Vaga de Manufacturing Science & Technology (MS&T) Process Sr. Analyst
1 vaga: | Publicada em 29/06
A combinar
Sobre a vaga
Manufacturing Science & Technology (MS&T) Process Sr. Analyst-2407018380WDescriptionKenvue is currently recruiting for:
Manufacturing Science & Technology (MS&T) Process Sr. AnalystThis position reports
into MS&T Manager and is based in São José dos Campos, Brazil Who we areAt we
believe there is extraordinary power in everyday care. Built on over a century of
heritage and propelled forward by science, our iconic brandsincluding
NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSONS® and BAND-AID® are category
leaders trusted by millions of consumers who use our products to improve their
daily lives. Our employees share a digital-first mindset, an approach to
innovation grounded in deep human insights, and a commitment to continually
earning a place for our products in consumers hearts and homes. What will you
doThe Manufacturing Science and Technology Process Sr. Scientist is 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. In this position, the
sr. scientist will be also responsible for providing technical guidance to
manufacturing plants, quality assurance and other supply chain areas in material
and manufacturing processes troubleshooting to guarantee reliability in base
business execution. Finally, will ensure all supported projects are defined,
planned, documented, and executed in the compliance manner to Regulatory
requirement, GMP, EHS&S and Corporate quality standards. 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.·Apply intensive and diversified knowledge of technical
principles and practices to influence business decisions based on sound scientific
rationale.·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.QualificationsWhat
we are looking for Required Qualifications · Bachelors 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. Desired Qualifications·Working experience in
pharmaceutical manufacturing processes development is preferred·Desired to be a
critical thinker with problem solving skills·Intermediate Spanish will be
considered a differential·Good communication, organizational, interpersonal and
influencing skills.Whatýýýs in it for you·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.Primary LocationLatin
America-Brazil-São Paulo-São José dos CamposJob FunctionR&D