Job Opportunity Details

Job ID Specialty Geographic Location City State Recruiter
2205494 Laboratory Management/Supervisor Atlanta GA KA Recruiting

In HouseID:
KM
Recruiter Email: alisha@ka-recruiting.com

Job Description

This is a Laboratory Management/Supervisor Opportunity Only!

Please fill out the form below to contact a Coalition Partner about this job.

() -



Company Name: KA Recruiting
Recruiter Name: Alisha Dynan
Contact Phone: 617-746-2742

Job Title: Quality System Specialist

(Only QUALIFIED Healthcare Professionals accepted) Laboratory Management/Supervisor - Full-time Quality System Specialist needed right outside of Atlanta!

Currently looking to hire a results-oriented and experienced Quality System Specialist to join our team. In this position, you will play a key role reviewing all Device history record documentation to ensure compliance to all applicable regulatory standards. This will involve using your detail-oriented abilities and knowledge of standard concepts, practices and procedures to provide quality input. If you have a solid background working in a comparable manufacturing environment, and the analytical capabilities that this position requires, please submit your resume for some more information!

Quality Assurance System Specialist (Manufacturing Compliance | Systems QA)

Responsibilities: As a Quality System Specialist, you will be responsible for reviewing and approving al documentation for serological, chemical and biological evaluations to ensure product meets specifications prior to distribution. This will include evaluations completed on final, intermediate and raw material products and for filling, labeling and packaging operations. Specific duties for this manufacturing operations compliance role include, but are not limited to:
- Performing batch record review, product disposition and quality issue resolution to maintain the flow of products and documents to meet site objectives
- Ensuring accuracy, integrity and completion of every page, reconciliation, and product yield computation
- Identifying mistakes, oversights, and incomplete data on batch records and reporting batch record deficiencies to Manufacturing for correction
- Understanding regulatory requirements thoroughly, including domestic and international standards applicable to our company and the consequences of nonconformance
- Writing, standard operating procedures, change orders, document change requests, and corrective|preventive action requests
- Maintaining a thorough understanding of our company policies and basic understanding of activities of all company departments
Representing our Sr. Quality Operations Managers and| or Quality Operation Managers in a variety of forums, as deemed necessary
- Efficiently making quality decisions, to include determination of a quality deviation, Product hold and disposition, etc. based on the specific circumstances that could affect product quality

Qualifications: We are looking for a highly organized and detail-oriented Quality System Specialist who combines exceptional analytical and problem-solving skills with the ability to quickly drive solutions while maintaining positive relationships. In addition, you should be able to work independently to manage and prioritize workload and assignments within a fast-paced manufacturing environment. It is also vital to this role that you display excellent verbal and written communication skills, as well as the ability to effectively build working relationships both internally and externally at various organizational levels of the organization. Specific qualifications for this medical device quality assurance role include:
* Bachelor’s degree in a related scientific field
* 5+ years of experience in a comparable manufacturing environment to ensure sound judgment and performance
* Computer proficiency including, MS Office Suite
* Intermediate mathematics skills
* Knowledge of quality assurance practices within the medical device industry, including FDA Quality System Requirements (QSR) and ISO 13485, as well as Canadian Medical Devices Regulations, and In Vitro Diagnostics Directive
* Ability to adhere to Regulatory and Compliance Standard operating procedures
* Experience and|or certification as a medical technologist, preferred

Offering competitive compensation and complete benefits!
For more information, please submit your resume for review.




  lblReferrer

Our Services Are Unparalleled

Home Office

Main Street,
Washington, WV 26181
304-699-5426

Texas Office

Main Street,
Arlington, TX 76010
817-277-1763