241 Osd Jobs - Page 9

Company: Strides Pharma Department: IPQA Profile: - Executive Office Locations: KRSG Plant, Bangalore Qualification – B. Pharmacy/ M. Pharmacy Experience – 2 to 6 years (Must have exposure to OSD) Job Description: • To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing. • QA overview for clean room behaviour and aseptic activity. • Review of batch processing records. • Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. • Review of documents of respective areas and logbooks for adequacy and completeness. • QA overview for receipt of material from warehouse to production. • IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. • Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records. • Preparation & Review of process validation protocols and reports. • Executing the validation/revalidation activity in the absence of authorized person. • Any job activity assigned by HOD • Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA Competencies: • Execute IPQA Excellence by setting clear benchmarks. • Smart Thinker and displays smart/ tactical moves & mental agility. • Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past. • Comes up with ideas which are different and can be used commercially, profitably and growth. • Support and guide subordinates by giving appropriate examples & feedback. Encourage team to come up with new ideas. • Proposes solution which has elements of sustainability.

Job Role : Sr.Manager Production (OSD) Job Location : Poanta Sahib Job Function : Formulations (OSD) Education : Graduate in Pharmacy (B. Pharm) Experience : 15 to 18 yrs Job Summary 1. Manufacturing and Packaging operations of Oral Solid Formulation. 2. Documentation operations of General Solid Oral Manufacturing and Packaging Department. 3. Ensure that Investigations, CAPA, Batch Records preparation completion schedule is prepared, tracked and, execution of schedule as per plan. 4. Review and production approval of documents like: I. Commercial product, stability batches, exhibit batches, characterization Batches - Master Batch manufacturing record and Master Batch Packaging record. II. Risk assessment, process validation protocol, Incident and Investigation report, CAPA Reports. III. Protocols & reports. V. Internal Quality Audit, Regulatory Quality Audit Compliance. VI. Change control, Standard Operating Procedure, and other documents including amendments. 5. Provide leadership and expertise to ensure achievement of production with respect to Quality outputs and commercial demands. 6. To ensuring that there are appropriate manufacturing and technical processes and procedures in place for the production. 7. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. The production records are evaluated and signed by a designated person. 8. In coordination with Quality head monitor the factor that may affect product Quality compliance of GMP, retention of records. 9. To approve the instructions relating to production operations, including the in-process controls, and to ensure their strict implementation. 10. To check the maintenance of the department, premises and equipment. To ensure that the appropriate process validations and calibrations of control 1. equipment are performed and recorded and the reports made available. 2. To ensure that the required initial and continuing training of production personnel for SOP, cGMP, personal hygiene are carried out and adapted according to need. 3. Optimization of the resources like men, materials and machines in manufacturing and packing area. 4. Ensure efficient collaboration and co-ordination between relevant departments like Warehouse, Engineering, PPIC, Quality Control, Quality Assurance, procurement and management. Supporting Compliance of internal quality/corporate quality/regulatory audit. Planning & execution of various activities viz. Gap Analysis, enhancement, SOPs, protocols and reports etc. To perform Risk Assessment with respect to investigations, internal / regulatory observation response, market complaints and for system improvements etc. 8. To co-ordinate with FDD, PDD (R & D) /MSTG for execution of trial/exhibit /Process validation batches and trouble shooting. 9. Procurement of New Suitable Equipment's required for process as per cGMP requirements. 10. Identify and implement improvements to the production process, yield. 11. To ensure protection of the product from contamination. And monitor quality standards of products. 12. Shall delegate authority to deputed deputies with satisfactory level of qualification and experience. 13. Coach and develop direct and indirect reporters through on going, example based performance feedback, annual performance reviews and provision of training and development opportunities. 14. Assure all time readiness department for regulatory agency inspections/internal audits and appropriate implementation of corrective actions regarding observations made by the agencies and internal audit teams. 15. Shall participate in Internal Quality Audit. 16. Responsible for ensuring market complaints, failures deviations are investigated and corrective and preventive actions are implemented as per set timeline. 17. Performs all work in support of our Corporate Values of pride- Humility, Integrity, passion and with accountability and diligence. Perform all work in accordance with all established regulatory and compliance and EHS requirements. Reporting Manager Comments

Jr. Officer - Plant Maintenance: Educational Qualification - D.E.E / D.M.E (Only diploma holders must apply.) Experience - 02 - 04 years in pharmaceutical manufacturing machine maintenance Job Responsibilities - 1. Day-to-day maintenance of manufacturing filling and Packaging machines used in formulation facility. troubleshooting, and repair of pharmaceuticals plant machinery, preferably hands on experience about ointment tube filling machines, liquid filling, labelling with OCR system and other packing machines like cartonators, check weighing machines, blister & strip packing machines etc. 2. Manufacturing machines like O intment Manufacturing vessels, Bottom entry agitators, RMG, FBD Compression machines and allied manufacturing machines like metal detectors dust extractors de - dusters counting machines washing machines and slat conveyor belts. 3. Diagnose and troubleshoot equipment malfunctions effectively and efficiently. 4. Optimize equipment performance to maximize output and minimize downtime. 5. P reventive and predictive maintenance on assigned equipment, recording data in log books and planners and schedules. 6. In addition to this added knowledge about utilities like boiler and AHU systems will be preferable.

