C&Q Specialists

Pinnaql, Inc.; Humacao (PR); Sur place; USD 85 000 - 105 000; Plein temps

Résumé du poste

Validation & Engineering Group Inc V&EG a Pinnaql company seeks C&Q Specialists to support equipment and systems in a biopharmaceutical facility. The specialists will execute field activities, document results and work with project teams to complete system qualification.

Responsibilities include developing, reviewing, and executing commissioning and qualification protocols; perform field walkdowns, installation verification, FAT/SAT/IQ/OQ activities, and ensure GMP-compliant

Qualifications

• At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facility.
• Experience with FAT SAT IQ OQ or comparable commissioning and qualification activities.
• Working knowledge of GMP requirements and controlled documentation.
• Strong field execution technical writing and teamwork skills.

Responsabilités

• Develop, review, and execute commissioning and qualification protocols.
• Perform field walkdowns, installation verification and functional testing.
• Coordinate with Engineering, Operations and Quality to complete qualification and system turnover.

Connaissances

Field execution

Technical writing

Teamwork

Description du poste

Validation & Engineering Group Inc V&EG a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical Biotechnology Chemical Food and Medical Devices industries in the following areas Laboratory Compliance Computer Engineering Project Management Validation and other services We are seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility The specialists will execute field activities document results and work with project teams to complete system qualification

C&Q SpecialistsDescription

Develop review and execute commissioning and qualification protocolsPerform field walkdowns installation verification and functional testingReview drawings specifications and vendor documentation against installed systemsDocument test results investigate discrepancies and support corrective actionsCoordinate with Engineering Operations and Quality to complete qualification and system turnover

Qualifications

• At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facilityExperience
• with FAT SAT IQ OQ or comparable commissioning and qualification activities
• Working knowledge of GMP requirements and controlled documentation
• Strong field execution technical writing and teamwork skills

At Validation & Engineering Group people always come first We believe that when youre empowered to do your best work bold ideas thrive and real progress happens This isnt just a job its an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose driven supportive team Excited to build something meaningful together We look forward to hearing from you 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