35 Formulations Jobs

Responsible for formulation development for OSD, external preparations, oral liquids, and injectables. Responsible for pre-formulation studies, prototype development, and scale-up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (A, C, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation.

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

This is a part-time on-site role for a Doctor Ayurvedic in Gurugram. You will be responsible for providing expertise in Ayurvedic practices and principles, finalizing the formulations on hair care products, and collaborating to promote company products on various social media platforms. Your role will involve having knowledge of various herbs and their usage in today's environment, arranging online consultations and follow-ups with customers on their issues, and providing a positive influence and comfort to the customers. You should also have knowledge about Panchakarma and various doshas, and assist in creating screening and diagnostic tests to reveal health and hair issues.,

As an R&D Specialist for Wipes and Diapers, your key responsibilities will include leading the development of new diaper and wipe products from concept to market launch. You will ensure that the products meet functional, quality, and regulatory standards. Collaboration with cross-functional teams such as Marketing, Production, Quality Control, and Supply Chain will be essential to align product concepts with consumer needs. Innovation will be a crucial aspect of your role, focusing on key product attributes like absorbency, softness, hypoallergenic properties, and biodegradability. Staying updated on market trends and consumer preferences, especially related to sustainability, skin health, and performance, will be necessary to drive product development. Your duties will involve analyzing consumer feedback and competitor products to identify improvement areas and new opportunities. Conducting in-depth research on emerging raw materials, manufacturing technologies, and packaging solutions will be required to enhance product performance and sustainability. You will be responsible for developing and testing new formulations and materials for both diapers and wipes, emphasizing natural, eco-friendly, and non-toxic ingredients. Evaluating the performance of substrates, absorbent cores, adhesives, and coatings used in diapers and wipes will be part of your role. Ensuring compliance with local, regional, and international regulations, such as FDA, CE, or relevant environmental regulations, will be crucial. Developing and executing testing protocols to ensure product safety standards and quality control procedures will also be a part of your responsibilities. Maintaining transparency and compliance with ingredient and material sourcing by working closely with suppliers will be essential. To qualify for this role, you should have a Bachelor's or Master's degree in Chemistry, Material Science, Biomedical Engineering, or a related field. Specialization in Personal Care, Cosmetics, or Consumer Goods is a plus. A minimum of 3-5 years of experience in product development or R&D in the wipes, diapers, or related industries is required. Demonstrated experience in working with raw materials such as nonwoven fabrics, absorbent cores (SAP), barrier films, and bio-based materials will be beneficial.,

As a Telecalling Executive at Swadeshi Ayurveda Products, located in Noida, Uttar Pradesh, you will play a crucial role in promoting and selling our Ayurveda products to both existing and prospective customers. Your primary responsibilities will involve leading telecalling initiatives, providing product recommendations tailored to customers" needs, and ensuring customer satisfaction through timely order processing. Additionally, you will be tasked with training and mentoring junior telecalling executives, maintaining comprehensive call logs and sales records in the CRM system, and following up on leads to achieve monthly sales targets. Your expertise in Ayurvedic ingredients, formulations, and product applications will be essential in handling customer queries effectively and suggesting product bundling strategies based on customer preferences. To excel in this role, you must have a minimum of 2 years of experience in telecalling or telesales of Ayurvedic or wellness products. Proficiency in Hindi is required, and knowledge of English is advantageous. Strong communication skills, a customer-oriented sales approach, and familiarity with CRM tools, Excel, and order entry systems are also essential for success in this position. We are looking for candidates with an energetic and self-driven personality, a passion for Ayurveda and natural wellness, and the ability to thrive in a fast-paced sales environment. If you possess these qualities and are capable of meeting sales deadlines and targets, we encourage you to apply for this full-time position. To apply for this role, please share your updated CV with Mr. Pushpendra V, HR Manager, via email at hr.sudarshannews@gmail.com or contact him at +91 78288 31975. Join us at Swadeshi Ayurveda Products and be a part of our dynamic team dedicated to promoting holistic wellness through Ayurveda. (Job Type: Full-time | Schedule: Day shift | Work Location: In person),

