Lonza Chemistry & Pharma Job - Production Supervisor Post

Lonza Chemistry & Pharma Job – Production Supervisor Post

Lonza hiring a Production Supervisor, Chemistry and Pharma job opening 2022. Chemistry supervisor vacancy, B Pharma & M Pharma job opening 2022. BSc job opening in Lonza. Interested and eligible candidates may check out all the details on the same below:

Job Title: Production Supervisor – GMR (Gel Melt Room)

Eligbility Criteria: 

  • B.Sc in Chemistry / B. Pharma / Master Degree in Pharmacy additional advantage with minimum 4 years of relevant experience in the production department in Pharma Industry.
  • Experience in handling GMP & GDP is a must.
  • Able to work in rotational shift working hours.

Key Responsibilities:

  • Efficiency within standard and agreed parameters in Gel Melt Room. Optimum utilization of man, material/equipment, etc. within agreed parameters.
  • Proper shift planning and managing idle time within agreed parameters. Control and Proper utilization of the consumables (Gelatin, Colors, Cleaning agents). Ensure the Safety & GMP in their shifts

GMR shift related

  • Responsible for shift-related operations in GMR (i.e. shift manning, leave, overtime, discipline, SOP compliance, etc.)
  • Ensure all procedures on the shop floor in the shift are being done and documented as per current SOPs.
  • Read and follow the Production Schedule and do the Planning of colour change /dish wash, melt charge, and GFT production accordingly.
  • Produce GFT as per set specifications and ensure no GFT is out of specification before GFT get transferred to the melt tank area.
  • Take immediate steps to file (wherever appropriate) and handle deviation if any.
  • Seek support from the supporting department for any correction in case of machine failure or utility disruptions etc. Follow up with the maintenance team and ensure necessary action is done.
  • Optimum usage of recyclable material, trim, and gel to ensure GUR is achieved as per target to ensure cost-effective production.
  • Understand gelatin melt process. Understand and work on and over graphic information in SCADA.
  • Understand usage, principle, operation, and maintenance schedule of all equipment and take action accordingly.
  • Understand and apply cGMP guidelines in Gelatin Preparation Room including labeling etc.
  • Maintain area and equipment in clean and organized form all the time as per GMP.
  • Ensure correct color of customized gel solution as it should be as per the standard sample, using spectra scan and avoid any downtime on account of color matching.
  • Ensure ageing time maintained for GFT is as per SOP always.
  • Get dispensing done as per the standard operating procedure.
  • Ensure issuance and storage of RM and in-process RM is done as per SOP along with proper labeling.
  • Ensure documentation is done on the shop floor and in a shift as per GDP and defined SOPs.
  • Control and minimize waste of RM including trim, recyclable capsule, gel, additives, and dyes to ensure cost-effective production.
  • Maintain a record of waste gel solution, trims, capsules. Ensure disposal of the material as per SOP and guidelines.
  • Maintain inventory supplies and take inventory of various items.
  • Handover shift and area in a form that reduces disruptions and does not affect quality/ costs etc.
  • Ensure changes, process improvement plans, revised procedures, and other changes are being implemented in shift post-training and ensure these are consistently maintained.
  • Ensure area in shift, remains presentable in a shift in terms of cleanliness, organized form, documentation, systems, etc.
  • Maintain 5S in the area.
  • Do other jobs as defined by HOD and be part of change management in general.

Environmental, Health & Safety:

  • Act in compliance with all laws, regulations, and policies on safety and environment, give feedback, make inspections and implement and follow up corrections.
  • Ensure safe working culture in shift including safe working habits, use of PPEs, etc.

Quality:

  • Ensure general GMP guidelines are being followed and motivate colleagues to do the same consistently.
  • Responsible for in-process quality control of work in progress.
  • Do follow-ups regularly to ensure the system in place.

Click Here To Apply Online

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