MCS Associate Quality Control - Aequor Technologies LLC
Thousand Oaks, CA 91320
About the Job
100% onsite ATO
Shift/Schedule - 8:30 - 5:30 pm (flex by an hour)
Ideal candidate: Minimum two years of Quality Control, Quality Assurance in a GMP or GLP environment (excluding internships) with strong skills in pipetting, documentation, and aseptic techniques. They must adhere to regulatory guidelines, perform routine lab procedures, and manage data. Flexibility, attention to detail, and strong communication skills are essential, along with the ability to handle multiple tasks and meet deadlines.
Job Details: Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Preferred Qualifications
? Ability to adhere to regulatory requirements, written procedures and safety guidelines
? Ability to evaluate documentation/data according to company and regulatory guidelines
? Ability to organize work, handle multiple priorities and meet deadlines
? Strong written and oral communication skills
? Must be detail orientated
? Must be flexible and adaptable to changing priorities and requirements
? Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
? Demonstrates understanding of when and how to appropriately escalate.
? May identify, recommend and implement improvements related to routine job functions.
? Must learn and comply with safety guideline and cGMPs.
Shift/Schedule - 8:30 - 5:30 pm (flex by an hour)
Ideal candidate: Minimum two years of Quality Control, Quality Assurance in a GMP or GLP environment (excluding internships) with strong skills in pipetting, documentation, and aseptic techniques. They must adhere to regulatory guidelines, perform routine lab procedures, and manage data. Flexibility, attention to detail, and strong communication skills are essential, along with the ability to handle multiple tasks and meet deadlines.
Job Details: Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Preferred Qualifications
? Ability to adhere to regulatory requirements, written procedures and safety guidelines
? Ability to evaluate documentation/data according to company and regulatory guidelines
? Ability to organize work, handle multiple priorities and meet deadlines
? Strong written and oral communication skills
? Must be detail orientated
? Must be flexible and adaptable to changing priorities and requirements
? Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
? Demonstrates understanding of when and how to appropriately escalate.
? May identify, recommend and implement improvements related to routine job functions.
? Must learn and comply with safety guideline and cGMPs.
Source : Aequor Technologies LLC
