Location : Westborough MA USA The Compliance Specialist will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at AIRM. The successful candidate will foster data integrity, quality, and compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts at Astellas to help ensure high quality standards and value delivery for our patients. This position is based in Westborough, MA and will require on-site work.

Location (mandatory): Westborough MA USA The Research Associate role will provide a supporting role for ongoing research activities.

Location : Weston, FL 33331 (Hybrid). The Accounts Receivable Clerk will be a temporary position to aid and assist the Collections Department with general duties including, but not limited to, phone calls, data entry, and administrative tasks.

Location (mandatory): Marlborough MA USA We are seeking a highly motivated Research Associate to support the analytical testing of cell therapy products to support development activities. The role requires hands-on laboratory work, including mammalian cell culture, flow cytometry, and PCR-based testing as well as data analysis. The Research Associate will work as part of a team under the guidance of Senior Project/Team Leads.

Location : Rochester, NY 14606 Microbiologist responsible for performing routine quality control testing of raw materials, in-process samples, and finished products. Ensures compliance with GMP, HACCP, and ISO standards through accurate microbiological analysis, documentation, and product release in SAP. Skilled in aseptic techniques, microbial identification, and supporting operations with timely QC results. We are looking for a Microbiologist for our Quality Control team to be responsible for supporting the Rochester Laboratory in a manufacturing setting. This includes routine Microbiological lab testing with accurate, timely recording of test results into the business integrated module as well as utilizing lab reference materials for information regarding testing.

Location : Plainsboro, NJ 08536. Panelists will participate in sensory evaluations of food, beverages, and odorant samples, both individually and in groups, under the guidance of a panel leader. Responsibilities include following detailed instructions, completing evaluations using ballots or digital devices, and contributing to group discussions. Applicants must complete sensory screening tests prior to panel admission, with compensation provided for participation. Requirements: No experience required. Must be able to commit to at least 1 year of testing. Sensory evaluations will occur every Wednesday from 9:30am to 12:30pm. Please note: the panel runs during business hours. Must be free of major food allergies and dietary restrictions. Should have good communication skills, willingness to take direction from panel leaders and work well within a team of other sensory panelists. Applicants should have an excellent sense of smell and of taste, as well as the ability to accurately describe what they taste and smell. Applicants should be free of aversions to nearly all common foods and beverages.

Location: Cincinnati, OH (Onsite) The Lab Technician performs a variety of chemical, biological, and physical tests required for research, development or quality control. This position compiles data for reports and assists in special studies in the laboratory and in the field.

Location : San Diego CA The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw materials, in-process, and finished goods for the Molecular Diagnostics Division. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products.

Location : Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.