A Chemical Engineer in the polyurethane and foam industry plays a crucial role in designing, developing, and optimizing chemical processes for manufacturing polyurethane-based products. You will be responsible for developing and optimizing polyurethane foam formulations for various applications. Additionally, you will conduct chemical process analysis to improve efficiency and product quality. Ensuring compliance with industry regulations such as REACH and fire retardant standards will also be a key aspect of your role. Collaboration with R&D teams to innovate new polyurethane materials and overseeing production trials to troubleshoot manufacturing issues will be part of your responsibilities. Working closely with suppliers to source raw materials like MDI, polyols, surfactants, and fire retardants is essential. Moreover, maintaining quality control and environmental certifications and providing technical support to production teams will be integral to your daily tasks. To qualify for this position, you should hold a Bachelors or Masters degree in Chemical Engineering, Materials Science, or a related field. Demonstrating expertise in polyurethane chemistry, including formulations and processing, is required. Prior experience in industrial production environments, strong problem-solving skills, and the ability to work in cross-functional teams are essential. Knowledge of chemical safety protocols and environmental impact assessments will be advantageous. This is a full-time, permanent position offering benefits such as leave encashment and Provident Fund. The work schedule is during the day shift, and the work location is in person.,

You will be responsible for machine setting, operation, and cleaning of machines according to the operating instructions and standard operating procedures. Your role will involve meeting the pilot production schedule and ensuring adherence to the delivery timeline. You will execute pilot-bio/clinical trial/trial batches as per manufacturing instructions and record process parameters during batch manufacturing, online documentation, log books, and status labeling. Adherence to quality and safety procedures & policies at manufacturing sites will be a key aspect of your responsibilities. As part of your duties, you will be responsible for the calibration of instruments as per the schedule and applicable procedures, carrying out in-process checks as per the instructions in the batch production record, and maintaining the pilot production area. Strict adherence to cGMP requirements, compliance with regulatory requirements, and following practices as per relevant SOPs are essential. Your role will also involve supporting the qualification of equipment and instruments and releasing them for regular usage. You will be responsible for the line clearance procedure of equipment and the area, following personal hygiene, safety requirements, and discipline on the shop floor, as well as adhering to applicable SHE procedures at the workplace. The position requires readiness to work in oncology & non-oncology formulation oral solid dosage forms. Qualifications: - ITI/diploma/BE in any discipline with 3-6 years of experience in Oral Solid dosage forms in the pharmaceutical industry. About the Department: Integrated Product Development Organisation: The Integrated Product Development Organisation at Dr. Reddys integrates deep science capabilities and cutting-edge technology to develop innovative, accessible, and affordable therapies for patients worldwide. The department is science-driven, innovation-focused, and committed to accelerating access to healthcare solutions globally. With end-to-end capabilities in API, Formulations, Clinical, Intellectual Property, and Regulatory Affairs, the department serves 55+ markets with innovative and generic products. Benefits Offered: Dr. Reddys actively supports career growth and professional development through personalized learning programs. The benefits at Dr. Reddys are on par with the best industry standards and include joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, and life coverage for yourself. Our Work Culture: At Dr. Reddys, employees come to work every day with the shared purpose of accelerating access to affordable and innovative medicines because Good Health Cant Wait. The company fosters a culture of empathy and dynamism, supporting individual ability while promoting teamwork and shared success. Dr. Reddys believes that diverse skills, bound by a common purpose and value system, can create magic in the healthcare industry. For more details, please visit our career website at https://careers.drreddys.com/#!/,

You will be responsible for the development of new products and optimization of existing formulas across different product lines such as solid dosage products (tablets, capsules) and other delivery forms (liquids, powders) for regulated markets including the US, Europe, and ROW. Your tasks will involve formulation and process development of oral dosage forms, troubleshooting unresolved formula issues, designing formulation trials, and evaluating stability data to finalize composition. Additionally, you will develop manufacturing processes for R&D formulations to ensure successful technical transfer for large-scale batches. In this role, you will write and review various documents such as master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, and QOS. Collaboration with other departments like Analytical Method Development, Regulatory Affairs, Quality Control, Quality Assurance, and Inventory Control will be essential to expedite the development and approval of new products by the FDA. Practical experience in development, technology transfer, and ANDA submissions for solid/liquid oral dosage forms (solutions, suspensions, tablets, capsules) for regulated and semi-regulated markets like the US, Europe, and ROW is a key requirement. The ideal candidate for this position should hold a minimum Master's Degree in Pharmaceutical Sciences and possess at least 1 year of relevant experience.,

