Manager/Sr. Manager, Global Compliance and Training

Role Summary

The Manager/Sr. Manager, Compliance and Training, will provide expertise in training design and execution for Beam and support overall training management. This role is responsible for developing, implementing, and administering global training while supporting the application of Global Quality Policies & Standards, Change Controls, and Deviation/Corrective and Preventive Action review and administration. The position supports compliance with 21 CFR 211.25 and GMP/GxP training requirements, delivering training, system support, and process guidance to Quality Systems users globally.

Responsibilities

• Develops, leads, and implements training initiatives that are aligned with business strategies.
• Design, develop and deliver instructional materials, both digital and physical, in an efficient, effective, appealing, engaging way.
• Manages the performance/effectiveness of quality system training programs.
• Work collaboratively on the GXP integrated digital landscape to support, resolve system technical issues and communicate best practices for electronic quality training systems.
• Assist in the refinement of system user training and support training delivery.
• Assist in improving and maintaining Beam’s overall Quality Management System (QMS), including policies and procedures, while keeping them current with emerging and changing regulations.
• Develops user requirements regarding Quality training systems and supports the generation/review/approval of computer system validation deliverables.
• Contributes to the generation, review, and approval of computer system test scripts.
• Support site and function audit preparations with respect to system functionality.
• Support development of harmonized/streamlined/standardized processes and supplemental documents (including Work Instruction creation or maintenance) governing management and usage of Quality Systems.
• Maintain system-related metrics and assist in analyzing training effectiveness based on those metrics.
• Ability to own appropriate and complete system Quality Events (Issues, Change Controls and CAPAs) to meet internal procedures and regulatory expectations.
• Provides quality assurance guidance in a professional and collaborative manner to stakeholders.

Qualifications

• University degree in scientific discipline/Life Sciences or equivalent experience in the biotech or pharmaceutical industry.
• 8+ years of relevant experience in a GMP and GXP environment with at least 3 years of demonstrated experience with the development, maintenance, and training oversight required.
• General knowledge of regulatory requirements for the pharmaceutical, biotechnology, or vaccine industry.
• Skilled in determining the state and needs of the learner and defining the end goal of instruction.
• Excellent interpersonal effectiveness, written/verbal communication, influencing, and negotiation skills.
• Ability to work independently.
• Excellent computer skills and advanced knowledge of Quality Systems.
• Direct experience with Quality Management Systems, Document Management Systems, Learning Management Systems, and Microsoft Office, including Word and Excel.
• Veeva experience required.
• Self-motivator with the ability to follow up on and complete multiple projects simultaneously.
• Formal or technical writing experience.
• Highly attentive to details and able to work well as part of a team.
• Demonstrates consistent judgment, quality, accuracy, speed, and creativity.
• Understands, selects, and uses appropriate risk management and root cause analysis tools.
• Takes initiative in making improvement suggestions to promote operational goals.
• Applies Quality concepts and company policies to resolve issues of moderate complexity in an effective manner.
• Facilitates designing processes with Quality built in from the beginning.
• Identifies and uses good judgement to handle out-of-compliance situations.
• Good listening and communication skills.
• Positive approach.

Additional Requirements

• This position is expected to be on-site three days a week.