963 Osd Jobs - Page 5

Site Master File, Validation Master Plan and execution as per Plan, Quality Manual & approvals, SOP & GMP GLP, OOT, OOS, CAPA Internal audit Regulatory requirement,market complaints. Product recall Validation of process, documentation in compliance

Responsibilities: 1. Lead QMS initiatives, ensuring compliance with regulatory standards. 2. Manage deviations, change controls, investigations, cleaning validations. 3. OSD / Injectable QMS 4. Audit Compliances, cGMP, ICH, 21 CFR Knowledge Health insurance Provident fund

Roles and Responsibilities Ensure compliance with cGMP guidelines during primary and secondary packaging operations. Conduct line clearance activities before commencing packaging operations. Verify batch records, including BMR/BPR, COA, and labeling. Maintain accurate records of production runs and productivity metrics.

Roles and Responsibilities Monitor machine performance and troubleshoot issues to minimize downtime. Ensure compliance with quality standards and regulations during production processes. Collaborate with team members to achieve daily targets and goals. Maintain accurate records of production data and inventory management.

Position Summary. Formulation Operator is responsible for carrying out manufacturing activities related to oral solid dosage (OSD) forms, including granulation, compression, and coating operations. The role ensures all processes are executed in compliance with GMP, SOPs, and safety guidelines while achieving required production targets and product quality standards. Key Responsibilities. 1. Granulation Operate and monitor granulation equipment (RMG, FBD, Blenders, Sifters). Perform material charging, mixing, wet granulation, drying, and sizing activities. Ensure granulation parameters are followed as per BMR/BPR. Conduct in-process checks such as LOD, bulk density, particle size, and granule...

Site Visit at the time of Manufacturing Compression Filling/ Visual/ Packing/ FG Stages of the final product ,Line clearance to be given in case needed in cases of any anomaly being observed & cleared thereafter Practical approach towards inspection Required Candidate profile Site Visit at the time of Manufacturing Compression Filling/ Visual/ Packing/ FG Stages of the final product ,Line clearance to be given in case needed in cases of any anomaly being observed IPQA/IPQC

The incumbent will be responsible for carrying out manufacturing activities in the Oral Solid Dosage (OSD) production area, including Compression, Coating, Encapsulation, and Bottle Packing (Primary & Secondary). The role ensures adherence to GMP, safety, and quality standards during all production processes. Sound knowledge of GMP documentation and BMR/BPR . Hands-on experience in compression, coating, capsule filling, and bottle packing operations . Basic understanding of equipment calibration, validation, and maintenance practices . Strong focus on quality, safety, and compliance . Good communication and teamwork skills. Role & responsibilities Preferred candidate profile

Operate Granulation machine Operate backpacking machine FBD, Multimill , Blender, Shifter, CVC line BMP/BPR filling Audit trial Preferred candidate profile Candidate must have experience in OSD formulation and USFDA/MHRA plant. Experience in SCDA system

Roles and Responsibilities Responsible for overall Quality System Review & Improvements Handling and control of Non-conforming products. Responsible for review & approval of key Quality System Procedures, Standard Operating Procedures & other Master Documents. GAP Analysis of the process and products. Identifying the scope of improvement based on trend analysis. Putting forward the suggestions for improvements to the Management. Participation in audits, compliance and Tracking of Audit Compliances/Status. Review & closeout of Change Controls, Deviation Complaints & CAPA. Participating in Impact assessment, investigation & approval of deviations. Review & Approval of change controls, Deviatio...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (02 07 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ Micro-biology ARD - OSD Experience: (02 06 Years) •HPLC/ FG/Analytical Method validation/ Stability PACKING Experience: (01-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer & Jr.Executive NOTE: Offering a Joining bonus only for QC Depart. for Immediate Joiners Instrument experience in HPLC / GC ...

Note: Walk In Interview at Vapi Date: - 23-11-2025 (Sunday) Designation: Store Officer-Sr. Officer Location: Sarigam Experience: 2 to 8 years in OSD Qualification: M.Sc. / B.Sc. / M.Com / B.Com / B.Pharm Required Candidate profile Roles and Responsibilities: -2 to 7 years of experience in receipt & dispensing activity, Inward & outward activity.

Company: Aurobindo Pharma APL HC-4 (Naidupeta Location) Work Location: Naidupeta (Plant) | Walk-in Venue: Hotel palm grove, East Sikkim Interview Date & Time: Saturday & Sunday, 22 November 2025 & 23 November 2025| 09:00 AM 05:00 PM Open Positions Production OSD (Granulation/Compression/Coating/Capsule Filling) • Executive/Sr. Executive: B.Pharm/M.Pharm, 2-6 years • TA/Sr. TA: ITI/Diploma/Degree, 2-8 years Production Oral Liquid / Nasal Spray • Executive/Sr. Executive: B.Pharm/M.Pharm, 2-6 years • TA/Sr. TA: ITI/Diploma/Degree, 2-8 years Packing OSD (Blister/Bottle) • TA/Sr. TA: ITI/Diploma, 2–8 years QC – IP/FP, Stability, Nasal • Executive/Sr. Executive: B.Pharm/M.Pharm/M.Sc, 2–6 years QA ...

