Skip to main content

Production Assistant Manager Job at GSK Rx India

 

Clinical courses

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

APPLY ONLINE>>

See All   B.Pharm Alerts   M.Pharm Alerts    Ph.D Alerts   Bangalore Alerts

See All   Other Jobs  in our Database

Subscribe to Pharmatutor Job Alerts by Email