About this opportunity
Scorpion Therapeutics lists this Manager, Quality Engineering Product Surveillance opportunity in marlborough, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Role
Lead Quality Engineering Product Surveillance to enhance product quality, investigate issues, and drive continuous improvement within a biopharma manufacturing context.
Key Responsibilities
Managing complaint handling systems.
Leading cross-functional investigations.
Implementing CAPA.
Analyzing complaint metrics.
Fostering a culture of accountability and operational excellence.
Collaborating with Engineering, Manufacturing, and Customer teams to resolve complex quality challenges.
Maintaining ISO 9001 compliance.
Focus on complaint investigation, CAPA, root cause analysis, and continuous improvement in a biopharma production setting, with an emphasis on customer-centric quality resolution.
Requirements
Bachelor's in Engineering, Life Sciences, or related field.
7+ years in Quality Assurance with at least 3 years in leadership.
Deep knowledge of ISO 9001, complaint management, root cause analysis, and QMS.
Experience with electronic quality management systems, audits, and cross-functional stakeholder engagement.
Preferred
Proficiency with business software including Salesforce.
Strong communication and technical writing skills.
Additional Details
Work setup and travel details are not specified.
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Worksite address
marlborough, MA, 01752, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.