Company DescriptionQRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http: //www. qrcgroup. com/ to learn more about our services and solutions!Job DescriptionTo support the installation of several manufacturing solid dosage equipment such as but not limited to: EncapsulatorCheckweigherCompression machineHardness testerEncapsulation machineAuxiliary equipmentMain activities should include: Verification of the equipment installed and configured at the vendor site (FAT). Implement the progression from FAT through IOQ in accordance with the CC strategy.
Installation at the manufacturing room for qualification activities. Qualification activities in the manufacturing room areas. Development of Standard Operating Procedures. Generation and routing of calibration and preventive maintenance forms. Development and approval of GxP and automation impact assessments. Provide alternatives to resolve documentation situations. Establish project communication and documentation controls. Assure consistent quality of activities that meets or exceeds the requirements. QualificationsBachelor in Science or related field5 years of experience as CSV consultant in regulated industry. Experience with MS Office applications (Word, Excel and MS Project)Excellent technical writing skills. Bilingual: English and Spanish, speaking and writing.
Additional InformationAll your information will be kept confidential according to EEO guidelines.
Customize your resume to highlight skills and experiences relevant to this specific position.
Learn about the company's mission, values, products, and recent news before your interview.
Ensure your LinkedIn profile is complete, professional, and matches your resume information.
Prepare thoughtful questions to ask about team dynamics, growth opportunities, and company culture.
