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Quality Assurance And Document Control Specialist Jobs

Quality Document Specialist Jobs
By Bluebird Staffing At Florida, United States
$80,000 Salary plus Benefits (Paid Relocation)
First 4-6 weeks on-site, then remote
• A diverse clinical background and in depth knowledge of pathophysiology is a must.
*** Must relocate or live in the State of Florida! ***
Quality Document Control Specialist
By Elevation Labs At Idaho Falls, ID, United States

About Us What do we consider our greatest asset? Our passionate team members. With a vision of creating quality skincare and cosmetic products for the most popular brands in the world, our founders ...

Document Control Coordinator - Quality Assurance
By Transmedics Inc At , Andover, Ma $24.35 - $29.33 an hour
Documentation Management Database experience preferred
Familiarity with a Quality Management System or other regulated environment
Assist Document Control Manager with Document Control PLM system in support of other departments
3-5 years’ experience working in a regulated industry; Quality Control experience strongly preferred
Strong organizational skills with the ability to work with a high degree of accuracy
Attention to detail with exceptional proof reading and quality control skills
Quality Assurance Document Specialist - Pharmaceutical
By Integrated Resources, Inc ( IRI ) At Cincinnati, OH, United States
File management (e.g., SharePoint and Playbook)
Cincinatti, OH - Hybrid schedule (3 days onsite, 2 days remote)
Develop in-depth knowledge of departments research processes, policies, and procedures
Acquire knowledge of department organizational structure
Maintain entries to research process trackers and summarization of information for reporting to senior leadership
Assist in development and maintenance of PUBSTRAT Adimn guidance documents & training
Quality Systems Specialist (Exp In Capa, Document Control, Supplier Quality&Qms) - Remote
By MillenniumSoft Inc At Tempe, AZ, United States
Demonstrate expert QMS skills and knowledge.
Intermediate to advanced computer skills and software applications, including experience with Microsoft Office tools (Outlook, Word, Excel, PowerPoint).
Works within the designated QMS element in accordance with process and procedural requirements.
Intermediate to advanced organizational and administrative skills.
Basic working knowledge of the regulations.
Bachelor’s Degree in a related area / technical field or comparable years of experience.
Document Control Specialist (Mdc Specialist) - Abiomed
By Johnson & Johnson At Danvers, MA, United States
Ensure that approved compliance policies, procedures and requirements are implemented or in place, as appropriate.
Review and collaborate with content creators to ensure their projects, programs or marketing activities consistently meet compliance requirement standards.
Bachelor's Degree and minimum of 2 years of experience or 5 to 7 years equivalent work experience.
Strong organizational skills; must be detailed-oriented.
Must have powerful editing/proofreading skills.
Results driven, self-motivated, and solutions-oriented ability to manage assigned tasks in an assertive, efficient, and timely manner.
Document Control Specialist, Quality Assurance
By Hays At Ladson, SC, United States
• Report on the progress of scanning project at appropriate daily management meetings.
Document Control Specialist, Quality Assurance – Contract – Ladson, SC – $10.00-$18.00/hr.
Our Client is seeking a Document Control Specialist, Quality Assurance in Ladson, SC .
• Responsibility over the conversion of 3000+ legacy hard copy quality records into digital file format.
• Work with a digital scanner, Microsoft Office & outlook to support the file conversion handling activity.
Nervous about an upcoming interview? Unsure how to write a new resume?
Quality Assurance / Document Control
By Sciecure Pharma Inc. At , Monmouth Junction, 08852, Nj
Assist in the timely completion of Quality Assurance tasks and responsibilities.
Use and manage Quality spreadsheets, tracking sheets and checklists.
Entry level candidate with some experience in Quality Department (QC or QA).
3 years of prior work experience in a Biotechnological, Pharmaceutical, or Clinical environment is required.
Superior attention to detail with strong organizational skills.
Become proficient in the following internal systems and activities: SOP's, Change Controls, Deviations, Corrective Actions, Training records, and record retention.
Quality Assurance Engineer (Section 508 Document Compliance Specialist)
By Criterion Systems, Inc. At , Remote
Required Experience, Education, Skills & Technologies
Preparing and testing documents to ensure compliance with Section 508 requirements.
Familiarity with alt text, tagging, color contrast, and the requirements of compliance and how to meet them.
Ensure all documents, capabilities, tools and work-flows are 508 compliant.
Demonstrated experience providing accurate 508 compliant documents
Strong interpersonal, communication, and customer service skills
Quality Specialist - Calibration, Document And Complaint Management
By Neogen At , , Mn
Manage the timely in-flow of customer complaints, the assignment of investigation responsibilities, and expedient processing and closure.
Manages complaints associated with multiple manufacturing sites.
Manages calibration due dates to ensure equipment does not become overdue.
Perform complaint analysis and summarize complaint investigation.
Work closely with investigators to ensure thorough and accurate investigations and drive the initiation of CAPAs when appropriate.
Coordinate the communication of investigation data to corresponding divisions as applicable.
Marketing Document Control Specialist (Mdc Specialist) - Abiomed
By Johnson & Johnson At , Danvers, Ma
Ensure that approved compliance policies, procedures and requirements are implemented or in place, as appropriate.
