Morepen Proprietary Drug Research Pvt Ltd (MPDRPL), a leading pharmaceutical research and development organization, is seeking a highly skilled and experienced Senior Medicinal Chemist to join our dynamic team. With a commitment to innovation and the advancement of healthcare, we are dedicated to discovering and developing ground breaking therapeutic solutions. Roles & Responsibilities Synthesis and scale-up of small organic molecules / intermediates / active ingredients on milligram to multikilogram quantities Planning of synthesis including retrosynthesis and literature search Process development & optimization of routes to advanced intermediates/finished products (chemical, physical and preparative). Planning, evaluating & documenting experiments, preparing tech transfer documents such as lab development reports Collaborating with cross functional project teams such as research, analytical, safety etc. Adhering to MPDRPL Environmental Health Safety (EHS), HR policies and work practices Knowledge & experience: · Postgraduate (M. Sc.) in organic chemistry with sound theoretical knowledge in organic synthesis Working experience for >= 1 year in chemical / pharmaceutical / agrochemical industry as a bench chemist or as an intern Why Join Us: Be part of a leading company in the pharmaceutical industry. Opportunity to influence and shape the company's product portfolio. Competitive compensation and benefits package. Professional growth and development opportunities. Application Process: To apply, please submit your resume and a cover letter detailing your experience and qualifications to jobs@morepenpdr.com. Show more Show less

Morepen Proprietary Drug Research Pvt Ltd (MPDRPL) , a leading pharmaceutical research and development organization, is seeking a highly skilled and experienced Senior Medicinal Chemist to join our dynamic team. With a commitment to innovation and the advancement of healthcare, we are dedicated to discovering and developing ground breaking therapeutic solutions. Roles & Responsibilities Synthesis and scale-up of small organic molecules / intermediates / active ingredients on milligram to multikilogram quantities Planning of synthesis including retrosynthesis and literature search Process development & optimization of routes to advanced intermediates/finished products (chemical, physical and preparative). Planning, evaluating & documenting experiments, preparing tech transfer documents such as lab development reports Collaborating with cross functional project teams such as research, analytical, safety etc. Adhering to MPDRPL Environmental Health Safety (EHS), HR policies and work practices Knowledge & experience: Postgraduate (M. Sc.) in organic chemistry with sound theoretical knowledge in organic synthesis Working experience for >= 1 year in chemical / pharmaceutical / agrochemical industry as a bench chemist or as an intern Why Join Us: Be part of a leading company in the pharmaceutical industry. Opportunity to influence and shape the company's product portfolio. Competitive compensation and benefits package. Professional growth and development opportunities. Application Process: To apply, please submit your resume and a cover letter detailing your experience and qualifications to jobs@morepenpdr.com. Show more Show less

