963 Osd Jobs - Page 6

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 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. Showcasing your leadership skills, you will drive the team towards successful project completion and client satisfaction. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the...

Experience into Granulation with RMG & FBP Machine Role & responsibilities Experience into Coating Operating Machine Preferred candidate profile

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operations - Control, monitoring, and recording To monitor and carry out maintenance of utility equipment and review planned preventive maintenance of utility and production equipment. To provide quality service system such as, potable water, Steam, compressed air and Vacuum. To maintain and update the HVAC system. To review and update all engineering SOPs and other related documents along with quality assurance. Collaborates in the planning of new facilities and equipment or their replacement. Prepare work authorisation. Develop plant layout and prepare plans for facilities and requirements. Est...

Job Purpose: To ensure compliance of all engineering systems, utilities, and equipment with current Good Manufacturing Practices (cGMP), regulatory requirements, and company quality standards. The Engineering QA Engineer will support qualification, validation, and periodic review activities to maintain a state of control across all engineering systems within the pharmaceutical manufacturing facility. Key Responsibilities: 1. Qualification & Validation Review and approve engineering qualification documents (URS, DQ, IQ, OQ, PQ) for equipment, utilities, and facilities. Participate in qualification/validation activities ensuring compliance with cGMP and internal procedures. Ensure traceability...

Preferred candidate profile Diploma in Mechanical/Electrical with minimum 1 year of experience in Pellet Production Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operate and monitor pelletization equipment as per SOPs. Maintain process parameters to ensure product quality. Perform equipment cleaning and changeover activities. Process data and maintain batch documentation. Follow GMP, safety, etc. Operate Fluid Bed Equipment and Spheroniser as per SOP, including cleaning and line clearance activities to ensure readiness for production. Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and moni...

About The Role Skill required: Tech for Operations - Application Architecture Implementation & Test Designation: Solution Architecture Manager Qualifications: Any Graduation Years of Experience: 13 to 18 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song"” all powered by the world's largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients...

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Own production execution and shift supervision; ensure line clea...

Key Responsibilities: Prepare and administer radiopharmaceuticals to patients under the supervision of a Nuclear Medicine Physician. Operate and maintain gamma cameras, PET-CT scanners, and SPECT systems for diagnostic imaging. Conduct imaging procedures, process images, and ensure data quality and patient safety. Follow strict protocols for radiation safety, waste disposal, and contamination control . Calibrate and perform routine maintenance on imaging equipment. Maintain accurate patient records, dosage logs, and equipment usage reports. Educate patients on the procedures and ensure comfort during tests. Collaborate with physicians, radiologists, and other healthcare professionals for acc...

Formulation, ROW Market

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 : Dassault Systemes ENOVIA V5 Good to have skills : NA Minimum 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. Your typical day will involve collaborating with various stakeholders to gather requirements, overseeing the development process, and ensuring that the applications meet the specified needs. You will also be ...

To perform physical and chemical, instrumental analysis of Raw Material, packaging material, Water samples, In Process, Finished Product Samples and Stability Samples. The candidate should have experience on HPLC, GC UV, IR and Dissolution testing. To perform a Release testing, Dissolution profile study, challenge study ,Hold time study, RLD sample analysis, validation, verification, method transfer activity and API-Verification as when applicable. To perform instrument calibration and working standard qualification. Responsible to adherence of GLP and Health, Safety Environment system in Laboratory. To perform the task assigned by the supervisor/HOD as and when required. Should have good wr...

Role & responsibilities : QC,QA & Production We are seeking a diligent and experienced candidates QC OFFICER TO EXECUTIVE (HPLC/GC/UV/RM/PM),LOGISTICS INCHARGE, PRODUCTION SR.OFFICER(OSD)(GRANULATION/COMPRESSION),QA(QMS/VALIDATION/IPQA)(DPI) Preferred candidate profile Quality control QA/QC/Production The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance (QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. The Saksham Success Enterprises Near Sunder Ayan by pass solan 17...

Education: M. Pharm (Pharmaceutics) Experience: 4-6 years Mandatory skills: Formulation Development for solid orals, liquid orals, Pellets, sachets, HME, Literature search , regulatory guidelines, RFIs/Clarifax response to health agency ICH/MHRA/TGA/HC, Drug/Excipients compatibility, Lab scale development hands on experience in scaling up (exhibit batches) & equipments in manufacturing (RMG/FBD/compression machine/coating/GPCG), team handling & documentation exposure MFR/BMR/BPR/PVP/HTSP/PDR/CDR (Preferably from Bangalore candidates who can join in 30 days)

Architect SCCM/Intune setups, manage full endpoint lifecycle, enforce policies, deploy apps/OS, automate patching, monitor via Power BI, troubleshoot issues, script with PowerShell, and integrate hybrid/cloud environments. Required Candidate profile Experience with SCCM & Intune; expert in infra design, Autopilot, AAD Join, Apple DEP, Win11 deployment, app packaging, and PowerShell automation for MDM, reporting, and troubleshooting.

