750 Osd Jobs - Page 6

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 1. To develop Stable and Bioequivalent solid oral products for EU, ROW (Rest Of World) and Domestic markets. 2. Technology transfer of developed products to plant level; this includes all TTD related works 3. To collect, compile of all data of plant batches and submit to regulatory department as per market specific requirement 4. To address agency's queries as per requirement 5. To extend support to plant for any trouble shooting

Excellent job opportunity for OSD Production - Machine Operator @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: 2-8 years Location : Moraiya, Ahmedabad Unit : 3 Education Qualifi...

Job Title: Manager Global Quality Sustainability, Training and Quality Culture Business Unit: Global Quality & Compliance Job Grade G10 Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: S...

Job Summary We are seeking an individual to oversee batch manufacturing, ensuring adherence to cGMP (Current Good Manufacturing Practices), providing training, and coordinating day-to-day activities. Responsibilities include minimizing machine downtime, managing subordinate staff, assuring compliance with standards and SOPs (Standard Operating Procedure), leading regulatory audits, compiling reports, ensuring safety norms, and budget management. Roles & Responsibilities • You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control. • You will be responsible for imparting general and cGMP ...

Having good communication skills Willing to work in Shifts Shall report to Executive / Sr. Executive for day to day activities Execution of allotted daily production activities in Solid Oral Section (Softgel) of Oncology & Hormone Block To perform all related activities as per cGMP and compliance To perform activities as per SOPs and to complete related documentation Planning and execution of daily production activities To operate the equipments in compounding area like compounding vessel and Filtration vessel etc. as per SOP To perform cleaning and sterilization of compounding vessel as per SOP

1) Understand and develop immediate release and modified release oral formulations for regulated markets (US and EU market); 2) Handling equipment’s for solid oral dosage forms. 3) Troubleshoot in existing products and optimize the process; Required Candidate profile 4) Knowledge of using Design Expert/Mini Tab QbD Software for development conduct experiments. 5) Preparing reports like PDR, specifications, stability protocols, DoE, Tech transfer & Reports.

A highly skilled professional responsible for management of market complaints/investigations at site, including receipt, logging, and further tracking. Timely follow-ups and effective communication within quality team and other relevant stakeholders. Ability to perform the investigations thoroughly. Strong capabilities in data interpretations and root cause identification. Ability to prepare risk assessments. Detailed investigation reports preparation/writeups skills. Initiating and managing CAPAs through Trackwise system, ensuring timely implementation and closure. Effective collaboration with cross-functional teams to support Field Alert Reports (FARs), product recall associated activities...

Department: Production Location: Plant ( Bavla) Shift: Rotational Shifts (Day/Night/General) To oversee and ensure smooth operation of sachet filling machines within the pharmaceutical production line, maintaining compliance with cGMP standards, safety protocols, and production targets. Key Responsibilities: Operate, monitor, and manage sachet filling machines (e.g., automatic sachet packing machines, multi-lane sachet fillers). Supervise and guide machine operators and contract manpower during shift operations. Ensure adherence to Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs) . Perform line clearance , conduct in-process quality checks , and maintain accurate p...

Department: Production Location: Plant ( Bavla) Shift: Rotational Shifts (Day/Night/General) To ensure smooth execution of capsule filling operations within the Oral Solid Dosage (OSD) manufacturing section, ensuring compliance with cGMP standards, safety protocols, and production targets. Key Responsibilities: Operate, monitor, and manage capsule filling machines (e.g., Bosch, ACG Pam, Fette, etc.) within the OSD manufacturing unit. Supervise and guide operators and contract workforce during production shifts. Ensure accuracy and completeness of Batch Manufacturing Records (BMRs) and adherence to Standard Operating Procedures (SOPs) . Perform line clearance , conduct in-process quality chec...

Role & responsibilities Operate and maintain labelling machines (including Pharma Pack) to ensure accurate and efficient labelling of pharmaceutical products. Verify correct batch details, expiry/manufacturing dates, and regulatory information on labels to ensure compliance with SOPs and GMP standards. Perform in-process quality checks to identify and segregate defective or non-conforming products. Maintain proper documentation of labelling activities and report any machine breakdowns, deviations, or quality concerns promptly to supervisors. Preferred candidate profile 2-8 years of relevant experience in labelling operations, preferably in the pharmaceutical industry. Hands-on experience han...

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 always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including s...

Roles and Responsibilities 1. As a Head Sales and Marketing, you will be responsible for handling Respiratory segment current business around 20 Crore for reputed pharma company based in Mumbai HQ. 2. Candidate will be responsible for handling P&L Budgeting and Top line and Bottom line for the Respiratory business. 3. Candidate will be responsible for handling 20 Cr per annum for Respiratory segment and implement new strategies and strengthening existing brands. 4. Candidate will be responsible for recruiting, training, and developing an entire new sales and marketing team for the new division and guide them to achieve derived targets and incentives. 5. Candidate is responsible for handling ...

