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We unite the people who make our world healthier by placing top experts with life sciences companies worldwide. Fast and reliably, with the perfect match.
Manufacturing Associate (M/F/D)
Performs and documents daily manufacturing operations in a cGMP environment, including operation of process equipment, execution of validation protocols, and revising cGMP documents. Ensures compliance with cGMP standards and maintains equipment and facilities. The MA should be detail-oriented with strong documentation skills. Maintains training levels to the required standard and supports other functions on site.
Tasks:
* Executes manufacturing processing steps and/or support activities, monitoring the process against the recipe & MFG documentation (90%)
* Participates in training activities, manages their individual training plan, and trains other associates as required. (5%)
* Executes validation protocols (3%)
* Performs other duties as assigned from time to time. (2%)
Qualifications:
* High school diploma or equivalent with typically 3-5 years relevant experience in related or non-related industry, or 2-3 years in Pharma/Biotech industry
* Bachelor's degree in a related field with 1-2 years of professional experience
* Bachelor's degree in a non-related field with typically 3-4 years of experience
Languages: English B1, German and/or French are assets.
Must have hands-on experience in Upstream Processing within Pharma/Biotech production, with a preference for aseptic techniques and a solid understanding of aseptic processes. Basic understanding of biotech processes required. Must understand the importance of accurate and timely documentation within a cGMP environment. Must be trained and skilled in operational and regulatory procedures of at least one manufacturing department. Basic automation knowledge or comfort with technology platforms is preferred.
Requirements:
Start: ASAP
Duration: 12 months
Seniority level
* Associate
Employment type
* Full-time
Job function
* Manufacturing
Industries
* Pharmaceutical Manufacturing
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