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, 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.
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, 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.
