Company Overview:
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.
Position Overview:
The incumbent will support the implementation and execution of core microbiology programs at Beam’s manufacturing facility in RTP, North Carolina. The NC manufacturing facility is a greenfield build and will be implemented in phases over a 6-8 Year period, with a focus on advanced therapeutic manufacturing technologies (cell and gene therapy modalities). The facility will start as a clinical phase manufacturing plant with the intent to move programs to commercial within the same facility. The incumbent will assist with the planning, implementation, and execution of microbiology workstreams in support of the facility startup plan. These workstreams and duties may include draft documentation for the microbiology programs, perform facility environmental monitoring (EM), conducting/drafting investigations, Gram staining, media growth promotion, endotoxin, bioburden and rapid sterility testing. The incumbent will work with colleagues in other Quality teams, as well as colleagues in manufacturing, engineering, validation to support the implementation of site contamination control goals and standards. The work schedule will provide support for site implementation activities and establishment of routine operations. Leveling for this position will be commensurate of experience.
Primary Responsibilities:
- Draft documentation for the microbiology programs (SOPs, WIs, Protocols, reports etc.)
- Conduct and draft investigations for the microbiology programs (EM excursions, lab deviations, product OOS’s, etc.)
- Support the implementation and execution of microbiology laboratory programs, including bioburden, endotoxin, and rapid sterility testing, method verifications, media growth promotion and gram staining.
- Support the implementation and execution of the environmental monitoring (EM) program.
- Review and approve laboratory data for the microbiology programs.
- Support the incoming testing and management of raw materials.
- Assist with the data analysis and trending program for EM data.
- Support the implementation of the disinfectant efficacy qualification program.
- Partner with CQV representative to support the implementation of QC lab equipment by providing technical assistance during the development and execution of IQ/OQ/PQ protocols.
- Provide assistance for the implementation of the site LIMS; support protocol execution when applicable.
- Additional duties as assigned.
Qualifications:
- Bachelor’s or Master’s degree in a scientific discipline.
- 2+ years’ relevant experience in the pharmaceutical/biotech industry.
- Excellent verbal and written communication skills.
- Strong writing skills.
- Strong team player that has a customer service approach and is solution oriented.
- Attention to detail and the ability to work equally well individually as within a multi-disciplinary team.
- Excellent time management skills.
- Consistent delivery of high-quality work at all times.
The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Skills Required
- Bachelor's or Master's degree in a scientific discipline
- 2+ years' relevant experience in the pharmaceutical/biotech industry
- Excellent verbal and written communication skills
- Strong writing skills
- Strong team player
- Attention to detail
- Excellent time management skills
What We Do
Beam Therapeutics, launched in 2018, is pioneering the use of CRISPR base editing to develop a broad portfolio of advanced genetic medicines. Our groundbreaking base editing technology allows us to make permanent, specific edits to single bases in DNA and RNA, without cutting the strands. Base editor therapeutics represent a new class of “precision genetic medicines,” combining precision targeting of the genome with precision control of editing outcomes. Our dream is to provide life-long cures for patients suffering from serious diseases. The Beam Team Is: • A community of fearless innovators • Rigorous and honest in our research • Listening with open minds • Committed to each other
