2048 Formulation Jobs - Page 36

Role & responsibilities 1. To develop Stable and Bioequivalent solid oral products for EU, ROW (Rest Of World) and Domestic markets. 2. Technology transfer of developed products to plant level; this includes all TTD related works 3. To collect, compile of all data of plant batches and submit to regulatory department as per market specific requirement 4. To address agency's queries as per requirement 5. To extend support to plant for any trouble shooting

As a Manufacturing Chemist, you will be responsible for overseeing and managing the formulation and production processes of cosmetic products. Your primary focus will be to ensure that all manufacturing activities comply with regulatory standards, product specifications, and quality norms, while maintaining efficiency and safety. **Key Responsibilities:** - Supervise and execute batch manufacturing of cosmetic products such as creams, lotions, talc, lip balm, etc. as per standard operating procedures (SOPs) and batch manufacturing records (BMR). - Ensure accurate weighing, mixing, heating, cooling, and filling of raw materials and ingredients as per approved formulations. - Maintain hygiene ...

Developing innovative products, enhancing existing formulations & ensuring that R&D projects align with market demands & company goals. involves coordinating with cross-functional teams to ensure successful product development and commercialization. Required Candidate profile B Tech Chemical/ Masters in Chemistry. 5-7 years of experience in R&D roles within a manufacturing environment, preferably in the construction chemicals industry. Analytical & problem-solving skills.

Role & responsibilities Candidate should hands on experience on Analytical instrumentation, knowledge of USP chapters, ICH Guidelines . Should have inclination for solving problems encountered during analysis.

Job Summary We are seeking an individual to oversee batch manufacturing, ensuring adherence to cGMP (Current Good Manufacturing Practices), providing training, and coordinating day-to-day activities. Responsibilities include minimizing machine downtime, managing subordinate staff, assuring compliance with standards and SOPs (Standard Operating Procedure), leading regulatory audits, compiling reports, ensuring safety norms, and budget management. Roles & Responsibilities • You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control. • You will be responsible for imparting general and cGMP ...

Role & responsibilities Conducting day- to-day Experiments. Monitoring of the experiments with observations. Calculation of moles & mole ratios. Calculation of molar yield. Familiar on properties of solvents, raw materials and catalysts like boiling point, melting point, density, freezing point etc Familiar on MSDS. Periodically checking the Lab instruments for their maintenance. The difficulties / problems arise during the experiment will be report to Seniors. Interaction with AR&D and stores departments for getting analysis results and raw materials in time. Maintenance of glassware and Equipment. Maintenance of lab clean and tidy cleaning and segregation of glassware. Storage of raw mater...

About the Company As an integral part of Advenza Global Limited Commercial team, the incumbent will be managing a large portfolio of complex projects. The primary responsibility will be developing the P2P finished formulation, Vials, stick packs, Capsules, Tablets etc. as well as Probiotics global/domestic business development and strategy deployment, while working with a range of internal stakeholders to create opportunities aligned with the organizations strategy plan. In this autonomous and entrepreneurial role, the incumbent will help achieve long term organizational objectives and priorities by leading definable and measurable commercial strategy goals and ensure that they are met. Role...

As a Cosmetic Chemist at Glexon Healthcare Pvt. Ltd., you will play a crucial role in formulating and developing new cosmetic products. Your responsibilities will include conducting stability tests, ensuring product compliance with industry standards, researching and sourcing raw materials, performing quality control tests, and collaborating with the production team to optimize manufacturing processes. Key Responsibilities: - Formulate and develop skin care, hair care, and personal care products - Conduct stability tests and quality control checks - Research and source raw materials - Ensure compliance with industry standards - Collaborate with the production team to optimize manufacturing p...

Role Overview: You will play a crucial role in contributing strategically to the overall success of Biotechnology R&D by driving innovation, enhancing team performance, and aligning with departmental/organizational goals. Your responsibilities will include ensuring the security of intellectual property for R&D, conducting literature searches using available databases, developing microbial consortia for wastewater treatment, and designing and executing experiments for protein purification using chromatography, filtration, and other downstream techniques. You will also be involved in developing, evaluating, and characterizing purification processes from lab to pilot scale, collaborating with c...

