Lab Tech II-Evening Shift - US Tech Solutions, Inc.
Waco, TX 76712
About the Job
Monday to Friday 4pm to 12 am
• Performing component and final product inspection, physical stability program, and maintaining documentation of inspection reports to support component, raw material and finished product release.
• Maintaining and tracking all incoming and outgoing FQA product with traceability through FQA Delivery logbooks and destruction of FQA Sample logbook.
• Destroying all FQA samples through approved methods.
• Maintaining and updating LMS training daily.
Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives. The incumbent must be willing to take temporary assignments as required.
Regulated Responsibilities (including cGMP and EHS)
Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA.
Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate.
Years of experience/education and/or certifications required: Experience: Technical Prefer three (3) to seven (7) years of experience in either Quality Control/Quality Assurance functions within the device, food, or cosmetic industry.
What are the top 3-5 skills requirements should this person have?
• non-degreed
• Organized
• Can follow instructions very well
• Able to lift 20 pounds
• Able to work Overtime/Weekends
• Able to adhere to the work schedule as any missed days will put our project behind.
• Performing component and final product inspection, physical stability program, and maintaining documentation of inspection reports to support component, raw material and finished product release.
• Maintaining and tracking all incoming and outgoing FQA product with traceability through FQA Delivery logbooks and destruction of FQA Sample logbook.
• Destroying all FQA samples through approved methods.
• Maintaining and updating LMS training daily.
Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives. The incumbent must be willing to take temporary assignments as required.
Regulated Responsibilities (including cGMP and EHS)
Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA.
Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate.
Years of experience/education and/or certifications required: Experience: Technical Prefer three (3) to seven (7) years of experience in either Quality Control/Quality Assurance functions within the device, food, or cosmetic industry.
What are the top 3-5 skills requirements should this person have?
• non-degreed
• Organized
• Can follow instructions very well
• Able to lift 20 pounds
• Able to work Overtime/Weekends
• Able to adhere to the work schedule as any missed days will put our project behind.
Source : US Tech Solutions, Inc.