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

Unison Pharmaceuticals is urgently seeking talented Production Supervisors for our OSD Production team. Apply now to become a part of our team!! Experience: 2-6 years Job Role : 1) Compression Supervisor 2) Granulation Supervisor Designation: Officer / Sr. Officer / Executive Qualification: B.Pharma/M.sc Location: Moraiya, Ahmedabad. No. of Openings : 3 Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career. Regards HR department

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-10 Yrs Job Location: Pashamylaram - Patancheruv Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

Role & responsibilities *Operate and maintain tablet compression machines, ensuring they run efficiently and produce tablets that meet quality standards. * Monitor the compression process to ensure tablets are produced according to specifications, conducting regular checks for weight, thickness, and hardness. * Identify and resolve any mechanical or process issues that arise during production to minimize downtime and maintain productivity. Preferred candidate profile ITI / Diploma or Graduate with 2-8 years of experience Perks and benefits Relocation allowance Travel allowance Initial accommodation Virtual Interview (Online Interview)

Job Title: Manager-Plant Maintenance Block A Position: Manager-2 Job Grade: G11A No. of Direct Reports (if any): 09 Function: Engineering & Projects. Location: Dadra Areas of Responsibility 1. To ensure 100% Maintenance of all Plant Machinery process Equipments (Granulation equipments-FBD, FBE, RMG, Blender, Tablet compression machine, Tablet Coating machines, Blistering machine, Cartonating machines, Packing Bottle machines, Inspection machine etc.) & its relevant. Ensure minimum time for the breakdown to be achieved 2. To ensure technician & staff deputed at breakdown, preventive & building maintenance works accordingly as per approved shift schedule. 3. To ensure the timely completion of the work orders, purchase orders & purchase requisition & ensure the work measurements are proper and timely bill booking & approval from the Block Head. 4. To involve & support in the modification/ongoing CAPEX as well as projects works for the right implementation of the equipment to ensure right & easy maintenance of the same in future. 5. To ensure the services vendor at site & loading/unloading, fabrication & civil works are carried out as per the GMP norms with safety norms also. AMC if any should be inline as per schedule. 6. To train the people & people management & ensure all have to trained in LMS system as well as applicable OJT in place as per the requirements. 7. To ensure Preventive maintenance & Breakdown maintenance program through SAP system. All records & schedule should be traceable as per SOP. 8. To handle all the stakeholders for their works & timely maintenance solution to each with defined timeline. 9. To coordinate with EHS Department for statuary complies & ensure the safety maintenance. 10. To ensure the critical spares/inventory/hardwares to be available for the maintenance purpose. 24x7 shift management & availability of the manpower’s for the maintenance & rectification works. 11. Implementation of Good Engineering Practices, Good Manufacturing Practices, Data integrity and Good Documentation Practices should be followed & no any noncompliance. 12. To Co-ordinate the internal engineering cross function section like utility, calibration & water system for getting the rectification & timely works completion relevant to process equipment/APU. 13. To prepare the investigation, root cause identification and derive CAPA in case of incident of system failures/out of specification observation and request change control, action item through Track wise (QMS) system. 14. Handling of EDMS, LMS, track wise accordingly & input to be done for the smooth system handling & documents handling accordingly. 15. Co-ordinate for the self-inspection/visit/audit at site & ensure proper walkout for the same while inside the premises/ process equipment area. 16. To handle observations & ensure timely compliances of observations/points same within timeline. 17. To handle the vendor/OEM as per requirements & ensure the GMP compliances accordingly. 18. To ensure all required drawings/layouts of AUTO CAD generated & approved . Status label, record shall be in place & current updated version of the SOP. Drawings/layouts regarding plant equipment & APU system Job Scope Internal Interactions (within the organization) All departments stakeholders External Interactions (outside the organization) External service vendor like fabrication, building maintenance vendors etc. Geographical Scope Any. Financial Accountability (cost/revenue with exclusive authority) To run the maintenance as per defined budget & control the inventory Job Requirements Educational Qualification B.E. Electrical (Preferably). Specific Certification Should know AUTO CAD, PCS system knowledge & Projects skills will add advantages. Skills Good trainer on SOPs, Good mentor to technical staff Experience 10-15 Years.

