As the MES Applications Manager for our Healthcare and Pharma department, you will be responsible for leading the development, implementation, and support of Manufacturing Execution Systems (MES) for our clients. You will work closely with clients to understand their requirements and collaborate with our teams to design, develop, and deploy customized MES solutions using Siemens Opcenter.
Key Responsibilities:
- Act as the primary point of contact for clients to understand their MES requirements and translate them into technical specifications
- Collaborate with our teams to design and develop customized MES solutions using Siemens Opcenter
- Manage the full software development lifecycle, including testing, deployment, and maintenance of MES applications
- Monitor and manage the performance of MES applications, ensuring they meet the required service levels and KPIs
- Provide guidance and support to the client's team during the implementation and post-implementation phases
- Work closely with the project management team to ensure timely delivery of projects within scope and budget
- Stay up to date with the latest MES technologies and provide recommendations to clients on how to improve their manufacturing processes
- Contribute to the development of our MES practice by sharing best practices, identifying new opportunities, and participating in training programs
Requirements:
- Bachelor's or Master's degree in Computer Science, Engineering, or a related field
- Minimum of 5 years of experience in developing and deploying MES solutions, preferably in the healthcare or pharmaceutical industry
- Strong technical expertise in Siemens Opcenter and other MES applications
- Experience in managing the full software development lifecycle of MES applications
- Excellent communication and interpersonal skills, with the ability to interact with clients and internal teams at all levels
- Strong problem-solving and analytical skills, with the ability to identify issues and propose solutions
- Ability to work in a team environment and lead a team of developers and analysts
- Strong project management skills, with the ability to manage multiple projects simultaneously
- Willingness to travel to client sites as required
Preferred Qualifications:
- Experience in working with clients in the healthcare and pharmaceutical industry
- Knowledge of regulatory requirements and guidelines related to manufacturing processes in the healthcare and pharmaceutical industry
- Experience in implementing MES solutions in a GxP environment
- Understanding of quality management systems, such as ISO 13485 or FDA 21 CFR Part 820
If you meet the above qualifications and are interested in this exciting opportunity, please submit your resume and cover letter to us for review. We look forward to hearing from you!
