1168 Uv Jobs - Page 45

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. Perks & Benefits Dynamic work environment Career development opportuniti...

Walk-in Drive @ Ahmedabad on 18th May'25 (Sunday) for Quality Control Department We are looking for suitable candidates for OSD Quality Control for Ahmedabad location Unit Interview Venue Details: Date: 18th May 25 (Sunday), Time: - 9:00 AM to 1:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd Survey No. 634,637-641 Village: Rajoda Tal: Bavla Dist: Ahmedabad -Gujarat - 382220 1) REQUIREMENT FOR OSD QUALITY CONTROL DEPARTMENT Total Experience: 02 to 7 years (Pharma experience only) Qualification: B.Sc./ M.Sc/ B. Pharm/ M. Pharm Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Desired Profile: Test RM, PM, in-process, finished & stability samples (various do...

Role: Officer / Executive - Quality Control Job Location: Nashik At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at every stage of life.We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here's how this role, wi...

Company Overview: We are a reputed pharmaceutical company specializing in the manufacturing of Oral Solid Dosage (OSD) formulations. Committed to high-quality standards and regulatory compliance, we are looking for a dynamic and experienced professional to join our Quality Control team. Job Purpose: The Assistant Manager Quality Control will oversee and manage day-to-day QC operations to ensure compliance with cGMP, GLP, and regulatory requirements for OSD manufacturing. This role is critical for maintaining product quality and supporting internal and external audits. Key Responsibilities: Supervise and lead a team of QC analysts and chemists in routine testing of raw materials, in-process s...

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC d...

VACANCY FOR TEAM LEADER - ANALYTICAL METHOD DEVELOPMENT (FORMULATIONS) - REGULATED MARKET Experience: 10 to 15 years Designation : Asst. Manager/ManagerEducational qualification : M.Sc Job profile : Need to work independently and should have handled a team of 6 to 8 members for method development and routine testing To guide and mentor analysts with practical training for developing analytical methods. SOP training and Analyst certification for new joinees within the team. Work allocation and planning of daily activities for the team subordinates Monitoring of routine analysis and trouble shooting To support site for critical trouble shooting and investigation Review of raw data , LNB and fi...

At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit 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...

GCS Medical College Hospital & Research Centre is looking for Executive - Quality to join our dynamic team and embark on a rewarding career journey. Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the l...

Sampling And Analysis of Raw Material , In Process Material And Finish Product Maintaining And Calibrating QC instruments Suggestions for improvement Strictly Follow Instructions given by HOD To Maintain And Provide document for Audit to Auditor Required Candidate profile Experience M. Sc / B. Sc / B. Pharma/ M.Pharm Must Have good knowledge of Chemistry , Analysis Work And Laboratory Instrument Effective Written , Verbal communication And MS Word Computer Knowledge

About The Role Role Finance and Administration CSR: 360 degree CFO Like responsibility in running functions and entities Will be responsible for managing accounts, compliances and Tax for ~ 3 not for profit entities Will support financial reporting for CSR Hybrid work structure for work life balance Requirement CA with 5-7 years of experience Deep understanding of financial, legal, tax and compliances matter .

Sampling And Analysis of Raw Material , In Process Material And Finish Product Maintaining And Calibrating QC instruments Suggestions for improvement Strictly Follow Instructions given by HOD To Maintain And Provide document for Audit to Auditor Required Candidate profile M. Sc-B. Sc - Chemistry -Dyes - Paint, Pigment Must Have good knowledge of Chemistry , Analysis Work And Laboratory Instrument Effective Written , Verbal communication And MS Word Computer Knowledge

Position: IPQA OFFICER Education: BSc. in chemistry, MSc. in chemistry or B.pharma / M.Pharma Experience: minimum 10 year in API pharmaceutical industries. Salary: 50 to 70 K per month Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600 Required Candidate profile Coordinate with regulatory authorities for inspections, licensing, and compliance documentation. Investigate quality incidents, deviations, and complaints, ensuring timely resolutions

Job Description: RESPONSIBILITIES. Timeliness and accuracy to meet turnaround time and that the daily test result is produced accurately and precisely. Information from the clients is kept as strictly confidential and never revealed to the third party Compliance to testing and environmental QA/QC procedures All analytical equipment, apparatus etc are to be appropriately maintained and calibrated as per the required schedule. Root-cause of all non-conformities or customer complaints are investigated and identified and appropriate corrective and preventive actions are taken. To go on client site for any environment analysis with required instruments. Responsible for effective implementation an...

