Self Care Senior Process Scientist - Singapore - Johnson & Johnson

Johnson & Johnson
Johnson & Johnson
Verified Company
Singapore

1 week ago

Wei Jie

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Wei Jie

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Description

The Regional Self Care Staff Process Scientist provides technical support in Manufacturing Science and Technology for a broad range of OTC drug products and other consumer health product categories (including devices, food, complementary medicine etc).

The individual possesses a deep understanding of the principles of manufacturing processes, material interactions and has a demonstrated passion for innovation and continuous improvement.

Working under mínimal direction, this individual collaborates cross-functionally with Operations, Marketing, Quality Assurance, Research and Development (R&D), Raw Material Centre and other functions as needed to lead and provide sophisticated technical support in the design, development, and implementation of technical solutions for cost reduction and critical initiatives.

This individual is expected to assess, determine and implement technical aspects of projects, report metrics, and interact with multi-functional teams to implement projects.


The Regional Staff Scientist will act as the single point of contact for triaging raw material changes within the MS&T Self Care team and lead the definition of the drug product impact assessment strategies.

In addition, the Staff Scientist will actively support the Director Process Science in execution of key strategic initiatives.


Duties & Responsibilities:


General:


  • Ensure quality and compliance in all actions by:
  • Attending GMP / EHS&S (Environmental, Health, Safety & Sustainability) training on the schedule designated for the role
  • Adhering to strict compliance with procedures applicable to the role.
  • Exercising the highest level of integrity in the tasks that they perform.
  • In a timely and prompt manner, identifying, reporting, and seeking correction for deviations noted in the workplace.
  • Accepting a behavior of employee involvement and commitment to doing the job right the first time.
  • Develops, uses and maintains contacts with key scientists across organization, external partners and companies to benchmark and drive innovative solutions or technical support.
  • Advocates and leads initiatives to drive execution excellence and timely realization. Identify and recommend new agile ways and riskbased approaches to accomplish goals and objectives.
  • Identifies and proposes opportunities and innovations, technical solutions or optimizations that can positively impact the products or business.
  • Designs, coordinates, and implements project tasks per established timeline including the execution of planned experiments (i.e., sample collection, inprocess testing, sample management, etc.).
  • Lead for technological transfer process for New Products Introduction, Products Improvements, and new raw material qualification.
  • Writes or approves SOPs based on the area of experience and training. Is a trusted voice for and provides technical advice on SOPs, policies, and procedures.
  • Oversees, prepares, reviews or approves technical memos, reports, analyzes and summarizes data, and recommends conclusions based on scientific rationale. Reviews and approves reports and confirms conclusions are based on scientific rationale.
  • Leads, reviews and implements change control deliverables/documentation, investigations, corrective/preventative actions, and new product release data collection and analysis.
  • Oversee, lead or carries out investigations related to product out of specification or process deviation, stability deviation, consumer complaints, and other investigations as applicable. Defines and conducts laboratory experimentation as needed related to investigations and root cause analysis
  • Leads technical aspects for solving critical supply issues, global change control (GCC), root cause analysis, and remediation for technicalrelated complex issues. Corrective Action and Preventative Action (CAPA) implementation and follow up to ensure CAPA effectiveness to address investigation and the root causes related to process deviation, stability, out of specification, out of trend, out of expectations, complaints and others as applicable
  • Champions and leads technical aspects for manufacturing process improvements through data analysis identification of critical process parameters, the proposal of alternate process modifications, assistance in conducting DOE to determine the best processes, assistance in conducting scaleup activities including pilotscale and validation as required.
  • Oversees and writes technical documentation including but not limited to Product Impact Assessment, Technical Justifications, manufacturing work instructions, INV reports, and other reports as applicable.
  • Works under mínimal direction. Provides direction and mentorship to other scientists and coops.
  • Decisions made at this level may have a significant impact in scope and authority.
  • Consults on business opportunities and problems.
  • May assist in process or equipment validation.

Qualifications:


Education:


  • A minimum of a Bachelo

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