606 Formulation Development Jobs - Page 13

Scientist, Job Title: Formulation Scientist, Cosmetics & Personal Care Products Location: Chennai (Onsite) Experience- 7+ Years Employment Type: Full-Time About the Role: We are seeking a highly skilled and innovative formulation scientist with hands-on experience in developing a wide range of cosmetic and personal care products, including soaps, detergents, shampoos, perfumes, creams, lotions, and other hygiene products. This is an exciting opportunity to work in a dynamic environment, contributing to new product innovations and process improvements from concept to commercialisation. Key Responsibilities: Research & Development: Design and develop new formulations for personal care and cosmetic products such as bar soaps, liquid hand washes, laundry detergents, face creams, body lotions, shampoos, conditioners, deodorants, and perfumes. Modify and optimize existing formulations to enhance product quality, efficacy, safety, and cost-efficiency. Product Testing & Analysis: Conduct routine stability, compatibility, and performance tests on raw materials and finished products. Ensure all products meet internal quality standards and comply with local/international regulatory requirements (BIS, FDA, etc.). Innovation & Trends: Stay abreast of the latest market trends, ingredient innovations, natural/organic alternatives, and sustainable formulation techniques. Generate innovative product concepts and technical solutions in line with consumer needs and company goals. Cross-Functional Collaboration: Work closely with the marketing, packaging, quality control, production, and procurement teams for product development, scale-up, and commercialisation. Provide technical support during pilot batches and full-scale manufacturing. Documentation & Compliance: Maintain accurate and detailed records of formulations, lab notebooks, test results, and stability data. Ensure documentation aligns with regulatory guidelines and supports product registrations if required. Required Experience Bachelor's degree, preferably in Chemistry or Science science-related Major Excellent olfactory capabilities (candidates will be required to complete an internal smelling test.) At least 7+ years of industry experience. Excellent communication skills (written/verbal) with all levels within the organization Strong project management skills, disciplined, and process-oriented Creative mind; able to come up with new ideas and concepts that are practical to implement Solid understanding of functional and technical capabilities, including knowledge of the consumers and different markets Can motivate, develop, and manage/mentor others Focused on execution and strategic thinking Embraces diversity.

Perform pre - formulation studies, R&D trials and support scale-up activities. Conduct R&D trials for oral solid dosage forms (tablets, capsules, etc.) Develop and optimize formulation to meet regulatory and quality requirements. Document and analyze trial data to improve formulation. Collaborate with cross-functional teams for technology transfer to manufacturing.

Role & responsibilities Product Innovation Support all innovation and savings projects for all Soap & Bar category for national and international business Design experiments to present proof of principal studies using DOE methods, formula chemistry and processing principles of mixing in home care application Suggest modifications based on technical learning and understanding. Plan and Make batches using different technology approach. Execute shelf-life studies for projects and carry out the storage studies adhering to the standard protocols. Derive technical conclusion from experimental data Defining the RM and FG specification for the innovation, Plan and execute consumer studies, stability studies and product performance studies Use digital available tools to store, process and share experimental data regularly. Quality Assurance and Supply chain support . Forge a partnership with supply chain procurement , packaging , plant quality and manufacturing teams to ensure implementation of winning formulation Perform analysis of complaint samples , track plant data and give inputs where required Competition Mapping Monitor the quality of competition product and try to gain an understanding of the product strategy R and D support services Maintain the pilot plant in good working condition Regularly plan for maintenance of equipment with concerned teams Maintain minimum agreed RM stock for pilot batches Preferred candidate profile Minimum Qualification - MSc Chemistry / BE Chemical Engineering / B.Tech. Chemical Engineering Minimum 2-4 years experience in R&D / Plant Quality Area of Specialization Product Development /Innovation Required Male candidates only. Looking for the candidates from FMCG industry- having experience into Home care, personal care, Fabric care . Contact HR Monika Gaud Job Location- Kasna (Greater Noida) Office Hours- 09:30 am to 06:00 pm 2nd & 4th Sat off

Modification and improvement in machine parts. Introduce new technology. Machine setting as per product requirement. Study design of products for making improvements. To support production by making process improvement, lean manufacturing. Should be able to read the engineering drawings and have knowledge about fits procedures. Job Specifications: Diploma/ Degree in Mechanical 5-6 years of relevant experience in a reputed firm Experience in SAP Excellent Communication Work experience in Production/ Production Engineering/ Technology Transfer is preferable.

