Support the Validation Engineering team at the Client Oceanside manufacturing facility, authoring, executing, and summarizing equipment qualification and cleaning validation activities.
Responsibilities
Support the Validation Engineering team at the Client Oceanside manufacturing facility
Author, review, and execute qualification protocols (IQ, OQ, PQ) for systems and equipment
Develop and execute Cleaning Validation (CV) and cleaning verification protocols
Evaluate validation test results against defined acceptance criteria
Support continuous improvement in validation processes
Requirements
B.S. or M.S. in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Biochemistry, or a related technical discipline
Support the Validation Engineering team at the Oceanside manufacturing facility by authoring, executing, and summarizing equipment qualification and cleaning validation activities.
Responsibilities
Author, review, and execute qualification protocols (IQ, OQ, PQ) for systems and equipment
Develop and execute Cleaning Validation (CV) and cleaning verification protocols, including sampling plans, visual inspections, and analytical test data coordination
Evaluate validation test results against defined acceptance criteria, resolve execution discrepancies via structured troubleshooting, and author protocol exceptions with cross-functional stakeholders
Support continuous improvement in validation processes
Document validation activities and maintain records
Provide technical expertise in pharmaceutical production processes, focusing on Cleaning Validation and Cleaning Process Lifecycle Management, supporting troubleshooting, decision‑making, and continuous improvement initiatives.
Compensation
Competitive salary (plus annual bonus, participation in company life insurance and private healthcare program).
Responsibilities
Act as subject matter expert for assigned processes, technologies, or Cleaning validation areas, and contribute to the relevant MSO systems within Process Technology & Transfers (PT&T).
Design, plan, execute, and evaluate cleaning validation and lifecycle activities, including monitoring data analysis and risk-based assessments.
Create, review, and update cGMP‑compliant cleaning validation documentation, including validation protocols, reports, and supporting documents.
Support the creation, assessment, and documentation of deviations and investigations, including root cause analyses and corrective and preventive actions.
Support inspections, audits, and regulatory interactions as a technical expert, maintaining permanent inspection readiness.
Author, review, and/or approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
Compensation
The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary.
Responsibilities
Author, review, and/or approve validation master plans, protocols, and reports
Perform a variety of Validation activities in compliance with Good Manufacturing Practices (GMP) and Validation Master Plan (VMP) requirements
Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities
Manage routine Quality systems such as Supplier Quality Management, Change Control, Quality Risk Management, Documentation, and Investigations, Annual Product Review and coordinate testing with functional groups
Maintain the Site Validation Master Plan and support validation as a Subject Matter Expert during customer and regulatory audits
Requirements
High school diploma (or equivalent) with 8+ years of experience
Associate’s degree with 6+ years of experience
BS with at least 2+ years of experience in pharmaceutical industry
Nice to have: Technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems
Chargé(e) Qualification/Validation Grands projets H/F Validation Nettoyage
Responsable de la validation des procédés et du nettoyage pour les projets industriels stratégiques de Virbac, basé à Carros (Ardèche).
Compensation
Rémunération fixe et avantages (Bonus, primes diverses, intéressement et participation, mutuelle et prévoyance, avantages CSE, participation aux repas d’entreprise…)
Responsibilities
Apporter son expertise en validation de procédés et de nettoyage
Élaborer les stratégies de validation et les analyses de risques
Vérifier et approuver les documents de validation
Rédiger les instructions de fabrication
Participer aux réunions stratégiques et opérationnelles
Lead validation initiatives for manufacturing equipment, processes, cleaning and computerized systems to ensure compliance with regulatory and quality standards.
Compensation
The estimated salary range for this position is $72,080.00 - $108,120.00 CAD annually, which reflects base salary as well as estimated target payout under the Management Incentive Compensation Plan.
Responsibilities
Lead the development, execution, and completion of validation programs for manufacturing equipment, processes, cleaning and computerized systems to ensure a validated state of control.
Author validation protocols and reports, analyze validation data, and apply statistical techniques to demonstrate compliance with regulatory and quality requirements.
Partner with Engineering, Production, Quality Control, and external vendors to plan, coordinate, and execute qualification activities including IQ, OQ, and PQ protocols.
Serve as a validation subject matter expert by providing technical guidance on process validation, cleaning validation, equipment qualification, computerized systems validation, and data integrity practices.
Support change control and quality system activities by assessing validation impacts, contributing to investigations, and leading resolution of validation-related non-conformances and corrective actions.
Requirements
Bachelor's degree in engineering, Chemistry, Microbiology, Pharmacy, Life Sciences, or a related scientific discipline.
The Process Engineer II is responsible for providing 1st shift engineering production support including implementing process and technology improvements, regular on-the-floor manufacturing support, collecting, monitoring, analyzing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market, investigating non-conformances, CAPAs, process performance drifts and implementing corrective and preventative actions, conducting technical assessments of change orders and Supplier Change Requests, and responsible for the initiation and follow-through of the change control processes.
Responsibilities
Implementing process and technology improvements
Regular on-the-floor manufacturing support
Collecting, monitoring, analyzing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market
Investigating non-conformances, CAPAs, process performance drifts and implementing corrective and preventative actions
Conducting Technical assessments of change orders and Supplier Change Requests
The CQV Engineer III is a mid-level career position that requires understanding of commissioning, qualification and validation (CQV) and the ability to handle multiple real-time complex projects while maintaining strong work ethic and client collaboration.
Responsibilities
Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
Independently interacts with client to assess and continuously reassess client needs
Performs quality GAP analysis
Authors technical and scientific reports
Demonstrates an understanding of project scope of work assigned
Requirements
Bachelor’s degree is required; an engineering degree is preferred
The Pharmaceutical Process Engineer leads or participates in various projects within a complex, globally oriented environment, focusing on polymerics production, packaging and distribution in a GMP environment.
Responsibilities
Defining, specifying, and purchasing new production equipment
Setting up, executing, and reporting qualifications for new equipment
Introducing new products, materials, or components to production departments
Setting up, executing, and reporting on process and cleaning validations
Setting up, executing, reporting, and/or coordinating investigations and changes for the improvement of existing installations and production processes
Requirements
HBO level education
Chemical Engineering
Mechanical Engineering
Other relevant field
Nice to have: Technically and technologically oriented
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