45 Capsules Jobs - Page 2

Roles and Responsibilities 1. Review of Technology data package and preparation of Gap analysis document. 2. Preparation of technology transfer protocol and report. 3. Co-ordination with FD for smooth Tech Transfer. 4. Monitoring of validation batches at production site. 5. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. 6. Review of MPCR and protocol. 7. Planning for Execution of Process design, Process qualification batch. 8. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. 9. Should be part of handling deviation, change control and failure investigations. 10. Process manufacturing parameters for Qualification batches Vs Commercial batches. 11. Preparation and reviewing of intended batch documents for regulatory submission. 12. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products.

Roles and Responsibilities Granulation: Operate and maintain granulation equipment (e.g., high shear mixers, fluid bed dryers). Perform wet and dry granulation processes, ensuring uniformity and consistency in batches. Monitor parameters like moisture content, particle size distribution, and granule flow properties. Compression: Operate tablet compression machines to produce solid dosage forms. Monitor compression parameters such as hardness, thickness, weight, and friability. Troubleshoot and adjust compression equipment to optimize production. Coating: Oversee the tablet and capsule coating processes, ensuring proper application of film coatings. Work with coating machines like pan coaters and fluid bed coaters. Monitor and control coating parameters such as spray rate, drying time, and temperature. Capsule Filling: Operate capsule filling machines to ensure accurate dosing of powder or pellets into capsules. Perform checks for capsule fill weight and ensure proper capsule sealing. Troubleshoot issues related to capsule filling, such as jammed capsules or weight discrepancies. General Responsibilities: Ensure all equipment is functioning properly and safely, adhering to preventive maintenance schedules. Maintain a clean and sterile environment in compliance with Good Manufacturing Practices (GMP). Perform in-process quality control checks to ensure that the products meet specifications. Document all activities, including batch records, machine logs, and quality checks in accordance with regulatory requirements. Collaborate with quality control and engineering teams to identify and resolve any production issues.onitor and control process parameters to ensure quality products meet specifications. Maintain accurate records of production data and perform routine maintenance tasks on equipment. Collaborate with team members to achieve daily targets and improve overall productivity. Ensure compliance with Good Manufacturing Practices (GMP) guidelines.

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.

We have been hired by a highly reputed and fast growing Pharma company to hire a "DGM - Formulation & Development' to be based at their plant located at Aurangabad . Details of the position are mentioned below: Role & responsibilities: Literature search/study and to prepare development trials strategies. Pre formulation study execution. Market/Innovator/reference product characterization. Execution and documentation of trial batches for prototype formulation development. Execution and monitoring of development stability studies. Execution of process optimization/scale-up batches. Technology transfer activities at site. Preparation/review of documents like BOM, MFR, compatibility study protocol & report, stability study protocol and report, PDR, etc as per requirements. Co-ordination with production, other relevant cross-functional departments/teams. Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc dosage forms aimed for ROW and domestic market. Should possess experience in handling various equipment like RMG, FBD/FBP, compression machine, roller compactor, coating machine, etc. Preferred candidate profile : Educational Qualification: M. Pharm Experience: 12 - 20 Years of relevant experience in a leading Pharma Company. Good Communication & Presentation skills Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak Director, Pharma Placements Inc. Mobile number: 98202 34987

