What are the responsibilities and job description for the Manufacturing Quality Assurance Technician position at Lornamead?
Lornamead is currently seeking a Manufacturing Quality Assurance Technician to join our team!
2nd Shift: Monday - Friday, 3p.m. - 11:30p.m.
Lornamead, Inc. manufactures and supplies hair care, skin care, oral care, and bath products in America. The company offers toothpastes, teeth whitening products and oral analgesics for drug chains, and national food retailers. The company is headquartered in New York, with a manufacturing facility in Tonawanda, New York. Lornamead is a US division of Meiyume who a global beauty company across major cities across the globe is.
Essential Functions:
Reporting directly to the Quality Assurance Manager, he/she will be responsible for quality oversight and assistance to production processes supporting departments and laboratory.
- Drive a culture of continuous quality improvement with presence in the manufacturing areas
- Perform routine quality checks in batching, filling, cartoning and warehouse areas to confirm adherence to procedures and cGMPs.
- Support in investigations and root cause analysis for incidents, investigations and consumer/customer complaints
- Documentation review of batch records, logbooks and other regulated documents for Good Documentation Practices and cGMP and procedural compliance
- Perform internal audits as scheduled, including write up of audit report and confirmation of previous corrective actions’ effectiveness
- Support change control process, as needed, to ensure documents are approved, trained and published (effective) in a timely manner.
- Performance of other duties assigned by Quality Management to ensure uniform quality assurance throughout the entire company
Education and Experience:
- Minimum of a High School Diploma with two (2) to three (3) years of work experience in field subject to current Good Manufacturing Practices
Knowledge, Skills and Abilities:
- Knowledge of cGMPs (FDA cGMP, CFR Parts 210 and 211, USP Chapters/Monographs) and experience in GMP processes and pharmaceutical document review to understand and guide process improvements.
- Strong computer skills, knowledgeable with standard Microsoft Office suite, email, document scanning, and strong Excel and Word experience
- Self-motivated and organized with minimum supervision.
- Ability to independently utilize critical thinking skills
Job Type: Full-time
Pay: $18.00 - $22.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person
Salary : $18 - $22
