Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
Validation & Engineering Group, Inc. (V&EG) is seeking a talented and dedicated individual for the position of QA Analyst (Senior & Mid-Level) in Biopharmaceutical Manufacturing. The Senior and Mid-Level QA Analysts will play a crucial role in ensuring GMP compliance and product quality within a biopharmaceutical manufacturing operation. Both roles will report to the QA Manager.
Responsibilities:
- Review batch records and release products
- Manage deviations, CAPAs, change controls, and investigations
- Participate in audits and inspections
- Guarantee GMP and FDA compliance throughout operations
Qualifications:
- Bachelor's degree in Science or related field
- Minimum of 5 years of experience in GMP within the pharmaceutical/biotechnology or regulated manufacturing sectors
- Proficiency in quality systems and documentation
- Advanced investigation and compliance leadership skills for the Senior role
- Strong QA foundation with potential for growth in the Mid-level role
Validation & Engineering Group, Proudly serving our clients since 1997.
Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.
Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.
Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.
At Validation & Engineering Group we provide professional expertise in the areas of:
•Audit and Assessment
•Automated Process Control System Qualification
•Equipment and Facilities Qualification
•Facilities Start-Up and Commissioning
•GAP Analysis
•Information Systems Computer Validation
•Packaging and Process Analysis
•Process & Cleaning Validation
•Project Management
•Quality Systems
•Risk Based Approach
•Regulatory Compliance
•Standard Operating and Maintenance Procedures
•Training
•Utilities Support and Qualification
In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.
Our Offices:
Puerto Rico:
Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico
Phone: (787) 622-0996
United States:
2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States
Phone: (770) 403-5802
