Engineering Specialist job in San Diego, CA
Vacancy has expired
San Diego, CA CorTech LLC
| Job Ref: | 344393 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 106.00/Per Hour |
| Remote: | No |
Location |
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| City: | San Diego, CA |
| Post Code: | 92121 |
| Map: |
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Description |
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CorTech is seeking to hire a Engineering Specialist for our client in San Diego, CA! Benefits Available! Weekly Pay! $106.00/Hour ? Provides engineering, validation and maintenance support to the decommissioning of QC equipment, facility and utilities at a site; equipment may include lab equipment such as cellometers, CX5, Densitometers, support systems such as SCADA, incubators, freezers bio-safety cabinets, offline bench-top instruments or facility/utility systems. ? Ensures equipment is decommissioned in a compliant manner through equipment life cycle. Help define and optimize equipment qualification strategy. ? Manages exit calibration, periodic reviews, specification updates ? Owns and manages changes to the lab equipment to maintain equipment in a validated state. ? Investigates any equipment or process deviations and developing corrective actions to prevent re-occurrences. Able to provide industry wide expertise for complex equipment and process investigations. ? Applies knowledge of engineering principles and best practices to ensure robust solutions. ? Provides mentorship to other process engineers. ? Leads small internal teams to help optimize engineering systems and processes. ? Obsoletes equipment specifications in standard documentation ? User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS). ? Other related job duties as assigned. Qualifications ? B.S. degree in Chemical, Electrical or Mechanical Engineering, or related technical field, with 5 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (9 years) in pharmaceutical or biopharmaceutical based GMP manufacturing operations. ? Excellent oral and written communication skills. Strong technical writing ability required. ? Working in a team environment, with excellent communication and organizational skills. ? Diverse experience in the development, automation, and manufacture of gene therapy products, medical devices, instruments, or biotechnology. ? In-depth knowledge of FDA regulations and GMP systems and experience providing engineering support in a highly regulated or pharmaceutical / biotech facility. ? Strong project management skill set with extensive experience in strategic / tactical planning, demonstrated ability to perform long-term project planning. ? Ability to prepare contingency plans and logically work through complex issues in a pressure filled atmosphere. ? Demonstrated ability to lead cross functional teams across manufacturing locations in a fast pace, dynamic team setting. ? Uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways. ? Full understanding of area of specialization; resolves a wide range of issues in creative ways ? Ability to work on problems of diverse scope where analysis of data requires evaluation of identifiable factors. ? Demonstrates good judgment in selecting methods and techniques for obtaining solutions. ? Networks with senior internal and external personnel in own area of expertise. | |
ref: (344393)
1011 days ago
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