Job Purpose
To ensure Packaging Lab processes are implemented including sampling and testing, material complaints handling (TPI), new material development with team and ensure its effective In -place and In-use that are aligned with GSK and Regulatory specifications around and bring improvement to make the processes more robust.
Education, Experience & Skills
B-Pharm/Pharm-D
Must have an experience of at least 3-5 years on the same (or equivalent) position
Computer literacy, minimum to access and utilize emails for official correspondence
Must have understanding on Pakistan Drug law/Labelling rules.
Use of MS-Office (Word, Excel, PowerPoint) at least to a moderate level
Good communication and presentation skills
Key Responsibilities
Packaging Material Disposition
To review Packaging Materials GRs/incoming materials and manage final disposition on time.
To ensure packaging material / components sampling and testing to meet the lead time.
To ensure compliance of the specification and standards with QMS and ensure the Quality of packaging material as per GSK and local regulatory standards.
To prepare the change control, drawing and specifications for new development or change in packaging materials initiated by site
To manage the activities assigned from time to time for the development of products related to packaging materials.
Preparation of monthly report of the section, Vendor complaints & rejection data for supply review meetings.
TPI:
To ensure and investigate on site for vendor complaints related to packaging materials.
To monitor and track the timely closing of the complaints.
To conduct the meeting with Supplier’s for on-line complaint and critical rejections in order to facilitate the supplier in CAPA so to avoid recurrence in future supplies.
Handling and reporting on-line complaints of packaging material, Complete investigations and RCA against the complains received, Review effective CAPA implementation and its compliance against the complaints
Others:
Participate Management Monitoring/ audits to ensure compliance and ensure level one audits are managed per GQMP/ GQPs at Operational Quality.
Participate in QMS gap analysis of packaging material procedures.
Preparation /Review of specifications /test methods, SOP’s of packaging material to ensure compliance
Participate in Pack Management and Artwork projects and initiatives in alignment with GPS.
To manage calibration, EHS, artwork control, change control & documentation related activities, to ensure compliance.
Manage and updated the Record Retention as department representative.
Role of department trainings representative.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
Contact information:
You may apply for this position online by selecting the Apply now button.
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