Commissioning & Qualification Engineer

Veg Group; United States; Hybrid; USD 65,000 - 85,000; Full time

Job summary

Veg Group is seeking a mid-level Commissioning & Qualification (C&Q) professional in Juncos, Puerto Rico to support Packaging operations within Process Development. The role focuses on executing C&Q activities for packaging equipment, ensuring compliance with regulatory standards.

The ideal candidate will have experience in the pharmaceutical industry and strong communication and problem-solving skills. The role may require work during 2nd and 3rd shifts to support project timelines.

Qualifications

• Mid-level experience in Commissioning & Qualification in pharmaceutical, biotechnology, or medical device industries.
• Familiarity with cGMP regulations and validation lifecycle is preferred.
• Ability to work independently and manage priorities.

Responsibilities

• Execute commissioning and qualification activities for packaging equipment.
• Support development and execution of C&Q documentation.
• Collaborate with Engineering, Quality, Manufacturing, and PD teams.

Skills

Commissioning & Qualification

Problem-solving skills

Communication skills

Ownership and accountability

Job description

Job Summary

We are seeking a mid-level Commissioning & Qualification (C&Q) professional to support Packaging operations within Process Development (PD). This role will focus on executing C&Q activities for packaging equipment and systems, ensuring compliance with regulatory standards while supporting project timelines. The ideal candidate is proactive, adaptable, and demonstrates strong ownership and initiative.

Key Responsibilities

• Execute commissioning and qualification activities for packaging equipment and systems within PD environments.
• Support the development and execution of C&Q documentation, including protocols, test scripts, and reports.
• Collaborate with cross-functional teams such as Engineering, Quality, Manufacturing, and PD to ensure alignment and project success.
• Assist in troubleshooting and resolving issues related to packaging systems during qualification activities.
• Ensure compliance with cGMP and internal quality standards.
• Maintain accurate documentation and provide timely updates on project progress.
• Support continuous improvement initiatives within packaging and qualification processes.

Qualifications

• Mid-level experience in Commissioning & Qualification within pharmaceutical, biotechnology, or medical device industries.
• Experience or exposure to packaging equipment and processes is preferred.
• Strong sense of ownership, accountability, and initiative.
• Ability to work independently and manage priorities in a dynamic environment.
• Strong communication and problem‑solving skills.

Additional Requirements

• Availability to work 2nd and 3rd shifts as required to support project timelines.

Preferred Skills

• Familiarity with cGMP regulations and validation lifecycle.
• Experience working in Process Development (PD) environments is a plus.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.