What are the responsibilities and job description for the Quality Control Inspector II position at BEPC Inc?
BEPC is looking for a Quality Control Inspector II in Newark, DE to join our fast-growing team of consultants!
W2 Contract: 12 months with opportunities for extensions based on business needs and performance.
Pay Range: $22.40-33.61/hr. plus we offer Medical, Dental, Vision and Life Insurance benefits!
Schedule: 100% Onsite, M-F 7:00AM to 4:00PM
Job Summary:
Performs inspections, checks testing and sampling procedures for product manufacturing processes. Carries out packaging line, manufacturing inspections and sampling and testing of incoming components and raw materials to ensure that company standards are met. Responsible for review and release of Device History Records. Monitors critical equipment and instrumentation. May assist with validating or troubleshooting testing methods, including assays. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated.
Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice. Applies acquired job skills and company policies and procedures to complete assigned tasks. Normally follows established procedures on routine work, requires instructions only on new assignments.
Essential Duties and Responsibilities:
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
· Maintain and promote a safe work environment at all times. Identify, address, and react to any unsafe or hazardous situation.
· Conduct inspections, including work in process and final inspection of finished goods to ensure manufactured products conform to specifications. Proficient in identifying and documenting defects, and corrections required.
· Record and maintain quality control records documenting testing and inspections.
· Participate in investigations into non-conforming products and corrective actions.
· Perform manufacturing process audits to ensure correct adherence to Standard Operating Procedures (SOPs) and Work Instructions.
· Initiate Non-Conforming Events (NCEs) within the Quality Management System and assists with investigations relating to non-conforming products.
· Responsible for cleaning, calibrating, and maintaining quality assurance equipment.
· Performs daily reviews of in-process and final test device history records and sales orders.
· Performs inspections to determine pass/fail criteria.
· Participate in Kaizen events and other continuous improvement initiatives.
· Complete all training requirements in a timely manner and maintain accurate training records.
· Regular and punctual attendance. Ability to adhere to standardized production schedule for position and ability to work overtime to support production needs as necessary.
Physical Environment:
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
· Sit; use hands to finger, handle or feel objects, tools, or controls.
· Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
· Lifting/moving and carrying products weighing up to 40 pounds.
· Exposure to moving mechanical parts, vibration and/or moderate noise levels.
· Safety Shoes with Impact and Compression Protection Must be worn in designated areas
· High voltage electronics, radiation. Ability to work in clean room, controlled environment, and/or dark room.
Qualifications:
· Education: High School (H.S./GED) or Associate Degree.
· Experience: Preferred Minimum Non-Technical Degree: 1-2 Years
· Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial.
· Previous quality assurance or manufacturing experience is beneficial.
· Experience in an FDA regulated medical device environment is beneficial.
Skills:
· Knowledge of Microsoft Office platform including Excel, Word, SharePoint, and OneDrive required.
· Ability to read, understand, and follow all written procedures.
· Ability to communicate effectively, both written and verbally.
· Ability to work both independently and as a member of a team.
· High-level of attention to detail and focus on quality.
· Detail oriented and accurate.
· Ability to use quality control tools such as measuring tapes, calipers, micrometers, scales, gauges, microscopes, etc.
· Ability to read and interpret basic schematics and blueprints required to ensure proper assembly.
· Understanding of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
USOPS
Job Type: Contract
Pay: $22.40 - $33.61 per hour
Benefits:
- Dental insurance
- Health insurance
- Life insurance
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Education:
- High school or equivalent (Required)
Ability to Commute:
- Newark, DE 19702 (Required)
Work Location: In person
Salary : $22 - $34