Role & responsibilities 1. Product Strategy & Lifecycle Management: Develop and implement strategic product roadmaps for OSD products in alignment with business objectives. Conduct market research and competitive analysis to identify trends, opportunities, and threats. Manage the product lifecycle from development to commercialization, ensuring alignment with customer and regulatory requirements. 2. Business Development & Customer Engagement: Collaborate with the sales and business development teams to identify and engage potential clients. Support contract negotiations, pricing strategies, and proposals for new business opportunities. Serve as the key point of contact for clients, addressing their technical and commercial inquiries. 3. Project & Cross-functional Coordination: Work closely with R&D, manufacturing, regulatory affairs, and quality assurance teams to ensure seamless product development and commercialization. Drive project timelines and ensure deliverables are met within budget and compliance parameters. Facilitate internal and external stakeholder communication to optimize project execution. 4. Regulatory & Compliance Oversight: Ensure all OSD products comply with global regulatory requirements (FDA, EMA, MHRA, etc.). Stay updated on evolving regulatory landscapes and provide guidance to internal teams and clients. Support dossier development and regulatory submissions for product approvals. 5. Financial & Performance Metrics: Monitor product performance, profitability, and cost-effectiveness. Track KPIs and generate reports on sales, market trends, and operational efficiency. Identify opportunities for cost optimization and revenue growth. Preferred candidate profile Bachelors or Masters degree in Pharmacy, Life Sciences, Chemistry, or a related field. MBA is a plus. 6+ years of experience in product management, business development, or project management within a CDMO, pharmaceutical, or OSD manufacturing environment. Strong understanding of formulation development, tech transfer, and regulatory requirements for OSD products.

Role & responsibilities To review and understand technology of product from R&D scientist and coordinate, plan activities with all concerns personnel/ dept. for successful transfer of the products, Monitor tech transfer at site and update documents. To review and understand technology of product from CRO and coordinate, plan activities with all concerns personnel/ dept. for successful transfer of the products, monitor tech transfer at site and update documents. To resolve manufacturing issues/trouble shooting batches at manufacturing sites for the products which are commercialized. Monitoring of redeveloped formulations for quality improvement at manufacturing site. To develop new products as per requirement from business development team which involves pre-formulation studies, competitor product evaluation, prototype formulation development and stability batches manufacturing, stability charging and monitoring, preparation of R & D dossier etc with satisfactory stability studies. To work on quality improvisation and redevelopment projects at R & D To revise technical documents like MFR, FP Specifications after validation batches for changes, if any. To check/verify the documents like Process Validation Protocol and Process Validation Summary Report, APQR. To maintain and follow organizations rules and regulation. Preferred candidate profile 2 - 5 Years of experience in R & D. Qualification: M. Pharm | B. Pharm Specific Skills: Experience of technology transfer from R & D to manufacturing site, should have work on multiple projects in parallel. Should have experience of new product development for solid, semisolid and liquid dosage forms. Perks and benefits Company bus service.

Role & Responsibilities: Head of Procurement for Finished Formulations Role: We are seeking an experienced leader for our procurement department specializing in finished formulations. This role demands expertise in the pharmaceutical industry, particularly in purchasing finished formulation products, and the ability to manage relationships with manufacturers and CDMOs effectively. Responsibilities: - Oversee and manage the procurement process for finished formulations, ensuring timely and cost-effective acquisition. - Build and maintain strong relationships with Contract Development and Manufacturing Organizations (CDMOs) involved in finished formulations. - Ensure thorough understanding and application of Certificates of Analysis (COA) to verify product quality and compliance. - Generate and manage purchase orders accurately, adhering to company policies and standards - Lead the procurement team, providing guidance and support to ensure departmental goals are met. - Address and resolve procurement challenges, including supply chain issues and vendor-related problems. - Negotiate favorable terms and rates with vendors and CDMOs to optimize cost and value. - Monitor market trends and industry developments to inform strategic procurement decisions. - Ensure all procurement activities adhere to regulatory standards and company policies. - Prepare and present detailed procurement reports to senior management, highlighting key metrics and performance indicators. - Work closely with other departments to align procurement strategies with overall business objectives. - Develop and implement strategies for procurement that support long-term business goals and operational efficiency. Requirements: - Proven experience in procurement of finished formulations within the pharmaceutical industry. - Strong relationships with API manufacturers and CDMOs. - Expertise in managing COAs and generating purchase orders. - Demonstrated leadership abilities and effective problem-solving skills. - Excellent negotiation skills and market insight. This role requires a seasoned professional with the ability to navigate complex procurement processes, maintain strong vendor and CDMO relationships, and lead a team effectively. Preferred Candidate Profile : - Over 5 years of experience in procurement for finished formulation products within the pharmaceutical industry. - In-depth knowledge of Certificates of Analysis (COA) and quality standards, with experience in generating and managing purchase orders for finished formulations. - Strong relationships with API manufacturers and Contract Development and Manufacturing Organizations (CDMOs) across India. - Comprehensive understanding of pharmaceutical finished formulations and industry trends. - Up-to-date with current market conditions and pricing for finished formulations. - Strong personality with excellent communication and email writing skills. - Proficient in price negotiation and convincing suppliers and CDMOs. - Capable of handling procurement challenges effectively, demonstrating responsibility and a pragmatic approach. - Ability to manage multiple procurement tasks efficiently and maintain detailed records. - Familiarity with regulatory requirements and adherence to company policies related to finished formulations. - Flexibility to adapt to changing market conditions and procurement needs. Perks and Benefits: - Positive work culture with a supportive and collaborative environment focused on professional growth. - Supportive colleagues and leadership committed to helping you succeed. - Access to timely assistance for any questions or issues. - Genuine and flexible leave policies to accommodate your personal needs. - Attractive incentive programs and performance-based bonuses. - Pathways for advancement, including in-house promotions and performance-based salary increases, without time constraints. - Opportunities to participate in team-building activities and outings. - Comprehensive health insurance coverage for you and your family, up to 15 lakhs. - Complimentary transportation services for convenience in your daily commute.

