Commissioning & Qualification Specialist at QRC Group, Inc

Turku, Southwest Finland, Finland -

Full Time

Start Date

Immediate

Expiry Date

12 Feb, 26

Salary

0.0

Posted On

14 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Commissioning, Qualification, Documentation, Validation, Regulatory Standards, GMP, FDA, Technical Support, Communication, Organizational Skills, Teamwork, Project Coordination, Risk Management, Data Entry, Protocol Development, Execution

Industry

Staffing and Recruiting

Description

Company Description QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions! Job Description Commissioning & Qualification Specialist is focused on providing technical and documentation support for validation and startup activities within the pharmaceutical industry. The selected candidate will work directly on-site, collaborating with cross-functional teams to ensure compliance with regulatory and operational standards. Key Responsibilities • Develop commissioning and/or qualification documentation including URS, FS, IQ/OQ/PQ protocols, and final reports. • Prepare executed binders, enter qualification data into the designated system, and deliver documentation to the document control area. • Provide technical information and support related to qualification protocols and documentation to internal teams. • Offer technical assistance to resources and management throughout the qualification process. • Maintain effective communication with project sponsors and stakeholders regarding project status, progress, and risks. • Coordinate with the client and/or end users to ensure tasks are completed with minimal disruption to daily operations and within the established project timeline. • Actively participate in the review, development, and execution of documentation related to commissioning and qualification activities at the customer site. Qualifications • Bachelor degree in Engineering, Life Sciences, or related fields. • Previous experience in validation, commissioning, or qualification projects in regulated industry. • Knowledge of documentation best practices and regulatory standards (e.g., GMP, FDA). • Strong communication, organizational, and teamwork skills. • Ability to work in dynamic, results-driven environments. Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The Commissioning & Qualification Specialist will provide technical and documentation support for validation and startup activities within the pharmaceutical industry. They will collaborate with cross-functional teams to ensure compliance with regulatory and operational standards.