- Ensure
compliance with ISO 9001, cGMP, GSDP, GSDPMD, customer requirements,
company and regional quality standards. - Develop,
review and maintain quality procedures and records to ensure compliance
with quality regulations and best practices. - Ensure
products meets all quality standards and are in compliance with the
necessary quality requirements/ regulations prior to product release. - Support
the execution of process or equipment validations, revalidations,
re-qualifications, and on-site projects. - Review
and execute validation protocols and summary reports and ensure that are
technically correct and comply with internal and external requirements. - Participate
in internal and external quality audits. - Participated
quality improvement projects. - Collaborate
with cross functional personnel to provide root cause investigation and
develop corrective actions to respond to internal and external audit
findings. - Brings
together staff of different disciplines and drives the group to plan.
formulate and agree on comprehensive quality procedures. - Provide
training regarding ISO9001, cGMP, GSDP and GSDPMD and standard operating
procedures. - To
facilitate analysis, creation of reports, forms and graphs for the QA
department. - To
ensure there is prompt and effective communication both internally and
externally to keep all interested parties informed proactively. This
includes but not limited to superiors, subordinates, colleagues,
principals and customers. - Performs
other duties as assigned when required.
Job
Requirements
Requirements
- Minimum
bachelor degree in science or engineering. - Minimum
of 2 years’ experience in quality assurance. - Ability
to work independently in a fast-paced environment. - Must
have excellent written and verbal communication skills in English. - Prefer
good technical manufacturing knowledge, ISO 13485, cGMP, Validation,
Quality Management System.
The successful candidates will receive
an attractive remuneration package, including contractual bonus and medical
& hospitalization benefits.
an attractive remuneration package, including contractual bonus and medical
& hospitalization benefits.
Please apply online/write/fax in with a detailed resume stating your current
and expected salaries and contact telephone numbers together with a
non-returnable photograph to the following address :
The Head of Human Resources
(Ref: QVE-0215)
Zuellig Pharma Sdn Bhd (4013-D)
No. 15 Persiaran Pasak Bumi
Seksyen U8, Perindustrian Bukit Jelutong
40150 Shah Alam
Selangor Darul Ehsan
Fax: 03-7859 1950
Zuellig Pharma Sdn Bhd (4013-D)
No. 15 Persiaran Pasak Bumi
Seksyen U8, Perindustrian Bukit Jelutong
40150 Shah Alam
Selangor Darul Ehsan
Fax: 03-7859 1950
Email : recruit-zpmy@zuelligpharma.com
Applications will be treated with the strictest confidence.
Only shortlisted candidates will be
notified.
notified.