We are hiring for the following 2 positions: Senior Executive- Quality Control RM Section Head- 5-8 Years of Experience Executive- Quality Control- Analytical Method Validation- 4-6 Years of Experience 1. Senior Executive- Quality Control- RM (Raw Material) Section Head Raw Material Testing and Release: Supervise and ensure the testing of raw materials (active pharmaceutical ingredients, excipients, packaging materials) according to approved specifications. Lead the RM team in the timely testing and release of raw materials for production use, ensuring no delays in manufacturing. Ensure that the testing of raw materials is compliant with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulatory standards. Supervision and Team Management: Lead, guide, and mentor a team of QC analysts in the RM section, ensuring effective training and development. Allocate tasks and manage workload distribution within the team to ensure smooth and efficient operations. Conduct regular performance appraisals, set objectives, and ensure team productivity and morale. Raw Material Specifications and Documentation: Review and ensure the accuracy and completeness of raw material specifications, test protocols, and related documents. Approve the testing methods and ensure compliance with the established standard operating procedures (SOPs). Ensure the proper maintenance of records related to raw materials, including stability studies, inventory control, and release certificates. Compliance and Regulatory Adherence: Ensure all raw materials and testing activities comply with the Indian Pharmacopeia (IP), USP, BP, and other regulatory standards. Ensure that all QC raw material processes are aligned with FDA, EMA, and other regulatory guidelines as applicable. Assist in audits (internal and external), and provide necessary data and reports during regulatory inspections. Equipment and Instrument Management: Oversee the calibration, maintenance, and qualification of equipment used in the RM section, ensuring accurate and reliable results. Ensure that the laboratory instruments and equipment are well-maintained and functioning optimally. Quality Control & Troubleshooting: Address any deviations, out-of-specification (OOS) results, or out-of-trend (OOT) findings related to raw material testing. Investigate and resolve any quality control issues, and recommend corrective and preventive actions (CAPAs). Lead root cause analysis and support the investigation of quality incidents related to raw materials. Vendor Management & Raw Material Supplier Interaction: Liaise with suppliers and vendors to ensure the timely and quality supply of raw materials. Participate in the selection and qualification of raw material suppliers and ensure they meet quality standards. Continuous Improvement and Efficiency: Identify opportunities for process optimization and recommend improvements to enhance operational efficiency. Ensure that the QC RM section continuously adheres to cost-effective practices, reducing wastage and improving turnaround time. Training and Knowledge Sharing: Train QC team members on analytical techniques, equipment usage, and quality control standards for raw material testing. Keep the team updated on industry trends, new regulatory guidelines, and best practices. Executive-Quality Control- Analytical Method Validation (AMV) Analytical Method Validation (AMV) : Conduct validation of analytical methods as per ICH, FDA, and other regulatory guidelines. Perform method development, optimization, and validation for raw materials, in-process materials, and finished products. Ensure adherence to validation protocols and documentation. Testing & Documentation : Oversee the execution of analytical testing for stability, release, and in-process samples. Review and verify analytical data, ensuring accuracy and completeness. Prepare and review validation reports, SOPs, and other related documentation. Compliance & Quality Assurance : Ensure compliance with GMP, GLP, ISO, and other relevant standards in laboratory activities. Support the QC team in audits (internal and external) and address any non-conformities. Ensure proper handling, storage, and disposal of chemicals, reagents, and samples in compliance with safety protocols. Equipment Maintenance : Coordinate with the maintenance team for the calibration and qualification of laboratory instruments. Perform routine checks and calibration of instruments used in testing and validation. Continuous Improvement : Actively participate in continuous improvement initiatives and training programs. Suggest and implement improvements in analytical methods and processes to enhance efficiency. Cross-Department Collaboration : Liaise with R&D, production, and regulatory teams to resolve technical issues. Assist in troubleshooting analytical issues in collaboration with the technical team