Job Role: Analytical Chemistry-Analyst Department : Analytical - BGRC Job Location : Bangalaore About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Core Purpose of the Role: This role involves method development, method validation, method transfer and R&D stability s...

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & ex...

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. po...

Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).

Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performi...

Core Responsibilities: o Download data from Systems and mapping the same as per the requirement, co-ordinating with different teams for the data and checking its accuracy o Preparing Daily, Weekly & Monthly MIS reports o Preparing presentations,dash board, Graphs and analytical reports o Co-ordinating with the branches for feedback and any query related to customer handling. Support the manager in rolling out the new projects and initiatives and also updating on the progress and its impacts Desired Experience: Minimum 0-3 years in the field. Graduate : Yes Masters/Postgraduate: Optional Location - mumbai,delhi,pune,bangalore,hyderabad,chennai

Sampling And Analysis of Raw Material , In Process Material And Finish Product Maintaining And Calibrating QC instruments Suggestions for improvement Strictly Follow Instructions given by HOD To Maintain And Provide document for Audit to Auditor Required Candidate profile Experience M. Sc / B. Sc / B. Pharma/ M.Pharm Must Have good knowledge of Chemistry , Analysis Work And Laboratory Instrument Effective Written , Verbal communication And MS Word Computer Knowledge

Key Responsibilities Perform analytical testing of raw materials, intermediates, and finished APIs using HPLC, GC, UV, and other analytical instruments. Execute analytical method validation, method transfer, and verification as per regulatory guidelines. Ensure compliance with cGMP, GLP, and regulatory standards (ICH, USFDA, EU, WHO) . Maintain accurate documentation, calibration logs, and test reports in compliance with company SOPs. Support investigations, OOS, OOT, and CAPA implementation . Coordinate with QA and Production teams for smooth project execution. Contribute to laboratory upkeep, safety practices, and audit readiness.

Tool Box Meeting Conducting daily toolbox meeting befor the shift starts Timeliness , No.of meetings conducted Manpower Allocation Allocating contract manpower in such a way that they would generate productivity of more than 60 MT/ group Standard v/s Actual Productivity Shift management Ensure loading & stabilization of material as per SOP SOP v/s Actual Reporting of breakages,cullet& not found material during the shift No.of times stock not updated Ensuring loading of correct material in truck as per Loading slip No.of Trucks wrong loaded Avoiding loose box generation in warehouse by closely monitoring the loading point & warehouse to reduce breakages No of breakages due to loose box Collec...

Safety Management SystemOf Manpower:- To follow SOP's for safety so as to build safe working environment in shift. No. of First aid cases/nearmiss. No. of time PPE not used by subordinates. No. of time PTW system not followed.Operation & Schedule Management To follow the Operation scheduled activities in order to provide & to ensure smooth operation of equipment & machine. No. of instance motor changeover schedule not followed. No. of instance of utilities failure. No. of times Reading not taken as per schedule. Report generation of Daily utilities consumption. No. of times Report is not generated on time.Daily routine Patrol checking as per schedule.No. of instance patrol checking not done ...

Roles and Responsibilities Conduct analytical testing using HPLC, GC, UV-Vis, ICP-MS, LCMS techniques to ensure product quality and purity. Develop and validate methods for analysis of pharmaceutical products according to cGMP guidelines. Collaborate with cross-functional teams to resolve method validation issues and implement changes as needed. Maintain accurate records of test results, instrument calibration, and maintenance schedules. Participate in continuous improvement initiatives to optimize laboratory processes and procedures.