Morepen Proprietary Drug Research Pvt Ltd (MPDRPL) , a leading pharmaceutical research and development organization, is seeking a talented and motivated Medicinal Chemist to join our innovative team. With a commitment to excellence and the advancement of healthcare, we are dedicated to discovering and developing breakthrough therapeutic solutions that improve patient outcomes worldwide. Roles & Responsibilities : Design and synthesize novel small molecule compounds with potential therapeutic applications Conduct structure-activity relationship (SAR) studies to optimize lead compounds for potency, selectivity, and drug-like properties Perform multi-step organic synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs) Analyze and interpret analytical data (NMR, MS, HPLC) to confirm compound identity and purity Maintain detailed laboratory notebooks and prepare comprehensive reports on synthetic methods and compound characterization Stay current with scientific literature and emerging trends in medicinal chemistry and drug discovery Support patent applications and intellectual property documentation Ensure compliance with laboratory safety protocols and MPDRPL Environmental Health Safety (EHS) guidelines Knowledge & Experience : Master's degree (M.Sc.) or Bachelor's degree (B.Sc.) in Organic Chemistry, Medicinal Chemistry, or related field 1-4 years of hands-on experience in medicinal chemistry, pharmaceutical research, or related chemical synthesis roles Strong foundation in organic synthesis, reaction mechanisms, and synthetic methodology Experience with modern analytical techniques including NMR spectroscopy, mass spectrometry, and chromatography Knowledge of structure-activity relationships (SAR) and drug design principles Familiarity with chemical databases, literature searching, and computational chemistry tools Understanding of pharmaceutical development processes and regulatory requirements Excellent problem-solving skills and ability to work independently as well as in team environments Strong communication skills and ability to present scientific data effectively Preferred Qualifications: Experience with parallel synthesis and library design Knowledge of ADMET properties and their optimization Familiarity with fragment-based drug discovery approaches Experience with process chemistry and scale-up activities Publications in peer-reviewed journals or patent applications Why Join us: Opportunity to work on cutting-edge drug discovery projects with significant therapeutic potential Access to state-of-the-art laboratory facilities and advanced analytical instrumentation Collaborative research environment with opportunities for professional growth and skill development Competitive compensation package with performance-based incentives Comprehensive benefits including health insurance, retirement plans, and professional development support Mentorship opportunities with senior scientists and exposure to diverse therapeutic areas Contribution to meaningful research that directly impacts patient health and well-being Application Process: To apply, please submit your resume and a cover letter highlighting your relevant experience and research interests to jobs@morepenpdr.com We are an equal opportunity employer committed to fostering an inclusive and diverse workplace environment.

💊 Job Title: Lead Formulation Scientist 📍 Company: Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) 📌 Location: Gagillapur, Hyderabad 📧 Apply at: jobs@morepenpdr.com 📞 +91 6302 451 459 About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and development of various dosage forms with major emphasize in oral dosage forms for ANDA/NDA submission. Build and guide a team to ensure on-time product delivery working in internal and external facility Ensure execution of lab-scale and pilot-scale batches as per QbD and DoE principles. Provide guidance to address formulation and process challenges and conduct technology transfer and ensure manufacturing of exhibit batch and process validation. Coordinate with all cross-functional teams including Analytical R&D, Regulatory Affairs, QA, Manufacturing and external parties to ensure product delivery. · Prepare/review technical documents such as batch records, protocols, reports, and Module 3 CMC documentation for regulatory filings. Ensure all time compliance for internal as well as external quality and safety audits. Present project update and data analytics for review with senior management and take Go/No-go decisions Internal infrastructure building as per the scope and budgeting for CAPEX. Hiring and talent retention. Knowledge & Experience Ph.D / M.Pharm in Pharmaceutics, Pharmaceutical Technology , or a related field. Experience: Ph.D with 6-8 years and M.Pharm with 8-12 years of experience in the area of formulation developments of generic product (ANDA) and/or Differentiated products (505b2) for various markets including US and EU. End to end knowledge in formulation design, development and filing of oral dosage forms (major experience) along with development of other dosage forms. · Strong knowledge in Deformulation, Preformulation, Reformulation and Formulation Optimization. Sound knowledge of FDA/EU/ICH guidelines for designing product spec and quality, QbD , BE studies and regulatory expectations for ANDA and/or NDA submissions. Strong data interpretation skills and familiarity with eCTD Module 3 documentation and dossier preparation. Ability to guide a team , fostering a positive work environment, and ensuring on time delivery of products addressing formulation and process challenges. Preferred Qualifications Exposure to semi-solid and or complex dosage forms Formulation developments of NCEs. Understanding of bioequivalence study design and in-vitro/in-vivo correlation (IVIVC). Involvement/participation in regulatory audits . Knowledge of analytical techniques used in drug product development Application of digital tools in formulation developments Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans . Application Process To apply, submit your updated CV and a cover letter highlighting your relevant experience to: 📧 jobs@morepenpdr.com MPDRPL is an equal opportunity employer committed to a diverse and inclusive workplace.

