750 Osd Jobs - Page 7

We have two urgent vacancies in SMT production 1) Assistant Manager - 6-10 Years Exp 2) Sr. Engineer - 3-6 Years Exp Company Name - Iljin Electronics(Amber Group) Location - Ecotech 3, Greater Noida Job Summary : Responsible for managing daily operations and team coordination in the SMT department. The role includes production monitoring, quality control, consumables and spare parts review, and regular audits to ensure smooth, efficient, and compliant SMT operations. Key Responsibilities : Engage in daily discussions with SMT staff and workers on production topics. Attend production meetings and analyze idle time. Review top consumables usage data and initiate corrective actions if needed. A...

Role & responsibilities Formulation Development of Oncology products Exposure of Regulated, Semi Regulated & India Markets FnD Documents like Product development report, , Specifications, MFC,BMR, Stability protocol, CCF , Deviation etc. Awareness of ICH/Regulatory guidelines pertaining to formulation development OSD Experienced candidates willing to work in Onco products can also apply Preferred candidate profile Qualification : M.Pharm with 2-5 Yrs of relevant experience. Interested candidates are requested to share their Cvs on vilshashah@torrentpharma.com

Job Description: We are seeking a highly skilled and experienced professional for the role of Formulation Development OSD , focused on regulated markets including USFDA, MHRA, EMA, and other global regulatory agencies. The ideal candidate will have a proven track record in developing and optimizing solid oral dosage forms (tablets, capsules) for submission and commercial-scale manufacturing. Key Responsibilities: Lead and execute formulation development projects for oral solid dosage (OSD) forms targeted at regulated markets (US, EU, etc.). Design and execute pre-formulation and formulation trials, optimization, and scale-up. Develop robust formulations and manufacturing processes based on Q...

Primary Packing Supervision 1.To see the packing line plan and work accordingly. 2.Checking of BOM against SAP BOM, SAP related work and verify the quantity dispensed accordingly. 3.Training to be given to the workmen & Operator in the concerned area as per the cGMP guidelines and maintaining Training record. 4.To Co-ordination with QA & QC dept. regarding the line clearance, samples collection and its release for further process. 5.Filling the online BPR & respective logbooks 6.Doing the entries in the daily format issued in respective areas 7.To co-ordinate for Preventive maintenance and calibration activities to be done. 8.Doing the BPR reconciliation, Effective Manpower handling, in proc...

Role & responsibilities Executive - Quality Assurance Preferred candidate profile Review of Equipment Qualification related documentation. Review of Computer System Validation related documentation. Exposure of Cleaning Validation. Exposure of Software like EDMS, LMS, Trackwise.

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP Document and Reporting Compliance Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. You will be responsible for overseeing the application development process and ensuring successful project delivery. Roles & Responsibilities:- Expected to perform independently and become an SME.- Required active ...

Title: OSD Maintenance Senior Manager Job Grade: G9B / Senior Manager Position Summary Responsible for utilities, air conditioning and maintenance of building & premises, maintenance of production, engineering equipment’s. To ensure the engineering activity such as Preventive Maintenance, Routine & breakdown maintenance , Calibration, Equipment. To ensure and maintain high degree of morale, discipline amongst the team. To ensure that all the systems and equipment are upgraded, Validated & Automated as per the procedures and requirements. To ensure that the subordinates are adequately trained for the job assigned Optimum utilization of resources. To ensure that optimum resources such as man, ...

Job Summary We are seeking an individual to oversee batch manufacturing, ensuring adherence to cGMP (Current Good Manufacturing Practices), providing training, and coordinating day-to-day activities. Responsibilities include minimizing machine downtime, managing subordinate staff, assuring compliance with standards and SOPs (Standard Operating Procedure), leading regulatory audits, compiling reports, ensuring safety norms, and budget management. Roles & Responsibilities • You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control. • You will be responsible for imparting general and cGMP ...

Planning and execution of production activities in Granulation, Compression, Coating & Capsule Filling area. Responsible for handling RMG, FBD, Coating, Compression & Capsule Filling Machine. Responsible for preparation and review of BMR & BPR. Ensuring daily cleaning activity & Machine preventive maintenance as per schedule. Handling of QMS activities like Change Control, Deviation & CAPA.

Role & responsibilities 1. Procurement Strategy & Planning Define and execute procurement strategy for Raw Materials (RM) & Packaging Materials (PM) aligned to business and production needs. Anticipate and ensure uninterrupted material availability for NPD, commercial batches, and technology transfers. Collaborate with cross-functions to prepare rolling forecasts and procurement plans. 2. Vendor Development & Relationship Management Source, evaluate, and onboard qualified suppliers in line with regulatory and quality benchmarks. Build long-term partnerships with local and global vendors to ensure supply reliability. Conduct vendor audits/assessments jointly with cross functional teams. Track...

Your role at PCI as part of the Batch File Review Team will involve compiling and reviewing batch documents across various process types such as OSD, Sterile, Biologics, Cell Therapy, and Gene Therapy. You will collaborate closely with internal and external stakeholders, preparing documentation for Quality Person (QP) review, coordinating corrections, and ensuring compliance with regulatory requirements. This position offers a diverse range of responsibilities and serves as an ideal foundation for those considering a future career as a QP. Key Responsibilities: - Compile and review batch documents, ensuring accuracy and completeness prior to QP review. - Collaborate with site personnel to ad...

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP Document and Reporting Compliance Good to have skills : NAMinimum 7.5 year(s) of experience is required Educational Qualification : 15 years of Education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. You will be responsible for overseeing the application development process and ensuring successful project delivery. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team to perform- Responsi...

