377 Osd Jobs - Page 9

Interpret medical images such as X-rays, MRIs, CT scans, and ultrasounds to diagnose and monitor various conditions Collaborate with referring physicians to provide accurate, timely diagnostic reports and recommendations for further evaluation or treatment Ensure the appropriate imaging protocols are followed and maintain compliance with safety and radiation regulations Supervise and guide radiologic technologists, review image quality, and ensure accurate patient identification and documentation Stay updated with advancements in radiologic technology and integrate new techniques to improve diagnostic precision and patient car

Job Description Version. no.: The Job Responsibilities of the position holder are : Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for Chemical and Instrumentation (Format No.BDI-QCSG004F19). Analysis of In process, SFG, Finished Goods, Raw material & stability sample, Analytical method validation/Verification, of OSD and LVP as per defined Protocol or procedure and related documentation as per GLP and GMP in time. Responsible for receiving sample and their documentation. Responsible Data entry in SAP. Responsible for sending the sample to outside laboratory and ensure their analysis as per requirement from Outside Commercial Lab as and when required. Calibration of instruments, as and when required. Preparation of volumetric solution, reagent, and test solution, as and when required. Ensuring the timely updation in the documents as per the Pharmacopeial amendments. Responsible for maintaining the resource in the quality control department. To ensure the compliance of the requirement of cGDP/cGDP and Data integrity while performing all activities in the laboratory. Ensuring the Compliance to EPD Global Guidelines. Facing internal and external audits and ensuring compliance. Implementation of GLP / GMP requirements. Coordinating and aligning the practices and procedures in line with the COBC requirements. SOP training in Isotrain of self-train within stipulated time. Any other task assigned by reporting manager. In absence of the position holder, the sub-ordinate Executive / Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working. Signatures _____________ Position holder ______________________ Authorized by JOB FAMILY: Operations Quality t

As a Senior Project Engineer , you play a pivotal role in the successful delivery of complex projects. With a minimum of 10 years of experience, you are responsible for overseeing and coordinating all technical and administrative project activities, ensuring the project objectives are met efficiently and within budget and time constraints. This senior role requires strong leadership and in-depth expertise across multiple project disciplines. Key Responsibilities : You lead the development and management of project plans, schedules, and budgets, ensuring alignment with project objectives and stakeholder expectations. You oversee coordination between engineering, procurement, and construction teams, ensuring all project requirements are thoroughly met. You conduct and oversee advanced technical evaluations, risk assessments, and feasibility studies to guide project decision-making. You monitor and drive project progress, proactively identifying risks and implementing corrective actions to ensure milestones are met. You lead the review of technical documentation, ensuring adherence to industry standards, safety regulations, and company policies. You act as key liaison with clients, contractors, and regulatory bodies, ensuring clear communication and collaboration across all project phases. You provide guidance and mentorship to the project engineering team, fostering a culture of continuous improvement and technical excellence. You mentor more junior project engineers and support their development Project Role: Package Manager Ref.: Project plans and GEMS. The Package Manager (PKM) is the front-line of the supply chain within the project and he/she is responsible to deliver the package to meet project requirements in terms of safety, budget, schedule and quality. The Package Manager (PKM) assumes the role of the Purchaser Representative in the Purchase Order (PO). The main responsibilities are: Serve as the Project Manager for the assigned packages, and act as the primary point of contact with the Supplier. Deliver the package in accordance with all project requirements, ensuring safety, quality compliance, adherence to schedule, and budget constraints. Manage all aspects related to the delivery of the package, including setting up, planning, and managing Package Health Checks. Ensure all project requirements are followed and executed in accordance with the contract, project management plans, and technical specifications. Ensure all relevant technical requirements are known and addressed by maintaining a close relationship with the PKE and the supporting team. Understand the technical requirements of the package by liaising with the Package Engineer (PKE). Developing and maintaining a close relationship with the engineering team to anticipate potential delays or changes. Manage the package interface with the Supplier and ensuring that the activities align with project priorities. Monitor package execution and proactively raising alerts to implement corrective action plans. Report package progress to the Project Management Team throughout the projects life. Control and closing all TQ, TD, NCR, VOR (in liaison with Engineering and Quality when required by PMT) of the assigned package(s). Ensure inspection is properly managed and close out all OWL, SOB, OSD, and Punch list items raised against the package. Prepare for package handover to the Completion/Construction Team, and organize handover sessions timely when applicable. Provide support and participating (if needed) in construction, integration, pre-commissioning, and commissioning activities. Ensure continuous improvement by sharing package best practices and lessons learned. Complete timely package close out of the PO. Qualifications Bachelor s degree in Engineering. Minimum 10 years of experience in project engineering within the oil and gas sector, with demonstrated expertise in large-scale projects. Strong leadership, problem-solving, and decision-making skills. Proficiency in project management tools and methodologies. SBM Offshore N.V. is a listed holding company that is headquartered in