Primarily responsible for supervision of Formulation & Development area and to monitor / Supervision and control over the operator / assistant operator in their designated premises at the site. Literature search, patents search and review the same as per product requirement. Innovator/ market sample characterization. Day to day execution planning of F&D trials for Domestic / ROW & other regulatory markets. Responsible for characterization, lab scale development, scale up, technology transfer and exhibit batches. Planning of pre – formulation studies for the Product development. Execution of development trials, achieving desired critical quality attributes, and manufacturing the stability batches. Improvement in existing formulations and possibility of new dosage forms. To ensure the timely completion of the assigned products Formulation Development and Technology Transfer. Coordination with analytical department for routine analysis of formulations and development. Preparation of technical documents like product development reports, master formula record and technology transfer documents.

Junior Scientist ?? Analytical Development (IP) Location: Hyderabad Experience: 2-5 years About the Role: Join our analytical development team to ensure high-quality analysis and method development for For . Ltd.. Get In Touch Page load link |pharmaceutical products. Key Responsibilities: Perform analysis using UV/HPLC, GC, and dissolution techniques. Validate test procedures (dissolution, assay, related substances, etc.). Maintain error-free documentation and calibrated instruments. Apply Now Location:Hyderabad Experience:2-5 years Phone: +91 040 2379 2190 Email: info@aizant.com |Business Inquiries: bd@aizant.com Development Pre-Formulation Formulation Development Analytical Development Regulatory Support & Dossier Compilation Manufacturing Clinical Trial Material Commercial Supplies Technology Transfer Clinical Research Bioanalytical BABE Clinical Trial Services Our Portfolio Co-Development Out-licensing About Us Quick Links Careers We are hiring Social responsibility Sustainability Environment, Health & Safety Knowledge Hub Contact Us Copyright 2025 All Rights Reserved | Aizant Drug Research Solutions Pvt

Junior Scientist Formulation Development (FFS & IP) Location: Hyderabad Experience: 2-5 years About the Role: Be part of our formulation development team, focusing on pre-formulation and formulation activities for innovative pharmaceutical products. Key Responsibilities: Plan and execute formulation development tasks. Prepare development documents (MFC, BMR, protocols, etc.). Ensure compliance with GLP and GDP standards.

Job Description OBJECTIVE: To maintain optimum quality in Formulation research and generation of quality data in Formulation Development department to support the development of a safe and quality product. RESPONSIBILITY : Formulation development of oral solid, Liquid, Parenteral and semisolid products by QbD Approach for Regulatory & ROW markets. To handle a team of 10 to 15 team members. Technical assessments of projects (Screening of Project, pipeline) Scientific literature Search and patents evaluation for strategic development. Technical screening of API, RM, PM sourcing for F&D activity. Formulation Development Strategy preparation with design around opportunities & developing Bio-equivalent products. Provides support and guidance in scale up/Technology transfer activities for new Formulation development Projects Assisting and ensuring timely completion of development activities at in-house R&D lab, (Pre-formulation studies, formulation development, stability studies etc.,) Guiding the F&D teammates to timely complete the development activities. Review and summarizing technical data for milestone assessments. Performing trending and monitoring of critical quality attributes/critical process parameters to maintain product quality. Responsible for review of analytical data (e.g. dissolution, assay, related substances, Blend uniformity, content uniformity etc.) Supporting regulatory team in health regulatory submission and query response. Maintain Evolet Healthcare Policy on Quality, Safety and Efficacy Value.

