Quality Records Specialist
NextPhase Medical Devices LLC
Job Description
Job Description
Job Summary:
The role of the Quality Control Technician is to perform and ensure the product documentation is complete, accurate and compliant to the ISO 13485 standards and FDA regulations.
Duties/Responsibilities
- Understand, support, and comply with the Company Quality System requirements.
- Maintain a safe and clean work environment.
- Follow the standard operating procedures and written work instructions.
- Openly communicate with the Company team members.
- Perform Device History Record (DHR) review for production and RGA products.
- Perform label inspection on product labeling.
- Generate product Certificate of Conformance (C of C) documents for production and RGA.
- Perform final acceptance of product before customer shipment
- Review sterilization process data and reports for compliance.
- Identify and support continuous improvement efforts with Supervisor.
- Take on special projects as assigned.
- Other duties as assigned.
Other duties
- Verifies work affecting quality independently and has the authority to perform these tasks as stated in the responsibilities section.
- Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
Qualifications:
- 3-5 years in a regulated manufacturing environment, experience in an ISO 13485:2016 manufacturing environment is preferred.
- Strong mechanical aptitude abilities.
- Ability to communicate effectively through oral and written communications.
- Ability to work with others collaboratively.
- Attention to detail to understand and meet the requirements.
- Strong organizational skills.
- Strong verbal communication skills.
- Demonstrated problem solving ability in a cross functional environment.
- Take responsibility for task and time management.
Physical Requirements:
This position requires working in an office setting. This includes sitting at a desk working on a computer
for long periods of time. It also could include lifting 40 pounds and standing for long periods of
time as well as walking the facility.
On-Site/Remote Attendance: This position requires 100% on-site attendance.
- Quality Systems Specialist II - Training processes and Learning Management System (LMS) Contract Client is a Medical Device company. Implementation... ...and communicate best practices to ensure training records are complete and accurate. Consult with Client's leaders,...SuggestedContract work
- ...Responsibilities Maintain Cosette Supplier Management Program under the direction of Supplier Quality Management Drive and maintain the Cosette Supplier Management Program to include supplier records and supplier CAPA Audits and reporting Risk assessments Create and update quality...Suggested
$60k - $68k
...Quality Assurance Professional If you are a Quality Assurance Professional looking for an opportunity to grow, Emerson has an exciting... ...Will Be: Review and verify technical document records to ensure they are in compliance with American Society of Mechanical...SuggestedWork experience placementLocal areaFlexible hours$60k - $68k
...If you are a Quality Assurance Professional looking for an opportunity to grow, Emerson has an exciting opportunity for you! We manufacture... ...WILL BE: Review and verify technical document records to ensure they are in compliance with American Society of Mechanical...SuggestedTemporary workWork experience placementLocal areaFlexible hours$70k - $80k
...Job Description Job Description Quality Assurance Specialist Are you passionate about pets? Do you have a strong eye for detail and enjoy... ...documentation. Maintain technical files, quality records, certifications, regulatory documentation, and supplier records...SuggestedWork at officeRemote work1 day per week- iAutomation in Franklin, Massachusetts, is seeking a Quality Coordinator to manage ISO 9001 documentation, calibration records, and compliance requests. The role focuses on maintaining records, coordinating multiple departments, and ensuring timely documentation flow. The...
$23 - $25 per hour
...Job Description Job Description HIV Services Quality Specialist (Administrative Assistant) Location: Case Management / Brockton COPE... ...Ability to manage multiple priorities and maintain accurate records • Strong critical thinking and problem-solving abilities...Flexible hours- Emerson Mansfield is seeking a Quality Assurance Professional to ensure ASME code compliance and maintain detailed documentation for customers in our Mansfield, MA facility. You will review records, approve supplier documentation, and coordinate with internal teams to...
- Jobtailor is seeking a quality assurance professional to maintain and drive the Cosette Supplier Management Program. The role focuses on CAPA audits, supplier records, and regulatory-aligned reporting, with cross-functional collaboration for supplier onboarding and ongoing...
- Emerson Mansfield is seeking a Quality Assurance professional to verify and document records ensuring ASME code compliance and internal QA standards. You will review supplier documentation and communicate across departments to resolve deficiencies while maintaining proper...
- Emerson Mansfield is seeking a Quality Assurance professional to review and verify technical records, ensure ASME code compliance, and prepare documentation packages that confirm customers receive exactly what they ordered. You will collaborate with multiple departments...
