Quality Associate
Quality Associate
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$ 55000 - 69000
1 Vacancy
Job Description
At Azenta new ideas new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
All we accomplish is grounded in our core values of Customer Focus Achievement Accountability Teamwork Employee Value and Integrity
Job Title
Quality AssociateJob Description
Position Title: Quality Associate
Location: South Plainfield New Jersey
Shift: M-F 9am-5pm
Intro
At Azenta new ideas new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
Azenta Life Sciences is a global leader in the life sciences space with headquarters in Burlington MA and offices and operations worldwide. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development clinical and advanced cell therapies for the industrys top pharmaceutical biotech academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis sample management and storage services informatics software and consumables with the largest installed base managing over 1 billion samples globally.
What Youll Do
- Review study records notebooks logbooks and electronic data for completeness accuracy and compliance to applicable SOPs.
- Coordinate corrections to laboratory documents and electronic data to ensure compliance with regulatory and in-house requirements.
- Conduct internal facility study and data audits.
- Provide support in customer audit preparation and documentation as needed.
- Monitor tracking systems such as instrument calibrations and maintenance and collaborate with relevant personnel or business units as appropriate.
- Support updates to various quality-related documents as required.
- Assist Senior QA personnel in applicable tasks related to the Quality System.
- Other duties as required.
What You Will Bring
- Bachelors Degree in Life Sciences or equivalent years of related work experience
- 1 years of experience in a GLP/cGMP environment
- Ability to react to situations with a sense of urgency and accountability
- Proficient in Microsoft Office especially Excel
- Strong verbal and written communications skills are essential
- Detail oriented with strong organizational skills
EOE M/F/Disabled/Vet
If any applicant is unable to complete an application or respond to a job opening because of a disability please email at for assistance.
Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race color age religion gender sexual orientation gender identity national origin disability or veteran status.
United States Base Compensation: $55000.00 - $69000.00The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience education (including licensure and certifications) qualifications performance and geographic location among other relevant business or organizational needs.
Required Experience:
IC
Employment Type
Full-Time
