Associate Director, Chemical Stewardship

Bristol Myers Squibb

10 - 15 years

50 - 55 Lacs

hyderabad

Posted:1 day ago| Platform:

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Skills Required

project management immigration software testing h1 lca analysis artificial intelligence kaizen tpm visa processing chemical regulations leadership product development h1b line balancing work permit system process automation communication skills

Work Mode

Work from Office

Job Type

Full Time

Job Description

Act as company leader and subject matter expert on global chemical registration requirements (e.g., REACH, K-REACH, MEE Order No. 12, TSCA) ensuring timely and accurate submissions in accordance with regional and national regulations. Deliver overall chemical compliance company wide.
Conduct regulatory monitoring and impact assessment (e.g., product development, market access) related to anticipated legislative shifts for chemicals of concern (e.g., PFAS, microplastics), including restricted substances and emerging contaminants. Provide strategic guidance on chemical stewardship policies and procedures.
Lead internal taskforces/cross functional teams related to chemicals of concern (e.g., PFAS) and advocate for science-based chemical stewardship by representing the company in external industry forums and regulatory working groups.
Design and improve internal chemical stewardship processes to enhance agility and minimize business risk.
Provide subject matter expertise to support product and company sustainability targets. Experience with Life Cycle Analysis (LCA) is a plus.
Prepare chemical stewardship communications for leadership and internal partners to embed awareness, enhance agility and minimize business risk.

Qualifications & Experience

Bachelors degree in chemistry, toxicology, product stewardship or related discipline required. Advanced degree preferred.
10+ years regulatory experience in chemicals (experience with complex portfolios and multinational organizations is highly valued). In-depth knowledge of global chemical regulations and registrations processes applicable for the pharmaceutical industry.
Proven ability to implement new regulations and establish effective internal processes.
Leadership experience with the ability to coordinate across teams and functions as well as work independently.
Strong communication and interpersonal skills and a demonstrated ability to influence senior management, third parties, thought leaders and regulatory agencies; acts with integrity.
Ability to innovate and encourages others to do so as well. Strives to enhance performance by doing things that are unique and leading edge; experience with AI and/or process automation is a plus.
Willingly embraces changes needed to adapt to new circumstances and uncertainties.

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