Job Title: MES ConsultantEmployment Type: ContractJob DescriptionMust Have Very strong experience in SyncadeThe Role Requires
- Relevant Pharma experience
- Possess a deep understanding and extensive experience in MES systems (preferably Syncade), data integration, networking, and proficiency in ERP systems (preferably SAP)
- Understanding of various client quality and manufacturing impacts involved with MES implementation.
- GxP systems implementation or software development life cycle as well as supporting project and validation methodologies (CSV).
- Experienced in operating withing a regulated environment, possessing understanding of GMP, 21 CRF part 11, and validation criteria.
- Proficiency in Syncade modules, including WF, OM, MM, ET and RA
- Solid understanding of integration methodologies between Syncade and other manufacturing systems (e.g. ERP, SCADA, PLCs)
- Familiar with the processes involved in biotech or pharmaceutical manufacturing, including operational workflow and EBR.
- MES recipe authoring or MBR development
- Electronic batch record (EBR) design or validation experience
- Experience leading people or complex projects
- Willingness to gain additional knowledge of the MOM platform and integration capabilities.
- Excellent analytical and problem-solving skills.
- Excellent written, verbal communication and presentation skills
Responsibilities (include But Are Not Limited To)
- lead the design, implementation, and configuration of electronic batch records within Syncade MES solution, ensuring alignment with business objectives and manufacturing requirements.
- Collaborate with cross-functional teams, including process experts, production supervisors, and IT professionals, to gather requirements and translate them into functional specifications.
- Configure Syncade modules including WF, OM, MM, ET and RA
- Conduct thorough testing and validation of project solutions, including integration with other manufacturing sys such as ERP, SCADA and PLCs
- Collaborate with vendors, consultants, and stakeholders to troubleshoot and resolve technical issues ensuring minimal disruption of the production process.
- Participate in internal and external audits/inspections.
- Completes required training assignments to maintain necessary technical skills and knowledge and to ensure compliance with cGMP requirements.
- Ability to provide training and technical guidance to engineers and end users.
Basic Qualifications
- Bachelor’s degree (engineering/ business informatics or equivalent exposure to the IT industry or business analysis)
- 10 years’ experience in working with the manufacturing industry/shop-floor (functional or technical) preferably in life-science industry
- BS or BA in biochemical engineering, chemical engineering, biotechnology, chemistry, biology, or equivalent with at least 5 years of relevant experience or
- MA/MS in biochemical engineering, chemical engineering, biotechnology, chemistry, biology, or equivalent with at least 5 years of relevant experience.
Vimerse is a fast growing IT Company having a team of well trained professionals and with a huge spectrum of services to offer. It s having Innovation and Reliability as its driving force. We are proud to say that with our fleeting yet diverse experiences we are able to become a partner of choice with an astonishing accomplishment and customer satisfaction for our clients.Our main motive is to provide professional support system to our clients aligned to their core business activity with an aim to provide cost effectiveness and optimum utilization of available resource while keeping pace with dynamic market conditions.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran statusMES Consultant – Remote
