43 Senior Quality Associate Jobs in Billerica, MA
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Senior Quality Associate
$103k-124k (estimate)
Full Time
4 Weeks Ago
Sorry! This job is no longer available. Please explore similar jobs listed on the left.
Azenta Life Sciences is Hiring a Senior Quality Associate Near Billerica, MA
Company OverviewAt 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 industry's 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.
How You’ll Add ValueThe Senior Quality Associate, CRS will provide quality assurance support for Customer and Regional sites. They will be expected to comply with, enforce, and be held accountable for GxP Practices and Quality Control Procedures.
What You’ll Do
Azenta Life Sciences participates in E-Verify®, and will provide the United States Federal Government with your form I-9 information to confirm you are authorized to work in the United States. For more information, please visit E-Verify® at www.dhs.gov/E-Verify. E-Verify® is a registered trademark of the U.S. Department of Homeland Security.
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 industry's 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.
How You’ll Add ValueThe Senior Quality Associate, CRS will provide quality assurance support for Customer and Regional sites. They will be expected to comply with, enforce, and be held accountable for GxP Practices and Quality Control Procedures.
What You’ll Do
- Independently schedule and host client audits and respond to audit findings in a timely manner.
- Conduct internal audits for all North American Azenta Life Sciences facilities, including regional and client sites.
- Assists with implementation and improvement of quality system globally within Azenta Life Sciences through gap analysis and remediation – as needed.
- Routinely reviews and approves equipment validation documents – such as temperature mapping, calibration, alarm validations, etc.
- Compiles the Management Review Meeting Presentation, including interpretation of data, charts, etc.
- Reviews Change Request for Global Operations
- Provides direction and leadership to ensure compliance with GxPs, ISO 9001, federal and local guidelines and regulations at Customer and Regional Sites.
- Provides regional QA support, as needed
- Acts as system administrator in Qualtrax®.
- Four-year degree, preferred Life Sciences/ Engineering
- 4 years’ experience in Quality Assurance
- Experience performing internal audits
- Experience with ISO 9001
- Strong analytical skills and the ability to think creatively
- Excellent leadership skills and the ability to work across the organization
- Strong communication, interpersonal, and collaborative skills
- Demonstrated high level of initiative and the ability to work independently
- Proficiency in Microsoft Office Products
- Experience in GxP facility preferred
- Experience with Continuous Improvement initiatives preferred
- Experience with project management preferred
- Six Sigma certification preferred
- May work with potentially infectious materials.
- Responsible for maintaining a clean work environment and enforcing and following Universal Precautions for bloodborne pathogens when working in areas considered to be potentially contaminated
- As an Equal Opportunity Employer, we do our utmost to ensure that there is no discrimination or bias against anyone applying for a job or in any phase of employment for reasons related to race, color, religion, gender, national origin or ancestry, age, disability, veteran status, military service, sexual orientation, genetic information, or gender identity.
Azenta Life Sciences participates in E-Verify®, and will provide the United States Federal Government with your form I-9 information to confirm you are authorized to work in the United States. For more information, please visit E-Verify® at www.dhs.gov/E-Verify. E-Verify® is a registered trademark of the U.S. Department of Homeland Security.
- The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
Job Summary
JOB TYPE
Full Time
SALARY
$103k-124k (estimate)
POST DATE
06/03/2024
EXPIRATION DATE
06/22/2024
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