Junior CQV Engineer - Biopharma Validation & Startup

MMR Consulting; Boulder (CO); On-site; USD 80,000 - 115,000; Full time

Job summary

MMR Consulting in Colorado is seeking a Jr. CQV Engineer to join a growing team. You will work with engineers on the design, commissioning, qualification, start-up and project management of biopharma processes, equipment and facilities.

The ideal candidate has 2–4 years of experience in commissioning/qualification/validation, familiarity with cGMP, and the ability to lead junior engineers. Travel to client sites in the greater Denver/Boulder area may be required.

Qualifications

• 2-4 years of experience in commissioning, qualification or validation in pharma/biotech.
• Knowledge of cGMP operations and regulatory expectations.
• Experience with validation project development and execution is preferred.

Responsibilities

• Provide technical guidance in commissioning, qualification and startup of pharmaceutical/biopharmaceutical equipment and facilities.
• Lead development of qualification deliverables (DQ, FAT, SAT, IQ, OQ, PQ).
• Perform field execution of qualification tests and protocols.
• Support development of Project Validation Plans to test system applicability.
• Lead qualification processes to ensure timely completion and compliance with specs.

Skills

CQV

Leadership

Project management

GMP

Education

Engineering degree

Tools

PCS/SCADA

Job description

MMR Consulting in Colorado is seeking a Jr. CQV Engineer to join a growing team. You will work with engineers on the design, commissioning, qualification, start-up and project management of biopharma processes, equipment and facilities.

The ideal candidate has 2–4 years of experience in commissioning/qualification/validation, familiarity with cGMP, and the ability to lead junior engineers. Travel to client sites in the greater Denver/Boulder area may be required.