234 Gdp Jobs - Page 4

Post- Manager - Supply Chain Location Pune Hadapsar , Magarpatta Experience - 08-10 yrs Skills - pharmaceutical supply chain management. Strong understanding of GMP, GDP Education - Bachelor's/Master's degree in Supply Chain Management, Business Administration Job Overview : The Supply Chain Manager oversees and manages the end-to-end supply chain operations, ensuring the timely delivery of pharmaceutical products while maintaining quality, compliance, cost efficiency, and customer satisfaction. JD Develop and implement supply chain strategies Manage warehousing, inventory management, and distribution activities. Ensure compliance with industry regulations and quality standards. Collaborate ...

Job Title: Senior Guidewire Digital Developer / Engineer Experience: 7 10 Years Employment Type: Full-Time (FTE) Notice Period: Immediate 45 Days Location: Hyderabad, Pune, Coimbatore, bangalore Job Description We are looking for an experienced Guidewire Digital Developer with strong hands-on experience in Guidewire Digital Portal (GDP) and related modules to join our team. The ideal candidate will have 7-10 years of experience in developing and implementing digital solutions for insurance platforms, with a specific focus on Guidewire's Digital products. Key Responsibilities Design, develop, and implement enterprise-level digital solutions using Guidewire Digital Portal (GDP) . Work across d...

Post Production Operator - Capsules Organization Context Position Title: Line Operator - Capsules Employee Name: Grade : DET Department: Manufacturing-Post Production Location: Aurangabad Reports to: Team lead/Hall In-charge Reported by: Job Objective Maintain line continuity, productivity, quality of product, reduce wastages and adherence to cGMP, GDP and safety in-shift for the allocated line(s). Primary responsibilities Strategic Planning Activities: Core: Check the allocated post production (ATS/Printing /camera)- line(s) in each shift as per the CTQ (critical to Quality) /CTP (Critical to Productivity) checklist Follow plan as per colour change note by ensuring minimal change over time ...

As a member of the Group Company's Capsules team, your primary responsibilities will include checking the allocated post production (ATS/Printing/camera) line(s) in each shift according to the CTQ (critical to Quality) / CTP (Critical to Productivity) checklist. You will be required to follow the plan for color change noted, ensuring minimal change over time at each subsection. It is essential to follow instructions from the shift lead to facilitate timely changeover by ensuring the availability of rollers/ink, etc. You will execute IPQC after every roller cleaning, checking rejections of cameras every hour to achieve zero defects. Operating cameras as per SOP to meet productivity and qualit...

As a member of our team at Meteoric Biopharmaceuticals, your role will involve various responsibilities related to Human Resources. You will be responsible for Talent Acquisition and Management, ensuring we have the right individuals on board to drive our organization forward. Additionally, you will oversee Onboarding and Offboarding processes, ensuring a smooth transition for new hires and departing employees. Employee Relations and Engagement will be a key focus of your role, as you work to foster a positive and inclusive work environment. Performance Management will also fall under your purview, as you support employees in reaching their full potential through feedback and development opp...

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. ...

Job Title: Senior Supplier Quality Location: Bengaluru, Karnataka, India Employment type: Part-time Job Summary: We are seeking an experienced Supplier Quality Professional Trainer with 10+ years of expertise in managing supplier quality assurance , supplier development, and compliance in regulated industries (pharmaceutical, biotech, or medical devices). The role involves ensuring suppliers meet company , industry, and regulatory standards by leading audits, driving quality improvement initiatives , and building strong supplier partnerships. Job Responsibilities: Develop and manage supplier quality strategies, policies, and risk management processes. Lead supplier qualification, selection, ...

As a Quality Control Inspector, your primary responsibilities will include ensuring effective implementation of IQC/PQC inspections, ensuring that capsules produced comply with dimension specifications, ensuring compliance with GDP and cGMP requirements, ensuring compliance with safety regulations, and ensuring CAPA compliance for customer satisfaction. You will be responsible for performing and reviewing In Process quality control checks to meet the required quality compliance as per specifications. Additionally, you will be involved in key interfaces such as inspection of attribute defects, checking moisture of capsules, inspection of print defects, online & offline printing machine line c...

