816 Formulation Development Jobs - Page 27

KEY RESPONSIBILITIES: Develop new processes, or refine existing ones, to optimize the scale up of lab batches in factory. plan, carry out and supervise process trials in laboratories & pilot trials. Develop tech transfer documents along with formulation team. Plan the scale up batches aligning with stakeholders. scale up the production process via trials, making changes to raw materials or components, and process parameters to ensure quality is maintained during large-scale production. To run the stability studies of pilot batches, assist the lab team in running stability studies. work with product pipelines at various stages of development and provide guidance on scalability. develop formul...

Role & responsibilities New Product Development/ R&D: Provide expert insights regarding the new formulations from AYUSH pharmacology with reference of scientific literature, standard textbooks & new scientific developments. Evaluate and analyse drug drug interaction if the ingredients are used from ayurveda, Unani, homeopathy or Nutraceuticals. Detailed knowledge of all classic ayurvedic formulations & good acumen of new Nutraceutical types with high bioavailability. Production: Conduct sample batch for human testing in the inhouse lab Technical Documentation: To make RM & FG specifications. To create label drafts, SOPs, Label content for ayush products and SOPs and regulations related to fo...

Job Title: Management Associate MPD – AMA Contract Resource Department: MPD-BB, AMA PHC Location: Andheri East Chakala, Mumbai Position Type: Full-Time, Contractual Vacancies: 1 Job Description: We are seeking a Management Associate to support the MPD – AMA team on a contractual basis. This role involves key responsibilities in pharmaceutical documentation, data management, and coordination to ensure efficient support to formulation and analytical development teams. Key Responsibilities: Setup of Enovia DSM for formulation parts and documentation. Compilation and tracking of stability study data for review and approval in Enovia. Raise and manage Change Controls in Veeva QA system for MPD de...

Role & responsibilities Conduct pre-formulation and formulation development of new pharmaceutical dosage forms (solid, liquid, semisolid, etc.). Perform compatibility studies for Drug-Excipient interactions. Design and execute laboratory-scale and pilot-scale trials . Develop and optimize manufacturing processes , ensuring scalability and reproducibility. Maintain batch manufacturing records (BMRs) and development reports . Support analytical development teams with stability and validation studies. Assist in technology transfer to production and contract manufacturing sites. Ensure adherence to GMP, GLP, and regulatory guidelines (e.g., USFDA, MHRA, WHO). Collaborate with cross-functional te...

Role & responsibilities Formulation development of Injectable FORMULATION for regulated market, USA and Europe. To carry out product development trials, process optimization trials, scale up trials and exhibit batches at manufacturing plant. Literature search of new products, to conduct pre formulation studies, other studies like Tubing studies, compatibility studies and filter studies. Preparation of development protocols, QbD/Risk assessment documents, technology transfer documents and product development reports. Ability to carry out investigations, troubleshooting exercises related to development, scale up and exhibit batches. Preferred experience on Lyo product and colloidal Iron produc...

Key Responsibilities: Search and review scientific information / literature Drafting, submitting applications with all necessary information to RA for related Licenses required for Product Development. Identify and propose formulation strategy for product development. Read, discuss and plan Developmental activities, bring Innovation in work and adopting Digital Initiatives while doing scientific work. Visualize the developmental needs of the product. Work along with Cross functional team towards to meet project milestones as per timelines. Use Scientific approach to mitigate challenges during development, scale up and Technology transfer of the product. Qualification M.Pharm/Phd(Pharmaceutic...

Role & responsibilities 1. Literature Search, Pharmacopoeia and Patent Search, Review and Discussion and Documentation. 2. Application of NOC, Test License, Manufacturing and Import License 3. Reference product Characterization, Manufacturing and Import License. 4. Reference product Characterization, Reverse Engineering and prototype development. 5. Preformulation study, Manufacturing of bench scale trials for formulation development. 6. Manufacturing of process optimization batches, scale up batches and submission batches. 7. Preparation of Bill of Material, Master Formula Record for manufacturing of submission batches. 8. Preparation of Product development Report for regulatory filing of p...

Off Targets is a leader in pharmaceutical innovation, committed to developing advanced therapeutic solutions that address unmet medical needs. We are looking for an experienced and dynamic professional to lead our Formulation Development department, driving the development of cutting-edge injectable drug products. Job Description We are seeking an accomplished R&D leader to head our Injectable Formulation Development function. The ideal candidate will bring deep technical expertise in complex injectable products and a strategic mindset aligned with 505(b)(2) development, regulatory planning, and IP differentiation. Key Responsibilities: Lead end-to-end formulation development of complex inje...

Role & responsibilities 1. Responsible to lead a team of 4-5 scientist for the development of drug products of Regulated Market (EU and UK) 2. Responsible for drug product development to exhibit batch execution and to support for regulatory filing. 3. Conduct Literature survey and compile the scientific data per product. Development of Rubust, bioequivalent formulation and processes through optimization by applying QbD principles. 4. Compilation and review of developmental data and exhibit batch stability data. 5. Should have good understanding on Reference Product Characterization, reverse Engineering, Bioequivalent Prototype development, Stability studies, Scale up activities. 6. Coordinat...

Essential Duties and Responsibilities: Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family. Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis. Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investiga...

