544 Oos Jobs - Page 8

Role & responsibilities Adequate knowledge of respective guidelines. i.e. ICH, USP,WHO, etc. Stability sample analysis by HPLC/GC/UV/Dissolution apparatus. Preparation of stability testing worksheets. Sample charge and withdrawal as per stability condition. Management of stability samples and stability chambers and maintain the schedule. Preparation of stability trend records and summarize the results Review the stability sample testing data. Review the stability analysis worksheet. Review the stability protocols, samples and stability chambers log records. Review of OOS/OOT and co-ordinate with respective concerns.

Job Description Maintenance of GLP in the Laboratory Upkeep of Housekeeping in the Laboratory. Ensuring activity logs are maintained for all critical instruments /equipment’s. Timely preparation of Laboratory Documents. Timely review of analytical data generated in laboratory. Ensuring Analytical Technology transfer from transferring lab as per approved protocol. Review and approval of incident , out of specification ,out of trend report and approval of QC related activities. Involved in QAMS activities such as change control, CAPA , incidents, deviation etc. Approval of stability summery report. Timely review of Quality control procedures and initiation for up gradation of same. Compliance ...

Roles and Responsibilities Conduct market complaint investigations, deviation management, and OOS/OOT handling according to established procedures. Ensure compliance with regulatory requirements through vendor qualification, equipment qualification, cleaning validation, water validation, injectable processing, and process validation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and maintain documentation related to quality control processes. Provide technical support for product testing and analysis. Desired Candidate Profile 4-8 years of experience in Quality Assurance (QA) or a related field within the pharmaceutical industry. ...

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong ...

Overview POSITION SUMMARY STATEMENT This position is having the primary purpose of ensuring compliance to the Herbalife requirements and adherence to HLF's global procedures in Quality assurance and control during the manufacturing and storage of Herbalife products in the Contract manufacturing location in India. How You Would Contribute Monitoring of process on set frequencies to ascertain compliance to Herbalife Quality procedure requirements Conduct periodic audits of the facility and operations associated with Herbalife, to help CM meet and improve the quality and hygiene standards as per Herbalife Quality standards, Ministry of Ayush, Ayurveda product standard and FSSAI GMP Guidelines. ...

HI, We have an opening for Assistant Manager - QC (Analytical Reviewer & QMS) in Nerul, Navi Mumbai Location. Experience - 10 - 15 yrs Qualification - M.Sc. (Chemistry/Analytical Chemistry) Interested Candidate may forward his resume on ankit02.kumar@usv.in Job Responsibilities: 1. Review of Logbooks, Test data sheets, and data generated in Quality control Analytical department. 2. Routine inspection of Quality control department to check and ensure compliance as per cGMP. 3. Routine inspection of QC schedule for execution. 4. Preparation and review of protocol and report for validation, verification, Characterization, hypothetical testing and Force degradation studies. 5. Initiation of devi...

Handle the Recovered Section. Assist in investigations related to out-of-specification (OOS), deviations, and laboratory incidents. Review and verify entries in logbooks, worksheets, and other controlled documents. Required Candidate profile Review analytical raw data, calculations, and reports for accuracy, completeness, and compliance with approved specifications and methods. Ensure all laboratory documentation meets regulatory

2–4 year experience in inventory(retail/e-commerce preferred) Strong analytical skills with advanced Excel/Google Sheets Effective communication, negotiation & project management skills Monitoring KPIs and optimizing stock levels (reducing OOS SKUs)

You will be responsible for the following tasks as Officer - API at Dishman Carbogen Amcis Limited in Bavla, Gujarat, IN: - Handling Manufacturing Compliance activities such as IPQA Activity - Managing QMS Documents including CAPA, OOS, and Change control - Handling APQR processes - Managing Batch release activities - Demonstrating strong communication skills - Having exposure to Regulatory audits If you possess the necessary qualifications and experience for this role, you are encouraged to apply.,

Your Role Design and implement seamless integration solutions between Teamcenter and enterprise platforms Develop custom BMIDE (Business Modeling Integrated Development Environment) extensions Configure Solid Edge and Teamcenter integration Create data mapping and synchronization strategies Develop interfaces between PLM, ERP, and CRM systems Ensure data integrity and consistency across multiple platforms Troubleshoot and resolve complex integration challenges Create comprehensive technical documentation Your Profile XML/JSON data mapping BMIDE customization Web services and API integration SQL and database integration Enterprise system architecture Integration middleware technologies Siemen...

Job Title: Senior Executive – R&D Quality, CMC QA (Analytical) Business Unit: Global Quality & Compliance Job Grade G11B Location : Gurugram 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: Rev...

Quality Control (QC) investigators are responsible for analyzing and investigating deviations from specifications, such as out-of-specification (OOS) test results complaints, and potential quality issues Required Candidate profile identified during manufacturing, which ensures product quality, safety, and regulatory compliance.

Perform daily, weekly, and monthly reconciliations of bank statements with internal accounting records. Investigate and resolve discrepancies in a timely and efficient manner. Record and monitor all cash transactions including bank fees, interest, and transfers. Collaborate with Accounts Payable and Accounts Receivable teams to ensure alignment of transactions. Maintain documentation and audit trails for all reconciliation activities. Prepare monthly reconciliation reports and assist with month-end and year-end closing processes. Liaise with banks to resolve any issues or discrepancies. Support internal and external audits by providing necessary reconciliation documentation. Identify opportu...

