Aequor Technologies
MCS Associate Quality Control
Aequor Technologies, Thousand Oaks, California, United States, 91362
100% onsite
Duration: 1-year
Monday-Friday, 8:00 AM-5:00 PM
Overtime: Occasional; ~once a month on a weekend (usually 1 day)
Ideal candidate has a Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry) and has lab and GMP experience in a regulated environment, preferably within pharma, biotech, or academia. Must possess skills in analytical testing such as HPLC or chromatography, along with basic Excel and Word proficiency for data entry in lab notebooks and electronic systems. Soft skills include strong communication, conflict resolution within a small team, and self-starting initiative. Candidates should demonstrate role longevity and commitment; patterns of short-term job hopping are a red flag.
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.
Ideal candidate has a Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry) and has lab and GMP experience in a regulated environment, preferably within pharma, biotech, or academia. Must possess skills in analytical testing such as HPLC or chromatography, along with basic Excel and Word proficiency for data entry in lab notebooks and electronic systems. Soft skills include strong communication, conflict resolution within a small team, and self-starting initiative. Candidates should demonstrate role longevity and commitment; patterns of short-term job hopping are a red flag.
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.