About Honasa - Honasa Consumer Limited (HCL) is the fastest-growing Beauty & Personal Care house of brands, creating the FMCG conglomerate of the future. Built on the values of Honesty, Natural ingredients, and Safe care, HCL addresses the needs of consumers through innovative products, evolved propositions, direct-to-consumer marketing, and e-commerce fulfillment. With brands like Mamaearth, The Derma Co., Aqualogica, and BBlunt, HCL currently serves over 500 cities across India, building an ecosystem that benefits both consumers and the community at large. The company is backed by leading investors such as Sequoia Capital India, Sofina SA, Fireside Ventures, and Stellaris Venture Partners. Job Title- AM - R&D Location- Mumbai (Thane) Key Responsibilities: Involved in all aspects of product formulation from the initial brief to final sign-off, and overseeing the manufacture of pilot batches and full-scale production. Lead the development of robust, stable, and effective formulations for manufacturing at third-party manufacturers and in-house facilities. Formulate products and conduct research and analysis to support manufacturing operations, production, product, and process development. Develop new formulations as per business demands and innovation requirements. Have in-depth knowledge of skincare and hair care products. Manage and execute development work for new products and the improvement of existing products. Lead technology transfer and scale-up operations to manufacture products in-house or at outsourced manufacturers. Conduct compatibility and product testing, shelf-life determination, process maintenance, and development. Maintain awareness of SOPs, cosmetic ingredients, GMP, and scale-up lab batches. Recommend ingredients and processes to improve the overall cost of each product and identify substitutes for raw materials. Responsible for research and development of new product formulations, from designing and formulating small batch lab prototypes to documentation, evaluation, and stability testing of a wide range of hair care products. Hands-on experience with surfactant-based formulations, in-depth knowledge of surfactants, conditioning agents, humectants, and different raw materials involved in hair care formulations. Provide technical leadership based on scientific principles for new products. Ability to work with ambiguity. Knowledge of regulatory and safety requirements for cosmetics. We are seeking a candidate who can bring technical leadership and innovation to our team, driving the development of cutting-edge personal care products Qualifications and Experience: B.Tech/M.Tech in Cosmetology, B.Sc./M.Sc. in Organic Chemistry, B.Pharm, M.Pharm. Relevant experience in the personal care industry is essential, particularly in skin and hair care.

Role & responsibilities Responsible for Pre-formulation studies for lab formulation development trials of solid orals, Oral Liquid, injectable, products, and Nutraceuticals product. To design strategy for projects through literature surveys. Respective API characterization, excipients characterization, drug and excipient study and its ratio. Worked on different manufacturing strategies for the development of products. To evaluate product for stability in manufacturing, monitor and review the stabilized batches. To study on existing formulations. Responsible for co-ordination, execution and monitoring of scale up activity, Responsible for Trial batches, Scale up batches, Optimization batches, Exhibit batches. Co- ordination with all cross-functional teams. TT sites and LL Sites To design/assist/support/ review for documents such as SOP, LNB, QQ, Risk assessment, PDR, MFR, Scale up BMR, stability protocol, qualification, validation documents, change controls, deviations, investigations and CAPAs etc. Preferred candidate profile

Role & responsibilities Visit customers and meet R&D and manufacturing sites to promote and support use of Client products and to follow up on pipeline projects. Keep the CRM database updated regarding Project pipeline, samples request etc. Follow the project through its various stages from sending literature, relevant articles, conducting onsite seminars, conducting R&D trials to scale up trials. Understand the key features and benefits of all Client products including Modified Release Technologies and Immediate Release film coatings and excipients. Recommend their application based on customers drug release, formulation and processing requirements. Coordinate the provision of Client product samples to the customer in a timely fashion in close cooperation with the sample lab. Provide clear and detailed instructions to the sample laboratory. Optimize customers processes to maximize the performance, efficiency and cost effectiveness of Client products. Capture all relevant details via Coating Trial Reports. Present technical information (oral and written) for both internal and external training seminars, coating schools and other product promotion events. Provide feedback on un-met customer needs and new product ideas to marketing and NPD groups. Seeking continually expand understanding of current, emerging and competitive pharmaceutical technologies. Guide the customers to our website in order to help them access standard documents (like COA, specs etc) from our 24X6 CSS system. Co-ordinate with Regulatory team for specific responses that R&D / regulatory teams might want in order to address regulatory body queries. Involve different resources (FTM / FCM / MDM / RSM / GM) for customer interaction to strengthen our relationship by value addition. Preferred candidate profile Preferred candidates from Pharmaceutical Industry