Post Production Operator - Capsules Organization Context Position Title: Line Operator - Capsules Employee Name: Grade : DET Department: Manufacturing-Post Production Location: Aurangabad Reports to: Team lead/Hall In-charge Reported by: Job Objective Maintain line continuity, productivity, quality of product, reduce wastages and adherence to cGMP, GDP and safety in-shift for the allocated line(s). Primary responsibilities Strategic Planning Activities: Core: Check the allocated post production (ATS/Printing /camera)- line(s) in each shift as per the CTQ (critical to Quality) /CTP (Critical to Productivity) checklist Follow plan as per colour change note by ensuring minimal change over time ...

Role & responsibilities Job description Perform protocol for drug excipient compatibility studies and submit the protocol for review and approval Complete lab. experiment hands-on independently (Lab scale to exhibit batch and query handling). Dosage forms experience: Injectables predominantly more than 90% in career. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development. Carry out /Support Scientific literature search (CVM/USFDA/Daily-med/publications). Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments. Compilation, int...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

It's more than a job When you work in Freight Logistics and Operations at Kuehne+Nagel, you play a key role in optimising processes and ensuring that inventory and shipments move efficiently. But that is not all. Your work also helps ensure that vital medicines reach patients on time and supports other essential deliveries, from wind turbines to semiconductors. At Kuehne+Nagel, our contribution counts in more ways than we imagine. ? The Quality Auditor is a vital member of the Integrated Logistics Team, responsible for ensuring quality and compliance throughout the supply chain. Reporting to the Integrated Logistics Quality Manager, they collaborate closely with the Excellence, Operations, P...

As a QC Executive LCMS at QbD Research and Development Lab Pvt. Ltd., your primary responsibility will be to perform quality control tests and analyses using LCMS technique. This full-time on-site role based in Thane requires you to ensure compliance with regulatory standards while carrying out analytical method development and validation. To excel in this role, you must have experience in the Pharmaceutical Industry, proficiency in LCMS troubleshooting, and a solid understanding of analytical method development and validation. Familiarity with regulatory standards, guidelines (GDP, GLP, GMP), and the ability to prepare and maintain analytical protocols, reports, and records are essential. A...

The primary responsibilities of this role include ensuring the quality of all incoming PM, RM, in-process materials, stability samples, and finished products. You will be responsible for sampling and testing all PM, RM, in-process materials, and finished products within the specified lead time. Additionally, you will be expected to prepare testing reports in a timely manner and ensure correct labeling on materials such as sampled, approved, and rejected. You will also be responsible for sampling and testing raw water and purified water as per specifications. Other responsibilities include checking the dye strength of stock color solutions, verifying preservative traces in equipment used for ...

The role involves ensuring CGMP compliance and supervising overall production activities of the manufacturing area of multiple assigned manufacturing lines. Additionally, the position requires reviewing and maintaining online documents. You will be responsible for the preparation, review, revision, control, and implementation of standard operating procedures. You will also handle the preparation and review of master production documents, protocols, reports, and various document management tasks such as BMRs and BPRs. Your duties will include managing Change Control, Deviations, CAPA, Investigations, and ensuring line clearance activities are conducted before operations like manufacturing, fi...

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

As an experienced professional in the field of Analytical R&D, your primary responsibilities will include the calibration of analytical instruments, preparation, and maintenance of solutions and reagents. You will be entrusted with the critical task of analyzing development batches, stability samples, and comparative dissolution profiles. Leading the analytical method development and validation processes, along with preparation of method development reports, will be a key aspect of your role. Your expertise will be crucial in conducting drug solubility studies of active pharmaceutical ingredients, as well as executing API and excipient comparability studies. You will be responsible for the d...

