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Quality Assurance Supervisor - Pharmaceutical Manuf.

Company: Task Management Inc
Location: Clinton
Posted on: November 23, 2020

Job Description:

My client is a Pharmaceutical Manufacturing company and needs a QA Supervisor with Pharmaceutical Manufacturing industry experience. JOB SUMMARY This Quality Supervisor professional is responsible for ensuring that the Quality Assurance auditing in our CT facilities (Centerbrook and Clinton) operates effectively and efficiently and is fully integrated with the company's business objectives. Day to day responsibilities include performing necessary inspection and testing required for product release, supporting the manufacturing operation, providing timely information and communicating with both internal and external customers. Successful candidate will present a high level of integrity and ethics, strong commitment to quality and a proven track record in quality assurance within GMP environment. ESSENTIAL JOB FUNCTIONS 1. Oversee the daily activities of the QA Associates providing direction of responsibilities and guidance for completing tasks as well as providing any necessary training. 2. Conduct packaging audit, ensuring final product meets packaging specifications and is within the allowed accepted quality limits (AQL) inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications. 3. Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications. 4. Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies. 5. In collaboration with other key personnel, review Quality SOPs and manufacturing records on a periodic basis and revise or create new documents as necessary. 6. Audit finishedcompleted batch production documents for procedural or mathematical errors and approve for release of product. 7. Communicate identified manufacturing deficiencies to key personnel (Machine Operator, Technical Director, Production Supervisorhellipetc.). 8. Coordinate packaging specifications review and approve Bill of Materials (BOM). 9. Perform all work in accordance with established Safety, cGMP and company procedures support company mission and values. 10. Other responsibilities as assigned. JOB REQUIREMENTS Three to Five (5) years of experience in Quality Assurance in the pharmaceutical manufacturing industry. Demonstrated current knowledge of cGMP regulations and industry standards. Minimum 3 years Supervisory experience Strong team player, demonstrated team attitude and behaviors. Excellent organizational skills ability to delegate. Working knowledge of MS Word and MS Excel. Strong writing skills. BENEFITS Dynamic working environment with a competitive benefit package including 401(k) with generous company match. - Medical Dental Insurance, Disability insurance, Life Insurance, ADD, 401k Retirement, Flexible Spending accounts, Company paid Holidays and vacation time, Employee Assistance Program and Educational Assistance. TO APPLY send resume to Lisataskmanagement. com (All one word) Job Type Full-time

Keywords: Task Management Inc, New England , Quality Assurance Supervisor - Pharmaceutical Manuf., Healthcare , Clinton, Northeast

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