Manufacturing Associate IV
at Biogen
Luterbach, so, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Dec, 2024 | Not Specified | 24 Sep, 2024 | 5 year(s) or above | Delta V,Languages | No | No |
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US Citizen | Student Visa |
H1B | CPT |
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Full Time | Part Time |
Permanent | Independent - 1099 |
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Description:
Job Description
REQUIRED SKILLS
- High school diploma or equivalent experience and typically 9-11 years relevant experience in Pharma/Biotech industry OR Bachelor degree in related filed with 5-6 years Pharma/Biotech professional experience OR Bachelor degree in not related field and typically 7-9 Pharma/Biotech years experience.
- Solid understanding of Delta V or Syncade or similar automated systems.
- Understanding of full Biotech process.
- Languages: English full B1, German and/or French an asset.
Additional Information
Responsibilities:
ABOUT THIS ROLE
As a Manufacturing Associate IV, you’ll perform processing steps and manufacturing support activities in our facilities in Luterbach (Solothurn). You will be the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. Your responsibilities include performing and documenting daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Embrace the opportunity to maintain equipment and facilities while actively supporting various functions on site.
WHAT YOU’LL DO
- 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, Capable of equipment and/or process changes.
- Actively participate in training activities, managing their individual training plan. Train other associates as required.
- Execute validation protocols.
- Capable of leading shift when supervisor is absent, and actively lead or participate in shift exchanges. Coordinate activities and daily schedules with cross-functional areas.
- Embrace additional duties that may be assigned, adding versatility to your skill set.
Qualifications
REQUIREMENT SUMMARY
Min:5.0Max:11.0 year(s)
Other Industry
Pharma / Biotech / Healthcare / Medical / R&D
Other
Diploma
Not related field and typically 7-9 pharma/biotech years experience
Proficient
1
Luterbach, SO, Switzerland