Job Title: Associate Manager – Manufacturing Execution Systems (MES)
Location: Visakhapatnam (Vizag), India
Employment Type: Full-Time
Posted: 2 Days Ago
Job Requisition ID: 4950273
About the Role:
We are seeking an experienced Associate Manager – MES to join our pharmaceutical manufacturing team in Vizag. The ideal candidate will bring a strong blend of technical expertise, manufacturing knowledge, and regulatory compliance experience to ensure seamless operations and digital integration in our sterile manufacturing facility.
Key Responsibilities:
Lead and manage electronic batch record (EBR) systems and associated software platforms (e.g., FTPS/AMPS, SAP, MLM).
Support and optimize manufacturing and packaging operations, including process design, workflow, and compliance adherence.
Drive regulatory readiness, including defending manufacturing processes during audits and inspections.
Collaborate with cross-functional teams (CFTs) to ensure effective communication and smooth operational integration.
Implement and maintain manufacturing and quality systems, ensuring adherence to global compliance standards.
Independently manage projects while fostering a collaborative team environment.
Required Qualifications & Experience:
Graduate or Postgraduate in Pharmaceutical Sciences, Engineering, or related disciplines.
Minimum 8+ years of experience in pharmaceutical manufacturing, preferably in sterile dosage form production.
Hands-on experience in electronic batch record design and working knowledge of MES-related software.
Strong understanding of manufacturing operations, quality systems, and regulatory compliance processes.
Excellent written and verbal communication skills with the ability to interact with multiple stakeholders effectively.
Preferred Qualifications:
Master’s degree in relevant field.
Prior experience with SAP and advanced EBR software platforms (e.g., FTPS, PAS|X).
Demonstrated knowledge of global pharmaceutical manufacturing standards and compliance frameworks.
Work Location: On-Premise – Vizag, India
Why Join Us:
This role offers the opportunity to work in a dynamic pharmaceutical environment at the intersection of technology and manufacturing. You will play a critical role in advancing digital manufacturing initiatives while ensuring regulatory compliance and operational excellence.
Equal Opportunity Statement:
We are an equal opportunity employer and comply with all applicable equal employment opportunity legislation in each jurisdiction in which we operate.
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