Role Purpose The purpose of the role is to resolve, maintain and manage clients software/ hardware/ network based on the service requests raised from the end-user as per the defined SLAs ensuring client satisfaction Do Ensure timely response of all the tickets raised by the client end user Service requests solutioning by maintaining quality parameters Act as a custodian of clients network/ server/ system/ storage/ platform/ infrastructure and other equipments to keep track of each of their proper functioning and upkeep Keep a check on the number of tickets raised (dial home/ email/ chat/ IMS), ensuring right solutioning as per the defined resolution timeframe Perform root cause analysis of t...

Job description Company: Strides Pharma Science Ltd Department: Production (Tablets) Position: Executive Job Location: Alathur, Chennai Qualification: M.Sc., B-Pharm, M-Pharm Experience: 2 to 6 Years Job responsibility: Shift Incharge, QMS Handling, SAP, Elog book, Hands on experience in Granulation, Compression, Coating. Regards, Srinidhi S HR Talent Acquisition

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 f...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAP Document and Reporting Compliance Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will engage in the design, construction, and configuration of applications tailored to fulfill specific business processes and application requirements. Your typical day will involve collaborating with team members to understand project needs, developing innovative solutions, and ensuring that appli...

Monitor and maintain documentation related to QMS activities, including SOPs, change controls, deviations, and CAPAs Handle market complaints by conducting root cause analysis and implementing corrective actions. Ensure implementation and compliance with Quality Management System (QMS) guidelines. Facilitate training programs for personnel on QMS procedures, regulatory requirements, and best practices. Ensure compliance with Good Manufacturing Practices (GMP) and company policies. Obtain line clearance as per BMR/BPR, SOP, and checklist. Follow and execute the daily plan efficiently. Coordinate with QA, QC, Engineering, and Stores to achieve daily productivity targets. Conduct the entire pac...

VS Hospitals is looking for RADIOLOGY TECHNICIAN to join our dynamic team and embark on a rewarding career journey Operate and maintain radiographic equipment to capture diagnostic images Position patients and adjust equipment settings to obtain optimal images Explain procedures to patients and address any concerns or questions Ensure the safety and comfort of patients during imaging procedures Collaborate with radiologists and other healthcare professionals to review images and assess the quality of results Follow established protocols and safety measures to minimize radiation exposure to patients and staff Process and analyze diagnostic images, ensuring accuracy and clarity Maintain accura...

Job Title: AQA Quality Assurance (LCMS, GCMS, ICPMS) Company: Energon Labs Location: Hyderabad Experience Required: 2 - 6 years Employment Type: Full Time, Permanent Role Overview We are seeking experienced professionals in Analytical Quality Assurance (AQA) to review and ensure compliance in analytical data generated through LCMS, GCMS, and ICPMS techniques. The role requires a keen eye for detail, strong knowledge of analytical methods, and the ability to uphold the highest quality standards. Key Responsibilities Review analytical data for LCMS, GCMS, and ICPMS techniques. Conduct electronic audit trail reviews for analytical instruments and ensure compliance. Review Analytical Method Vali...

Job Title : Executive / Sr. Executive Formulation Development Entity : Evonik India (Evonik India Research Hub) Work Location : Thane PRINCIPLE ACCOUNTABILITIES: Conduct formulations experiments, coordinate for analysis of samples and carry out the required stability studies. Troubleshoot technical problems related to the manufacturing processes and formulations independently, in order to meet the project goals. Guide fellow scientists and trainees on technical matters. Manage a Quick run innovation project independently. Communicate with the project manager(s) and other stakeholders. Presentations with due connect to the overall technical and business goals. Coordinate with analytical depar...

As the Plant Head at our Baddi location, you will be responsible for overseeing operations with a focus on OSD. Your main responsibilities will include: - Leading and managing the plant operations - Ensuring compliance with safety regulations and quality standards - Developing and implementing strategies to improve plant efficiency To excel in this role, you should have: - Minimum of 5 years of experience as a Plant Head - Strong stability record in previous roles Please note that this is a full-time position with a day shift schedule. If you are interested in this opportunity, please send your resume to admin@addiibiotech.com or contact 7719715392. (Note: No additional details of the compan...

Roles and Responsibilities Develop new products and formulations for OSD (Oral Solid Dose) applications. Conduct research and development activities to improve existing products' quality, stability, and efficacy. Prepare technical documentation and reports on product development progress. Collaborate with cross-functional teams to ensure successful product launches.

Roles and Responsibilities Ensure compliance with cGMP guidelines during all stages of product development. Design and optimize formulations that meet regulatory requirements and customer needs. Collaborate with cross-functional teams to ensure successful technology transfer from R&D to manufacturing scale-up. Conduct research on solid oral, liquid oral, injectable, OSD, and other dosage forms to improve existing products or develop new ones. Develop new products from concept to launch, ensuring timely delivery of high-quality formulations.

Role & responsibilities : Required technician for osd packing department machine experience required into HV1 cartonator, cvc packing, blister packing machine, sachet

Greetings!!!! We are seeking experienced professionals in Regulatory Affairs US Market (CMC, Module 3) with expertise in Formulation, for our Hyderabad-based R&D Centre. Regulatory Affairs US Market (CMC) with strong exposure to ANDA/NDA submissions and post-approval changes. Key Responsibilities: Hands-on experience in US Regulatory Affairs for ANDA & NDA (Approved and Tentative) submissions. Responsible for filing supplements : CBE, CBE-30, PAS, Controlled Correspondence, Annual Reports/Updates. Planning, reviewing, and timely submission of assigned projects in compliance with FDA guidelines . Strong interpretation of FDA queries and drafting of high-quality responses. Review and preparati...