For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.
General Information:
* Start date: 01.02.2025
* End date: 31.01.2026
* Extension: Possible
* Workplace: Solothurn
* Workload: 100%
* Remote/Home office: Not available
Job Summary:
Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documents. Ensuring compliance to cGMP as well as maintaining equipment and facilities. The MA is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
Tasks & Responsibilities:
* Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation.
* Perform troubleshooting/investigation of equipment and process issues.
* Revise documents as instructed and manage equipment and/or process changes.
* Actively participate in training activities, managing their individual training plan, train other associates as required.
* Execute validation protocols.
* Lead shifts when the supervisor is absent, and actively leads or participates in shift exchanges.
* Coordinate activities and daily schedules with cross-functional teams.
* Perform other job duties as assigned.
Must haves:
* High school diploma or equivalent experience and typically 3-5 years of relevant experience in related / non-related industry or 2-3 years of experience in Pharma/Biotech industry.
* Bachelor's degree in a related field with 1-2 years of professional experience; or a Bachelor's degree in a non-related field with 3-4 years of experience.
* Languages: English B1, German and/or French an asset.
* Basic understanding of the Biotech process, able to follow and comply with written procedures and protocols.
* Solid understanding of the requirements within correct and timely documentation within a cGMP environment.
* Trained and skilled in all operational and regulatory procedures of at least one manufacturing department.
* Basic understanding of automation or comfort with technology platforms.
* Ability to independently document and record job-related information.
* Good verbal and written communication skills.
If this sounds like you, we'd love to hear from you! Submit your CV today and join a leading pharmaceutical company driving innovation.
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