Strides Pharma is conducting walk in interview on 23rd Mar 2025 (Sunday) in Bangalore for below positions. Department: Packing Qualification: B.Pharm/M.Pharm Work Location: Bangalore Experience: 2-5 years in Oral Solid Dosage Key Responsibilities Planning and execution of batch packing activities such as Dispensing & Line clearance. Expertise in handling Blister, Bottle and Sachet packing machineries like BQS, CAM, Maspack, Auto Cartonator etc. Handling of QMS activities like Change Control, Deviation, OOS, OOT, CAPA etc. Department: Maintenance Engineering Qualification: Diploma/B.E/B.Tech (Mechanical/Electrical/Instrumentation) Work Location: Bangalore Experience: 2-7 years Key Responsibilities Responsible to conduct Preventive Maintenance and Breakdown Maintenance of production and packing equipment's like Fluid bed driers (FBD), Compression machines, Coating machines, Blenders, Rapid mixture grinders (RMG), Capsule filling machines, Blister packaging, Bulk counting lines, Sachet filling lines, Serialization equipment's, inspection systems. Troubleshooting knowledge of PLC, HMI, IPCs, SCADA systems. Knowledge on Digital platform SAP & TrackWise to handle PM/BD and QMS documents. Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

Roles and Responsibilities Ensure primary packaging material meets quality standards. Perform blister packing operations according to SOPs. Conduct bottling activities with precision and efficiency. Manage secondary packaging processes effectively. Maintain accurate records of production data.

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

Role & responsibilities Analytical Development Laboratory (ADL) Position: Executive Experience: 03-08 Years Qualification: M.Pharm / M.Sc Job/ Skill Set HPLC/GC/IC method development, feasibility, verification, equivalency, validation for API, complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis Dissolution development, comparative dissolution, multimedia dissolution and statistical evaluation and report preparation Good understanding and hands on experience of analytical instruments like HPLC,IC, GC etc. NI/GI & NDSRI with LCMS/GCMS expertise, Solid state characterization and API sameness study Hands on experience on in-vitro Studies, E&L, Solid State characterization, IVPT/IVRT, Impurity characterization, sameness study Welversed with USP/EP/BP/IP and various current regulatory guidelines (ICH/EMEAVFDA) Pertorm maintenance and calibration of lab instruments / equipment Contact Details: Email : nitinsingh@torrentpharma.com, devalmodi@torrentpharma.com, vilshashah@torrentpharma.com

Job Title: Research Scientist - P.HD (Formulation-OSD) Location: Dholka (Ahmedabad) Experience: 2-3 Education: M.Pharm + P.HD Job Description To develop Stable & Bioequivalent for solid oral products for Europe, ROW & Domestic Markets. Technology transfer of developed products to plant level, this includes all TTD-related works. To collect and compile all data and submit to respective regulatory agencies. To address DCGI/ regulatory agency queries as per requirement. To extend support to plant for any commercial trouble shooting. Interested candidate can share there CV on disha.bhalani@cadilapharma.com

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 department for getting forms and logbooks 4. Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments 5. Coordination and participation of internal department audits / sponsor or client audits 6. Coordination with purchase/sourcing department for procurement of materials 7. Participation in qualification of equipments/instrument pertaining to the department 8. Compilation, interpretation and review of analytical results and stability data 9. Submission of documents and coordination with liaison personnel for procuring required licenses for carrying out the development work 10. To initiate the project and allot the product identification codes 11. Preparation of Master formula card (MFC), scale up BMR, process evaluation plan, exhibit batch protocols, stability protocol, Dissolution profiling report, Assessment report, Tablet sub division study summary report and all documents related to Formulation development. 12. To drive all concerned documents from formulation development to exhibit batches and then to commercialization through document management system. 13. Coordinate to prepare the specifications for raw materials, in-process and finished product. 14. Preparation of product development reports (PDR) 15. Preparation of summary reports for exhibit and process evaluation batches. 16. Initiation of Change controls. 17. Initiation of document/ mandatory revision/withdrawal control form. 18. Initiation of departmental incidents. 19. Conducting departmental trainings. 20. Calibration of instrument/equipment pertaining to the department. 21. Preparation and processing of department SOPs/Guidelines/Operating instructions. 22. Preparation of summary reports for exhibit and process evaluation batches Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

Roles and Responsibilities Manage process engineering activities for OSD (Oral Solid Dose) injectable products, ensuring compliance with regulatory requirements. Lead a team of engineers to design, develop, test, and commission electrical systems for sterile manufacturing facilities. Collaborate with cross-functional teams to ensure smooth operation of production lines and maintain high-quality standards. Develop and implement process improvements to increase efficiency, reduce costs, and enhance productivity. Ensure effective communication among team members, stakeholders, and senior management.

Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have in depth knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 8 to 15 Years

Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

Role & responsibilities : In process activity in production and packing area, Perform Line clearances activities as per defined instruction in SOP , Continuous monitoring of GMP and cGMP compliance at shop floor, Perform calibration of IPQA instrument on time. Issuance, review and control the change management activities i.e. implementation, post implementation review and proof verification. Preferred candidate profile : Must be B. Pharm Fresher (2024 Batch) Perks and benefits : Stipend : 2,20,000/- LPA

Roles and Responsibilities Develop and implement training programs to enhance employee skills and performance. Conduct Training Needs Identification (TNI) and Gap Analysis to identify skill gaps in employees. Design and deliver soft skills training sessions, including communication, leadership, teamwork, time management, etc. Collaborate with stakeholders to develop customized learning solutions for specific business needs. Monitor the effectiveness of training programs through evaluation metrics such as ROI analysis.

Literature search, preformulating studies, RLD characterization. Planning and execution of lab scale batches, recording the detailed observation of trials in laboratory notebook. Initiation of stability study and data compilation. Understanding and knowledge of process flow of solid orals. (Tablets , capsules) Involve in the all studies required for the different regulatory bodies formulation techniques such as wet granulation , direct compression, top spray granulation . Co-ordination with cross functional department to work for timely product development.

-We are looking out candidates for different sections and positions in Quality Assurance department. Such as IPQA, QMS, Lab QA, AMV QA. Interested candidates can share their resumes on a.salunkhe@v-ensure.com & n32admin@v-ensure.com Role & responsibilities 1) IPQA - In process Checks. - Line clearance - Review of BMR, BPR 2) QMS - Handling and review of Change control, deviations, CAPA of different departments. - Document issuance, archival, retrieval. - Facing the Audits. 3) Lab QA & AMV QA - Managing Analytical QA activities. - Review of documents related to QC i.e. Raw material, finished products, stability. - Review of documents of Method validation, Assay. Preferred candidate profile - Candidates must have experience in Pharma formulation plant. - Must have good communication skills. - Candidates from Regulatory plant will be given preference. - Immediate joiners will be preferred. Perks and benefits Best in the industry

• Responsible for Defining and Implementation of Quality Management system and Quality Assurance processes across OSD and CMO/ CRO locations. • Ensuring compliance with all cGMP requirements in line with global and Indian regulatory requirements • Handling all Regulatory audits, Client Audits, Internal Audits • Responsible for Qualification /Audit of CxP Vendors and CxP service providers • Responsible for GxP Training • Responsible for providing all documentation and other necesary support for Regulatory for product registrations and life cycle management • Responsible for providing all documentation and other necessary support for Business / Marketing, Customers • Responsible for management of Deviations, OOS, Complaints, Changes, Qualifications, Validations • Responsible for Licenses, Certifications and compliance (Indian FDA / CDSCO)

About The Role : Experience in designing, implementing, and managing SCCM and Intune solutions. Strong understanding of endpoint management concepts, including device provisioning, software distribution, patch management, and security. Experience with Microsoft Endpoint Manager (SCCM and Intune) integration, configuration, and administration. Familiarity with modern management concepts, such as cloud-based management, autopilot, and zero-touch deployment. Experience working with PC/Mac infrastructure as an engineer level SCCM & Intune Certification Experience with system provisioning and imaging using tools such as DEP and SCCM. Experience with managing 802.1x on MacOS/Windows (for wifi and wired network connections). Experience with end point management client software deployment (SCCM + Intune), inventory, antivirus and end point security solution Familiarity with configuration profile and working with preference files (.plist) Experience with Azure/AWS Network troubleshooting Background in server administration, networking, troubleshooting, scripting, automation Experience with Active Directory including user and group management, group policies Experience with desktop operating systems including Windows 10/11 and OS X Scripting via PowerShell, BASH, and others Excellent analytical, problem-solving, and communication skills. Primary skills SCCM Intune OSD Secondary skills Azure AWS Active Directory

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.

Roles and Responsibilities Conduct pilot plant scale up activities to commercialize new products. Ensure successful transfer of technologies from lab to production scale. Develop formulations for solid oral products using OSD technology. Troubleshoot issues related to formulation development and scaling up. Collaborate with cross-functional teams for tech transfer projects.