750 Osd Jobs - Page 9

Responsible for formulation development for OSD, external preparations, oral liquids, and injectables. Responsible for pre-formulation studies, prototype development, and scale-up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (A, C, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation.

QC Chemist (Formulation OSD) Role & responsibilities Job Role: - Analysis of Raw Materials & Packing Materials - Sampling & analysis of Water, In-process, Finished products, Stability, and Swab Analysis Experience: 1 to 5 years Education: B. Pharm / M. Sc in Chemistry, Organic Chemistry, General Chemistry, Pharmaceutical Chemistry, or Industrial Chemistry Work Location: Bangalore Preferred candidate profile

Role & responsibilities Hiring for OSD Formulation Site, Mohali Punjab Production Technician & Officers ( Granulation/ Compression/ Coating/ Capsule/ Packing) Quality Control Analyst (Officer/Senior Officer) Analyst Role must have exposure-HPLC with empower software, GC & Dissolution in FG/Stability Lab Preferred candidate profile Mandatory USFDA Plant Exposure Production Technician- ITI/Diploma QC Analyst- B.SC/M.SC in Chemistry Note- Sun Pharma does not seek payment of any kind from a prospective candidates for employment with Sun Pharma or authorise any agency or any individual to collect or charge any fees or charges for recruitment. Please be cautious while dealing with any recruitment ...

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. uality Management Systems (MS): Implementat...

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. Quality Management Systems (MS): Implementa...

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 ...

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. ...

Job Title: Packing Supervisor OSD (USFDA Approved Plant) Job Location: Dadra Job Summary The Packing Supervisor will oversee and manage the packaging operations of oral solid dosage pharmaceutical products in compliance with USFDA, cGMP, and company standards This role ensures timely execution of packing activities, adherence to quality and safety norms, and coordination with cross-functional teams to meet production targets, Key Responsibilities Supervision & Operations Oversee day-to-day packaging operations for OSD products, Ensure compliance with USFDA, cGMP, and SOPs during all packing activities, Monitor and maintain the integrity of batch records and documentation, Quality & Complianc...

Job Description Position: Technical Lead - SCCM Experience: 6 to 9 years Location: Noida Education: B.E./ B.Tech./ .MCA Primary Skills: SCCM, MECM, Intune, OSD, SCCM Infra Key Responsibilities Lead and resolve escalated MECM-related incidents and service requests. Design, deploy, and manage MECM infrastructure and client configurations. Package, test, and deploy applications across enterprise environments. Manage MECM with Intune for co-management scenarios. Perform OS deployments. Collaborate with security and infrastructure teams to ensure endpoint health and compliance. Managing OS & Boot Images Required Skills & Qualifications 6+ years of hands-on experience with MECM/SCCM in enterprise ...

Role Purpose The purpose of this role is to support delivery through development and deployment of tools. Do 1. Provide tool design, development and deployment support for the project delivery a. Interact with the internal project or client to understand the project requirement from a tool perspective b. Design the solution keeping in mind the tool requirements, current tools available as well as details on licenses required etc. c. Provide budget and timeline estimates for the tool development/ deployment as required d. For any new tool development, identify sources for development (internal or 3rd party) and work with the project managers on the development of the tool keeping in mind the ...

Walk In Drive for Engineering Services Department In Formulation Division @ Kothur Department:- Engineering Services OSD Skills- OSD ( Electrical | Mechanical) | Sterile Mechanical | HVAC | Water System Qualification :- ITI | Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulations Work location :-MSNF-II, Kothur Interview Date- 13-09-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- Unit-II Kothur, Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8787 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan C...

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

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.

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.

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

Role & responsibilities: To perform line clearance, area clearance & daily IPQA activities. To review BMR/BPR/BCR, validation protocols. To perform sampling activity at manufacturing facility. To perform facility round at shop floor. Collection of control sample and Stability sample. Issuance of LMR, BMR, ECR and maintaining the record product wise. Issuance of Finished product label & maintaining the record.

Candidate having minimum 3 to 5 year experience in Granulation, Compression & Coating section in pharmaceutical industry. Interested candidate can call on this mobile no-+91-78310 31890, 9816336040 Food allowance Health insurance Annual bonus Provident fund

ensure compliance with cGMP, cGLP, SOPs & regulatory norms. Prepare/review QMS docs (SOPs, CAPA, Deviation, OOS, Complaints). Oversee production, resource planning, validations, in-process checks & documentation (BMR/BPR). Coordinate with QA/QC/

Interview for BSC Chemistry Fresher for Packing Department for Large Formulation Pharma Company No MSC Candidates Contract Base Job Call on 9727755967 / 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Packing Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

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...

JOB DESCRIPTION Designation: Executive Job Location: Bangalore Department: EAM About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D pr...

Greetings!!!! We are looking for a QA - Manger - OSD _Chennai Location Job Description: Responsible for BMR, batch release, validations, qualifications, SOPs, GMP compliance. Handle audits, QMS (Deviation, OOS, OOT, CAPA), and technology transfer. Exposure to analytical operations will be an added advantage. Strong experience in OSD / Liquid formulation QA required. Key Skills: QA, Quality Assurance, BMR, Batch Release, Validation, GMP, SOP, QMS, Audit, Deviation, OOS, OOT, CAPA, Pharma QA. Salary: As per market standards Note: Immediate joiners preferred. Interested Candidates Kindly share your updated cv to uma@bvrpc.com

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 h...

Role & responsibilities Perform granulation process operations as per SOP and batch requirements. Handle RMG (Rapid Mixer Granulator) machine for mixing and wet granulation. Operate and monitor FBD (Fluidized Bed Dryer) machine for drying granules. Ensure cleaning and maintenance of equipment (RMG, FBD, and associated accessories) as per cGMP and safety guidelines. Record operational parameters, cleaning logs, and maintain proper documentation. Follow SOPs, GMP, and safety protocols during operations. Coordinate with production and quality teams for smooth batch execution. Preferred candidate profile Experience: 14 years in Pharma Production (Granulation). Hands-on experience in RMG & FBD op...

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.