China Job Openings
Kenvue
Process Science Assistant Manager, OTC China
November 17, 2024
Description
nsure quality and compliance in all actions:
o Attend GMP training on the schedule designated for role and as appropriate for role.
o Adhere to strict compliance with procedures applicable to role.
o Exercise the highest level of integrity in the tasks performed.
o In a timely and prompt manner, identify, report and seek correction for deviations noted in the workplace.
o Embrace a behavior of employee involvement and commitment to doing the job right the first time.
o 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.
o Promoting an environment of employee engagement in the workplace.
o Seeking prompt identification, reporting and correction of deviations in the workplace as noted by employees.
nsure quality and compliance in all actions:
o Attend GMP training on the schedule designated for role and as appropriate for role.
o Adhere to strict compliance with procedures applicable to role.
o Exercise the highest level of integrity in the tasks performed.
o In a timely and prompt manner, identify, report and seek correction for deviations noted in the workplace.
o Embrace a behavior of employee involvement and commitment to doing the job right the first time.
o 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.
o Promoting an environment of employee engagement in the workplace.
o Seeking prompt identification, reporting and correction of deviations in the workplace as noted by employees.
- Execute technical projects in accordance with the site, MS&T and Jn J policies and procedures
- Provide support to the China Cluster Lead in the progress of key projects impacting revenue growth, quality improvements, compliance remediation, and cost reduction. Effectively collaborate with cross-functional leaders to optimize business results. Provide support & guidance to resolve issues impacting timely completion and achievement of project goals.
- Partners with the Validation Co E to execute site Process and Cleaning Validation activities
- Partners to deliver and execute key projects according to critical processes including, but not limited to, Tech Transfer, Characterization, and Validation.
- Support effective product lifecycle and knowledge management in close collaboration with the Regional and Global MS&T and technical need state leaders.
- 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.
- Take the responsible for EM site management from Technical aspect, including help management team to qualify EM site, to execute Pre-DD, full DD and related mitigation plan. Also support EM quality department to do the further on-site technical support on-time.
Qualifications
- Education: Bachelor’s degree (or equivalent) in Chemistry, Pharmacy, or Engineering is required. M.S., or Ph.D in Chemistry, Pharmacy, or Engineering is preferred. Reference experience minimums noted below.
-
Experience: 5+ years of industry experience is required. Relevant experience includes product/process development of pharmaceutical/OTC /Medical Device products, manufacturing of pharmaceutical/OTC/Medical Device products; R&D, Technical Services, Quality & Compliance, Validation experience or Engineering in pharmaceutical/OTC field.
Experience on the solid and semi-solid product technology is preferred.
Primary Location Asia Pacific-China-Shanghai-Shanghai
Job Function Process Engineering
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