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C&Q Specialist

QRC Group

Job Location:

Juncos - Puerto Rico

Monthly Salary: Not provided by the employer

Experience Required: 4years

Posted: 19 September 2026 (Yesterday)

Application Deadline: 17 December 2026

Vacancies: 1 Vacancy

Job Summary

We are seeking a C&Q Specialist with expertise in execute qualification activities around an OEM-driven retrofit to an existing GMP manufacturing isolator.

Responsibilities:

Prepare and maintain all commissioning documentation.
Coordinate execution with contractor and vendors.
Maintain commissioning status reports.
Coordinate closure of deficiencies.
Participate in project meetings.
Support turnover to Operations and Maintenance.
Maintain commissioning records.
Provide editable electronic copies of all deliverables.
Provide final PDF copies of all approved deliverables.

Requirements

Bachelor Degree in Science or Engineering or related field.
Background in pharmaceutical products manufacturing environmental specially in sterile packaging area.
Experience in commissioning and qualification.
Strong knowledge of cGMPs regulations.
Startup and operational readiness experience.
More than 5 years of experience in commissioning related projects.
Experience in digital validation solutions.
Good skills writing validation/commissioning and technical documentation in English and using MS Office applications.
Bilingual (English & Spanish)