TSMS Scientist

PUB316308

About this job

  • Branche: Pharmaceutical
  • Area of expertise: Project Management & Services
  • Location: Charlottetown

What is required?

  • Hours per week: 40
  • Education level: Academic Master

About this role

About this role

We’re hiring a Technical Services Manufacturing Science (TSMS) Scientist for our client, a large pharmaceutical company producing medicines and vaccinations for pets and livestock. The TSMS Scientist 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 standard. This is a two year contract role, reporting to the Charlottetown, PE office.

  • Maintains overview of fermentation process performance through data trending and front-line support of commercial manufacturing operations.
  • 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.
  • Participate in product and process related technical investigations and root-cause analyses of process deviations, complaints, and OOS/OOE events.
  • Work with cross-functional manufacturing and quality teams in execution of technical protocols, development activities, and scale-up / technology transfer programs.
  • Develop / execute projects to address process issues and deliver on improvement opportunities.
  • Provide support for upstream cell/viral culture manufacturing processes.
  • Participate 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, risk assessments, 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.
  • Support other operational programs and initiatives as required

Requirements

Requirements

  • MSc. in Engineering, Bio/Pharmaceutical Technology, Chemistry, Microbiology, or similar scientific degree desired. Bachelor’s-level degree with equivalent work experience will also be considered.
  • Minimum 3-5 years’ experience in the pharma/biotech industry, with emphasis on fermentation processes. Cell and viral culture experience a plus.
  • Proven understanding of biopharmaceutical production processes.
  • Demonstrated knowledge and experience with operations in a commercial cGMP manufacturing facility.
  • Proven success in working within multi-disciplinary project teams with excellent communication, problem-solving, and critical-thinking skills.

Benefits

Benefits

Why work with Brunel? We are proud to offer exciting career opportunities from over 100 offices globally in 42 countries. Advancing your career takes time and effort – let us match you to your ideal position.

Join the Brunel Family

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Join the Brunel Family

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.

Start applying immediately

Start applying immediately

Sending an application is quick and easy. Just make sure you have the required documents ready to go.

  • Certifications (optional)
  • Job references (optional)
  • Motivation Letter (optional)
  • Resume
Apply now

Any questions remaining?

Your consultant, Chris Kapusta is happy to clarify anything about this vacancy. When reaching out, use the pub number:
PUB316308

Account manager

Chris Kapusta
Brunel Canada - Calgary
c.kapusta@brunel.net

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