Job Description

Position Description:

To support in the production process of veterinary biologics according to a defined production schedule following Good Manufacturing Practices,guidelines and specific outlines of production to meet market demands for aquaculture products.

Functions, Duties, Tasks:

Comply with company quality and safety standards, adhere to safety first and quality always mindset.



Ensures production operations comply with safety requirements, Good Manufacturing Practices, Standard Operating Procedures, and manufacturing documentation.



Ensures the product produced according to their approved Outline of Product/Product Dossiers and to Good Manufacturing Practices guidelines to meet market demand for the aqua products.



Drive & model behaviours in alignment with company principles with a particular emphasis on speaking up for safety & quality.



Provides technical leadership to cross functional technical team.



Demonstrates direction including adherence to standard calendar including Huddles and Gemba's.



Facilitates the daily huddle meeting, ensures cross functional attendance, metrics delivery and action completion / accountability.



Provides routine update to control tower on key issues, mitigations, and schedule adherence.



Facilitates cross functional team meetings, including routine balanced scorecard review, continuous improvement project prioritization and improvement delivery accountability.



Works with cross functional process team to deliver one schedule including all production and maintenance activities.



Works with Supply Chain to manage raw material issues / Bill of material improvements.



Holds routine 1:1's with supervisor(s) and completes performance management and development discussions.



Ensures that performance management and/ development discussions are completed for Production Technicians and Process Technicians.



Guide significant deviation investigations using structured root cause analysis



Reviews revisions to batch records, Standard Operating Procedure, qualification documents for the production operations.



Implements small operational changes including writing change controls, ensuring compliance to procedure.



Provides input to user requirement specifications (URS) documents for key capital projects.



Acts as production lead for Capital projects ensuring the operational readiness plan is defined and completed on time.



Escalates significant issues and potential solutions to the Operations Director.



Other duties as required.

Minimum Qualifications:

Must have a Bachelor's degree in a life science (e.g., Biochemistry, Chemistry, Chemical Engineering, Biochemical Engineering, Biology).



5-10 years of experience in the manufacturing industry is preferred.



Mininum 3-years previous supervisory experience.



Expertise performing investigations and writing deviations.



Expertise in completing production documentation (i.e., deviations, Standard Operating procedure, Correctice Actions & Preventive Actions, etc.).



Intermediate/expert computer skills using MS Office (Word, Excel, Power Point), SAP and experience is required.



Excellent interpersonal skills, both communications and written.

Preferred Qualifications:

Thorough technical understanding of quality systems and regulatory requirements.



Have a strong resiliency to change in the manufacturing environment.



Lean or Six sigma experience.

Other Information:

Role will be available for contact 12 hours a day 7 days a week for emergency situations.



We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.



The Company is required to provide a reasonable estimate of the salary range for this job in certain provinces within Canada. Final determinations with respect to salary will consider a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education. Expected CAD salary range: $73,000- $124,100. Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, and vacation.



All candidates are required to have adequate and legal work authorization to work in Canada, prior to applying for posted positions. Only candidates with valid work authorization, not requiring company sponsorship in the course of their employment with our company will be considered in the recruitment process.



Current Employees apply HERE



Current Contingent Workers apply HERE

Secondary Language(s) :

Description du poste:

Soutenir le processus de production de produits biologiques veterinaires selon un calendrier de production defini en suivant les directives cGMP (Bonnes pratiques de fabrication)et les plans de production specifiques pour repondre aux demandes du marche pour les produits aquacoles.

Fonctions, Devoirs, Taches :

Respecter les normes de qualite et de securite de l'entreprise, adherer a la mentalite de securite d'abord et de qualite toujours.

S'assure que les operations de production respectent les exigences de securite, Bonnes pratiques de fabrication, les Procedures operatoires normalisees et la documentation de fabrication.

S'assure que le produit est fabrique selon leur plan approuve de produit/dossiers de produit et selon les directives Bonnes pratiques de fabrication pour repondre a la demande du marche pour les produits aquatiques.

Encourager et modeliser des comportements en alignement avec les principes de l'entreprise, en mettant particulierement l'accent sur la prise de parole pour la securite et la qualite.

Fournit un leadership technique a une equipe technique interfonctionnelle.

Demontre un leadership, y compris l'adhesion au calendrier standard, y compris les Huddles et les Gemba.

Facilite la reunion quotidienne de huddle, assure la presence interfonctionnelle, la livraison des metriques et l'achevement des actions / responsabilite.

Fournit une mise a jour de routine a la tour de controle sur les problemes cles, les attenuations et le respect du calendrier.

Facilite les reunions d'equipe interfonctionnelles, y compris la revision de la carte de pointage equilibree de routine, la priorisation des projets d'amelioration continue et la responsabilite de la livraison des ameliorations.

Travaille avec l'equipe de processus interfonctionnelle pour livrer un calendrier unique incluant toutes les activites de production et de maintenance.

Travaille avec la chaine d'approvisionnement pour gerer les problemes de matieres premieres / ameliorations de la nomenclature.

Tient des reunions individuelles de routine avec les superviseurs et complete les discussions sur la gestion de la performance et le developpement.

S'assure que les discussions sur la gestion de la performance et/ou le developpement sont completees pour les techniciens de production et les techniciens de processus.

Mene des enquetes sur les deviations significatives en utilisant une analyse des causes profondes structuree

Examine les revisions des dossiers de lots, des procedures operatoires normalisees, des documents de qualification pour les operations de production.

Met en oeuvre de petits changements operationnels, y compris la redaction de controles de changement au besoin, en assurant la conformite aux procedures.

Fournit des contributions aux documents (User requirement specifications) pour les projets d'investissement cles.

Agit en tant que responsable de la production pour les projets capitaux en s'assurant que le plan de preparation operationnelle est defini et complete a temps.

Escalade les problemes significatifs et les solutions potentielles au directeur des operations.

Autres taches selon les besoins.

Qualifications minimales:

Doit avoir un diplome de licence. De preference en sciences de la vie (par exemple, biochimie, chimie, genie chimique, genie biochimique, biologie).



5-10 ans d'experience dans en environnement de fabrication.



3-5 ans d'experience prealable en supervision.



Experience dans la realisation d'enquetes et la redaction de deviations.



Experience dans la completion de la documentation de production (c'est-a-dire, deviations, Procedures operatoires standards, Actions et mesures preventives.).



Competences informatiques intermediaires/expert utilisant MS Office (Word, Excel, Power Point), SAP et experience requise.



Excellentes competences interpersonnelles, tant en communication qu'a l'ecrit.

Qualifications preferees:

Comprehension technique approfondie des systemes de qualite et des exigences reglementaires.



Avoir une forte resilience au changement dans l'environnement de fabrication.



Experience Lean ou Six Sigma.

Autres informations:

Le role sera disponible pour contact 12 heures par jour, 7 jours par semaine pour les situations d'urgence.



Nous sommes fiers d'etre une entreprise qui embrasse la valeur de rassembler des personnes diversifiees, talentueuses et engagees. La facon la plus rapide d'innover est de rassembler des gens de diverses opinions dans un environnement inclusif. Nous encourageons nos collegues a remettre en question avec respect les problemes de reflexion et d'approche de l'un et de l'autre. Nous sommes un employeur souscrivant au principe de l'egalite d'acces a l'emploi et nous sommes determines a