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Assistant Quality Supervisor - Rock Hill, United States - Cirtec Medical
Description
Job DescriptionJob Description
JOB SUMMARY
This position is primarily responsible to motivate the team to meet production, quality goals, and objectives. Provide complete, timely, and informative communication to all shifts. Ensure that Production Control schedule is followed and contribute to all teams achieving monthly production schedules and quality goals.
ESSENTIAL RESPONSIBILITIES
Assesses risks and seeks appropriate assistance from Quality
Manager/Supervisor.
Ensures safety guidelines are understood and followed at all times.
Resolves quality problems and documents issues for discussion in meetings with Management, Engineering and Quality.
Recommends quality changes to Quality
Manager/Supervisor.
Gives and receives employee feedback.
Identifies training and cross-training needs and ensures completion of training records for work cell.
Facilitates team participation.
Review schedule with supervisor and work towards meeting shipment dates-while ensuring quality standards are being maintained.
Ensures rejections are documented and communicated to Production & Inventory Control as needed to support accurate inventory counts.
Shop cleanliness and tidiness:
Work cell is responsible for cleaning the area daily in accordance with established procedures.
Will have authority to shut down production for out-of-control situations, contact necessary personnel to solve problems, request additional resources and move resources to other areas for temporary assignments.
Complies with company, quality, and safety standards, policies, and procedures.Provides leadership, mentoring and supervision of Quality Inspectors.
Works extended hours or weekends as needed.
Complies with company, quality and safety standards, policies, and procedures.
Other duties as assigned.
This is not a remote position.
An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
REQUIRED QUALIFICATIONS
High school diploma or GED.
Minimum 5 years' experience in a quality inspection in a manufacturing environment.
Minimum 2 years' experience in a leadership role.
Prior experience in a Contract Manufacturing Operation (CMO) is preferred.
Relevant experience in leading team performance and regulatory compliance.
Be able to read, write and speak fluent English.
Basic understanding of computer monitor, keyboard and hard drive.
Intermediate MS Office – must be able to create a variety of charts and reports to support quality activities.
WORKING ENVIRONMENT
Work is performed in a manufacturing environment. The noise level in the work environment is usually moderate.
The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
EEO STATEMENT
Cirtec Medical Corporation is an Equal Opportunity
Minority/Female/Individuals
with
Disabilities/Protected
Veteran and Affirmative Action Employer
Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law.
Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.#LI-PS1
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