Senior Training Manager, Quality Assurance

Posted 2 Days Ago
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Sioux Falls, SD, USA
In-Office
Senior level
Biotech • Pharmaceutical • Agriculture
The Role
Develop, implement, and continuously improve GxP training and personnel qualification programs. Manage LMS/eQMS training systems, ensure inspection readiness, create role-based curricula and competency frameworks, link training to quality systems (deviations, CAPA, change control), and drive cross-functional compliance and training effectiveness.
Summary Generated by Built In
The Senior Training Manager-QA is responsible for the strategic development, implementation, and continuous improvement of the company’s GxP training and personnel qualification program to ensure compliance with current Good Manufacturing Practices (cGMP) and global regulatory requirements. This role oversees the design and execution of training systems, curricula, and qualification processes to ensure that all personnel are appropriately trained, qualified, and competent to perform their roles.
The Senior Training Manager partners cross-functionally with Quality Assurance, Manufacturing, Quality Control, and other departments to ensure training programs are aligned with regulatory expectations, quality system requirements, and business objectives. This position plays a critical role in inspection readiness by ensuring training programs are risk-based, role-specific, effective, and fully compliant.
Duties and Responsibilities (Responsibilities include but are not limited to):
  • Lead the development and continuous improvement of the company’s GxP training and personnel qualification program, ensuring alignment with regulatory requirements and internal quality standards
  • Oversee and administer training systems (LMS/eQMS), ensuring accurate training assignment, tracking, compliance, and data integrity across all functions
  • Ensure inspection readiness of all training programs, including leading training-related activities during regulatory inspections and audits and defending training processes
  • Establish and maintain role-based training curricula and competency frameworks, including training effectiveness strategies and performance-based qualification
  • Drive cross-functional collaboration and continuous improvement, ensuring training programs are integrated with quality systems (deviations, CAPA, change control) and aligned with business and regulatory expectations
Supervisory Duties:
  • This position does not have supervisory responsibilities.
Education/Experience/Skills:
  • BS/BA in life sciences, education, or related field required
  • Minimum of 3-5 years of experience in a regulated (GxP) environment, with significant experience in training, quality systems, or personnel qualification programs
  • Demonstrated experience developing and managing training programs in a pharmaceutical or biotech environment
  • Strong knowledge of cGMP requirements, regulatory expectations (FDA, EMA), and applicable training requirements (e.g., personnel qualification)
  • Experience with Learning Management Systems (LMS) and/or electronic Quality Management Systems (eQMS)
  • Strong understanding of quality systems (e.g., deviations, CAPA, change control) and their linkage to training
  • Demonstrated knowledge of quality risk management principles (ICH Q9) and their application to training programs
  • Proven leadership and cross-functional collaboration skills
  • Strong analytical skills, including the ability to trend data and evaluate training effectiveness
  • Excellent communication and presentation skills
Working Environment and Travel:
While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee must regularly lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus.
Normal office environment with some exposure to lab areas. The noise level in the working environment is usually moderate.
Occasional travel may also be expected, as needed.
ADA: 
The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.
SAB BIO is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. SAB BIO is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets
 

Skills Required

  • BS/BA in life sciences, education, or related field
  • Minimum of 3-5 years experience in a regulated (GxP) environment with significant experience in training, quality systems, or personnel qualification programs
  • Demonstrated experience developing and managing training programs in a pharmaceutical or biotech environment
  • Strong knowledge of cGMP requirements and regulatory expectations (FDA, EMA)
  • Experience with Learning Management Systems (LMS) and/or electronic Quality Management Systems (eQMS)
  • Strong understanding of quality systems (deviations, CAPA, change control) and linkage to training
  • Knowledge of quality risk management principles (ICH Q9) and application to training programs
  • Proven leadership and cross-functional collaboration skills
  • Strong analytical skills, including trending data and evaluating training effectiveness
  • Excellent communication and presentation skills
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The Company

What We Do

SAB Biotherapeutics is a biopharmaceutical company that operates pharmaceutical sites focused on high-standard bovine care. The company manages specialized livestock husbandry and executes pharmaceutical protocols, such as plasmapheresis, to produce therapeutic bioproducts, ensuring optimal animal welfare and operational efficiency across its facilities.

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