Senior Manufacturing Technician Upstream and/or...

at  Recrutis

Bern, BE, Switzerland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Jul, 2024Not Specified28 Apr, 20245 year(s) or aboveFood Industry,Pharmaceutical Industry,It,Chemical Industry,Languages,Delta VNoNo
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Description:

For one of our major clients, a World Leading Biotech, we are currently looking for Senior Manufacturing Technicians Upstream or Downstream to support the production ramp up of our client.

JOB SUMMARY:

Perform and document daily manufacturing operations in a cGMP environment, including operating process equipment, executing validation protocols, and revising cGMP documentation. Ensure compliance with cGMP standards while maintaining equipment and facilities. This role requires strong attention to detail and expertise in automated systems and process controls. Additionally, provide support to other functions on site and maintain training to the required level.

MINIMUM EDUCATION REQUIREMENTS:

Relevant education from the chemical industry, food industry, pharmaceutical, or biotech industry.

MINIMUM EXPERIENCE REQUIREMENTS:

  • High school diploma or equivalent experience and typically 9-11 years relevant experience in Pharma/Biotech industry OR
  • Bachelor’s degree in a related field with 5-6 years Pharma/Biotech professional experience OR
  • Bachelor’s degree in an unrelated field and typically 7-9 Pharma/Biotech years’ experience.
  • Good understanding of Delta V or Syncade or similar automated systems.
  • Understanding of full Biotech process.
  • Languages: English B1, German and/or French are assets.
    Got what it takes? Apply now and join us in making a difference in the pharmaceutical industry

Responsibilities:

  • Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation (65%).
  • Perform troubleshooting/investigation of equipment and process issues (10%).
  • Revise documents as instructed, capable of equipment and/or process changes (5%).
  • Actively participate in training activities, managing your individual training plan. Train other associates as required (5%).
  • Execute validation protocols (5%).
  • Capable of leading shifts when the supervisor is absent and actively lead or participate in shift exchanges. Coordinate activities and daily schedules with cross-functional areas (5%).
  • Perform other job duties assigned from time to time (5%).


REQUIREMENT SUMMARY

Min:5.0Max:11.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Diploma

Pharma/biotech industry or

Proficient

1

Bern, BE, Switzerland