Be part of the Next Industrial Revolution - Behind every SaaS Product is a Team
InVimachem,we’reusing technology to empower the people who manufacture medicines for our world. Since 2015, we have been developing the industry’s only AI-enabled MES platform purpose-built for Life Sciences-combining MES,IIoT,and Pharma 4.0 capabilities into a single, modern system that helps pharmaceutical and biotech manufacturers scale faster,operatewith greater flexibility, and deliver high-quality, life-savingmedications.
Today, we are going through one of the most excitingperiodsinour company's history. We are growing rapidly globally and expanding our EU-based MES consulting team,seekingan experienced,ambitiousLeadMES Consultant to joinus.
Our culture is fast-paced, entrepreneurial, and rewarding.We'vebeen recognized as a "Great Place to Work" for multiple consecutive years by fostering an inclusive and mission-driven culture. If you are passionate aboutcutting-edgesoftware and global MES engagements, the future is bright for you atVimachem, and we want to hear from you!
This position is a fully remote position for EU-based candidates, with up to 25% travel for on-site customer visits.
About The Role
As aLeadMES Consultant, you willleverageyour deep understanding of bothVimachemsolutions and the Life Sciences manufacturing industry to driveoperational and delivery excellenceacrosspharmaceutical and biopharmaceutical manufacturing organizations. You will be a part of a highly motivated, growing team that analyzes and improves business processes throughVimachemsolutions, ensuring alignment with industry best practices inLifeSciences manufacturing.
What will you do as aLeadMES Consultant?
- Act as the lead technical consultant on client projects from process analysis and design through configuration, testing, deployment, go-live, andhypercare.
- Consult customers and prospects to prepare their companies for digital transformation.
- Remote or on-site analysis, design, improvement, documentation, and maintenance of pharma/biopharma clients’ manufacturing processes.
- Design, configure, and test digital workflows usingVimachem’sno-code/low-code MBR Designer.
- Work closely with sales executives to effectively progress opportunities through the pipeline and secure the "technical win”.
- Develop,presentand deliver high-impact technical demonstrations of theVimachemsolutions (Demos, technical presentations, technical discussions, etc.)
- Collaborate with clients' QA, Production, and IT stakeholders at client sites to align MES implementation with operational and regulatory requirements.
- Test and troubleshoot system behavior and provide guidance to client teams.
- Contribute to internal best practices and knowledge base.
- Organize and teach best practice product workshops remotely or at customer sites.
- Investigate client issues and communicate key insights and findings to the product team.
- Analyze and enhance the efficiency, stability, and scalability of theVimachemPharma MES platform through working with Product and Engineering teams to provide client feedback and support continuous platform improvement.
- Contribute as amarket and customer expertin annual sales strategy and planning,providing insights on industry trends, customer needs, and competitive landscape.
- Help develop and answer RFx (RFI, RFP, RFQ), technical assessments, technical and security questionnaires.
- Lead in the scoping and estimation of implementation projects delivered by theVimachemProfessional Services Team.
- Proven experience managing high-performing teams. This role will lead a growing team of MES consultants across theVimachemPharma MES platform, ensuring alignment, accountability, and professional development through structured bi-annual performancereviews.
The main qualifications for theLeadMES Consultant role are:
- At least 5 years of experience working in Pharma / Biopharma manufacturing (Pharma, Biotech, or Cell & Gene Therapy) or with Pharma / Biopharma clients.
- At least 5 years of hands-on experience with MES platforms (e.g.,WerumPAS-X, Rockwell, EmersonSyncade, Siemens OpsCenter, or similar) with hands-on experience in functional configuration and EBR design.
- Atleast 2 years of experienceindeliveringdemonstrations and training ofMES platforms within the Life Sciences industry.
- Strong understanding of GMP workflows, batch record design, and regulatory requirements in pharmaceutical production.
- Experience with integrationtoproduction and packaging equipment, LIMS, ERP, or SCADA systems.
- Excellent communication skills and the ability to work with cross-functional teams and international clients.
- Ability to travel up to 25% based on theVimachemmodules and the clients you serve.
- ABachelor'sdegree in a STEM (Science, Technology, Engineering, or Math) discipline or Life Science field or equivalent.
- Hands-on pharmaceutical manufacturing experience is a strong plus.
- Fluency in French, Italian, or Spanish is a strong plus.
AtVimachem, we know that even exceptional candidates sometimes hesitate to apply. Ifyou’reexcited about this role butdon’tmeet every single requirement, we encourage you to apply -we’dlove to explore your potential fit.
What’sin for You
Our team is a strong, diverse, hard-working team that values families, personal well-being, and meritocracy. We believe amazing results require amazing effort and commitment, and we perform bi-annual performance reviews and continuous feedback to ensure we reward our top performers.
Benefits of working with us include:
- Competitive salary and performance bonus.
- Employee Stock Option Plan (ESOP).
- Modern work environment with an open culture towards improvements andnew ideas.
- Benefits packageincludingHealth insurance, Life insurance, Short-term Disability, and Long-term Disability.
- Continuous training, company workshops, and events.
- A buddy will support you with onboarding.
We are an equal opportunity employer and value diversity at our company. We do not discriminateon the basis ofrace, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Help us build an inclusive community that will transform Life Sciences manufacturing.
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