Positive Employment is currently recruiting for a Compliance lead for our client local government organisation based in Bristol.
The successful candidate will lead responsibility and technical expert for compliance across the Technical Service for gas, electrical, lifts and legionella ensuring resident safety.
Oversee the repair, continuity, improvement and maintenance of all building services to our blocks of flats; the installing and servicing of domestic heating and hot water systems, and leading on innovative transition to new forms of heat and energy generation.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
The duration of the contract will be 23 months with a start date in July or August 2024.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
About the Role: In this role, you will provide technical support and process operation for the Process Research and Development team.
You will work as part of a team in a laboratory setting, supporting chemists and engineers, and ensuring the smooth and safe execution of laboratory work.
Building and maintaining effective relationships between team members, contractors, customers and stakeholders to ensure the efficient delivery of work for statutory compliance and remedial work.
A large housing association has an urgent need for a statutory compliance surveyor
You will be working within the building compliance team and the role will include To assist the Asset Management Team in all aspects of delivery of the Planned Investment and Capital Programmes including compliance requirements for passive and active fire protective works, electrical remedial works, asbestos, plumbing and heating
A specialist, international Pharmaceutical company is actively seeking a Regulatory Affairs Manager due to their successful company growth and dedication to innovate new products.
The role reports directly to the Head of Regulatory Affairs and is responsible for pre-approval regulatory activities that support the delivery of the company's strategic plans.
This is an excellent opportunity to work across a number of product ranges in a growing company that is expanding globally with a focus on delivering medicines to the paediatric market.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.