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 that includes a suite of gene editing and delivery technologies and is in the process of building 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 potential 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:

We are seeking an experienced Process and Cleaning Validation subject matter experts to provide Validation support for development of the process and cleaning validation programs, strategies to be applied to early processes entering these validation programs, and expertise in validation project management and technical document preparation as needed.

Key Responsibilities:

• Design and implement approaches for validation studies, using knowledge and input from Process Development, Analytical Development, Manufacturing, MST/ENG, and Quality partners.
• Develop and execute validation master plans and/or project plans, protocols, and reports for process and cleaning validation activities.
• Conduct risk assessments and gap analyses of existing validation programs to identify areas for improvement.
• Evaluate equipment design and manufacturing process procedures to establish scientifically sound acceptance criteria for PQ studies.
• Support regulatory submission efforts and inspection preparation and address validation-related observations related to process and cleaning validation.
• Train client personnel on validation principles, methodologies, and best practices.
• Author, Review and approve validation documentation to ensure compliance with cGMP requirements.
• Provide technical expertise in cleaning agent selection, residue detection methods, and recovery studies.
• Support technology transfer activities and process scale-up initiatives involving Process or Cleaning Validation Programs for internal and external manufacturing initiatives.

Required Qualifications:

• Bachelor's degree in Engineering, Chemistry, Pharmaceutical Sciences, or related field.
• Minimum 6 years of experience in biopharmaceutical industry supporting manufacturing in a process validation, cleaning validation, process engineering, MST, process development, or other manufacturing support related capacity.
• Experience with quality risk management tools and methodologies.
• Technical writing and documentation skills.
• Project management and communication abilities.
• Must be able to travel up to 25%.

Preferred Qualifications:

• Experience working with LNP processes and/or process equipment.
• Experience with managing a team of direct reports.
• Knowledge of FDA, EMA, and ICH guidelines related to process and cleaning validation or knowledge of how to find/access these regulations.
• Understanding of process design/characterization, equipment design, and CIP/COP systems.
• Familiarity with analytical method development and validation.
• Familiarity with statistical analysis and validation lifecycle approach.