Functions
Life science quality & regulatory affairs
Quality and Regulatory Affairs is involved at every step along the value chain. The life science industry must comply with stringent laws and regulations which govern the testing, safety and reliability of drugs and devices before they can be administered.
Our dedicated Quality and Regulatory Affairs function – staffed by expert talent consultants with in-depth Quality knowledge – provide cutting-edge talent solutions to life science industry leaders and emerging start-ups in the following specialisms.
Expertise
Quality & regulatory affairs specialisms
Good Practice (GxP)
Helping to build teams who are able to adhere to and apply best practice across the life science value chain.
Regulatory Affairs
Connecting with industry specialists who can obtain approval for new products while ensuring itl is maintained for the entire product lifecycle.
Quality Assurance (QA)
Collaborating with experts responsible for all matters influencing the quality of goods or services across the value chain.
Quality Control (QC)
Engaging with top performers who can oversee the sampling, testing, documentation and release procedures of goods and services.
Supplier Quality
Engaindividualsging with skilled who can build and manage relationships with suppliers, ensuring goods or services meet quality requirements.
Other
Specialism not listed? These are only some of our quality and regulator affair specialisms. Get in touch for more information.