Team Lead Sterile
GSK
Karachi, Sindh, PK
3d ago
source : Mehnat Mazdoori

Site Name : Pakistan - Sindh - Karachi Posted Date : Jun 8 2021 Job Purpose The purpose of this job is to supervise the manufacturing and filling operations of Lactam Sterile, so the products are delivered and supplied in full and on time to the patients at the end of our supply chain.

Educational Requirement Minimum Level of Education : Pharm-D Area of Specialisation : Industrial Pharmaceutics Experience Requirement 2-3 Years Key Responsibilities

  • Ensure strong compliance in Quality, EHS, Legal and other critical parts of the business related to the area responsibility.
  • Drive performance to improve quality and EHS standards in the area responsibility (Sterile Manufacturing), in accordance with GSK’s strategic objectives and with applicable law.
  • Drive a culture of transparency and total disclosure.
  • Production

  • To make and agree daily / weekly / monthly production plan for Sterile.
  • To supervise manufacturing operations of sterile to achieve the production plan on time
  • Maximum utilization of resources for delivery of quality products and to improve KPIs.
  • Labor allocation
  • Update respective production visual boards
  • Effectively implement GPS within the area of responsibility in manufacturing department
  • Embed OE culture within the area of responsibility in manufacturing department
  • Identify, develop and implement improvement / Operational Excellence (OE) projects to generate cost savings (Strategy Deployment).
  • Involve in investigations into incidents and ensure root cause is identified
  • Implement appropriate corrective and preventive actions are implemented
  • To Ensure SAP manufacturing data postings.
  • Training Rep

  • Provide training on new SOP’s to down the line staff
  • Maintain the training record of down the line staff
  • Ensure trainings are provided before the given deadline
  • Change Control

  • Involve in origination of change controls
  • Attend change control meetings and provide valuable information as required
  • Quality Compliances

  • Have knowledge of Aseptic manufacturing and its guidelines.
  • Involve in right first time performance
  • Maintain the department in Inspection Ready’ state all the time.
  • Raise deviation as needed
  • Make certain 100% relevant SOPs are In-place In-use.
  • Conduct L1 inspection against approved schedule and record observations in the tracker.
  • Prepare and implement CAPA and monitor the timely closures of observations related to L1, L2, L3 & L4
  • Support the team in L2, L3 & L4 audits.
  • Ensure Data integrity compliance and improve the DI control (ALCOA principle) at Lactam Sterile Manufacturing.
  • Conducting Risk assessment & CRAs.
  • Ensure the embedding of living safety culture
  • Ensure EHS standards compliance by conducting EHS L1 audit; record observations, prepare CAPA and monitor timely closures.
  • Ensure LOTO application on respective machines.
  • Contact Information You may apply for this position online by selecting the Apply now button. Important notice to Employment businesses / Agencies GSK does not accept referrals from employment businesses and / or employment agencies in respect of the vacancies posted on this site.

    All employment businesses / agencies are required to contact GSK's commercial and general procurement / human resources department to obtain prior written authorization before referring any candidates to GSK.

    The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business / agency and GSK.

    In the absence of such written authorization being obtained any actions undertaken by the employment business / agency shall be deemed to have been performed without the consent or contractual agreement of GSK.

    GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses / agencies in respect of the vacancies posted on this site.

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