2048 Formulation Jobs - Page 2

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries....

Roles and Responsibilities Should Have Formulation Experience. 1. Responsible for product registration in ROW (AFRICA, ANZ, ASIA, LATAM, CIS &, MENA). 2. Responsible and involving in the regulatory audits and coordinating with the auditors/customers. 3. Preparation, compilation and review of dossiers for RoW region in CTD /country specific format. 4. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. 5. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. 6...

Role & responsibilities Responsible for handling of CMO projects of solid orals and injectable products from project initiation to commercial launches Responsible for handling of site transfer projects that and will be SPOC for all projects that will be executed at CMO Responsible for preparation of project tracker and monitoring of project timelines as per set milestones Responsible for handling of activities related to new product launches from CMO sites for US/EU & Canada territories Should be able to coordinate with QP labs for method transfer activities and commercial releases Should be able to coordinate between customers, internal cross functional teams and CMO partners for project ac...

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries....

Roles and Responsibilities Should Have Formulation Experience. Having vacancies in RoW (ASIA , MENA, LATAM, AFRICA) Regions Responsible for product registration RoW (ASIA , MENA, LATAM, AFRICA) Regions region Preparation, compilation and review of dossiers for region in eCTD/CTD/country specific format. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. Responding to queries with in the time lines receive...

Role & responsibilities CMC and Labelling: Preparation of ANDAs in eCTD format for various type of formulations Review of the technical documents such as Specifications, BMR, MFC, Able to work on All type of CTD section write-ups Hands on experience on life cycle management activity (AR, CBE, CBE-30 and PAS) Through knowledge on ICH guidances Should able to handle Module -I related activities Able to review Drug substance DMF and should prepare a due diligence eCTD Related activities: Complete knowledge on eCTD related publishing activities Practical knowledge on PDF attributes such as book marking, intra inter hyper ink, file destination TOC’s etc., should adhere to FDA published latest gui...

Job Summary We are seeking a highly motivated Formulation Development professional with 37 years of experience to support formulation development activities for oral solid and liquid dosage forms. The role involves working in a CRO/CDMO environment, supporting multiple client programs including big pharma and innovative companies, with a strong focus on scientific rigor, minimal-intervention clinical batch manufacturing, and effective cross-functional communication. Key Responsibilities 1. Design, develop, and optimize oral solid dosage forms (IR, MR, modified release) and oral liquid formulations for preclinical and clinical studies. 2. Execute formulation development, scale-up, and clinica...

Handle procurement of raw & packaging materials for pharma formulations (Tablets, Liquids, Ointments), vendor management, negotiations, inventory control, GMP compliance, and coordination with Production, QA, QC & Finance. Required Candidate profile Pharma Purchase professional with 8–10 yrs experience in sourcing raw & packaging materials, vendor management, price negotiations, inventory control, ERP exposure, and GMP compliance.

JOB DESCRIPTION Job title (Manager/ Sr. Manager-Pharmacy) (Lucknow) MAX OVERVIEW: Max Healthcare Institute Limited (MHIL), founded in 2000, is one of India’s largest private hospital chain with 22+ healthcare facilities. Being the India's most valuable listed healthcare organizations, we have driven innovation and excellence in healthcare for 25 years. With a workforce of 35,000+, including 5,000+ clinicians and 12,000 nurses/paramedics, we deliver advanced care across key locations including Delhi NCR (Saket, SMART, Patparganj, Vaishali, BLK, Shalimar Bagh, Dwarka, Gurugram, Panchsheel Park, Noida) Mumbai, Mohali, Bathinda, Dehradun, Lucknow, and Nagpur. We also operate Max@Home–among India...

Officer/Sr.Officer in IPQA Qualification: B Pharm/M Pharm Required Candidate profile Experience-:-1 to 3 years experience into IPQA hiring for leading pharma company near vadodara

responsible for monitoring stock levels, ordering supplies, coordinating shipments, and maintaining accurate inventory records, ensuring that stock levels are always optimal to meet business demands.

Immediately required for reputed Pharma Industry @Pardi, Valsad Post: Purchase Trainee Qual: MBA in Supply Chain Management Exp: Fresher or 01 Yrs Salary: As per candidates Ms Nimitha 9662780300 & Whatsapp

Dear All, We are seeking a highly motivated and talented Formulation R&D Scientist to join our innovative team. The ideal candidate will have a strong foundation in formulation development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 6-8 Years Job Responsibilities: 1. Plan and execute Pre-formulation and formulation activities and ensure the timely execution of project related tasks in coordination with team members. 2. Actively participate in the literature search and preparation of formulation development strategy. 3. Coordinate with QA departm...

