Production Technician

Sanofi•Pearl River, NY

1d•$24 - $32•Onsite

About The Position

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Primary responsibility of the incumbent will be operation of general manufacturing equipment under close supervision in accordance with current relevant quality standards or standardized procedures and within safety guidelines in the production of Flublok Drug Substance in the downstream processing (Clarification and Purification) and buffer preparation areas of the cGMP commercial manufacturing facility. Requires good documentation skills and attention to detail. Duties will include the operation, maintenance, cleaning and sanitization of all downstream processing equipment such as stainless-steel vessels including transfer lines, ancillary equipment (tube welders, tube sealers, peristaltic pumps), use of water-for-injection (WFI) point of use taps, etc. Activities will include executing techniques such as large-scale centrifugation, depth filtration, chromatography column purification and packing, tangential flow filtration, and clean-in-place and steam-in-place of process equipment. Other duties will include the cleaning and preparation of workspaces and biosafety cabinets. The incumbent should be proficient in aseptic technique, preventive maintenance, and changeovers for area equipment, including biosafety cabinets, magnetic mixers, in-process testing equipment (pH / conductivity meters and turbidity meters). Secondary responsibilities will be to aid in the troubleshooting of problems as they arise in downstream and buffer preparation areas. Business needs may also require database entry, cross training and operations in flex areas. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Requirements

High School Diploma with at least 1 year of work experience
Bachelor’s Degree with no prior experience
Training within a cGMP manufacturing environment is preferred
General knowledge of cGMP, GDP, SOP’s
English fluent, both written and spoken
Good communication and social skills
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job and include the ability to stand over intervals of several hours at a time, ability to bend, squat, and reach, and ability to lift, push, or pull various amounts of weight up to approximately 50 lbs.
Based on production schedules, different start time scenarios may occur, requiring a flexible work schedule for the candidate.
Ability to accommodate production requirements that may require 50+ hour workweeks, including 2nd shift or split shift hours, extended day hours and weekends.

Nice To Haves

Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process is desired but not required

Responsibilities

In depth understanding of techniques and processes being executed on routine basis.
Responsible for all aspects of downstream and buffer preparation including equipment preparation (CIP and SIP), appropriate use of raw materials and components (FIFO), weighing and dispensing of raw materials and intermediate solutions, material sampling for applicable analytical testing, filter integrity testing, etc.
Responsible for the operation and maintenance of ancillary equipment such as pH / conductivity meters, turbidity meters, tube welder, tube sealer, peristaltic pumps, etc.
Interacts with other departmental personnel to assist in resolving manufacturing quality issues.
Technician should have the ability to manage and analyze manufacturing data.
Ability to take initiative to identify issues, troubleshoot, propose solutions, and keep management informed.
Ensure good documentation practices (GDP) in execution and reviews of production records.
Responsible for all required cGMP training including additional training assigned by their manager.
Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.
Follows established SOPs for the flow of materials, personnel, and equipment in and out of the cGMP facility.
Work a flexible work schedule, weekends and holidays as required, and as needed by department.
Work with Compliance regarding notification of deviations and CAPAs as they occur and provides information during investigations.
Other duties as they are required.