750 Osd Jobs - Page 13

Job Title: QC Microbiology Analyst Job Location: Bangalore Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assign...

Required Skills Technology | Network Monitoring Tools | Traverse Domain | IT in Banking | Customer Support Behavioral | Aptitude | Communication Technology | Network Monitoring Tools | Solarwinds Behavioral | Aptitude | Information Processing Education Qualification : Any Graduate Certification Mandatory / Desirable : Technology | IT Certifications | Microsoft Certification | Microsoft Windows Server Networking Fundamentals Details: 1. SCCM Administration - Working knowledge of SCCM administration and related dependent components like AD, DNS, BitLocker, Group Policies etc. 2. Patch Management: a. Deployment of monthly updates on every patch Tuesday following the Change process b. Provide th...

Role & responsibilities Plan, execute, and review Validation Protocols and Reports (Process, Cleaning, Analytical Method, and Computer System Validation). Execute and review Equipment Qualification activities (IQ/OQ/PQ, Re-qualification). Support preparation and maintenance of Validation Master Plan (VMP) . Ensure compliance with cGMP, FDA, MHRA, WHO, and other international regulatory guidelines. Coordinate with cross-functional teams (Production, Engineering, QC, R&D) for smooth execution of validation activities. Conduct risk assessments and gap analysis for equipment, utilities, and processes. Review and maintain SOPs, protocols, and technical documentation related to validation. Handle ...

Role & responsibilities Operate and monitor tablet compression machines (e.g., Cadmach, Fette, Korsch, or equivalent). Set and adjust machine parameters (RPM, compression force, weight, thickness, hardness, etc.) as per BMR. Ensure proper tooling installation, changeover, and maintenance of punches & dies. Perform in-process checks (IPC) like weight, thickness, hardness, friability, and appearance. Record all operational activities in BMR, logbooks, and other documents as per GDP. Ensure line clearance, cleaning, and preventive maintenance of machines. Report deviations, breakdowns, and abnormalities to supervisors/engineering. Adhere strictly to cGMP, GDP, EHS, and safety guidelines during ...

Role & responsibilities Operate and monitor tablet coating machines (Auto Coater/Conventional Pan) as per batch manufacturing records (BMR). Perform coating processes (aqueous/organic) ensuring uniformity and quality standards. Set and monitor machine parameters (spray rate, pan speed, inlet/outlet temperature, atomizing pressure, etc.). Carry out equipment cleaning, calibration, and preventive maintenance. Record all operational details in BMR, logbooks, and related documents. Coordinate with QA/QC for in-process checks and ensure compliance. Report deviations, breakdowns, and abnormalities immediately. Maintain proper stock of coating materials and consumables. Follow cGMP, GDP, safety, an...

Role & responsibilities Operate RMG, FBD, Multi Mill, and related granulation equipment as per BMR and SOP. Carry out wet granulation, drying, sizing, and blending processes. Set machine parameters and monitor process conditions (impeller/chopper speed, inlet/outlet temperature, drying time, etc.). Prepare and handle binder/solution as per production requirement. Ensure proper cleaning, line clearance, and preventive maintenance of equipment. Record production activities in BMR, logbooks, and other documents as per GDP. Coordinate with QA/QC for in-process checks (LOD, particle size, etc.) and implement corrective actions. Report any deviations, equipment breakdowns, or abnormalities promptl...

Excellent job opportunity for Production Supervisor @Unison Pharmaceuticals Pvt Ltd, Moraiya, Ahmedabad 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. Experience : 2 to 6 years Job Role : Production Supervisor Designation : Officer / Sr. Off...

The ideal candidate will be responsible for sourcing, negotiating, and managing supplier relationships to ensure the timely and cost-effective acquisition of goods and materials necessary for our export operations. Oversee purchase order management, documentation, and compliance with export regulations. Manage and lead the procurement team, ensuring training, motivation, and performance management. Purchase of finished product tablets / Capsules / Injections / Surgical items from Third Party Manufacturing. 8 to 10 Pharma Finished goods procurement, preferably with exposure to CMO coordination .

