Manufacturing Associate 4, Drug Product Filling (1st Shift)

Position Overview The manufacturing associate in Drug Product Manufacturing will have a primary task for operation of filling line including all tasks related. This role will also support projects which influence manufacturing processes for DPM including training of others. This position will also support and assist in scheduling daily manufacturing activities for the team. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours or shift rotation. Job Description What You’ll Do During the project phase Participate and support testing activities, such as FAT, PQ etc. as well as other related activities Support and contribute to the preparation of the documentation package as e.g., "Standard Operating Procedures", "Work Instructions" Contribute to the preparation for operational readiness related to bulk drug product manufacturing Possible assignments include: Supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes as well as testing and commissioning support Travel up to 0-25% (international or domestic) may be required during the project phase In operations Lead, execute and document manufacturing processing steps and/or manufacturing support activities as well as process monitoring and control Perform operations of the Drug product filling line Execute validation protocols according to cGMP Standard Operating Procedures (SOPs) Own the establishment of processes and trainings to become a trainer for coworkers Maintain compliance of GMP documents and ensure own training level is complaint and maintained Support and/or assist senior level associates or supervisor with scheduling daily activities on drug product manufacturing floor, as needed This role requires shift work (weekend and potential for nights) Perform other duties as assigned Basic Requirements High School Diploma or GED 6+ years of direct experience in a manufacturing environment Preferred Requirements Associate's Degree + 4 years of direct experience in a cGMP manufacturing environment OR BA/BS + 2 years of direct experience in a cGMP manufacturing environment Equivalent Military training or experience Experience on specific unit operations (ex: Viral Filtration and Bulk Dispensing) Understanding of manufacturing run cadence and order of shift activities Knowledge of cGMP, safety and operational procedures A high degree of knowledge and expertise of the operation of specific production equipment Working Conditions & Physical Requirements Be exposed to an environment that may necessitate respiratory protection Be exposed to noisy environments Have a normal range of vision Climb ladders and stairs of various heights Experience prolonged sitting, standing, walking, bending, stooping and stretching throughout the shift, up to 12 hours Use hand-eye coordination and manual dexterity sufficient to operate a computer keyboard, telephone, calculator, and other office equipment is required May be required to lift up to 50 pounds on occasion EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (View email address on click.appcast.io). #J-18808-Ljbffr Merck & Co.