Quality Assurance Systems Specialist (18-Month Contract)

Job Description

The success of a company depends on the passionate people we partner with. Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing, producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well‑being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Health is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Job Title: Quality Assurance Specialist

Responsibilities

At campus level, ensure that the quality system is implemented and followed according to the right level of quality defined by the Global Systems QA organization.

Right level of Quality & Strategy

• Assist the Operational QA manager for the investigation relating to their product

QMS & Documentation

• Ensure corporate harmonized requirements are implemented in the local QMS.


• Participate in the definition, set‑up and follow‑up of the local CAPA System.


• Participate in the definition, set‑up and follow‑up of the document control strategy for local QMS.


• Participate in the definition and set‑up of the local archival system.


• Participate in the definition, set‑up and follow‑up of the QMS training process in line with corporate standards.


• Participate in the definition of local other systems (eg. qualification, change control).

Community Building and Activation

• Act in the Global QA practices harmonization


• Represent the QA Systems locally and the campus in the QA systems community.

Audits and Inspections

• Define the annual self‑inspection schedule together with relevant SMEs.


• May perform self‑inspections.

Other Responsibilities

• Deviation Investigation – Investigate deviations, determine root cause, and document results. Determine and/or complete CAPA as required. Collect and analyze deviation trend data.


• CAPA/Change Control – Complete CAPA and administrate change control process as assigned.


• Training – conduct or assist in training activities within the relevant area of expertise.

Other duties as assigned.

Competencies

• Drive Ambition & Accountabilities


• Influence Others


• Collaborate with Empathy


• Engage & Develop


• Shape Solutions out of Complexity


• Client Focus

Qualifications

• Post‑secondary degree/diploma in biolofical sciences or related field preferred.


• Post‑secondary degree/diploma in Quality Assurance/Control ideal.


• 3 years in a Quality Assurance role in which you were involved in the development and administration of quality assurance systems.


• Previous experience in pharmaceutical or similar industry.


• Previous experience within a GXP environment.

Disclosures

• This requisition is for a current opening at our Guelph, ON facility


• Targeted compensation range is between $60-70k annual salary but may vary dependent upon education, skills and experience

Qualifications

• Post‑secondary degree/diploma in biolofical sciences or related field preferred.


• Post‑secondary degree/diploma in Quality Assurance/Control ideal.


• 3 years in a Quality Assurance role in which you were involved in the development and administration of quality assurance systems.


• Previous experience in pharmaceutical or similar industry.


• Previous experience within a GXP environment.

Your profile

• Post‑secondary degree/diploma in biolofical sciences or related field preferred.


• Post‑secondary degree/diploma in Quality Assurance/Control ideal.


• 3 years in a Quality Assurance role in which you were involved in the development and administration of quality assurance systems.


• Previous experience in pharmaceutical or similar industry.


• Previous experience within a GXP environment.