Role & responsibilities Actively supports launch and sustenance of Baxter commercial product globally. Support all commercialized project related requirements related to Baxter manufacturing sites and CMOs Globally. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of product design governance documents for a particular product family. Make sure the relevant documents for various product families are available to support risk management, change control processes and design integrity. A very good understanding of Quality Risk Management for pharmaceutical products is required per ICH Q9 and ensure sustenance of Baxter commercial products gl...

Role & responsibilities 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 updation in Excel Sheet. Ensure GMP practice in Laboratory routinely. Documentation of stability batches. Calibration of instruments in the labo...

Responsibilities: Review IP landscape reports, non-infringement& FTO analysis Devise strategies for patent non infringement and invalidations Collaborate with R & D Scientist to explore design around strategies for P-IV & NCE products Conduct IP due diligence for product selection/ new opportunity identification. Support RA for patent certification, PIL clearances and declaration Monitor, review and manage ANDA litigations Conduct patentability searches, draft and file patent applications and manage prosecutions Ensure timely and effective task delivery through strategic planning prioritisation and execution.

Urgent hiring for Research Scientist Formulation R&D (OSD) Location: Roorkee Department: Formulation & Development (F&D) Industry: Pharmaceuticals – OSD & Liquid Job Description: We are hiring a Research Scientist – Formulation R&D for its Roorkee facility . The candidate must have strong experience in formulation development, technology transfer , and scale-up activities for regulated and semi-regulated markets . Key Responsibilities: Execute and support formulation development and scale-up for OSD products Conduct technology transfer from R&D to production Prepare and review MFC, MFR, PDR , and tech transfer documentation Develop and optimize exhibit and validation batches Ensure complianc...

PDR . ; SOPs.; CHANGE controls, deviations , incidents ; Master formula card, drug excipient study reports ; regulatory and customer audits. .Apply the Test Licenses and Narcotic-related licenses. Provident fund

Role & responsibilities: Formulation development Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Pre-formulation studies lab formulation development trials of solid oral Literature survey, to design strategy for the formulation of the projects Day to day execution of the planned batches in laboratory Technology transfer activities to production Required Candidate profile email:-sunil@flamingopharma.com

Responsibilities: * Conduct formulation research & development. * Collaborate with R&D team on new product launches. * Develop protein-based food products. * Optimize food processing techniques. Food allowance Annual bonus

Job Description Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will...

Role & responsibilities 1. Performing Stability analysis, Method transfer and Method Validation. 2. Develop formulations for solid oral dosage forms (Tablets, Capsules) with expertise in compression, granulation, coating, OSD, and formulation development. 3. Conduct production monitoring activities to ensure compliance with quality standards. Desired Candidate Profile 4. Strong understanding of tablets, capsules, compression, granulation, coating processes; knowledge of OSD technology an added advantage. 5. Preparation and review of Method Transfer Protocols, Validation protocols and all related protocols, procedures and reports. 6. To carry out analytical method development, method validati...

Job Description: Head of Research & Development (R&D) Location: Pune, India Company: Star Engineers Pvt. Ltd. Position- Head - Research & Development (R&D) Location- Pune, India Experience- 20+ years in R&D, with at least 10 years in a leadership role in automotive electronics Reporting To - Managing Director / CTO / CEO Industry Preference - Automotive, Electronics Manufacturing, or Related Industries Educational Qualification - B.E./B.Tech (Electronics/Electrical/Embedded Systems) + M.Tech/Ph.D preferred Travel - Automotive Electronics, APQP, or Mechatronics Employment Type - Full-time, Permanent Travel - Occasional (Domestic and International, for customer/partner collaboration) Role Purp...

* Conduct market research on ingredients & trends * Develop new products through R&D process * Transfer technology from lab to production line * Collaborate with cross-functional teams on formulations * Making Samples as per requirements Provident fund

Job Description: We are seeking a highly motivated and experienced professional for our Formulation and Development team in the R&D department. The ideal candidate will have a strong background in formulating Solid Oral dosage forms (OSD), Liquid orals, Semi solid or Topicals and experience in product development, scale-up, and technology transfer . Key Responsibilities: Literature review and Patent search Preparation of master formula card, Qbd product development report & other protocols. Design and develop formulations for new and existing pharmaceutical products. Conduct pre-formulation studies and compatibility testing. Execute lab-scale and pilot-scale batch manufacturing. Coordinate w...

Responsible for managing & operating all testing Labs & achieving revenue from all labs as defined by the management Responsible for implementation of quality policy throughout the labs Reviewing the contracts for new test methods as per the company norms Effective coordination with internal teams and other operational department or labs Ensures all lab staff have adequate resources to perform all aspects of work required Ensures all lab staff are adequately trained to safely perform all required job functions and that competency records are maintained Ensures corporate policy & procedures in the laboratory Provides employee motivation and champions the quality system, including, calibration...

Key Responsibilities: Lead cross-functional project management activities across Quality, Regulatory, different R&D ancillary functions, and manufacturing sites. Be a bridge between development teams, QA, RA, and other key departments. Coordinate development and tech transfer projects and ensure timely completion of tasks. Identify and resolve plant/site-related issues efficiently. Ensure project timelines and quality standards are met. Ideal Candidate Profile: 6-10 years of relevant experience in pharma project management. Strong communication and stakeholder management skills. Proven ability to multitask and drive teams towards results. Relevant technical exposure to QA/RA/R&D functions is...