1455 Formulation Jobs - Page 8

Role & responsibilities A Packing Head in the nutraceutical industry oversees all packaging operations, ensuring that products are packed efficiently and in compliance with strict quality and regulatory standards . The role involves strategic planning, team leadership, and process optimization to meet production targets and maintain product integrity. Core responsibilities Operational management: Lead and supervise the packaging department's daily activities, including planning and executing packing schedules to meet production demands. Quality and compliance: Enforce and uphold Good Manufacturing Practices (cGMP), FDA, and other relevant regulatory requirements. Review and approve batch pac...

Roles and Responsibilities (5 days working) Dossier (CTD, ACTD & Country Specific Format) review for Latam, ASEAN, CIS & African countries. Collaborate with various departments within the organization, such as Plant (QA, QC, Production, Packing & Purchase) and R&D, to gather the necessary inputs for regulatory submissions. Compilation and timely submission of Dossiers to the respective regulatory authorities in the assigned countries. Planning, monitoring, review, strategy & delegation of the below mentioned activities for Countries: New Product Registration, Re-Registration, Retention, Tender. Handling of queries from various regulatory authorities/consultants. Post Approval Changes GMP (Co...

Role & responsibilities Leading a team of PHD & master graduates in areas of natural products identifying & executing new researching projects aligning with company goals Monitoring & maintaining lab instruments to ensure minimum down time Working with manufacturing teams for trouble shooting process related issues Working with other teams to support multi-disciplinary research projects.

Responsibilities Key Deliverables Benchmarking and formulation of Quality Targets for New Products, timely Product evaluations to assess gaps and driving corrective actions. Product and Process Failure mode avoidance in project such as 7QC-tools, FMEA, DVP, DFA/ DFM, Risk analysis and Product quality design reviews throughout the product development phase. Generating Quality indicator dashboard for Senior Management reviews highlighting key quality risks and proposed contingency plans. Working closely with various stakeholders to capture customer latent needs and ensuring deployment during the product development. Driving Teams towards implementation of various Product and Process improvemen...

Oversee daily workflow, schedules, assignments of security staff Assist managing physical security of site through guarding service, monitor optimum functioning of physical security devices controls Inspiring performance excellence on the part of security service team members Conducts regular walk-throughs, security inspections for assigned facilities. Implement and ensure adherence to stringent audit scheduling, with findings documented communicated Ensure 100% Training of all security guards Perform initial risk assessments of site operations, propose mitigation measures Respond, assist in emergency response, workplace incidents Perform trend analysis, data mining using various in-house to...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / IPQA (OSD) / Documentation (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. / B.Sc. MICROBIOLOGY (Officer / ...

Company: Strides Pharma Science Ltd Department: SCM (Procurement) Position: Assistant Manager Job Location: Bangalore Qualification: B. Pharm, BSC or MSc, M. Pharm. (Science background is preferable) Experience: 6 to 10 Years Key responsibilities Identification and qualification of Sources for new API and excipients. Arrange the alternate source samples of Excipients & API along with working standards, Impurities, Specification, COA and MOA. Arranging Pre-requisite documents and sharing the same with CFTs for Initiating the AVD project. Follow up with vendors for getting required technical documents. Check and raise request for vendor/manufacturer code creation. Create quality info Record an...

Job Overview: The Product Development Leader (PDL) for Oral Solid Dosage (OSD) will play a pivotal role in leading the development of oral solid dosage forms such as tablets and capsules from early formulation stages through to commercialization. This position requires strong leadership skills in overseeing product development strategies, managing cross-functional teams, ensuring timely project execution, and maintaining compliance with regulatory standards. The PDL will work closely with formulation development, analytical services, regulatory affairs, and manufacturing departments to deliver high-quality pharmaceutical products. Roles & Responsibilities: Formulation Development and Optimiz...

