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Form of workI'm a recruiting consultant with Artech and I'm hoping I can help you find the perfect next opportunity for your career goals. You very well could be happy in your present role, but might be looking for a more challenging project or maybe you want to explore opportunities outside your comfort zone. I am currently recruiting for a QA Associate Specialist – Document Control for one of the largest Pharmaceutical companies in the US. Below are the specs for the role:
Job description:
Job Title: QA Associate Specialist – Document Control
Location: Bothell, WA
Duration: 12 months
Rate: $44/hr
Job Description: Job Title: Quality Assurance Document Control (QADC) Associate Specialist
Location: Bothell, WA*Onsite
Top Skills:
- 1 to 3 years of Document Control experience in a regulated environment
- 1 to 3 years of EDMS Experience(Veeva or similar Electronic Doc Management System)
- 1 to 3 years with MS Office 365(Specifically Word styles and formatting)
**PLEASE DO NOT SUBMIT CANDIDATES THAT HAVE PREVIOUSLY BEEN DISQUALIFIED FOR THIS ROLE**
PURPOSE AND SCOPE OF POSITION:
The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, including the document change control process, issuance and reconciliation of batch records, batch related forms, product labels, and management of archival and retention of GMP records.
REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:
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
DUTIES AND RESPONSIBILITIES:
Primary responsibilities include:
• 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
WORKING CONDITIONS (US Only):
Employees holding this position will be required to perform job-related duties supporting the Manufacturing Operations, related to batch documentation to support the various Manufacturing shifts. Weekend and off-shift support may be required.
Additional Job Requirements
Click “APPLY” to send your resume for this role or you can send an email to me at Garvita.Sharma@artech.com. You can also reach me directly at 973.933.4852.
Artech has been an employer-of-choice for 27 years, proudly serving over 80 Fortune 500 companies. We have dedicated professionals that will help you with your next career move. Our recruiters will listen carefully to your career goals and then match your skills and aspirations to various open roles. There is nothing we are more passionate about than finding candidates a rewarding job that makes them happy. Artech is an EEO Employer.