Role & responsibilities Timely completion of designs, and Process engineering deliverables. Adherence to Dept./Discipline Working Instructions and Quality Systems. Overview of work progress and work-hour usage. Working within company budgets Meet client expectations and maintain long-term relationship with client. Attend to clients feedback and any complaints Preferred candidate profile A degree in Chemical Engineering Discipline with Minimum 18 to 25 years in Process Department of a consultancy organization or technical services department of a Pharmaceutical/ Biotech/Lifesciences. Candidate should possess knowledge in carrying out basic and detailed engineering work. The experience can be ...

Role & responsibilities Key Responsibilities: Perform routine and preventive maintenance of electrical panels, motors, MCCs, PLCs, and field instruments in formulation (Granulation, Compression, Coating, Capsule filling, Blister packing, etc.). Attend to electrical breakdowns in production equipment with minimum downtime. Assist in installation, commissioning, and qualification (IQ/OQ/PQ) of new formulation machines. Maintain logbooks, calibration records, and preventive maintenance schedules as per SOPs. Ensure adherence to GMP, safety, and electrical compliance standards. Support in audits (regulatory, safety, internal, and external). Monitor and maintain compliance of electrical safety st...

Roles Open: QA (QMS, Validations and AQA): Qualifications, Process/Cleaning Validation, QMS (Change Controls, Deviations, CAPA, Complaints, and OOS) RA (Regulatory Affairs): CTD Preparation/Review, Regulatory Queries, Tech Transfer Documents. Required Candidate profile QA Executive / Sr. Executive (QMS & Validations) AQA Executive / Sr. Executive (Analytical QA) RA Executive / Sr. Executive – Regulatory Affairs

We have requirement for Formulations AR&D. Exp: 2 to 16 Years Designation: Executive to Senior Manager Work Location: CRAMSN Research Park, Pashamylaram, Patancheru, Hyderabad. Interested can share there CV's to mail: manishankar.dadi@msnlabs.com

Roles & Responsibilities 1. To support and execute formulation development of mAbs 2. Conducting stability studies as per ICH guidelines. 3. Acquisition, recording, analysis and compilation of data in prescribed formats. 4. Responsible for maintenance and documentation of the developmental work carried out. 5. Supporting procurement/installation of appropriate equipment’s and consumables required for work, whenever applicable. 6. Capturing and compilation of the data generated contemporaneously in eLN (electronic Lab Notebook) and getting the same verified by the manager of the team regularly. 7. Ensuring proper usage and maintenance and calibration of equipment: entering the usage in log bo...

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 ...

Role & responsibilities Lead Generation and Account Management: Generate leads and convert them into business through effective account management, specifically focusing on hospital business . Develop and manage strong relationships with corporate hospitals and healthcare professionals in your assigned territory. Sales Effectiveness: Ensure consistent sales performance by meeting call averages, coverage, and daily activity reporting. Continuously achieve monthly and annual sales targets. Marketing & Brand Building - monthly basis: Execute marketing strategies like Promotion Campaigns , Continuing Medical Education (CME) , and Patient Experience Programs to enhance brand image and recall. Con...

Job Title: QMS Manager Business Unit: Global Quality Compliance Job Grade G10 / Manager 1 Location : Mohali Educational Qualification: M.Sc / B.Pharm / M.Pharm Experience: 12+ yrs Quality Management System 1. Implement, operate, monitor and maintain Quality Systems which enable operations on site to occur in an efficient manner and in compliance with Global Quality Standards and cGMPs. 2. Review and Archival of Quality System documents. 3. Follow up for timely closure of Quality Management System documents. 4. Participating in the investigation analysis for Complaints and Audit finding, moreover responsible for providing batch disposition decision as per the outcome of PQC investigation. 5. ...

