GSK (GlaxoSmith )Hiring
Executive - External Supply Quality Graduate in Science / Pharmacy discipline
Apply Now
Job Purpose :-
•To ensure support
to business by management of Raw and Packaging material supplier management.
•To support
resolution of supplier related complaints by acting as interface between
procurement, site Q representatives and Supplier Quality Ops.
•To support
Business in introducing new vendors (API, Excipients & Primary packing
materials) and coordinating for validations and stability strategies through
change management process.
•To Provide
support to CMO sites with respect to Microbial method.
•To support
Analytical method, transfer w.r.t Microbial method at new/existing sites to
support Product transfers.
•To support MERPs
team, For implementation of MERPs process.
The Key
responsibilities of this role are as follows:
Supplier
Management:
• To ensure that
the RM, PM used for manufacturing GSK products are only obtained from GSK
approved manufacturers and suppliers.
• Preparation of
Approved Supplier list on timely basis and updating as and when required.
• To prepare
adequate Risk Assessment / STP for usage / discontinuation of material from
disapproved and conditionally approved supplier.
• To provide
information to CMOs and site representatives about usage or discontinuation of
material from disapproved suppliers.
• To Conduct LIC
for the supplier disapprovals.
• To support Site
Q representatives for disposition of materials required for production.
• To maintain
supplier complaint log with all the relevant details.
• To ensure that
all supplier related complaints are resolved in stipulated time period in
coordination with suppliers.
• To identify
repeat complaints from RM/PM supplier and follow-up with Procurement / ES
technical / Supplier Quality Ops for resolution and support.
• To follow up
with supplier quality Operation for escalated complaints.
• To provide
continuous support to improve business performance by support to Procurement
function and Supplier Quality Ops., where required.
• To provide the supplier
complaint KPI to SQOps.
• To provide Data
collection form to SQA&C as the pre-audit data collation details for
supplier audit.
• Approval of
SQOPS change control related to supplier change control details relevant to ES
site suppliers
Others
• To raise Change
controls/Deviation related to revision of Approved Supplier List.
• Preparation /
Revision of SOP as per QMS gap assessment.
• Ensure a site of
inspection readiness for above mentioned activities.
• To perform the
activities assigned by the supervisor as and when required.
Minimum Level of Job-Related
Experience required
Preferably 1 to 5
years’ experience in Corporate Quality Assurance and in Pharmaceuticals
formulations, in Supplier Management, , Documentation and SOP management.
Demonstrated
experience in managing w.r.t microbial method transfers and method
verification.
Other Job-Related
Skills/Background
Good knowledge of
Microbiological and QC analysis/ Documentation/ Regulatory requirements and
Quality Management System.
Effective verbal
and communication skills, collaborative team member & team leader.
Capable to work
independently.
Educational Background
Graduate in
Science / Pharmacy discipline
Area of
Specialization
Quality Assurance
/ Pharmaceutical Sciences/ Microbiology
TO APPLY CLICK HERE
FOR MORE JOB UPDATES
No comments:
Post a Comment