Based in Auckland New Zealand, Alpha Laboratories (NZ) Ltd is the leading manufacturer of dietary supplements and complementary medicines products into the Asia Pacific Region. This is a great opportunity to take your career to the next level with a leading manufacturer in the region.
Quality Assurance Manager
This position has overall responsibility for the day-to-day management and delivery of QA functions at both Alpha’s manufacturing sites. You will provide leadership and management to the QA team to implement and improve on Alpha’s quality assurance systems, for stringent compliance to company’s standards and cGMP requirements.
We are seeking dynamic, goal orientated individual with a keen eye for detail who wish to further their career in a cGMP manufacturing environment with a leading company.
Relevant qualification & QA management experience is essential
Key responsibilities and tasks include:
Day-to-day management and leadership of the QA team
Auditing/disposition functions for material and product release for the manufacturing site according to the relevant marketing authorizations with technical and compliance checks on manufacture and testing
Reviewing and approving all key quality systems
Timely resolution of quality related issues through investigations in order to support the timely release of materials and products
Partner with production and other internal teams to build robust working relationships and to provide feedback for effective, efficient and compliant operations
Perform and support the immediate and longer term service delivery of defined aspects of Quality Assurance, including participation in improvement plans to meet the agreed goals and KPI’s
The ideal candidate for this role would have:
A relevant Science or related degree.
Experience in the complementary medicine, dietary supplement or related industries
Excellent relationship managements skills, and demonstrated communication and negotiation skills
Sound understanding and knowledge of cGMP quality systems, practices and principles for manufacture of complementary medicines
Sound understanding and knowledge of RMP requirements (APA 1999) for manufacture and export of products containing animal and dairy ingredients
Disciplined approach with eye for detail and demonstrated problem-solving and decision-making skills
Strong customer focus and a “can do” outlook
Strong ability to multi-task and proven ability to meet deadlines
A strong commitment to team success
If you are a self-motivated person and have the above qualities this is a great opportunity. If this sounds like you please apply today to firstname.lastname@example.org