What are the responsibilities and job description for the Sr. Validation & Compliance Engineer position at Jobs via Dice?
Location: Topeka, KS
Salary: $55.00 USD Hourly - $60.00 USD Hourly
Description: Our client is currently seeking a Sr. Validation & Compliance Engineer
Job Title : Sr. Validation & Compliance Engineer
Location : Indianapolis, IN | Kansas City, KS
Worksite : Onsite
Duration : 6 months
Job Description:
We are seeking experienced Sr. Validation & Compliance Engineers to support Commissioning & Qualification (C&Q) activities in pharmaceutical manufacturing environments. This role is ideal for professionals with 3-10 years of CQV experience who thrive in regulated environments and enjoy cross-functional collaboration.
Qualification:
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Salary: $55.00 USD Hourly - $60.00 USD Hourly
Description: Our client is currently seeking a Sr. Validation & Compliance Engineer
Job Title : Sr. Validation & Compliance Engineer
Location : Indianapolis, IN | Kansas City, KS
Worksite : Onsite
Duration : 6 months
Job Description:
We are seeking experienced Sr. Validation & Compliance Engineers to support Commissioning & Qualification (C&Q) activities in pharmaceutical manufacturing environments. This role is ideal for professionals with 3-10 years of CQV experience who thrive in regulated environments and enjoy cross-functional collaboration.
Qualification:
- Experience Level: Mid to Senior (3-10 years in CQV within pharmaceutical manufacturing)
- Expertise: Strong knowledge of FDA/EMA regulations, GMP, and risk-based validation practices
- Skills: Excellent documentation, problem-solving, and cross-team communication abilities
- Commissioning & Qualification: Develop, execute, and document IQ/OQ/PQ protocols for equipment, utilities, and facilities.
- Documentation: Author and review qualification documents, test scripts, deviation reports, and summary reports.
- Risk-Based Approach: Perform commissioning and qualification activities aligned with FDA, EMA, and internal quality standards.
- Cross-Functional Collaboration: Work closely with engineering, QA, validation, and operations teams throughout the C&Q lifecycle.
- Technology Transfer: Support process validation and handover to manufacturing.
- Deviation & CAPA: Participate in investigations, CAPA implementation, and continuous improvement initiatives.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Salary : $55 - $60