Quality Systems & Document Control Specialist
The Davis Companies
The Davis Companies in Massachusetts, Burlington, is seeking a motivated Document Control & Quality Systems Coordinator to join our manufacturing quality team. You will manage controlled documents, coordinate corrective actions, support internal and external audits, and ensure ISO 9001 (ISO 13485 preferred) compliance. This on-site role offers a clear path for growth in a fast‑paced industrial environment with strong emphasis on precision and traceability. #J-18808-Ljbffr The Davis Companies
- Target PR Range: 25-35/hr DOE Document Control Specialist, Quality Summary: This rolewill work closely with members of the Document Control team and... ...in document control and electronic document management systems. Strong attention to detail and organizational skills,...Quality
$30 - $34 per hour
Document Control Specialist - Quality (CR/511742) Bedford, Massachusetts Salary: USD30 - USD34 per hour A biotech organization located in Bedford, MA... ...in Document Control and Electronic Document Management systems Strong attention to detail and organizational skills Ability...QualityHourly payMonday to Friday$80k - $100k
...Determines how to improve and maintain the change control system and associated processes by means of lean and operational... .... to ensure the appropriate changes are properly documented and implemented. Manages the quality manual system document facilitation working cross...Quality- ...The desired candidate will have prior documentation experience, preferably in a medical device company. Specific... ...limited to: filing; copying and scanning of Quality documentation in an effective and efficient filing system to ensure accuracy and immediate availability...QualityImmediate start
- Planet Pharma seeks a Document Control Specialist, Quality, to support document management lifecycle at our Bedford, MA site. The role emphasizes issuing... ...and collaboration with internal teams to uphold quality systems and regulatory standards. #J-18808-Ljbffr Planet PharmaQuality
- Tandym-Group is assisting a biotech client in Bedford, MA to hire a Document Control Specialist - Quality to manage controlled documents and archival within a GxP environment. The role focuses on SOP adherence, document reconciliation, and preparation for audits, with a...QualityMonday to Friday
- ...Clinical Document Management Specialist IV A Few Words About Us - Integrated Resources, Inc is a premier... ...centers on delivering only the best quality talent, the first time and every time... ...of Electronic Document Management Systems Advanced computer proficiency Demonstrated...QualityFlexible hours
- ...Document Control Specialist Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic... ...batch records (80-90%) Will work in SharePoint document system, Trackwise, and SAP program. Will pull the batch...Work at office
$160k - $195k
...target muscle and the central nervous system (CNS) to address the root cause of disease... ....Role Summary:The Associate Director, Quality Management Systems is a key member of... ...for key elements of the QMS including document control, records management and training ensuring...QualityLocal area$27 - $29 per hour
...Document Processing Specialist BerryDunn is currently seeking a Document Processing... ..., document management systems, and collaboration tools to... ...adhere to company policies, quality assurance standards, and... ...revisions, and implement version control measures to ensure...QualityHourly payWork at office- ...Dyne Therapeutics, based in Waltham, MA, seeks an Associate Director, Quality Management Systems to design and scale a global QMS for commercial operations. You will own document control, records management, and training, ensuring systems are inspection-ready and aligned...Quality
$85k - $200k
...are valued, seen, and heard. How you’ll make an impact: The Quality Systems role is responsible for managing the operational... ...Kymera’s Quality Management System, with primary ownership of document control, training program management, and quality systems compliance...QualityWork at office- ...creativity.Position Summary:The Manager, Quality Management Systems & Validations is responsible for... ...Actions (CAPAs), and Change Controls) as well as the continuous improvement... ...approval of validation protocols and documentation.Working cross-functionally with other...QualityLocal area
- ...engineering, manufacturing, field service, and marketing. You will manage the software library, ensure documentation integrity, and drive lean improvements to the change control system. The role requires a Bachelor’s degree and at least 3-5 years in document management or change...
