606 Formulation Development Jobs - Page 23

WALK -IN INTERVIEWS FOR FORMULATION SCIENTISTS ON 31ST MAY 2025 AT OUR R&D , KANDIVALI (W), MUMBAI. Designation : Research Associate / Research Scientist Department : Formulation & Development Qualification : M.pharma. / Ph.D. Experience : Candidates having 3 to 8 years experience in Product development of Solid Orals, Onco OSD, Liquid Orals and Sterile formulations. Markets handled: Regulated / ROW / Domestic. CARRY YOUR UPDATED RESUME & PASSPORT SIZE PHOTO AT THE TIME OF INTERVIEW.

Roles and Responsibilities 1. Review of Technology data package and preparation of Gap analysis document. 2. Preparation of technology transfer protocol and report. 3. Co-ordination with FD for smooth Tech Transfer. 4. Monitoring of validation batches at production site. 5. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. 6. Review of MPCR and protocol. 7. Planning for Execution of Process design, Process qualification batch. 8. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. 9. Should be part of handling deviation, change control and failure investigations. 10. Process manufacturing parameters for Qualification batches Vs Commercial batches. 11. Preparation and reviewing of intended batch documents for regulatory submission. 12. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products.

Job Title: Research & Development (R&D) Specialist Location : Jammu (Manufacturing Unit) Experience : 4-5 years in Nutraceuticals & Herbal Products Salary : Negotiable Job Summary:- We are hiring an R&D Specialist for our Jammu plant to lead product formulation, innovation, and compliance for Nutraceutical & Herbal Products. The role involves developing new formulations, optimizing processes, ensuring quality standards, and collaborating with production teams for seamless execution. Key Responsibilities:- Formulation & Development Create and optimize nutraceutical and herbal formulations while ensuring GMP, FSSAI, and AYUSH compliance. BOM (Bill of Material) & Costing– Prepare BOM and costing for finished formulations. Process Optimization– Conduct stability studies, pilot batches, and troubleshoot manufacturing challenges. Regulatory & Quality Compliance– Maintain documentation and assist in regulatory approvals. Innovation & Research– Identify new ingredients and enhance product efficacy, stability, and cost-efficiency. Collaboration– Work closely with Production, QA/QC, and Regulatory teams for smooth scale-up. Qualifications & Experience:- B.Pharm/M.Pharm, M.Sc. in Food Tech/Biotech or related field. 4-5 years of R&D experience in Nutraceuticals & Herbal Products (Manufacturing Unit). Strong knowledge of GMP, FSSAI, AYUSH, and regulatory guidelines. Expertise in formulation, stability studies, and process validation. How to Apply? Send your resume to hr@adexapharma.in or contact 7827305246 .

Looking for F&D Executive who has experience into Nutra / Farm

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Job Title: Senior Manager Formulation Development (Generic Finished Formulations) Department: Research & Development (R&D) Formulation Development Reports To: Head – Formulation Development / Vice President – R&D Job Purpose: To lead and manage the development of generic pharmaceutical finished dosage forms (oral solids, liquids, injectables, topical, etc.) from concept through scale-up, technology transfer, and regulatory submission. Responsible for ensuring robust, cost-effective, and regulatory-compliant formulations aligned with company strategy and market requirements. Key Responsibilities: Formulation Development & Optimization Lead the design and development of generic formulations for multiple dosage forms. Ensure development of stable, bioequivalent, and patient-friendly products. Drive pre-formulation studies, excipient compatibility, and optimization of manufacturing processes. Regulatory & Compliance Oversee preparation of product development reports, QbD documents, and regulatory submission modules (CTD/ANDA dossiers). Ensure compliance with CDSCO, USFDA, EMA, Health Canada, ENVISA and other global regulatory requirements. Provide technical support during regulatory audits and queries. Technology Transfer & Scale-up Lead pilot scale and exhibit batch manufacturing. Oversee technology transfer to manufacturing sites and ensure successful scale-up. Collaborate with Production, QA, and QC for smooth handover of products. Team Leadership & Project Management Manage and mentor formulation scientists and technical staff. Allocate resources, monitor project timelines, and ensure delivery as per business goals. Foster cross-functional collaboration with Analytical R&D, RA, Supply Chain, and BD teams. Innovation & Cost Optimization Identify and evaluate novel excipients, technologies, and platforms for product differentiation. Drive cost-effective formulation strategies without compromising quality and compliance. Monitor market trends, competitor products, and technological advancements. Key Skills & Competencies: Strong technical expertise in formulation science (solid oral dosage forms essential; additional knowledge of liquids, injectables preferred). Deep understanding of QbD, ICH guidelines, and global regulatory expectations. Proven experience in bioequivalence-oriented development. Strong leadership, people management, and project management skills. Excellent problem-solving, analytical, and decision-making abilities. Effective communication skills (written & verbal) for cross-functional and regulatory interactions. Education & Experience: M.Pharm / Ph.D. in Pharmaceutics / Pharmaceutical Technology. Minimum 10–15 years of experience in formulation development of generic finished dosage forms. Hands-on experience in developing products for regulated markets (US, EU, Canada). Proven track record of successful ANDA/NDA/MA submissions and approvals. Work Location: Ahmedabad, Gujarat Company Profile: Alpine Pharma Research is a group company of Alpine Health in USA which is a licensed pharmaceutical distributor based in Secaucus, New Jersey, USA that serves independent pharmacies across the US. Alpine Health offers a full range of generics, OTC's, diabetic supplies, vials and pharmacy supplies. Alpine Pharma Research in India is focused on developing high quality products for regulated and no-regulated healthcare markets including USA, India and ROW region. Based in Ahmedabad the company has its own manufacturing facility of medical plastics and is also developing OTC formulations for worldwide market. The company aims to have a portfolio of products that cater to pharmaceutical and healthcare industry across the globe.

