Manufacturing Manager Production
Resume:
OGUNMEFUN,
Adewale Babatunde
Contact
Address:
**, ******** ******** ****** ******* Lagos
Phone:
Email:
************@*****.***
LinkedIn:
linkedin.com/ogun4success.com
Education and Qualifications
Lagos State University (LASU)
(2012-2014). Master’s in
business administration
(MBA)
Yaba College of Technology,
Yaba. Lagos (1997-1999)
HND Biochemistry. (Upper
Credit Credit)
Languages
English Language
Yoruba Language
Hobbies
Time out with family and friends -
great way to unwind, destress, and
keep the mind sharp.
Skill Highlights
Project Management
Excellence (eDM) in Problem Solving.
Flexibility
Teamwork
Profile (Product Process Owner)
A decisive and result oriented professional equipped with extensive experience in operations and Quality management, Operational excellence (Lean Six Sigma) and Technical background. Employs excellent leadership skills and multi-tasking strengths in overseeing, coordinating and controlling production activities. Demonstrated ability to improve process/operations performance, reduce waste, reduce costs hence increase productivity. Working Experience
- Production Chemist
Doyin Industries Limited, Orile (August 2001- December 2003)
- Asst. Production Manager
Doyin Industries Limited, Orile (August 2003- December 2005)
- Production Supervisor
Glaxosmithkline Nigeria Plc. Agbara. (January 2006 – March 2009)
- Manufacturing Manager
Glaxosmithkline Nigeria Plc. Agbara. (April 2009 – December 2009)
- Packaging Manager
Glaxosmithkline Nigeria Plc. Agbara. (January 2010 – February 2013) Product Process Owner (OHC/OTC Value Stream)
Glaxosmithkline Nigeria Plc. Agbara. (October 2018 – till date)
Recognized as the principal point of contact for all aspects of product(s) knowledge, performance and end to end process, including critical quality attributes (CQAs) and critical process parameters (CPPs).
Well-versed in aspects of Product Quality Lifecycle Management (PLM), Technical Risk Assessment (TRA), Product Control Strategy (PCS) and translation to standard work as batch manufacturing instructions, Continued Process Verification (CPV) and Process Robustness Assessment.
Ensures QbD principles are applied and a robust and well understood process and product control strategy are transferred during technical transfer, full scale development and commercialization of new products from other sites, and subsequent transfers to third party manufacturing sites.
Maintains accountability for the product throughout its lifecycle, influencing the manufacturing process, analytical process, pack and associated specifications including technical input to the lifecycle validation approach for the product.
Responsible for assessing the product quality, impact of any change (AL1/2/3) that can impact CQAs/CPPs via review and update of TRA and PCS.
Provides leadership and establishes key relationships within site across Operations, Technical, Quality and Engineering for the product(s), above site with other Product Owners and Category team.
Provides technical leadership and input into root cause analyses to support the investigation and resolution of product complaints and deviations, in conjunction with Quality and operations
Production Manager (Oral Health Care Manufacturing and Packaging Line) Glaxosmithkline Nigeria Plc. Agbara. (April 2013 – September 2018)
Plan, organize and monitor all aspect of manufacturing and packaging of toothpaste with strict compliance to Current Good Manufacturing Practice rules to meet supply plans, budgets, safety standards, acceptable quality and ensure delivery of major KPI’s
(CTP, ZAPs, CAPA closure, Deviations, Product Complaints etc.)
Actively participate in all manufacturing and Packaging activities involved in New Product Introduction, New Packaging Material Development and New Process Installation.
Coordinate Trials and all (Manufacturing and Packaging) Process / Equipment Validation in accordance with Validation Master Plan as well as calibration. This includes data generation, collation and logical interpretation
Audit and review of relevant documents such as operating procedures (SOPs) to reflect actual practice (in place and in use) and eliminate data integrity.
Propose, initiate and implement process improvements. Identify and resolve performance improvement issues with aid of tools such as JDIs, PDCA, STAR etc.
Support and ensure compliance to QMS and EHS policies and standards in order to minimize accidents and quality failures.
Control of cost and materials wastages below approved waste factor in BOM through effective labor utilization, pragmatic equipment and Value Engineering. Certifications
HACCP
MFG/PRO QAD Enterprise for manufacturing organization
Introduction to STATISTICA
Lean Sigma
Trainings
Product Life Cycle Management
Validation Lifecycle
Technical Risk Assessment (TRA)
Material Risk Assessment (MRA) overview
New Product Introduction and Artwork Process
Documentation (Data Integrity Train the trainer)
Introduction to Stability Analysis
Introduction to Statistica
Quality Workflow CARISMA 3 (Deviation, Change Control and CAPA effectiveness)
GSK Production System: To ensure Zero waste, Zero defects and Zero Accident.
Excellence deviation management eDM and Investigation Handling. (RCA)
Audit. (Self-Inspection: Level 1 and Monitoring Audit: Level 2)
MFG/PRO QAD Enterprise for manufacturing organization
Lean Manufacturing concepts and tools.
Awards
Silver Award: Recovery of N5M above set target on the production line.
Best Employee of the year 2010 (Senior Staff Category)
Bronze: Global Employee Recognition Award
Excellent knowledge and demonstration of process understanding that delivered the site out of quality remediation and delivered compliance of our EHS.
Bronze: Process ownership during the Environment Health and Safety Audit Achievements
Introduction of Sensodyne Variants and Macleans Fresh gel (Blue), both were successfully launched into the Market post satisfactory trial and process Qualification.
Introduction of new pack size of Panadol Extra (4s X 25) by carrying out the trial, qualification and other process involved in delivery of the product.
Increase in number of products with CQAs having PpK > 1.0
Achieved waste reduction on the toothpaste line from initial 9% to 0.7% by identifying and correcting the defect on the sensor mark orientation.
Reduced materials write off in production department from N2.8M to N0.8M through effective receipt, reconciliation, control, monitoring and other OE tools
Key player during the transition period of the manufacturing Upgrade, from glass bottling line to PET line.
Part of the pioneering team in the delivery of seven HACCP plans for the site following the requirements in the site’s GQP 1207 and codex Alimentarius in 2011. References
Pharmacist Adekunle Adeyemi Miss.Titilayo Fashedemi Operations Manager, Technical /NPI Manager,
GlaxoSmithKline Nigeria Plc. GlaxoSmithKline Nigeria Plc. Agbara Agbara
Ogun State Ogun State
Tel: 080******** Tel: 081********
Groups/Site Committees
Member,
Product Technical
Review Team (Panadol)
Member, Product
Technical Review Team
(Toothpaste)
Member, Site
Production Planning
Team.
Member, Site waste
diagnostic Team.
Member, GSK
Production System
Council (GPS)
Member, Site Value
Engineering Team (VE)
Member, Site Quality
Management system.
(QMS)
Member, Community of
Practice (Technical)
Member, Site Quality
Council. (SQC)
Member, L1 and L2
Auditor
Member, Environment
Health and Safety
Council (EHS)
Projects
Unification of Macleans
Shippers
Unification of ALS
Shippers
Use of Chipboard for
Macleans unit boxes
against FBB (With
savings of £18)
Glucose Waste
Reduction
Flow Project Review
(VSM of Oral Health
Care)
Reduction in Site
consumables spend.
Continuous
Improvement
Framework (CIF) on NM
700 Toothpaste Filling
Machine.
OEE improvement on
the NM700 Line from
45% to 65% in two
different cycles
Energy and Water
Management
Contact this candidate