The responsibilities and duties of this role include: - Performing sampling and analysis of Raw materials, Packing materials, In process, Intermediate, and Finished products. - Conducting calibration of Quality Control instruments. - Carrying out Stability/Holding time studies. - Managing Reference Standards and qualifying Working Standards. - Ensuring Analyst qualifications are met. - Conducting Analytical Method Validation. - Managing Control samples (Retain sample). - Conducting OOS investigations (Phase-1). The ideal candidate should have: - 2-3 years of experience in Pharmaceutical Quality Control. - Educational background in M.Pharmacy/B.Pharmacy/M.Sc. (Chemistry)/B.Sc. (Chemistry). - ...

Role & responsibilities To supervise all IPQA/QMS function activity on daily basis and update to Section Manager. To conduct and participate in CAPA meetings and review summary report of the same within defined time period monthly. To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, and take corrective actions. To ensure the investigation for complaints and deviations and CAPA after reviewing instruments. To prepare, review, Implement and update SOPs according to current regulations systems. To review Master Batch Document (MBD) / Master Packing Document (MPD) and get approval in advance from Head of Department of Production & QA. To train/...

In this role, your responsibilities will include analyzing customer inputs and understanding requirements such as Design Specifications, P&IDs, Control Narratives, IO list, Instrument Index, Operating Philosophies, Cause & effect diagrams, FGS layouts, etc. You will need to follow Emerson FSM process and maintain all SIS-related documentation of the assigned activities as per safety lifecycle requirements. Ensuring compliance to IEC61511/other standards as per the assigned scope in the project, raising Technical Queries, developing Safety System SW Design, performing I/O to Safety Logic Solver Assignment, defining Software Concepts, third party interfaces, developing SW library, project-spec...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

Job Title: Quality Assurance Manager Location: Rabale, Navi Mumbai Experience: 10 15 years Department: Quality Assurance Employment Type: Full-time Reports To: Quality Head About Fusion Scientific Laboratories Fusion Scientific Laboratories is a USFDA and EMA accredited pharmaceutical laboratory based in Rabale, Navi Mumbai , offering world-class services in Formulation Development , Analytical Solutions , and Integrated Pharmaceutical Services (CDMO) . We partner with pharmaceutical companies globally to deliver compliant and innovative solutions across the drug development lifecycle. Position Overview We are looking for a highly experienced Quality Assurance Manager to lead quality oversig...

As an Associate R&D (DQA) at our company located in Jhagadia, you will play a crucial role in the Research & Development department. You are required to have a qualification of M.Sc. in Chemistry or a related science field along with a minimum of 4 years of experience, preferably in the pharmaceutical industry. Your primary responsibilities will include reviewing Lab Validation Protocols/Reports (CRD) and Method Development/Validation documents (ADL), as well as reviewing specifications and STPs for raw materials, intermediates, and finished products. Additionally, you will be supporting DMF filings, stability studies, and regulatory documentation, preparing/reviewing SOPs, logbooks, and ens...

The VP of Supply Chain at Piramal Critical Care (PCC) plays a pivotal role in overseeing and developing the Global Supply Chain operations under the strategic direction of the Executive Committee (Excom) and the EVP of Global Operations. In this position, you will be responsible for managing External Supply Operations, end-to-end Global Planning, Logistics, Procurement, revenue forecasting, and Supply Chain Operations across the three regions where PCC operates. As the VP of Supply Chain, you will collaborate with key stakeholders both internally and externally. Internal stakeholders include Regional Supply Chain heads, Excom Vice Presidents, Sales General Managers, and Alliance Management H...

As an Executive/Senior Executive in the R&D Quality-CMC QA department at Sun Pharmaceutical Industries Limited in Gurugram, your primary responsibility will include reviewing various R&D documents such as stability data, analytical reports, method qualification reports, method verification reports, method validation protocols & reports, working standard/impurity standard profile, analytical data of pilot bio batches, and method transfers protocol & report. You will also be required to review lab events, deviations, change control, CAPA, and associated investigation reports before Technology Transfer. Additionally, you will support and participate in failure investigations to resolve root cau...