Roles and Responsibilities Manage warehouse operations, including inventory management, storage, and dispatch. Coordinate with production team to ensure timely delivery of raw materials (RM) and packaging materials. Ensure accurate recording of stock levels, orders, and deliveries using ERP systems. Desired Candidate Profile Experience: 2-5 years Qualification: B.A/ B.Sc./ B. Com Must have experience in OSD Formulation Warehouse operations Should be willing to work in shift operations Interested candidates can share their updated CV to jahnavi.kodali@granulesindia.com

Role & responsibilities To lead Regulatory affairs team engaged in dossier preparation in CTD and ACTD formats. Responsible for final review of dossier before submission. Reviewing artwork for products as per relevant regulatory authority requirements. Coordination with F&D, QA, QC & Store for documentation In-depth knowledge of pharmaceutical documentation & regulatory guidelines. To coordinate with technical team for documents required for dossier. Country Experience Preferred: CIS, LATAM Dosage Form Experience: Soild Oral + Injectable Preferred candidate profile

Good Background in chemistry Hands on experience in product development Communication & teamwork skill Exposure to Scale up process chemical analysis techniques like HPLC, GC, along with wet analysis like titration etc. 2 to 5 years of experience in R&D - Synthesis & ADL.

As an experienced and research-oriented dermatologist or physician with a solid background in medical or clinical ops, you will be working with one of India's fastest growing digital health platforms to develop condition-specific treatment solutions for millions of users. Your primary responsibilities will include: - Providing high-quality medical care & dermatologist consultation online - Collaborating with in-house doctors to envision condition-specific solutions - Offering research-based data to the Product Formulation Team - Maintaining experimental results for pilot studies - Supervising production batches - Creating product concepts based on common skin & hair concerns in dermatology -...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Th...

Role Overview: As a Consultant in Blending & Tank farm, your main responsibility will be producing various product blends as per specifications provided by the Commercial team. You are expected to meticulously follow blend sheets, batch records, and outlined procedures to ensure accurate production of product blends and lot combinations. It is crucial to accurately pull specified streams and lots, document all actions, oils, lots, locations, and weights of oil used in production. Utilizing Good Manufacturing Practices (GMP) to prevent contamination and enhance production efficiency is a key aspect of your role. Collaboration with other blending specialists and manufacturing personnel is esse...

Role Overview: You will be responsible for conducting IP evaluation of Formulation & Drug-Device combination products. Additionally, you will be preparing claim charts, structuring FLBs, and providing litigation support. Your role will involve creating IP through Patent filing for the 505(b)2 range of products. You will also offer IP support to the Central Portfolio Team for the USA & International Market, including Due diligence for new business opportunities. Tracking pending patent applications, OB listings, competitors" ANDA, and litigation strategy to assess their impact on the pipeline and keeping Senior Management informed will be part of your responsibilities. Key Responsibilities: -...

Key Responsibilities 1. Lead the development, formulation, and optimization of construction coatings such as: Waterproofing coatings (acrylic, PU, epoxy, hybrid systems) Protective and decorative coatings (cementitious, elastomeric, primers, sealers) Floor coatings and industrial protective coatings 2. Evaluate and select raw materials (polymers, additives, pigments, fillers) for performance, cost-effectiveness, and sustainability 3. Conduct application trials, performance testing, and benchmarking against market standards 4. Troubleshoot coating performance issues during formulation scale-up and application at customer sites 5. Collaborate with cross-functional teams (Production, QC, Market...

Responsible for Water sampling, Sample receipt of raw materials, in process, finished product and stability samples. Responsible for Chemical analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for sample management and coordination with team for smooth operation of samples release activity. Monitoring and review of Temperature monitoring data record of equipment and clean room. Monitoring of differential pressure in Laboratory. Analysis of Raw Material/ In process samples/ cleaning samples/ Intermediate samples/Finished product/water sample / Packaging materials/ Formulation finished products and management/traceability of Reserve samples and ...