Hello. We re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we re improving everyday health for billions of people. By growing and innovating our global portfolio of categoryleading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What s more, we re achieving it in a company that we re in control of. In an environment that we re co-creating. And a culture that s uniquely ours. Care to join us. It isn t a question. With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we re uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It s an opportunity to be part of something special. Job Purpose The primary purpose of the Lead Scientist - Innovation and Incubation role is to develop and optimize formulations for new and existing products, ensuring they meet regulatory and quality standards. This involves conducting research and experiments to evaluate the stability, efficacy, and safety of formulations. The role also requires collaboration with cross-functional teams, including marketing, regulatory, and manufacturing, to ensure successful product development and launch. This role involves working closely with cross-functional teams to drive innovation and deliver consumer-centric solutions. Key responsibilities Develop and optimize formulations for new and existing products, ensuring they meet regulatory and quality standards. Conduct research and experiments to evaluate the stability, efficacy, and safety of formulations. Collaborate with cross-functional teams, including marketing, regulatory, and manufacturing, to ensure successful product development and launch. Maintain accurate and detailed records of all formulation activities and experiments. Stay updated with the latest advancements in formulation science and incorporate new techniques and technologies into the development process. Troubleshoot and resolve any issues related to formulation and product performance. Provide technical support and guidance to junior scientists and other team members Qualifications and skills PhD / Masters degree in Pharmaceutical Sciences, or a related field from reputed institutions. Minimum 15 yrs of proven experience in formulation development, preferably in the pharmaceutical or consumer goods industry. Strong understanding of formulation principles, techniques, and regulatory requirements. Why Haleon? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability,Development, and Teamwork. As Haleon focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness Diversity, Equity and Inclusion At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. . We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Care to join us. Find out what life at Haleon is really like www.haleon.com/careers .

We have an urgent opening with our esteemed client. Our client is one of the only startup in India that started out by first building a Research Lab and a Manufacturing Facility. Our cluent is a well known brand in Beauty and Personal Care industry. Experience : Min 8 years+ experience of working on formulations in haircare, skincare & suncare categories. Location : Manesar (Shuttle available from Metro Stations of Gurgaon) Roles & Responsibilities : 1) Should have at least 8-12 years of experience of working on formulations in haircare, skincare & suncare categories. 2) Have previously worked on product development lifecycle from Idea generation to product launch & post launch monitoring. 3) Should have technical knowledge of different raw materials & their interactions in haircare/skincare/suncare formulations. 4) Ensure all the formulations meet global regulatory standards. 5) Ensuring if there are any changes in the regulatory landscape of raw materials, actives formulations to be adjusted so that compliance is in place. 6) Understand, follow & help in developing protocols/test methods used to measure functional and aesthetic performance of products - Analyze and evaluate competition. 7) For any products to be manufactured in 3 rd parties, ensuring stability is done in house & approved. 8) Alternate vendors/Cost optimization 9) Intellectual property/Trademarks As the requirement is a bit urgent, an early response on this would be highly appreciated. Alternatively, if you know someone suitable and available please refer. Regards, Shakil