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Preferred Skills: Technology->Performance Testing->Performance Testing - ALL->Performance Prediction Model

Educational Requirements MCA,MSc,MTech,Bachelor Of Science,Bachelor of Engineering,BCA,Bachelor Of Technology (Integrated) Service Line Microsoft Practice Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Additional Responsibilities: Ability to work with clients to identify business challenges and contribute to client deliverables by refining, analyzing, and structuring relevant data Awareness of latest technologies and trends Logical thinking and problem solving skills along with an ability to collaborate Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Technical and Professional Requirements: Primary skills:Technology->Mobile Device Management->Intune Preferred Skills: Technology->Mobile Device Management->Intune->Intune

Role & responsibilities 1. Development of stable, bioequivalent pellets dosage form (IR/ SR/ DR/ ER/ MUMPS) 2. Efficient technology transfer of pellets projects from R&D to plant level. 3. Closely working with Plant tea for trouble shooting of ongoing commercial pellets projects. 4. Oversee all aspects of pellets dosage form including planning, execution, and innovation strategy. 5. Evaluation and implementation new technology for pellets product development. 6. Collaborate with internal team and external partners for project success. Preferred candidate profile 1. Strong expertise in pellets dosage product development and its technology transfer to plant. 2. Strong analytical and problem-solving skills with a proactive approach. 3. Ability to align R&D strategies with business goals, 4. Excellent communication and stakeholder management abilities.

Job description Manufacturing Chemist Company Name - Fixderma India Pvt. Ltd. Job location - Neemrana ( Rajasthan ) Male Only. Only Derma skin care / hair care industry candidate needs to apply. Company Website - www.fixderma.com www.fclskincare.com Job Summary A Production Chemist is responsible for the formulation, testing, and manufacture of chemical products that meet quality standards and regulatory requirements. Key Responsibilities Formulate and develop chemical products using scientific principles and technologies. Conduct laboratory experiments to optimize product formulations and processes. Perform physical and chemical analyses of raw materials and finished products to ensure compliance with specifications. Conduct stability testing to determine product shelf life. Develop and validate analytical methods to quantify product constituents. Provide technical support to production personnel, including troubleshooting of manufacturing processes. Conduct laboratory investigations to identify root causes of production issues and implement corrective action plans. Compile and maintain documentation of laboratory experiments and results, including batch records and standard operating procedures. Ensure compliance with regulatory requirements and safety protocols. Collaborate with cross-functional teams to support new product development projects. Interested candiates can apply at hr2@fixderma.com

As Service Associate -Payroll,you will be supporting the end-to-end payroll related activities while ensuring you are in adherence to the policies and processes. Your primary responsibilities include: Process any payroll data in accordance with legal, IBM and the customer requirements related to personal data protection Ensure the timeliness of payroll processing (sending inputs to payroll services providers, approving payrolls) Ensure the timeliness of payroll payments processing (requesting uploads and payments releases, uploading payroll payments into the bank system, monitoring the rejected payments) Carry out the validation of payroll inputs and the reconciliation of output files and properly handle any discovered errors/discrepancies Monitor execution of compliance activities if required Perform any activities related to electronic payslips handling Communicate any risks to payroll process or deadlines in accordance with escalation paths Interact with employees, client, payroll stakeholders or third party providers to process payroll data and ensure the correct and timely pay Report the status of payroll cycle in a timely and accurate manner Support year end processes or any other country specific processes not related to monthly payroll cycle Initiate and actively supporting any continuous improvement activities or other process and/or tools improvements using the existing change management channels Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise 2-3 years’ experience in payroll operations for any International IT / ITES Company Good communication skills in English both oral & written Strong knowledge of MS Excel and MS Word Ability to pre-empt potential issues and reprioritize work to meet ever changing needs of customers both internal and external; proactively follows up with key customers on resolution and action plans Ability to think through complex issues and situations and develop robust, well thought out solutions which meet the need of the business Effectively Works with Others - Works well with internal customers and external suppliers and can positively influence others in problem solving and work process improvements Excellent Customer Service skills – ability to communicate to all people at all levels within the organization. Must have the ability to resolve difficult customer service issues High degree of numeracy skills with meticulous attention to details Team work – the ability to work well within the team is key to this role Preferred technical and professional experience Ambitious individual who can work under their own direction towards agreed targets/goals. Ability to work under tight timelines and have been part of change management initiatives. Proven interpersonal skills while contributing to team effort by accomplishing related results as needed Enhance technical skills by attending educational workshops, reviewing publications etc.

Role & responsibilities Product Formulation : Develop and optimize formulations for solvents and petrochemical products, ensuring they meet customer specifications and industry standards. Research and Development : Conduct R&D to innovate new products and improve existing formulations, keeping up-to-date with market trends. Manufacturing Oversight : Collaborate with production teams to scale up formulations, ensuring efficient and cost-effective manufacturing processes. Quality Control : Establish and oversee testing protocols to ensure all products meet quality standards and regulatory requirements. Customer Interaction : Work closely with clients to understand their needs, provide technical support, and tailor. Preferred candidate profile Education: B.Tech/M.Tech in Chemical Engineering, Petrochemical Engineering, Polymer Science, or related fields. Experience: 5 to 10 years in R&D, product development, or formulation in petrochemicals, specialty chemicals, transformer oils, lubricants, or related industries . Experience in scaling formulations from lab to production is highly desirable. Technical Skills: Expertise in product formulation and optimization. Hands-on knowledge of chemical analysis and quality control methods. Familiarity with manufacturing processes, industrial equipment, and safety standards. Soft Skills: Strong analytical and problem-solving abilities. Effective communication skills for liaising with cross-functional teams and clients. Ability to innovate and adapt in a dynamic industrial environment. Additional Preferences: Prior experience in transformer oils or specialty lubricants . Knowledge of regulatory compliance and industry standards.

Role & responsibilities We are looking for a passionate and self-motivated fresher to join our Formulation & Development team. The candidate will assist in the development of new formulations and support various stages of the drug product development cycle under the supervision of senior Assist in pre-formulation studies and compatibility testing of APIs and excipients. Support formulation trials for dosage forms liquids Operate and maintain F&D lab equipment such as granulators, blenders Assist in scale-up , process optimization , and technology transfer activities. Prepare and maintain batch manufacturing records (BMRs) , lab notebooks , and experimental reports . Conduct stability studies as per ICH guidelines and assist in sample preparation and documentation. Follow GMP and GLP guidelines strictly while working in the lab. Coordinate with analytical development, regulatory, and production teams during the development lifecycle. Preferred candidate profile Good understanding of pharmaceutical formulation techniques . Knowledge of pre-formulation, excipient selection , and dosage form design . Awareness of regulatory guidelines (ICH, USFDA, WHO, etc.) Ability to learn and operate F&D lab instruments. Strong documentation and report writing skills . Interested candidate can share their CV at Anee.Silas@otsukapharma.in

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Sr Analyst Qualifications: Master of Pharmacy Years of Experience: 5 to 8 years Language - Ability: English(International) - Advanced About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The incumbent will perform the regulatory operations tasks of bookmarking and hyper linking for granular components (documents) of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components.Collect, collate and evaluate the scientific data gathered as part of R & D. Advise on legal and scientific restraints and requirements. Ensure the organization`s products comply with current regulations. Example; Build regulatory submission strategy, author CMC documents, and health authority packages etc. What are we looking for? Adaptable and flexibleProblem-solving skillsAgility for quick learningStrong analytical skillsAbility to meet deadlines Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualification Master of Pharmacy

