About the role
As a Senior MES Recipe Author – Syncade, you will make an impact by implementing recipe changes and supporting the systems that enable reliable pharmaceutical manufacturing operations.
You will be a valued member of a collaborative Manufacturing Execution System (MES) team supporting a large multinational biotechnology manufacturing facility in Cork. You will work across Electronic Batch Records, Weigh and Dispense, and Equipment Management modules within the Emerson Syncade MES solution.
In this role, you will:
- Manage the ServiceNow incident queue, investigating and resolving MES issues in a timely manner.
- Initiate and implement change-control activities in accordance with site quality standards, procedures and Good Manufacturing Practice requirements.
- Configure, test and deploy MES recipes and system changes, producing high-quality documentation that is clear and maintainable.
- Create computer system validation documentation and perform system and integration testing in line with site procedures and project schedules.
- Collaborate with business users and cross-functional teams to understand requirements, recommend improvements and deliver effective MES solutions.
Work model
We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role’s business requirements, this is a hybrid position requiring three days a week at our client’s site in Cork, Ireland. Regardless of your working arrangement, we are here to support a healthy work-life balance through our various wellbeing programmes.
The working arrangements for this role are accurate as of the date of posting. This may change based on the project you’re engaged in, as well as business and client requirements. Rest assured, we will always be clear about role expectations.
What you need to have to be considered
- Three to five years of experience supporting IT applications, including troubleshooting, incident management, change control, design documentation, test-case development and system or integration testing.
- Experience in MES recipe authoring, ideally using Emerson Syncade.
- Experience implementing or supporting application changes within a Good Manufacturing Practice-regulated environment.
- Knowledge of programming, Visual Basic, configuration management and the deployment of developed code.
- Strong written and verbal communication skills, with the ability to collaborate effectively with business users and cross-functional teams.
These will help you stand out
- Experience working with Electronic Batch Records, Weigh and Dispense, or Equipment Management modules.
- Knowledge of Microsoft SQL Server.
- Experience producing computer system validation documentation within a pharmaceutical or biotechnology manufacturing environment.
- A strong understanding of quality-control requirements within pharmaceutical production.
- The flexibility to participate in out-of-hours support as the role evolves.
We’re excited to meet people who share our mission and can make an impact in a variety of ways. Don’t hesitate to apply, even if you only meet the minimum requirements listed. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and exciting things to this role.
关于高知特 (Cognizant)
高知特(Cognizant)（纳斯达克代码：CTSH）作为一家AI Builder和相关技术服务提供商，致力于通过打造全栈AI解决方案，帮助企业将人工智能投资转化为实际价值。公司凭借深厚的行业经验、流程优化和工程技术专长，将企业独特的业务场景融入科技系统，赋能组织释放人才潜能，推动切实成果，并帮助全球企业在瞬息万变的环境中保持领先。如需了解更多详情，敬请访问 cognizant.ai 或关注@cognizant。
补充雇佣信息
薪酬信息截至本职位发布之日为准。Cognizant 保留在适用法律允许的范围内随时修改该信息的权利。
申请人可能需要通过现场面试或视频会议的方式参加面试。此外，候选人在每次面试时可能需要出示其当前所在州或政府签发的有效身份证件。
Cognizant 是一家提供平等就业机会的雇主。在招聘过程中，您的申请和候选资格不会因种族、肤色、性别、宗教、信仰、性取向、性别认同、国籍、残疾、遗传信息、怀孕、退伍军人身份或任何其他受联邦、州或地方法律保护的特征而受到影响。
