What are the responsibilities and job description for the Validation Engineer - 2nd Shift position at Amneal Pharmaceuticals?
Job Description
Description:
The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes.
Essential Functions:
Education:
Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.
Description:
The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes.
Essential Functions:
- Design, review and execute validation document activities such as Factory acceptance test (FAT), Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment /utilities/facilities and generate reports which summarize results, specification and its acceptance criteria
- Performs re-qualification of equipment, facility and utilities as required
- Responsible for creating validation project and validation progress reports - weekly and monthly
- Participate in evaluation of failures and out of specification results impacting compliance with quality, safety and other design requirements
- Provide Technical Inputs and develop strategy for various domestic and international Site Transfer projects. Provide regular status updates to the department and program management.
- Closely works with the maintenance & facility teams to complete new equipment installation, commission and validation as per project requirement.
- Performs engineering assessment and writes investigation reports for non-conformance
- Assists with engineering projects and performs other duties as assigned.
Education:
- Bachelors Degree (BA/BS) BS: in Pharmaceutical manufacturing, Engineering, Science or relevant field - Required
- 2 years of experience in engineering, pharmaceutical industry, cGMP environment
- Proficient in MS Office. - Advanced
- Excellent technical writing skills - Intermediate
- Excellent oral and written communication skills. - Advanced
- Must be able for follow direction and execute assigned work independently, after initial training is completed - Advanced
- Ability to work both independently and in conjunction with a team - Advanced
- Read, understand and verify piping & instrument diagram, engineering layout, drawing and documents
Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.