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The Analyst II, QC Microbiology supports the Microbiology Department by conducting quality-related testing on pharmaceutical products while ensuring compliance with SOPs and cGMP.

The Senior Specialist, Supply Chain Planning manages supply chain analytics, reporting, process improvements, and inventory analysis to support multiple teams and ensure compliance with regulatory standards.

The Associate II, Quality Assurance ensures compliance with GMP in biomanufacturing, manages quality systems, and collaborates with teams to uphold regulatory standards and execute necessary documentation.

The Specialist II in Supply Chain manages logistics for temperature-controlled shipments, oversees export compliance, and improves delivery performance. Responsibilities include scheduling, monitoring, and SOP development for shipping operations.

The Automation Engineer II role involves optimizing, validating, and maintaining automation systems in a biomanufacturing setting while collaborating across departments and ensuring compliance.

The Senior Analyst, QC Microbiology performs microbiological testing and ensures GMP compliance, authors SOPs, and leads investigations in QC processes.

The Quality Control Systems Engineer oversees LabVantage LIMS, leading enhancements and validations, ensuring compliance and effective system operations in a regulated environment.

The Process Engineer III - Serialization leads projects for serialization systems in pharma production, ensuring compliance and continuous improvement while mentoring junior engineers and supporting manufacturing.

The Reliability Engineer III is responsible for developing reliability strategies, optimizing maintenance plans, performing RCA, and collaborating across departments to ensure effective asset management in a biomanufacturing environment.

The Senior Specialist, Product Complaints manages product quality complaints evaluations and investigations, ensuring compliance with regulations and improving processes across departments while providing training.