3rd Shift Quality Assurance Technician
About The Position
TempToFT 3 rd Shift Quality Assurance Technician Rate: $21/hr + $1/hr shift differential Hours: 10:30pm-6:30am, Sunday Night-Thursday Night Cincinnati, OH C-D Responsibilities: - Provide oversight of the label area including receipt, approval, issuance, counts, accountability and inventory. - Perform QA functions to include daily manufacturing cGMP inspection and balance/scale checks; product disposition; preparation of CoA/CoM; preparation, revision and issuance of SOPs; preparation, revision and issuance of packaging instructions/specifications and provide support to internal and external customers in compliance with government regulations and customer requirements. - Provide support during customer and regulatory audits. - Provide support to the incoming inspection when necessary. - Maintain Master Manufacturing Records in accordance with regulatory requirements. - Conduct quality investigations as directed and prepare findings. - Provide support to internal and external customers. - Compile all required reports and documents on the performance of the above duties. - Serve as back-up to QA incoming inspection when needed. - Perform or assist with internal audits in compliance with cGMP regulations. - Combination: sit – 50% stand/walk – 50%. - Other projects or duties as assigned. Requirements: - Bachelor degree in Science or related field to meet FDA requirements for sign offs. - 2+ years of quality experience. - Knowledge and understanding of quality principles and cGMP compliance in a manufacturing environment. - Working knowledge of various testing apparatus beneficial. - Detail oriented and well organized; strong math, writing, and reasoning skills. - Self-starter with ability to work and think independently. - Effective communication and interpersonal relationship skills. - Proficiency in Microsoft 365 (Office-Word and Excel). - Writing skills with the ability to create procedures, packaging instructions and specifications, cGMP documentation. - Ability to interact and impact quality on the manufacturing floor and support customer requirements. - Ability to effectively balance and prioritize multiple tasks, deadlines and interruptions simultaneously. - Lifting: Up to 40 pounds. - Pass drug test and background check. If you possess the skills we are looking for and ready to make a positive impact, apply NOW! We look forward to connecting soon!
Requirements
- Bachelor degree in Science or related field to meet FDA requirements for sign offs.
- 2+ years of quality experience.
- Knowledge and understanding of quality principles and cGMP compliance in a manufacturing environment.
- Working knowledge of various testing apparatus beneficial.
- Detail oriented and well organized; strong math, writing, and reasoning skills.
- Self-starter with ability to work and think independently.
- Effective communication and interpersonal relationship skills.
- Proficiency in Microsoft 365 (Office-Word and Excel).
- Writing skills with the ability to create procedures, packaging instructions and specifications, cGMP documentation.
- Ability to interact and impact quality on the manufacturing floor and support customer requirements.
- Ability to effectively balance and prioritize multiple tasks, deadlines and interruptions simultaneously.
- Lifting: Up to 40 pounds.
- Pass drug test and background check.
Responsibilities
- Provide oversight of the label area including receipt, approval, issuance, counts, accountability and inventory.
- Perform QA functions to include daily manufacturing cGMP inspection and balance/scale checks; product disposition; preparation of CoA/CoM; preparation, revision and issuance of SOPs; preparation, revision and issuance of packaging instructions/specifications and provide support to internal and external customers in compliance with government regulations and customer requirements.
- Provide support during customer and regulatory audits.
- Provide support to the incoming inspection when necessary.
- Maintain Master Manufacturing Records in accordance with regulatory requirements.
- Conduct quality investigations as directed and prepare findings.
- Provide support to internal and external customers.
- Compile all required reports and documents on the performance of the above duties.
- Serve as back-up to QA incoming inspection when needed.
- Perform or assist with internal audits in compliance with cGMP regulations.
- Combination: sit – 50% stand/walk – 50%.
- Other projects or duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