We are Hiring for Formulations/NPD For Chennai location. Job Title: Formulations/NPD Job Location : Chennai Experience: 1-6 years Job Responsibilities & Duties: Developing new biobased surfactant formulation for textile auxiliaries, cleaning products for home care & institutional applications, Cosmetics & personal care products. Product optimization studies in the formulation lab & executing application trials for product development in the textile application lab across various stages of fabric processing. Planning for daily experiments. Developing customized SOPs and testing parameters for bio-based applications developed. Collaborating with marketing team to run troubleshooting experiments for market products and existing applications. Thorough knowledge and experience in handling of lab testing equipment and analytical instruments. Through knowledge of surfactant chemistry & formulations. Well aware with analytical skills including titration, preparation of standard solutions, standard calibration methods, etc. Experience in overall handling of a surfactant-based formulation lab Job requirements: A successful candidate will have: Qualification: M.Tech./M.Sc. in Chemical/Surfactant /Oleochemicals Experience: 1 - 5 years essentially having worked in R&D with a formulation or Surfactant chemicals company Thorough knowledge of Surfactant chemistry & Formulations Experience in handling various types of formulations & allied chemistries Thorough understanding and experience in handling various chemicals used in cleaning products Experience in Lab to Plant Scale successful implementation of various recipes Good Communication Skills Looking for candidates who can join immediately or within 30 days. Interested candidates please send me your resume over Parmar.Hardik@adecco.com.

Essential Duties and Responsibilities: Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family. Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis. Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation. Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety. Provide support to analytical team by providing the required product solution/placebo solution samples. Execute batches in laboratory, assess the study outcome to support the compendial product change requirement. Ensure response to customer queries, agencies query, market compliance. Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance. Responsible for ensuring the availability of required licenses and materials (raw material, packaging materials) in laboratory. Qualifications: Educational Qualification: Masters in Pharmaceutics or equivalent Hands on experience in laboratory batch execution and drive the towards the expected result. Good communication skills for effective liaison and teamwork Problem-solving skills, analytical skills and attention to detail Excellent organizational skills and the ability to work on several tasks or projects concurrently Presentation skills - for presenting ideas and findings to colleagues and customers Ability to work well independently, with minimum supervision Drive, enthusiasm and self-motivation

Desired Candidate Profile 2-6 years of experience in pharmaceutical industry or related field (Ayurveda/ Herbal / Nutraceuticals). BAMS degree from recognized institution (Any Specialization). Strong knowledge of Ayurveda principles and practices. Excellent communication skills with ability to build rapport with customers.

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Sr Analyst Qualifications: Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The incumbent will perform the regulatory operations tasks of bookmarking and hyper linking for granular components (documents) of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components.Coordinate the essential documentation and resources required for the filing of global applications. Understand, manage & process electronic submissions that include original application filings, Life Cycle Management submissions such as CMC, Ad-promos, amendments, annual reports, SPL submissions, etc. What are we looking for? Agility for quick learningAdaptable and flexibleAbility to work well in a teamAbility to perform under pressureAbility to meet deadlines Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualification Master of Pharmacy

Looking for a dedicated and compassionate individual to join our team as a Baby Care Taker in Lucknow. The ideal candidate will have excellent communication skills, a strong passion for childcare, and the ability to work effectively with young children. Roles and Responsibility Provide high-quality care and support to babies and infants. Develop and implement engaging activities to promote cognitive, social, and emotional development. Build strong relationships with parents and caregivers to ensure comprehensive care. Collaborate with other healthcare professionals to achieve optimal outcomes. Maintain accurate records of patient progress and communicate effectively with families. Participate in ongoing training and professional development to stay updated on best practices. Job Requirements Strong knowledge of child development principles and practices. Excellent communication and interpersonal skills. Ability to work effectively with diverse groups of people. Compassionate and empathetic approach to working with children and their families. Strong organizational and time management skills. Familiarity with digital marketing concepts and strategies is an added advantage.

