Senior Engineer
Planet Pharma · Irvine, CA · 1 wk ago
EngineeringContract
About the role
This position focuses on equipment and fixture validations, protocol development, and documentation related to manufacturing and inspection processes.
Responsibilities
- Protocol development for equipment and fixture validations (IQ/OQ/PQ/TFIQ)
- Execution of equipment and fixture validations (IQ/OQ/PQ/TFIQ)
- Report writing of equipment and fixture validations (IQ/OQ/PQ/TFIQ)
- Drafting of procedures and documents related to the manufacturing and inspection of product
- Drafting / revising procedures and documents related to the management of manufacturing / inspection areas
- Planning and executing on deliverables with team members
Qualifications
- Bachelor's degree in engineering required
- 5-7 years experience required
Skills
- Creativity, verbal and written communication skills, analytical and problem-solving ability
- Team player and detail oriented
- Previous experience with validations, protocol development and technical writing
- MS Office Suite proficiency
Pay
Target PR Range: 48-58/hr DOE