You are looking for a Pharmaceutical Purchase Executive with over 3 years of experience in procurement, vendor coordination, and inventory management. Your responsibilities will include managing the end-to-end procurement process for pharmaceutical products, negotiating with suppliers, issuing purchase orders, maintaining purchase records, monitoring stock levels, ensuring compliance with regulations, and developing relationships with vendors. Additionally, you will work closely with the QA/Regulatory team, provide regular reports on purchase costs, lead times, and vendor performance. You should have a minimum of 3 years of experience in a similar role within the pharmaceutical industry, a strong understanding of pharmaceutical products and compliance requirements, proficiency in purchase/inventory management software, excellent negotiation and communication skills, and the ability to manage multiple vendors efficiently. Attention to detail and accuracy in documentation are key requirements. It is essential that you are currently based in Mumbai and available for in-office work. Preferred qualifications include a D. Pharm / B. Pharm degree or a background in pharmaceuticals, familiarity with GST billing, regulatory documentation, and import procurement, as well as experience in handling bulk procurement or contract manufacturing orders. You will receive a competitive salary with performance-based incentives, work in a professional and growth-oriented environment, and have the opportunity to collaborate with renowned pharma companies and vendors. This is a full-time, permanent position with benefits such as paid sick time, paid time off, provident fund, and bonuses based on performance. The work location is in person, with a day shift and fixed schedule.,

As a Formulations Scientist located in Hyderabad, India, you will be responsible for developing oral solid dosage forms of both Non-DEA and DEA substances. Your key functions will include conducting Literature Search, Pre-Formulation, and Formulation Design to ensure the development of stable, Bioequivalent, and Manufacturable generic solid oral formulations. Your responsibilities will involve being a mentor and motivator to your team. You will be tasked with developing robust formulations and processes for immediate release and modified release tablet and capsule dosage forms. Additionally, you will evaluate patents, develop non-infringement strategies, and have the capability of developing Paragraph IV products. You will be required to oversee the scale-up and optimization of the manufacturing process, execute pre-exhibit and exhibit batches, and handle the technology transfer from R&D to production to meet project timelines. Your role will also involve planning and contributing to project-related scientific/technical activities, authoring technical documents for regulatory filings, and interacting with API manufacturers, CROs, and CMOs as necessary. Furthermore, you will work collaboratively with cross-functional groups to execute change controls associated with Manufacturing and Packaging master records, SOPs, and protocols. You will be responsible for creating and reviewing SOPs, ensuring documentation and test results accuracy and compliance with SOPs/GMP requirements, and coordinating with Regulatory Affairs for ANDA filings and Supplements filing. To qualify for this position, you should hold a Masters degree with a minimum of 15 years of experience or a Ph.D. in Pharmacy with at least 5 years of relevant experience in oral solids product development within the generic pharmaceutical industry. Experience in Generic R&D and a successful track record of AND submissions are essential. Knowledge of modified release dosage forms is advantageous. Candidates should possess self-motivation, excellent written and verbal communication skills, as well as good interpersonal and project management skills.,

You will be a key member of our team as a MSc synthesis organic and polymer chemist with a passion for Research & Development. In this role, you will contribute to the innovative work carried out at our chemical manufacturing company. Your primary responsibilities will include studying chemical compounds, formulations, as well as developing new and improving existing products and processes. This is a full-time position with a day shift schedule, and the work location will be on-site.,

You will be joining our team in the aerosol industry as a Sales Executive, where your primary responsibility will be to identify new business opportunities, cultivate client relationships, and drive sales growth. To excel in this role, you must possess a deep understanding of aerosol products, exceptional communication skills, and a strong passion for sales. Your key responsibilities will include: - Sales & Business Development: Targeting potential customers across various industries and devising effective sales strategies. - Client Relationship Management: Building and nurturing strong relationships with both new and existing clients, understanding their needs, and providing tailored solutions. - Product Knowledge & Promotion: Showcasing aerosol products to clients, keeping abreast of industry innovations, and collaborating with the marketing team on promotional activities. - Sales Operations & Reporting: Generating and presenting sales reports, managing pricing and negotiations, and ensuring seamless coordination with production and logistics teams. To be considered for this role, you should have: - Education: Bachelor's degree in Business Administration, Marketing, Chemistry, or related field. - Experience: 2-5 years of sales experience, preferably in the aerosol, FMCG, or chemical industry. - Skills: Proficiency in negotiation and communication, ability to develop and implement sales strategies, and knowledge of aerosol products, formulations, and applications. Self-motivation, target-driven mindset, and proficiency in Microsoft Office and CRM software are also essential. This is a full-time position located in Hosur, Narsapura, Chennai, and offers a competitive salary based on experience along with commission/incentives. If you are enthusiastic about sales and have a background in the aerosol industry, we welcome you to apply and become part of our dynamic team.,

