Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.

Job purpose

The role will provide structured assistance across document management, complaints handling, reporting, and general administrative activities. Securing this support will improve operational efficiency, strengthen compliance, and enable QA professionals to focus on high-value quality and oversight responsibilities. The Quality Department operates in a highly regulated environment with increasing demands related to documentation, customer assurance, and quality reporting. QA administrative workload has grown significantly, particularly in areas such as complaints management, CMO scorecard development, and compliance checks.

Responsibilities

The Quality Associate support will initially provide approximately 20 hours per week of support across the following key areas

Document Creation and Execution Support

Preparation, formatting, and maintenance of QA documentation within Veeva
Coordination of document lifecycle activities including review and version control
Ensuring adherence to internal documentation standards

Complaints Management Support

Initiating and tracking of customer complaints
Supporting data entry, documentation, and follow-up activities
Assisting in maintaining audit-ready complaint records

CMO Scorecard Development

Supporting data collection and consolidation for CMO performance metrics
Assisting in the preparation and formatting of scorecards and reports
Maintaining consistency and accuracy in reporting outputs

Distribution and Quality Disposition Support

Coordinating distribution of quality-related documents and communications e.g. disposition returns
Supporting quality disposition processes and maintaining executed record logs e.g Temperature excursions
Facilitating communication between internal and external stakeholders as needed

Bona Fide Customer Checks

Conducting verification checks on customers
Maintaining accurate and traceable records of compliance activities
Supporting QA in meeting regulatory and internal compliance requirements

General Administrative Support (Ad Hoc)

Event and meeting organization
Additional administrative duties as required

Qualifications

Required Qualifications

Bachelor’s degree in Life Sciences, Biotechnology, Chemistry, Engineering, or a related scientific discipline
Approximately 5 years of hands-on experience in a life sciences Quality environment (biotech, pharmaceutical, medical device, or regulated healthcare industry)
Demonstrated experience supporting Quality Assurance (QA) and Quality Management System (QMS) activities
Strong working knowledge of GxP requirements (e.g., GMP, GDP) and regulated documentation practices
Proven experience with document creation, formatting, execution, and lifecycle management within an electronic document management system (e.g., Veeva Vault or similar)
Experience supporting complaints management processes, including documentation, tracking, and maintenance of audit-ready records
High attention to detail with the ability to maintain accurate, compliant, and traceable records
Strong organizational and time management skills, with the ability to manage multiple tasks and prioritize effectively in a part-time (approximately 20 hours/week) support role
Excellent written and verbal communication skills, with the ability to interact professionally with internal and external stakeholders
Proficiency with Microsoft Office tools (Word, Excel, PowerPoint), particularly for data consolidation, tracking, and reporting

#LI-HYBRID

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.

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 talentacquisition@cytokinetics.com

Please visit our website at: www.cytokinetics.com

Cytokinetics is an Equal Opportunity Employer

Contractor – Sr. Quality Associate

Job Description