Role: Scientist Peptide Chemistry. Qualification: M.Sc. Organic Chemistry with 2 to 6 years of experience on Synthetic and Analytical knowledge and experience of Peptide molecules. Areas Of Responsibility: Synthesis and Characterization of peptides Plan and execute the synthesis of peptide molecules with adequate purity and quantity as per project requirements. Develop good trouble shooting skills and comply with IPM and Safety norms. Developing appropriate methods for special functionalized peptides. Preparing key intermediates by solution phase synthesis which would be used as building blocks for synthesis of final target molecules. IN ORDER TO: successfully synthesize and deliver target compounds as per project specifications. Data Interpretation: To interpret the analytical data in identifying the synthesized targets and key intermediates. IN ORDER TO: successfully characterize the synthesized targets. Safety Compliance To follow the lab safety and industrial hygiene practices.

Hiring professionals with expertise in the analytical method development and characterization of biologic molecules. Hands-on experience with analytical techniques such as HPLC, UPLC, Capillary Electrophoresis, and Mass Spectrometry is required. Experience in method development, qualification, and transfer is highly desired. Guiding and mentoring juniors is a plus. Preferred candidate profile

Role: Product Manager Department: DPEx Role Band: S - equivalent to Indigo Location: Miyapur, Hyderabad No. of Positions: - 01 Context: APSL has embarked on an organization wide initiative of Business Transformation Process Excellence leveraging Digital, Analytics Automation. The DPEx team plays a key role in understanding business processes, suggesting solutions and planning executing these solutions to create direct impact on business KPIs. The Product Manager is expected to lead many such initiatives within the organization. The product manager should understand the business requirements, map processes, translate business process requirements into business requirement specifications and drive business excellence initiatives. He/she should work collaboratively with cross functional teams (CFTs), own/co-own drive internal projects products. What makes this assignment interesting Broader understanding of APSL business context and scenarios Opportunity to own create new business platforms and drive impact on PL Insight into the Business workings process related to RnD labs (PRD, ARD, FRD, Process Engineering, Drug Discovery labs (MedChem, DMPK, Animal Toxicology, Cellular Molecular Biology, etc.)) Value chain analysis and understanding of latest trends in business applications. Key Responsibilities: Lead Digital initiatives end-to-end from ideation to execution and adoption Responsibility to own the business metrics and its delivery through direct and vendor-led work around internal products Develop clear roadmap strategy to improve business KPIs and user experience Participate in business user requirements and understand the key operational data challenges of the organization. Prepare business processes documents, URS and recommendations related to proposed solution. Adoption tracking and reporting to senior management. Develops functional specifications and system design specifications for client engagements. Oversee development of solution prototype. Ensures issues are identified, tracked, reported on and resolved in a pro-active manner. Communicates needed changes to development team. Technical Requirements: Must have good technology inclination, exposure to business applications like ELN, Empower, etc. Must have hands-on experience in Designing, solutioning executing Digitization projects/products, process improvement projects Should have played a BA+ Product Manager role for at least 3-5 years Good understanding of business processes in at least one of the functions like Pharma RD , Lab Automation, Drug discovery development. Exhibits confidence and an extensive knowledge of emerging industry practices when solving business problems. Knowledge in Product management background and familiar with PMI project methodologies and SDLC. Must have hands-on experience in process mapping, creating URS specification documents project management. Education Experience: BTech + MBA would be preferred. Prefer minimum 3-5 years of experience in Product Management of business applications around Pharma RD Services, CDMO, Discovery or in a consulting firm.

