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Sanofi Group Analytical Chemist in Chattanooga, Tennessee

R2744831 Analytical Chemist II

  • Location: Chattanooga, TN

  • Job type: Full time

About the job

At Sanofi Consumer Healthcare , we have one overarching mission - to work passionately, challenging ourselves and our industry every day, to build a healthier future by helping people, help themselves, bringing “Health in Your Hands”.

Our teams are building trusted & loved brands that connect with hundreds of millions of consumers worldwide, enabling better self-care for individuals and communities, while also contributing to a healthier planet. To fulfill this mission, we are embarking our consumers, our customers, healthcare professionals, and our employees in this journey because this is what will make us become the “Best Fast-Moving Consumer Healthcare (FMCH) Company In & For the World”.

We strive to act as a force for good by integrating sustainability along our business and employees’ mission and operate responsibly from both a social and environmental point of view.

To achieve this, we need strong talent who will help us shape the future of our Consumer Healthcare business and challenge our industry. At Sanofi Consumer Healthcare, we aspire to create a work environment where people can thrive, grow, and be at their best every day. Our priority is working with integrity to improve the health and well-being of people and communities where we operate, working towards making a positive impact in the world.

Our Team:

Sanofi is immediately hiring an Analytical Chemist to focus on prioritizing and expediting strategic projects for product life cycle and COGS optimization. It includes all Analytical Chemist I duties, plus creating methods for lifecycle management and technical compliance.

This Analytical Chemist will report directly to KSOL and with a dotted line to the QA Associate Director, it involves generating documentation for methods, stability studies, and cleaning studies under QA guidance. Additionally, it conducts and designs testing for evaluating, maintaining, and approving raw materials for Sanofi CHC products.

Main responsibilities:

Analytical Chemist responsibilities include executing and maintaining methods and techniques for lifecycle management and problem-solving in support of quality assurance, quality control, and operations. This involves supporting methods and protocols for validation programs and writing reports for validation projects. Strong written articulation of theoretical, mathematical, and practical aspects of methods is crucial. Also, may lead teams and operates with minimal supervision, guided by KSOL and the Associate Director, QA. Demonstrating potential for progression to opportunity to advance after some time in the role.

  • Execution of methods and techniques for the raw material evaluation program

  • Maintenance and possibly development of methods and techniques for the accelerated stability program

  • Development and execution of methods for technical compliance of currently marketed products

  • Provides support for projects related to transfer of products to a CMO or to the site

  • Management of method validation projects

  • Management of raw material evaluation projects

  • Preparation of Validation reports

  • Tracking progress of all projects

  • Transfer and Validation of compendial methods

  • Written development of the theory, mathematics, and practical execution of compendial and in-house methods

  • Written preparation of reports, change requests, GMP documentation with strong attention to detail

  • Design of testing of materials for approval for use in Sanofi CHC products

  • Detailed working knowledge of instrumentation and maintenance

  • Support of laboratory personnel

  • Troubleshoot and solve problems within AQA and across departments

  • Interaction with vendors to compile necessary documentation and supplies

  • Other duties as assigned

This description is representative but not inclusive of all position responsibilities. You may be asked from time to time to complete tasks not listed within the contents of this document, but that are relative to the goals of the business.

About you

  • Bachelor’s degree from an accredited college in Chemistry, Pharmaceutical Sciences, or closely related field required.

  • 4+ years of analytical experience.

  • GMP experience required

  • Wet chemistry experience required.

  • HPLC, GC, IC, ICP, AA, and UV preferred.

  • This position requires extensive use of computer equipment.

  • Must have a demonstrated proficiency in Microsoft business software to include Excel, Word, and Outlook.

  • Strong verbal and written communication skills are required.

  • Experience with Chemstation and Openlab software is desired.

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Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video (https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at sanofi.com (https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness) !

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