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation Interview Date:-30-08-2025 - Saturday Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur, MSN Unit -V R K Puram. Venue Location :- MSN Laboratories Pvt Ltd| Formulation Unit -2 | Kothur | Sy. No 1277&1319 -1324| Nandigama|Rangareddy| Telangana - 509216 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

The R&D Chemist for Cosmetic & Ayurvedic Products will be responsible for formulating safe and innovative skincare, haircare, and personal care products using natural and Ayurvedic ingredients. You will play a key role in developing formulations, conducting stability testing, and ensuring compliance with regulatory standards and brand objectives. Your expertise will contribute to product scale-up and the creation of high-quality products that align with industry trends and customer preferences. Key Responsibilities: - Develop formulations for a range of products using natural and Ayurvedic ingredients such as creams, lotions, serums, oils, and cleansers. - Research and evaluate herbal actives to ensure product safety and effectiveness. - Prepare lab-scale and pilot batches, conduct product trials, and optimize formulations. - Perform stability testing in accordance with Ayurvedic and cosmetic standards. - Maintain accurate records of formulation processes, results, and observations. - Ensure compliance with AYUSH guidelines, BIS standards, and relevant cosmetic regulations. - Collaborate with cross-functional teams including packaging, QA/QC, marketing, and production. - Support product claims substantiation, label ingredient verification, and regulatory documentation. - Assist in sourcing and evaluating new raw materials and herbal extracts. - Stay informed about industry trends, natural ingredients, clean beauty innovations, and global regulations. Requirements: Education: B.Pharm / M.Pharm (Ayurveda/Pharmaceutics) / M tech/ B tech, B.Sc / M.Sc (Cosmetic Science, Chemistry, or relevant field) Experience: 0-3 years in R&D (Ayurvedic, Herbal, or Cosmetic industry); freshers with hands-on project/internship experience may be considered. Knowledge: - Ayurvedic pharmacopoeia, herbal actives, natural preservation systems - Cosmetic safety, stability protocols, and regulatory compliance (AYUSH, BIS, FDA, etc.) Skills: - Strong understanding of formulations and ingredient functionality - Creative problem-solving and documentation - Attention to detail and quality consciousness To apply, please share your CV at deepak.kaushik@ridhisidhi.org or contact us at 9056766684. This is a full-time, permanent position suitable for fresher candidates as well. Work Location: In person,

Traya Health is an innovative health and wellness company specializing in holistic hair care solutions that combine cosmetic, ayurvedic, and pharmaceutical approaches. The mission of Traya Health is to provide effective, science-backed treatments that address the root causes of hair concerns through personalized care regimens. As the Research & Development Team Lead at Traya Health, you will play a crucial role in driving the company's product innovation strategy across cosmetic, ayurvedic, and pharmaceutical categories. This position requires a unique blend of scientific expertise, creative problem-solving, and cross-functional leadership to develop groundbreaking hair care formulations that align with the holistic treatment philosophy of Traya Health. Your key responsibilities will include leading the end-to-end development of new products, from conceptualization to market launch, ensuring alignment with consumer needs and company strategy. You will be tasked with developing and optimizing formulations for hair care products by integrating Ayurveda, Allopathy, and modern science. Ensuring regulatory compliance, overseeing clinical trials and efficacy studies, and collaborating closely with marketing, manufacturing, and quality assurance teams will also be part of your role. As the ideal candidate for this position, you should have a background in FMCG/Pharma with an understanding of Ayurveda. A PhD or Master's degree in Cosmetic Science, Pharmaceutical Sciences, Chemistry, Biology, or related field, along with a minimum of 10+ years of experience in R&D within personal care, pharmaceutical, or related industries is required. You should have a proven track record of successful product development and commercialization, experience managing cross-functional R&D teams and projects, and a strong understanding of hair biology, scalp conditions, and treatment modalities. Furthermore, your leadership skills should include exceptional critical thinking and problem-solving abilities, strong project management capabilities, outstanding communication skills, and a collaborative mindset to work effectively in a matrix organization. Experience in personalized or customized product development, clinical testing, digital tools for formulation management, natural and sustainable ingredient sourcing, and knowledge of Indian regulatory environment for personal care and pharmaceuticals would be considered desirable qualifications for this role. If you are a dynamic and experienced professional with a passion for innovation and scientific excellence in the field of hair care product development, we invite you to join Traya Health as the Head of Research & Development and contribute to our mission of providing holistic solutions for hair concerns.,

