Current jobs related to Quality Assurance Manager - Cambridge - Tenneco Inc.
-
Quality Assurance Operations Manager
2 hours ago
Cambridge, Massachusetts, United States R&D Partners Full timeJob DescriptionThe Quality Assurance Operations Manager plays a vital role in ensuring the quality of drug products manufactured by external Contract Manufacturing Organizations. This position requires a strong understanding of Good Manufacturing Practice (GMP) regulations and the ability to work collaboratively with cross-functional teams.Main...
-
Director of Quality Assurance Management
4 weeks ago
Cambridge, Massachusetts, United States Marengo Therapeutics, Inc. Full timeAbout the RoleThis is an exciting opportunity for a seasoned quality professional to join our team as Director of Quality Assurance Management. As a key member of our operations team, you will be responsible for establishing and maintaining appropriate development phase GMP/GLP compliance. Your expertise in material/product disposition activities, testing...
-
Quality Assurance Specialist
3 hours ago
Cambridge, Massachusetts, United States RadNet Full timeJob Title: Quality Assurance SpecialistJob Summary:The Quality Assurance Specialist at RadNet supports the organization's Quality Management System in product maintenance, development, and growth.Key Responsibilities:Lead document management, including configuration management.Manage the complaint management process, including investigations and customer...
-
Quality Assurance Operations Manager
10 hours ago
Cambridge, United States R&D Partners Full timeJob DescriptionJob DescriptionOverview The Manager of Quality Assurance Operations will work within the DP / CMC / Alliance QA Operations team and is responsible for providing support to all GMP aspects of drug product (DP) manufacturing, CMC and alliance management. This role will work cooperatively with their counterparts in Quality Operations to...
-
Manager GMP Quality Assurance
1 week ago
Cambridge, United States Beacon Hill Life Sciences - Boston Full timeJob DescriptionJob DescriptionOur Client is searching for a dynamic Manager GMP QA – Clinical to join a growing QA team. Looking for someone who cares about this important work, and who’s driven to connect to our mission of helping these patient communities. The Manager GMP QA Clinical will be responsible for supporting and maintaining high quality...
-
Quality Assurance Lead
3 weeks ago
Cambridge, Massachusetts, United States Third Rock Ventures Full timeKey ResponsibilitiesThe Quality Assurance Lead will be responsible for developing and implementing quality assurance procedures to ensure that all analytical methods and data meet regulatory requirements. This includes overseeing CDMOs for phase-appropriate analytical method development, qualification, validation, and transfer for in-process testing, drug...
-
Quality Assurance Professional
5 days ago
Cambridge, Massachusetts, United States Voyager Therapeutics Full timeJoin Our TeamVoyager Therapeutics is a rapidly growing biotech company looking for a Quality Assurance Specialist to join our team. This is an exciting opportunity to be part of a dynamic organization that is making a difference in the field of gene therapy.The successful candidate will have a strong background in quality assurance and compliance, with a...
-
Quality Assurance Lead
3 weeks ago
Cambridge, Massachusetts, United States Jobot Full timeWe are seeking a seasoned professional to fill the role of Senior Director of Quality Assurance (GMP) and lead our quality assurance efforts.The estimated salary for this position is approximately $180,000 per year, reflecting the industry standard and the specific requirements of this role.Your key responsibilities will include:Developing and implementing...
-
Quality Assurance Manager
4 weeks ago
Cambridge, Massachusetts, United States Disability Solutions Full timeJob OverviewWe are seeking a highly skilled and experienced Senior CAPA Manager to join our team at Disability Solutions. As a key member of our Patient Safety and Quality organization, you will be responsible for managing and leading cross-functional teams in driving CAPA activities from issue identification to closure.In this role, you will manage project...
-
Senior Manager Quality Assurance Operations
2 weeks ago
Cambridge, Massachusetts, United States Marengo Therapeutics, Inc. Full timeAbout Marengo Therapeutics, Inc.Marengo Therapeutics is a pioneering biopharmaceutical company dedicated to developing innovative therapeutics that activate the right immune response to promote lifelong protection against cancer. Our team is passionate about making a meaningful difference in the lives of patients and their loved ones.Job OverviewWe are...
-
Director of Quality Assurance Biotechnology
3 weeks ago
Cambridge, Massachusetts, United States Jobot Full timeJob SummaryWe are a publicly traded biotechnology company developing innovative treatments for chronic dermatological diseases. Our team is seeking a seasoned Senior Director of Quality Assurance (GMP) to provide expert guidance on quality oversight for our clinical development programs and manufacturing processes.The ideal candidate will have extensive...
-
Quality Assurance Manager
3 weeks ago
Cambridge, Maryland, United States Interstate Corrpack LLC Full timeJob Title: Senior Quality Control SpecialistAbout the RoleWe are seeking a highly skilled and experienced Senior Quality Control Specialist to join our team at Interstate Corrpack LLC in Cambridge, MD. This is an exciting opportunity for a motivated professional to take on a challenging role that will involve managing day-to-day quality operations,...
-
Validation and Quality Assurance Professional
3 weeks ago
Cambridge, Massachusetts, United States WHITE COLLAR TECHNOLOGIES INC Full timeAbout the RoleWe are looking for a talented Validation and Quality Assurance Professional to join our team at White Collar Technologies Inc. As a key member of our team, you will play a crucial role in ensuring the quality and compliance of our services.The salary for this position is $90,000 - $115,000 per year, depending on experience.Job DescriptionIn...
