Scientist, Formulation 12-18 Months

2 weeks ago

Guelph, Ontario, Canada Kenvue Full time

Scientist, Formulation 12-18 Months W

Description


Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), is currently recruiting for a Scientist, Formulation for a Months contract with the potential to extend.

This position reports into the Senior Manager, Process Science and is based in Guelph, Canada.

Who We Are


At Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), we believe there is extraordinary power in everyday care.

Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S 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.

Join us in shaping our future-and yours

Watch us here:

What will you do?


Under the Guidance of the Senior Scientist(s) and the Departmental Manager - this role will plan, coordinate, and execute development and validation studies to document that manufacturing processes are consistently executable and meet the required specifications and regulatory expectations.


The position will also comply with all Kenvue (a division of Johnson & Johnson) policies and quality standards, health, safety and environmental regulations, and regulatory requirements (e.g.

Health Canada and the United States FDA).


Collaborate with Quality & Compliance, Plant Operations, and MS&T Engineering (if applicable) and coordinate the development, creation, review, and approval of process development and validation documents (protocols, reports, and validation assessments).


Key Responsibilities***- Design process implementation plans covering Feasibility, Characterization, and Validation depending on the nature of the Project, and oversee the execution of the development and validation batches within manufacturing.


  • Perform sampling and physical testing requirements for development and process validation batches
  • Prepare technical documents according to established format guidelines in support of department activities. Control the circulation of work in progress and maintains active and historical documents
  • Coordinate with all impacted departments (e.g. Planning, Quality & Compliance, and Plant Operation) and oversees the execution of all Process Development activities
  • Collate, analyze, and process data. Reviews data and documents pertinent to their technical area of focus
  • Perform other duties assigned by Senior Scientist, or Manager
Qualifications

Required:

  • A Bachelor's Degree (B.Sc.) with >2 years experience or a College Diploma coupled with >6 year experience in a pharmaceutical/OTC manufacturing environment will be considered.
  • A minimum of 2 years of prior experience in pharmaceutical/OTC process development is strongly preferred.
  • Good understanding of Granulation, Compression, and/or Coating principals.
  • Ability to evaluate scientific data.
  • Ability to take ownership for or work independently on project activities.
  • Excellent communication and presentation skills
  • Ability to influence and facilitate groups with diverse perspectives and bring teams to consensus / alignment.
  • Strong leadership, organization, decision making and interaction management skills.
  • Advanced computer skills, specifically in Microsoft Word, Excel, and Adobe Acrobat.
  • Strong technical writing, verbal communication, interpersonal and problemsolving skills

Desired:

  • Degree in Chemistry, Biology, Pharmaceutical Formulation or B. Eng. (Chemical)
  • Knowledge of process excellence
  • Previous project management experience

Other:

  • This position may require up to 10% domestic travel
  • Heavy lifting (up to 22 kg) may be required
  • Disposition of waste
  • Exposure to dust, fumes and noise
  • Corrosive, flammable, and toxic material handling may be required
Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies.

Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success.

We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.

LI-TA1

Primary Location NA-CA-Ontario-Guelph

Organization Johnson & Johnson Inc.

Travel Yes, 10 % of the Time

Job Function Product Development

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