.Pfizer Manufacturing Associate Support in Bothell, United States Why Patients Need YouOur breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.What You Will AchieveThe North Creek Manufacturing Facility at Pfizer is seeking a highly motivated Manufacturing Associate that desires the opportunity to significantly contribute to the development and commercialization of transformative cancer therapies. The Manufacturing Associate will use their training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP Facility.How You Will Achieve ItUtilize standard operating procedures and documents cGMP activities within batch records and logbooks applying good cGMP documentation and data integrity practices.Complete setup, use, and cleaning (as necessary) of cGMP production equipment.Proactively works with senior associates, subject matter experts, and management to achieve training competency in production operations.Maintains a clean and orderly production area. Positively engages and collaborates with other team members to ensure daily production tasks are completed promptly.Ensure work executed in compliance with company and regulatory quality policy and systems.Participates and supports a culture of continuous improvement. Effectively collaborates with cross functional partners such as Quality Assurance, Quality Control, Supply Chain, and Facilities.Job Duties May include:Media and buffer compounding, assembly and movement of materials and equipment into staving and production areas, wipe-down and sanitization of equipment/materials prior to and post-transfer, preparation and sterilization of parts and assemblies (including manual wash, equipment wash, and autoclave), stocking of materials, gowning, and supplies, and ensuring cleanliness and audit -readiness of the GMP Manufacturing areas.Perform cell culture operations safely and compliantly in accordance with OSHA and cGMP guidelines. Cell Culture operations include but are not limited to, dispensing and sampling of raw materials, media preparation, small scall passaging, set-up and operation of single use bioreactor, product sampling, and depth filtration harvest set-up and operations.Perform Downstream and Conjugation operations safely and compliantly with OSHA and cGMP guidelines. Operations include but are not limited to, dispensing and sampling of raw materials, buffer preparation, column packing, UF/DF, chromatography, viral inactivation and filtration, product sampling, and formulation of bulk drug substance and intermediate
