ACL Digital
Senior Executive – US TAG at ACL (Pharmaceuticals, Life Sciences and Medical Devices)
Job Title:
Engineer/Validation/Mechanical
Location:
Thousand Oaks CA
Duration:
12 Months
Description:
Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Note:
Onsite USTO - Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed. Bippharm or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office. Heavy on documentation and manual disassembly role.
Responsibilities
Support senior staff in initiation, design, and delivery of projects.
Gather user requirements and translate them into technical documentation.
Perform engineering studies and assessment for CCIT system installations.
Field evaluate existing systems and recommend engineering design.
Develop technical documentation related to CCI testing and execute protocols.
Qualification
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience.
Solid modeling (Solid Works - preferred).
Technical Writing.
Working in a team.
Seniority level Mid-Senior level
Employment type Contract
Job function Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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Engineer/Validation/Mechanical
Location:
Thousand Oaks CA
Duration:
12 Months
Description:
Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Note:
Onsite USTO - Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed. Bippharm or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office. Heavy on documentation and manual disassembly role.
Responsibilities
Support senior staff in initiation, design, and delivery of projects.
Gather user requirements and translate them into technical documentation.
Perform engineering studies and assessment for CCIT system installations.
Field evaluate existing systems and recommend engineering design.
Develop technical documentation related to CCI testing and execute protocols.
Qualification
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience.
Solid modeling (Solid Works - preferred).
Technical Writing.
Working in a team.
Seniority level Mid-Senior level
Employment type Contract
Job function Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
#J-18808-Ljbffr