180 Formulation Development Jobs - Page 2

Execute process development activities for pharmaceutical products at laboratory scale Design and implement experiments to optimize manufacturing processes for increased efficiency and product quality Conduct and analyze data from characterization and optimization studies Prepare the documents like PIS, sampling plan and risk matrix for pilot scale batches (Confirmatory batch and exhibit batch manufacturing) Troubleshoot process issues and implement corrective actions Collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs Author and review technical reports, batch records, and standard operating procedures Ensure compliance with cGMP regulations and company policies Participate in technology transfer activities to support scale-up and exhibit batches. Stay current with industry trends and emerging technologies in pharmaceutical process development Present findings and recommendations to group leader. Contribute to continuous improvement initiatives within the department Qualification M. Pharmacy Additional Information

Characterization of marketed product wrt market requirements Knowledge of ICH stability conditions and compilation of analytical data Preparation of documents like PDR, stability protocol, development report writing FDR/PDR Required Candidate profile Candidate should perform literature search Looking candidates for PDR (Formulation & Development ) Dept. Candidate should have experience in solid oral dosage (Regulated Market- USA/EU/ South Africa)

-New Product Development for various ice cream flavors & Frozen Desert -Design SOPS for all the products variants required for R&D -Improve existing formulations for taste, nutrition & shelf life -Collaborate with production and quality teams

We are hiring for Production Assistant Manager & Executive to work with our manufacturing operations, ensuring consistent production of high-quality branded generics across our diverse portfolio of oral liquids, solids, and topical dosage forms. This is a critical role for our organization, and the ideal candidate will be a strategic leader with a proven track record of driving productivity improvements, operational excellence, optimizing efficiency, and ensuring strict adherence to cGMP compliance. Responsibilities: • Oversee the day-to-day operations of all production departments, including: Oral Liquids Manufacturing Solid Dosage Manufacturing Collaboration with Quality Control, Quality Assurance, Engineering, Warehouse, Production Planning, Marketing, Finance and Research & Development • Manage relationships with key stakeholders, including R&D, Quality Assurance, and Supply Chain teams. • Identify and implement new technologies and processes to improve production efficiency and product quality. • Prepare and present production reports and metrics to leadership team.

Job Description Literature search and patent review of products Responsible for formulation development of DPI, SMI pMDIs formulations for US, EU, ROW, CSI and IRF markets. Responsible for planning and execution of development- Pilot / Scale-up and Exhibit activities for pulmonary formulations. Responsible for preparation of timelines, costings for ongoing projects. Responsible for preparation and compilation of project related documents in compliance with quality and regulatory requirements. Responsible for lab maintenance and upkeep of the laboratory and equipment s Responsible for analytical data and interpretation for way forward Responsible for procurement and control of innovators samples and maintaining their records. Responsible for Coordination with planning, engineering department and purchase department for product related activities Responsible for Preparation of department SOPs, guidelines, product related protocols and tech transfer documents along with DQA, CQA and regulatory team. To provide timely support for cross functional activities like regulatory queries, clinical development, technical support to manufacturing plants and intellectual property related inputs and feedback. To provide support for launching and troubleshooting of approved products. Work Experience 12 years + Education Masters in Pharmacy or Pharmacy Doctorate in Pharmacy or Pharmacy Competencies

