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Production Assistant Manager Job at GSK Rx India

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Production Assistant Manager Job at GSK Rx India

GlaxoSmithKline Pharmaceuticals Ltd is one of the oldest pharmaceuticals company and employs over 5000 plus people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders.

Post : Assistant Manager - Production

Job description
People Leadership
• Working with the team to continuously improve the capability of both the individuals and the overall team to increase their performance towards targets.
• Improve people capability by imparting trainings as per training curricula defined.
• Ensuring development plans and PDPs are undertaken on a regular basis  using the 70:20:10 and GSK methods. This includes ensuring that the  training required is identified, recorded using the appropriate method  and ensure that the training is undertaken using local processes. 
• Coaching and providing development to improve the behavior/performance  of individuals and the team to ensure that the expectations are being  met. This will include holding people to account for the duties that they  are responsible. 
• NMS PDP completion & doing coaching / counseling of people to  ensure adherence to stds for safety, quality & delivery.
• Disciplinary, Absence management, Grievance procedures as appropriate  in site.
• Role modelling the expected behaviors and standards for all staff in  the area.

Performance management and Problem solving
• Fully deploying performance management process within area ensuring  accurate and timely data is used.
• Real time issue identification and resolution involving staff.  Including  running of GSK Problem solving process with staff and necessary  Support Functions, line side.
• Current state analysis and “TOP 3 issues” identified with aligned  target conditions/actions using Lead and Lag measures to track and  improve.
•  Actively engage team in Gemba Kaizen.
•  Ensuring that the appropriate Deviation procedure and problem solving  processes are used to avoid reoccurrence of issues.
•  Ensuring the area returns to standard after a safety, quality  or performance/output deviation/incident in a controlled manner.
• Ensuring that they understand the cost budget for the area and the  impact that they and their team can have on this.
• Coordination & monitoring of department consumables & inventory.

Process management
•  Process confirmations against the 4M’s Material, Manpower, Method,  Measurement.
•  Required to manage safety, quality, compliance and output.    This includes being well prepared to have a good shift/batch/day/etc.
•  Ensuring adoption and adherence to the Leader Standard Work, and the  application of Standard Work for roles within the area by staff.
•  Being highly visible during times in the shift when there is more risk for  issues e.g. Line changeovers and providing guidance and resolving  problems as they arise.
•  Ensuring alignment to and providing data for the tiered accountability  meetings within the area and on site.  Following through on resulting  actions in a timely fashion.
•  Ensure cGMP, regulatory, QMS, EHS, internal and external audit compliance.
•  Conduct monthly L1 audit of EHS & Quality as per schedule to identify  gaps & timely closure of actions.
•  Active engagement in Governance review meetings for the area e.g.  Safety meetings, TIP review.
• Input to GSK systems e.g. BPCS, Trackwise, CDMS, Workday etc.
•  Preparation of weekly production plan and scheduling of activities with  effective utilization of man, materials, process and machineries for better  efficiency and productivity.
•  Proactive planning of required resources, Raw material / Packing  Material and non-coded item required to perform the day to day activity  in work area.
•  Supervise the manufacturing processes & documentations  (BMR /Log book / Check list etc) of various production activities.
•  To ensure safety checks like PSSR /guard interlocking. 
• Ensure the equipment / instruments are with in calibration due date.
• To ensure that manufacturing is carried out according to SOP, BMR  &  cGMP practices are followed to ensure all time inspection readiness  (Area & facility up keep & cleanliness, status labelling, good  documentation practices etc)
• To identify risk proactively in area which could have impact on  safety, quality & delivery.

Candidate Profile
• B.Pharm / M.Pharm / BE / M.Sc. (Science Graduate)
• 1+years Manufacturing / Packing pharmaceutical products.
• Manufacturing / Packing pharmaceutical products.
• Resource Planning
• Problem Solving
• Effective communication skills
• Ability to build relationships (Team  building ) at all levels and across functions.
• Have Influencing skilled & IR issue handling

Additional Information
Experience :
1+ years
Qualification : B.Pharm / M. Pharm / BE / M.Sc
Location : Nashik
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :
Quality Control
Req ID : 298782
End Date : 10th August, 2021


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