Principal Scientist ytical NPD

About the job

Job Description

Kenvue is currently recruiting for

Principal Scientist Analytical NPD This position reports into Associate Director and is based at Mumbai .

Who We Are

At Kenvue we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science were the house of iconic brands including NEUTROGENA AVEENO TYLENOL LISTERINE JOHNSONS and BANDAID that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22000 diverse and brilliant people passionate about insights innovation and committed to deliver the best products to our customers. With expertise and empathy being a Kenvuer means to have the power to impact life of millions of people every day. We put people first care fiercely earn trust with science and solve with courage and have brilliant opportunities waiting for you! Join us in shaping our futureand yours. For more information click here .

What You Will Do

The Principal Scientist will lead analytical activities for complex new drug products from preformulation studies through process validation studies including preformulation studies method development and validation stability studies and process evaluation analysis. This individual will work with crossfunctional teams to define requirements deliverables and milestones to meet regulatory requirements and assure business goals are met. This individual will potentially supervise or oversee a team of analysts supporting analytical project activities including allocation of resources and prioritization across multiple activities or projects.

Key Responsibilities

Identify evaluate and implement new analytical technology as required for project activities.

Issue review and approve technical documents including analytical method development histories method validation protocols and reports and stability reports in compliance with standard operating procedures and regulatory requirements.

Participate on crossfunctional teams and recruit and mentor analytical Scientists.

Required Qualifications

• Minimum MSc B Pharm M. Pharm Ph.D. or equivalent science stream with minimum 1012 years of work experience
• A focused degree in Chemistry or Pharmaceutical Chemistry is preferred.
• Experience in working within Pharmaceutical or OTC environment is required.
• Experience with HPLC and UPLC is required. Experience with Atomic Absorption Ion chromatography and/or Gas Chromatography is preferred.
• Previous experience in working with Formulations Quality and New Product Development teams is preferred.
• Experience managing others is preferred.
• Experience working with LIMS systems and other documentation systems is preferred.
• Strong knowledge of GMPs is required.
• Experience interacting with the FDA EPA and/or DEA during audits and inspections is preferred. Broad knowledge and experience with regulatory requirements including ICH FDA and compendia (e.g. USP JP EP etc.) is highly preferred.
• Strong written and oral communication skills are required.
• It is preferred that this candidate have strong technical writing skills with understanding of compliance both from quality and regulatory standpoint.
• This individual will be able to work independently while managing multiple priorities successfully.
• The ability to influence others without direct line authority is highly preferred.

Whats In It For You

Competitive Benefit Package

Paid Company Holidays Paid Vacation Volunteer Time Summer Fridays More!

Learning Development Opportunities

Employee Resource Groups

This list could vary based on location/region

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Remote Work :

No