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New · posted Oct 15

Cytokinetics · Pharmaceuticals

Manager, Quality Systems - GxP Training

  • South San Francisco, CA
  • Hybrid
  • Contract
  • Manager
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Deadline

Open until filled

The role

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.

The Manager of GxP Training, Quality Systems supports the administration, development, and continuous improvement of the company’s GxP training program. This role manages and executes assigned day-to-day GxP training activities, ensuring that training assignments, curricula, systems, and learning materials remain accurate, effective, and aligned with regulatory requirements, business needs, and established departmental priorities.

As a GxP Training subject matter expert, the Manager contributes to the development and implementation of learning initiatives across multiple delivery methods, including instructor-led training, virtual training, eLearning, and system-based training.

This position reports to the Senior Manager, Quality Systems, GxP Training and supports the execution of the company’s broader GxP training strategy.

What you need

  • Bachelor’s degree in life sciences, business, education, communications, technical writing, or a related field, or an equivalent combination of education and relevant experience.
  • 6+ years of combined experience in GxP Training, Document Control, Quality Systems, or related functions in the biotechnology or pharmaceutical industry.
  • 2+ years of recent experience administering Veeva Vault Training.
  • Working knowledge of GxP regulations, quality systems, and GxP training compliance requirements.
  • Strong technical writing, presentation, and facilitation skills,  with the ability to communicate complex information clearly and accurately.
  • Strong project management, communication, and stakeholder management skills.
  • Excellent organizational skills, with strong attention to detail and ability to manage multiple priorities and work effectively in a fast-paced environment.
  • Able to develop engaging and compliant training, as well as delivering training to employees at all levels of an organization.
  • Demonstrated curiosity and interest in continuous learning, with the ability to research and evaluate relevant industry trends and evolving best practices and apply or recommend them, as appropriate.
  • Experience supporting regulatory inspections, internal audits, and customer audits.
  • Experience monitoring training metrics, contributing to continuous improvement initiatives, and inspection readiness.

Preferred Experiencenice to have

  • Education, certification, or practical experience in instructional design, adult learning, learning and development, or related discipline.
  • Familiarity with eLearning and video-based training tools such as Articulate 360, Camtasia, or similar authoring platforms.
  • Experience translating regulatory requirements and technical concepts into practical, learner-focused training materials.

What you'll do

  1. Execute assigned goals and initiatives that advance the continuous improvement of GxP training processes, standards, and business practices.
  2. Ensure GxP functional roles and associated curricula are appropriately targeted, relevant, and routinely reviewed for accuracy and compliance.
  3. Create, review, and refine GxP functional training assignments, learner roles, and curricula, and recommend opportunities for improvement to the Senior Manager.
  4. Develop or contribute to clear and effective GxP training materials using instructor-led, virtual, and eLearning formats, as appropriate.
  5. Collaborate with GxP and non-GxP departments to align training objectives and activities where responsibilities overlap.
  6. Monitor open GxP training assignments, coordinate follow-up activities, and report training metrics.
  7. Exercise judgment when interpreting existing procedures and administering the GxP LMS and associated training processes within established procedures and delegated authority.
  8. Partner with IT and business stakeholders to ensure training systems support user and organizational needs.
  9. Collaborate with Document Control to promote effective integration and consistent user experience across the EDMS and LMS.
  10. Support inspections, audits, and responses to training-related observations or requests.
  11. Manage assigned projects and deliverables based on established timelines and priorities.
  12. Ensure training processes remain inspection-ready and compliant with applicable FDA, EMA, ICH, and other GxP regulatory requirements.
  13. Provide Document Control coverage, as needed.

Pay

Cytokinetics didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.  

Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.

Where you'll work

South San Francisco, CAHybridOpen in Maps (opens in a new tab)

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Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers

Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.

Here are some ways to check for authenticity:

  • We do not conduct job interviews through non-standard text messaging applications

  • We will never request personal information such as banking details until after an official offer has been accepted and verified

  • We will never request that you purchase equipment or other items when interviewing or hiring

  • If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at [email protected]

Job intelligence

The context around this role

Live data · October 15, 2026

Salary intelligence

How the pay compares

Manager roles in California25 roles publishing pay

Middle half $156,000 to $181,000, median $165,500

Manager roles in the US105 roles publishing pay

Middle half $126,000 to $167,500, median $153,000
Annual base pay
Annual base payLowMedianHigh
California$156,000$165,500$181,000
All US$126,000$153,000$167,500

Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Cytokinetics's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $79K median227 open
  2. One step back

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $123K median353 open
  3. This role

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $153K median136 open
  4. Next step

    Director

    Often: Director, Quality · Associate Director, Clinical Quality Assurance

    $209K median114 open
  5. Later

    VP & Executive

    Often: Vice President, Quality Assurance · AVP

    $302K median15 open

Skills DNA

What this role leans on

How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 16 linesLab testing and methods: 1 lineDocumentation and SOPs: 8 linesQuality systems and risk: 6 linesData and digital systems: 1 lineCollaboration and leadership: 23 linesGMPLab testingDocumentationQuality systemsData systemsTeamwork
  • Collaboration and leadership23
  • GMP and compliance16
  • Documentation and SOPs8
  • Quality systems and risk6
  • Lab testing and methods1
  • Data and digital systems1

Company hiring pulse

Cytokinetics on Regulatory Jobs

12
Open roles
11
Distinct roles
2
Locations

By discipline

  • Regulatory6 50%
  • Quality4 33%
  • Compliance & Safety2 17%

By level

  • Director5 42%
  • Manager5 42%
  • Senior & Principal2 17%
See all 12 Cytokinetics roles

More roles at Cytokinetics

All 12 Cytokinetics roles

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Manager, Quality Systems - GxP Training at Cytokinetics

Open until filled.

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    Manager, Quality Systems - GxP Training at Cytokinetics — South San Francisco, CA | Regulatory Jobs