Manufacturing Associate III

Swisslinx AG; Bezirk Solothurn; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Swisslinx AG is seeking a technically adept professional to support daily manufacturing activities in a cGMP-regulated production environment in Switzerland. You will perform and document operations, operate process equipment, and assist with validation protocols while ensuring compliance with quality standards.

The role requires hands-on experience, meticulous documentation, and the ability to collaborate across functions to maintain safe, compliant operations and ongoing training at the site.

Qualifikationen

• 3–5 years of relevant experience in pharmaceutical/biotech or other cGMP-regulated manufacturing.
• Hands-on experience supporting manufacturing operations and operating process equipment.
• Good understanding of cGMP requirements and compliant documentation practices.
• Experience supporting validation activities and working with validation protocols.
• Strong attention to detail and very good documentation skills.

Aufgaben

• Perform and document daily manufacturing operations in accordance with cGMP requirements.
• Operate manufacturing and process equipment.
• Support the execution of validation protocols and related manufacturing activities.
• Review and revise cGMP documentation where required.
• Ensure compliance with cGMP standards, internal procedures and quality requirements.
• Support the maintenance of manufacturing equipment and facilities.
• Maintain the required level of training and ensure all assigned training is completed on time.
• Collaborate with and support other functions across the site as needed.
• Contribute to the smooth and efficient running of daily manufacturing operations.
• Maintain accurate and complete documentation throughout all manufacturing activities.

Kenntnisse

cGMP experience

Documentation

Attention to detail

Team collaboration

Equipment operation

Training management

Jobbeschreibung

• Start: ASAP until 28/02/2027 with possible extension

You will support daily manufacturing activities within a cGMP-regulated production environment, ensuring that operations are performed safely, accurately and in compliance with applicable quality standards and procedures.

Requirements

• Perform and document daily manufacturing operations in accordance with cGMP requirements.
• Operate manufacturing and process equipment.
• Support the execution of validation protocols and related manufacturing activities.
• Review and revise cGMP documentation where required.
• Ensure compliance with cGMP standards, internal procedures and quality requirements.
• Support the maintenance of manufacturing equipment and facilities.
• Maintain the required level of training and ensure all assigned training is completed on time.
• Collaborate with and support other functions across the site as needed.
• Contribute to the smooth and efficient running of daily manufacturing operations.
• Maintain accurate and complete documentation throughout all manufacturing activities.

Competences

• 3–5 years of relevant experience within pharmaceutical, biotechnology or another cGMP-regulated manufacturing environment.
• Hands-on experience supporting manufacturing operations and operating process equipment.
• Good understanding of cGMP requirements and compliant documentation practices.
• Experience supporting validation activities and working with validation protocols.
• Strong attention to detail and very good documentation skills.
• Ability to work reliably within established procedures and quality systems.
• Comfortable working collaboratively with different functions across a manufacturing site.
• Strong sense of responsibility and commitment to maintaining a safe and compliant working environment.

Maybe not for you, but for someone else?