Engineer-Process Validation

US Tech Solutions; Boulder (CO); On-site; USD 80,000 - 100,000; Full time

Job summary

A global staffing firm is seeking a Process Validation Engineer to ensure the consistent implementation of compliance within a pharmaceutical manufacturing facility. The ideal candidate will have a BS/BA degree in engineering, at least three years of industry experience, and proven abilities in understanding equipment design, multi-tasking, and thorough documentation. This role involves overseeing trial runs, testing process parameters, and developing knowledge of equipment functions.

Qualifications

• Minimum of three years of experience in the pharmaceutical industry.
• Proven ability to understand equipment design and functions.
• Excellent ability to document details of work performed.

Responsibilities

• Ensure consistent implementation of corporate and regulatory compliance.
• Oversee trial runs of production or related processes.
• Work with project engineers to understand equipment capabilities.
• Test critical process parameters for reliability and quality.
• Develop knowledge of equipment function, design, and utilization.
• Present updates and reports to staff and regulatory agencies.

Skills

Understanding of equipment design

Multi-tasking skills

Documentation skills

Education

BS/BA degree in engineering or related field

Job description

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website www.ustechsolutions.com.

We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.

Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.

Job Description

• The Process Validation Engineer will ensure consistent implementation of corporate and regulatory compliance of validation activities within a pharmaceutical manufacturing facility.

Primary functions of the role include :

• Oversees trial runs of a production or production- related process to substantiate the validity of the equipment/process and completion of all associated documentation.
• Works with project engineers and other support groups to have an in-depth understanding of new and existing equipment capabilities.
• Tests critical and key process parameters to assure reliability, quality and proper documentation to support the associated process and results.
• Develops a working knowledge within assigned area of responsibility of equipment function, design, and utilization.
• Presents updates, reports and presentations as necessary to the department, plant staff and regulatory agencies.
• Provides a key role in assuring the integrity of the manufacturing process.

Qualifications

Requirements :

• BS/BA degree required in engineering or an engineering related field
• Minimum of three years of experience, preferably in the pharmaceutical industry.
• Proven ability to understand equipment design and functions to assure appropriate utilization and validation of the process.
• Excellent multi-tasking skills and the ability to document details of the work performed are required.