturing. Mentoring and training junior team members and actively participating in knowledge transfer. Participating in sampling activities or being on-call, including potential weekend duties. Requirements: Educational background in a relevant discipline. 2-5 years of experience in the pharmaceutical or biotech industry. Minimum of 2 years of practical experience in the GMP manufacturing of biologics (upstream or downstream). Expert knowledge in specific unit operations for biologics manufacturing. Understanding of GMP principles and the ability to work under pressure in a complex environment. Preferred Skills and Experience: Bachelor’s or Master’s degree in a relevant discipline. Familiarity with quality management and compliance systems (e.g., Trackwise, SAP QM, VeevaVault). Experience with automated systems (DeltaV) or electronic batch records (MES). Previous experience with process development or scale-up activities. Ability to work efficiently as part of a team and independently on projects. If you are interested, please submit your updated CV for consideration. #J-18808-Ljbffr
Process Engineer - II Arbeitgeber: Whatjobs
Kontaktperson:
Whatjobs HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Process Engineer - II
✨Tip Number 1
Make sure to familiarize yourself with GMP guidelines and the specific unit operations relevant to biologics manufacturing. This knowledge 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 and biotech industry, especially those who have experience in GMP environments. Engaging with them can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Highlight any experience you have with quality management systems like Trackwise or SAP QM. Being able to discuss your familiarity with these tools can set you apart from other candidates.
✨Tip Number 4
Be prepared to discuss your approach to continuous improvement initiatives and how you've contributed to process optimization in previous roles. This shows that you're proactive and results-oriented.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Process Engineer - II
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Process Engineer - II position. Understand the key responsibilities and required skills, especially those related to GMP manufacturing and biologics.
Tailor Your CV: Customize your CV to highlight relevant experience in the pharmaceutical or biotech industry, particularly your practical experience in GMP manufacturing. Emphasize any specific unit operations you are familiar with.
Craft a Strong Cover Letter: Write a cover letter that connects your background and skills to the requirements of the role. Mention your experience with continuous improvement initiatives and your ability to work under pressure in complex environments.
Highlight Team Collaboration: In your application, emphasize your ability to work as part of a team and your experience mentoring junior members. This is crucial for the role, as collaboration with Quality Assurance and other stakeholders is a key responsibility.
Wie du dich auf ein Vorstellungsgespräch bei Whatjobs vorbereitest
✨Showcase Your GMP Knowledge
Make sure to highlight your understanding of GMP principles during the interview. Be prepared to discuss specific experiences where you successfully applied these guidelines in previous roles, especially in biologics manufacturing.
✨Demonstrate Problem-Solving Skills
Since troubleshooting is a key part of the role, come prepared with examples of challenges you've faced in upstream or downstream processes. Explain how you approached these issues and what the outcomes were.
✨Emphasize Team Collaboration
This position requires working closely with Quality Assurance and other stakeholders. Share examples of how you've effectively collaborated with cross-functional teams in the past, and how you contributed to continuous improvement initiatives.
✨Prepare for Technical Questions
Expect to be asked about specific unit operations and technologies relevant to biologics manufacturing. Brush up on your technical knowledge and be ready to discuss any automated systems or electronic batch records you've worked with.