As an Application Development Technical Specialist at Avient Corporation, you will play a crucial role in leading new applications, generating specifications, and replicating successful applications across local and global markets. Your responsibilities will include introducing new products to customers, collaborating with the global team on grade translation and technology transfer, addressing customer processes and complaints, designing and developing demo tools, publishing technical bulletins, conducting application-related testing, providing training on Avient materials, and modifying grades to meet customer requirements. Your active participation in resolving customer complaints and supporting R&D and sales teams through comprehensive testing plans and data analysis will be essential. To excel in this role, you should have a minimum of 4-6 years of customer-facing experience in technical service and application development, strong analytical skills, and the ability to manage complex projects across diverse teams. Your primary duties will involve leading customers and business teams in generating new business through application development, developing formulations for new applications, preparing product specifications, providing technical support to customers and commercial teams, troubleshooting processing challenges, leading and coordinating plant technical trials, developing demo tools, publishing technical bulletins, and acting as a reservoir of technical information. Additionally, you will be responsible for ensuring all activities align with safety and health principles and understanding customer needs to select the right material solutions based on functional and service requirements. You will be required to have a Master's degree in Polymer Science/Engineering, Material Science, or a related field, with 4-6 years of experience in a customer-facing role. In-depth knowledge of engineering plastics and thermoplastic elastomers, industry awareness in healthcare, automotive, or consumer sectors, exceptional communication and presentation skills, strong business acumen, analytical mindset, self-motivation, complex problem-solving skills, high technical aptitude, and excellent organizational skills are also essential for this position. You should be willing to travel across India on short notice, with up to 40% travel time. Moreover, you will be expected to comply with all applicable Environmental, Health, Safety, and Security (EHS&S) requirements at Avient, integrating EHS&S into all aspects of operations and reporting all incidents immediately. The job may involve physical demands such as standing, sitting, walking, bending, climbing ladders and stairs, lifting, pushing, or pulling up to 50 pounds, and exposure to manufacturing environments with loud noise levels and personal protective equipment. Your adherence to ethical business policies, proactive approach, teamwork, and ability to translate customer needs into solutions will be critical for success in this role.,

At YSK Labs, we are dedicated to shaping pharmaceutical innovation by pioneering SMART APIs that bring enhanced value to Active Pharmaceutical Ingredients (APIs) and redefine the realm of formulations. Our journey of innovation involves meticulous research, development, and manufacturing of cutting-edge solutions that lay the foundation for superior formulations. Our flagship achievement, the Directly Compressible Granules (DC Granules), represents a breakthrough semi-formulated state of APIs. These granules revolutionize the formulation process by eliminating the need for granulation and extensive processing. With an impressive annual production capacity of 400-500 metric tons of DC Granules, we are committed to reshaping the landscape of pharmaceutical manufacturing. We are currently seeking Area Managers at Lucknow, Varanasi, Gorakhpur, Kanpur, Meerut/Ghaziabad, Agra/Bareilly, Dehradun/Roorkee, Haldwani, and Regional Managers at Lucknow/Varanasi, Dehradoon/Haldwani to cover the whole Uttaranchal & Western UP regions. Ideal candidates should have a minimum of 2 years of experience working in Branded Generics in Cardiac-Diabetic & General segments, with a focus on covering Retailers/Chemist & Dispensing Doctors. We are looking for dedicated individuals who can contribute to our mission of transforming pharmaceutical possibilities. If you are passionate about pharmaceutical innovation and meet the above requirements, please send your Photo Resumes to the following email IDs: rajesh.vns94@gmail.com, marketingnorth@ysklabs.com, info@ysklabs.com, hrysklabs@gmail.com. Job Type: Full-time Benefits: - Cell phone reimbursement - Provident Fund Schedule: - Day shift - Performance bonus Work Location: In person Application Deadline: 29/09/2025 Expected Start Date: 01/09/2025,