Position Overview : We are seeking a skilled and strategic-minded General Manager to lead our External Manufacturing division. The successful candidate will play a pivotal role in coordinating and optimizing our external manufacturing operations, ensuring seamless collaboration with partners, and maintaining the highest standards of quality, compliance, and efficiency. Key Responsibilities: Coordinate and facilitate effective communication between third-party vendors and internal stakeholders to ensure the fulfillment of company requirements and timely query resolution. Review production plans and coordinate with demand planning, supply planning, and Contract Manufacturing Organizations (CMO). Circulate production plans to vendors and oversee their timely execution in alignment with export requirements. Monitor and proactively manage the quality of Ryvis Pharma products, implementing measures to prevent any quality issues that may arise. Explore alternate vendor development options for critical SKUs. Create purchase orders for materials and services needed for production. Lead efforts for packaging changes and product improvements in collaboration with relevant teams. Manage the end-to-end coordination of goods dispatch and QA release, addressing any associated queries and concerns. Take ownership of coordinating and resolving queries raised by the QA team. Facilitate CMO site audits and ensure compliance with standards. Manage market complaints by coordinating between CMO sites and our QA team, including investigating reports and implementing CAPA arrangements. Oversee the creation of product codes and vendor codes. Manage product shifts between CMO units, including evaluation, QA, and R&D approval, as well as site-to-site product transfers. Collaborate with internal stakeholders to prepare and release new artworks in response to changing regulations. Coordinate with vendors and arrange necessary documents for the company's tender business. Initiate change controls for CMO products and maintain vendor records. Coordinate supplier payments, resolving invoicing, taxation, and other discrepancies. Analyze cost sheets, validate prices, negotiate with third parties, and finalize rates. Ensure the timely delivery of committed products to support monthly sales closing. Generate monthly MIS reports for sales and purchase details of third-party products. Maintain and update the CMO Material Master Product List and Vendor Master List monthly. Identify opportunities for cost savings against the budget and implement necessary measures. Proactively manage product risks to ensure continuous alignment with business requirements and supply. Qualifications: Bachelor's degree in Pharmaceutical Sciences, or related field. An advanced degree (MBA, MSc, PhD) preferred. Proven experience (10+ years) in pharmaceutical manufacturing, with a focus on external manufacturing and/or loan license manufacturing. Strong understanding of cGMP regulations and global regulatory requirements for pharmaceutical manufacturing. Demonstrated experience in managing external partners and contract negotiations. Exceptional leadership skills with the ability to inspire and lead cross-functional teams. Excellent communication, interpersonal, and problem-solving skills. Strategic thinker with a track record of driving process improvements and operational excellence. Ability to thrive in a fast-paced, dynamic, and evolving pharmaceutical industry. Experience: Experience in managing supplies of more than 100 finished goods from multiple CMO sites. Experience in implementing multiple projects at CMO sites. Experience in managing production for export orders. Benefits: Competitive salary commensurate with experience. Opportunity to work in a senior management role within a rapidly growing pharmaceutical company. Collaborative and dynamic work environment. If you are a results-driven professional with a proven track record in pharma external manufacturing and are excited to take on a leadership role, we encourage you to apply. Please send your updated CV along with the requested details to hrdept@ryvispharma.com Age: Qualification: Current Company: Current Designation: Current CTC: Expected CTC: Years of Experience: Notice Period: Current location: Reason for Job Change:

Role & responsibilities Formulation and Development Oral Solid Dosage US market

JOB DESCRIPTION Job Title: Junior Analytical Development Scientist Oral Solids Job Location: Bangalore Department : Analytical Development Drug Product About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always. Core Purpose of the Role: Analytical development supporting Formulation development Routine analysis of samples Method development Instrument calibrations Documentation Report preparation Miscellaneous lab responsibilities Role Accountabilities: Candidate should have very good educational and theoretical background. Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC Knowledge of any other instruments than the above will be added advantage. Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: 1 to 3 years) Skills and Capabilities: Technical/functional Skills: Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line Behavioral Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Education: M.Pharm / M.Sc Equal Opportunity Employer . #LI-JK1

Job Tile: Pharmaceutical Proposal Specialist Job Location: Bengaluru About Syngene: Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Framing the drug product proposal for oral, injectable and topical formulations and project for early and late phase molecules. Role Accountabilities Be single point of contact for all formulation development and manufacturing RFI/RFPs from clients Tracking the RFI and RFP received from clients to completion Work closely with RFX team in commercial to ensure all RFI/RFPs are completed as per agreed upon timelines Circulate the RFI/RFP to respective team lead (AD/FD/Production) for their review Collecting the review comments from respective team lead and further sharing with BD to take inputs from client Coordinating with different stake holder like EHSS/QA/license team/ Regulatory team to address any quire on RFI/RFP Collaborating with cross-functional teams (scientists, clinicians, regulatory affairs) to craft a compelling proposal that aligns with the companys strategic goals and addresses the clients specific requirements. Ensuring proposals are accurate, well-organized, and professionally presented, including thorough quality checks before submission. Frame the drug product proposal based on the queries responses from client (this seems like a repeat) Maintain list of open proposals for OU head review Play active part in the cadence calls with commercial team. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Demonstrated Capability Education Experience 4-8 years in formulation development, proposal writing in to pharma industry. Skills and Capabilities The candidate should have excellent communication skill Good hand hold on MS excels and word Should have through understanding on drug product development and manufacturing flow, which can add lot of ease to understand RFI/RFP received from client. Education M. Pharm or M. S in pharmaceutics Equal Opportunity Employer .

