Job Description
- Lead site production and engineering projects, serving as the primary project coordinator. Maintain continuous tracking and oversight of all projects.
- Plan and oversee all new and retrofit projects related to oral formulations at the manufacturing site.
- Responsible for development of SOPs, quality standard, development, and execution of Qualification protocols with following site QMS procedures.
- Responsible for overseeing and managing a team of vendors and contractors.
- Conduct techno-commercial evaluations of consultants, vendors, and contractors.
- Coordinating with statutory authorities for relevant approvals.
- Complying with operational and personnel standards, regulatory and statutory requirements to ensure efficient, reliable, and uninterrupted operation.
- Ensure the project is delivered within the approved budget and timeline.
- Ensure smooth handing over of the project to end-users, coordinate and ensure deliverables as per plan.
- Ensure to maintain the highest standards for cGMP requirements for the manufacturing site.
- Ensuring timely MIS and updates to the management.
- Ensure to meet required the regulatory requirements (e.g. HSA, FDA etc.) and keep the site audit ready all the time.
- Achieve financial objectives through efficient utility operation, cost improvement actions and optimal cost options.
Qualification:
- Bachelor or Master’s degree in engineering with a minimum of 8-10 years of relevant experience.
- Prefer candidates who are certified Project Management Professionals.
- 5-10 years of experience in the green field / brown field area project management.
- Experience handle the project from USD 5-25 million.
- Proficiency or experience in the Microsoft project software and project tracking.
