- Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations
- Perform data analysis and final result reporting to support product lot release with adherence to turnaround times.
- Perform all activities with respect to GMP/GDP compliance
- Support thorough GMP investigations for out of specification test results and other quality events
- Support technical problem solving for issues pertaining to GMP Quality Control
- Support product stability programs including execution of stability testing, stability data analysis and trending, and final reporting of stability data
- Assist in the generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs and change controls
- Perform peer review of laboratory data and logbooks
- Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
- Support Health Authority inspections
- Provide input to functional laboratory team meetings
- Other responsibilities as assigned
- Bachelor's degree in a relevant discipline (biological sciences or equivalent).
- Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role
- Experience with two or more of the following: Flow Cytometry, Cell based ELISA, NC200
- Successfully interface with multi-disciplined teams
- Extremely detail-oriented with strong technical skills.
- Ability to effectively manage multiple priorities involving aggressive, changing timelines at a high level of productivity
- High level of ownership and accountability
- Demonstrate sense of urgency; ability to recognize time sensitivity
- Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
- Experience with cell therapy products
- Shift Sunday through Thursday
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
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Molecular Biologist - Dubai, United Arab Emirates - Actalent
Description
Description:
The QC Analyst, Cell Based Immunology will:
Additional Skills & Qualifications:
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: