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MSAT Principal Scientist
MSAT Principal Scientist6046-JANSSEN SUPPLY GROUP. Legal Entity • Spring House, Pennsylvania, USA
MSAT Principal Scientist

MSAT Principal Scientist

6046-JANSSEN SUPPLY GROUP. Legal Entity • Spring House, Pennsylvania, USA
8 days ago
Job type
  • Full-time
Job description

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

Job Function :

Supply Chain Engineering

Job Sub Function : Process Engineering

Job Category :

Scientific / Technology

All Job Posting Locations :

Spring House Pennsylvania United States of America

Job Description :

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way. Learn more at today for this exciting opportunity to be part of our growing team!

Preferential areas NC Greenville. Alternatively Titusville Horsham Malver area at one of the JNJ campuses with regular site visits to NC.

As a Principal Scientist in Global MSAT your primary role is as Drug Product Technical Owner (DPTO) with specific responsibility for significant program / brand. The DPTO is the voice of MSAT in the Value Chain Team and Virtual Management Team (VMT) and is responsible for the technical aspect of the Lifecycle Management structure and strategy of DP during their commercial lifespan.

Key Responsibilities :

  • Represents MSAT and the technical team in the VCT and VMT and provides the required manufacturing technical support
  • Participates in the VCT / VMT to develop the long-term supply strategy including scenario development and E2E impact analysis
  • Supports the VCT / VMT to identify improvement / innovation opportunities to build project business cases and to prioritize projects (product related)
  • Coordination of all product-related technical activities
  • Supervises technical process and product performance
  • Identifies and implements opportunities for active decrease in manufacturing COGs
  • Implements or follows-up on execution of technical projects
  • Deploys the platform standardization policy as appropriate
  • Supports failure investigations (escalation of quality or compliance events)
  • Reviews technical product & process risk profile and criticality analysis
  • Implementing and supporting new platforms innovations or changes in life cycle management products
  • Provides this expertise as well to External Manufacturing related to the Biotherapeutics Platform

Qualifications

Education :

  • A minimum Bachelors degree is required
  • Experience and Skills :

    Required :

  • A minimum 8 years of relevant experience and BS degree or equivalent OR 5 years with advanced degree MS / MBA / Ph.D. or equivalent.
  • Experience of process validation. Preferably in the field of large molecule Drug Product.
  • Prior experience leading Tech Transfer- and Launch activities (Internal or external partners)
  • Detailed technical knowledge of biopharmaceutical manufacturing site unit operations
  • Manufacturing experience within a GMP regulated environment
  • Excellent interpersonal and communication skills
  • Shown leadership in providing integration of activities and information across multifunctional groups and matrix teams
  • Knowledge of technical aspect of the lifecycle strategy of products
  • Science-based risk approach and regulatory intelligence experience
  • Ability to influence and lead peers superiors and external partners.
  • Preferred :

  • Experience in Life Cycle Management DP development and project management.
  • Document Mgmt. systems such as TruVault etc. SAP MS Office applications TrackWise / COMET Planisware MS-project Minitab or similar statistical software
  • Other :

  • Ability to travel up to 20%; depending on project needs to NC areas
  • For more information on how we support the whole health of our employees throughout their wellness career and life journey please visit .

    Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law.

    We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

    Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center ( ) or contact AskGS to be directed to your accommodation resource.

    Required Skills : Preferred Skills :

    Agile Decision Making Business Savvy Coaching Corrective and Preventive Action (CAPA) Crisis Management Critical Thinking Disruptive Innovations Emerging Technologies Industrial Hygiene Lean Supply Chain Management Organizing Process Control Process Engineering Product Costing Program Management Project Scheduling Science Technology Engineering and Math (STEM) Application Technical Research

    The anticipated base pay range for this position is :

    $ 102000-$ 175200 USD

    Additional Description for Pay Transparency :

    Subject to the terms of their respective plans employees and / or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs : medical dental vision life insurance short- and long-term disability business accident insurance and group legal insurance. Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys long-term incentive program. Subject to the terms of their respective policies and date of hire Employees are eligible for the following time off benefits : Vacation 120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year Holiday pay including Floating Holidays 13 days per calendar year Work Personal and Family Time - up to 40 hours per calendar year Parental Leave 480 hours within one year of the birth / adoption / foster care of a child Condolence Leave 30 days for an immediate family member : 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below. Experience :

    Staff IC

    Key Skills

    Machine Learning,Python,Data Science,AI,R,Research Experience,Sensors,Drug Discovery,Research & Development,Natural Language Processing,Data Analysis Skills,Toxicology Experience

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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    Principal Scientist • Spring House, Pennsylvania, USA

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