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Form of workJob Description
QA LABEL SPECIALIST
SUMMIT, NJ
SUMMIT, NJ
Shift Sun-Wed 1pm to 11pm.
100% Onsite.
Pay ranges between $40.00 - $46.00 an hour.
Required Skills:
- Bachelor's degree or equivalent .
- Minimum of 1 year of relevant labeling experience in a cGMP/FDA regulated environment .
- Some document management experience .
- Crystal reports experience preferred .
- Strong communication and customer service skills.
- 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) .
- Develop and improve label issuance processes to drive operational efficiency .
- 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 be able to complete tasks independently and communicate with manager on decisions outside of established processes and the ability to build an internal network .
- To succeed in this role, you will have a strong attention to detail and an analytical mindset.
Project Description:
- The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, including the coordination, issuance, reconciliation, and management of production labels and records.
- Supports all activities for the Quality Assurance Label Control group.
- Responsible for issuing clinical and commercial in-process and final product labels for labeling operations.
- Responsible for ensuring accurate printed information on labels in compliance with health authority requirements.
- Coordinates with production teams to ensure timely issuance of labels.
- Performs training of label control and issuance requirements for internal personnel as needed.
- Ensures standard operating procedures (SOPs) related to job responsibilities define the steps necessary to complete tasks, etc. Writes, reviews and updates SOPs as required.
- Carries out plans and actions to support new drug product launches, new market and other quality management activities as assigned.
- Provides support during internal and health authority inspections and audits of facility.
- Knowledge of quality processes, including label control and issuance, change control, product complaints, deviations, investigations and CAPA management.
- Performs supplemental investigations/projects as required by Management.
- Maintains knowledge of current GMPs and regulatory guidelines.
- 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.
This 6+ month position starts ASAP.
Please E-MAIL your resume (attachment to email) with rate and availability to Supriya: supriya@AlphaConsulting.com
ALPHA'S REQUIREMENT #23-00791
W2 ONLY MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE
