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Tulex Pharmaceuticals
Quality Assurance Manager
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Based on New Jersey data
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What they do
A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.
$109,830 / year median in New Jersey
-1% projected decline
Job Description
Job Overview We are seeking a highly skilled and detail-oriented Quality Assurance Manager to lead our quality assurance initiatives. As the Quality Assurance Manager, you will oversee the development and execution of testing strategies, ensure adherence to industry standards, and drive continuous improvement in product quality. Requirement B.S. in Chemistry or Life-sciences field with Minimum of 7 Year's quality assurance experience in Pharmaceuticals. Supervisory role for 2 years is necessary. Previous experience with FDA inspections is preferred. ASQ certifications like CQA/CQM is preferred. Must have good work ethics and attitudes. Must have good communication and interpersonal skills. Paying attention to details is required. Duties Responsible for daily QA operations including production, packaging and warehouse and QA documentation. Write, review, update, approve and train SOP's to ensure cGMP compliance, as required. Review and approve raw materials and components and approve quality control documents, including drug products release and stability samples. Ensure thorough and compliant investigations, including Deviations, Root cause analysis and CAPAs. Confirm the timely closures by following up with concerned departments. Supervise the Change control program. Assist in writing, review and approval of Qualification documents (IQ/OQ/PQ). Manage and track employee training matrix and respective training files. Participate in writing the Annual Product Reviews. Conduct qualification audits on vendor / supplier as well as internal audits. Act as a secondary contact for FDA inspections. Train QA employees on job functions, assign the daily tasks, supervise, follow-up and conduct performance reviews for direct reports. Initiate and lead projects for continuous improvements and efficiencies. Coordinate with inter/intra departments to meet the company timelines and resolve issues. Attend required training courses, conferences, meetings, and seminars as necessary. Perform any other activities as required or assigned by management.
Pay:
$90,000.00 - $120,000.00 per yearBenefits:
401(k) Dental insurance Retirement plan Tuition reimbursementWork Location:
In personBenefits
- Financial Aid/Assistance
- Dental Insurance
- 401(k) Plans
- Other Retirement and Savings