Dishman Carbogen Amcis is looking for Senior Executive - API QC to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel an...

We are seeking a highly motivated QA Test Developer with 5 to 7 years of hands-on experience in test automation, primarily using Python and PyTest to work on containerized storage solution. The ideal candidate is enthusiastic about quality, has strong problem-solving abilities, and is ready to take ownership of their work in a fast-paced, collaborative environment. The candidate delivers assigned work of increasing scope and complexity with high quality and on time, applying learned skills, new technologies, and innovation to improve team code quality and quantity. Negotiates effectively, as needed, to deliver outcomes.. You will be part of a QA team responsible for ensuring the quality of o...

As a Senior Executive/Executive in the Stability Section at Kimia Biosciences, you will play a crucial role in maintaining stability schedules, handling inward and withdrawal of stability and hold time samples, preparing stability reports, extrapolating stability data, determining shelf life, and being aware of OOS, lab incidences, as well as data integrity issues. Key Responsibilities: - Maintain stability schedules - Handle inward and withdrawal of stability and hold time samples - Prepare stability reports - Extrapolate stability data and determine shelf life - Be aware of OOS, lab incidences, and data integrity issues Qualifications Required: - Must have experience in maintaining stabili...

As a Document Controller at Ferring India Laboratories, your role involves handling the issuance, control, and retrieval of documents. You will be responsible for scanning and uploading approved paper-based documents in Veeva Vault. Additionally, maintaining master copies for SOPs, including issuance, control, and retrieval of SOPs will be a key part of your responsibilities. Your key responsibilities will include: - Managing and conducting training sessions - Organizing training programs - Maintaining vendor audit and technical agreement planners - Preparing and reviewing SOPs, Protocols, and other cGMP documents - Tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with sta...

We are looking for a skilled SAP CRM-C4C professional with 9 to 20 years of experience. The ideal candidate will have expertise in SAP C4C and be able to work effectively in a fast-paced environment. Roles and Responsibility Manage and implement SAP C4C solutions for clients. Collaborate with cross-functional teams to identify business requirements and develop solutions. Provide training and support to end-users on SAP C4C functionality. Troubleshoot and resolve technical issues related to SAP C4C. Develop and maintain documentation of SAP C4C configurations and customizations. Ensure data integrity and security in SAP C4C implementations. Job Requirements Strong knowledge of SAP C4C modules...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Requisition for Executive for the implementation and monitoring of GLP in TIC. Skills Required : Good Laboratory Practice, Quality Assurance, MS Office Package, Communication Skills Roles and Responsibilities : Preparation of documents related to applying GLP (Good Laboratory Practices). Ensure the upkeep and maintenance of the laboratory by implementing GLP. Ensure compliance with GLP standards. Logbook management, sample management, SOP management, and other document management related to GLP. Any other work related to Quality assurance assigned by the manager. GLP-trained person or experience working in GLP labs. Must have good verbal and written skills.

Key Responsibilities: Manage all Analytical Quality Assurance (AQA) activities. Review, approve, and close Quality Management System documents related to QC. Act as Single Point of Contact (SPOC) for submission activities Dossier, Regulatory, Variation filings. Handle customer communications related to QA. Review manufacturing, packing, analytical reports of submission/validation batches. Review Stability data and ensure submission compliance. Ensure compliance of Stability Studies and Control Sample Handling at site. Ensure adherence to GDP/GLP. Monitor compliance of Gowning/De-gowning in QC lab. Authorize written procedures, amendments, and related documentation. Ensure SOP compliance acro...

We are looking for a skilled professional with 6-15 years of experience to join our team as an Allegro QA/Developer in PAN India, including Bangalore, Hyderabad, Pune, Chennai, and Noida. The ideal candidate will have expertise in designing Allegro-based functional prototypes and functional modeling of business flows. Roles and Responsibility Design and develop Allegro-based functional prototypes and models. Document functional design, data design, and setup in Allegro. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code using Allegro. Troubleshoot and resolve technical issues related to Allegro. Participate in code ...

About The Role 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 : IT Infrastructure Operations Good to have skills : NA Minimum 5 year of experience is required Educational Qualification : 15 years full time education Position Summary The IT Infrastructure Architect will design, implement, and optimize enterprise-level solutions across Operating Systems, Databases, Site Reliability Engineering (SRE), and Middleware platforms. The role requires deep technical expertise, strategic planning, and leadership to ensure high availability, scalability, performance, and secu...

Skills Required: Graduate / PG in management With a minimum of 4-7 years of experience in managing the Admin function. Must have hands on experience into Advance Excel Key Responsibilities Making MIS Reports of collated data Meticulously working on the data collated from various sources of department and preparing comprehensive reports Ensuring the precision of the reports Preparing Delivery Files Extensive work on Excel Preparing necessary dashboards for day to day operations Monitor & analyses data for business trends & prepare monthly revenue & collection report Provide cross functional quality oversight from a compliance perspective fo testing and disposition, quality investigations, val...

Roles and Responsibility Conduct thorough reviews of patient data to ensure accuracy and compliance with regulatory standards. Analyze complex data sets to identify trends and patterns that inform business decisions. Develop and implement effective data visualization techniques to communicate insights to stakeholders. Collaborate with cross-functional teams to design and implement process improvements. Provide expert guidance on data management best practices to junior team members. Stay up-to-date with industry developments and emerging trends in health data analytics. Job Requirements Strong understanding of healthcare operations and regulations. Proficiency in data analysis and visualizat...