What are the responsibilities and job description for the Senior Validation Engineer position at Piper Companies?
Piper Companies is seeking a Senior Validation Engineer to join a leading pharmaceutical manufacturing company located in Lynwood, Ca. This role is 100% onsite. The Senior Validation Engineer will oversee the validation and coordination of machinery and process operations within the plant.
Responsibilities of the Senior Validation Engineer include:
Keywords: commissioning, qualification, decommissioning, production, validation standards, validation criteria, procedures, protocol, validation test equipment, detail-oriented, quality assurance, innovation, documentation, communication, collaboration, risk management, time management, GMP, problem solving, medical device, hardware, adaptability, technical writing, project management, FDA, Oracle, QMS, statistical tools , biological sciences, engineering, tests, instruments, quality director, quality engineer, supplier quality engineer, validation specialist
Responsibilities of the Senior Validation Engineer include:
- Manage end to end, hands on, validation for products, processes, equipment and packaging
- Supports all qualification tasks related to manufacturing equipment – IQ/OQ/PQ
- Provide decisions on validation strategies and performance issues
- Prepare, review and organize validation protocols and reports
- Schedule and oversee validation tasks across all shifts
- Support inspections and ensure GMP compliance
- 5-7 years of experience in a similar liquid pharmaceutical industry role, including experience in validation, tech transfer and leadership
- Knowledge of FDA guidance and Validation for process, equipment, and cleaning.
- Proficiency in Office 365, Oracle, QMS, statistical/validation tools
- Strong technical writing, verbal and written communication skills
- Ability to manage multiple tasks, work independently, and thrive in a fast-paced environment with changing priorities
- Bachelor's degree in chemical or Biological Sciences/Engineering required
- Salary Range: $85,000 - $95,000 **Depending on experience**
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays
Keywords: commissioning, qualification, decommissioning, production, validation standards, validation criteria, procedures, protocol, validation test equipment, detail-oriented, quality assurance, innovation, documentation, communication, collaboration, risk management, time management, GMP, problem solving, medical device, hardware, adaptability, technical writing, project management, FDA, Oracle, QMS, statistical tools , biological sciences, engineering, tests, instruments, quality director, quality engineer, supplier quality engineer, validation specialist
Salary : $85,000 - $95,000