Role & responsibilities Responsible for conducting literature search and preparing literature review presentation. To conduct Physico-chemical analysis of API and preformulation studies. To prepare prototype formulations based on preformulation studies. To optimize Product composition and Processes and prepare batches for Stability Studies. To indent the project requirements like API, excipients, toolings and Packing Materials. Process development, Optimization, validation and successful transfer to manufacturing location. Preparation of process development report. Responsible for the setting up the R&D scale equipment in the Research Laboratory Responsible for checking the calibration of Equipment /Instruments as per the schedule. Responsible for the preparation of SOPs (Standard Operating Procedures) Responsible for the preparation MFR, MPR, Stability & hold time study protocols, filling of lab note books, compilation of PDR. Maintain GMP and Safety procedures in the Laboratory. Sufficient Knowledge of Regulatory Guidelines (WHO, EU, US and emerging markets) Up-date the Project status on regular basis to the concerned Superior. Patent analysis and selection of non-infringing route. Preparation of Investigation Reports Coordination with all interfaces for successful Product Development Must possess good knowledge of GLP requirements Preferred candidate profile Qualification :- M. Pharm, Pharmaceutics Age :- Between 23 years to 35 years Experience :- Minimum 2-3 years in Formulation Development. Exposure / Knowledge of HPTLC preferably in the field of Ayurvedic / Herbal Analysis, Export related Documentation would be an added advantage. However, Freshers can also apply Exposure in Ayurvedic/ Herbal Industry will be an preferred advantage, though not mandatory.

Role & responsibilities 1. To prepare and review Packaging Material specifications, Standard test procedure, Master Packaging card, Pack Strategy, Intended Master Packaging card, packaging development reports etc. 2. To review Trade dress and Stability study protocol. 3. To Evaluate Innovator pack and compile the report. 4. To oversee and to evaluate the packing materials availability for stability studies for FRD in comparison with the innovator samples for Bio studies. 5. To check and approve artworks of printed packaging components for all regulated markets. 6. To initiate the change control activities for any changes in Packaging development activities. 7. To attend to the regulatory queries and to provide the required data & documents to regulatory affairs. 8. To support the technology transfer of products with packaging specific activities. 9. To provide tentative BOMs for the required product pack for tentative cost estimation of the planned product packs. 10. To provide packaging development technical support to Quality control, Purchase, Marketing, Regulatory Affairs and other allied departments. 11. To provide Documentation support for all the activities in compliance to cGMP. 12. Tracking the projects for ongoing and upcoming product of packaging development. 13. Development of Vendor & Blister change parts for product execution. Preferred candidate profile 1. The candidate should have a Degree/ a PG diploma in Packaging Development from a reputed institute with 4 to 6 years of relevant experience in R&D. 2. Should be well-versed in US Regulatory guidelines concerning Packaging 3. Should know Coraldraw, Adobe Illustrator.

1. Ophthalmic product development from pre-formulation, various drug delivery technologies, formulation, process & scale up manufacturing towards commercialization 3. Supervision and execution of manufacturing of Pre exhibit/ Exhibit batch Required Candidate profile Qualification- M. Pharm Must have experience into F& D Reg Market into Ophthalmic is must Target company -Send only FD- Opthal – Reg market candidates only

1. Ophthalmic product development from pre-formulation, various drug delivery technologies, formulation, process & scale up manufacturing towards commercialization 3. Supervision and execution of manufacturing of Pre exhibit/ Exhibit batch Required Candidate profile Qualification- M. Pharm Must have experience into F& D Reg Market into Ophthalmic is must Target company -Send only FD- Opthal – Reg market candidates only

R&D Executive (Food Technologist) with 3+ yrs experience in NPD, formulation, and tech transfer for nutraceuticals. Expertise in FSSAI compliance, ingredient selection, and product development. Location: Mohali. B. Tech in Food Tech required.

At Nouryon, our global team of changemakers takes positive action every day, to reach higher goals collectively and individually. We create innovative and sustainable solutions for our customers to answer societys needs – today and in the future. Purpose of the Job Design experiments and execute lab work for prioritized projects. Provide application support and training to sales team, customers and distributors. Support Sales Team with join visits to key markets / customers. Coordinate with global technical teams to facilitate sharing of information. Stay abreast of technical developments in the industry. About the job (Job Responsibilities) To provide technical support for Personal Care and Pharmaceutical Applications in India, SEA and ANZ, with a team of 2 direct reports. Develop an understanding of the benefits of Nouryon products versus competition in formulation and generate data to support value proposition. Design experiments, perform lab work and develop solutions to solve customer problems or to meet technical targets for prioritized projects. Lead and guide the Personal Care technical team in India and Singapore Keep abreast of customer needs, patent literature, market trends and drivers, to anticipate and test new applications and formulations for Nouryon’s product. Work with global teams to implement global/regional application programs, as well as developing relevant local programs. Provide technical training to customers / distributors and sales teams as required Present technical presentation in market seminars / in-house workshops to promote products and technologies. Build connections with stakeholders in the Personal Care Industry. We believe you bring (Education & Experience) Minimum 10 years of experience in application development in Personal Care, either at end user or ingredient supplier. Postgraduate or above majoring in Chemistry, Chemical Technology, Polymers or Cosmetic Sciences. Graduate with more relevant technical experience in the same or similar areas could be considered. Good problem-solving skills, ability to work independently. Good listening and communication skills. Good interpersonal skills and ability to work with people at different levels. Strong desire to acquire new technical knowledge, strong intention to learn new things and perform. Ability to work and communicate across cultures. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ We look forward to receiving your application! We kindly ask our internal candidates to apply with your Nouryon email via Success Factors. We’re looking for tomorrow’s Changemakers, today. If you’re looking for your next career move, apply today and join Nouryon’s worldwide team of Changemakers in providing essential solutions that our customers use to manufacture everyday products such as personal care, cleaning, paints and coatings, agriculture and food, pharmaceuticals, and building products. Our employees are driven by the wish to make an impact and actively drive positive change. If that describes you, we will gladly make way for your ambitions. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment. Visit our website and follow us on LinkedIn . #WeAreNouryon #Changemakers

As a Research and Development (RD) Asst. Manger in Hair Care, you will play a pivotal role in the creation and testing of new hair care. You'll work closely with scientists, chemists, and other team members to ensure the smooth operation of lab processes and the development of innovative hair care range. This role requires a keen eye for detail, a passion for cosmetics, and the ability to adhere to strict quality and safety standards. Responsibilities: Lab Operations: Execute laboratory experiments and procedures. This includes preparing hair care product, conducting/monitor stability tests, and performing quality control checks. Formulation Development: Create formulation basis product brief from the scratch to the finalization. Follow established protocols and document all experimental procedures and outcomes accurately. Ingredient Selection: Collaborate with RD team members to research and evaluate cosmetic ingredients for efficacy, safety, and regulatory compliance. Contribute insights on ingredient functionality and compatibility in formulations. Testing and Analysis: Conduct various tests and analyses to assess the performance, stability, and safety of cosmetic products. This may involve viscosity measurements, pH testing, microbial analysis, and sensory evaluations. Documentation and Reporting: Maintain detailed records of experimental procedures, formulation recipes, test results, and other relevant data. Prepare reports and presentations summarizing RD activities and findings for internal review and regulatory purposes. Equipment Maintenance: Operate and maintain laboratory equipment and instrumentation, ensuring proper calibration and functionality. Notify appropriate personnel of any equipment malfunctions or maintenance needs. Compliance and Safety: Stay updated on industry regulations, guidelines, and best practices related to cosmetic formulation and testing. Follow safety protocols and procedures to minimize risks in the laboratory environment. Qualifications: Bachelor's degree in Chemistry, Chemical Engineering, Cosmetology, or a related field. Previous 4-6 years of experience in a hair care division, preferably from Loreal or Unilever. Strong understanding of cosmetic science, formulation principles, and ingredient functionality. Familiarity with laboratory techniques and instrumentation used in cosmetic analysis and testing. Excellent organizational skills and attention to detail. Effective communication and collaboration skills, with the ability to work well in a team environment. Knowledge of regulatory requirements for cosmetics, such as FDA regulations and EU Cosmetics Regulation, is a plus. Attributes: Passion for cosmetics and beauty products. Analytical mindset with a problem-solving orientation. Adaptability and willingness to learn new techniques and technologies. Commitment to quality, safety, and compliance. Creative thinking and innovation in product development.

PRINCIPLE ACCOUNTABILITIES: Conduct formulations experiments, coordinate for analysis of samples and carry out the required stability studies. Troubleshoot technical problems related to the manufacturing processes and formulations independently, in order to meet the project goals. Guide fellow scientists and trainees on technical matters. Manage a Quick run innovation project independently. Communicate with the project manager(s) and other stakeholders. Presentations with due connect to the overall technical and business goals. Coordinate with analytical department for analysis of formulation samples. In-time documentation of experiments, trial reports, stability studies and other technical documents as per the standard system and operating procedures. Material destruction coordination within RCI for destruction of experimental materials quarterly with due documentation in place. Play active role in protection of IP for the organization by coordinating with IP department. Update project specific technical details in project management system periodically. Generate new technical ideas of business relevance. Execution and reporting of additional administrative KRAs as assigned. KNOWLEDGE BASE Describe knowledge in practical procedures, work skills, specialized knowledge, and scientific disciplines, required to perform all the requite tasks and assignments on the job. Master’s in pharmacy or equivalent, with minimum 2 years of experience in carrying out formulation development and administrative activities in lab. Sound technical knowledge related to the oral drug delivery domain. Knowledge of handling of APIs such as hormones and anticancer drugs would be preferred. Advanced analytical skills to help troubleshoot the technical problems encountered during project execution.

Good Analytical handGood management skill to handle the team members and good coordination skill with team members job Discription: Should have worked for Regulated market product development (ANDA)Providing technical expertise/scientific input on formulation development strategies for ANDA / 505(b)2 Preparation and practical execution of formulation development Batches using QbD concept Assisting to client during meetings with in a scientific manner Preparation of Technology Transfer documents, Development Reports Documents in eCTD format Monitoring and Execution of Scale up and Exhibit Batches (e.g.process development, implementation of new formulation techniques) and ensuring complex data are interpreted in a scientifically correct way, which can help for development of robust formulation Identifying potential stability and performance issues with prototype formulations and overcome the same Streamlining the activities associated with a wide variety of formulation technologies to shorten Formulation Lab turnaround times and improve the quality of formulations

Greetings of the day !!! Yutika Natural, as the name suggests, The Love For Henna started in 1930 with the agriculture of Henna in the Pali District of Rajasthan. Taking this love forward, the company commercially established itself in 1988 with a vision to streamline the orthodox Mehendi business & manufacture superior quality natural herbal henna-based products. Keeping the vision in mind it pioneered the Mehendi Cone concept, simplifying its application & trade. For more details, you can log in to www.yutikanatural.com We have an opening in R&D Department Position: R&D Scientist Job Location: Nashik Experience: 3-5 Years Job Description: Formulation and Development for Tablet/Capsule/Ointments etc. Good Knowledge in Tablet/Capsule/Ointments etc. Well Known R&D Protocols for Product Development. Stability Protocols, Documentation, BMR, MFR, BPR, Material and Machine Handling etc. Thanks & Regards, Priya Jain | Assistant Manager- Human Resource Yutika Natural Private Limited | Nashik, Maharashtra India. Official Mob No. +91 (9109904703), Email: priya@yutikanaturals.com

