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
Responsible for providing technical support to operations in terms of equipment/system initial validation and equipment/system requalification’s.
Compensation
Salary Range: $60,966 -$85,694
Responsibilities
Drafts protocols and executes equipment commissioning, qualification, and requalification’s per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results.
Analyzes data, composes a final report and circulates for approval.
Executes equipment validation studies to include protocol preparation, scheduling, protocol execution, and final report preparation.
Participates in presentation of results to Regulatory Agency when necessary.
Programs and operates department analytical instruments (such as temperature/humidity dataloggers) to perform controlled temperature/humidity chamber qualifications (examples lyophilizers, warehouses, sterilizers, incubators, etc.).
Provides technical support for operations regarding equipment/system initial validation and requalification within a cGMP-compliant environment.
Compensation
Salary Range: $60,966 - $85,694. Final pay determinations will depend on various factors, including but not limited to experience level, education, knowledge, skills, and abilities.
Responsibilities
Drafts protocols and executes equipment commissioning, qualification, and requalification’s per Standard Operating Procedures (SOPs).
Coordinates and communicates all testing with affected functional groups and evaluates test results.
Analyzes data, composes a final report and circulates for approval.
Executes equipment validation studies to include protocol preparation, scheduling, protocol execution, and final report preparation.
Participates in presentation of results to Regulatory Agency when necessary.
Supervisor overseeing daily manufacturing shift activities in the IGIV Purification area of Grifols Canada Therapeutics (GCT) facility, ensuring quality, safety, delivery, and productivity objectives are met.
Responsibilities
Lead and direct daily manufacturing shift activities ensuring all tasks are assigned and followed up
Ensure quality or preventative maintenance notifications are issued and investigated in a timely manner
Ensure manufacturing schedules, products and materials are delivered
Train IGIV Purification personnel on process activities, safety requirements and cGMP requirements
Identify technical and non-technical development gaps and implement plans and targets
Lead operational initiatives for deployment, validation, and lifecycle management of restaurant equipment and back‑of‑house solutions.
Compensation
A reasonable estimate of the current base pay range for this position is $85,000.00–$122,500.00. You are also eligible for annual cash bonuses and equity awards based upon performance and other factors.
Responsibilities
Lead equipment deployment initiatives from pilot through enterprise implementation
Manage project plans, milestones, risks, dependencies, and stakeholder communications
Develop tracking tools, reporting systems, and governance structures
Support restaurant openings, remodels, menu innovation and transformation programs
Drive asset lifecycle management, recovery and disposition programs
Requirements
Bachelor's Degree (BA/BS) from 4-year college or university
Nice to have: experience in restaurant or food service industry
Nice to have: experience with Smartsheet
Nice to have: experience with reporting tools
Nice to have: experience with workflow management platforms
Support the Quality Control Bioassay laboratory by planning, executing, and validating analytical testing for biologic products, managing documentation, and leading quality initiatives.
Compensation
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 78,724.45USD -106,509.55 USD
Responsibilities
Assist with planning and execution of equipment installation and qualification
Operate QC bioassay analytical testing for biologic products including ELISA and cell-based methods
Lead transfer, qualification, and/or validation of complex biologic procedures
Author, revise, and review documents and reports including SOPs, safety assessments, methods, trend reports, qualification/validation summary reports, technical reports, and method assessments
Assist with planning, scheduling, and execution of daily activities
Requirements
High school/GED + 4 years of Quality Analytical testing experience
Associate’s + 2 years of Quality Analytical testing experience
Bachelor’s + 6 months of Quality Analytical testing experience
Master's
Nice to have: GMP pharmaceutical production facility experience
Lead and manage quality control bioassay operations during the second shift, ensuring GMP compliance, data integrity, and efficient testing of biologic products.
Compensation
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 78,724.45USD -106,509.55 USD
Responsibilities
Assist with planning and execution of equipment installation and qualification
Operate QC bioassay analytical testing for biologic products including ELISA and cell-based methods
Lead transfer, qualification, and validation of complex biologic procedures
Author, revise, and review SOPs, safety assessments, methods, trend reports, and technical reports
Plan, schedule, and execute daily activities
Requirements
High school/GED + 4 years of Quality Analytical testing experience
Associate’s + 2 years of Quality Analytical testing experience
Bachelor’s + 6 months of Quality Analytical testing experience
Master's
Nice to have: Experience in GMP pharmaceutical production facility with classified areas
Lead a team to deliver on Key Safety, Quality, Delivery and Cost Results in a high volume, fully automated manufacturing environment producing Pen Needle products.
Responsibilities
Lead a team of engineers and/or technicians to provide direct support to the production and maintenance teams to resolve daily issues and assist with troubleshooting.
Champion a data-driven approach to investigate and resolve process issues.
Drive structured problem-solving with the technicians.
Continuously strive to improve efficiency of the equipment by standardising and optimising equipment setup, upgrading equipment to improve process capability where necessary.
Carry out frequent reviews of the preventative maintenance schedules to ensure that they are effective at mitigating equipment failure and improving uptime.
Superviseur, Purification IGIV SupervisorGrifols · Montreal, Canada