End-to-end management of regulatory submissions for finished dosage forms. Prepare & compile high-quality dossiers (Modules 1–5). Coordinate cross-functional teams, handle queries, ensure compliance, and support lifecycle mgmt of products.

- To Internalizing the S.O.P. - Selection of good quality product. - To receive the quotation from different company. - As per doctor requirements check the comparative rates. - Procurement of medicine. - Negotiation for scheme with supplier/manufacture.. - Purchase order approval. - Recruitment of new pharmacist. - Train the new staff. - Supervision on present staff. - Attending the M.R. for new molecule & new brand. - Audit of medicines at nursing station for their expiry &storage condition. - Training programmed on medication safety for concerned staff. - Assisting Pharmacist in routine work whenever required. - Second check on gate pass. - Manage require staff in all areas all the time. ...

Regulatory Affairs professional with knowledge of D&C Act, Rules, and FSSAI regulations. Experienced in Domestic Market only.

Responsible for schedule adherence & maintaining project schedule live in SAP. Formulation and custodian of plant master, KPM and project schedules. Drive OTD within business To create SAP project structure to ensure that complete, fit for purpose, definition of customer date and technical requirements are fully reflected in PS at the time of release. Attend internal order review meeting ensuring that project and commercial priorities are clearly communicated to appropriate departments and feedback taken in to accounts when adjusting finalized PS. To succeed in this role, you will need: Work experience: Minimum 10-15 years of relevant experience of planning and scheduling Strong SAP knowledg...

Liaise with Client Service Advisors to fully understand the Client s business and insurance requirements Contribute to the formulation of the Service Plan, Reports, Presentations, and any other client documents etc, as required Support Client Service Advisors to prepare for the internal renewal strategy meeting Preparation of draft comprehensive marketing presentations and the renewal report, working with the Client Service Advisors to learn and develop technical skills Arrange and take part in internal discovery meetings Establish and develop effective working relationships with Insurers and where appropriate, liaise with Insurers as per agreed parameter and process to support deliver clien...

Role & responsibilities To be well versed about coordination and collaboration with Quality functions of third party manufacturing (CMO) sites and CMO team for compliance of product, facility, systems, procedures. and for documents required from third party for various purpose; review, RA submission etc. Must have knowledge and know how on regulatory pathway for registration of product as per third party and or loan license norms/rules and requirement of documentation for regulatory submissions. Incumbent is expected a good reviewer and investigator To know the function of oversight of CMO sites for batch/lot releases as applicable form the manufacturing (Feed supplements and Pharma products...

Responsibilities: * Manage production schedules & resources effectively * Oversee liquid oral, syrup & suspension formulations * Ensure GMP compliance at all times * Handle manpower efficiently

JOB RESPONSIBILITIES: Job Title: Manager/Sr. Manager Exp- 10- 15 Years Ability to handle prior art/patentability / invalidation and FTO searches. Making of Landscape preparation and patent monitoring of drug products for the proposed Active Pharmaceutical Ingredients (API). -Conducting Infringement/FTO Analysis for API for countries of interest and provide clearances to CRD. Freedom to operate analysis-Drug product-based, Technology-based and packing based. Orange book patent analysis-critical non-infringement strategy. Collaboration with R&D scientists, analysts regarding patent issues. Taking of attorney opinions for proposed invalidity or non-infringement study wrt the proposed route of s...

Roles and Responsibilities Develop analytical methods for OSD products using techniques such as HPLC, GC, UV, etc. Conduct formulation research and development of injectable products. Prepare protocols, SOPs, and reports related to formulations and analysis. Collaborate with cross-functional teams to ensure successful product launches. Ensure compliance with regulatory requirements throughout the product lifecycle. Independently handling the Stability analysis of dosage forms. Has knowledge on Validation of the methods. Forced Degradation studies. Desired Candidate Profile Sound Knowledge about analytical method development and Stability analysis of dosage forms 2. Hands on experience in usi...

