Aditi Consulting
MCS Associate Quality Control
Aditi Consulting, Thousand Oaks, California, United States, 91362
Shift/Schedule:
8:30 - 5:30 pm (flex by an hour) Job Description:
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 oriented 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 guidelines and cGMPs. Top 3 Must Have Skill Sets:
Analytical testing experience GMP/GDP knowledge/experience Pay Transparency:
The typical base pay for this role across the U.S. is: $21.00 - $ 23.00 /hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance. Seniority level:
Associate Employment type:
Contract Job function:
Quality Assurance Industries:
Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr
8:30 - 5:30 pm (flex by an hour) Job Description:
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 oriented 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 guidelines and cGMPs. Top 3 Must Have Skill Sets:
Analytical testing experience GMP/GDP knowledge/experience Pay Transparency:
The typical base pay for this role across the U.S. is: $21.00 - $ 23.00 /hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance. Seniority level:
Associate Employment type:
Contract Job function:
Quality Assurance Industries:
Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr