606 Formulation Development Jobs - Page 11

New & existing product development, Innovation, Renovation, Quality improvement, Productivity, Upscaling, commercialization, supplier and new ingredients evaluation. External communications with labs & other service provider. Preparation of MMI Required Candidate profile 4+ years of Experience in R & D in Dairy industry Ready to relocate to Umbre, Khopoli with family on long term basis Male applicant would be preferrable

Job Description: R&D Head (Cosmetics and Skincare) Job Title R&D Manager (Cosmetics and Skincare) Eligibility Criteria (Experience, Qualification, Skills)Qualification Advanced degree (Master's or Doctorate) in Ayurveda, Herbal Sciences, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field Experience Minimum 12 years of in research and development, with significant exposure to cosmetics, homecare, or FMCG industries. Proven track record of leading successful product development projects and teams. Skills required Expertise in cosmetic chemistry, formulation techniques, and product innovation. In depth Knowledge of Cosmetics and homecare products and properties Leadership and strategic planning abilities. Communication and stakeholder management skills. Problem-solving and decision-making capabilities. Project management and organizational skills. Ability to inspire and motivate a multidisciplinary team. Market knowledge Job Location Jaipur Key Responsibilities Provide strategic leadership for setting the R&D vision Provide technical expertise and guidance to the Cosmetics and homecare R&D team Oversee all aspects of cosmetics and homecare product development Collaborate with internal (cross functional team) and external stakeholders Manage R&D budgets and resources effectively Ensure regulatory compliance and quality standards Establish KPIs metrics and benchmarks Drive continuous improvement and innovation Job description Provide vision, direction, and strategic guidance for the company's R&D efforts in cosmetics and homecare products Develop and implement R&D strategies aligned with business objectives, to address market needs and capitalize on emerging opportunities Lead, mentor, and inspire a multidisciplinary team of scientists, researchers, and technicians, fostering a culture of excellence, innovation, and collaboration. Oversee the entire product development lifecycle, from conceptualization and formulation to testing, validation, and commercialization. Drive collaborative research initiatives, joint ventures, and technology transfer agreements to enhance the company's R&D capabilities and accelerate innovation Ensure that all R&D activities comply with applicable regulatory requirements, quality standards, and industry best practices. Develop and manage the R&D budget, allocating resources effectively and efficiently to support priority projects and initiatives. Establish key performance indicators (KPIs), metrics, and benchmarks to monitor and evaluate the performance and impact of R&D initiatives. Stay abreast of market trends, consumer preferences, competitor activities, and technological advancements in the cosmetics and homecare segment.

Job Title R&D Head (Food & Nutraceuticals) Eligibility Criteria (Experience, Qualification, Skills) Qualification: Advanced degree (Masters or Doctorate) in Food Science, Nutrition, Biochemistry, or B.Tech. in Biotechnology, food technology, or related field Experience: Minimum 15 years of experience in research and development within the food industry, with a significant focus on Ayurvedic products. Proven track record of leading successful product development projects and teams. Skills required Expertise in Ayurvedic principles and their application in food product development. Knowledge of food science, formulation, and product innovation. Leadership and strategic planning abilities. Communication and stakeholder management skills. Problem-solving and decision-making capabilities. Project management and organizational skills. Ability to inspire and motivate a multidisciplinary team. Market knowledge Key Responsibilities Lead and oversee all R&D activities related to Ayurvedic food and wellness products Provide technical expertise and guidance to the R&D team Oversee all aspects of product development in the food segment Collaborate with internal (cross-functional team) and external stakeholders Manage R&D budgets and resources effectively Ensure regulatory compliance and quality standards Establish KPI metrics and benchmarks Drive continuous improvement and innovation Job description Provide visionary leadership and direction for the R&D function, setting strategic priorities and objectives in alignment with the company's mission and business goals. Develop and implement R&D strategies aligned with business objectives, to address market needs and capitalize on emerging opportunities Lead, mentor, and inspire a multidisciplinary team of scientists, researchers, and technicians, fostering a culture of excellence, innovation, and collaboration. Oversee the entire product development lifecycle, from conceptualization and formulation to testing, validation, and commercialization. Drive collaborative research initiatives, joint ventures, and technology transfer agreements to enhance the company's R&D capabilities and accelerate innovation Ensure that all R&D activities comply with applicable regulatory requirements, quality standards, and industry best practices. Develop and manage the R&D budget, allocating resources effectively and efficiently to support priority projects and initiatives. Establish key performance indicators (KPIs), metrics, and benchmarks to monitor and evaluate the performance and impact of R&D initiatives. Stay abreast of market trends, consumer preferences, competitor activities, and technological advancements in the sector.

