Publié hier
Validation Associate
@ Resolute Workforce Solutions
Brantford, Ontario
Salaire :
55 000 $–65 000 $ par année
Responsabilités :
- Provide Quality support for New Product Development (NPD) and Existing Product Development (EPD) projects, including cleaning validation activities.
- Develop validation protocols and final reports for equipment, facility, cleaning, process, and computerized system qualifications.
- Maintain and update the Master Validation/Qualification Plan and manage calibration and preventive maintenance programs, coordinating with contractors to…
- Develop and implement SOPs and support the review and approval of QMS documents, including deviations, change controls, CAPAs, complaint investigations, and…
- Coordinate regularly with Production and QA teams to support operational planning and activities.
- Assist in preparing validation-related sections of Annual Product Quality Reports (APQRs).
Résumé des exigences :
- Resolute Workforce Solutions, a staff augmentation subsidiary of Brevitas Consulting Inc., provides qualified professionals to support the workforce requirements of organizations in the…
- Please review the site location and associated logistics, including commuting arrangements, accessibility, and any site-specific requirements, when considering these opportunities.
- Develop validation protocols and final reports for equipment, facility, cleaning, process, and computerized system qualifications.
- Maintain and update the Master Validation/Qualification Plan and manage calibration and preventive maintenance programs, coordinating with contractors to ensure compliance.
- Follow all Occupational Health and Safety Act requirements, regulations, and safety procedures, and perform other duties as assigned by the Associate Manager, Quality.
- Bachelor's degree in Science, Engineering, or a related field from an accredited university; Master's degree preferred.
Outils et compétences
Avantages mentionnés
Source et dates
Type de source non vérifié · zoho
- Date publiée par l’employeur
- 2026-11-06
- Première détection par notre source
- 2026-11-07
- Mise à jour du dossier source
- 2026-11-07
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Resolute Workforce Solutions
Profil d’entreprise sauvegardé
Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.
Your Consulting & Resourcing Partner
Description complète de l’entreprise
Resolute Workforce Solutions' mission is to provide our clients and candidates with the best possible employment experience. We hold accountability and integrity as our core values and live by them every day. Our team has years of hands-on experience in project management, operational process improvement, organizational change management, quality, compliance and technical assurances. We service pharmaceutical, biotech, financial, oil & gas, chemical, food & beverage and medicinal marijuana. Our Services - Engineering Engineering design and project management have become a critical component of organization success as organization span over multiple countries and business processes become increasingly complex. We are looking for candidates with skills in design development, risk management, project controls, and project management. Roles: Engineers, Project Coordinators/Managers, Reliability Engineers, Process Improvement, etc. - IT & Information Solution Information Technology and Information Solutions implementation starts with a robust business process modeling, which forms the basis of design for a solution, a strong project management, and quality assurance practices through the life cycle. Understanding the organizational and technical environments to build context specific process models is essential. Roles: Computer System Validation, Security Infrastructure, Business Analysts, Business Intelligence, etc. - Quality & Compliance Abiding to a strict regulatory environment that is increasingly demanding and rigorously enforced has become problematic. Consequently, organizations are struggling to achieve and maintain an ongoing state of compliance and thus, the ability to supply products to the market. Roles: Technical Writers, Cleaning Validation, Process Scientist, Lead Investigators, Lab Technologist, etc.
- Abonnés LinkedIn
- 7 472
- Personnes associées sur LinkedIn
- 14
- Bureaux déclarés
- 70 E Beaver Creek Rd, Suite 24, Richmond Hill, Ontario L4B 3B2, CA
- Catégories d’activité
- Employment
- Recruiting
- Staffing Agency
- Autres noms enregistrés
- Resolute Workforce Solutions
- Spécialités
- Recruitment
- Pharmaceutical
- Financial Recruitment
- Sourcing
- Reference Checks
- Biotech Recruitment
- Leaders
- Operations Staff
- Consultants
- Food & Beverage
- Medicinal Marijuana
- IT
- Quality & Compliance
- and Engineering
- Le profil indique une agence de recrutement
- Oui
- Investissement total déclaré
- 0
La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.
