Stepan is a growing, Illinois-based chemical manufacturing corporation with facilities located throughout the United States and abroad. Our expertise in chemical manufacturing and global reach are driving factors in our long-term relationships with customers. With a commitment to ensuring a safe, secure and sustainable work environment for our employees, customers, visitors and communities, we continuously improve our management systems to achieve incident-free performance. Due to our continued ...
Director of Quality
Responsible for establishing a corporate quality assurance system and team that promotes customer satisfaction and that positively impacts the financial performance of H.D. Smith Specialty Solutions and supporting umbrella organizations. Champion continuous improvement efforts and corrective action initiatives to establish an effective Quality Management System (QMS); initiate and implement quality improvement activities as appropriate (e.g., Kaizen, Six Sigma) ...
SUMMARY OF POSITION:
Plans and executes activities pertaining to the evaluation and disposition of products received from raw material and component suppliers and/or is engaged in the qualification and approval of suppliers of purchased components. Issues and supports supplier corrective actions and the failure analysis processes.
1. Coordinate and perform incoming inspection activities.
2. Make determination of acceptable material and physically / systemically release ...
PSI CRO AG - Home-based - Southeast Region - Oncology Experienced
PSI is expanding rapidly in the US and seeking highly motivated CRAs. At PSI, we believe employees are our greatest assets.
Responsibilities: Project activities and monitoring functions associated for Phase I-IV clinical research studies. Comprehensive understanding of the drug development process, Good Clinical Practices (GCP), and relevant regulations. Demonstrates a high level of communication skills and provides clinical and ...
Seeking degree in chemistry, biology, engineering or similar and leadership track record in biological pharmaceutical manufacturing quality compliance who is expertly familiar with biopharmaceutical manufacturing operations, documentation management, training, and auditing.
*** Supervising RA and QA associates and contractors.
*** Oversight of corrective and preventive actions.
*** cGMP and GMP Document management.
*** Coordinating and maintaining cGMP and GMP training program.
Our client has an outstanding career opportunity for Formulation Scientist located in Aurora (IL) USA. This role is responsible for driving and generating innovative chemistries for state-of- the-art CMP consumable technologies and new slurry technology development.
Responsibilities include the following:
Drive, plan, and conduct innovation activities focused on obtaining a fundamental understanding of the formulation and manufacturing of CMP consumables, leading to new and improved ...
Jan 13 -
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