Formulation - Research & Development - Pellets exp is must , Comply with GMP’s, SOP’s,regulatory documentation.,Develop Robust formulations & Evaluate patents and develop non-infringement strategiesScale up and optimization of manufacturing process.

A Pharma Industry Jhagadia, Bharuch Formulation Development Chemist (AAD-010-N1C) Qualification: M.Sc Agrochemicals/Chemistry Experience: 4 to 6 Years Salary: No bar for right candidate Candidate must have knowledge of surfactant/surface chemistry. He must have Experience and knowledge of formulation equipment and general analytical equipment in developing Ag formulations with a knowledge of pesticide formulations. He will be accountable for accomplishing work commitments and deliverables. Good computer skills, proficiency in Microsoft office is important. Click to Apply

As a Production Chemist in the nutraceutical industry, you will leverage your 5-7 years of experience to lead the production of various products such as tablets, capsules, proteins, and pre-workout blends. Your responsibilities will include ensuring strict compliance with industry regulations and Good Manufacturing Practices (GMP), guiding formulation and development of new products, monitoring quality control processes, and collaborating with cross-functional teams to enhance manufacturing efficiency. Your expertise in nutraceutical ingredients, manufacturing processes, and quality control standards will be crucial in overseeing the production process and driving process optimization. You will be responsible for ensuring product efficacy, stability, and regulatory compliance through your deep understanding of ingredient functionality and interactions. Your role will also involve troubleshooting and resolving production issues related to blending, mixing, encapsulation, and tableting. Additionally, you will maintain comprehensive records of batch production, train and supervise production staff, and ensure that all raw materials and finished products meet defined specification requirements. To qualify for this position, you should have a Masters degree in Pharmaceutical Sciences or Food Science & Technology, along with hands-on experience in tablet and capsule manufacturing, protein and pre-workout product blending, and knowledge of GMP and regulatory requirements in the nutraceutical sector. Strong leadership, communication, and team management capabilities are essential, along with excellent troubleshooting and problem-solving skills. Preferred skills include experience with sports nutrition and pre-workout formulations, as well as familiarity with stability testing and shelf-life analysis. This is a full-time role with health insurance benefits, requiring a night shift schedule and an expected start date of 20/01/2025.,

As an Assistant General Manager (AGM) in Formulation Development for Injectable products, you will be responsible for the development, scale-up, and validation of simple and complex Injectable dosage forms for various markets including US, EU, India, Canada, Brazil, and others. This role is based at the Matoda plant in Ahmedabad. Your key responsibilities will include: - Developing Injectable dosage forms for multiple markets - Scaling up and transferring technology for Injectable dosage forms - Designing formulation strategies and drug product development roadmaps - Reviewing trials processes, development records, and technology transfer documents - Analyzing stability data of products under development and validation batches - Handling regulatory queries and conducting studies as required - Organizing resources, facilitating communication, and coordinating timely drug product development with internal departments and external vendors - Troubleshooting product issues and actively participating in failure investigations - Providing technical guidance to subordinates and ensuring adherence to good laboratory practices and safety regulations - Following Good Documentation Practices and Data Integrity requirements during all GxP operations - Ensuring understanding and application of Data Integrity requirements and consequences for non-compliance - Reviewing GxP data in compliance with Data Integrity requirements specific to the job description You may also be required to perform any other activities designated by your supervisor to support the overall objectives of the organization.,

Develop & improve formulations for industrial paints, coatings, primers & related products. Conduct research on raw materials & pigments to enhance product quality & performance. Monitor market trends & competitor products for continuous innovation. Required Candidate profile Strong knowledge of resin chemistry, pigment dispersion & paint formulation techniques Proficiency in computer applications Resolve customer complaints through testing ofthe retained sample