Job Description: We are seeking an experienced Intune & Endpoint Management Administrator with deep expertise in Microsoft Intune, Endpoint Manager, SCCM, and device management . The ideal candidate will have extensive knowledge of device enrollment, application packaging, security policies, and troubleshooting across Windows, Android, iOS/iPadOS, and macOS environments. Key Responsibilities: Microsoft Intune & Endpoint Manager: Manage Intune/Endpoint Manager Admin Center Console for device enrollment, app protection policies, and app proxy . Configure and troubleshoot Windows Autopilot and Intune update rings . Work with Samsung Knox (KME) and Apple Business Manager for enterprise device ma...

Roles and Responsibilities Develop analytical methods for OSD products using techniques such as HPLC, GC, UV, etc. Conduct formulation research and development of injectable products. Prepare protocols, SOPs, and reports related to formulations and analysis. Collaborate with cross-functional teams to ensure successful product launches. Ensure compliance with regulatory requirements throughout the product lifecycle. Independently handling the Stability analysis of dosage forms. Has knowledge on Validation of the methods. Forced Degradation studies. Desired Candidate Profile Sound Knowledge about analytical method development and Stability analysis of dosage forms 2. Hands on experience in usi...

Job Title: Executive/Sr Executive Process Engineering OSD Business Unit: Sun Global Operations Job Grade G12A/G11B Location : Guwahati At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: Diagnose malfunction...

Vibonum Technologies, (the Althera Group), is an innovation-driven pharmaceutical manufacturing company specializing in cutting-edge solutions in Oral Solid Dosage (OSD) forms. We are committed to excellence, compliance, and global quality standards in our product delivery. We are seeking an experienced and visionary Project & Engineering Leader to lead Projects & Engineering function, specifically for our OSD (Tablets/Capsules) operations. The ideal candidate will be responsible for driving technical excellence, overseeing all engineering and project management activities, managing teams, budgets, and projects, and collaborating with stakeholders. Role & responsibilities Should be experienc...

We are looking for a skilled professional with 5-10 years of experience to join our team as an Enovia Expert in Bangalore, Hyderabad, Pune, and Chennai. The ideal candidate will have a strong background in design and development using the Enovia 3D Exp. 2020/21/22x platform. Roles and Responsibility Design and develop applications using Java, J2EE, and other relevant technologies. Implement end-to-end projects and migrate data from legacy systems. Collaborate with cross-functional teams to ensure successful project delivery. Develop and maintain technical documentation for applications and systems. Troubleshoot and resolve issues related to application performance and functionality. Provide ...

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

Job Summary We are looking for an individual to oversee day-to-day production operations, including guiding and coaching employees, ensuring equipment safety and maintenance, and executing batch manufacturing activities. Responsibilities also include documentation review, maintaining product quality, coordinating training, conducting initial incident investigations, and managing process orders.The person must having skill to operate and do the trouble shooting of Scantech Laser Tablet Drilling machine. Roles & Responsibilities • You will be responsible for overseeing execution of day-to-day production activities. • You will be responsible for guiding and coaching employees, monitoring their ...

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.

Walk-in Interview for Zydus Lifesciences Limited at Ahmedabad| 28th September 2025|Sunday We are recruiting for our Moriaya, Ahmedabad Unit . Walk-in Interview Details Interview Date : 28th September 2025 Interview Timings: 9:00 AM 4:00 PM Interview Location: Zydus Healthcare Ltd, Block 2, 3, 4, 5, Sigma Commerce Zone, Nr. Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad 380015. Job Location: Moraiya, Ahmedabad Education Qualification: ITI / Diploma / BE / B.Sc / M.Sc / B.Pharma / M.Pharma Experience: 2 – 8 Years Quality Assurance (IPQA) : Officer to Sr. Executive: IPQA in process (Mfg. & Pkg.) Engineering: Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumenta...

As a Technical and Development professional, your role will involve a variety of responsibilities and qualifications to excel in the field. **Role Overview:** You will be expected to have a Degree in Architecture from an institute recognized by the Council of Architecture. Your expertise will include in-depth knowledge in Layout development and general process requirements of pharmaceutical / Life Science Pharmaceutical production facilities. This includes but is not limited to facilities for API, Sterile Products, OSD, Bio-Pharma, Gene Therapy products, and related R&D labs. Additionally, you should have the ability and initiative to learn new types of facilities as required by client requi...

Manage QMS docs per regulatory standards. Prepare, review QRA, validation, complaints, audits, PQR, SMF, manuals. Align with teams, support audits, SOPs, training, reviews, and drive continuous improvement. Perks and benefits Bachelor's Accommodation and Travelling benefit.

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Open Positions: Operators & Supervisors OSD Production & Packing (Onco & Non-Onco) Experience: 0 to 6 Years (Freshers graduated in 2024/25 are eligible) Qualifications: I.T.I / Diploma / B. Pharmacy / M. Pharmacy Key Responsibilities: Operate equipment's in Granulation (RMG, FBD, ACG, GEA), Compression (GEA, Sejong), Coating (NEOCOTA), Capsule Filling (Bosch, MG02), Blister Packing (CAM NMX, HV1, BQS, IMA/ACG), and Bottle Packing (CVC, Optel) lines. Supervise production lines, including Granulation, Compression, Coating, and Packing (Blister/Bottle). Good verbal and written English communication skills 2. Tr...