Management Manufacturing

TODEWALE K. SURIJ

TODEWALE K. SURIJ

Contact: +**4-771-***-****; E-Mail: **.********@*****.***

Alternate E-Mail: **.********@*****.**.**

Skype ID: surij.todewale4

MANAGEMENT PROFESSIONAL

LVP, SVP Manufacturing Operations Production Planning Project Management

Manufacturing Excellence CAPA, Deviation, URS, BMR, SOPs, RA, Audits

Manufacturing Supervisor offering over 8 years of professional experience in

Manufacturing, production planning, project packaging operations in injectable, LVP and

Ophthalmic management, materials management with cross functional exposure Quality

Assurance, profit sharing operations. Proven abilities to enhance the production process

operations, optimize resources and capacity utilization, escalate productivity and

operational efficiencies. Currently associated with Rasan IV Pharmaceutical co.,

Sulaymaniyah, Kurdistan as a Manufacturing Supervisor. Resourceful techniques for

maximum utilization of manpower/equipment. Conversant with techniques like Lean

manufacturing, OEE, 5S, Six Sigma, Kaizen, 5S. A keen planner with skills in

conceptualization and effecting process initiatives to enhance plant capacity and efficiency

and productivity. Well conversant with TQS, Kaizen, Safety Norms, First Aid.

Co-coordinating projects for the set up facilities with accountability for strategic utilization

and deployment of available resources to achieve KPI objectives. Well organized with a

track record that demonstrates self motivation, creativity and initiati ve. Believe in leading

from the front.

PROFESSIONAL FORTE

GENERAL MANAGEMENT

Planning Execution Conceptual layout New Initiatives

Formulation Man power requirement Project Management

Material Management Leadership Inventory Controls

Techno Commercial Operations Coordination

PRODUCTION/ TECHNICAL EXPERTISE

Inventory Management Production Management Process Enhancement

Qualification Validation Quality Assurance

Commissioning KPI Administration

New Product Development Training & Development

HIGHLIGHTS

1. Reward and Recognition for reducing the primary packing material consumption.

2. Appreciation for improving the productivity and decrease the percentage of breakdown.

3. Appreciation for 100% OTIF (on-time in full) and 100% CSI (customer satisfaction index)

EMPLOYMENT DETAILS

1. Since June' 20, 2013; Rasan Pharmaceuticals, Sulaymaniyah, Iraq as a Manufacturing Supervisor.

Accountabilities: 1. Responsible for Overall manufacturing operations

2. Area and equipments' qualification and validation.

3. Risk Management and Documentation.

4. All shop floor operations such as manufacturing of bulk, aseptic filling,

sterilization as per cGMP requirements, local FDA and regulatory norms.

5. Knowledge of Six Sigma, Kaizen, Lean manufacturing, 5 S and OEE tools and

their implementation at shop floor to increase the productivity and reduce

rejection.

6. Documentation - BMR and SOPs, protocols and URS preparation

7. Registration documents preparation.

8. Techno commercial comparison of Equipments / Machines.

9. Prepared conceptual layout of manufacturing area.

10. Mentoring to technicians and officers.

2.Since Oct. 2008 to May 2013; Piramal Healthcare Ltd, Indore, MP as a Manufacturing

Executive.

Accountabilities: 1. Execution of monthly production plan.

2. Handled four FFS lines (Weiler, USA)

3. Manufacturing, filtration and filer integrity.

4. Execution of ANDA products and BMR preparation.

5. Troubleshooting of BFS machines.

6. Preparation of BMR, SOPs, URS and protocols

7. Compliance to observations and CAPA.

8. Change control initiation and handling of deviations.

9. FFS / BFS project handled successfully.

3. Since Aug. 2006 to Sept. 2008; J B Chemicals and Pharmaceuticals Ltd, Ankleshwar, Gujarat

as a Officer Manufacturing.

Accountabilities: 1. Manufacturing, filtration, aseptic filling.

2. Terminal sterilization of ampoules and vials.

3. Supervises the Vial line BOSCH

4. Process simulation

5. Validation of Depyrogenating and Sterilizing Tunnel

6. Qualification and report compilation.

7. Timely submission of BMR and maintaining GMP records.

8. Independently operates machines- Washing, filling and its change over.

9. Operated Multi Column Distillation Plant, Pure steam generator.

10. Training to the sub-ordinates and new comers.

DOCUMENTATION: Includes Review, Preparation and Completion of

Standard Operating Procedure and FMEA (Risk Analysis).

Audit / Observation compliances.

Handling of Market complaint / Recall

Batch manufacturing record

Qualification and Validation

Deviation, CAPA, RCA and change control.

Quality Records and Equipment logs.

TRAINING ATTENDED

Underwent the following training programmes

Online and class room training to subordinates on various aspects of cGMP &

SOP’s.

Fire Safety

First Aid

Leadership

Communication and Presentation skills

Manufacturing and quality control of Injection and Ophthalmic.

Emotional Excellence

EXPOSURE TO AUDITS: INCLUDING INTERNAL AUDIT EXPOSURE TO

Medicinal Control Council Of South Africa

Irish Medicinal Board

ISO 9000, ISO14000 and ISO 13485

WHO

TGA

MHRA

USFDA

CORE COMPETENCIES:

Project Management

Quality Management

Production Planning

Team Management

Training

Mentoring

5S,Lean Mfg, Six Sigma

Drive for Quality

OEE and Productivity

PERSONAL DETAILS:

Father’s Name : TODEWALE K. SURIJ

Date of Birth : 06 July, 1983

Marital Status : Single

Expected Salary : Negotiable.

Valid Passport No. : K3561256 (Valid up to 2022).

ACADEMIC CREDENTIALS

2012 MBA in Production and Operations Management from IIBMS, Mumbai.

2006 B. Pharmacy from SRTM University, Nanded.

2002 HSC from SANV, Pune Board.

IT SKILLS

Proficient in MS-Office and Windows

SAP for products in data processing

AUTOCAD (only basic) for layout with dimension and understanding of drawings

Note: References will be provided upon request.

Contact this candidate