Key / Primary Responsibilities : Receive approved PDRF from S&M Initiate literature review and data collection for ingredients and comparative market brands for new product development Studying RM, Pack size, Research Ingredients, Claims & USPs. Creating tentative formulation with RM Costing On costing approval initiate procurement of RM samples support Purchase with identifying vendors / suppliers for new RM. Calculating Timelines wrt lab trials – Pilot Batch Manufacturing to product launch in market Initiate lab trials – circulate product samples within internal team for evaluation – Minimum 75 - 80% positive feedback / evaluation criteria for finalizing the formulation – reformulation in specific cases Handing over 3 to 4 final samples to marketing for sample approval along with sample approval form. Initiate accelerated stability study parallel with lab trials – fine tunings if required wrt stability reports & protocols Accuracy in formulation documentation. Data support for Specification reports to ADL (as per to Standards) eg: BIS – Bureau of Indian Standards Support RA for FDA related product documentation Prepare BMRj – SAP updating of MFC (Master Formula Card) – Documentation transfer from F&D to QA (eg: HALAL) Ensure successful technology transfer from F&D to Production – minimum 3 batches – handle all tech transfer issues – revised documentation Handle all routine cosmetic production issues F&D Lab – Maintaining lab equipment, data, sample coding, RM Store at F&D lab, Raising PO – Support QA with data for creating new RM codes Miscellaneous – Prepare and submit MIS report, Maintaining 5-S system.

Microgen Pharma India we are into manufacturing of Disinfectant and hygiene range of products. We also manufacture Anaesthesia, Critical care, Derma and OTC cosmetic and lotion. Our company has WHO GMP certificate.

Lead new product development (NPD) projects from concept to commercialization for silicone/rubber-based biopharma consumables, tubing, and components. Conduct research on materials, formulations, and process improvements aligned with market trends Required Candidate profile M.Tech / B.Tech / M.Sc in Polymer Science, Rubber Technology, or related field. Hands-on knowledge of extrusion, molding, compounding, and testing equipment. Familiarity with QMS, GMP

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

F&D of Solid, Liquid and Topical dosage forms End-to-end formulation & development of Herbal Nutraceutical products Tech transfer and coordination - manufacturing, trial batches & troubleshooting Stay updated on FDA guidelines & industry practices

Role & responsibilities Analytical Research & Development (ARD) [FORMULATIONS] Experience in method validation, Method development and method transfer of new analytical methods by HPLC. Develop, optimize and validate new analytical methods for key starting materials, Intermediates and Active Pharmaceutical Ingredient products. Preparation of analytical method validation protocol, raw data and analytical method validation report as per ICH requirements. Manage and execute transfer of analytical methods from AR&D to internal QC. Analytical regular support for Process development team. Analytical regular support for Alternative vendor development projects. Perform hands on Residual solvents Unknown peak identification and quantification by GC troubleshooting. Maintenance of lab compliance such as calibration schedules etc. Performing a Qualitative and Quantitative tests which include analysis of raw materials, APIs and in process samples. Adequate Knowledge in Wet Lab Analysis. Formulations Research & Development [FRD] Entrusted with the task of conducting research and support activity In Formulation Department and handling various projects like Oral Solid Dosage forms (Tablets, Capsules), Liquid Dosage forms etc. Proactively involved in formulation of Robust, Stable. Cost effective, Time effective various enzyme preparations s/a Solid Oral Dosage Forms like Tablets (Dispersible, Film coated, and IR) & Capsules. Preparation of Product Development Report, Master Formula Card, various SOPs etc. Actively involved in planning, review of analysis related activities, Installation and calibration of various analytical instruments. Scale-up and technology transfer of Softgel capsules, Spray drying and Beadlets technology. Product improvement and cost reduction of existing products. Coordination with marketing and analytical team or successful completion of projects Trouble shooting and quality improvement of existing products Preparation and review of Master manufacturing document (MMD), NPD documents, batch manufacturing record (BMR), product development report (PDR) , HACCP plan and Technology Transfer documents. Process Research & Development (PRD) [API] Monitoring and planning of experiments with team. Recording the daily lab experiments as per cGMP and preparing weekly planning report. Preparation, identification, characterization and control of process related impurities and GTIs. Ability to complete the project with in stipulated time lines. Developing chemical processes for APIs and intermediates. Optimizing and validating the process at the lab,pilot and plant scale. Adequate response to the queries raised by competent regulatory bodies. Preparation of process development report(PDR) and technical packages. Co-ordinating with cross functional teams, collecting the data and supporting in the preparation of product development report. Identify & solve the plant related queries such as OOS OOT, CAPA. Obey & follow the safety norms. If interested, please share your resumes to jayakishore.gollapalli@srikrishnapharma.com