Job Summary: We are seeking a skilled and motivated Research Assocate to join our Formulation & Development (F&D) Oral Solid Dosage (OSD) team. The ideal candidate will be responsible for the design, development, and optimization of oral solid dosage forms (tablets, capsules, etc.) from concept to commercial scale. The role involves conducting pre-formulation studies, formulation trials, process optimization, and technology transfer to manufacturing sites while ensuring compliance with regulatory and quality standards. Key Responsibilities: Design and develop robust formulations for oral solid dosage (OSD) products, including tablets, capsules, and modified-release systems. Conduct pre-formu...

About The Role Project Role : Technology Support Engineer Project Role Description : Resolve incidents and problems across multiple business system components and ensure operational stability. Create and implement Requests for Change (RFC) and update knowledge base articles to support effective troubleshooting. Collaborate with vendors and help service management teams with issue analysis and resolution. Must have skills : Application Packaging Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Technology Support Engineer, you will engage in a dynamic work environment where your primary focus will be on ...

Sampling of Finished Products.Sampling activities of Rinse/Swab during cleaning validation.Issuance of BPCR, PCOCR, BPR, BLR, and SDR Handling, Storage and destruction of reserve sample and document as per SOP. Review BPCR. Required Candidate profile Issue critical QA documents including Analytical Work Reports, Specifications, Testing Methods, and Logbooks. Handling of dispatch activity. Checking cleanliness of equipment and give line clearance. Perks and benefits Transportation

Role & responsibilities : Job Description: To take plant round for monitoring of entire production operations and confirm quality conformance to specifications in shift. To issue and control of SOPs, BMRs, BPRs, BCRs and also finished product label/product container seals /sealing of the containers as the part of IPQA activities. To review BMRs, BCRs and analysis records before release of API. To perform sampling of APIs, maintain its records and ensure the cleaning of sampling tools. To provide line clearance at the time of product changes over. To perform the documentation control activity at site. To monitor/Maintain/Review of Records and Handling of controlled/Retained samples of Interme...

Formulation (Tablet): Technician (ITI/ SSC/ HSC): Fette & Sejong Compression, Glatt & PAM Glatt Coater, Viswill Camera Inspection Machine & Granulation equipment operator Technical Assistant (B. Pharm): Experience in Online documentation, BMR, QMS. Formulation (Packing): Technician (ITI/ SSC/ HSC): BQS / Romaco Blister Packing Machine, Auto Cartonator Machine, CV and Contact Bulk packing machine operator Technical Assistant(B. Pharm/ B.Sc): QMS, Track & Track system (Optel / ACG) with serialization system

ear Candidate, We are seeking a Senior Executive/ Assistant - Regulatory affairs Europe) to join our team, He/ she will be responsible for Dossier compilation, preparation, Life cycle management, Pre approval, Post approvals. based at Govandi Location. Markets : Europe Dosage Form : OSD/ Sterile Key Responsibilities: Collate/prepare and file dossiers in a timely and accurate manner for formulations/ drug products to get licenses from various targeted markets. Prepare the checklist for documentation for regulatory filings as per current regulatory requirements (country specific). Collate and conduct first-level review/overview of relevant standard technical documentation like stability, TTD, ...

Role & responsibilities Operate and monitor tablet compression machines as per production schedule and SOPs. Set up machines by ensuring correct tooling installation, parameters, and batch changeover. Conduct in-process checks such as weight variation, hardness, thickness, friability, and appearance. Maintain proper documentation like BMR/BPR, logbooks, and online records as per cGMP requirements. Ensure continuous machine operation with minimal downtime and timely troubleshooting of minor issues. Perform cleaning of equipment before and after batch operations as per CIP/SIP guidelines. Coordinate with QA, Maintenance, and Production teams to ensure smooth batch execution. Follow safety prot...

Role & responsibilities Job Summary: The Senior Operator Granulation is responsible for the operation and monitoring of granulation equipment in the production of pharmaceutical formulations. This role ensures that the granulation process is carried out efficiently, safely, and in compliance with GMP and company standards to meet production targets and product quality requirements. Key Responsibilities: Operate and monitor granulation machines and associated equipment according to batch manufacturing instructions and SOPs.Ensure adherence to Good Manufacturing Practices (GMP) and safety protocols during production.Perform routine checks and adjustments to maintain process parameters within s...

Responsibilities: * Lead quality control team, ensuring compliance with HPLC methods & OSD standards. * Prepare technical documentation, audit documents & manage regulatory compliance.

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 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will be responsible for designing, building, and configuring applications to meet business process and application requirements. You will collaborate with teams to ensure successful project delivery and implementation. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team...

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Dassault Systemes ENOVIA V5 Good to have skills : Dassault Systemes 3DEXPERIENCE ENOVIA Customization Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Lead, you will engage in the development and configuration of software systems, either managing the entire process or focusing on speci...

* Manage comprehensive system & program for a startup OSD manufacturing facility * To assist in project design, execution, validation & commissioning. * To coordinate with vendors and other CFTs for qualification. * Coordinate with QA & R&D. Required Candidate profile * Candidate with 14 years of exp in Pharma industry. * Qualification: B.Pharm / M.Sc. * Knowledge about Tablets, Capsules,& Powder filling. * GMP * Good communication skills in English.

About The Role 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 : NA Minimum 7.5 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. Your day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities:- Expected to be an SME- Collabo...