The Manager - Nasal Spray Formulation Development will lead the development of innovative nasal spray formulations, driving projects from concept to commercial scale-up. You will focus on the design, development, and optimization of nasal spray drug products, ensuring regulatory compliance and meeting quality standards. Leading a team of formulation scientists, you will collaborate with cross-functional teams to deliver high-quality, cost-effective nasal spray formulations for global markets. Key responsibilities include having relevant experience in developing and technology transferring Nasal Sprays, Dry Powder Inhalers, and Soft Mist Inhalers dosage forms for regulated markets like EU and US. You will be responsible for preparing and reviewing literature search reports for drug substances and products, proposing formulation strategies, guiding executives for development batches in the lab, providing expert input into formulation and process studies, and ensuring compliance with specifications. Additionally, you will evaluate vendors for packaging material, monitor stability studies, prepare Technology Transfer documents, coordinate with stakeholders, and adhere to GLP and GMP. Qualifications and Skills required for this role include an M.Pharm or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field with specialization in drug delivery systems or formulation science preferred. You should have 8-10 years of hands-on experience in formulation development, with at least 5 years focused on nasal spray or inhalation formulations. Technical expertise in nasal spray formulation techniques, drug-excipient interactions, device development, particle size distribution, viscosity, and droplet characteristics is essential. You should possess strong project management skills, experience in working with cross-functional teams, and knowledge of regulatory requirements for nasal spray formulations. Leadership qualities, excellent communication and presentation skills, problem-solving abilities, and a knack for innovation are crucial for this role. The work environment will primarily be based at the R&D center, with occasional travel to manufacturing sites, vendors, and regulatory meetings.,

As a Formulation and Development Officer for our client based in Vatva, Gujarat, you will be responsible for various key tasks. Your primary duty will involve the development of formulations for all dosage forms such as tablets, capsules, ointments, creams, gels, oral liquids, injectables, and novel drug delivery systems for different markets including regulated, domestic, and ROW markets. This includes activities like document review, planning, and conducting stability studies of R&D batches. Additionally, you will be required to provide technical support for the scale-up and technology transfer to manufacturing processes. You will play a crucial role in troubleshooting formulation-related issues that may arise during production, ensuring a smooth manufacturing process. To qualify for this position, you should hold a Bachelors or Masters degree in Pharmacy. If you believe you possess the necessary qualifications and skills for this role, we encourage you to share your updated CV with us. We look forward to reviewing your application and will reach out to you promptly.,

Position Title: Team Member Formulation & Development – Tech Transfer ( Officer / Executive ) - OSD Department: Formulation & Development - Tech Transfer Location: Vadodara Reports To: Manager – Formulation & Development – Tech Transfer Job Overview: The Team Member will support the successful transfer of products from development to manufacturing by ensuring process accuracy, documentation integrity, and adherence to quality standards. This role involves close collaboration with cross-functional teams, participation in validation processes, and troubleshooting to optimize manufacturing efficiency. Key Responsibilities: Process & Documentation: Prepare Technology Transfer Dossiers (TTD) and ensure the accuracy and completeness of all transfer documents, including SOPs and batch records. Validation Support: Assist in process and equipment validation activities, ensuring alignment with manufacturing and regulatory requirements. Risk Management: Identify potential risks during technology transfer and collaborate with relevant teams to implement mitigation strategies. Collaboration: Work closely with cross-functional teams, including R&D, Quality Assurance, and Production, to ensure a seamless transfer process. Troubleshooting: Resolve issues encountered during the transfer process and manufacturing runs, and implement practical solutions. Training: Support and participate in training programs for team members to ensure understanding of processes and compliance requirements. Compliance: Ensure adherence to all regulatory and quality standards throughout the transfer process and during manufacturing. Reporting: Maintain accurate and comprehensive project documentation to support future references and regulatory inspections. Key Skills: Technical Skills: Knowledge of GMP, process validation, and regulatory standards. Familiarity with product development, manufacturing, and technology transfer processes. Soft Skills: Strong communication and collaboration abilities for effective teamwork. Analytical thinking and problem-solving skills to address challenges. Attention to detail to ensure accuracy and compliance. Qualifications & Experience: Education: B. Pharm or Master of Science (M. Sc). Experience: 4-7 years of experience in product development, manufacturing, and technology transfer. Skills: Hands-on expertise in GMP, validation processes, and adherence to regulatory guidelines.