We are looking for a meticulous and experienced Technology Transfer Manager to spearhead the efficient transfer of technology for solid dosage forms at Evertogen Life Sciences . This pivotal role involves overseeing the seamless transition of OSD products from R&D or third-party development to our manufacturing plant, ensuring successful scale-up, unwavering regulatory compliance, and adherence to the highest quality standards. The ideal candidate will champion the preparation and review of critical technical documents, including technology transfer protocols, BMR/BPR, and process validation reports, while actively coordinating with cross-functional teams such as QA, QC, RA, and Production. This role demands a proactive individual adept at troubleshooting technical challenges, participating in scale-up batches, and driving continuous improvement initiatives. If you are passionate about optimizing pharmaceutical manufacturing processes, possess a strong understanding of QbD principles, and thrive in a collaborative environment, we encourage you to bring your expertise to Evertogen and contribute to our mission of delivering high-quality, affordable medications to the global market. Your contributions will directly impact our ability to meet client needs and maintain a diverse product portfolio. Job Details: Industry : OSD Formulation (Pharmaceuticals) Department : Technical Transfer Role : Assistant Manager Tech Transfer Location : Jadcherla Compensation : Up to 15 LPA Experience : 8+ years Employment Type : Full-time Qualification : M.Pharm / B.Pharm / M.Sc. in Pharma or related field Responsibilities: Technology Transfer Execution & Documentation: Lead technology transfer projects for solid dosage forms, ensuring adherence to timelines and quality standards. Develop technology transfer protocols covering critical process parameters and quality attributes. Oversee preparation and review of essential documentation (Technology Transfer Plans, Gap Analysis Reports, Process Flow Diagrams, BMR, BPR, Process Validation Reports). Coordinate cross-functional activities (R&D, Manufacturing, QA, RA) for seamless transfer and scale-up. Monitor process performance, addressing deviations or challenges. Maintain detailed records of technology transfer activities, ensuring compliance and data integrity. Ensure documentation adheres to cGMP, regulatory requirements (US FDA, EU EMA), and internal standards. Manage document archival and retrieval. Process Validation & Scale-Up: Participate in process validation activities for robust manufacturing processes of OSD Formulations. Analyze process data to identify CPPs and CQAs for process control strategies. Troubleshoot technical issues during scale-up and validation, implementing corrective actions. Evaluate the impact of process changes on product quality. Collaborate with engineering and production to optimize manufacturing processes. Ensure compliance with validation lifecycle management. Quality & Regulatory Compliance: Ensure compliance with cGMP, regulatory requirements (US FDA, EU EMA), and internal standards. Conduct risk assessments and implement mitigation strategies. Participate in audits, addressing findings and implementing corrective actions. Maintain understanding of regulatory requirements and best practices in OSD Formulation. Oversee CAPA implementation. Promote a culture of quality and compliance. Technical Troubleshooting & Continuous Improvement: Lead troubleshooting during initial commercial batches, identifying root causes and solutions. Apply problem-solving methodologies to address technical challenges in OSD Formulation. Identify process improvement opportunities. Utilize SPC tools to monitor process performance. Implement Lean Six Sigma principles. Champion continuous improvement. Cross-Functional Collaboration & Stakeholder Management: Coordinate with QA, QC, RA, and Production teams. Facilitate communication and collaboration among teams. Manage stakeholder expectations. Build relationships with internal and external partners. Generate progress reports, highlighting milestones, challenges, and risks. Present technical data to teams and management. Lead meetings to discuss project status and make decisions. Act as a liaison between R&D, Manufacturing, and stakeholders. General Expectations and Past Experiences: Possess 8+ years of hands-on experience in technology transfer within OSD manufacturing, demonstrating a strong understanding of the entire process lifecycle. Demonstrate proficiency in preparing and reviewing critical technical documents such as technology transfer protocols, BMR/BPR, and process validation reports. Exhibit a thorough understanding of Quality by Design (QbD) principles and their application in pharmaceutical manufacturing. Showcase strong technical troubleshooting skills with the ability to identify and resolve issues during scale-up and commercial manufacturing. Proven ability to coordinate and collaborate effectively with cross-functional teams, including QA, QC, RA, and Production. Demonstrate a solid understanding of regulatory guidelines (US FDA, EU EMA) and CGMP compliance requirements for pharmaceutical manufacturing. Experience risk assessment methodologies and CAPA management systems in a pharmaceutical setting.

