Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

Validation Specialist at QRC Group, Inc

Carolina, , Puerto Rico -

Full Time

Start Date

Immediate

Expiry Date

28 Jul, 26

Salary

0.0

Posted On

29 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation Engineering, Manufacturing Process, Life Cycle Validation, IQ, OQ, PQ, Technical Writing, Oral Solid Dosage, Equipment Qualification, Regulatory Compliance, Pharmaceutical Industry, Medical Devices, Chemical Industry

Industry

Staffing and Recruiting

Description

Company Description QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions! Job Description Sr. Validation Specialist support of manufacturing process and equipment upgrades, replacements, and modifications in the manufacturing, or manufacturing support environment. Experience in: Manufacturing Process Methasys Validation Life Cycle Validation IQ, OQ, PQ Process and Reports Oral Solid Dosage (OSD) Qualifications Equipment’s Qualifications Requirements Bachelor’s Degree and 5 years of directly related experience in related field. Technical Writing Bilingual (English and Spanish) Technical Expertise areas of Validation Engineering in Manufacturing Environment Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The Validation Specialist will support manufacturing process and equipment upgrades, replacements, and modifications. They are responsible for executing validation life cycle activities including IQ, OQ, and PQ processes and reports.