Looking candidates for PDR (Formulation & Development ) Dept. 5-10 years of relevant experience in solid oral dosage (Regulated Market US & Europe) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Head - Research & Development (R&D) Job Location: Ambernath Reports to: Technical Director Experience: 20+ Years Industry: Specialty Chemicals / Surfactants Role Overview We are seeking a dynamic, solution-oriented R&D Head to lead our innovation and development initiatives. This is a strategic and execution-heavy role, responsible for spearheading customized product development, aligning innovation with market needs, engaging directly with customers, and driving value creation from lab to plant to market. Key Responsibilities Lead the R&D function across product development, application support, process innovation, and scale-up for surfactants and specialty chemicals. Drive market-linked innovation translate customer needs into technically feasible, scalable solutions. Work closely with sales and marketing to support business goals through product innovation and application development. Engage directly with key customers (domestic and international) to co-develop solutions and build trust-based relationships. Drive market intelligence within the R&D team to proactively anticipate industry trends and customer expectations. Deliver on commercial targetswork alongside leadership to convert R&D into business outcomes (e.g., creating 2 crore+ value within 24 months). Build and mentor a high-performing, agile, and hands-on R&D team. Lead from the frontdrive accountability, discipline, and delivery mindset in the lab. Ensure strong collaboration across manufacturing, QA/QC, procurement, and regulatory to support smooth scale-up and commercialization. Represent the companys technical strength in key customer meetings, industry forums, and technical panels. Ideal Candidate Profile Education: Masters degree (M.Sc.) in Chemistry or Chemical Engineering; ICT alumni preferred. PhD is a plus but not mandatory. Strong academic or technical background in oleochemicals, surfactants, and oils is essential. Experience: Minimum 20 years in R&D leadership roles in reputed chemical manufacturing companies. Strong grounding in applied research, scale-up, and product customization. Demonstrated success in engaging with customers, converting needs into high-value solutions. Key Skills & Attributes: Excellent communication and presentation skillscan translate complex chemistry into customer value. Strong business acumenunderstands commercial implications of R&D decisions. Highly organized, task-driven, and result-oriented. A natural team leader, who inspires, coaches, and sets a high standard. Ready to travel extensivelyboth within India and internationally. Passionate about problem-solving and delivering real-world impact through innovation. What You Get at Viswaat End-to-end exposure: From lab bench to boardroom, plant to market. No silos: Collaborative, integrated way of working. Opportunity to create visible value in a growing environment.

Role & responsibilities 1. Formulation & Development for Emerging Market & Regulated Market 2. Execution of Lab Trial batches & Tech Transfer activities at site. 3. Lab note book writing & documentation ensuring compliance with regulated guidelines. Preferred candidate profile Experience in Tablet, Capsules, Pellets, ER, SR and DR product development for emerging market M.Pharm Only

Job Summary We are seeking a dynamic and experienced Project Manager in Research & Development team for comprehensive project management support throughout the project lifecycle, including initiation, planning, execution, monitoring, and successful filing or project launch with all regulatory requirements and launches as per business and market requirements. Responsibilities also include creating and maintaining detailed project information, ensuring effective coordination between cross-functional teams (CFTs), facilitating smooth workflow, and ensuring seamless communication. Regular and accurate status reporting is essential, along with serving as the single point of contact (SPOC) for external partners and vendors for third-party assignments. Roles & Responsibilities You will be responsible to collaborate with stakeholders to draw up a comprehensive project plan and establish clear timelines for each milestone. Organize project kick-off meetings and ensure adherence to the Design and Start of Development (DSN) phase gate protocols in coordination with the Quality Assurance (QA) team. You will be responsible to develop the Project Development Charter (PDC) in collaboration with the Portfolio team, incorporating the project's overall budget allocation for each year. You will be responsible for project planning & scheduling for timeline tracking and alignment with stakeholders. Interaction with cross functional team for task monitoring, ensuring the licenses availability for all markets, availability of raw material for development, assisting the team for readiness for pilot studies and go -to-plant readiness. You will be responsible for identifying issues for de-bottlenecking. Coordination for Pre-clinical and clinical/regulatory strategy finalisation for differing markets to ensure timely product development for scale-up and registration/Exhibit batches leading to filing and launch. You will be responsible to ensure timely project updates via MIS reports and regular presentations to senior management, facilitating task completion for timely milestone achievement. Implement project schedule optimization and risk management strategies, while effectively managing budgets and prioritizing activities for seamless project progression. You will be responsible for project monitoring and control by ensuring effective risk identification and debottlenecking, prioritize activities as needed, and promptly address and resolve issues by engaging the relevant teams, including budget enhancement and execution area allocation. You will be responsible to monitor costs against deliverables, resolve conflicts, manage changes during the project lifecycle, and make key decisions based on evolving business scenarios. You will be responsible to facilitate urgency for priority project delivery, oversee coordination with external manufacturing partners, and provide support to Regulatory Affairs (RA) for document tracking and filing. Additionally, ensure timely closure of Quality Assurance (QA) and Quality Control (QC) issues, dossier filing. You will be responsible to facilitate post-filing activities, including additional batch planning, sample preparation for studies, and document preparation, while ensuring effective coordination for a successful product launch and maintain adequate stock levels at the Global Distribution Centre to meet business and market needs. Qualification Educational qualification: Masters in Pharmacy / MBA Minimum work experience: 6-8 years of experience with at least 2-3 years in Project Management experience. Background: Formulation development or Regulatory department. Skills & attributes: Technical Skills Broad understanding of pharmaceutical requirements for different geographies (US, EU, Canada). Certification in Project Management/Training in Project Management. Experience in MS projects/any other project planning software. Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Position: Research Scientist - Cosmetic Products- Formulation Development - Regulated market Experience : 5 to 10 Years Qualification : B. Tech/M.Tech in Cosmetics or M. Pharm Description : 1) Hands on experience on formulation development of Cosmetic products like Sun screen lotions & creams, Face wash, Moisturizers, Shampoos, Conditioners etc.. 2) Product development design and planning. 3) Preparation of various study protocols for development studies. 4) Handling Technology transfer activities. 5) Timely escalation to senior management and take guidance of process. Please share your updated CV along with CTC details at jobs.hr@ipca.com