Major Activities Support in the formulation of AMI Business HSSE strategy, guidelines and procedures in line with overall Apraava Energy s policies and monitor adherence to the same to drive a strong HSSE culture and maintain a high safety standard. Work closely with the State AMI Operations Lead to develop, drive and implement state & site-specific AMI HSSE Management System, Strategy, guidelines & procedures, checklists etc. in line with AMI HSSE Plan and Corporate HSSE policies, procedure, guidelines & expectations. Develop state & site specific HSSE targets for leading & lagging HSSE indicators and monitor its implementation. Prepare Risk Assessment, Job Safety Analysis and get it implem...

" Jubilant Biosys is looking for Research Associate II - In Vivo, DMPK Location : Bengaluru Experience : 3 to 5 years Qualification : M Pharmacy Key Responsibilties : Read and understand various in vivo study protocols Good knowledge of various in vivo animal models employed in DMPK arena Handling of laboratory animals (mice, rats, guinea pigs, rabbits, hamsters etc.) Conduct various in vivo ADME studies (IV and PO studies, excretion studies etc.) Ability to administer compound via various routes in rodents (IV, PO, IP, SC, tropical, intravitreal etc.). Should be adept at conducting IV studies employing infusion pumps Should be able good at rodent cannulations (jugular, carotid, femoral) and...

Responsibilities & Key Deliverables As a Senior Lead Engineer - Materials Technology within Mahindra & Mahindra Ltds Automotive Division, you will play a pivotal role in advancing the application of adhesives and sealants across multiple automotive domains, including BIW (Body in White), Trims, Seating, and Powertrain. Your expertise will be critical in selecting, specifying, and validating materials that meet stringent performance, durability, and manufacturing standards under real-world conditions. You will lead cross-functional teams to develop innovative material solutions driving cost optimisation, lightweighting, and process simplification. Your responsibilities will include overseeing...

Job Title: Sterile Manufacturing, Filling Supervisor Department: Formulation production Job Location: Bengaluru, India About Syngene: Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to s...

Role & responsibilities Strategic Leadership: Provide overall direction, leadership and vision for the Dahej Plant. Drive operational excellence and continuous improvement initiatives. Ensure adherence to corporate goals, compliance, and sustainability objectives. Regulatory & Compliance: Ensure strict compliance with USFDA and other international regulatoryguidelines. Lead and support inspections, audits, and regulatory submissions. Establish and maintain robust quality systems and EHS practices. Operations Management: Oversee end-to-end plant operations including Production, Quality, Engineering, Maintenance, Supply Chain, HR, IT, and Administration. Drive productivity, efficiency, and cos...

Role Overview: You will be responsible for conducting primary research and literature review on skincare, haircare, or cosmetic ingredients and technologies. Developing and testing prototypes, optimizing formulations, and conducting stability and compatibility testing will be key aspects of your role. Collaboration with cross-functional teams from ideation to launch, preparing product briefs and regulatory documentation, and analyzing consumer trends and competitor benchmarks will also be part of your responsibilities. Key Responsibilities: - Conduct primary research and literature review on skincare, haircare, or cosmetic ingredients and technologies. - Develop and test prototypes in-house ...

Role & responsibilities Ability to develop novel robust agrochemicals formulations like EC, SC, WG, WP, Microencapsulation, SSF, SE, Microbial formulation etc. Identifying new formulations for the Pesticide (Insecticide, Fungicide, Herbicides, Bio stimulants, PGR, secondary metabolites and biopesticides) Define the experimental program that include the development of new pesticide formulations, Procedures/standards. Identification and realization of cost-saving and cost-reduction opportunities by developing innovative formulations. Design, prepare and develop stable and compatible agricultural formulations for use in crop protection. Contribute ideas aimed at advancing existing technologies ...