Responsibilities:

Ÿ Ensure quality and
compliance in all actions:

² Attend GMP training
on the schedule designated for role and as appropriate for role.

² Adhere to strict
compliance with procedures applicable to role.

² Exercise the highest
level of integrity in the tasks performed.

² In a timely and
prompt manner, identify, report and seek correction for deviations noted in the
workplace.

² Embrace a behavior
of employee involvement and commitment to doing the job right the first time.

² Ensuring employees
under the position’s scope of responsibility are trained in required procedures
for the execution of their role and maintain current with training requirements
during the year.

² Promoting an
environment of employee engagement in the workplace.

² Seeking prompt
identification, reporting and correction of deviations in the workplace as
noted by employees.

Ÿ Execute technical
projects in accordance with the HA and Kenvue policies and procedures.

Ÿ Provide support to
the in progress key projects which impacting revenue growth, quality
improvements, compliance remediation, and cost reduction. Effectively
collaborate with cross-functional team to optimize business results. Provide
support to resolve issues impacting timely completion and achievement of
project goals.

Ÿ Partners with the
Validation CoE to execute site Process and Cleaning Validation activities

Ÿ Partners to deliver
and execute key projects according to critical processes including, but not
limited to, Tech Transfer, Characterization, Validation and EM site Hyper care.

Ÿ Support effective
product lifecycle and knowledge management in close collaboration with the
Regional and Global MS&T and technical need state leaders.

Ÿ Partner with
Research and Development to establish and maintain processes for planning,
developing, and commercializing new products resulting in well-characterized,
validated, highly capable, cost-effective manufacturing processes.

Qualifications:

Ÿ Bachelor’s degree or above.

Ÿ Minimum 5 years (8 years preferred) in a pharmaceutical company, specifically in a technical department (not R&D).

Ÿ Strong understanding of GMP and mandatory experience in process and cleaning validation.

Ÿ Excellent communication skills.