Manufacturing Execution System (MES) Developer at Tekhqs

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

23 Aug, 26

Salary

0.0

Posted On

25 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

MES Implementation, Recipe Authoring, Electronic Batch Records, System Integration, Validation, GMP, 21 CFR Part 11, GAMP5, ISA-95, SQL, APIs, SCADA, PLC, ERP, SAP, LIMS

Industry

IT Services and IT Consulting

Description

Job Summary We are looking for an experienced Manufacturing Execution System (MES) Developer with 6+ years of experience in Pharma Manufacturing and Digital Transformation projects. The ideal candidate should have hands-on expertise in MES implementation, recipe authoring, electronic batch records, system integration, validation, and deployment within regulated pharmaceutical environments. Experience with platforms such as Werum PAS-X, FactoryTalk PharmaSuite, Emerson Syncade, or Siemens Opcenter will be highly preferred. Key Responsibilities Design, develop, configure, and implement MES solutions for pharmaceutical manufacturing environments. Develop and maintain: EBR (Electronic Batch Records) MBR/GMBR/PMBR Recipes and workflows Perform recipe authoring and process modeling in MES platforms. Integrate MES with SCADA, PLC, ERP, SAP, LIMS, and automation systems. Support MES deployment, testing, troubleshooting, and production go-live activities. Execute validation activities including IQ/OQ/PQ and ensure compliance with GMP and 21 CFR Part 11. Collaborate with cross-functional teams including Manufacturing, QA, Validation, Automation, and IT. Support change control, deviation management, and system documentation. Participate in Pharma Digital Transformation initiatives and continuous improvement projects. Provide technical support and issue resolution during project execution. Required Skills & Experience 6+ years of experience in MES development/implementation. Strong experience with one or more MES platforms: Werum PAS-X Rockwell PharmaSuite Emerson Syncade Siemens Opcenter Experience in Pharma or Life Sciences industry is mandatory. Strong understanding of: GMP GAMP5 21 CFR Part 11 ISA-95 concepts Hands-on experience in: Recipe Authoring EBR/MBR Design Validation Documentation Batch Execution System Integration Experience with SQL, APIs, and automation systems is preferred. Excellent communication and stakeholder management skills. Ability to work independently in remote/global project environments. Preferred Qualifications Bachelor's degree in Computer Science, Engineering, IT, or related field. MES certifications or Pharma automation certifications are a plus. Experience working with international pharma clients is preferred. Nice to Have Exposure to Pharma 4.0 initiatives Cloud or IIoT integration experience Agile project delivery experience Knowledge of serialization or manufacturing analytics

Responsibilities

Design, develop, and implement MES solutions and electronic batch records for pharmaceutical manufacturing environments. Integrate MES with automation systems and ensure compliance with GMP and 21 CFR Part 11 regulations.