💊 Job Title: Lead Formulation Scientist 📍 Company: Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) 📌 Location: Gagillapur, Hyderabad. 📧 Apply at: jobs@morepenpdr.com 📞 +91 6302 451 459 About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and development of various dosage forms with major emphasize in oral dosage forms for ANDA/NDA submission. Build and guide a team to ensure on-time product delivery working in internal and external facility Ensure execution of lab-scale and pilot-scale batches as per QbD and DoE principles. Provide guidance to address formulation and process challenges and conduct technology transfer and ensure manufacturing of exhibit batch and process validation. Coordinate with all cross-functional teams including Analytical R&D, Regulatory Affairs, QA, Manufacturing and external parties to ensure product delivery. · Prepare/review technical documents such as batch records, protocols, reports, and Module 3 CMC documentation for regulatory filings. Ensure all time compliance for internal as well as external quality and safety audits. Present project update and data analytics for review with senior management and take Go/No-go decisions Internal infrastructure building as per the scope and budgeting for CAPEX. Hiring and talent retention. Knowledge & Experience Ph.D / M.Pharm in Pharmaceutics, Pharmaceutical Technology , or a related field. Experience: Ph.D with 6-8 years or M.Pharm with 8-12 years of experience in the area of formulation developments of generic product (ANDA) and/or Differentiated products (505b2) for various markets including US and EU. End to end knowledge in formulation design, development and filing of oral dosage forms (major experience) along with development of other dosage forms. · Strong knowledge in Deformulation, Preformulation, Reformulation and Formulation Optimization. Sound knowledge of FDA/EU/ICH guidelines for designing product spec and quality, QbD , BE studies and regulatory expectations for ANDA and/or NDA submissions. Strong data interpretation skills and familiarity with eCTD Module 3 documentation and dossier preparation. Ability to guide a team , fostering a positive work environment, and ensuring on time delivery of products addressing formulation and process challenges. Preferred Qualifications Exposure to semi-solid and or complex dosage forms Formulation developments of NCEs. Understanding of bioequivalence study design and in-vitro/in-vivo correlation (IVIVC). Involvement/participation in regulatory audits . Knowledge of analytical techniques used in drug product development Application of digital tools in formulation developments Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans . Application Process To apply, submit your updated CV and a cover letter highlighting your relevant experience to: 📧 jobs@morepenpdr.com MPDRPL is an equal opportunity employer committed to a diverse and inclusive workplace.

💊 Job Title: Lead Formulation Scientist 📍 Company: Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) 📌 Location: Gagillapur, Hyderabad. 📧 Apply at: jobs@morepenpdr.com 📞 +91 6302 451 459 About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and development of various dosage forms with major emphasize in oral dosage forms for ANDA/NDA submission. Build and guide a team to ensure on-time product delivery working in internal and external facility Ensure execution of lab-scale and pilot-scale batches as per QbD and DoE principles. Provide guidance to address formulation and process challenges and conduct technology transfer and ensure manufacturing of exhibit batch and process validation. Coordinate with all cross-functional teams including Analytical R&D, Regulatory Affairs, QA, Manufacturing and external parties to ensure product delivery. Prepare/review technical documents such as batch records, protocols, reports, and Module 3 CMC documentation for regulatory filings. Ensure all time compliance for internal as well as external quality and safety audits. Present project update and data analytics for review with senior management and take Go/No-go decisions Internal infrastructure building as per the scope and budgeting for CAPEX. Hiring and talent retention. Knowledge & Experience Ph.D / M.Pharm in Pharmaceutics, Pharmaceutical Technology , or a related field. Experience: Ph.D with 3-8 years or M.Pharm with 5-12 years of experience in the area of formulation developments of generic product (ANDA) and/or Differentiated products (505b2) for various markets including US and EU. End to end knowledge in formulation design, development and filing of oral dosage forms (major experience) along with development of other dosage forms. Strong knowledge in Deformulation, Preformulation, Reformulation and Formulation Optimization. Sound knowledge of FDA/EU/ICH guidelines for designing product spec and quality, QbD , BE studies and regulatory expectations for ANDA and/or NDA submissions. Strong data interpretation skills and familiarity with eCTD Module 3 documentation and dossier preparation. Ability to guide a team , fostering a positive work environment, and ensuring on time delivery of products addressing formulation and process challenges. Preferred Qualifications Exposure to semi-solid and or complex dosage forms Formulation developments of NCEs. Understanding of bioequivalence study design and in-vitro/in-vivo correlation (IVIVC). Involvement/participation in regulatory audits . Knowledge of analytical techniques used in drug product development Application of digital tools in formulation developments Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans . Application Process To apply, submit your updated CV and a cover letter highlighting your relevant experience to: 📧 jobs@morepenpdr.com MPDRPL is an equal opportunity employer committed to a diverse and inclusive workplace.

