Proccess Engineer; m​/w​/d

Process Engineer (m/w/d)
-100%

Location
:
Grenchen (SO), Switzerland

Type of Contract
:
Permanent position

Start date: in alignment with the candidate’s availability

The Process Engineer is responsible for supporting and improving manufacturing processes to ensure product quality, compliance, and operational efficiency. This role will lead non-conformance (NC), CAPA, audit observation investigations and ensure accurate documentation. Additionally, the Process Engineer will drive process optimization initiatives, update work instructions, and collaborate cross‑functionally to maintain compliance with internal procedures and regulatory requirements.

• Lead and document investigations of quality issues (non-conformances (NCs), CAPAs, Audit observations) including product bounding and disposition, root cause analysis, definition of corrective and preventive actions and compliance with quality standards.
• Lead cross-functional investigation teams for quality issues ensuring timely completion of investigation and implementation of corrections, corrective and preventive actions.
• Prepare, review, and maintain documentation related to NCs and process improvements in line with regulatory and company requirements.
• Serve as subject matter expert (SME) for deviations in internal and external audits.
• Analyze manufacturing processes and identify opportunities for optimization to improve quality, cost efficiency, and throughput.
• Revise and update work instructions, standard operating procedures (SOPs), and other process documentation to reflect changes and improvements.
• Ensure compliance with applicable industry standards, quality management systems, and regulatory requirements (e.g., ISO, FDA, GMP).
• Collaborate with cross-functional teams (Quality, R&D, Production, Supply Chain, etc.) to support product and process improvements.
• Provide technical support and training to production personnel to ensure proper execution of validated processes.
• Support continuous improvement initiatives and contribute to the development of best practices within the manufacturing environment.

Process Engineering Supervisor II

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or related field.
• Proven experience in manufacturing or process engineering, or quality engineering (experience in regulated industries such as medical devices, pharmaceuticals, or aerospace preferred).
• Strong knowledge of NC/CAPA processes.
• Familiarity with regulatory and quality standards (e.g., ISO 13485, FDA 21 CFR Part 820, GMP).
• Excellent problem-solving, analytical, and documentation skills.
• Proficiency in process improvement tools and methodologies (Lean, Six Sigma preferred).
• Strong communication and teamwork skills with the ability to influence and drive results.
• Proven experience in project leadership.
• Fluent in English. Fluency in German is preferred.

• Attention to detail and strong organizational skills.
• Ability to manage multiple tasks and priorities in a fast-paced environment.
• Continuous improvement mindset and proactive approach to problem-solving.
• Commitment to quality and compliance.

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access  site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to  with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail.

Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.