Manufacturing Science and Technology Process Lead

Há 6 horas

São Paulo, São Paulo, Brasil Johnson & Johnson Tempo inteiro
Job Title: Manufacturing Science and Technology Process Sr. Scientist

We are seeking a highly skilled Manufacturing Science and Technology Process Sr. Scientist to join our team in São José dos Campos, Brazil. As a key member of our MS&T team, you will be responsible for leading and executing local and regional projects for development of manufacturing processes, reformulations, and continuous processes improvement for solid, liquid and semi-solid pharmaceutical presentations.

Key Responsibilities:
  • Technically lead life cycle management projects for technology transfers, cost reduction, BCP development, manufacturing processes optimization or new technology implementation, working with multi-functional teams at local, regional and global levels.
  • Execute technical activities related to life cycle management projects including, but not limited to historical data review, product and manufacturing process assessment, development plan and other technical documents elaboration, pilot and/or trial execution, specifications and standard procedures review, etc
  • Technically support manufacturing processes validations, cleaning & sanitization validations and production campaigns development.
  • Provide technical support to investigations, CAPA and troubleshooting events related to raw material, product composition, manufacturing process design or consumer complaint, by conducting root cause analysis and historical data evaluation
  • Work in close collaboration with local, regional and global teams to guarantee compliance, processes harmonization and leverage of best practices across manufacturing sites Kenvue networking.
  • Be responsible for coaching and promoting development of less experienced teammates.
  • Manage expenses related to execution of life cycle management projects and report progress to MS&T regional leader.
Qualifications:
  • Bachelor's degree in Chemistry, Pharmacy, Chemical Engineering or correlated areas is required
  • At least 5 years' experience within the pharmaceutical or related industry.
  • Advanced English is required.
  • Experience with pharmaceutical or related industry processes and systems including product development, validation, technology transfer and life-cycle management of products
  • Experience in technical writing, cGMP ́s, ANVISA / COFEPRIS / FDA / ICH regulations
  • Knowledge of regulatory requirements in Brazil (it is a plus previous experience with ICH, FDA, etc.)
  • Knowledge in statistics (DOE, process capability, control charts, etc)
  • Demonstrated leadership skills to align multi-functional team members on delivering project deliverables
  • Ability to manage complexity and to work collaboratively with critical stakeholders at local, regional and global levels.
What We Offer:
  • Competitive Benefit Package
  • Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More
  • Learning & Development Opportunities
  • Employee Resource Groups

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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