Current jobs related to Quality Assurance Engineer - Mahwah - Impact Business Group Inc
-
Associate Engineer, Quality Assurance
2 weeks ago
Mahwah, United States The Judge Group Full timeOur client is currently seeking a Associate Engineer, Quality Assurance or a 12 month + contract. Medical device experience is highly preferred.Read, Understand, Document and Approve PPAPUnderstand and Approve FAI, DCP, PFMEA, IGS and Mfg. ProceduresAbility to articulate with SuppliersAbility to investigate nonconformances and CAPAs with suppliersKnowledge...
-
Quality Assurance Specialist
7 days ago
Mahwah, New Jersey, United States Actalent Full timeJob SummaryWe are seeking a highly skilled Quality Assurance Engineer to join our team in Mahwah, NJ. As a key member of our organization, you will be responsible for ensuring the quality and integrity of our products.
-
Quality Assurance Engineer
2 weeks ago
Mahwah, NJ, United States Joulé Full timeJob Title: Quality Assurance Engineer Location: Mahwah, NJ Type: Contract Responsibilities The role must follow clearly defined procedures and tasks as well as defined guidelines to aid in decision making for maintain engineering quality. Requirements Read, Understand, Document and Approve PPAP Understand and Approve FAI, DCP, PFMEA, IGS...
-
Quality Assurance Engineer
4 weeks ago
Mahwah, United States Impact Business Group Inc Full timeOur client, a Global Leader in the Medical Device Industry has an immediate opening for a Quality Assurance Engineer (QMS Specialist) for a 12 month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail-oriented Top...
-
Quality Assurance Engineer
3 weeks ago
Mahwah, United States Impact Business Group Inc Full timeOur client, a Global Leader in the Medical Device Industry has an immediate opening for a Quality Assurance Engineer (QMS Specialist) for a 12 month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail-oriented Top...
-
Quality Assurance Engineer
2 weeks ago
Mahwah, United States Actalent Full timeDescription Read, Understand, Document and Approve PPAP Understand and Approve FAI, DCP, PFMEA, IGS and Mfg. Procedures Ability to articulate with Suppliers Ability to investigate nonconformances and CAPAs with suppliers Knowledge on Supply chain, Operations and Production Knowledge on any PLCM ( OnePLM, Windchill, SAP) Knowledge on any Production Software...
-
Specialist, Quality Assurance
1 month ago
Mahwah, United States The Judge Group Full timeOur client is currently seeking a Specialist, Quality Assurance for a 12 month + contract.Candidates MUST be fluent in English and French.Prefer candidates that can work a hybrid schedule in Mahwah, NJ but open to remote if they meet all of the qualifications. Primarily responsible for facilitating document and product related changes in accordance with...
-
Mahwah, New Jersey, United States Impact Business Group Inc Full time**Quality Assurance Engineer Role at Impact Business Group Inc**At Impact Business Group Inc, we offer a unique opportunity for a highly skilled Quality Assurance Engineer to join our team. This 12-month contract position will be based in a globally renowned medical device industry leader. With a focus on quality and regulatory compliance, you will have the...
-
Senior Quality Assurance Specialist
4 weeks ago
Mahwah, United States Joulé Full timeJob SummaryWe are seeking a skilled Quality Assurance Specialist to join our team at Joulé. As a key member of our quality assurance department, you will play a critical role in ensuring the highest standards of quality in our products and services.About the RoleThis is a contract-to-hire opportunity for a Quality Assurance Associate II who will work on...
-
Biopharmaceutical Quality Assurance Lead
2 weeks ago
Mahwah, New Jersey, United States Joulé Full timeJob OverviewJoulé is seeking a highly skilled Biopharmaceutical Quality Assurance Lead to join our team. In this role, you will be responsible for ensuring compliance with regulatory agency requirements and implementing quality control measures.
-
Quality Assurance Specialist
2 weeks ago
Mahwah, New Jersey, United States Joulé Full timeJob TitleQA Associate IIAbout the RoleWe are seeking a highly skilled QA Associate II to join our team at Joulé. As a key member of our quality assurance department, you will be responsible for supporting daily tasks that are essential for maintaining and improving quality systems and adhering to client-specific procedures.Key ResponsibilitiesDocument...
-
Laboratory Quality Assurance Manager
4 weeks ago
Mahwah, New Jersey, United States Joulé Full timeJob OverviewJoulé is seeking an experienced Laboratory Quality Assurance Manager to oversee the quality of our analytical laboratory operations.About the RoleThis key position will be responsible for ensuring compliance with regulatory agency requirements, enforcing a quality culture throughout the department, and maintaining audit readiness within the...
-
Quality Assurance Associate
3 weeks ago
Mahwah, United States Kelly Full timeJob DescriptionKelly Science is seeking a Quality Assurance Associate to join a growing company located in Mahwah, NJ for a 6+ month contract. Pay: $26-28/hourShift: Monday-Friday 8am-5pmEmployment Type: Full Time: 6+ month contract Job Duties Include:\tReviewing all incoming batch records (including controlled substances) to ensure compliance with...
