Jobs In West Greenwich, Rhode Island

Process Development Bioprocess Senior Engineer

**Job Description** Do you want to help shape the future of biopharmaceutical manufacturing? Are you interested in working with a diverse product portfolio of life changing products in a dynamic working environment? Would you like to work with a highly motivated team of process science professionals to positively impact patients’ lives? Would you like to […]

Associate Manufacturing – Nights

The Associate Manufacturing is a hands-on role in one of the two manufacturing facilities on site at Amgen Rhode Island. Successful candidates will join the AR30 team, focused on operational readiness and start-up. The on-boarding phase for this role will last 2 weeks, during which time successful incumbents will be on an administrative schedule (Monday […]

Associate Manufacturing – Nights

The Associate Manufacturing is a hands-on role in manufacturing on site at Amgen Rhode Island. Successful candidates will join the AR30 team, focused on operational readiness and start-up. The on-boarding phase for this role will last 2 weeks, during which time successful incumbents will be on an administrative schedule (Monday through Friday, approximately 8am to […]

Quality Control Associate

QC for Manufacturing – Team B Associate Quality Control **Job Summary:** Under minimal supervision, the Quality Control Associate will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment. 1. Perform sample collection and sample handling to support GMP […]

Engineer

Job Description The Engineer reports to the Senior Manager of the Downstream Process Engineering group. Working under direction, the position is responsible for providing process engineering support at the Amgen Rhode Island site. Specific duties include: + Provide technical support to commercial manufacturing as required + Working closely with multiple disciplines, including manufacturing, engineering, utility […]

Associate of Manufacturing

The Associate Manufacturing is a hands-on role in one of the two manufacturing facilities on site at Amgen Rhode Island. Successful candidates will join the AR30 team, focused on operational readiness and start-up. The on-boarding phase for this role will last 2 weeks, during which time successful incumbents will be on an administrative schedule (Monday […]

Non Clinical CMS Statistician

Amgen is seeking a Senior Quality Engineer (Non Clinical CMS Statistician) to be part of the Global Quality Engineering (GQE) team. We are pursuing highly motivated, mid-level career candidates, who are passionate practitioners of non-clinical statistics. The successful candidate will contribute to Amgen’s pipeline of new molecules and commercial products, that are treating serious illnesses […]

Engineer

**Job Description** The Engineer reports to the Senior Manager of the Downstream Process Engineering group. Working under direction, the position is responsible for providing process engineering support at the Amgen Rhode Island site. Specific duties include: + Provide technical support to commercial manufacturing as required + Working closely with multiple disciplines, including manufacturing, engineering, utility […]

Associate Manufacturing – Nights

D Shift: 7pm to 7am, rotating nights Under general supervision, Associate will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will […]

Associate Manufacturing – Days

**Shift Schedule: 7:00am – 7:00pm Rotating Days** Under general supervision, Associate Manufacturing will perform operations in the Manufacturing area, specifically Inoc/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical […]

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