963 Osd Jobs - Page 7

Role & responsibilities Job Role : Compression/Coating/Inspection-Supervision 1. To follow the production plan and work accordingly. 2. 3. To check BMR against SAP BOM and verify the quantity dispensed as per BMR. To coordinate with and take follow-up from QA Department regarding Line Clearance, in process checks, sample collection and its release for further process. 4. 5. 6. To make online SAP entries. To maintain dies and punches inventory record. To maintain online documentation related to production activities like BMR, log books & daily records. 7. 8. To ensure Preventive maintenance and calibration activities as per schedule on time. Completion of BMR and all related documents & in- p...

Technology Transfer: Execute transfer of OSD products (tablets, capsules) from development to manufacturing sites. Process Development: Establish and optimize manufacturing processes for scale-up and commercial production. Validation & Compliance: Support process validation, risk assessments, and ensure adherence to GMP and regulatory guidelines. Cross-functional Collaboration: Work closely with R&D, QA, QC, and production teams to ensure seamless execution. Documentation: Prepare technical reports, SOPs, and validation protocols. Preferred candidate profile

Lead Engineering, Maintenance, Utilities & Projects at OSD plant. Ensure equipment uptime, regulatory compliance (USFDA/MHRA/WHO), safety, cost control & timely CAPEX execution while driving reliability, energy efficiency & team excellence. Food allowance Health insurance Annual bonus Provident fund

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 o Instrument experience in HPLC / G...

Design, plan, perform, interpret and report the analytical results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within global ARD. Expertise in analytical method development, method validation as well as technical and strategic background. Manage technical lab/plant activities. Execute the analytical experiments in line with TRD vision. Ensure full portfolio support in line with GDD, NTO and NIBR plans. Maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned. About the Role Major accountabilities Provide analytical and technical support to PHAD/project t...

Description: Primary Skills:Windows 10, Intune, Autopilot and App packaging Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade :C Level :To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) :No Remote work possibility :Yes Global Role Family :To be defined Local Role Name :To be defined Local Skills :Microsoft Intune Languages Required::ENGLISH Role Rarity :To Be Defined

Description Hiring manager / EMP id nitin.relekar@capgemini.com/408700 Primary Skill:M365 - SOE administration, System configuration, Windows OS Secondary Skill:ITIL Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade C Level To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) No Remote work possibility No Global Role Family To be defined Local Role Name To be defined Local Skills system configuration Languages RequiredENGLISH Role Rarity To Be Defined

Role & responsibilities Follow the SOP of GMP, GDP, Data Integrity and Safety principles within the team. Ensure for the Operation, Cleaning and Maintenance of Compression machine, Combo Metal Detector with De-duster, Tablet Inspection Belt and its allied equipment as per SOP. Ensure for the Operation, Cleaning and Maintenance of Blender, Multimill, Sifter, Bin, Equipment washing Machine and its allied equipment as per SOP. Ensure for the Operation, Cleaning and Maintenance of Automatic Air Jet Bottle air and vacuum cleaning machine, Automatic eight head pick & place type screw capping machine, Automatic eight head inner plug pressing machine, Salt Conveyor, Packing conveyor Belt, Turn Table...

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! Intas Pharmaceuticals is a leading, vertically integrated global pharmaceutical company headquartered in Ahmedabad, India, with a strong presence in over 85 countries. Driven by innovation and quality, Intas is committed to developing and manufacturing affordable medicines that improve lives across the world. We are pleased to announce a Walk-In Drive for our SEZ Plant for professionals experienced in Oral Solid Manufacturing operations including Granulation Compression Coating Experience Required: - 3 to 10 Years Qualification Required: - B.Pharm. / Diploma / ITI Walk-In Drive Interview Details: - Date: Sunday, 9th November 2025 Tim...

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...

Job Description for Executive - Quality Assurance, Pharma Educational Qualification B. Pharm / M. Pharm from a reputed university Experience 1 to 4 years of similar experience in a regulatory-approved OSD manufacturing large unit. Quality Management/Continuous Improvement Line Clearance and shop floor compliance Assisting in the Complaint Investigation system at site Assisting in the Qualification and validation system, change control system, deviations Preparing reviewing the Annual Product Quality Review Review of Batch Manufacturing Packing Records Coordination of cGMP Training activity. Compliance Ensure adherence to company Quality Standards, Local FDA MHRA regulations, by Understanding...

Aster Medcity is looking for Senior Specialist to join our dynamic team and embark on a rewarding career journey Perform initial diagnoses and prescribe the best treatments possible, Must explain complex conditions in simple terms. Diagnosing and treating conditions that affect women, such as certain types of cancer and conditions like menopause Working with expecting mothers to explain the childbirth process Performing routine checkups with patients Providing childbirth and postpartum care for new mothers Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all det...

