Document Control Specialist

Document Control Specialist

12 May 2024
Washington, Bothell, 98011 Bothell USA

Document Control Specialist

Job Title: Document Control Specialist Location: Bothell, WA Hours/Schedule: Sunday - Thursday 10:00pm - 6:30am Compensation: $50.00 - $56.53/hr Type: Contract, Potential for extension or conversion to permanent Responsibilities

Issuing production batch records, labels, and other controlled documents to support manufacturing operations

Responsible for the organization of cGXP controlled document files within the Document Center and ensure that records are readily retrievable and sent off to final archive facility as needed.

Assist with managing the Document Center Archive room

Managing an electronic document system for the JuMP site which includes reviewing and approving document change requests, troubleshooting and and releasing documents to an effective state

May write and revise document control procedures including participating in the development and roll-out of document control tools

Follow Policies, SOPs and work instructions to support the document approval process, assign effective dates and training workflows, and archive documents and document change requests

Assist with cross-training of Document Control personnel and customers to ensure adherence with procedures

Execute the process and procedures for identifying, collecting, distributing and filing the controlled documents for the site

Support internal and external audits and regulatory inspections. This may require data gathering, interviewing or escorting auditors during the audit. Assist with document retrieval /organization support during regulatory inspections

Perform Document Control metric reporting and analysis for the local site data. This may require the use of relational databases and reporting tools to collate and analyze quality data

Provide communication as to the status of Quality Systems deliverables to customers, management and stakeholders

Requirements

Education:

Bachelor’s degree or equivalent

Experience Basic Qualifications:

Minimum of 1 year of relevant document control management experience in a cGMP/FDA regulated environment

Strong communication and customer service skills.

Some technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles

Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System)

Must demonstrate the following behaviors consistently: Innovative, proactive, and resourceful; committed to quality and continuous improvement

Able to prioritize, manage time well, multi-task, and troubleshoot effectively

Ability to work effectively and collaboratively at a fast pace with cross functional departments to finalize time-sensitive deliverables

Possess project management skills.

Experience interacting with FDA or other regulatory agencies strongly preferred

Strong knowledge of cGMPs and domestic regulatory requirements

Knowledge of manufacturing quality (manufacturing, packaging, facilities, critical systems, validation, etc.)

Must complete tasks independently, notify manager of decisions outside of established processes and the ability to build an internal network

Some labeling experience strongly preferred

Benefits

System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Related jobs

  • Innova Solutions is immediately hiring for a QA Associate Specialist - Document Control Position type: Full-time Contract Duration: 10 Months Location: Bothell WA 98021 (Onsite) As a QA Associate Specialist - Document Control, you will: Responsible for the organization of cGXP controlled document files within the Document Center and ensure that records are readily retrievable and sent off to final archive facility as needed. Assist with managing the Document Center Archive room Thorough Knowledge of Records Management, Scanning and organization functions Follow Policies, SOPs, and work instructions to support the document approval process, assign effective dates and training workflows, and archive documents and document change requests Experience Required: 5+ years of experience with the following: Library Science MS Office including Word, Adobe, Visio. Document Scanning experience. FDA Documentation & Compliance like 21 CFR Part 11/CGMP Ability to manage competing priorities. Accuracy and Attention to Detail Experience Basic Qualifications: Minimum of 5 - 8 years of relevant document control records management experience in a cGMP/FDA regulated environment Strong communication and customer service skills. Experience with Part 11 adherence regarding scanning of records and electronic archiving. Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System) Must demonstrate the following behaviors consistently: Innovative, proactive, and resourceful; committed to quality and continuous improvement Able to prioritize, manage time well, multi-task, and troubleshoot effectively Ability to work effectively and collaboratively at a fast pace with cross functional departments to finalize time-sensitive deliverables Possess project management skills. Strong knowledge of cGMP and domestic regulatory requirements Must complete tasks independently, notify manager of decisions outside of established processes and the ability to build an internal network Vinay Bhatiya Associate- Recruitment PAY RANGE AND BENEFITS: Pay Range: $48.00 - $52.00 per hour. Pay range offered to a successful candidate will be based on several factors, including the candidate\'s education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS:Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: One of Largest IT Consulting Staffing firms in the USA - Recognized as #4 by Staffing Industry Analysts (SIA 2022) ClearlyRated® Client Diamond Award Winner (2020) One of the Largest Certified MBE Companies in the NMSDC Network (2022) Advanced Tier Services partner with AWS and Gold with MS Website: 

  • Job Title: Quality Assurance Specialist

  • Looking at the challenges the world is facing today Philips’ purpose has never been more relevant. So, whatever your role, if you share our passion for helping others, you’ll be working towards creating a better and fairer future for all.

  • Job Title: Quality Assurance Specialist

  • Overview

  • Description

  • The VeriSight Clinical Specialist will represent our Philips’ VeriSight Pro 3D ICE (Intracardiac Echo Catheter), to Interventional Cardiologists and Electrophysiologists. Within Philips, this is an entirely new sales and clinical team to commercialize our groundbreaking new VeriSight Pro 3D ICE catheter. VeriSight is redefining how structural heart and EP procedures can be done. The first ICE catheter to miniaturize the same 3D imaging technology that powers TEE, VeriSight offers best-in-class 2D and 3D imaging.

Job Details

Jocancy Online Job Portal by jobSearchi.