Job Summary: We are looking for a dynamic and skilled R&D Manager to oversee the development of innovative and high-quality cosmetic and personal care products. The ideal candidate should have hands-on experience in formulation development, strong knowledge of cosmetic regulations, and the ability to lead projects from concept through commercialization. Key Responsibilities: Product Development: Lead the formulation and development of skincare, haircare, and personal care products, ensuring alignment with brand goals and consumer expectations. Project Management: Manage multiple R&D projects, timelines, and deliverables across various product categories. Formulation & Testing: Supervise lab trials, stability studies, performance testing, and scale-up processes. Documentation & Compliance: Prepare and maintain formulation records, product dossiers, and ensure regulatory compliance (BIS, FDA, EU, etc.). Raw Material Evaluation: Source and evaluate new raw materials in collaboration with procurement and suppliers. Team Supervision: Manage and mentor junior chemists, technicians, and interns within the R&D lab. Cross-functional Coordination: Collaborate with marketing, QA/QC, production, and packaging teams to ensure product feasibility and quality. Innovation & Trends: Stay updated with market trends, consumer insights, and technological advancements to fuel innovation. Qualifications & Experience: Bachelors or Master’s degree in Cosmetic Technology, Chemistry, Pharmaceutical Sciences, or related field. 5–8 years of hands-on experience in the cosmetic or personal care industry. Solid understanding of formulation chemistry, manufacturing processes, and cosmetic regulations. Proficiency in managing lab operations, stability testing, and product documentation. Preferred Skills: Experience in natural/organic/clean beauty product development. Familiarity with global cosmetic ingredient standards and labeling regulations. Strong organizational, analytical, and communication skills.

Preferred candidate profile : Experience or Education in Pulp , Paper and Cellulose Technology Experience Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertical Job Responsibilities: 1) Lead overall raw materials, product lab tests process and the present the results in a right format and time. 2) Perform the validation tests for new test methods. 3) Regularly evaluate market samples and maintain proper records for the same. 4) Responsible for the preventive maintenance, calibration and proper functioning of the lab equipment. 5) Document knowledge, make the clear report and maintain the security of the result as required by RSPL policy. 6) Maintain expertise in at least one area of the company's technology as a Researcher for Feminine Care products. 7) Skillful handling of critical lab test equipment especially for those of Sanitary Napkin testing and evaluation. 8) Experience into pulp, paper & Non- woven. Number of positions : 5 This position belongs to HCD Vertical. Job Location- Kasna Industrial Area, Greater Noida Office Timings- 09:30 am to 06:00 pm 2nd & 4th Saturday are off. 1)We need Fresher Candidates M. Sc. (Cellulose & Paper Technology) 2)We need any Post Graduate candidates with experience of 2 to 3 Years into pulp, paper and non woven. (Can consider textile industry experience as well) Contact HR: Ms. Nancy Goyal Email- nancy.goyal@rsplgroup.com

Design and develop formulations for generic drug products (solid orals) Experience in technology transfer Prepare and review Master Formula Records (MFR), Batch Manufacturing Records (BMR), and technology transfer documents.

Role & responsibilities Lead Pre Formulation studies for solid orals, oral liquids, external preparations, injectable products, and nutraceuticals. Design project strategies through comprehensive literature surveys. Conduct API and excipient characterization, drug and excipient ratio studies, and explore various manufacturing strategies. Develop and finalize QQ formulas in alignment with the requirements of the Business Development (BD) team. Coordinate with BD team to ensure timely project execution. Finalize specifications for finished products. Evaluate product stability during manufacturing, monitor stabilized batches, and prepare related reports. Enhance existing formulations and explore new dosage forms possibilities. Procure innovator products, conduct comparative characterization studies, and test products. Prepare product development reports (PDRs), identify critical material attributes (CMAs), critical process parameters (CPPs), and critical quality attributes (CQAs) for robust product development using Quality by Design (QbD) principles. Execute development studies and prepare comprehensive study reports. Optimize formulations and processes using QbD methodologies. Respond to queries related to commercial and under development products promptly. Ensure effective technology transfer of F&D products. Review and authorize documents related to stability, inuse stability, forced degradation, and Bioequivalence (BABE) protocols. Authorize formulation related activities for BABE projects and lead BABE projects as required. Perform any other tasks assigned by the Head of Department (HOD) or management. Preferred candidate profile Pharma industries only Formulation THANKS YOU REGARDS MILAP RATHOD (74868 29377) whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Looking candidates for PDR (Formulation & Development ) Dept. 2-7 years of relevant experience in solid oral dosage (Regulated Market) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

