Über
Newark, DE, United States
Join Hologic as a
Quality Engineer
in a regulated medical device environment, responsible for ensuring products, processes and systems meet internal quality requirements and external regulatory standards (e.g., FDA, ISO). The position supports Operations, Engineering and R&D, focusing on defect prevention, continuous improvement, and robust manufacturing practices.
Knowledge
Quality Management Systems (QMS) for medical devices
GMP, GDP principles and basic regulatory frameworks
Medical device Quality System Regulations (21 CFR 820), ISO 13485, MDD (beneficial)
Risk management, risk assessments and documentation updates
Nonconformance (NCE), CAPA, SCAR, MRB processes
Inspection, testing and validation methods for products and processes
Statistical analysis and scientific method (beneficial)
Basic understanding of microbiology, molecular biology, biochemistry, chemistry, or related fields (beneficial)
Nucleic acid amplification and detection technologies (beneficial)
Company quality system requirements and standards
Skills
Strong computer literacy: word processing, spreadsheets, databases
Ability to develop and implement procedures, inspection procedures and test methods
Excellent technical writing; able to produce clear quality reports and detailed procedures
Ability to read, analyze and interpret technical procedures, standards, journals and regulations
Effective presentation and communication skills
Good interpersonal skills; able to work with all levels, including in potentially adversarial situations
Familiarity with Oracle and Agile systems (beneficial)
Certified Quality Engineer (beneficial)
Behaviors
Models and champions quality values and best practices
Acts with urgency in identifying and resolving quality issues
Uses sound judgment within defined procedures and practices
Focuses on defect prevention, reduction of variation and waste, and continuous improvement
Maintains productive internal and external working relationships
Stays current with industry and technical developments through literature review
Works independently on routine tasks, seeking guidance for new or complex assignments
Engages proactively in cross-functional forums (MRB, NCE, CAPA, SCAR) and regulatory interactions
Experience
2-5 years with Bachelor's degree; 1-2 years with Bachelor's in a technical field; 0-2 years with a Master's degree
Working in regulated environments, ideally FDA-regulated or medical devices (beneficial)
Supporting Operations, Engineering and R&D in product and process development
Participating in audits and inspections (facility, supplier, Notified Body, FDA)
Handling nonconformances, complaints, root cause analysis and corrective actions
Reviewing and approving ECOs, product changes, verification/validation and sustaining engineering documentation
Why join Hologic?
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
The annualized base salary range for this role is $97,600-$152,700 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
Agency and Third-Party Recruiter Notice
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
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Sprachkenntnisse
- English
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