Join our team as a Sales Coordinator for Food Ingredient Raw Materials at our Navi Mumbai location! If you are proactive, detail-oriented, and passionate about the food industry, we are looking for you! Your responsibilities will include supporting our sales team with customer inquiries and order processing, engaging with customers through calls and follow-ups, handling inquiries from platforms like IndiaMART and our website, coordinating product samples, facilitating trial orders, and maintaining accurate records while assisting in preparing sales documents. To excel in this role, you should possess excellent communication skills in Hindi and English, hold a Bachelor's degree in Commerce, Arts, or Science (freshers are welcome, prior experience is a plus), have strong organizational skills, attention to detail, and proficiency in sending emails and making phone calls. If you have knowledge of food ingredients and formulations for dairy, bakery, health drinks, and meat/fish processing, it will be considered an advantage. In return, we offer a competitive salary of up to 3.5 LPA (all-inclusive), a 3-month probation period with a performance review, opportunities for growth in a dynamic industry, and a friendly and collaborative work environment. The work timings for this position are from 9:30 AM to 6:30 PM, Monday to Saturday. If you are ready to take the next step in your career and contribute to the food ingredient distribution industry, apply now by sending your applications to kratika@shunyatattva.co.in. We look forward to welcoming you to our team! Regards, Dhanashree Salunke HR Executive Shunya Tattva Management Consultants 8291999522,

You will be responsible for overseeing daily operations in the rubber mixing area to ensure smooth workflow and adherence to production schedules. You will work closely with Production, QA, and R&D teams to drive continuous improvement initiatives. Analyzing mixing cycle times, energy consumption, and material utilization will be essential to enhance operational efficiency. Your role will involve implementing best practices for cost reduction while maintaining high quality standards. It will be crucial to ensure proper maintenance of mixers, mills, and other equipment to minimize downtime. Moreover, you will supervise and mentor operators and technicians in the mixing area, ensuring their compliance with safety protocols and regulatory requirements. You will also prepare reports for senior management and provide improvement strategies. To succeed in this role, you should lead with an outside-in mindset, placing customers at the center of all operations. Upholding Gates ethics and core values will be key to developing talents with the right skills, knowledge, and behavior. Advocating for performance-based rewards will drive accountability for sustainable growth. Additionally, designing a contemporary and innovative learning environment will help attract a diverse talent pool. In terms of supervisory responsibilities, you will have 3+ direct reports and manage a generally homogeneous team. You will adapt plans and set priorities to meet service and operational challenges. Your role will involve performance management and people development responsibilities for managers or associates, as well as providing subject matter guidance to associates, colleagues, and customers. The ideal candidate for this position should have 10-15 years of experience and a strong knowledge of 6-Sigma, policies, and procedures such as kaizens, kanbans, Error-Proofing, TPM, SMED, SPC, 5-S, APQP, and Quality concepts. You should possess expertise in rubber mixing processes, formulations, and materials, along with hands-on experience with internal mixers like Banbury and Kneader, as well as open mills. Strong leadership and team management skills are essential, coupled with problem-solving and process optimization expertise. Familiarity with ISO, IATF, or other relevant quality standards, as well as proficiency in data analysis and production planning tools, will be advantageous for this role.,

You should be able to stay at Morbe (Panvel) where food & accommodation will be provided. Key Responsibilities: Prepare and dispense Ayurvedic medicines as per doctor's prescriptions. Maintain proper records of stock, formulations, expiry dates, and inventory control. Assist in the preparation of traditional formulations (asavas, arishtas, churnas, kwathas, etc.). Ensure compliance with Ayurvedic pharmacopoeia and GMP (Good Manufacturing Practices). Monitor storage conditions of medicines and raw materials. Guide patients on dosage, timing, and method of taking medicines. Maintain cleanliness and hygiene of the pharmacy area. Collaborate with Ayurvedic doctors and therapists for treatment protocols. Manage procurement and vendor relationships for Ayurvedic raw materials and medicines. 13 years of experience in an Ayurvedic pharmacy or clinic preferred. Job Types: Full-time, Permanent Benefits: Food provided.,

