Job title: Quality Assurance Technician III - 3rd shift

• Location: Onsite in Chattanooga, TN
• 3rd Shift - Sunday-Thursday 10:30 pm - 7 am

About the job

Opella, the Consumer Healthcare business unit of Sanofi, is the purest and third-largest player globally in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market.

We have an unshakable belief in the power of self-care and the role it can play in creating a healthier society and a healthier planet. That's why we want to make self-care as simple as it should be by being consumer-led always, with science at our core. Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands.

This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers. We are also proud to be the first major fast-moving consumer healthcare company to achieve B Corp certification. Join us on our mission. Health. In your hands.

The Quality Assurance Technician III will support overall compliance related to cGMP regulations in all routine functions performed by the Quality Assurance Technicians, including review of batch packaging records, oversight to packaging operations, and component inspection and disposition.is

This is a 3rd Shift position - Sunday-Thursday 10:30 pm - 7 am

Main responsibilities:

• Support auditing of packaging operations including filling, cartoning, and display assembly to assure they are performed in compliance with cGMP's. Assure that the documentation is accurate and approved in a timely manner.
• Support the testing and disposition of packaging components.
• Approve audit portion of Batch Packaging Records.
• Provide support for regulatory site inspections.
• Participate in the necessary training for all levels reporting to the Senior Manager, Production Quality.
• Provide back-up to Senior Manager of Production Quality as needed to support the overall quality objective.
• Perform verifications of balances, Magna Mikes, and Web Tech machines as applicable.
• Maintain all roll stock and insert labeling as applicable to cGMP's.
• Attend daily QDCI Level 2 meetings.

About you

• Education & Experience: You must have a high school diploma or GED and at least two years of relevant work experience.
• Desired Qualifications: Knowledge of cGMPs and all applicable SOPs applicable to the quality role. Knowledge of SAP.
• Physical Ability: You need to be able to lift 10 to 20 pounds regularly and up to 50 pounds occasionally, and stand, walk, and bend for 8 to 10 hours per day.
• Special Requirements: You are required to comply with dress code regulations, be willing to undergo necessary training, and work in conditions with exposure to product, dust, grease, and packing machinery hazards.
• Pre-employment Testing: You need to complete the required pre-employment testing.

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.

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