Inspection and Packaging Operator

Sanofi; Ridgefield (NJ); On-site; USD 35,000 - 55,000; Full time

Job summary

An innovative global healthcare company is seeking an Inspection and Packaging Operator to ensure the quality and compliance of prefilled syringe products. This role involves meticulous inspection, documentation, and teamwork to uphold the highest standards of safety and efficiency. Join a supportive team dedicated to improving lives through science, where you will have opportunities for career growth and development. Enjoy a comprehensive rewards package that values your contributions and promotes well-being, including extensive health benefits and parental leave. If you are detail-oriented and thrive in a collaborative environment, this is the perfect opportunity for you.

Benefits

Health and wellbeing benefits

Parental leave

Career growth opportunities

Qualifications

• 2-3 years experience in manufacturing or inspection roles required.
• Fluent in English, both written and spoken.

Responsibilities

• Maintain batch record documentation and logs as required.
• Perform visual inspection of vials and syringes according to standards.
• Conduct reconciliation of materials used during inspection.

Skills

Ability to follow written and oral instructions

Teamwork

Knowledge of current Good Manufacturing Practices

Knowledge of Production Inspection Process

Knowledge of Manufacturing Packaging Process

Ability to quickly learn new processes

Good vision (correctable to 20/20)

Detail-oriented

Time Management

Ability to lift, push, or pull ≤ 50 lbs

Basic math proficiency

Computer knowledge

Education

High School Diploma or GED

Job description

Job Title: Inspection and Packaging Operator

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.

The Prefilled Syringe (PFS) Inspection Area is responsible for the staging, reconciliation, inspection, and packing of prefilled syringe products produced on the site. This includes hyaluronic acid (HA) based medical device products as well as pharmaceutical based products. In support of our main functions, additional responsibilities include maintaining compliance with all applicable Regulatory requirements relative to FDA, cGMP Regulations, Company’s SOPs, and Safety Regulations, accurate documentation on batch production records and logs, and cleaning production 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?

Main Responsibilities:

• Maintains batch record documentation and logs as required by corporation and regulatory agencies.
• Timely report at work-stations.
• Timely and accurate batch record entries.
• Checking and confirming accuracy of staged components.
• Perform visual inspection of vials and syringes according to established standards.
• Identify any inspection failures and report them immediately.
• Conduct reconciliation of materials used during inspection.
• Perform packing of inspected products.
• Perform daily safety walkthroughs and reporting results to management.
• Use of computers for data entry and reporting purposes and to obtain training.
• Achieve required quality, safety and efficiency targets.
• Perform packaging operations as required.
• Perform routine daily and monthly cleaning in production area.

About You

Skills

• Ability to follow written and oral instructions.
• Must be able to work effectively in a team-based environment.
• Knowledge of current Good Manufacturing Practices - 3 years.
• Knowledge of Production Inspection Process – 2 years.
• Knowledge of Manufacturing Packaging Process – 2 years.
• Ability to quickly learn new processes.
• Good vision (must be correctable to 20/20).
• Must be detail-oriented.
• Time Management.
• Able to support a flexible schedule and have a willingness to work overtime.
• Ability to lift, push, or pull various amounts ≤ 50 lbs.
• Proficient in performing basic math.
• Computer knowledge.

Basic Qualifications

• High School Diploma or GED
• 2 - 3 years of experience required
• Fluent in reading, writing and speaking English.

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.