The Quality Manager will be responsible for execution of quality related activities through all stages of project. Lead development and implementation of policies, procedures. Implementation of GMP activities, standards, compliance initiatives and regulations.
DUTIES & RESPONSIBILITIES:
Quality Manager should have hands on experience in QA/QMS ideally within a manufacturing or highly regulated environment. Develop implement procedures and conduct audit as required.
Develop and follow quality aspects of pharmaceutical development in an outsourcing environment, including the quality aspects of process and formulation development, manufacturing, analytical testing and packaging areas
You are required to perform quality activities, Validate protocols, Specification review, batch record review and release to ensure timely delivery of finished products to support the clinical development plan as well as commercial sales plan
Quality manager should be able to perform supplier quality management activities, Confirmation of compliance, conduct quality audits, inspection and site inspection test plans.
Quality experience in QA/QMS experience ideally within a manufacturing or highly regulated environment.
Good communications management experience skills.
CQI membership (preferable)
If you think this could be the new and exciting challenge for you, and you want to learn more please get in touch today.
Founded in 1958, Belcan has become a global technological leader and established go to Engineering Services provider, working within many industries including Aerospace, Defence, Marine, Nuclear, Automotive and Cyber Security.
This vacancy is being advertised by Belcan.