Validation Engineer

Job Description

Job Description

Validation Engineer

12+ month contract

Lewisville, TX (Onsite)

Designs, engineers, and implements quality systems to ensure regulatory compliance and quality improvements. This includes designing, planning, and executing validation activities for Over the Counter (O.T.C.) Drugs in accordance with Food & Drug Administration (FDA) regulatory guidelines. Supports quality engineering initiatives (i.e., conducting process capability studies and process improvement investigations), to improve quality, capacity, and efficiency while reducing costs. Independently plan, perform and / or coordinate validation projects to ensure timely completion. Draft and coordinate execution of validation documents for Equipment Qualification (IQOQPQ), Process Validation and Cleaning Validation / Verification. Draft / or provide technical guidance for SOPs / Work Instructions and other master documents. Remain current with industry and regulatory agency trends. Provide technical leadership for deviation investigations. Analyze data and provide recommendations for improvements in manufacturing process, and equipment. Prepare protocols and other technical documents, and participate in the interpretation of data, collaborating with other departments. Other responsibilities as directed.

Responsibilities

• Interfaces with personnel in Quality Assurance Laboratories (Microbiology (QCM) and Chemistry (QCA)), Process Development, Product Integrity, Engineering, Contract Services, Regulatory Affairs, Package Engineering, Scheduling, Packaging, Processing and Central Weigh to design, plan, write protocols, execute, document results, and gain the required approvals for all validation activities. Validation activities include, but are not limited to product processing, product packaging, and utilities.
• Collaborates with Site / Corporate Engineering or Process Development and directs all Qualification activities for newly purchased equipment.
• Develops validation master plan, qualification, and validation schedule. Ensures that validation / qualification projects and timelines are structured in accordance with FDA regulatory guidelines. Informs Quality Assurance management of status of validation projects on a regular basis.
• Plans and organizes all validation execution activities, including scheduling validation runs, collecting and analyzing data, and documenting results. Coordinates with management, the allocation of all resources towards validation efforts.
• Compiles validation and other technical work in report format for future use, including building a technology base of pertinent continuous quality improvement related issues and solutions. Implements re-validation process improvements as required.
• Interfaces with personnel in Quality Assurance, Packaging, Processing, etc. to identify potential areas for product quality and process improvement.
• Identifies the source of variation in all manufacturing processes and seeks to reduce unnecessary variation, through the use of various statistical and quality improvement tools (i.e. experimental design, statistical process control).

Experience

Estimated Min Rate : $28.00

Estimated Max Rate : $40.00

What’s In It for You?

We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include :

Note : Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit https : / / www.yoh.com / applicants -with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice :   https : / / www.yoh.com / privacy -notice

Company Description

Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.

Company Website : https : / / www.yoh.com /

Company Description

Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day & Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website : https : / / www.yoh.com /