Product Manager, Manufacturing Execution & Batch Lifecycle

Team: Product Management

Location: Hyderabad

Commitment: Full-Time

Workplace Type: onsite

Responsibilities:

Product Strategy & Roadmap 

• Own and evolve the product roadmap for Electronic Batch Records (EBR) and adjacent batch execution workflows, grounded in customer discovery, regulatory intelligence, and competitive market analysis 

• Prioritize platform capabilities through structured discovery—customer interviews and feedback, EAP programs, and on-site manufacturing observations 

• Translate evolving FDA CSA, EU Annex 11, 21 CFR Part 11, ALCOA++, and ICH Q10 expectations into actionable roadmap input 

• Partner with other Product Managers to ensure coherent positioning and continutiy across the platform 

Voice of the Market 

• Serve as an internal authority on batch execution, review-by-exception, and deviation workflows across pharma, biotech, and CDMO segments 

• Support Sales and Pre-Sales in customer discovery, product demonstrations, and competitive evaluations against incumbents 

Delivery & Execution 

• Author product requirements—solution definition, mock-ups creation, use-case documentation—that translate batch manufacturing workflows into buildable software specifications 

• Manage Early Adopter Program (EAP) and early release cycles  

• Partner to define governed-AI use cases 

Go-to-Market & Commercialization 

• Partner with Marketing and Sales Enablement on product launches, competitive positioning, and solution messaging 

• Develop narratives grounded in manufacturing and regulatory credibility 

Requirements:

Manufacturing Execution Domain Knowledge 

• 5+ years of hands-on experience in pharmaceutical, biotech, or CDMO manufacturing operations—batch execution, manufacturing sciences (MSAT), site QA, manufacturing IT, or technical operations 

• Direct, working familiarity with electronic batch records, review-by-exception, deviation management, and batch release workflows in a regulated environment 

• Working knowledge of MES/eBR platforms and the manufacturing data substrate  

• Familiarity with MES, LIMS, ERP, QMS, eLogbooks, and GxP-regulated informatics 

• Working knowledge of GxP regulatory frameworks: 21 CFR Part 11, EU Annex 11, ALCOA++, FDA CSA, and ICH Q10 

Product Management 

• 3+ years in product management or a closely adjacent role within a life sciences software, MES, or industrial SaaS company 

• Proven ability to translate complex manufacturing and quality workflows into clear, prioritized software requirements 

• Strong communication skills—credible with floor operators, site QA leaders, and C-suite executives alike 

• Experience with Agile/Scrum delivery nice to have 

 

Education 

• B.Sc., M.Sc., or Ph.D. in Chemical Engineering, Pharmaceutical Sciences, Industrial Engineering, Computer Science, or a related discipline 

• Equivalent experience considered where manufacturing execution domain expertise is clearly evidenced