View all jobs
MCS Associate Quality Control
Thousand Oaks, CADescription:
Note:
100% onsite standard core hours some flexibility may be needed for overtime.
Ideal candidate: the MCS Associate Quality Control role is good for a early-career professional with a strong foundation in laboratory techniques, aseptic handling, and quality control principles. They should possess hands-on experience with pipetting, assay execution, and documentation, ideally gained through academic coursework, internships, or industry experience. Experience working with 96-well plates, plate readers, biosafety cabinets, or cell lines is highly desirable. While two years of industry experience in a GMP or GLP environment is preferred, candidates with strong laboratory training in microbiology or cell biology will also be considered. The candidate should be detail-oriented, adaptable, and eager to learn within a regulated QC setting. Since the role requires extensive training, long-term commitment is essential, making candidates who seek stable career growth within the organization more favorable. Additionally, flexibility to work occasional overtime or weekends is necessary to support fluctuating workloads.
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
"This posting is for Contingent Worker, not an FTE"
Note:
100% onsite standard core hours some flexibility may be needed for overtime.
Ideal candidate: the MCS Associate Quality Control role is good for a early-career professional with a strong foundation in laboratory techniques, aseptic handling, and quality control principles. They should possess hands-on experience with pipetting, assay execution, and documentation, ideally gained through academic coursework, internships, or industry experience. Experience working with 96-well plates, plate readers, biosafety cabinets, or cell lines is highly desirable. While two years of industry experience in a GMP or GLP environment is preferred, candidates with strong laboratory training in microbiology or cell biology will also be considered. The candidate should be detail-oriented, adaptable, and eager to learn within a regulated QC setting. Since the role requires extensive training, long-term commitment is essential, making candidates who seek stable career growth within the organization more favorable. Additionally, flexibility to work occasional overtime or weekends is necessary to support fluctuating workloads.
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.
- Basic Qualifications
- Bachelor degree and 2 years of Quality Control, Quality Assurance OR related experience OR Associate degree and 6 years of Quality Control, Quality Assurance OR related experience OR High school diploma / GED and 8 years of Quality Control, Quality Assurance OR related experience
- Pipetting, Documentation, Aseptic Technique
"This posting is for Contingent Worker, not an FTE"