To involve from start and investigate level 2 & 3 incidents, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To Involve in valid OOS and other cases as relevant, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To review level 1B incidents and give feedback for improvement. To periodically trend level 1A incidents and highlight/escalate key observations. To review any other referred reports associated with incidents/events in association with sites. To possess high level of integrity to have unbiased, independent and objective closure of incidents and maintain high level of confidentiality and have the tenacity to get to the root cause. To use Rubrics template for investigation report writing. To provide appropriate support to site in preparing for or during regulatory inspection for investigations. Qualification B Pharmacy Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Role & responsibilities Experience: 3-6 years Specialization: soft gel Key Responsibilities: Formulation Development : Design and optimize Softgel formulations for pharmaceutical and nutraceutical applications. Process Optimization: Conduct proof-of-concept studies, scale-up trials, and technology transfers. Regulatory Compliance: Ensure formulations meet ICH, FDA, and GMP guidelines. Analytical Coordination: Work with analytical teams to develop and validate testing methods. Troubleshooting: Address formulation challenges related to solubility, stability, and encapsulation. Documentation: Maintain accurate records, prepare technical reports, and contribute to regulatory submissions. Collaboration: Work with manufacturing, quality assurance, and regulatory teams to ensure seamless product development. Qualifications: Education: Masters degree (M. Pharm / industrial Pharmaceutics) or equivalent in Pharmaceutical Sciences Experience: 3 to 6 years in Softgel formulation R&D. Technical Expertise: Strong knowledge of gelatine-based and alternative encapsulation technologies. Regulatory Knowledge: Familiarity with ICH guidelines, GMP, and regulatory requirements. Analytical Skills: Ability to interpret analytical data and troubleshoot formulation issues. Communication: Strong technical writing and presentation skills. Preferred candidate profile Experience in Soft Gel

Responsibilities: Responsible for formulation and process development of Injectable dosage forms. Troubleshoot and problem-solve unresolved or new formula issues. Design and execute formulation trials to finalize formulation composition. Provident fund

1. Product development: Utilize extensive experience in the pharmaceutical industry to lead comprehensive reviews of literature, evaluation of finished products, and acquisition of scientific insights. Conduct pre-formulation trials, laboratory experiments, and meticulously document findings in detailed reports. Oversee lab and scale-up trials with precision, ensuring seamless execution while meticulously preparing all necessary documentation and reports. Take charge of preparing protocols, batch records, and other essential documents to maintain stringent quality standards. Lead process evaluation, exhibit batch execution, and prepare comprehensive reports with meticulous attention to detail. Monitor stability studies as a crucial component of development work, ensuring compliance with regulatory standards. Prepare vital reports including Product Development Reports (PDR), stability reports, and interim development reports with a focus on accuracy and compliance. Undertake additional activities as assigned by superiors to drive project success. 2. System development: Create laboratory systems and documentation such as SOPs, IQ/OQ/PQ, Documents, training record and other related documents. Planning of product development activities. Review of required specification of in-process & finished product specifications. Ensure timely procurement of APIs & other materials required for lab trials/exhibit batches. 3. Improvements: Participate actively in continuous learning initiatives in alignment with organizational practices and under the guidance of supervisors, while actively contributing to the continuous improvement efforts of the organization Cost reduction of existing products or development of cost effective formulations. 4. People Related: Foster effective coordination with other departments to facilitate smooth completion of tasks, promoting a collaborative work environment. Note: Candidates with prior experience in oncology are preferred. Interested candidates can share their profile on praveen.kunchapudi@granulesindia.com

Medicamen Biotech - SRL Pharma R&D Centre Required Formulations Profile Designation: Executive/ Scientist Qualifications: M. Pharma - Pharmaceutics Vacant Post: 6 Nos. Experience: 4 to 8 Years Please share profile on uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in Formulation USFDA exposer prefer Preparation of Pharmaceutical Development Report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience