Job Purpose
The purpose of this job is to supervise the packaging operations of Tablets department so the products are delivered and supplied in full and on time to the patients at the end of supply chain.
Education, Experience & Skills
Pharm- D / Bachelor’s Degree or equivalent experience
2 to 3 years relevant experience
Key Responsibilities
Ensure strong compliance in Quality, EHS, Legal and other critical parts of the business related to the area responsibilities
Drive performance to improve quality and EHS standards in the area responsibility, in accordance with GSK’s strategic objectives and with applicable law.
Drive a culture of transparency and total disclosure. Supervise third party service providers in accordance with GSK requirements.
Production:
To make and agree daily/weekly/monthly production plan for TabletsSKUs
To supervise inspection & packaging operations of Tabletsto achieve the production plan on time
Maximum utilization of resources for delivery of quality products and to improve KPIs
Labour allocation
Update respective performance boards
GPS:
Effectively implement GPS within the area of responsibility in Packaging department
Monitor department OPEX and ensure consumables and overtime within target
OE:
Embed OE culture within the area of responsibility in packaging department.
Identify, develop and implement improvement/Operational Excellence (OE) projects to generate cost savings (Strategy Deployment).
RCA:
Involve in investigations into incidents and ensure root cause is identified.
Implement appropriate corrective and preventive actions are implemented.
DMERP:
To ensure DMERP packaging data postings
TRAINING:
Provide training on SOP and OJT to employees working in Tablets area
Prepare and maintain L2 curricula
Maintain employees training record
QUALITY COMPLIANCE:
Ensure right first time performance
Maintain the department in ‘Inspection Ready’ state all the time
Raise deviation as needed
Originate Change controls where required.
Make sure 100% SOPs are In-place In-use in Ampoule & Eye drops Packaging
Conduct L1 inspection against approved schedule
Prepare CAPA and monitor the timely closures of observations related to LI, L2, L3 & L4.
Support the team in L2, L3 & L4 audits.
EHS:
Conducting EHS general Risk assessment, Ergonomics Risk assesssment & CRAs.
Ensure the embedding of living safety culture with in the department.
Ensure EHS standards compliance by conducting EHS L1 audit, record observations, prepare CAPA and monitor timely closures.
Ensure LOTO application in Packaging area machines
DATA INTEGRITY:
Ensure data integrity compliance and improve DI controls (ALCOA + principles) in Tablets department.
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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