ASST QA MANAGER [JOHOR BAHRU]
KEY DUTIES & RESPONSIBILITIES
To support and perform Manager-delegate role in leading the Department to fulfil quality objectives and ensure the regulatory and customers’ requirements are met.
To ensure that the QA/QC systems and quality standards of products are maintained and constantly improved.
To support the operation of the Department effectively and efficiently with regard to timely release of in-coming materials, intermediates and finished products.
To review and approve various GMP/QA/QC, technical documents, artwork and release / reject of material for use in production and finished product for sale with delegation from the Head of Department.
To assist in handling quality-related matters, change control, non-conformances, manufacturing deviations, and product complaints.
To assist in managing resources, and to keep up-to-date with the latest developments in relevant technical and regulatory information.
To manage and support Regulatory Authority and Customer audits.
To provide technical documentation in support of new product registrations, and maintenance of product registrations.
To participate in vendor audit, supplier approval, quality improvement and new product development projects.
Any other project / assignment that will be advised / directed by the superior.
ACADEMIC QUALIFICATION / TRAINING / EXPERIENCE REQUIRED
A good Degree in Chemistry/Pharmacy/ Microbiology
Minimum 3 years of relevant working experience in management of quality assurance, quality control and regulatory submission, preferably in pharmaceutical manufacturing industry.
Familiar with GMP, PICs guidelines and other regulatory guidelines.
Team player with good analytical skill, good application knowledge and experience, and good communication and interpersonal skills.
Kindly contact the Mr Hanafi at +60 19-785 1503 for further details or send your resume to [ firstname.lastname@example.org ]