MES Program Manager
MES Program Manager
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Job Description
The Role:
- MES Program Manager
- Hybrid (Witney UK). The role will require regular onsite working so you should be commutable to the Witney (Oxfordshire) location.
- The role is expected to commence in Q4 2024 or Q1 2025
- Contract or PermanentOpportunity
Role Brief:
The successful candidate will be responsible for the delivery of new and updated integration functionalities for Manufacturing Execution Systems for use in production. Responsibility also includes oversight on alignment of Manufacturing Information Systems with Global Operating Specifications.
Skills Brief:
- Provide support for all MES applications particularly POMSNet.
- MES experience with focus on workflow S95 & S88 standards and integration from the control layer to MES in pharma & biopharma industries
- Engage in workshops with various stakeholders including Business Quality Compliance and product SMEs to align with process flow related to recipe designs.
- Collaborate with leaders from Operations Supply Chain Engineering IT and Quality to ensure efficient MES site support.
- Ensure adherence to relevant Policies and Procedures and contribute to the creation of Work Instructions and Procedures to maintain compliance.
- Coordinate and execute process and equipment projects relevant to MES.
- Validate new processes and generate technical documentation for your areas of responsibility.
- Construct test and validate recipes that involve integration with systems like SAP databases and PLCs.
- Design author develop and configure Electronic Batch Records (EBR).
- Implement MES solutions and seamlessly integrate them with ERP and control equipment.
- Thoroughly document MES configurations and validate Electronic Batch Records (EBRs).
- Develop Project Charter including Scope Statement Budget and other project assets aligned to the PMO governance framework.
- Develop and execute an effective Communications Plan for internal/ external stakeholders to always ensure clear visibility to project progress.
- Drive internal & client deliverables to maintain project schedules and budget adherence.
- Perform Risk and Change Management activities throughout the project lifecycle.
- Manage project teams through all stages of the project (indirect/ direct).
- Ensure Project Quality is maintained to the highest standard.
Person Brief:
Candidates must have a level 8degree qualification with minimum of five years relevant industry experience in pharmaceutical or biotechnology manufacturing environments. The ideal candidate will have excellent collaboration and communication skills with the ability to work in a fast paced dynamic environment. In addition to this strong attention to detail including the ability to proofread documents and to accurately translate customers requirements into meaningful enduser instructions consistently is required.
You should have a mix of strong and relevant technical skills and proven client and project management skills. The candidate should have experience with POMS system and strong C# coding and SQL Database knowledge. PTL XML and Power Automate knowledge is desirable.
Ideally you will have35 Years experience in project managing OT projects in a GMP environment
A PMP / Prince / PgmP Certification is essential for the role.
The candidate should be based in or near to Oxfordshire UK and able to travel onsite to the Witney location as required.
Opportunity Brief:
This is an excellent opportunity to work with clients who are global leaders in their field helping to develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development and wellness along with a competitive and rounded compensation package which rewards high performers.
Company Brief:
SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers including many of the worlds top multinational companies in the medical device and pharmaceutical sectors achieve their Six Sigma and OEE targets.
Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway Limerick Leinster and Florida USA.
We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users OEMs and Technology providers.
Find out more about working at SL Controls our Sustainable Development Goals and our Diversity Equity and Inclusion policy.
Employment Type
Full Time