Resolute Workforce Solutions' mission is to provide our clients and candidates with the best possible employment experience. We hold accountability and integrity as our core values and live by them every day. Our team has years of hands-on experience in project management, operational process improvement, organizational change management, quality, compliance and technical assurances. We service pharmaceutical…
| Champ | Valeur |
|---|---|
| Secteur | Staffing and Recruiting |
| Taille | 51-200 employees |
| Siège social | Richmond Hill, Ontario |
| Type d’organisation | Privately Held |
| Spécialités | RecruitmentPharmaceuticalFinancial RecruitmentSourcingReference ChecksBiotech RecruitmentLeadersOperations StaffConsultantsFood & Beverage |
| Offres sur Jobsy | 6 |
| Voir la page |
About Resolute
Resolute Workforce Solutions, a staff augmentation subsidiary of Brevitas Consulting Inc., provides qualified professionals to support the workforce requirements of organizations in the pharmaceutical and life sciences sectors.
We have been retained by a pharmaceutical manufacturing company to support its increased production demands through the provision of qualified resources at its manufacturing facility in Brantford, Ontario. All positions associated with this engagement are site-based and require personnel to work on-site. Please review the site location and associated logistics, including commuting arrangements, accessibility, and any site-specific requirements, when considering these opportunities.
Role Overview
We are looking for a highly motivated and energetic professional to join our team as a Validation Associate in Brantford, ON (Onsite).
Responsibilities:
- Provide Quality support for New Product Development (NPD) and Existing Product Development (EPD) projects, including cleaning validation activities.
- Develop validation protocols and final reports for equipment, facility, cleaning, process, and computerized system qualifications.
- Maintain and update the Master Validation/Qualification Plan and manage calibration and preventive maintenance programs, coordinating with contractors to ensure compliance.
- Develop and implement SOPs and support the review and approval of QMS documents, including deviations, change controls, CAPAs, complaint investigations, and training records.
- Coordinate regularly with Production and QA teams to support operational planning and activities.
- Assist in preparing validation-related sections of Annual Product Quality Reports (APQRs).
- Follow all Occupational Health and Safety Act requirements, regulations, and safety procedures, and perform other duties as assigned by the Associate Manager, Quality.
Qualifications:
- Bachelor's degree in Science, Engineering, or a related field from an accredited university; Master's degree preferred.
- Minimum 5 years of experience in Quality Engineering, QA/QC, or Validation within a pharmaceutical manufacturing GMP/cGMP environment.
- Certified Quality Engineer (CQE) certification is an asset. Experience with GC, HPLC, laboratory equipment, and microbiological testing is preferred.
- Thorough knowledge of GMP/cGMP, GLP, regulatory standards, and proficiency in MS Word, MS Excel, and electronic systems.
- Strong organizational, time management, multitasking, and problem-solving skills, with the ability to manage high workloads, work under pressure, and drive continuous improvement.
- Excellent interpersonal, verbal, and written communication skills, with good judgment and the ability to collaborate effectively with internal teams and external contacts.
- Overtime may be required based on production needs and must be approved by Management.
Note: The annual salary range is $55,000–$65,000, depending on qualifications and experience.
Benefits
Upon successful completion of probation, you will also be enrolled in our benefit programs:
- Life Insurance
- Accidental Death
- Long Term Disability
- Dental and Healthcare
To Apply:
Click the “I’m interested” button below, or
E-mail your resume in MSWord or pdf format to [email protected] with the following details in the e-mail's Subject Line: Validation Associate: FIRST NAME, LAST NAME.
We thank all applicants in advance; however, we will only contact the candidates whose qualifications match closely to the job requirements.
We welcome and encourage applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.
Review our Candidate Privacy Policy for more information.
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