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Associate Scientist

Thousand Oaks, CA
Top 3 Must Have Skill Sets:

GMP (or GLP) experience and
familiarity working with regulated documents
Lab management skills
Ability to work independently and as part of a team with internal and external clients, self motivation, adaptability, and a positive attitude
Excellent communication (oral and written) and attention to detail; excellent project management skills including the ability to manage project resource requirements, and ability to elevate relevant issues to project lead and line-management

Day to Day Responsibilities:

Management of equipment; maintain inventory, enter and track work orders, work with maintenance and vendors for equipment repair
Maintain list of active assets including equipment information, equipment procedures, calibration and preventive maintenance records, scheduling, etc.
Assist/coordinate new equipment procurement and installation
Perform tasks related to safety and compliance initiatives in the lab; inspections and observation resolutions
Coordinate regular lab clean-up and general lab housekeeping
Management of inventory levels of commonly used reference standards and reagents.
Author, review, and data verify technical documents
Ensure compliance with SOPs and policies

Summary

Management of equipment; maintain inventory, enter and track work orders, work with maintenance and vendors for equipment repair
Maintain list of active assets including equipment information, equipment procedures, calibration and preventive maintenance records, scheduling, etc.
Assist/coordinate new equipment procurement and installation
Perform tasks related to safety and compliance initiatives in the lab; inspections and observation resolutions
Coordinate regular lab clean-up and general lab housekeeping
Management of inventory levels of commonly used reference standards and reagents.
Author, review, and data verify technical documents
Ensure compliance with SOPs and policies
Strong computer, scientific, and organizational skills
GMP (or GLP) experience and familiarity working with regulated documents
Experience entering, reviewing and verifying data in regulated systems
Excellent communication (oral and written) and attention to detail; excellent project management skills including the ability to manage project resource requirements, and ability to elevate relevant issues to project lead and line-management
Ability to work independently and as part of a team with internal and external clients, self motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Ability to participate in global cross-functional teams and work effectively in a highly matrixed team environment
Prior experience working with Maximo and LIMS systems is preferred

Education:

B.S. in Biology, Chemistry, Engineering, Pharmaceutical Sciences, Life Sciences, or related degree, and at least 2-3 years in a related scientific field

"This posting is for Contingent Worker, not an FTE"
 

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