Role & responsibilities 1. To undertake literature search & preparation of report for a new development project. 2. To execute development trials as part of prototype development till technology transfer of new drug products at the manufacturing sites. 3. To guide & supervise development trainees or associates during development of new formulations. 4. To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. 5. Material Master creation of Material code/ Vendor code in ERP. 6. MIC creation of Raw material / Packing material / Finished products in ERP. 7. Applying Test / Import / Manufacturer Licenses 8. Involving all Development QA a...

Compilation and submission of eCTD dossier for new product application & post approval submission Query response, PAS,CBE and annual report, drug listing Review of artwork and submission of labelling section Maintain product life cycle.

Job Description: Formulation Development candidate - OSD will be responsible for designing, developing, and optimizing advanced drug delivery systems in oral solid dosage forms such as tablets, capsules, and controlled-release formulations. This role requires expertise in pharmaceutical formulation, process development, and a thorough understanding of regulatory requirements. Formulation Development: Design and develop OSD formulations for oral solid dosage forms, including immediate release (IR), extended release (ER), and modified release (MR) products. Perform pre-formulation studies, including solubility, stability, and compatibility evaluations. Technology Integration: Implement innovat...

":" Job Title: IT Administrator Job Summary: As an Intune Administrator at VE3, you will play a pivotal role in orchestrating a secure and efficient digital workplace environment. Your expertise will be instrumental in managing end-user client devices, backend infrastructure, and ensuring a seamless operational framework. We value candidates with a robust understanding of Intune, exceptional troubleshooting acumen, and a forward-thinking approach to innovation and automation in operational protocols. Requirements Key Responsibilities: Frontend Workplace Management: Administer remote management of end-user client devices. Execute device lifecycle management and timely OS patching. Workplace A...

To initiate action for purchasing based on requirement. To discuss and influence for receiving commercial offer. To prepare Purchase orders based on final decision from OSD lead and QTS. To perform Vendor Registration Process To initiate action for purchasing based on requirement. To discuss and influence for receiving commercial offer. To discuss and negotiate with vendor. To prepare purchase based on final decision from OSD lead and QTS Preparation of gate pass, Picklist for raw material withdrawal from store, transport request Raw material movement for vendors as per PO for manufacturing Need to develop new Vendors for boiler attachment and NPP manufacturing To Coordinate with other depar...

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 4 Years Skills :- Supervisor :- Granulation | Compression | Coating | Cartornator| Packing Operators :- Granulation | Compression | Coating | Cartornator| Packing Division :- Formulation Interview Date:- 23-08-2025 Interview Time :- 9.00AM TO 2.00PM 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 candidate those ...

Role & responsibilities 1. To develop stable solid oral products for Domestic Markets and ROW Markets. 2. Technology transfer of developed products to plant level, this includes all TTD-related works. 3. To collect and compile all data and submit to respective regulatory agencies. 4. To address DCGI/ regulatory agency queries as per requirement. 5. To extend support to plant for any commercial trouble shooting. Preferred candidate profile Only Ph.D candidates

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma & M.Sc with relevant experience Designations: Jr. Officer, Officer & Jr.Executive • PRODUCTION: Compression, Granulation, Coating. Qualification & Experience: (01 - 04Years) •ITI, Diploma & B.Sc with relevant experience Designations: Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: Hotel: HOTEL EVERGREEN oAmbala - Chandigarh Expy, Near Bus stand, Bhagat Singh Nagar, Dera Bassi, Sheikhpur Khurd, Punjab 140507 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documen...

Role & responsibilities Hiring for OSD Formulation Technician- Granulation/Compression/Capsule/Coating/Compression/Packing QC/Microbiologist Supervisor- Analyst Role Preferred candidate profile B.sc/ M.SC in Chemistry, Microbiology is required for QC/Micro position ITI/Diploma Experienced Technician required Mandatory USFDA Plant Exposure required 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 agency or anyone asking you to pay money representing himself to be representing Sun...