Contractor – Sr. Quality Associate
Cytokinetics INC - Dublin, Dublin, Ireland
Posted Apr 20, 2026
Benefits
- Parental leave
- Not verified
- Non-birth-parent leave
- Not verified
- Family-building benefits
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- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
- Not verified
- Relocation assistance
- Not verified
- Childcare support
- Not verified
- Learning budget
- Not verified
- Verification
- Not verified last checked Jun 13, 2026
- Salary
- Not verified
- 401(k) match
- Listed Source: EMPLR_CONTRIB_INCOME_AMT. source Last checked Jun 13, 2026.
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Schedule
- Shift type
- Not verified
- Weekend work
- Not verified
Application
- Cover letter
- Not verified
- Assessment
- Not verified
- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Contractor – Sr. Quality Associate Dublin, Dublin, Ireland 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
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Apply link verified; last checked Jun 13, 2026.
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