What are the responsibilities and job description for the QC Technician position at Global Pharma?
Job Role: QC Technician
Job Location: Covington GA 30014
Hours/ Week: 40
Shift: 2nd Shift 3:00pm - 11:30pm OT
Shift: 1st shift 6 am - 2:30 pm OT
Job Description:
This position is responsible for ensuring the quality of products processed for Interventional Access Systems (BAS Kitting) at the client's office
The QC Technician will ensure that all procedures, inspection protocols, and specifications are adhered to in accordance with product requirements and meets visual, physical, and/ or dimensional requirements.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Performs visual, dimensional, and functional inspections on a wide variety of products in accordance with internal procedures and Product Specifications.
- Accurately prepares inspection paperwork and result in the documentation.
- Verifies Documentation of product lot records to ensure compliance with product specifications and good documentation procedures.
- Prepares non-conformance (MRR/Rejection) notices (where appropriate).
- Performs re-work functions in accordance with procedures and internal protocols
- Utilizes sampling plans to determine inspection levels for routine quality inspections
- Trains on all applicable procedures as it relates to the Quality Technician role
- Participates as needed as a quality representative for small team activities for process improvements
- Cross trains to provide quality control coverage as needed in support of business needs/ strategies.
- Other duties as applicable or assigned.
- Seen as a Champion of Quality as it relates to the execution of the QMS
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Have previous experience in a regulated environment (ISO, FDA) (preferred)
- Proficient in the use of personal computers with a basic level of keyboarding skills
- The ability to utilize measurement equipment (calibrated rulers & weights, calipers, etc. ) is a plus
- Must be detail-oriented
- Self-starter must be able to work independently with little direct supervision
- Responsible decision-maker, ability to reason and make sound decisions
- Experience with Continuous Improvement, Problem Analysis, Root Cause Investigation
- Understands Quality sampling plans and must be able to read and understand AQL inspection plans
- Experience in performing quality inspections in process or within a lab environment.
EDUCATION and/or EXPERIENCE
- High School Education or equivalent
- One to two (1-2) years related Quality Control experience or equivalency
SKILLS
- Ability to read and communicate well with individuals at all levels of the organization.
- Must read and interpret sampling plans
- Ability to perform basic math problems. Basic aptitude test required.
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
PHYSICAL DEMANDS
While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is frequently required to use hands to finger, handle or feel. The employee is occasionally required to stand and reach with hands and arms and lifts and/or moves up to 50 pounds. The employee is required to meet with other personnel in other areas of the building. Specific vision abilities required by this job include close vision
Job Type: Full-time
Pay: $16.00 - $17.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
- Night shift
- Overtime
Education:
- High school or equivalent (Preferred)
Experience:
- Quality control: 2 years (Preferred)
- Root Cause Investigation: 2 years (Preferred)
- measurement equipment: 2 years (Preferred)
Work Location:
- One location
Work Location: One location