Interim Validation Consultant

Sector: Pharma, Medical device, Biopharma

Current Salary Range: 550 per day

Location  Bournemouth

About the Candidate

A highly experienced quality/validation/project/test professional with extensive experience of delivering the full project lifecycle, from gathering requirements and assessment of risks through to handover to business as usual (BAU). Initially working within an application testing environment, has developed knowledge and experience in ensuring quality and compliance at the highest level in a range of industries, including pharmaceutical (commercial and manufacturing), CMO, Bio Pharma, Medical Devices. Performed audit reviews and re-validation of both systems and equipment. Extremely analytical, logical, methodical, accurate and meticulous, individual. Excellent communication and interpersonal skills, problem solving skills.

What Makes them great?

Exemplary Leadership in Compliance: Demonstrated consistent adherence to stringent quality standards and regulations like GMP, GCP, and CSV, ensuring robust compliance and validation across diverse manufacturing environments.

Expertise in Validation and Quality Engineering: ASQ-certified Quality Engineer with extensive experience in executing equipment qualifications and process validations in the pharmaceutical sector, ensuring alignment with GMP and CQV requirements.

Effective Project Management: Successfully led mid-sized to large projects related to process equipment and clean utilities, exhibiting strong team leadership and resource allocation skills, resulting in timely project delivery.

Their Experience

Validation, CSV, CQV

Other Details