- 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
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Quality Lab Associate I - Round Lake, United States - Actalent
Description
Description:
What are the top three to five technical skill requirements? Strong knowledge in principles of analytical chemistry proficient in advanced wet chemistry techniques analytical chemistry instrumentation experience e.g. HPLC pH KF AA GFAA titrations etc.
Summary
The position may be responsible for analytical testing validation/verification and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake IL Stability Laboratories within Product Quality serving multiple global businesses.
This role is essential for supporting the global commercial product teams and/or product development teams. The position may interface with multiple functions. The individual in this position must: 1 Effectively demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance. 2 Display basic technical understanding of related disciplines. 3 Conduct routine/non-routine experiments with minimal assistance.
A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.
Essential Duties and Responsibilities.
Under direction conduct critical chemical physical and biological analyses on finished product stability samples. May also support testing of raw materials initial in-process and final product samples from the manufacturing facility as required. Work under minimum supervision.
Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to conduct validations.
Complete all testing including special project / protocol testing in a timely and appropriate manner to meet project schedules.
Maintain data integrity and ensure compliance with company SOPs and specifications FDA cGxP and QSR regulations.
Participate with management to investigate deviations and write exception documents.
May perform advanced biological and chemical assays requiring precise analytical skills and understanding of chemistry principles.
May perform review of test data which includes overall documentation practices. May perform review functions in LIMS or other computerized systems.
May participate in cross functional teams which impact production increase efficiency solve problems generate cost savings and improve quality and provide new product support.
Maintain laboratory supplies and laboratory safety requirements to ensure audit readiness at all times.
Perform equipment maintenance and calibrations as required. Troubleshoot and resolve instrument problems with some assistance.
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:
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.
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