Ardelyx

Senior Quality Training Specialist

Ardelyx$119K — $145K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences, quality, education, or a related field with 8+ years of experience in Quality or training in pharmaceuticals/biotech.
  • Experience in developing and facilitating instructor-led or virtual training programs with strong engagement skills.
  • Knowledge of adult-learning principles with experience crafting training materials and assessments.
  • Understanding of GxP principles and Quality Management Systems related to training and compliance.
  • Experience with managing an electronic Learning Management System (LMS) and validated systems is preferred.
  • Strong communication, organizational, and project management skills with an ability to collaborate cross-functionally.
  • Analytical mindset with problem-solving skills and a focus on continuous improvement.

Responsibilities

  • Develop and facilitate various Quality training programs, including onboarding and recurring training.
  • Collaborate with subject matter experts to create effective training content and guide internal trainers.
  • Apply adult-learning principles to design impactful training experiences and assess their effectiveness.
  • Identify training needs and maintain training compliance across the organization.
  • Develop Quality Training documents in line with QMS requirements.
  • Implement process improvements for Quality Training and documentation systems as needed.
  • Analyze training metrics to assess compliance risks and suggest enhancements for training programs.
  • Support audits and inspections with necessary training documentation and subject matter expertise.

Benefits

  • 401(k) plan with generous employer match
  • 12 weeks of paid parental leave
  • Up to 12 weeks of living organ and bone marrow leave
  • Equity incentive plans
  • Health plans (medical, prescription, dental, vision)
  • Life insurance and disability coverage
  • Flexible time off policy
  • Annual Winter Holiday shut down
  • At least 11 paid holidays
Full Job Description
Description

Position Summary:

The Senior Quality Training Specialist is responsible for the development, administration, delivery, and continuous improvement of the Quality Training program within the Quality Management System (QMS). This role independently develops and facilitates training for employees across the organization and partners with Quality, functional subject matter experts, and business stakeholders to ensure employees have the knowledge and skills necessary to perform their responsibilities in accordance with applicable procedures, regulatory requirements, and Company standards.

The Senior Specialist serves as a key subject matter resource for Quality training processes with responsibility for training delivery, curriculum management, compliance monitoring, training effectiveness, and continuous improvement. This role requires a strong facilitator who can translate complex Quality and compliance concepts into clear, engaging, and practical learning experiences.

This position is hybrid-based requiring 2-3 days onsite in our Waltham, MA Headquarters.

Responsibilities:
  • Develop, coordinate, and facilitate instructor-led, virtual, and other Quality training programs, including onboarding, recurring QMS training, and training associated with new or revised processes, procedures, and systems
  • Partner with subject matter experts to develop effective training content and learning materials and provide guidance and coaching to internal trainers to support consistent and engaging training delivery
  • Apply adult-learning principles and appropriate instructional techniques to create effective learning experiences and evaluate training effectiveness through assessments, feedback, observations, and performance metrics
  • Partner cross-functionally to identify training needs, maintain appropriate curricula, monitor training compliance, and ensure personnel training and qualification requirements are effectively implemented
  • Develop and maintain Quality Training procedures, work instructions, job aids, training materials, and other supporting documentation in accordance with QMS requirements
  • Identify and implement process improvements for Quality Training and GxP documentation systems in accordance with QMS requirements
  • Generate and analyze training metrics and trends to identify compliance risks, evaluate program effectiveness, and recommend and implement continuous improvement opportunities for training processes and systems
  • Support training-related investigations and CAPAs, internal and external audits, regulatory inspections, and other QMS activities by providing records, documentation, metrics, and subject matter expertise
  • Maintain current knowledge of applicable GxP requirements, regulatory expectations, industry practices, and learning methodologies, and recommend and implement opportunities to improve the effectiveness and efficiency of the Quality Training program

Qualifications:
  • Bachelor's degree in life sciences, quality, education/training, instructional design, business, or related discipline with 8+ years of experience in Quality, Quality Systems, training, learning and development, or a related function, within the pharmaceutical or biotechnology industry.
  • Demonstrated experience developing and facilitating instructor-led and/or virtual training, with strong presentation, facilitation, and audience-engagement skills
  • Strong knowledge of adult-learning principles and experience developing effective training materials, presentations, job aids, and knowledge assessments
  • Strong working knowledge of GxP principles, Quality Management Systems, and regulatory expectations related to employee training, qualification, documentation, and data integrity
  • Experience administering or supporting an electronic Learning Management System (LMS), including curricula, assignments, training records, compliance monitoring, and reporting; experience with validated/GxP systems preferred
  • Strong written and verbal communication, interpersonal, organizational, and project management skills, with the ability to collaborate and influence effectively across functions and organizational levels
  • Demonstrated analytical and problem-solving skills, attention to detail, and a continuous-improvement mindset, with the ability to manage multiple priorities independently and exercise sound judgment in a dynamic environment
  • Experience supporting audits, regulatory inspections, investigations, or CAPAs is preferred


The anticipated annualized base pay range for this full-time position is $119,000 - $145,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.

Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.

About Ardelyx

Ardelyx, Inc. is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of innovative, minimally systemic therapeutic agents that work exclusively in the gastrointestinal (GI) tract to treat GI and cardio-renal diseases. The company was founded in 2007 and is headquartered in Fremont, California.
Learn more about Ardelyx
Size
86 employees
Market Cap
$433.1 million
Industry
Net Income
-$94.3 million
Founded
2007
5 Year Trend
-20.6%
Revenue
$7.5 million
NASDAQ

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