Quality Document Control Specialist

Metric Bio; Houston (TX); On-site; USD 50,000 - 80,000; Full time

Job summary

An exciting pharmaceutical company in Houston is seeking a Quality Document Control Specialist to enhance their document control system. In this role, you will be responsible for cleaning the system, rewriting Standard Operating Procedures (SOPs), and building training curriculums. This position offers a unique opportunity to contribute to quality assurance in a dynamic environment. The contract is for 6 months with the potential for a permanent position, making it an ideal opportunity for those looking to grow in the pharmaceutical industry. Join a team dedicated to excellence and innovation in pharmaceutical manufacturing.

Qualifications

• 2-5 years of GMP experience in a life science setting.
• Experience in cleaning Document Control System and rewriting SOPs.

Responsibilities

• Assist in cleaning the document control system and rewriting SOPs.
• Build curriculums and manage CAPAs and deviations.

Skills

GMP experience

Document Control System cleaning

SOP rewriting

Curriculum building

CAPAs

Deviation management

Spreadsheet experience

Job description

Metric Bio has partnered up with a very exciting Pharmaceutical company located in Houston, Texas looking for a Quality Document Control Specialist. You will assist in cleaning the document control system, rewriting SOPs, and building curriculums.

Responsibilities:

• 2-5 years of GMP in a life science setting
• Experience cleaning Document Control System
• Experience rewriting SOPs
• Experience building curriculums
• CAPAs, Deviation, and Building spreadsheet experience

This is a 6 month Contract with the possibility for a Contract to Permanent position.

Seniority level

Associate

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing