Backed by GV.
About the role
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Bachelors or Advanced degree in a scientific discipline
- 12+ years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and quality. Must have Biologics experience
- 3+ years of Quality management experience with a successful track record in managing CDMOs as well as internal QA systems in a virtual environment
- Understanding of worldwide requirements of cGMP and quality systems for commercial and clinical products
- Excellent verbal and written communication skills, detail-oriented personality and ability to work and drive change across functions
- Experience interacting with regulatory health authorities at pre- and post-approval inspection
More about this role
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
The Associate Director of Product Quality Assurance (PQA) will be responsible for phase appropriate quality oversight of internal and external manufacturing and analytical activities. These activities include analytical testing performed by Beam staff in Cambridge as well as that performed by external partners at contract test...
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