Dear Candidate, We have urgent opening for "Key Account Manager" for a leading distributor of Pharma Excipients company for Mumbai locations. Job Description: - The primary responsibility will be to manage and grow sales of excipients, at new and existing customers and to expand and advance the pipeline projects. - The role will be home/office based in India and requires significant travel. - The Account Manager will report to the Director Business development. Responsibilities : - Manage an assigned territory for Marketing and sales - Manage and grow sales of excipients, APIs and drug delivery platforms at established accounts and distributors and develop business at new customers. - Expand and advance pipeline through close collaboration with R&D, business development, purchasing and operations in the Region Pharma industry. - Explore opportunities for Pharma Solutions projects at major pharma customers. - Support introduction of new products on territory as per launch plan from Marketing. - Develop strong relationships and deep contacts at all levels throughout customer organizations with a focus on technical and business development groups. This will be led in close collaboration with the Region Technical Development Manager. - Increase exposure and market leadership through seminars, technical conferences and participation in industry organizations in close coordination with Asia Pacific TDM (meetings, trade shows, seminars). - Negotiate pricing and contracts, track and report on industry trends, monitor competitor activities and market share, submit new product ideas and assist with resolving customer issues. - Complete, update and execute the annual territory plan covering key accounts, territory objectives, target accounts and strategies. Develop specific Global Account Plans as needed. - Submit the Monthly /annual territory sales budget and forecasts. - Attend trade shows, industry conferences and local pharma organizations to keep current with industry trends and identify new opportunities. - Enter call reports, contact information and market data in Excel. - Support the team with demand planning as needed. - Collaborate with Customer Service/S&OP to optimize customer satisfaction. Skill Set Requirements : - Degree in Pharmaceutical Science (Master of Pharmacy) Chemistry, , or related scientific discipline. - Technical Enough to understand Product positioning and Make first level presentations - Minimum 1-year experience in developing new business and selling APIs and ingredients to Pharmaceutical manufacturers. - Comfortable in technical/scientific aspects of pharmaceutical development. Knowledge of pharmaceutical Quality and Regulatory requirements. - Multilevel sales contacts at the top pharmaceutical accounts in territory. - Strong interpersonal and negotiating skills. Willing to make cold calls and seek out key decision makers. - Ability to gain the trust of customers by connecting their strategic needs with capabilities. - Extensive travel required - minimum 75% of the time. - Excellent verbal and written communication skills. - Strong organization and planning skills. - Analytical skills and ability to use market research to recommend pricing and prepare offers. - Team player - Experienced in working in a global organization and multicultural teams. - Open minded, willing to listen and to share ideas generated internally and by customers. - Excellent follow-up skills. - Driven, self-motivated, results oriented individual with the ability to work under limited supervision. - Motivated by fast evolving environment and challenges Kindly forward the updated resume along with CTC Details on yogeeta@shauryahc.in Regards