Role & responsibilities To perform and be responsible for all the activities and documentation of formulation and filling process development and should have strong knowledge of optimization of different vaccine formulations, stabilizer selection, excipient selection, selection and preparation of adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, LNP formulation and preparation, aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting for existing vaccines. To perform all the activities and documentation of the formulation and filling process, development and execution of clinical drug product manufacturing for the clinical batches, planning and execution of media fill activities Prepare and Maintain R/D lab documents, equipment and area qualifications as per GMP requirements and Responsible for preparation of process validation and technology transfer protocols as per GMP requirements and co-ordinates with QA, QC, Engineering department for viral vaccine development activities. Responsible to ensuring proper hygiene and entry exit procedures in the respective formulation and filling section and preparation of adjuvant, buffer solutions and other materials & ensuring proper arrangements for their preparation and supply. To coordinate with the central warehouse department for receipt and entry of RM and PM materials. Preparation / supervision of disinfectant solution, cleaning solution, integrity testing of hydrophobic and hydrophilic filters, sanitization and disinfection activities of R/D formulation department. Responsible for QMS such as deviations, MDD, investigation, observation and ensuring its timely closure. Preparation of standard operating procedure and Batch manufacturing records, QRM and protocol related to R/D formulation and filling section. To supervise washing, drying, packing and sterilizations of materials required for R/D development and GMP clinical batch preparation. Preferred candidate profile PhD/MSc in science (Biotechnology, Biochemistry and Microbiology), masters degree in pharmacy or engineering with biotechnology. Candidate should have experience in vaccine industry Candidate should be able to work on bench and this position has one reporting.

Role & responsibilities: Preferred candidate profile :

Designing and developing new pharmaceutical formulations based on project objectives. Modifying existing formulations to improve performance or address specific needs.

Assist in formulation development of parenteral/ Injectable dosage forms. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Injectables- Share CV- stuti.naik@enaltec.com

Job Description 1. Collate and present literature review on preformulation, physico-chemical characterization, stability, bioavailability / pharmacokinetics of molecules to aid complex generic product development. Application of fundamental understanding of Pharmaceutical Sciences, Biopharmaceutics, Pharmacokinetics & Biostatistics in generic formulation design. 2. Lead the effort towards reconstruction/ reverse engineering of innovator formulation including preformulation studies, evaluation of API & in-house formulation using modern analytical, imaging and characterization techniques. 3. Responsible for brain storming with team and clarification of ideas aimed at development of discriminatory and bio-relevant dissolution methodologies, review and validation of data generated from this effort with the objective of providing the formulation team tools that aid in systematic deduction of formulation variables and improving the BE hit rates. 4. Supervise & perform preformulation studies for complex generic formulations and develop innovative methods to perform RLD characterization studies to aid development of formulation/manufacturing strategies for complex generic products. 5. Lead the team in developing prospective in vitro/in vivo model for new projects- Connecting RLD design and reported in vivo (PK) results to build targeted dissolution profile & dissolution methodologies before initiation of actual development. 6. Perform retrospective/ prospective biopharmaceutical modeling of in vitro/in vivo data of complex generics with an objective of establishing IVIVR/C. Dissection and meta-analysis of pilot/ pivotal BE data- Using systematic deduction & statistical approaches. 7. Document methods and results from dissolution studies, biopharmaceutical modeling, preformulation studies and RLD characterization experiments. And to prepare reports/presentations for project discussions with the formulation development group Work Experience PhD with 3-5 years experience/ Fresh PhD/ Post Doc in Pharmcokinetics (PK) and Biopharmaceutics to consider as M1 Education Masters Doctorate in Pharmaceutical Technology Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

Formulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Responsibilities Qualifications -M. Pharm