$22 - $27 per hour
...with AS9100 standardsFollow established procedures to support quality system updates and changesLearn and apply basic continuous improvement... ...team membersRecords ManagementMaintain and organize quality records (digital and physical) for accuracy and accessibilityEnsure...Work at officeLocal areaWorldwide- A healthcare consulting company is seeking a Quality Systems Specialist II to implement training processes and manage the Learning Management System (LMS). The ideal candidate will monitor training programs, support the development of procedures, and have a Bachelor’s...Contract work
$32.28 per hour
Our client, a leader in the food industry, is seeking a Quality Specialist to join their team. As a Quality Specialist, you will be part of the Quality Assurance department supporting food safety initiatives and compliance efforts. The ideal candidate will demonstrate...Temporary workShift work$94k - $151.8k
...our employees and recognize their merit. Job Function: Quality Job Sub Function: Supplier Quality Job Category: Professional... ...Synthes is recruiting for a Supplier Quality Performance Specialist. Johnson & Johnson announced plans to separate our...Local areaImmediate start$90k - $210k
We are seeking an innovative and highly motivated Senior Quality Validation Specialist, who will contribute significantly to the growth of the Cellares... ..., test protocols, CAPAs, deviations, change control records, and additional site based technical documentation and activities...- ...Key Responsibilities Quality Data, Analysis & Reporting Collect, analyze, and interpret quality and operational data to identify... ..., Systems & Compliance Maintain quality documentation, records, and improvement logs Support internal audits and quality system...
$42 - $52 per hour
...Description Provide quality oversight for manufacturing operations, ensuring compliance with cGMP regulations and internal procedures... ...and drug product batches. Review and approve batch production records, testing records, and manufacturing documentation. Support...Contract workTemporary work$90k - $210k
...We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This... ...and revise test methods Maintain required training and training records and provide training to qualify other associates Participate in...- Position Overview An entry level quality assurance position. Responsibilities include, but are not limited to: assisting with the organization... ...drafting/editing/routing; creation and completion of cGMP/GLP records and archival activities; and assisting QAU Management with...
- ...engaged in manufacturing and supply of soft gels and value-added manufacturing. As a Quality Assurance Associate, you will be responsible for... With Supervision, reviewing documents/records and providing batch release authorization to 3PL service provider for products...Work at officeLocal area
- Job Title: Quality & Food Safety Specialist Duration: 12 Month+ Contract Work Location: Bridgewater, NJ / HYBRID Work Schedule: FT / M-F 8am - 5pm Pay Rate: $25-28/Hour on W2 Job Description Our client is seeking a Food Safety & Quality Compliance Specialist to support...Contract work
$55k - $65k
Quality Assurance (QA) Associate Full Time Clerical Bridgewater, NJ, US 4 days ago Requisition ID: 1168 Salary Range: $55,000.00 To $6... ...role include the following: With Supervision, review documents/records and provide batch release authorization to 3PL service provider...Full timeContract workWork at office- An entry level quality assurance position. Responsibilities include, but are not limited to: assisting with the organization and implementation... ...drafting/editing/routing; creation and completion of cGMP/GLP records and archival activities; and assisting QAU Management with...Contract workRelocationShift work
- Our client in Massachusetts is seeking a Quality Specialist to join their team within the Quality Assurance department, supporting food safety initiatives and compliance efforts. The ideal candidate will have a strong scientific background, attention to detail, and proactive...
$71.7k - $83.2k
...about Careers at Organogenesis What You Will Achieve: The QA Specialist performs quality activities in support of new product production and... ...validation approvals. How You Will Achieve It: Review batch records and test records and perform final product inspection/...Temporary workFor contractorsImmediate startFlexible hours- ...Job Description Job Description Title: QA Associate, Quality Operations Location: Norton, MA Duration: 6months+ Pay: $4... ...production activities. Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents...
- ...Job Description Job Description Title: Quality Control Operations Analyst I Duration: 12 months Location: Norton MA This... ...supervision, following established SOPs Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely...Permanent employmentContract work
$50.47k - $63.09k
...Description R&D Partners is seeking to hire a Quality Control Analyst I in Norton, MA.... ...SOPs Maintain up-to-date training records, adhere to the testing schedule, and ensure... ...click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D...- Cellares is seeking a Senior Quality Validation Specialist at our Bridgewater facility to ensure quality assurance oversight of all validation processes. You will be responsible for approving complex documentation and maintaining standards in a GMP environment. Successful...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Records Specialist. Be the first to apply!