Formulation Development, OSD ,

Qualification: Bsc Chemistry/Bpharma Experience : 0 to 5 Years CTC: Up to 4.5 LPA Work Location : Ankleshwar Experince in OSD, Tables, API send cv on sdpbharuch@gmail.com with Sub : Production Ankleshwar Call on 9712914207 Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar No Charges Share with Friends & Colleagues

Job Title: Radiology Technician Company Name: Manipal Hospitals Location: Yelahanka Job Description: We are looking for a skilled and dedicated Radiology Technician to join our team at Manipal Hospitals in Yelahanka. The Radiology Technician will be responsible for performing diagnostic imaging procedures, such as X-rays, CT scans, and MRI scans, while ensuring the highest level of patient care and safety. The ideal candidate will possess strong technical skills, attention to detail, and a compassionate approach to patient interactions. Key Responsibilities: - Prepare and educate patients for radiological procedures, ensuring comfort and understanding of the process. - Operate imaging equipment to obtain diagnostic images as per physicians' orders. - Ensure proper positioning of patients and equipment to achieve optimal imaging results. - Maintain equipment and ensure it is functioning correctly, reporting any malfunctions or issues as needed. - Maintain accurate patient records and document all procedures performed. - Adhere to safety protocols and infection control measures to protect patients and staff. - Collaborate with physicians and other healthcare professionals to discuss results and imaging procedures. - Stay current with advancements in radiology technology and practices. Skills and Qualifications: - Bachelor’s degree or diploma in Radiologic Technology or a related field. - Valid radiologic technologist license or certification. - Proficiency in operating radiology equipment including X-ray, CT, and MRI machines. - Strong knowledge of radiographic techniques and procedures. - Excellent communication and interpersonal skills for patient interaction. - Attention to detail and strong organizational skills. - Ability to work in a fast-paced environment and manage multiple tasks. - Commitment to ongoing professional development and adherence to ethical standards. Tools and Equipment: - X-ray machines - Computed Tomography (CT) scanners - Magnetic Resonance Imaging (MRI) machines - Patient management software - Radiation protection equipment - Imaging processing systems If you are a driven and committed professional looking to make a difference in the field of radiology, we encourage you to apply and become a part of the Manipal Hospitals team. Roles and Responsibilities About the Role: As a Radiology Technician at Manipal Hospitals, you will play a crucial role in providing high-quality imaging services. Your primary responsibility will be to operate imaging equipment and perform diagnostic procedures. You will ensure patient comfort and safety during examinations, while also maintaining the highest standards of image quality. About the Team: You will join a dedicated team of healthcare professionals who are committed to providing excellent patient care. The radiology team at Manipal Hospitals comprises experienced technicians, radiologists, and support staff, all working collaboratively to ensure effective communication and efficient workflow. The team fosters a supportive and educational environment for professional growth. You are Responsible for: - Performing a variety of imaging procedures including X-rays, CT scans, and MRI scans. - Ensuring proper positioning of patients to obtain optimal images. - Maintaining and calibrating imaging equipment to ensure accurate results. - Assisting in the preparation and care of patients before, during, and after procedures. - Adhering to safety protocols and infection control measures. To succeed in this role – you should have the following: - A diploma or degree in Radiologic Technology or a related field. - Certification from a recognized professional body, such as the American Registry of Radiologic Technologists (ARRT). - Strong technical skills and knowledge of imaging equipment and safety procedures. - Excellent communication and interpersonal skills to interact effectively with patients and team members. - Attention to detail and the ability to work in a fast-paced environment.

To ensure that all raw materials (API & excipients) are sampled, tested, and released. Key Responsibilities: 1. Sampling & Receipt 2. Testing & Analysis 3. Documentation & Release 4. Compliance & Audit Readiness 5. Instrument Handling Required Candidate profile Candidate must have experience in handling team of minimum 10 members. Candidate must have experience into routine analysis of raw material and QMS knowledge.