Experience in production of Tablet and capsule (Granulation, compression, coating and capsule filling). Issuance of BMR & BPR and QA authorization. Dispensing of Raw Material and Packing Material. Team handling. Documentation and SOP handling.

As an AGM Production in a pharma formulations company, you'll be responsible for : leading and optimizing the production process (planning and execution) ensuring adherence to GMP standards, managing resources, and achieving production targets while maintaining quality and cost effectiveness Responsible for: Technical Operation, Production, planning, vendor development with follow up, costing, projects management, quality, installation and expansion of operations Achievement of Production planning and accountable to ensure optimal utilization of all resources including manpower, machinery and raw materials Identifying potential bottlenecks and deviations, implementation corrective action to ensure that production targets are met within stipulated time and budget constraints Follow up with various departments for control to ensure smooth operation at the production lines /leading different plant audits Analyzing daily reports to plan further production keeping keen eye on deadlines as well as ensure order delivery as per agreed plan with keen eye on Quality. Implementation of inventory control measures to reduce obsolete stock. facilitating value engineering initiatives at the suppliers end to reduce cost of rejection of suppliers and in process production material. Performing analysis, root cause analysis, best practices for productivity improvement in production, repetitive problems (rework -rejection), Cost reduction and process updating. Preparing strong and reliable MIS reports to Streamline material management, Cost saving, Vendor quality assurance operations for facilitating the decision-making process in liaison with Management Able to handle the production as a Leader and must be good at people management at plant Preferred candidate profile B. Pharma/M, Pharma with minimum 15 years of core experience in production (tablets and capsules- allopathic & nutraceuticals), minimum 5 years at a leadership level at plant Leadership with people management with strong technical expertise Proven ability to work efficiently in both independent and team environments Must be a dynamic and positive as a leader

Department - Quality Analyst Position : Executive / Senior Executive Experience : 3 to 6 Years Qualification : MSc/Bsc/Bpharma/Mpharma Location : Jaipur Experience in Tablet/Capsule/Liquid Oral Formulation. Immediate Joiner Preferred

