A

August Bioservices

US-based CDMO for end-to-end drug development

Manager Training Program

Instructional Design & Curriculum DevelopmentConfirmed live in the last 24 hours
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in life sciences, engineering, education, organizational development, business, or a related field; equivalent relevant experience may be considered.
  • Five or more years of experience in pharmaceutical, biotechnology, medical device, or another regulated manufacturing environment, including at least two years in training, quality, operations, or a related leadership role.
  • Working knowledge of current Good Manufacturing Practice principles, controlled documentation, data integrity, deviations, corrective and preventive actions, change control, and inspection readiness.
  • Experience administering a learning management system and producing reliable compliance reports.
  • Demonstrated ability to design, deliver, and evaluate adult learning for technical and procedural content.
  • Strong written and verbal communication, facilitation, project-management, and cross-functional influencing skills.
  • Advanced degree or professional certification in instructional design, adult learning, quality, or organizational development.
  • Deep familiarity with Good Manufacturing Practice, Good Documentation Practice, FDA 21 CFR regulations, and EU regulations.
  • Experience supporting sterile, biologic, solid-dose, active pharmaceutical ingredient, packaging, laboratory, or warehouse operations.
  • Experience with electronic document management, quality management, and learning platforms.
  • Experience managing direct reports, external vendors, training budgets, or enterprise learning projects.
  • Ability to lift up to 25 pounds at times.

Responsibilities

  • Own and continuously improve the site training system, including governance, procedures, curricula, qualification pathways, metrics, and periodic review.
  • Ensure training assignments, completions, retraining, and qualification records are accurate, timely, traceable, and inspection ready.
  • Develop and maintain role-based learning plans for GxP, technical, safety, quality-system, and compliance requirements.
  • Partner with process owners and subject-matter experts to convert procedures, process changes, deviations, corrective and preventive actions, and regulatory commitments into effective training.
  • Oversee the learning management system and associated data integrity, access, reporting, and change controls, including eQMS administration for tracking training, such as MasterControl.
  • Establish standards for instructor-led training, on-the-job training, train-the-trainer programs, knowledge checks, practical demonstrations, and qualification sign-off.
  • Evaluate training effectiveness using assessments, observation, performance trends, deviation data, audit observations, and stakeholder feedback.
  • Provide training metrics and risk-based insights to site leadership and governance forums, and escalate overdue or ineffective training as appropriate.
  • Support internal audits, customer audits, and regulatory inspections by presenting the training system and retrieving supporting records.
  • Lead, coach, and develop training specialists, coordinators, instructional designers, and qualified trainers, where applicable.
  • Manage training vendors, materials, schedules, facilities, and budget within approved requirements.
  • Promote a culture of continuous learning, quality ownership, and right-first-time execution.
  • Meet training program outcomes for on-time completion of assigned training and retraining; timely qualification for new and transferred employees; training-record accuracy and audit readiness; effectiveness of curricula, trainers, and qualification methods; reduction in recurring errors or deviations linked to knowledge or skill gaps; and timely completion of training actions arising from changes, corrective and preventive actions, and commitments.
  • Sit for prolonged periods at a desk and work on a computer.

About the Company

August Bioservices

US-based CDMO for end-to-end drug development

August Bioservices is a US-based CDMO that provides end-to-end drug development and manufacturing from preclinical to commercial stages. It manages all steps in a single program, including research, development, testing, laboratory services, and sterile fill/finish, while following cGMP standards. It differentiates itself with a hybrid model that combines large-CDMO scale and capabilities with a strong focus on customer service and integrated workflows. Its goal is to help clients bring safe and effective drugs to market efficiently by delivering comprehensive development and manufacturing under one roof.

Company size
51-200
Company stage
Series B
Total funding
$88.6M
Headquarters
Nashville, TN
Founded
2017

Recently Posted Jobs

Explore more opportunities at August Bioservices

See more jobs