As a Polymorph Screening Scientist at Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL), your primary responsibility will be to lead the screening and selection of solid forms for drug candidates. You will play a crucial role in improving the physicochemical properties of active pharmaceutical ingredients (APIs) by overseeing polymorph screening activities. It is essential to identify the most stable and bioavailable forms of drug substances for regulatory submissions. Collaborating with cross-functional teams, you will mentor junior scientists and drive advancements in solid-state drug discovery. Your key responsibilities will include overseeing the screening of potential polymorphs, solvates, and hydrates for APIs, interpreting and analyzing solid-state data, scaling up identified novel polymorphs, collaborating with various teams to align polymorph selection with drug formulation strategies, preparing regulatory-compliant data for filings, troubleshooting any issues related to polymorph stability, and ensuring accurate documentation and reporting of experimental protocols and findings. The deliverables expected from you include the identification and characterization of stable polymorphs and crystal forms for drug candidates, detailed screening reports, regulatory-compliant data for solid-state forms, and methodologies for high-throughput screening, scaleup, and solid-state characterization. To qualify for this role, you should hold a Ph.D. in Pharmaceutical Sciences, Solid state Chemistry, Chemistry, or a related field, with a focus on solid-state chemistry or materials science. Alternatively, a Master's degree with equivalent experience will be considered. You should have a minimum of 6+ years of industry experience in solid-state chemistry, polymorph screening, or pharmaceutical development and proven expertise in solid-state characterization techniques and polymorph screening methods. Proficiency in solid-state characterization methods, high-throughput screening techniques, and knowledge of computational techniques for polymorph prediction are essential technical skills required for this role. In addition to technical skills, you should possess excellent problem-solving, troubleshooting, and decision-making skills. Effective communication skills, both written and verbal, are crucial for presenting complex data to diverse audiences. Being detail-oriented with strong organizational and documentation skills will contribute to your success in this role at MPDRPL.,

💊 Job Title: Junior Medicinal Chemist 📍 Company: Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) 📌 Location: Gagillapur, Hyderabad. 📧 Apply at: jobs@morepenpdr.com 📞 +91 6302 451 459 About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and optimize Route of Synthesis (RoS) for novel medicinal drugs. Synthesize and purify medicinal compounds using advanced laboratory techniques. Conduct laboratory experiments to test the efficacy and safety of synthesized compounds. Analyse data from various analytical techniques to assess compound quality and properties. Improve the physicochemical properties of existing drugs to enhance performance and stability. Collaborate with other scientists and departments to advance drug development projects. Follow strict health and safety guidelines to ensure a safe working environment. Review and interpret the structure and purity of chemical compounds using modern analytical tools. Knowledge & Experience Bachelors in Medicinal Chemistry with Master’s in Medicinal Chemistry, Organic Chemistry, or a related field With M.Sc. (2 to 4 years of Experience) At least 2 years of hands-on experience in chemical synthesis within a pharmaceutical or biotech setting. Proficiency in modern synthetic techniques and analytical methods (e.g., NMR, HPLC, MS). strong problem-solving skills and the ability to design efficient synthetic routes. Excellent laboratory skills, including safe handling of chemicals and operation of laboratory equipment. Ability to work collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Detail-oriented with strong organizational skills. Commitment to continuous learning and staying current with scientific advancements. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans . Application Process To apply, submit your updated CV and a cover letter highlighting your relevant experience to: 📧 jobs@morepenpdr.com MPDRPL is an equal opportunity employer committed to a diverse and inclusive workplace.