- Conduct critical chemical and physical analyses on Raw Materials Initial In-process and Final products and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision.
- Use sophisticated laboratory instrumentation HPLC FTIR UV GC etc and computer systems to collect and record data.
- Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles.
- Maintain data integrity and ensure compliance with company SOPs and specifications FDA GLP QSR and cGMP regulations.
- Participate in functions involving teams which impact production increase efficiency solve problems generate cost savings and improve quality.
- Perform laboratory and manufacturing audits as required. Audit and update as required plant SOPs.
- Perform equipment maintenance and calibrations as required.
- Document the completion of testing in Notebooks Controlled documents Forms and LIMS and maintain accurate and complete quality records.
- Follow understand and comply with Baxter SOPs and policies on cGMPs and safety. Maintain a clean safe and organized lab area and potentially assume responsibility to ensure that others maintain their lab areas.
- Investigate deviations and write exception/OOL/OOS/OOT documents.
- Support improvement projects and drive efficiency through utilization of LEAN management principles i/e/ 6S Kaizens etc.
- Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues recommend solutions when issues arise.
- Maintain and meet the highest standards in quality customer service and regulatory compliance.
- 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
Quality Lab Associate I - Pleasant Prairie, United States - Actalent
Description
Summary:
The Position encompasses the biological chemical and physical analyses on pharmaceutical products biologics and drugs through all stages of the manufacturing process from incoming raw materials to finished goods and environmental monitoring programs. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.
Essential Duties and Responsibilities:
Qualifications:
Must not be color blind
Education and/or Experience:
Bachelors degree in Chemistry or Science related degree with 6 months or more of experience
Skills:
HPLC, Lab, chemistry
Additional Skills & Qualifications:
Chemistry or Biochemistry degree with 0-6 months experience
HPLC
GMP
Experience Level:
Entry Level
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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