Manufacturing Associate III

Swisslinx; Bezirk Solothurn; Vor Ort; CHF 90.000 - 110.000; Vollzeit

Zusammenfassung

Swisslinx is seeking a Manufacturing Associate III to support daily cGMP-regulated production in Solothurn. You will perform manufacturing operations, operate equipment, and ensure compliance with quality standards. Start ASAP until 28/02/2027 with possible extension.

You will document activities, support validation, maintain training, and collaborate with cross-functional teams to keep production running smoothly and safely.

Qualifikationen

• 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.

Aufgaben

• Perform and document daily manufacturing operations in accordance with cGMP requirements.
• Operate manufacturing and process equipment.
• Support the execution of validation protocols.
• Review and revise cGMP documentation as required.
• Maintain accurate documentation throughout all manufacturing activities.
• Collaborate with other functions across the site as needed.
• Contribute to the smooth and efficient running of daily manufacturing operations.
• Ensure compliance with cGMP standards and quality systems.

Kenntnisse

cGMP knowledge

Operations execution

Process equipment

Validation support

Documentation skills

Training maintenance

Cross-functional collaboration

Jobbeschreibung

Job Description

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.

About The Customer

• Role: Manufacturing Associate III
• Location: Solothurn
• Start: ASAP until 28/02/2027 with possible extension
• Workload: Full time

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.