Role & responsibilities : Experienced in In process-checks, Line clearance, sampling, Environment monitoring, Documentation, process monitoring, Strong knowledge of GMP, regulatory guidelines (e.g., FDA), and quality assurance practices. Excellent analytical skills and attention to detail

Production - Experience in operation & supervision of compression, granulation, & coating machine Maintenance - Working in OSD formulation plant, Plant Maintenance compression, granulation, coating & packing QC - Handling instrument like HPLC dissolution, GC, IR, UV, QMS & material testing

Role & responsibilities Leadership & Department Setup. Formulation Development (Tablets). Coating Expertise. Project Management & Execution. Regulatory & Documentation. Innovation & Continuous Improvement Preferred candidate profile Deep expertise in tablet formulation and coating applications Strong understanding of polymers, coating materials like HPMC, PVA, acrylic polymers, etc. Ability to lead and build a scientific team from ground zero Hands-on experience with development and troubleshooting Strong documentation and regulatory knowledge Excellent project management and cross-functional coordination Strategic mindset with a problem-solving approach

Head Engineering (Pharma OSD) – Manage maintenance, utilities, HVAC, water systems, CAPEX, TPM, compliance (USFDA/MHRA/WHO), energy efficiency & safety. Lead team, ensure uptime, audit readiness & cost control in formulation plant. CV @ 9106329670 Office cab/shuttle Food allowance Health insurance Annual bonus Provident fund

Looking for a motivated professional with hands-on experience in production planning, inventory control, and international supply chain management within the pharmaceutical industry. What Youll Do: Plan and execute production schedules based on demand & capacity Manage raw materials and finished goods inventory Coordinate overseas procurement, import/export logistics & compliance Collaborate with cross-functional teams (Manufacturing, QA, SCM) Support global audits and drive process improvements What Were Looking For: 2–6 years’ experience in PPIC/Supply Chain (Pharma exp is mandatory) Bachelor’s in Supply Chain / Business / related field ERP/SAP proficiency & strong analytical mindset Excel...

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 Required::ENGLISH Role Rarity :To Be Defined

Walk In Drive For Production OSD In Formulation Division @ Burgula Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 6 Years Skills :- Supervisor :- Granulation | Compression | Coating | Cartonator | PackingAutocartonator Operators :- Granulation | Compression | Coating | Cartonator | Packing Division :- Formulation Interview Date:- 15-11-2025 Interview Time :- 9.00AM TO 4.00PM Work Location & Venue Location:- MSNF Unit-VI Burgula X5R8+CXH, Mothighanapur, Burgul, Telangana 509202 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for ca...

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | BA | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Operator: Compression | Coating | Granulation | Capsule Filling Manufacturing: Supervisor | Shift IN charge Packing operators: Cartonator | Auto Cartonator | Packing Supervisor | Blister Packing | Bottle Packing Division :- Formulation Interview Date:- 15-11-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur Venue Location:- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , ...

Walk In Drive for Production OSD Department In Formulation Division @ Mekaguda Qualification :- Diploma | B Tech | B Sc | B Pharmacy | M Sc | M Pharmacy Experience:- 2 to 8 Years Interview Date:- 15-11-2025 (Saturday) Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-04-Mekaguda 37XJ+W82, Mekaguda, Telangana 509228 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidates those who have experience in Manufacturing:- Capsule Filling | Granulation | Liquid | Roll Compactor Packing:- ...

About The Role Project Role : Tech Delivery Subject Matter Expert Project Role Description : Drive innovative practices into delivery, bring depth of expertise to a delivery engagement. Sought out as experts, enhance Accentures marketplace reputation. Bring emerging ideas to life by shaping Accenture and client strategy. Use deep technical expertise, business acumen and fluid communication skills, work directly with a client in a trusted advisor relationship to gather requirements to analyze, design and/or implement technology best practice business changes. Must have skills : SAP Document and Reporting Compliance Good to have skills : NAMinimum 12 year(s) of experience is required Education...

Job description You will be responsible for, 1. Candidate will be based at corporate office of reputed pharma company at Mumbai and will handle & coordinate with all Regulatory Affairs functions related to plant, R&D International Business of company also for export to USA, EU, Emerging Market. 2. Prepare registration dossier for procuring certificates/license from local FDA, DCGI and FSSAI. This would entail thorough familiarity with FDA, & FSSAI online portal, Drug Act and its various Schedules. 3. Co-ordinate with QA and R&D departments for technical documents (manufacturing documents like batch records, specifications, analytical methods, validation reports, and Stability data) required ...