Dr. Reddy’s Laboratories: Process Engineer API — Hyderabad, India

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.

The position and its setting

Dr. Reddy’s Laboratories lists Process Engineer API in Hyderabad, India, under reference REF25418M. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Employment type: Full-time
• Employer listing date: 23 October 2026
• Job Family: Engineering & Science
• Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

• Be responsible for development and Scale-up of processes for new products, Technology Transfer & Process Validation of the product at plant scale
• Be responsible to work in collaboration with Chemistry team & provide necessary inputs during Design of Experiments (DoE) studies & further process optimization
• Be responsible to develop detailed process understanding & ensure scale-up feasibility using fundamental studies of reaction kinetics, Crystallization, Process Safety, Process analytical technology (PAT)
• Be responsible to ensure appropriate facility/equipment/technology mapping at in house/SBP plants
• Be responsible to draft the process for scale up i.e Kilo lab, Critical Process Parameter (CPP) and validation batches in co-ordination with Cross Functional Teams
• Be responsible for Technology Transfer & Scale-up of Active Pharmaceutical Ingredient (API) and engineering optimization studies with minimal guidance
• Be responsible for supporting Drug Master Filing (DMF), address regulatory queries related to process engineering, and demonstrate awareness of process validation, GMP, and GLP aspects to facilitate smooth regulatory filing
• Your role will involve staying familiar with the Intellectual property (IP) landscape and relevant literature, participate in industry forums, and disseminate knowledge within PE teams, applying existing knowledge and technologies during development
• Be responsible for proactive planning & timely completion of Process Engineering tasks in alignment with project goals
• Be working collaboratively in cross functional team to drive Process Engineering activities

Essential requirements and candidate background

• Educational Qualification: B.tech in Chemical engineering
• Minimum Work
• 3+ years of experience
• Skills & Attributes & Critical Exposures
• Functional Skills:
• Automation
• Artificial Intelligence
• Business Analytics
• Data Quality
• Digital Product Management
• Predictive Modeling
• User Experience (UX) Design
• Workflow Management Systems
• Resident Skills:
• Agile Methodology
• Data Analysis
• Program Management
• Behavioural Skills:
• Attention to Detail: Demonstrates precision and accuracy in documenting processes, validating systems, and ensuring compliance with regulatory standards
• Problem-Solving Mindset: Proactively addresses technical challenges by applying analytical thinking and collaborating with cross-functional teams

Preferred experience and additional strengths

• Exposure: digital tools for manufacturing and quality improvement, including process automation and integration with MES and QMS is preferred
• Exposure: regulatory requirements (e.g., FDA, ISO) in manufacturing settings, particularly in relation to digital solutions, is preferred
• Exposure: digital tools and technologies such as ERP systems and data visualization tools is preferred

Location, schedule and contract conditions

• Work arrangement: On-site
• Advertised location: Hyderabad, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Process Engineer API vacancy is not an offer for reference REF25418M; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Dr. Reddy’s Laboratories

Applications follow the official employer page linked below.

Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF25418M.

Compare your qualifications and experience with the essential conditions for the Hyderabad, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• APIs
• AI/ML
• GMP
• ISO
• GLP
• chemistry
• pharmacy
• data analysis
• AI
• manufacturing
• compliance