A global CDMO in pharmaceutical manufacturing, specializing in process development and cGMP production in cell culture, microbial fermentation, and gene therapies, is looking for a Microbiology Data Reviewer. The Data Reviewer will provide technical reviews and maintain data integrity for a new project. This role is ideal for someone in Quality Control (QC) seeking exposure to Quality Assurance (QA) without fully transitioning into QA. The individual will perform technical reviews, including examining Standard Operating Procedures (SOPs) based on client standards.
ResponsibilitiesPerform technical reviews of data and documentation.Ensure data integrity and compliance with client standards.Review Standard Operating Procedures (SOPs).Collaborate with the QC team to ensure accurate data management.Assist in maintaining quality and compliance across the project.Essential Skills2-3 years of experience in a GMP laboratory.Experience performing kinetic endotoxin testingExperience with LIMS and Trackwise is idealProficiency in data review and documentation review (experience can be from peer review)Bachelor's or Master's degree in science, preferably in chemistry, biology, pharmaceutical sciences, or related technical field.Additional Skills & QualificationsStrong attention to detail.Excellent time management skills.Ability to work collaboratively in a team environment.
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.
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