We are looking for an experienced Pharmaceutical Manufacturing Validation Engineer to join our clients team in Houston!

Description: Validation Engineer II
Shift: Mon - Fri onsite 1st shift

W2 contract only * We cannot accept C2C at this time.

Requirements:

• 3 plus years experience doing pharmaceutical equipment/computer system validation.
• Local Houston candidates only.

Job Duties:

• Develops validation plans, qualification protocols, compiles and analyzes data, drafts summary reports, and reviews validation documentation to ensure that system are qualified in accordance with applicable regulatory agencies specifications/requirements.
• Assures that all validation documentation meets or exceeds the regulatory expectations.
• Entry level experienced with equipment and/or computer system validation.
• Able to work on validation discrepancies or investigations.
• Performs temperature mapping studies.
• Perform other duties as assigned.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.