As a key member of the New Product Development team, your primary responsibility will be to drive innovation by coming up with new ideas for products that resonate with our customers. You will collaborate closely with the Sales Team to implement customer-driven ideas and prepare formulations that meet the new product specifications and requirements. Your role will involve guiding the R&D team in preparing samples, conducting customer trials, and obtaining customer approval. In this role, you will be instrumental in designing formulations based on inputs provided by the Sales Team and working closely with the R&D executives to prepare samples and prototypes. You will be responsible for testing these samples to ensure they meet planned specifications and standards, as well as customer requirements. Additionally, you will refine formulations based on customer feedback and document them for repeatability. Your involvement in customer meetings alongside the Sales Team will be crucial as you provide technical information about ingredients and formulations, understand customer requirements, and support the Sales Team in addressing customer queries. You will also engage in technical visits to customer locations, where you will assess technical requirements, offer solutions, and provide detailed technical information about products and technologies to customers. Furthermore, your role will involve troubleshooting any issues with product performance or application during customer visits, offering expert advice and support to the internal R&D team, gathering customer feedback to refine products, and documenting findings from technical visits for continuous improvement. To be successful in this role, you should hold a degree in Cosmetic Science, Biotechnology, or Chemistry, along with a minimum of 8 to 10 years of experience in the personal care industry, focusing on research and development for skincare, haircare, and body care products. You should have in-depth knowledge of personal care products, ingredients, and technologies, as well as strong analytical skills and experience in product testing and analysis. Understanding regulatory requirements and compliance in the personal care industry, excellent communication and interpersonal skills, and proficiency in relevant software applications are also essential. If you are a driven individual with a passion for innovation in the personal care industry and possess the required qualifications and experience, we invite you to join us in this exciting full-time opportunity.,

As an In Vivo PK scientist at Syngene, your primary responsibility will be to conduct in vivo pharmacokinetics studies in rodents. With 5-8 years of post-qualification experience and a background in M. Pharm or M.V. Sc. (Pharmacology & Toxicology), you will play a crucial role in documenting lab notebooks online, managing compounds, and ensuring compliance with environment, health, and safety (EHS) practices. Your role will involve conducting pharmacokinetic studies in rodents, preparing study protocols and reports for submissions, and analyzing pharmacokinetic data using tools like Phoenix WinNonlin. You should be well-versed in surgical procedures such as cannulation of jugular, femoral, and portal veins in rats, as well as the collection of vital organs during tissue distribution studies. In addition to your technical skills, you are expected to be a team player with a willingness to take on new challenges, demonstrate commitment to work and timelines, and maintain a learning attitude. Strong communication skills and a proactive approach to work are essential for success in this role. At Syngene, safety is of utmost importance, and you will be required to adhere to safety protocols and EHS requirements at all times to ensure individual and lab/plant safety. By championing effective EHS practices and fostering a culture of excellence, integrity, and professionalism, you will contribute to Syngene's core values and commitment to quality and compliance. If you are a motivated individual with a passion for pharmacokinetics and a dedication to safety and quality standards, this role offers an exciting opportunity to make a significant impact in the field of in vivo PK studies.,

Job Title: Sales Support Back Office (Plastics & Polymers) Job Summary: We are looking for a detail-oriented and proactive Sales Support Executive Back Office to assist our sales and commercial team with timely updates on polymer prices, raw material databases, formulation support, additive and pigment pricing, and cost-saving initiatives. The ideal candidate should have a strong understanding of how to do product costings in excel & SAP Key Responsibilities: Monitor and update daily/weekly PolymerPrices (PE, PP, PVC, PET, etc.) from reliable sources. Maintain and organize the Raw Material Price File for sales and procurement reference. Support the sales team with costing sheets,formulations Update and track Additives, Pigment &Dyes Prices Monthly for accurate product pricing. Collaborate with the R&D and technical teams on formulation changes and customer-specific requirements. Maintain and update pricing databases. Prepare MIS reports related to price trends and material cost fluctuations. share your profile hrmumbai@kandui.in

Job Title: Sales Support Back Office (Plastics & Polymers) Job Summary: We are looking for a detail-oriented and proactive Sales Support Executive Back Office to assist our sales and commercial team with timely updates on polymer prices, raw material databases, formulation support, additive and pigment pricing, and cost-saving initiatives. The ideal candidate should have a strong understanding of how to do product costings in excel & SAP Key Responsibilities: Monitor and update daily/weekly PolymerPrices (PE, PP, PVC, PET, etc.) from reliable sources. Maintain and organize the Raw Material Price File for sales and procurement reference. Support the sales team with costing sheets,formulations Update and track Additives, Pigment &Dyes Prices Monthly for accurate product pricing. Collaborate with the R&D and technical teams on formulation changes and customer-specific requirements. Maintain and update pricing databases. Prepare MIS reports related to price trends and material cost fluctuations. share your profile hrmumbai@kandui.in

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-28-06-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.