1 month ago
Keele Newcastle Depending on experience Permanent
This is an outstanding career development opportunity for an individual looking to develop a career within validation. Working in exclusive partnership with one of our longest standing clients, we are now helping them expand their quality team, specifically within validation.
Our client is a leading biopharmaceutical company that has continued to grow throughout recent years. Having opened up another GMP facility in 2020, the plans for expansion are continuing this year and as such, opportunity for growth and development is very realistic.
Working with the Validation Leader to manage the Validation system
Oversee and manage delivery of validation to GMP standards
Generation and review of validation documents
Carrying out equipment validation in a GMP cleanroom area
Qualifications and experience
Degree level qualification in scientific subject
Minimum 2 years+ work experience in a GMP biopharma or pharma company is essential
Applicants should have demonstrated responsibility or leadership in a previous role (e.g. SOP writing, review/modification of protocols, training others, project management or process implementation etc.)
Some validation exposure would be a benefit but can be trained
Excellent communication and written/ verbal language
QA, quality assurance, officer, administrator, auditor, QC, MHRA, FDA, notified bodies, GMP, GLP, healthcare, biotechnology, pharmaceutical, biopharma, CSV, validation, validate, training, development.
Harris Lord is acting as a recruitment agency for this role