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Sanofi Group Production Technician Buffer in Pearl River, New York

*Must be flexible to work 1st or 2nd shift (Most likely a 2nd shift position) with holidays, weekends, and overtime as per business needs*

Primary responsibility is the execution of SOPs and Batch Records in the downstream processing and buffer preparation areas of the cGMP manufacturing facility. Duties include operation, maintenance, cleaning, and sanitization of all downstream processing equipment. Activities will include executing techniques such as large-scale chromatography column purification and packing, depth filtration and tangential flow filtration, and clean-in-place and steam-in-place of process equipment. The associate is trained and able to perform environmental monitoring including air, water, and steam sampling and as needed helps in training new employees and cross-training. Secondary responsibilities will be to aid in the troubleshooting of problems as they arise in the downstream and buffer preparation areas.

KEY ACCOUNTABILITIES:

  • In-depth understanding of techniques and processes being executed on a routine basis

  • Basic understanding of the BEVS manufacturing Process

  • Interacts with other departmental personnel to assist in resolving manufacturing quality issues

  • Employees are responsible for training on, understanding, and following documented procedures that apply to their departments that support the Quality System.

  • Maintains records and documentation in accordance with a cGMP environment. Follows established SOPs for the flow of materials, personnel, and equipment in and out of the cGMP facility

  • Stay current on all assigned cGMP training

  • Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.

  • Follows instructions on notification of deviations as they occur and provides information during investigations.

  • Lifting up to 50 pounds

EDUCATION/EXPERIENCE:

  • High School degree with at least 1-2 years of experience or training in a cGMP manufacturing environment or a BS with no experience

  • Knowledge of cGMP

  • English fluent, both written and spoken

  • Good communication and social skills

  • Self-starting, flexible, and positive attitude

As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.

According to the CDC, an individual is considered to be “fully vaccinated” fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SP

#LI-SP

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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