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15887en
- Contract
- English
- Associate
- Engineering & Technical Services
- Mittelland
- Healthcare & Life Sciences
Skills
Pharma, Manufacturing, GMP, Process Equipment, USP, DSP, Validation Protocols, Biotech, DeltaV, Syncade, Upstream, Downstream
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On behalf of our client, an international Biotechnology company based in Solothurn, Swisslinx is looking for Senior Manufacturing Associates. This is initially a 12 months contract position (extension possible) with a great opportunity to bring your proven knowledge and expertise to an organization that offers a dynamic working environment.
Start Date: As soon as possible
Location: Solothurn
Work type: On site
Workload: 100%
Duration: 12 months
Extension: Possible
Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation
- Ensure compliance to cGMP as well as maintaining equipment and facilities
- Maintain training to the required level and support other functions on site
- Execute manufacturing related work as per procedures and policies
Your profile:
- High school diploma or equivalent experience and typiically 4-5 years in related industry or 5-6 years Pharma/Biotech industry OR Bachelor degree in related filed with 3-4 years Pharma/Biotech professional experience
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Languages: Conversational English (minimum B1 level)
- Detail-oriented with strong understanding of automated systems and process controls
To apply or for any further information, please do not hesitate to contact Alina Peeva, senior recruiter: alina.peeva@swisslinx.com
Start Date: As soon as possible
Location: Solothurn
Work type: On site
Workload: 100%
Duration: 12 months
Extension: Possible
Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation
- Ensure compliance to cGMP as well as maintaining equipment and facilities
- Maintain training to the required level and support other functions on site
- Execute manufacturing related work as per procedures and policies
Your profile:
- High school diploma or equivalent experience and typiically 4-5 years in related industry or 5-6 years Pharma/Biotech industry OR Bachelor degree in related filed with 3-4 years Pharma/Biotech professional experience
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Languages: Conversational English (minimum B1 level)
- Detail-oriented with strong understanding of automated systems and process controls
To apply or for any further information, please do not hesitate to contact Alina Peeva, senior recruiter: alina.peeva@swisslinx.com
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