Manufacturing Associate II
at Biogen
Luterbach, so, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Aug, 2024 | Not Specified | 30 May, 2024 | 1 year(s) or above | Regulated Industry,Languages,Delta V | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job Description
REQUIRED SKILLS
- High school diploma or equivalent experience and typically 3-5 years relevant experience in related or non-related industry or 2-3 years experience in Pharma/Biotech industryOR
- Bachelor degree in related filed with 1-2 years professional experienceOR
- Bachelor degree in not related field and typically 3-4 years experience
- Languages: English B1, German and/or French an asset
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Good verbal and written skills are required to ensure proper description of any issues.
Additional Information
Responsibilities:
ABOUT THIS ROLE
As a Manufacturing Associate II, you will perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents. Your responsibilities also involved ensuring compliance to cGMP as well as maintaining equipment and facilities. The Manufacturing Associate II is detail-oriented and possess strong documentation skills. In addition to that, it is expected to maintain training level to the required level and support other 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 and train other associates as required.
- Execute validation protocols
- Capable of leading shift when supervisor is absent, and actively leads or participates in shift exchanges.
- Coordinate activities and daily schedules with cross-functional areas.
Qualifications
REQUIREMENT SUMMARY
Min:1.0Max:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Diploma
Pharma/biotech industryor
Proficient
1
Luterbach, SO, Switzerland