Why this role stands out
Gain invaluable hands-on experience in a GMP-regulated laboratory environment with Beam Therapeutics' Quality Control Co-op role, supporting cutting-edge gene editing technologies. This position is perfect for an energetic and detail-oriented individual eager to contribute to a values-driven organization at the forefront of precision genetic medicine. Apply now to develop critical skills and be part of a team dedicated to creating life-long cures.
Quick overview
Job description
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:
Beam is looking for a highly energetic co-op to join our growing quality control team. The co-op will provide operational, administrative, and laboratory support to the QC organization. This role is intended to support PLI readiness, method lifecycle activities, laboratory organization, reagent traceability, and quality-system-related activities while providing hands-on exposure to a GMP-regulated laboratory environment.
Responsibilities:
- Assist in procurement, tracking, and management of reagents and materials.
- Assist with method lifecycle activities, including feasibility runs and troubleshooting of analytical methods and laboratory instruments under supervision.
- Organize, document and archive historical data sets.
- Support quality event documentation (e.g., Deviation, CAPA, Change Control).
- Assist in reviewing data generated by other analysts to ensure accuracy and compliance.
- Learn about key functions in pharmaceutical development and manufacturing, including analytics, stability testing, manufacturing processes, and quality systems.
- Gain hands-on experience with analytical methods and techniques commonly used in the pharmaceutical and biotech industries.
Qualifications:
- Pursuing a BS or MS in biological sciences or a related field (Biochemistry/Biophysics, Cell Biology/Molecular Biology, Chemistry)
- Completed entry level biology, chemistry and biochemistry courses
- Completed of biology, chemistry and biochemistry lab courses.
- Knowledge of ICH/USP guidelines is highly desirable.
- Must be a team player, comfortable working collaboratively and thriving in a fast-paced environment.
- Applicants must be currently enrolled in a degree-granting college or university program and maintain their student status throughout the duration of the co-op to be eligible.
Hourly pay will will be determined based on several factors, including but not limited to, relevant experience, skills, and education.
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