-
Senior Quality Assurance Leader
5 days ago
Cambridge, Massachusetts, United States Amylyx Pharmaceuticals Inc Full timeAs a leader in the pharmaceutical industry, Amylyx Pharmaceuticals Inc is committed to delivering innovative solutions to address complex medical challenges. We are seeking a talented Senior Quality Assurance Leader to join our team and drive excellence in quality management.This role will be responsible for developing and implementing quality management...
-
Senior Quality Assurance Lead
3 weeks ago
Cambridge, Massachusetts, United States Jobot Full timeAbout the RoleWe are seeking a highly experienced GMP Quality Director to join our team. As a key member of our quality leadership group, you will provide strategic direction and oversight for our quality assurance programs, ensuring compliance with regulatory requirements and industry standards. Your primary focus will be on supporting the development and...
-
Director, GxP Quality Assurance
1 week ago
Cambridge, United States AIRNA Full timeCOMPANY OVERVIEWAIRNA is a biotechnology company with a mission to transform lives, one RNA edit at a time. AIRNA is pioneering the discovery and development of RNA editing therapeutics to realize the therapeutic potential of base editing for patients with rare and common diseases. RNA editing modality is poised to lead the next generation of RNA...
-
Director, GxP Quality Assurance
1 week ago
Cambridge, United States AIRNA Full timeCOMPANY OVERVIEWAIRNA is a biotechnology company with a mission to transform lives, one RNA edit at a time. AIRNA is pioneering the discovery and development of RNA editing therapeutics to realize the therapeutic potential of base editing for patients with rare and common diseases. RNA editing modality is poised to lead the next generation of RNA...
-
Quality Assurance Professional
7 hours ago
Cambridge, Massachusetts, United States Voyager Therapeutics, Inc. Full timeThe Quality Assurance Specialist will actively contribute to the implementation and maintenance of our company's Quality Systems Manual. This position is responsible for conducting GMP compliance audits as directed, with oversight of GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing...
-
Quality Assurance and Compliance Specialist
3 days ago
Cambridge, Massachusetts, United States Proclinical Staffing Full timeQuality Assurance and Regulatory ComplianceWe are seeking a highly skilled Clinical Trial Quality Oversight Specialist to join our team at Proclinical Staffing.Key Responsibilities:Review and implementation of regulatory requirements.Development of quality policies and procedures.Collaboration with internal stakeholders to ensure quality standards are...
-
Clinical Quality Assurance Expert
1 day ago
Cambridge, Massachusetts, United States LanceSoft Full timeJob OverviewLanceSoft is seeking a highly skilled Clinical Quality Compliance Specialist to join our team. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of compliance and quality in our clinical trial delivery systems.Key ResponsibilitiesLead the clinical trial delivery system inspection readiness...
Quality Assurance Manager
1 week ago
'Own Your Career' supports Tenneco's People Model, ensuring that we both "Select the Best" and "Build & Develop" internal talent.
It is our commitment to develop and promote great talent within the Tenneco team.
JOB TITLE:
Quality Assurance Manager
LOCATION NAME:
Cambridge, Ohio
REPORTS TO:
Plant Manager
DEPARTMENT:
Quality Department
SUMMARY OF POSITION:
Plans and manages the activities in the quality assurance and process engineering areas. Coordinates plant technical activities based upon quality and process requirements.
Directly or indirectly supervises exempt and non-exempt employees in the quality department. Provides technical support and quality assurance to a $20 MM per year facility. Budgetary responsibilities include $500 M per year in labor/benefits.
PRINCIPAL ACCOUNTABILITIES:
- Select, train, supervise, and evaluate staff.
- Allocate personnel and financial resources within area to achieve plant and divisional goals and objectives.
- Act as a liaison between ceramic development and the plant to bring laboratory developments into production while evaluating and engineering compliance to quality and productivity targets.
- Act as liaison between product engineering/assembly plants and local production/quality personnel to ensure engineering developments are production ready and at statistically capable levels.
- Determine appropriate corrective actions and process engineering improvements to correct shortcomings in quality.
- Develop and maintain the plant's quality management system in compliance with ISO 9000 / IATF 16949.
- Produce and maintain quality manual and aid affiliate plants as required.
Minimum Educational Requirements:
- Bachelor's degree in Ceramics, Engineering, or similar degree or equivalent knowledge in quality assurance.
- Certified manager of quality/organizational excellence through ASQ.
- ISO 9000 and/or IATF 16949 lead auditor.
Minimum Experience Requirements:
- 5 years of experience in quality control, process control, or engineering capacity.
- Industrial or automotive experience (tier 1 or OEM experience).
- 3 years minimum of demonstrated ability to create positive change.
- Ability to directly or indirectly manage and develop professionals.
- Gauging and gauge tracking experience.
- Utilizing APQP Process.
- Process improvement in reducing scrap (e.g., ceramic powder, bent bores, defects and decorating, Isostatic pressing, firing ceramics and decorating process).
- Reducing defects and working with internal and external customers.
- Excellent verbal and written communication skills.
- Excellent interpersonal relationship skills.
- Union shop experience preferred.
- Dimensional Control Engineering background preferred.
- Expert with implementation and execution of IATF 16949 (ISO a plus).
- Experience using Plex Quality System Modules or similar.
- Bulk process experience.
We are committed to the safety and health of our employees. We adhere to protocols, ensuring a safe work environment for all.
#J-18808-Ljbffr