Job Summary: Walter Bushnell is seeking a Research Associate Formulation with experience in Solid Oral Products to join our R&D team . The candidate will be responsible for formulation development, process optimization, and ensuring regulatory compliance for solid dosage forms. Key Responsibilities: Develop and optimize formulations for solid oral dosage forms (tablets, capsules, granules, etc.). Conduct pre-formulation studies, excipient compatibility tests, and stability studies . Perform process development, scale-up, and technology transfer for new formulations. Prepare and maintain technical documentation, protocols, and reports as per regulatory guidelines. Ensure compliance with cGMP, ICH, and regulatory standards for formulation development. Collaborate with analytical, regulatory, and manufacturing teams for successful product development. Troubleshoot formulation and process-related challenges to improve product stability and quality. Qualifications & Skills: Education: M. Pharm / B. Pharm in Pharmaceutics or related field. Experience: 4-5 years in formulation development of solid oral products . Strong knowledge of cGMP, ICH guidelines, and regulatory requirements . Hands-on experience in process optimization, scale-up, and tech transfer . Proficiency in documentation and regulatory compliance . How to Apply: Interested candidates can share their resumes at akanksha.jaiswal@walterbushnell.com . For further details, you can directly reach out at 7042636289 .

Recruiter Details Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and monitoring standard operating procedure (SOP) and current Good Manufacturing Practice (cGMP). To ensure effective implementation of RFT and Data integrity policy. Maintenance, upkeep of the department, premises and equipment. To maintain discipline in the section To protect product and material against spillage and deterioration Monitoring and Safely operating the machine as per SOP, with minimum rejection & maximum output. Improvement, continuous review and up gradation of existing SOPs & work systems and to ensure their strict implementation. To track execution of cleaning activity of non-product contact/indirect product contact surfaces Discussion of the day-to-day work with Section Head. To Co-ordination with other sections and departments. Check and monitor for cleanliness and environmental conditions of area w.r.t. temperature, relative humidity, differential pressure, microbial control, fly control and AHU handling (SCADA). To ensure that all materials and finished products are stored under the appropriate conditions as per specification and in an orderly fashion to permit batch segregation and stock rotation. To perform study as per various Study Protocol in areas. To perform activities such as Cleaning, Line Clearance, Operation, PPM and Calibration of equipment and area as per roles and responsibilities. To cooperate for investigation of deviations, OOS, OOT and complaints observed as per Standard Procedure. To perform timely entries of data and completeness of Batch Manufacturing Record, Checklist, Logs and Protocols on Issued Documents. To perform activities such as Calibration, Sanitization, Maintenance of DM Store, Inprocess store and Cleaned equipment Area. Maintain and monitor inventory required in Department and Scrap the damaged inventory. To transfer Inprocess and Finished goods to Inprocess store. Checking raw material is dispensed for manufacturing of batches and Issuance of batches for processing of next stage and also ensure Preparatory set up work prior to start of manufacturing activity. To monitor and maintain correct Status labelling of containers, equipments, area and materials. Identification, classification, finding, quarantine and destruction of rejects generated during manufacturing process. Calibration of equipment, instruments and weighing balances and PPM as per schedule and maintaining records of the same. To Operate SAP system, PRAMAAN (E-Log), LMS, Trackwise and Cipdox system based on roles and rights Provided in the application. To involve in the training conducted in the section (Scheduled training, Training on changes, Miscellaneous) and also as per the nominations given by Section Head/ Department Head. Participating in Process Validation and Cleaning Validation in co-ordination with Quality Assurance. Preferred candidate profile Candidate with a B. Pharm full time degree along with minimum 7 years of experience in softgel manufacturing

Role & responsibilities Batch manufacturing must have worked in Beta and cepha section Preferred candidate profile 3years+ experience in OSD-Beta and cepha section face to face interview preferred

Managing the production of tablets. Role and responsibility of Pune and Nigeria tablets manufacturing plant 4 to 5 months in Pune and similarly then in Nigeria. Additional healthy allowances will be paid while of trip to Nigeria Required Candidate profile Applicant should be strong in handling the production of tablets entirely. African regulatory bodies