Greetings From Immacule Lifesciences Pvt Ltd! We are conducting Mega Walk-In Drive for both OSD & Sterile Injectable Manufacturing on Sunday (22/06/25). Requirements: Positions : Officer to Assistant Manager Experience : 2 - 10 Years in Pharma Industry Job Location : Nalagarh, Baddi Departments: Production & Packaging OSD : ( Granulation, Compression, Coating, Capsule, Blister, Alu - Alu, Strip, AutoCartonator) Sterile : Manufacturing, Filling & Sealing, Autoclave, CNC, Vial Washing, Tunnel, Lyophilization Quality Control OSD & Sterile : Instrumental and chemical analysis i.e RM/PM/FG/ Validation/ Micro/ Stability and having competency on instruments like HPLC, GC. Quality Assurance OSD &Sterile : IPQA/QMS/Validation/Qualification/Documentation/Audit Compliance/Training/Vendor Qualification/Micro Compliance/Media Fill/PV/CV/ APQR with thorough knowledge of cGMP norms. Engineering: Sterile : Process Equipment's like Vial Washing, Vail Filling, Tunnel, Autoclave, HVAC, BMS & EMS Boiler & Water System. OSD : Plant Maintenance, HVAC, Utilities & Water System Candidates who are not able to attached the Walk-In drive, please send your resume to hr@acmegenerics.in / career@acmeformulation.com

Roles and Responsibilities Collaborate with cross-functional teams to identify market trends, competitor analysis, and customer needs to inform sales strategies. Provide backend support to the sales team by managing data entry, documentation, and reporting tasks efficiently. Ensure timely delivery of high-quality products to customers while maintaining excellent communication skills throughout the process. Identify areas for improvement in existing processes and implement changes to increase productivity and efficiency. Desired Candidate Profile 2-4 years of experience in pharmaceutical or nutraceutical industry with a focus on domestic marketing or CDMO services. Strong understanding of formulation development, OSD (Oral Solid Dose) manufacturing processes, and regulatory requirements. Excellent documentation skills with attention to detail; ability to manage multiple projects simultaneously under tight deadlines.

Role & responsibilities: To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head. To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor it's progress constantly. To organize, supervise and control the activities of Technology Transfer department. To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department. To check and update various documents and records, ensure production records filled online during batch manufacturing. To check and maintain housekeeping of the department. To enforce latest developments in GMP, SOP's etc. To observe and report to the seniors of Product / Material / Machine for their abnormal identified behaviour during production process. To counter check Raw Materials Dispensing and to recheck the material prior to their use in production processes. To ensure that the Quality, Health, Safety, Environment policy and procedures are followed. To prepare documents of New Product (ANDA) and site shift products (which includes CCF, MFC, BMR, QFR, ISP, PPQP, QRM, ESR TT Protocol, TT Report & PPQR (not limited to). To prepare documents for MES activity. To check, (i) Sampling request to Quality Assurance Department (ii) Material requirements requisitions (iii) Received batch from RM department To check / verify, (i) Daily Work in progress status. To achieve required production targets as per the budgetary norms. Handling of change parts. To ensure proper follow of company's rules and regulations. To ensure that all documents are complete in all respect prior to next stage of processing. To write requisition slips of Auxiliary Materials / Stationary materials etc. of daily use. To procure and control the utilization of such materials. To maintain optimum stock level of such materials for smooth functioning of department. To carry out any additional responsibility entrusted from time to time. Monitoring of Production process at each stage. To understand and follow all written procedure and manufacturing instructions mentioned in the respective batch record or any other quality document before starting production activity. To monitor constantly the CAPA of deviations, OOT and OOS to complete within time frame. To perform the investigation within timeframe related to quality system i.e. deviation, OOT and OOS. To be in communication with TRC and it's cross functional team for coordination and knowledge sharing of new site transfer products. To ensure that all SOP trainings are fulfilled on periodic basis. To coordinate activities like visit, document transfer and monitoring (but not limited to) related to manufacturing of products at CMO site. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh WERE HIRING | Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh Tablet/Pellet Coating Operators (2-7 yrs) | Key Responsibilities • Run tablet / pellet coating machines (Glatt, Gansons, ACG, etc.). • Mix coating solution and load materials as per the batch sheet. • Set and watch basic machine settingspan speed, temperature, spray rate. • Do simple in-process checks (weight gain, colour, appearance) and note results. • Fix small issues like blocked spray guns or wrong settings; call maintenance if bigger problems arise. • Keep all records, logbooks and tags up-to-date, neat and accurate. • Clean the machine and area after every batch; get line-clearance before the next product. • Follow cGMP, safety and PPE rules at all times; report any deviations. • Work closely with QA, engineering and warehouse teams for smooth flow. • Share ideas to cut waste, improve yield and speed up the process; help train new helpers/operators. Have hands-on experience on Glatt, Gansons, Sejong or Bohle auto-coaters? US-FDA approved OSD facility and accelerate your pharma journey! ITI / Diploma / Any Graduation Exposure to cGMP & global audits How to Apply Email your CV (Subject: Coating Operator 2-7 Yrs) to: naidupetahr@aurobindo.com OR WhatsApp to: +91 80968 88868 Immediate / 30-day joiners preferred.