Review and collaborate with content creators to ensure their projects, programs or marketing activities consistently meet compliance requirement standards.
Bachelor's Degree required and 2 years’ experience preferred.
Strong organizational skills; must be detailed-oriented
Must have powerful editing/proofreading skills.
Results driven, self-motivated, and solutions-oriented ability to manage assigned tasks in an assertive, efficient and timely manner.
Quality Assurance/Document Control Specialist
By Sorenson Forensics At , Salt Lake City, 84115, Ut
Minimum 2 years experience working in a Quality environment within an ISO accredited company.
You will also be uploading your resume and other certification documents you might hold.
We are excited to meet you and learn more about your qualifications.
Perform document control and distribution of controlled documents using Sorenson Forensics electronic database.
Update and maintain company documents, policies, and necessary forms to ensure company documents remain accurate and current.
Perform maintenance to ensure the quality and functionality of lab equipment and reagents.
Document Control And Training Specialist (Remote)
By The Geneva Foundation At , $47,800 - $65,000 a year
Collect and consolidate input from SMEs, management, and other team members to ensure compliant documents in the document management system
Actively participate in change management committee meetings; participate in continuous improvement initiatives
Minimum 2 years of relevant experience in a similar position
Experience in writing technical documents and procedures
Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects
Must have demonstrated competence in use of computing equipment with strong working knowledge of Microsoft Office 365 Suite
Quality Assurance/Quality Control (Qa/Qc) Associate And Document Control
By Inspired Spine Enterprise LLC At , Burnsville, 55337, Mn
Ability to exercise independent judgment and employ basic reasoning and self-management skills.
Proof-read and edit documents for Quality Management System
Complete training and documentation as required for Quality Management System to maintain compliance with FDA and ISO regulations
Attention to detail is a critical skill for this position
Work with specialized software/system to administer document control
Scan, Maintain and Organize certificates and records from deliveries, manufacturing and inspection
Associate Document Quality Specialist (Contractor)
By Amicus Therapeutics At , , Nj
1-4 years of experience at a pharmaceutical company or CRO is required.
Experience in the quality checking of regulatory submission documents
High attention to detail, advanced writing and speaking competency, and excellent organizational skills
Must have the ability to prioritize, manage time well, multitask, and troubleshoot
Positive and proactive communication skills, strong interpersonal and customer service skills, and the ability to work independently
Preferred location is Remote (with a hybrid work approach).
Quality Assurance Document Control
By Intellectt Inc At Philadelphia, PA, United States
Includes review of material status, protocol conformance, clinical design layout, ensuring blinding techniques are followed.
Exercises sound judgment and analytical in thought
Challenges status quo and initiates improvements
Quality Specialist, Document Control
By West Pharmaceutical Services At , Scottsdale, 85260, Az
Experience with Medical Device Product Development Life Cycle Activities, Verification / Validation Activities, Risk Management, DHF Activities
Preferred Knowledge, Skills and Abilities:
Review documents for accuracy & completeness, including data verification activities to cGMP requirements.
Minimum 3-5 years of experience in regulated Quality Assurance / Quality Control
Relevant work history and/or experience may be considered in lieu of degree.
Experience with managing Document Control activities within a regulated industry
Quality Specialist, Document Control, Gsc, Houston Tx/Or Us Remote
By Baker Hughes At , Houston, 77073, Tx
At least 5 years of experience in technical writing/documentation
Excellent oral and written communication skills with strong command of the English Language
Highly proficient writing skills including grammar, punctuation, spelling, formatting, etc.
Additional elected or voluntary benefits
Processing and publishing documentation in accordance with QMS procedures.
Managing workflow activities and role mapping with business leads.
Quality Assurance Associate Ii - Document Control
By Seagen At , Bothell, Wa $71,000 - $92,000 a year
Knowledge of physical and electronic Document Management workflows and principles
Experience with applicable software (e.g., Learning Management System, electronic Quality Management System, data analytics, etc.)
Process documents in electronic Document Management System
Back-up the Records Management job function as required
Participates in cross-functional teams to implement, update, or upgrade systems or processes related to the management of GMP records
Participates in continual improvement activities within Document Control and GMP Records management
Sr. Quality Assurance Specialist - Training And Document Control
By PBS Biotech At Camarillo, CA, United States
Support the company’s efforts for CGMP qualification and ISO Certification.
Provide assistance to internal and external customers in support of departmental functions related to Training and Quality Management Systems.
Help manage document control processes and systems for compliance with internal procedures and policies as well as regulatory requirements.
Help oversee the creation and management of document format and content templates.
Help establish and maintain records management system including secure storage, retrieval, retention, and destruction.
Support the deployment, maintenance, and continuous improvement of electronic Learning Management Systems (LMS) and Electronic Document Management System (EDMS).