Description of the job: Certification may be one of the best kept secrets in Engineering. Perceived as purely regulatory by some, this discipline in fact provides a complete overview of the aircraft development process, from the initial project application to the continued airworthiness of the in-service fleet. You will join the Airworthiness & Certification department. This dynamic department, is composed of Certification Engineers, Airworthiness Engineers and Designated Signatories, currently based in India and EU. This team provides technical expertise in the field of certification, in-service airworthiness and continued airworthiness. It contributes to Type Certification (TC), change to ...

Role & responsibilities RM & PM receiving and documentation of the same. Proper arrangement of the received COA of RM and PM. Sampling of received RM and PM, sending the samples to ADL for analysis. Preparation of indent for trial activity and ensure the availability in defines time. Taking of daily trial batches, discussion of issue with immediate supervisor. Entry of trial batches in lab notebook and preparation of BMR for stability batches. Maintaining the files pf individual products like RM & PM COA, Trial COA and stability reports after updating in excel sheet. Ensure GMP practice in laboratory routinely. Documentation of stability batches. Calibration of instruments in the laboratory....

Role & responsibilities Support regulatory strategy, registration, and lifecycle management for Pharma products in ROW markets. Prepare, review, and submit regulatory dossiers (CTD/eCTD) as per regional guidelines. Coordinate with regulatory agencies, distributors, and affiliates for approvals and query responses. Maintain regulatory documents, product information, and ensure compliance with health authority requirements. Monitor regulatory updates for ROW markets and share impact with stakeholders. Manage post-approval submissions including variations, renewals, and compliance updates. Work with cross-functional teams (R&D, QA, Supply Chain, Commercial) on regulatory matters Preferred candi...

Role & responsibilities Support regulatory strategy, registration, and lifecycle management for Pharma products in ROW markets. Prepare, review, and submit regulatory dossiers (CTD/eCTD) as per regional guidelines. Coordinate with regulatory agencies, distributors, and affiliates for approvals and query responses. Maintain regulatory documents, product information, and ensure compliance with health authority requirements. Monitor regulatory updates for ROW markets and share impact with stakeholders. Manage post-approval submissions including variations, renewals, and compliance updates. Work with cross-functional teams (R&D, QA, Supply Chain, Commercial) on regulatory matters Preferred candi...

Should be capable of performing ultrasonography. Attend rostered sessions/ perform work according to the weekly timetable. Provide clinically appropriate assessment, interpretation and reporting on imaging following accepted professional guideline

Urgent Openings in the Production department. 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. (A) Production Operator: Experience: 2-8 years Location : Moraiya, Ahmedabad Education Qualification : ITI/Diploma Industry : Pharma - OSD No. of va...

We are expanding!! You are invited to join one of the fastest growing pharma companies 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. Department: Quality Control Section: HPLC Analysis of OSD products Experience: 2-7 years Design...

Role & responsibilities 1. Managing Formulation development of New or existing formulations for ROW/ Regulated market as per business requirements including Oral Solids (Tablet & Capsules) IR tablets, Sustained release tablets, extended release tablets, Bilayer tablets, Capsule etc. & External preparations like Gels, Pastes, Creams, Ointments etc. 2. Leading team of FDL Officers, Technicians & workers by proper FDL planning and execution of each Project including creation of theoretical formulation, Pre-formulation studies, Trials, Optimization trials, Stability, Scale-up batches etc. 3. Conducting intellectual searches for technical information through a variety of resources, including the ...

Designation: Apprentice Department: Formulation Technology Transfer Preferred candidate profile: Candidates should have brief knowledge about the Formulation Technology Transfer department. Basic concepts should be cleared which you have studied during your qualification. Qualification: B. Pharma / M. Pharma Selection Criteria: Candidates should have 60% and above in 10th & 12th both. And in graduation or post graduation candidate should not have any kind of ATKT/Backlog in any of the semesters above 55% is required in both B. Pharma / M. Pharma. Stipend: Rs. 15,000 p/m Interested candidates please share your updated CV's on akshitsharma@torrentpharma.com .

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

Responsibilities: * Manage international client relationships * Execute B2B lead generation strategies * Acquire new clients globally * Develop international business opportunities * Lead OSD formulations sales abroad

- Provide remote QMS support for global sites, handling OOS, OOT, deviations, incidents and change controls. - Review documentation for compliance & drive continuous improvement. - Ensure timely investigation, analysis & change control initiation. Required Candidate profile - 9+ years of QC/QA experience in regulated pharma co. - Reviewing OOS, OOT, APQR & lab incident investigations, change controls & managing deviations - Strong knowledge of USFDA, EU & Health Canada

Roles and Responsibilities - Ensure quality control processes are followed by the team. - Conduct regular inspections to identify areas for improvement. - Develop and implement quality standards, procedures, and documentation. - Collaborate with cross-functional teams to resolve quality issues. - Analyze data to track trends and improve overall product quality.