Alembic Group is looking for Assistant Manager - Formulation Development to join our dynamic team and embark on a rewarding career journey Ensuring company policies are followed. Optimizing profits by controlling costs. Hiring, training and developing new employees. Resolving customer issues to their overall satisfaction. Maintaining an overall management style that follows company best practices. Providing leadership and direction to all employees. Ensuring product quality and availability. Preparing and presenting employee reviews. Working closely with the store manager to lead staff. Overseeing retail inventory. Assisting customers whenever necessary. Organizing employee schedule. Ensuring that health, safety, and security rules are followed. Ensuring a consistent standard of customer service. Motivating employees and ensuring a focus on the mission. Maintaining merchandise and a visual plan. Maintaining stores to standards, including stocking and cleaning. Completing tasks assigned by the general manager accurately and efficiently. Supporting store manager as needed.

Alembic Group is looking for Senior Manager - Formulation Development to join our dynamic team and embark on a rewarding career journey Delegating responsibilities and supervising business operations Hiring, training, motivating and coaching employees as they provide attentive, efficient service to customers, assessing employee performance and providing helpful feedback and training opportunities. Resolving conflicts or complaints from customers and employees. Monitoring store activity and ensuring it is properly provisioned and staffed. Analyzing information and processes and developing more effective or efficient processes and strategies. Establishing and achieving business and profit objectives. Maintaining a clean, tidy business, ensuring that signage and displays are attractive. Generating reports and presenting information to upper-level managers or other parties. Ensuring staff members follow company policies and procedures. Other duties to ensure the overall health and success of the business.

Alembic Group is looking for Junior Executive - Formulation Development to join our dynamic team and embark on a rewarding career journey They work under the guidance of senior executives and managers to support the organizations goals and objectives Must have excellent written and verbal communication skillsMust be able to analyze complex problems and develop effective solutions Managing internal and external communication, including preparing reports, presentations, and other materials

Alembic Group is looking for Executive - Formulation Development to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Role & responsibilities • Responsible for specific developmental projects assigned by HOD or seniors • Carrying out experiments, analysis etc. to establish the product quality and process, as guided by HOD or seniors. • Maintaining the progress of new products development in the form of monthly / daily report, as the case may be. • Responsibility to work together with PBL / pilot plant for new developed product. • Arrangement of lab developed sample for customer validation, as suggested by HOD or seniors. • To take care of all analytical equipment and reagents available in the lab. • Preparation and standardization of reagent solution required for analysis. Preferred candidate profile

RM and PM receiving and documentation of the same. Proper arrangement of the Received COA of RM and PM. Sampling of Received RM and PM, sending the samples to ADL for analysis. Preparation of indent for trial activity and ensure the availability in defined time. Taking of daily trial batches, discussion of issue with immediate supervisor. Entry of trial batch data in lab notebook and preparation of BMR for stability batches. Maintaining the files of individual products like RM and PM COA, Trial COA and Stability Reports after updating in Excel Sheet. Ensure GMP practice in Laboratory routinely. Documentation of stability batches. Calibration of instruments in the laboratory. Literature search and review for the newly identified products for EU/UK/Raw market. SOP preparation and submission to DQA. Ensure utility in good condition in laboratory during all development batches. Adhere Good Manufacturing Practice and Good Laboratory Practice throughout lifecycle of the product. Technically sound in development of Injectable/ Oral solid products and semisolid and liquid dosage forms. If additional knowledge of regulatory documents preparation is essential

Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientists for DOM/EMB market at our dedicated R&D center. Department : Formulation Development Formulation : Solid Orals Market : Domestic / Emerging Experience Required : 4-7 years Designation : Sr. Officer / Executive Location: R&D Center, Moraiya, Ahmedabad. Roles & responsibilities (Not Limited to): To perform detailed Literature and Patent Search, preparation of Summary and Product Development. Strategy documentation. API Characterization and Reference Product Evaluation. Formulation development of Oral solid Product (planning, execution, scale-up and exhibit batch). Execution of scale-up and exhibit batches for developed dosage form. Coordination with cross functional departments like DQA, IPR, RA, ADL,TT, Packaging Development, Production, QA and QC for product development related activities. Perks & Benefits: Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills & experience, we encourage you to apply for this position. Interested candidate can revert with their resume on career@unisonpharmaceuticals.com Regards, Team HR Unison Pharmaceuticals Pvt Ltd

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. 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.