Validation Manager
Location:
Livingston Type:
Permanent
Entrust Resource Solutions are supporting their client in Livingston in their search for a Validation Manager. This role oversees all aspects of the Validation Program to ensure that validation processes and procedures are in compliance with ISO9001; ISO13485; 21 CFR 600; IVDD 98/79/EC; IVDR 2017/746 and other appropriate regulations and standards. This includes site safety requirements and applicable GxP and Good Manufacturing Practices (GMP).
What do we need from you?
Bachelor's Degree in a quality or science-related discipline (chemistry, biology, or medical technology) or equivalent professional training. 5 years experience in a drug manufacturing, medical device, biologics or related industry. Experience in supervising and motivating personnel, managing by objectives and conducting personnel appraisals/performance reviews. Previous experience should demonstrate expertise in cGMP, FDA regulations, SOP development, as well as an understanding of Validation and Data Integrity Principles. Six Sigma Qualified (Green Belt or above). Strong analytical and problem-solving skills, including presentation of results into meaningful reports. Competent in the use of IT technology, such as Microsoft Word, Excel, and PowerPoint. Good communication skills (written and verbal) with the ability to collaborate and present at all levels and functions of the organisation.
To find out more about this exciting opportunity, please contact Lynsey today on (phone number removed) or send an up-to-date copy of your CV to (url removed).
#J-18808-Ljbffr
Livingston Type:
Permanent
Entrust Resource Solutions are supporting their client in Livingston in their search for a Validation Manager. This role oversees all aspects of the Validation Program to ensure that validation processes and procedures are in compliance with ISO9001; ISO13485; 21 CFR 600; IVDD 98/79/EC; IVDR 2017/746 and other appropriate regulations and standards. This includes site safety requirements and applicable GxP and Good Manufacturing Practices (GMP).
What do we need from you?
Bachelor's Degree in a quality or science-related discipline (chemistry, biology, or medical technology) or equivalent professional training. 5 years experience in a drug manufacturing, medical device, biologics or related industry. Experience in supervising and motivating personnel, managing by objectives and conducting personnel appraisals/performance reviews. Previous experience should demonstrate expertise in cGMP, FDA regulations, SOP development, as well as an understanding of Validation and Data Integrity Principles. Six Sigma Qualified (Green Belt or above). Strong analytical and problem-solving skills, including presentation of results into meaningful reports. Competent in the use of IT technology, such as Microsoft Word, Excel, and PowerPoint. Good communication skills (written and verbal) with the ability to collaborate and present at all levels and functions of the organisation.
To find out more about this exciting opportunity, please contact Lynsey today on (phone number removed) or send an up-to-date copy of your CV to (url removed).
#J-18808-Ljbffr
