Job Information
Actalent Quality Control Analyst in Vernon Hills, Illinois
Quality Control AnalystMUST HAVE
Bachelor's Degree in Chemistry, or Biology with a Chemistry Minor.
1-2 years of experience with UPLC/HPLC.
Experience with Microsoft Office (Word, Excel).
Pharmaceutical/FDA exposure.
Experience with cGMP.
Proficiency with Empower software
Job Description
We are seeking a dedicated Quality Control Analyst to join our team. The successful candidate will operate the materials management system, prepare mobile phase, samples and standards for use in procedures, and maintain proper waste disposal handling and record keeping. The role involves participating in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs, analyzing and interpreting experimental outcomes, preparing and assembling documentation, and collaborating with management for assigned tasks, including technology transfer.
Responsibilities
Operate the materials management system integrating receiving, quarantine, release, inventory, and disposal mechanisms.
Prepare mobile phase, samples, and standards for use in procedures, preventing waste or loss of materials.
Maintain proper waste disposal handling and record keeping.
Participate in the execution and optimization of Standard Operating Procedures (SOPs) for equipment and instrumentation per cGMPs.
Correctly analyze and interpret the outcome of experiments.
Prepare and assemble documentation such as entries into laboratory notebooks and maintain proper records per relevant SOPs and policies.
Collaborate with supporting management for assigned tasks, including technology transfer.
Learn regulations, legal requirements, policies, and procedures relevant to areas of responsibility.
Apply knowledge to ensure safe and compliant practices, manage risk, and maximize opportunities for projects to succeed.
Become proficient with UPLC, Empower, and various other analytical instruments and software packages.
Perform routine analytical tests of excipients, APIs, finished products, compounded sterile preparations, and stability samples.
Create and maintain clear and concise lab records and documentation.
Ensure the timely execution of lab analysis and related documentation.
Support daily analysis and stability study activities with significant supervision.
Work Environment
The QC Analyst will work in a clean, state-of-the-art laboratory facility as well as spend time in the office. The position involves testing samples from compounding. Our Client, founded in 2011, is a majority women-owned fully-integrated laboratory powered by advanced information technology to facilitate rapid drug development. The emphasis on automation of critical laboratory processes minimizes human error within the testing and analysis process. The company provides a full range of rapid testing and support services focusing on pharmaceutical products and compounded sterile or nonsterile preparations. The development activities span six major industries. The work environment is flexible, offers excellent training, and growth opportunities in a small company with a family feel.
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About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.