TSMS Scientist

PUB322151

About this role

About this role

We’re hiring a Technical Services Manufacturing Science (TSMS) Scientist for our client, a largepharmaceutical company producing medicines and vaccinations for pets and livestock. The TSMS
Scientist provides front-line support to commercial vaccine manufacturing operations, as well asdelivering process improvement and tech transfer projects, in compliance with GMP and applicable
regulatory guidelines and standard. This is a two year contract based role with the potential forextension

• Maintains overview of fermentation process performance through data trending and front-linesupport of commercial manufacturing operations.
• Use scientific and statistical analysis tools to improve process understanding, ensuremanufacturing 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 ofprocess 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, internalinspection bodies, and to Health Authorities.
• Author and assist in preparation and critical review of technical documents, APRs/PQRs, riskassessments, 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 similarscientific 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 fermentationprocesses. Cell and viral culture experience a plus.
• Proven understanding of biopharmaceutical production processes.• Demonstrated knowledge and experience with operations in a commercial cGMPmanufacturing facility.
• Proven success in working within multi-disciplinary project teams with excellentcommunication, 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

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:
PUB322151

Account manager

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

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