Responsible for the development and dossier deliverable of genreic application for projects assigned with in the team for Europe ,Canada Australia. Preparation ,review and approval of test licenses Import license applications. Planning and procurement of RMPMs/ RLDs and inventory control at R&D for development. Preparation and review of RMPMs/Justification of Specifications/Cleaning validation report/Risk assessment report/ stability protocol/CDRs/Technology Transfer dossiers. Review of MFRs/BMRs/BPRs/PVPs/HTS, product specific questionnaire, Protocol; and report etc. for scale up and registration batches Timely and Appropriate Reponses for CMC and Bio deficiencies from regulatory agencies for filed products and review of R&D documents for regulatory and quality audits.

Walk-in Drive @ Bangalore on 22nd June 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles. Venue: Strides Pharma Science Ltd. (R&D office): 165/2, 3rd Main Road, Oppo. Kalyani Magnum Tech Park, JP Nagar 4th Phase, Bengaluru-560076 Open Positions Department: Production Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production Department: Packing Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Bangalore Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-7 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Bangalore Key Skills: Analysis of Raw Material, Finished products, In Process, Stability Samples, for Capsules & Tablets with expertise in HPLC. Department: Formulation Development Experience: 4-7 years Qualification: M.Pharm Job Location: Bangalore Key Skills: Planning & Execution of Lab scale experiments. DOE, Quality by Design, Product Development, Stability Protocol, Regulatory Market. Department: Engineering Process Maintenance Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Bangalore Key Skills: Maintenance of RMG, FBD, Compression, Coating, Capsule filling, Blister Packing, Sachet Filling line, Bottle Packing Machines. Department: Engineering Projects & Utility Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Bangalore Key Skills: Installation, Commissioning, Equipment Qualification, DQ, IQ, OQ, PQ, Utility, Water System, HVAC, AHU, Chiller, Air Compressor, Cooling Tower, PLC, SCADA, HMI Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Raw Materials, Packaging Materials. To ensure that the proper maintenance of department, premises and equipment. Preferred candidate profile B. Pharm / M. Sc in Chemistry or Organic Chemistry or General Chemistry or Pharmaceutical Chemistry or Industrial Chemistry Experience: 3 to 6 years

Role & responsibilities Lead and manage the Quality Control team to ensure timely and accurate analysis of finished products (OSD & Injectables). Review and approve analytical reports, ensure compliance with GLP and cGMP standards. Oversee operations involving HPLC, GC, UV, IR , and other sophisticated instruments. Ensure proper implementation of MPCL and maintain all microbiological standards in compliance with regulatory guidelines. Handle all regulatory audits (USFDA, MHRA, WHO, etc.) and prepare necessary documentation. Manage OOS/OOT investigations and ensure CAPA implementation. Coordinate with cross-functional teams (QA, production, regulatory affairs) to ensure product quality. Train and mentor junior staff; ensure continuous skill development within the QC team. Manage documentation including SOPs, specifications, STPs, and logbooks. Preferred candidate profile B.Pharm / M.Pharm / M.Sc in Chemistry or equivalent. 12 15 years of relevant experience exclusively in the pharmaceutical industry (OSD & Injectables) . Strong knowledge of GLP, MPCL, and finished product QC . Proven team leadership and people management skills. Experience in handling regulatory inspections and audits. Good communication and documentation skills.

