Danaher Corporation Laboratory Compliance Associate in Lodi, CaliforniaAt Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing.
Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges.
Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings.
As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.The Laboratory Compliance Associate will be responsible for supporting the manufacturing and quality control labs, which includes but is not limited to cleanliness, organization, restocking inventory, regular audits for GLP/GMP compliance, and process improvements.
The person in this position is expected to generate creative, practical, and functional ideas for process improvements and facilitate these concepts into action with feedback from the manager.This position is part of the Laboratory Compliance, Maintenance, and Safety team and is in Lodi, CA, on-site day shift Saturday-Wednesday.In this role, the Laboratory Compliance Associate (P1) is expected to:Keep manufacturing and laboratory environment and practices compliant with guidelines set forth by company and regulatory agencies.Implement GMP and GLP practices/procedures and serve as a functional expert in the area of lab compliance.Perform regular lab inspections audits (i.e., Manufacturing and QC) to ensure adherence to company policies, guidelines, SOPs, and Biosafety program.Analyze and report lab inspections audits to appropriate management and follow up on corrective and preventive actions.Maintain laboratory contamination surveillance and decontamination program to ensure amplicons and other ANA (Amplifiable Nucleic Acids) contamination are prevented.The essential requirements of the job include:Bachelor's degree with 0-2 years of related work experience OR 5 years of related work experience.Knowledge and/or hands-on experience with GMP test sample collection and sampling.A 24/7 production and laboratory working environment, including modified shift times, overtime, and weekends.Must be able to follow cGMP, GLP, FDA, and ISO standards.Excels in a fast-paced team environment, is able to multi-task, is highly self-motivated, and is goal-oriented.Strong interpersonal skills, highly collaborative within a multi-discipline team, and contributes to a supportive and positive work environment.The salary range for this role is $59,900-$81,800.
This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting.
We may ultimately pay more or less than the posted range.
This range may be modified in the future.This job is also eligible for bonus/incentive pay.At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology.
We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve.
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