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Project Details

Consultant - Pharma Manufacturing (Generics)

Top tier management consulting firm

 Mumbai / Navi Mumbai, Delhi / NCR, Kolkata, Chennai, Bangalore, Pune, Hyderabad, Agra, Ahmedabad , Jaipur, Kota, Nagpur, Nashik, Rajkot, Surat, Thane, Vadodara

Posted on:  12/02/2019

Cinque Terre

Starts on:  26/02/2019

BROAD CATEGORY

Manufacturing/Operations

SUB CATEGORY

Large project management, Quality assurance, Manufacturing/Operations head, Process Engineering / Process excellence,

INDUSTRY

Pharmaceuticals

Company Details

A top tier strategy consulting firm advising clients in private, public and not-for-profit sectors around the world.

Assignment Details

Our client, a top tier management consulting firm, is looking to engage with a consultant having Pharma Manufacturing background for a short-term project with their client- a leading Pharma company.

Roles and Responsibilities include:

• Oversee and advise on procedures used to clean pharmaceutical production equipment and facilities
• Execute procedures for and strategise on changeovers for the manufacturing vertical of the client
• Identify and assists in the corrective actions of processing related issues
• Perform required in-process product quality checks and documents accurately.
• Execute procedures to complete tasks in a safe and efficient manner.
• Work in collaboration with the consulting team and the end client in helping determine methods and procedures on old and new assignments
• Effectively communicate issues to supervisor.
• Ensure adherence to all compliance/regulatory mandates and quality requirements.
• Assists in the identification and implementation of continuous improvement opportunities

This is a full-time on-site assignment based in Ahmedabad for a duration of 4-6 weeks.

Skills Required

- Atleast 7 years of experience in Pharmaceutical Manufacturing (Generics)
- A pharmaceutical background and technical training is compulsory
- Demonstrated ability to work in both independent and team environments.
- Proficient in reading and writing English to understand work instructions and document results.
- Demonstrated ability to operate pharmaceutical processing equipment.
- Demonstrated understanding of the unit operations and the ability to assist with on-the-job training of manufacturing trainees and operators.

Assignment Duration

2 month(s)

Capacity Required

Full Time

No. of Positions

1

Nature of Work

On-Site

Profile Requirements

Experience: 10+ years

Qualification: Graduate

fleXpertise required

Contract ManufacturingTotal Quality Management (TQM)Lean ManufacturingEnvironmental CompliancesOperations ManagementLean MethodologiesProcess ImprovementCapacity PlanningGood Manufacturing Practices (GMP)Medical GenericsIndustrial ControlsQuality Control

ESTIMATED BUDGET

-

 

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