Senior C&Q/Validation Engineers-Gmp/Pharma
By Process Engineering Specialists At Illinois, United States
Participate in the CQV of process/FUE and cleaning validation.
Using the process automation system for the commissioning and validation of process equipment.
Protocol Development (IQ,OQ, PQ) / protocol review for process equipment/FUE and/or cleaning validation.
Interface with client personnel and with outside vendors when necessary while performing the above.
If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony ([email protected]).
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Sound knowledge of GAAP, SEC reporting, a plus
Review of client books and records, reconcile account balances to supporting schedules
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Prepare non-public company’s financial statements, footnotes and necessary support
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Responsible for highlighting unusual relationships from basis analysis for financial statements and account balances
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Ability to contribute unique Telecoms domain technical knowledge or insights.
Ability to work across multiple-projects in the department as well as own project responsibilities.
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Exemplary communications and relationship building skills including cross-cultural working.
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Are you an experienced Senior Validation Consultant looking for a new challenge? We are looking for a highly motivated individual to join our team and help us ensure the quality of our products. You will be responsible for developing and executing validation plans, protocols, and reports. You will also be involved in troubleshooting and resolving validation issues. If you are looking for an exciting opportunity to make a difference, then this is the job for you!

A Senior Validation Consultant is responsible for providing technical expertise and guidance to clients in the areas of validation, compliance, and quality assurance. They are responsible for developing and implementing validation strategies, plans, and protocols, as well as providing technical support to clients.

What is Senior Validation Consultant Job Skills Required?

• Knowledge of validation principles, processes, and best practices
• Ability to develop and implement validation strategies, plans, and protocols
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to manage multiple projects and prioritize tasks
• Knowledge of regulatory requirements and industry standards
• Proficiency in Microsoft Office applications

What is Senior Validation Consultant Job Qualifications?

• Bachelor’s degree in a related field
• 5+ years of experience in validation, compliance, and/or quality assurance
• Experience in the pharmaceutical, biotechnology, or medical device industries
• Knowledge of FDA, EU, and other regulatory requirements
• Certified Validation Professional (CVP) certification is preferred

What is Senior Validation Consultant Job Knowledge?

• Knowledge of validation principles, processes, and best practices
• Knowledge of regulatory requirements and industry standards
• Knowledge of FDA, EU, and other regulatory requirements
• Knowledge of cGMPs, GLPs, and other quality systems

What is Senior Validation Consultant Job Experience?

• 5+ years of experience in validation, compliance, and/or quality assurance
• Experience in the pharmaceutical, biotechnology, or medical device industries

What is Senior Validation Consultant Job Responsibilities?

• Develop and implement validation strategies, plans, and protocols
• Provide technical support to clients in the areas of validation, compliance, and quality assurance
• Monitor and review validation activities to ensure compliance with regulatory requirements and industry standards
• Prepare and review validation documents such as protocols, reports, and SOPs
• Train and mentor staff on validation processes and best practices
• Develop and maintain relationships with clients and vendors
• Ensure compliance with cGMPs, GLPs, and other quality systems