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You will be updated with latest job alerts via emailBasic Qualifications:
High School/GED 4 years of Quality work experience OR
Associates degree 2 years of Quality work experience OR
Bachelors degree 6 months of Quality work experience OR
Masters degree
Preferred Qualifications:
Degree in a related scientific field such as Chemistry Microbiology Molecular Biology Physics or Engineering or Information Systems.
3 years of relevant experience in the GMP commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry.
Previous laboratory experience.
Strong knowledge of validation of LIMS & LMES/CIMS.
Experience in a lead role providing guidance to team members.
Knowledge of related regulatory/industry considerations compliance issues and/or scientific discovery.
Strong written and verbal communication skills including technical writing and presentation.
Familiar with authoring or owning change control records.
Experience with equipment and method validation verification and transfer including the change control process.
Interact effectively with variety of communication and working styles and ability to work well in teams.
Thrive!
What you can expect of us
As we work to develop treatments that take care of others we also work to care for our teammates professional and personal growth and wellbeing.
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Full Time