Walk-in Interviews: Process R&D & Process Engineering | 28th June'25 | Hyderabad Are you a seasoned Process R&D Scientist or Process Engineer driven by the intricacies of pharmaceutical scale-up and optimization? Aurigene Pharmaceutical Services Ltd, a leading CDMO at the forefront of drug development, is strategically expanding its core technical teams. We are seeking distinguished scientific and engineering professionals whose expertise will directly shape our advanced API development and manufacturing processes. This is an invitation to leverage your specialized knowledge and make a tangible impact within a high-growth environment. Positions Available: 1) Scientist - Process R&D (API) - Qualification & Experience: M.Sc . (Chemistry) with 3 - 6 years of experience - Responsibilities: Driving process optimization, scale-up (mg to kg), technology transfer, analytical interpretation (IR, NMR, Mass, GC, HPLC), documentation, and troubleshooting - Added Advantage: Flow chemistry experience 2) Team Member - Process Engineering - Qualification & Experience: B.Tech . Chemical Engineering with 3-6 years of - industrial experience - Responsibilities: Ensuring process feasibility, safety & compliance during scale-up, executing technology transfer, overseeing batch operations, and leading cost optimization initiatives Walk-in Interview Details: Date: Saturday, 28th June, 2025 Time: 9:00 AM to 12:00 PM Venue: Aurigene Pharmaceutical Services Ltd, Bollaram Road, Jaya Prakash Narayan Nagar, Miyapur, Hyderabad, Telangana 500049 Please remember to bring: - Your updated resume - Latest appraisal letter - Last 3 months' salary slips We look forward to meeting passionate individuals ready to make an impact!

Job Description: We are seeking a highly motivated and skilled Medicinal Chemist with the industrial experience of 2 to 5 years to join our dynamic research and development team in Bengaluru. The candidate will be responsible for the design, synthesis, and characterization of novel chemical entities (NCEs) in accordance with client specifications and internal guidelines, contributing significantly to our drug discovery programs. Key Responsibilities: Synthesize and characterize novel NCEs efficiently and independently, adhering to client specifications. Apply broad knowledge of modern organic chemistry and synthetic methodologies to complex chemical problems. Execute various synthetic reactions, including but not limited to: heterocyclic chemistry, metal-catalyzed reactions, air/moisture-sensitive reactions, and hydrogenations, carrying out multi-step synthesis as required. Utilize a wide range of techniques for synthesis and purification, including chromatographic methods (e.g., MPLC, HPLC). Perform spectroscopic characterization of novel compounds using techniques such as NMR, LCMS, HPLC, and IR. Maintain accurate and up-to-date Lab Note Books in accordance with client specifications and internal guidelines. Generate final reports and other scientific documents as needed. Demonstrate a strong understanding of systems and processes pertaining to safety, health, and environmental regulations. Strictly adhere to EHS (Environmental, Health, and Safety) guidelines, maintaining a zero-tolerance policy for non-compliance. Required Candidate Profile: Education: M.Sc. in Organic Chemistry or Chemistry. Experience: 2 to 5 years of experience in Synthetic Chemistry (Small Scale). Interview Details (Walk-in Drive): Date: 5 th July'25 Time: 9:00 AM to 3:00 PM Interview Venues: Bengaluru: Aurigene Pharmaceutical Services Ltd. 39-40 Hosur Road KIADB Industrial Area, Phase 2, Electronic City, Bengaluru, Karnataka 560100 Hyderabad: Aurigene Pharmaceutical Services Ltd. Bollarum Road, Jaya Prakash Narayan Nagar, Miyapur, Telangana 500049, India Mandatory Documents to Carry for Interview: Your latest resume. Last three months' salary slips. Salary revision letter (if applicable). 3 Passport-size photographs. Note: The final job posting location will be Bengaluru, regardless of the interview location.

Role & responsibilities To perform in vitro ADME assays (solubility, metabolic and plasma stability, CYP inhibition, plasma protein binding studies etc.) Design, conduct and report data from in vitro metabolism studies using various cellular and subcellular systems, e.g., microsomes, hepatocytes, recombinant CYPs/UGTs and transfected cells. Perform assays using automated workstations. To design, program and implement study protocols in automated workstations. Ability to integrate metabolism and other supporting ADME data to predict druggability outcomes. To lead a group of 2-5 members and train juniors for the ongoing assays and technologies. Maintain labs & comply with SHE/regulatory guidelines. Preferred candidate profile Masters with 10+ years of PhD with 2+ years industry experience in Invitro ADME assays.

To perform in vitro ADME assays (solubility, metabolic and plasma stability, CYP inhibition, plasma protein binding studies etc.) Design, conduct and report data from in vitro metabolism studies using various cellular and subcellular systems, e.g., microsomes, hepatocytes, recombinant CYPs/UGTs and transfected cells. Perform assays using automated workstations. To design, program and implement study protocols in automated workstations. Ability to integrate metabolism and other supporting ADME data to predict druggability outcomes. To lead a group of 2-5 members and train juniors for the ongoing assays and technologies. Maintain labs & comply with SHE/regulatory guidelines.