mRNA Manager QC
mRNA Manager QC
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Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob Description
Job Description
Thermo Fisher Scientific Inc. is seeking a dynamic and transformative leader to fill the role of mRNA Manager QC. This position is ideal for an individual with the ability to maintain and improve the quality of mRNA products to international standards. Join us in our mission to build a healthier safer world leading a dedicated QC team and implementing advanced analytical techniques.
Key Responsibilities:
Leadership:
- Lead the QC team towards improvementfocused goals.
- Set clear expectations and provide valuable timely feedback.
- Develop innovative problemsolving techniques and foster a wastefree environment.
Quality Control:
- Lead all aspects of our QC laboratory coordinate planning task prioritization comprehensive analyses and insightful report delivery.
- Ensure our QC Chemistry QC Biotechnology and QC Microbiology teams provide timely scientifically validated results in line with international regulatory guidelines and customer needs.
Technical Expertise:
- Supervise complex biological and physical characterization techniques including LCMS UPLC/HPLC molecular biology tests Endotoxin and Sterility tests.
- Implement QC processes in alignment with international mRNA quality standards set by globally recognized regulatory bodies.
Regulatory Compliance:
- Ensure the of qualification/validation protocols batch release and stability testing in accordance with regulatory standards.
- Improve and maintain quality systems for ongoing compliance and auditreadiness.
Collaboration & Innovation:
- Facilitate collaboration across departments to improve operational efficiency.
- Foster innovation in the PD lab embracing brand new QC methodologies.
Planning for longterm success:
- Lead the development and implementation of QC plans to drive the success of our mRNA business.
- Find opportunities to improve processes and introduce standard methodologies to improve QC operations.
Qualifications:
- Advanced degree (Ph.D. MSc or equivalent) in Chemistry Biochemistry Molecular Biology or a related field.
- 10 to 15 years of experience in QC or manufacturing in the biopharmaceutical industry.
- Proven leadership skills with the ability to build and lead highperforming teams.
- Extensive knowledge of international regulatory guidelines (FDA EMA etc. QC methodologies and manufacturing practices.
- Strong analytical and problemsolving skills with the ability to manage complex projects to completion.
- Excellent communication skills with the ability to facilitate effective crossfunctional collaborations.
Embrace this chance to create a significant impact in the scientific community. Apply today and lets explore the future together.
Join us!!
Required Experience:
Manager
Employment Type
Full-Time
