Manufacturing Scientist
vor 11 Stunden
We are a global biopharmaceutical company dedicated to bringing meaningful innovation to global health. Our team works with partners in healthcare to touch the lives of over a billion people every day, throughout the world. With more than 260 operating companies in over 60 countries, we employ approximately 134,000 people. Our worldwide headquarters is located in New Brunswick, New Jersey, USA.
Job Description
This role supports a routine GMP manufacturing process with a focus on downstream process steps (chromatography, diafiltration/ultrafiltration). The successful candidate will support routine GMP manufacturing, help troubleshoot and improve processes, verify data, and trend it. Additionally, they will write SOPs, train operators, and create technical documents like risk assessments and reports. As a subject matter expert, they will investigate quality issues and initiate change controls.
Main Responsibilities:
- Support routine GMP manufacturing and downstream process steps.
- Troubleshoot and improve processes.
- Verify and trend data.
- Write SOPs and train operators.
- Create technical documents like risk assessments and reports.
- Investigate quality issues and initiate change controls.
Qualifications:
To succeed in this role, you will need a Master's or Bachelor's degree in bio-engineering, biotechnology, biology, or biochemistry. You should have experience in GMP-compliant biotechnological manufacturing or development, particularly in chromatography and diafiltration/ultrafiltration. Excellent problem-solving and analytical skills are essential. Fluency in English and German is required, and teamwork, communication, and interpersonal skills are highly valued.
Benefits:
We offer a dynamic, progressive, and collaborative work environment. If you are interested in working for a global leading pharmaceutical company, please submit your application today.
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