-
Senior Quality Assurance Specialist
4 weeks ago
Mahwah, New Jersey, United States The Judge Group Full time**The Judge Group: A World-Class Staffing Solutions Provider**We are seeking a highly skilled and experienced Senior Quality Assurance Specialist to join our team. This is a fantastic opportunity to work with a renowned staffing solutions provider.About the Role:This 12-month + contract position will be based in Mahwah, NJ, with flexibility to work remotely...
-
Manufacturing Quality Manager
6 days ago
Mahwah, New Jersey, United States Actalent Full timeResponsibilitiesDevelop and implement quality control processes to ensure compliance with industry standards and regulationsCollaborate with cross-functional teams to identify and resolve quality issuesConduct regular audits and inspections to ensure adherence to quality standardsRequirementsBachelor's degree in Engineering or related fieldMinimum 5 years of...
-
Engineering Process Lead
7 days ago
Mahwah, New Jersey, United States Actalent Full timeAbout the RoleThe Quality Assurance Engineer will be responsible for developing and implementing quality control processes to ensure compliance with industry standards and regulations. This role requires a strong understanding of engineering principles and a keen eye for detail.
-
Associate Supplier Quality Engineer
2 weeks ago
Mahwah, United States Ledgent Technology Full timeWe are seeking an Associate Supplier Quality Assurance Engineer for a project with our client, which is a medical device manufacturer in Mahwah, NJ. Pay Rate Range: $33.33/hr. - $43.33/hr.Description/Comment:Read, Understand, Document and Approve PPAPUnderstand and Approve FAI, DCP, PFMEA, IGS and Mfg. ProceduresAbility to articulate with SuppliersAbility to...
-
Manufacturing Quality Engineer
2 weeks ago
Mahwah, United States Kelly Science, Engineering, Technology & Telecom Full timeManufacturing Quality Engineer • Location: Mahwah, NJ• Type: W2 contract (NO C2C OR THIRD PARTY)• Length: Until 1/2026 (Contract extension expectation)• Pay Rate – $40 - $48 hourly depending on experience• Work Authorization - Must be able to work in the U.S. with approved authorization status.What You'll Do:Read, Understand, Document and Approve...
-
Quality Assurance Manager
7 days ago
Mahwah, New Jersey, United States Joulé Full timeJob Summary:We are seeking a highly skilled QC Micro Lab Supervisor to join our team at Joulé. As a key member of our Quality Control (QC) Microbiology department, you will be responsible for overseeing daily operations, ensuring compliance with cGMP requirements, and driving process improvements. If you have a strong background in microbiology and...
-
Associate Engineer, Manufacturing Engineering
2 months ago
Mahwah, United States The Judge Group Full timeOur client is currently seeking a Associate Engineer, Manufacturing Engineering for a 12 month + contract. ****HYBRID****This function will be directly supporting the EUMDR project on Site.Requirements: • Education and Special Training Required: Bachelor's Degree in Engineering or relevant field of study Qualifications and Work Experience Required • 1-3...
Quality Assurance Engineer
1 month ago
Our client, a Global Leader in the Medical Device Industry has an immediate opening for a Quality Assurance Engineer (QMS Specialist) for a 12 month + Contract. Our client offers results-driven people a place where they can make a difference - every day You will also have the opportunity to work with other like-minded, self-directed and detail-oriented Top Talents in an extremely collaborative and professional environment.
Primarily responsible for facilitating document and product related changes in accordance with our clients change management procedures and relevant regulatory requirements for medical devices.
Fluent in English and French
Key Responsibilities:
Facilitate the change management process for document and product related changes.
Perform administrative activities related to Stryker's learning management system.
Assist with the migration of QMS related documentation from local document management systems to PLM system (Windchill).
Ensure QMS documentation reflects actual business activities while remaining compliant with applicable internal and external regulatory requirements including but not limited to Site, Division, Corporate, FDA, ISO, MDD, MDR and individual country requirements.
Drive Good Manufacturing Practices and Good Documentation Practices.
Identify and implement improvement opportunities to increase the efficiency and effectiveness of the QMS and associated documentation.
Develop and deliver training for QMS areas of expertise.
Engage with IT team in relevant PLM system discussions.
Qualifications:
BS in a science, engineering, business or related discipline.
Minimum of 3 years experience in a regulated industry using electronic document/change management systems preferred. Knowledge / competencies
Fluent in English and French
Proficient in Microsoft applications including but not limited to Word, Excel, Power Point, etc.
Thorough knowledge and understanding of US and International Medical Device Regulations.
Strong knowledge of Quality Systems (CAPA, audits, Management Review, Quality Planning, etc.)
Ability to plan, organize, and implement multiple concurrent tasks.
Strong interpersonal skills, written, oral communication and negotiations skills. Must demonstrate the ability to effectively communicate up/down and across different levels of the organization.
Analytical and problem-solving capabilities with the ability to draw insights from data quickly and to define executable actions.
Demonstrated ability to work in cross-functional team environments.
Basic understanding of compliance risk situations.