Expanding into new markets through efficient registration pipelines Delivering high-performance, eco-friendly solutions tailored to local needs Building long-term relationships based on trust, reliability, and regulatory excellence

Experience: Freshers or candidates with up to 2 years of experience. Interest in animal nutrition, feed technology, or food production is essential Skill: Understanding of animal nutrition and feed formulation Basic knowledge of food safety and quality standards (HACCP, ISO, FSSC) Observation skills and attention to detail in production environments Good teamwork and communication abilities Interest in production, quality, and R&D activities related to pet foods Role: Support production and quality operations at the Petfoods plant. Monitor product batches for nutritional and quality standards, assist in formulation trials, ensure hygiene and safety compliance, and contribute to R&D activitie...

,in-processthe ,for leading,for leading,problem-solvingResponsibilities We are looking for a senior professional AGM with a range of 15 to 20 years of experience in Analytical Method Validation for regulated markets. The role involves leading API and excipient method validation across multiple dosage forms and managing a team of 30, including three senior managers. The ideal candidate must be technically strong, experienced in US/EU compliance, and hold an M. Pharm, M.Sc., or Ph.D. Role & responsibilities: Accountable to lead the team for AMV of OSD, Nasal, Injectables, Ophthalmic and Topical dosage formulations. Responsible for RM & PM characterization and documentation. Generate qualificat...

We are seeking a highly motivated and experienced Shift Chemist to join our team. The successful candidate will be responsible for running production shifts, conducting chemical analysis, and ensuring product quality and consistency on their designated shift. Qualifications: Bachelor s degree in Chemistry or a related field (MSc in Chemistry is a plus) Minimum of 5 years of experience in a laboratory setting, preferably in the manufacturing of unsaturated polyester resins Strong knowledge of chemical analysis techniques and laboratory equipment Excellent attention to detail and ability to work independently Ability to work on a rotating shift schedule including daytime and night-time shifts ...

Job Title: Executive I (Mechanical )- Plant Engineering, Pharma Formulations Plant Maintenance Pharma Formulations Basic Minimum Qualification Diploma in Mechanical OR ITI in Fitter from a reputed Institute Experience: 5 to 8 years of working experience in a Pharmaceutical Formulations plant. Location: Ankleshwar Site . Job Description and KEY ACCOUNTABILITIES Carrying out preventive maintenance of equipment as per schedule. Attending breakdown maintenance as per the work order received and log related activities in SAP/HANA PM Module for packaging machines and formulation equipment. Maintaining tools/tackles properly. Assisting the superior in implementing modifications / small projects. Up...

Roles & Responsibilities 1. Responsible for monitoring of basic norms of cGMP, ALCOA+ Principle, data integrity, GDP & to maintain his personal health hygiene. 2. To review and approve the analytical reports for raw materials, packing material, In-process, Finished product and release or reject raw materials, packing materials, In-process and finished product in the Supply Chain Management system. 3. To review and approve/reject the Certificate of Analysis of RM, PM & finished product. 4. To perform audit trial review for QC & Microbiology instrument CDS and non CDS. 5. To handle different types of activity in SCM, New LIMS, HRMS, Mysetu, Newtronics ICDS 3.1, DMS, EDMS, LMS, Empower , AMS So...

Hiring Global Licensing Manager for a Pharma brand Location : Gurgaon Reports to : Managing Director /WTD We are seeking an experienced and dynamic Global Licensing Manager Existing /New Products to lead the identification, evaluation, negotiation, and acquisition of licensing opportunities in line with the companys global growth strategy. This role will focus on early to late-stage pipeline assets, New Formulation Generic Products and commercialized products in the pharmaceutical and biotech sectors. Key Responsibilities: Opportunity Identification: Identify and evaluate global out -licensing and co-development opportunities for new pharmaceutical products across therapeutic areas, includin...

Description External Job Description Primary Responsibilities: To work on development / modification of formulations meeting the project objectiveDesigning the shade formulation and matching the shade as per the project requirementDesigning the product specification for implementation on plantCarrying out the details testing as per the protocol and generating the data for long term performance as wellSupporting plant for the standardisation of formulationSupporting sales & marketing team, supply chain, plant Qualifications: Essential B Tech, MSC in Chemistry Desired Knowledge in Solvent based Paints & Shade Matching Additionally, basic knowledge on Resin Chemistry & paint raw materials Shoul...