We are seeking a dedicated Purchase Executive/Senior Executive/ Assistant Manager for our pharmaceutical formulation company. The primary responsibility of this role is the procurement of finished pharmaceutical products from external manufacturers (loan license manufacturers/contract manufacturers) while ensuring appropriate inventory management and timely delivery in line with agreed targets. Job Opening: Purchase Executive/Senior Executive/ Assistant Manager - Pharmaceutical Formulation Company Location: Goregaon, Mumbai Role & responsibilities : 1. Material Procurement: - Manage the procurement of raw materials, including APIs, excipients, colors, coating materials, etc. - Oversee packing materials (Primary foil, cartons, leaflets, glass & HDPE bottles, PET bottles, etc.) and tertiary materials (shippers, BOPP tape, shrink wrap, etc.). 2. Supplier Management: - Conduct the vendor qualification process and manage overall supplier responsibilities. - Update forecasts, place purchase orders, and monitor delivery follow-ups with suppliers. 3. Internal Coordination: - Act as the main point of contact for operational tasks with both suppliers and internal teams. - Participate in internal cross-functional meetings related to operational purchasing issues. - Provide timely information regarding product availability to relevant departments . 4. Support and Development: - Assist the Manager responsible for supplier and category management and development. - Maintain and update product information for purchased products. 5. Purchase Order Management: - Raise purchase orders and coordinate with suppliers to ensure timely deliveries. - Communicate with related departments regarding required materials and services. 6. Experience Requirements: - Candidates should have substantial experience in procurement for pharmaceutical raw materials, packing materials, capital purchases, and spare parts. - Familiarity with APIs, excipients, colors, coatings (raw materials); foils, cartons (packing materials); as well as shippers, BOPP tape, and shrink wraps (tertiary materials) is essential. 7. Vendor Communication and Negotiation: - Communicate with existing and new suppliers for inquiries and quotations. - Conduct price negotiations to ensure efficient acquisition of goods at fair prices. 8. Material Management: - Oversee the placement of purchase orders, follow up with suppliers and transporters for timely stock maintenance, vendor development, and new product development. - Manage rejected materials, including rebooking and coordinating with vendors to ensure material quality. 9. Issue Resolution and Auditing: - Resolve all queries raised by the production plant with timely feedback from vendors. - Conduct vendor audits and maintain records for internal and external audits. Desired profile :- Excellent communication skills are essential. ERP experience is a plus. A Bachelor's degree is preferred. Total work experience of 3-5 years is ideal. Qualification:- B.Pharm or equivalent Graduate, Diploma in Materials Management, MBA in Operations/Supply Chain will be an advantage.

Responsible for the establishment, implementation and maintenance of the Integrated Management System. Ensure Statistical analysis of various initiatives and establish efficacy. Analyze Rejections – take corrective actions & ensure implementation. Required Candidate profile Monitor performance by gathering relevant data and producing statistical reports Knowledge of Standard Deviation, Bell Curve, Time & motion study etc. Basic Analytical & 7 Qc tools. Perks and benefits Highest Monthly Salary, Bonuses, Canteen, Transp.

To receive the patient / customer with a smile and greet them To maintain good relations with customers/doctors To receive and transcribe prescriptions from customers and advise the dosage of medicines to the patients and give counseling if required Required Candidate profile Education : D Pharmacy / B Pharmacy

Production, shift operation, manufacturing of tablets, pharmaceutical products, quality, packing, pharma products. Required Candidate profile B Pharm/ D Pharm with 3 to 8 years exp in Pharma industry, tablets manufacturing industry, ready to work in Thrissur.

In-Process Quality Assurance During Production Activity Including Line Clearance And Sampling At Different Stages Of Processing/Packing As Per Pharma API Review of Master Documents such As BMR / BPR Test Batch Monitoring Process Validation Protocol Required Candidate profile Experience with reputed API or Bulk Drugs Unit Co-Ordinate with Plant QA And RA for PDR related activities To Review Specification, MOA And Analytical Data Good Computer And Communication skill Etc