Project Manager at NNIT
Cavan, County Cavan, Ireland -
Full Time


Start Date

Immediate

Expiry Date

15 Jun, 25

Salary

0.0

Posted On

15 Mar, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Integration, Workflow, Mes, Implementation Experience

Industry

Information Technology/IT

Description

SKILLS BRIEF:

  • Significant experience with POMSnet is essential and only candidates with this experience will be considered.
  • Some experience with the Aquilla version of POMSnet would be advantageous
  • Authoring and/or implementation experience with the POMSnet MES software package.
  • Experience in C# coding and SQL database knowledge.
  • MES experience with focus on workflow, S95 & S88 standards and integration from the control layer to MES in pharma & bio-pharma industries.
  • A minimum of 3 years experience with MES technology in Life Sciences, Pharma or Biotech manufacturing environments.
  • Strong project management experience in Life Sciences, Pharma or Biotech manufacturing environments is essential and ideally you will have a recognised Project Management qualification.
Responsibilities

THE ROLE:

  • Project Manager - MES
  • Hybrid. The role will require onsite presence for set activities and as required. Remote working is possible for other activities but you therefore must be based in Ireland and able to commute onsite as required
  • CavanContract or Permanent Opportunity
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ROLE BRIEF:

The successful candidate will be responsible for the delivery of new and updated integration functionalities for the Manufacturing Execution Systems for use in production. Responsibility also includes oversight on alignment of Manufacturing Information Systems with Global Operating Specifications.

Core Responsibilities:

  • Support the development of test plans with POMS.
  • Implementing, testing and deploying the changes as per requirement.
  • Design, create, write and execute, test and validation protocols, risk assessments, and system documentation.
  • Design, create, write and/or make all required changes to ensure equipment and product procedures are aligned to MES processes and vice versa.
  • Provide support to other MES system users as required to ensure business continuity.
  • Documentation of all activities in line with cGMP requirements.
  • Change management: Raising change requests based on the MES Application modification / upgrade requirements from the Business.
  • Work as part of a team in designing and developing electronic batch records / workflows within the MES solution.
  • Support, troubleshoot and resolve issues within the system.
  • Identify and drive continuous improvement opportunities within the MES.
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