Pharma CQV Validation Engineer

Dormont Manufacturing Co; United States; On-site; USD 75,000 - 100,000; Full time

Job summary

Dormont Manufacturing Co is seeking candidates for a technical position focused on developing documentation for CQV activities. This role demands a Bachelor's degree in a science or engineering field along with 2–4 years of experience in a regulated industry. Responsibilities also include writing and executing protocols, managing work plans, and collaborating on various pharmaceutical projects.

Join a diverse team committed to excellence and integrity, dedicated to making a difference in the industry. Candidates with backgrounds in utilities and pharmaceutical manufacturing will find a unique opportunity here.

Qualifications

• 2–4 years’ experience in commissioning in a regulated industry.
• Familiarity with facilities and equipment startup.
• Experience with pharmaceutical manufacturing processes.

Responsibilities

• Develop documentation for CQV activities.
• Write and execute protocols at client sites.
• Plan and coordinate work with small teams.

Skills

Commissioning and qualification experience

Documentation development

Problem-solving in utilities

Education

Bachelor’s degree in a science or engineering field

Tools

ISPE Baseline Guide 5

Job description

Dormont Manufacturing Co is seeking candidates for a technical position focused on developing documentation for CQV activities. This role demands a Bachelor's degree in a science or engineering field along with 2–4 years of experience in a regulated industry. Responsibilities also include writing and executing protocols, managing work plans, and collaborating on various pharmaceutical projects.

Join a diverse team committed to excellence and integrity, dedicated to making a difference in the industry. Candidates with backgrounds in utilities and pharmaceutical manufacturing will find a unique opportunity here.