$41.3k - $51.6k
...responsible for monitoring and maintaining the accuracy, integrity, and quality of Advancement's alumni and donor records. Accurate and... .... Testing of new and existing database integration systems and features. Research records for special lists and report...QualityFull timeWork at office$170k - $218k
...The Role The Director of Quality Assurance will oversee GMP QA operations for both internal... ...Agenus electronic Quality Management System (eQMS) platform and systems and enable compliant electronic and paper-based document control and archiving for the Agenus Enterprise...QualityContract work- ...in Bedford, MA is seeking a senior QA leader to manage the Quality Management System and Validation programs. The role ensures compliance with... ...functional teams. You will oversee Deviations, CAPAs, Change Controls, and QA Validations, drive continuous improvement, and...Quality
$30 - $40 per hour
...Quality Assurance Specialist (Entry-Level) Location: Burlington, MA and Cambridge, MA... ...reviewing and verifying Quality Control (QC) data, ensuring documentation accuracy, and supporting batch... ...initiatives related to quality systems and documentation processes....QualityFull timeContract workTemporary work- ...QA Documentation Associate A Few Words About Us Integrated Resources,... ...on delivering only the best quality talent, the first time and every... ...of the Company Quality Systems and apply it in their daily... ...cataloging and filing of Quality Controlled data and documents....Quality
- Werfen is seeking a QS Specialist I to support the Quality Management System, ensuring GMP compliance and FDA/ISO standards adherence. You will assist CAPA... ...organization. Responsibilities include maintaining quality documents, tracking metrics, and coordinating with affiliates...Quality
$103.5k - $162.69k
...that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionTitle: Manager, Quality Systems & Data Analytics, R&D GMP QualityLocation: Lexington, MAAbout the role:As a Manager, Quality Systems & Data Science, you will play...QualityMinimum wageTemporary workLocal area$93k - $160k
...electromechanical medical devices. This role helps oversee our Quality Management System and provides Quality Engineering support across... ...SOPs, work instructions, forms, test protocols, and other controlled documents Support document control and records management...Quality- Werfen is seeking a Quality Systems Specialist I to assist in planning, coordinating, and improving the Quality Management System to ensure GMP, FDA and ISO compliance. You will support CAPA, audits, quality agreements, and management review activities under supervision...Quality
- Responsible for maintaining quality standards for Ocular’s pharmaceutical and medical... ...associated with Supplier Quality Management, Document Control, Training, Internal Auditing, and... ...reporting to the Sr. Director of Quality Systems and Compliance. Principal Duties and...QualityFull time
$68.9k - $131.1k
...ahead of tomorrow’s threat. Our team solves tough, meaningful problems that create a safer, more secure world.The Raytheon Quality Management System (QMS) is a collection of business processes focused on consistently meeting customer requirements and enhancing customer...QualityTemporary workWork experience placementWork at officeRemote workFlexible hours- ...Plates). Will also be responsible for documenting, computing, compiling, interpreting, reviewing... ...and/or implementing changes in controlled documents. Must learn and comply with safety... ...procedures, building monitoring systems and laboratory log books. Skills: Lab experience...QualityWork experience placementInternship
- ...seeking a detail-oriented and motivated Quality Associate to join our team. In this... ...clients. Key Responsibilities: ~1. Document Control & Data Governance ~ Lifecycle... ...administration of the Document Control system, including the formatting, routing, and...QualityTemporary workInternshipWork at office
$77k - $86k
...Job Summary: The Quality Assurance (QA) Specialist supports the effectiveness... ...of the Quality Management System (QMS) by coordinating key... ...procedures Manage the Documents of External Origin program... ...Initiate, revise, and review controlled documents including SOPs,...QualityHourly payWork at officeFlexible hours$185k - $209k
...diseases of the central nervous system and the eye that are caused... ...: The Associate Director, Quality Systems will support the development... ...releases and manage Change Controls for configuration changes to... ...inspections (back-room document management) Possess a flexible...QualityTemporary workFlexible hours- ...role: We're looking for a passionate Systems QA Test Engineer to join our QA team within... ...from testing activities to measure the quality of the product. Identify tools, fixtures,... ...industries. Experience testing motion control equipment, motors, sensors, vision systems...QualityFull time
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