What are the responsibilities and job description for the Commissioning & Qualification Professional position at Hired by Matrix?
At-a-Glance:
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company. If so, our client is hiring a Commissioning & Qualification Professional.
Position Type:
- Contract
- Onsite
Required
- Bachelor’s degree in Engineering, Life Sciences, or a related technical field
- 5 years of experience in commissioning, qualification, and/or validation within the pharmaceutical or biotech industry
- Hands-on experience in aseptic manufacturing environments
- Strong knowledge of GxP, FDA regulations, and validation lifecycle requirements
- Experience with black utilities (e.g., WFI, clean steam) and/or laboratory analytical equipment qualification
- Familiarity with electronic validation systems such as Kneat is highly preferred
- Prior experience supporting large-scale pharmaceutical manufacturing projects is a plus
- Strong technical writing, communication, and problem-solving skills
- Ability to work both independently and in a collaborative team environment
Responsibilities:
- Commissioning & Qualification (C&Q) professionals to support aseptic manufacturing operations within a regulated life sciences environment.
- Role will focus on executing commissioning, qualification, and validation activities for critical systems, utilities, and laboratory equipment to ensure compliance with GxP and regulatory requirements.
- Execute commissioning and qualification (C&Q) activities for aseptic manufacturing equipment, utilities, and systems
- Develop and/or review protocols including IQ, OQ, and PQ documentation in alignment with regulatory standards
- Support startup and validation of black utilities (e.g., WFI, clean steam, process gases)
- Perform qualification activities for laboratory analytical instruments and equipment
- Collaborate cross-functionally with engineering, quality, validation, and manufacturing teams
- Ensure all activities comply with GxP, FDA, and applicable industry guidelines
- Utilize electronic validation systems (e.g., Kneat) for protocol execution and lifecycle documentation
- Troubleshoot issues during commissioning and qualification phases and support resolution efforts
- Maintain thorough and accurate documentation to support audits and inspections
Salary : $60