Role & responsibilities Collaborate on formulating and analyzing research strategies tailored to market and customer demands. Oversee commercial activities, securing approvals from manufacturers and our supply team. Assist in selecting manufacturers based on available equipment and machinery for specific products. Finalize quality and quantity formulas and product specifications, submitting them to manufacturers. Coordinate the preparation and arrangement of registration samples and artwork. Liaise with manufacturers to ensure commercial production aligns with our quality and quantity standards and product specifications. Collect and review documents from manufacturers. Coordinate with external laboratories for sample and product analysis according to our standards. Finalize active pharmaceutical ingredient (API) selection based on approved specifications submitted to relevant health authorities. Review and submit Product Information Files (PIFs) to manufacturers. Submit final quality and quantity standards and product specifications for new product launches. Coordinate with external F&D support teams. Review analytical data received and support regulatory affairs (RA) team with query responses. Arrange API and working substance samples, as well as analytical data like HPLC and certificates of analysis (COAs) for the F&D team. Review all documents from external sources and provide them to the RA team. Assist the supply team in sourcing API and primary material specifications. Review manufacturers' and Opes Healthcare's certificates of analysis for finished products. Provide troubleshooting support during new and existing product launches. Plan and execute plant visits during commercial production activities. Update management on critical changes, incidents, and market complaints. Review and approve all GMP documents including SOPs, change controls, deviations, batch manufacturing and packing records, process study protocols/reports, qualification documents, specifications, and standard testing procedures (STPs). Approve apex documents such as the Quality Manual, Validation Master Plan (VMP), and Site Master File (SMF). Design, review, and approve the Quality Management System (QMS) and associated documents. Drive initiatives for continuous improvement and operational excellence. Collaborate with other departments to ensure effective implementation of the designed quality management system. Manage activities related to registration batch manufacturing. Preferred candidate profile pharma THANKS YOU REGARDS MILAP RATHOD (7486829377) HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Position Overview We are seeking an innovative and experienced Assistant Manager for Product Development to lead the creation, development, and launch of cutting-edge skin and hair care products. This role will oversee the end-to-end product developmentprocess from concept ideation to formulation, testing, scale-up and market launchensuring alignment with brand vision, consumer needs, and industry trends. The ideal candidate has expertise in cosmetic science and a passion for creating high-quality personal care products. Key Responsibilities Product Innovation : Drive the development of new skin and hair care products by identifying market trends, consumer insights, and technological advancements. Collaborate with R&D and marketing teams to define product concepts and specifications. Project Management: Manage multiple product development projects simultaneously, ensuring timelines, budgets, and deliverables are met. Coordinate with cross-functional teams, including packaging, manufacturing, and regulatory affairs. Quality & Compliance: Ensure all products comply with global or local regulatory standards (e.g., FDA, BIS, EU Cosmetics Regulation) and internal quality benchmarks. Oversee stability testing, efficacy validation, and safety assessments. Vendor Collaboration: Partner with raw material suppliers, contract manufacturers, and external labs to source ingredients, troubleshoot formulation challenges, and support production scale-up. Market Launch Support: Work closely with marketing and sales teams to provide technical insights, product claims, and training materials for successful product launches. Scale-Up & Technology Transfer: Oversee the transition of formulations from lab-scale to full production, ensuring seamless technology transfer to manufacturing teams. Address technical challenges during scale-up to maintain product integrity and performance. Collaborate with plant teams to optimize processes and resolve scale-up challenges. Sustainability Focus: Incorporate sustainable practices and ingredients into product development, aligning with company goals and consumer demand for eco-friendly solutions. Key Requirements: Education: Min of Masters degree in Chemistry, Cosmetic technology or a related field. Experience: Minimum of 6 -10 years of Hands-on experience in product development within the skin and hair care or personal care industry. Technical Expertise: Strong knowledge of cosmetic formulation, raw materials (e.g., surfactants, emollients, actives), manufacturing processes, claim studies, label requirements. Regulatory Knowledge: Familiarity with global cosmetic regulations and safety standards (e.g., FDA, EU, COSMOS, etc.). Analytical Mindset: Data-driven decision-maker with experience in interpreting consumer feedback, clinical testing results, and market research. Communication: Excellent verbal and written communication skills, with the ability to present technical concepts to non-technical stakeholders and manufacturing teams Plant Support Experience: Proven track record of working with manufacturing plants, conducting site visits, and providing technical support during production ramp-up. Preferred Skills: Experience with clean beauty, natural, or organic product lines. Background in sensory evaluation or consumer and claim testing methodologies. Understanding of packaging compatibility and design for personal care products. Key Competencies: Innovation and creativity Attention to detail Problem-solving and critical thinking Time management and prioritization Team collaboration