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Serán BioScience

CDMO offering drug formulation & manufacturing

Manager – cGMP Training and Learning Programs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBend, OR, USANo salary listed

About the Job

Requirements

  • Thorough understanding of FDA, EU, ICH, and cGMP training requirements.
  • Strong knowledge of Quality Management Systems.
  • Experience designing qualification and competency programs.
  • Experience working in a GMP facility.
  • Strong presentation and facilitation skills.
  • Exceptional organizational and project management skills.
  • Ability to influence personnel across all organizational levels.
  • Strong analytical and problem-solving capabilities.
  • Proficiency with Learning Management System platforms, Microsoft Office, and electronic quality systems.
  • A bachelor's degree in Life Sciences, Education, Organizational Development, Quality, Engineering, or a related discipline is required.
  • A minimum of 5–8 years of experience in pharmaceutical, biotechnology, medical device, or CDMO environments is required.
  • A minimum of 3 years of experience managing GxP training programs or quality systems is required.
  • Experience supporting client audits and regulatory inspections.
  • Experience administering electronic learning management systems.
  • Demonstrated understanding of cGMP regulations and personnel qualification requirements.
  • Must be able to lift up to 15 pounds at a time.
  • Must be authorized to work for an employer in the United States.

Responsibilities

  • Manage and continuously improve the organization's GxP Training Program to ensure personnel are trained, qualified, and capable of performing assigned responsibilities in compliance with applicable regulatory requirements and internal Quality Management System procedures.
  • Oversee training governance, curriculum development, learning management systems, training compliance, employee qualification programs, training effectiveness assessments, and inspection readiness related to personnel competency.
  • Serve as the site subject matter expert for GxP training requirements and partner with all functional departments to establish sustainable training programs that support clinical and commercial manufacturing operations.
  • Lead and develop the Training department, provide mentoring, coaching, and professional development for technical staff, provide performance evaluations, and handle employee discipline in accordance with company policy.
  • Establish departmental goals aligned with organizational quality and operational objectives.
  • Conduct performance reviews and ensure staff maintain appropriate training and GMP qualifications.
  • Foster a culture of quality ownership, compliance, and continuous improvement.
  • Oversee the daily workflow of the department.
  • Own and maintain the corporate GxP Training Program.
  • Develop and maintain training policies, procedures, and governance practices.
  • Ensure training processes comply with applicable GxP regulations and industry requirements.
  • Establish systems supporting employee onboarding, qualification, retraining, and continuing education.
  • Monitor organizational training health and compliance.
  • Manage training coordinators and training administrators as applicable.
  • Provide guidance and support to departmental trainers and subject matter experts.
  • Develop training governance and site-wide training standards.
  • Support qualification of trainers and training owners.
  • Establish departmental objectives and performance metrics.
  • Lead continuous improvement initiatives within the training function.
  • Maintain and optimize electronic Learning Management System processes.
  • Ensure training assignments are current, accurate, and aligned to job responsibilities.
  • Oversee user access, curricula management, and training workflows.
  • Partner with Information Technology and system administrators on system validation, upgrades, and enhancements.
  • Ensure data integrity and inspection readiness of training records.
  • Develop and maintain role-based training curricula for all cGMP functions.
  • Ensure curricula accurately reflect required competencies and job functions.
  • Collaborate with department leaders to define qualification requirements.
  • Periodically assess training requirements to ensure continued effectiveness and compliance.
  • Support creation of learning paths for new and existing employees.
  • Develop and maintain personnel qualification programs.
  • Ensure qualification requirements are documented and consistently applied.
  • Establish qualification standards for critical GMP activities.
  • Coordinate qualification and requalification activities.
  • Monitor ongoing competency requirements.
  • Establish mechanisms to evaluate training effectiveness.
  • Develop tools to assess employee comprehension and competency.
  • Monitor trends related to human error and training-related deviations.
  • Collaborate with management to identify performance gaps and targeted learning opportunities.
  • Drive continual improvements to training methodologies.
  • Manage GMP onboarding programs for new employees.
  • Ensure timely completion of required training prior to independent work.
  • Coordinate cross-functional participation in onboarding activities.
  • Standardize onboarding processes across departments.
  • Maintain training records in a state of continuous inspection readiness.
  • Support client audits, internal audits, and regulatory inspections.
  • Coordinate retrieval and presentation of training records during inspections.
  • Ensure training-related observations are addressed through effective remediation plans.
  • Partner closely with Quality Systems personnel to ensure appropriate training support for the Quality Management System and ensure training impacts are appropriately assessed and implemented when quality systems change.
  • Develop and maintain training performance metrics and dashboards.
  • Provide routine reporting to leadership and Management Review.
  • Promote a culture of ownership, accountability, and compliance.
  • Develop educational programs that strengthen quality culture across the organization.
  • Identify opportunities to improve learning effectiveness and employee engagement.
  • Support implementation of modern adult-learning principles and workforce development strategies.
  • Adhere to consistent and predictable in-person attendance.

About the Company

Serán BioScience

CDMO offering drug formulation & manufacturing

Serán Bioscience is a contract development and manufacturing organization that helps pharmaceutical companies develop and manufacture drugs. It offers preformulation, formulation and dosage-form development, spray drying and particle engineering, plus cGMP manufacturing and analytical quality control. It relies on flexible, client-tailored services and a broad technical toolkit to support a range of clients from startups to large pharma. Its goal is to enable efficient, compliant drug development and production with rigorous quality standards.

Company size
51-200
Company stage
Growth Equity (Venture Capital)
Total funding
$200M
Headquarters
Bend, OR
Founded
2016

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