Inspection Packaging Operator Associate
Sanofi

Job Info

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Job Title: Inspection Packaging Operator Associate

Location: Ridgefield, NJ

About the Job

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.

This position is responsible for performing routine tasks, operating equipment, and troubleshooting in the area of automated Syringe Inspection and Syringe Packaging. This position supports execution of the production plan.

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?

Main Responsibilities

• Operate and troubleshoot high-speed automated Inspection and Packaging equipment. Typical tasks include loading vials/syringes onto automated inspection equipment, changing label reels, replenishing packaging items (e.g. inserts, labels, cartons, trays, shippers), operating syringe assembly machine, thermoformer, cartoner, case palletizer, serialization equipment, and wrapping pallets.
  
• Participate in line changeovers and continuously strive to minimize line downtime and maximize OEE%.
  
• Perform batch record reviews, logbook reviews, and SAP transactions.
  
• Perform OJT (On-the-job) training of less experienced Operator and ensure compliance with cGMPs and SOPs.
  
• Perform routine Quality and Safety inspection walk-throughs of the production areas.
  
• Schedule and coordinate periodic cleanings of equipment and packaging rooms.
  
• Will serve as witness of routine unit operation tasks for batch record signing. Maintains all associated documentation for operations being performed.
  
• Will be assigned formal FMEAs, RAs, CAPAs, CCRs and NCRs as needed.
  
• Implements and maintains production schedules based upon intra-departmental information.
  
• Generally receives minimal instructions on all assignments with some supervision. Takes initiative to identify issues, troubleshoot, propose solutions, and keep management informed.
  
• Other duties may be assigned as required.
  

About You

Basic Qualifications

• HS Diploma or GED and 3-5 yrs experience
  
• A degree in science, engineering or a related discipline and 1-3 years experience
  
• BS degree in science, engineering, or a related discipline and 0-3 years experience
  

Terms of employment

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, majority of the work activities are performed while standing.

• Ability to stand over intervals of several hours at a time
  
• Ability to bend, squat, and reach
  
• Ability to lift, push or pull various amounts of weight
  
• Ability to pass the required visual acuity test (wearing corrective lenses if needed)
  

Based on production demands and personnel availability, different start time scenarios or additional hours may be required so a flexible work schedule is required for the candidate. Core Work hours for the available shifts are as follows:

1st Shift, 5 AM to 1:30 PM.

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
  
• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
  

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.

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