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TSMS Scientist

locationCharlottetown - Prince Edward Island (PE),


Job Description:

Interested in joining a cause-driven, customer focused company dedicated to positively impacting the health of animals, people and the planet? Search our job listings below.

Position Description*: Provides front-line support to commercial vaccine manufacturing operations, as well as delivering process improvement and tech transfer projects, in compliance with cGMP and applicable regulatory guidelines and standards.
Functions, Duties, Tasks:
Primary Activities:

  • Work with manufacturing and quality teams in execution of technical protocols, development activities, and technical transfer programs.
  • Use scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes are capable and operating in a state of control, and identify opportunities for process improvements.
  • Develop / execute projects to address process issues and deliver on improvement opportunities.
  • Participate in product and process related technical investigations and root-cause analyses of process deviations, complaints, and OOS/OOE events.
  • Provide support in resolution of technical and compliance issues, technical answers to QA, internal inspection bodies, and to Health Authorities.
  • Author and assist in preparation and
critical review of technical documents, APRs/PQRs, PFDs, batch records, SOPs, protocols, and reports.
  • Demonstrate strict adherence to cGMP standards and Elanco policies and procedures. Maintain “safety first and quality always” mindset.
  • Other duties as required.
  • Minimum Qualifications (education, experience and/or training, required certifications):

    • MSc. in Engineering, Bio/Pharmaceutical Technology, Chemistry, Microbiology, or equivalent scientific degree.
    • Minimum 3-5 years’ experience in the pharma/biotech industry, with emphasis on downstream purification processes.
    • Expertise in molecular biology and nucleic acid platform technologies.
    • Proven understanding of biopharmaceutical production processes.
    • Demonstrated knowledge and experience with operations in a commercial cGMP manufacturing facility.
    • Proven success in leading multi-disciplinary project teams with excellent communication, problem-solving, and critical-thinking skills.

    Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

    Job Types: Full-time, Permanent

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