Roles & Responsibilities: Develop and execute regulatory strategies for the registration and lifecycle management of pharmaceutical products in ROW markets. Compile, review, and submit high-quality regulatory dossiers (CTD/eCTD format) in compliance with regional authority requirements. Interact with local affiliates, regulatory agencies, and distributors to ensure timely approvals and resolve queries or deficiencies. Maintain regulatory documentation and product information to ensure compliance with health authority regulations. Monitor and analyze changing regulatory landscapes in ROW regions and update stakeholders on impact. Support cross-functional teams including R&D, QA, Supply Chain, and Commercial in regulatory matters related to ROW. Manage post-approval changes (variations), renewals, and other lifecycle submissions. Participate in audits and inspections, ensuring regulatory readiness and compliance. Train and mentor junior regulatory staff, if applicable. EXPERIENCE: 8 10 years of experience in Regulatory Affairs in ROW markets. Strong knowledge of regulatory guidelines (ICH, WHO, local agency requirements). Experience with dossier preparation (CTD/eCTD) and handling agency queries. Understanding of regulatory requirements across key ROW territories. Project management and stakeholder communication skills. SKILLS: Familiarity with registration processes for both generics and branded formulations. Experience in working with third-party manufacturers and CROs. Hands-on experience with regulatory tracking tools and systems.

We are seeking a skilled professional for the role of Formulation Development (FRD) in Quality Assurance (QA) to join our team in Hyderabad. The ideal candidate will have hands-on experience in QA within the production department, specifically related to formulations in the Oral Solid Dosage (OSD) segment. Role & responsibilities Ensure compliance with quality standards in the production department related to formulations Oversee and support QA activities in manufacturing processes Prepare and review documentation including Master Formula Records and other QA-related documents Collaborate with cross-functional teams to maintain and improve product quality Participate in audits and implement corrective actions when necessary Preferred candidate profile Minimum 2 years of experience in QA within the pharmaceutical production department, preferably with OSD formulations Knowledge and exposure to QA manufacturing industry practices Strong documentation skills including preparation of Master Formula Records Detail-oriented with a thorough understanding of quality compliance Good communication and teamwork skills

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) We have opening for Formulation R&D Department. Position : Executive or Sr Executive 1)Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Good Communication Skills Ref to Friends or colleagues Please share update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation

Job Title : Capsule Filling Operator OSD (2-8 Yrs) Company : Aurobindo Pharma Ltd – Unit IV Location : Naidupeta, Tirupati (AP) Key Skills : Capsule Filling, Bosch/ACG Pam/IMA, BMR, cGMP, Hard-Gelatin Education : ITI / Diploma / B.Sc / B.Pharm Apply To : ganesh.janne@aurobindo.com | WhatsApp 8096888868

Great Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientist - Technology Transfer - EU market at our dedicated R&D center. Department : Formulation Development - Technology Transfer Formulation : Solid Orals Market : Europe Experience Required : 4-7 years Designation : Sr. Officer / Executive / Sr. Executive Location : R&D Center, Moraiya, Ahmedabad (Transportation from specific route if Ahmedabad is provided) Roles & responsibilities (Not Limited to): Execution of Scale-up, exhibit batches, validation batches for Regulated market products Feasibility trial, evaluation, execution of commercial validation batches for site variation contract manufacturing projects Document preparation, review related to SU/EB and validation batches Perks & Benefits: Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility 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 R&D and possess the required skills & experience, we encourage you to apply for this position. Interested one can revert with their resume on career@unisonpharmaceuticals.com Regards, Team HR

Qualification: Bsc Chemistry/Bpharma Experience : 0 to 5 Years CTC: Up to 4.5 LPA Work Location : Ankleshwar Experince in Pharma Company Prefer Like OSD, Tables, API send cv on sdpbharuch@gmail.com with Sub : Production Ankleshwar Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar No Charges Share with Friends & Colleagues

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

Roles and Responsibilities Ensure compliance with BPR review, batch manufacturing, and batch planning processes. Conduct granulation activities according to OSD requirements. Perform formulation tasks as per BMR guidelines. Collaborate with cross-functional teams for smooth production operations. Desired Candidate Profile 2-6 years of experience in pharmaceutical industry with expertise in Production Manufacturing (OSD). Bachelor's degree in Pharmacy (B.Pharma) from a recognized institution. Strong understanding of Batch Manufacturing Record (BMR), Batch Processing, and Tablets processing.

Roles and Responsibilities Operate compression machines to produce tablets in OSD manufacturing process. Ensure accurate weight control during compression operations. Monitor machine performance and troubleshoot issues as needed. Maintain cleanliness and organization of production area. Collaborate with team members to achieve production targets. Desired Candidate Profile 1-4 years of experience in pharmaceutical production, preferably in compression operations. Strong understanding of formulation, compression, and manufacturing processes. Ability to work accurately with precision instruments and equipment. Basic knowledge of tablet coating techniques would be an added advantage.