Responsibilities: Responsible for developing new features and functionality for the various mechanical and chemical processes. Primary responsibility includes mathematical model formulation, implementation on simulation software. This includes but is not limited to developing/maintaining library of process unit operations in steady state, transient & simulation utilities on the tools. Responsible for delivering top notch quality product. Be part of entire product development life cycle: idea inception, application/feature design, implementation adhering to coding standards, test, and address customer feedback. Responsible for interfacing with relevant Internal and external stakeholders throu...

Job Summary: Responsible for smooth technology transfer from R&D to manufacturing. Key Responsibilities: Coordinate tech transfer activities for new products. Prepare and review TT documents and protocols. Support scale-up, validation, and trial batches. Liaise with R&D, QA, QC, and production teams. Ensure compliance with regulatory requirements. Support audits and regulatory submissions. Qualifications & Skills: B.Pharm/M.Pharm with 5-8 years experience. Strong knowledge of formulation and process transfer.

Responsibilities: Responsible for developing new features and functionality for the various mechanical and chemical processes. Primary responsibility includes mathematical model formulation, implementation on simulation software. This includes but is not limited to developing/maintaining library of process unit operations in steady state, transient & simulation utilities on the tools. Responsible for delivering top notch quality product. Be part of entire product development life cycle: idea inception, application/feature design, implementation adhering to coding standards, test, and address customer feedback. Responsible for interfacing with relevant Internal and external stakeholders throu...

Huron is a global consultancy that collaborates with clients to drive strategic growth, ignite innovation and navigate constant change. Through a combination of strategy, expertise and creativity, we help clients accelerate operational, digital and cultural transformation, enabling the change they need to own their future. Join our team as the expert you are now and create your future. Huron is a global consultancy that collaborates with clients to drive strategic growth, ignite innovation, and navigate constant change. Were seeking a Data Science Manager to join the Data Science & Machine Learning team in our Commercial Digital practice, where youll lead advanced analytics initiatives that ...

COMPETENCIES Proven experience in strategic planning, business development, and market analysis. Strong analytical and problem-solving skills. Excellent leadership and team management abilities. Effective communication and interpersonal skills. Proven ability to drive revenue growth and achieve business targets. Knowledge of industry trends and competitor dynamics. Results-oriented with a focus on achieving measurable outcomes. >Science graduate, MBA preferable > Minimum 10 - 15 years in sales & business development. >Should have the prior experience of handling Sales in concerned entire zone. >Strong people management skills should have handled a large team in prior experiences. Lead the na...

experience in quality management roles within the mineral industry or Bentonite, Limestone, Clay dolomite, etc. Thorough understanding of quality management principles, methodologies, and tools.Research and Development, Quality Control and Assurance. Required Candidate profile has exposure in the R&D department. having strong technical skills. having strong experience in the Industrial minerals sector.

Key responsibilities: Oversee daily operations, manage personnel, and provide technical and strategic direction for the QC department. Develop, implement, and maintain quality control systems and ensure all processes adhere to company standards and regulatory requirements. Supervise the analysis of raw materials, in-process samples, finished products, and stability samples. Review analytical data, protocols, and reports. Thorough knowledge in handling all analytical instruments, analytical methods, HPLC, method validation and method development. Ensure strict adherence to GMP, GLP, and Good Documentation Practices (GDP). Prepare and review various documents, including standard test procedure...

Division Department Sub Department 1 Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Perform unit operations as per SOP and unit processes as per batch manufacturing record Optimize the utilization of available resources for achieving production in shift Maintain equipment, facility and block premises as per SOP for audit readiness Key Accountabilities (2/6) Provide suggestions for optimization of processes to manufacture quality product Identify the deficiency in area and errors in documen...

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other sup...

Role Overview: You will be joining a dynamic team at Swarna Fertilizer and Chemical Private Limited, a leading manufacturer and importer of Agro Chemical Technical and formulations, including Pesticide, Fertilizer, and Bio Stimulant in the Agro-Chemical Industry. Key Responsibilities: - Formulate and ensure quality control of agro chemicals and fertilizers such as Pesticide, Biostimulant, Micronutrients in various forms like EC, SC, WDG, WP, CS, ZC. - Analyze raw materials and finished goods according to ISO specifications using equipment like HPLC, GC, AAS, UV, Tritation, PH Meter, etc. Qualifications Required: - M.Sc in Chemistry - Minimum 1-3 years of experience in formulating agro chemic...

Division Department Sub Department 1 Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Perform unit operations as per SOP and unit processes as per batch manufacturing record Optimize the utilization of available resources for achieving production in shift Maintain equipment, facility and block premises as per SOP for audit readiness Key Accountabilities (2/6) Provide suggestions for optimization of processes to manufacture quality product Identify the deficiency in area and errors in documen...