552 Oos Jobs - Page 14

Manage QMS activities: Change Control, Deviation, CAPA, OOS, OOT, Lab Events. Conduct Risk Assessments, SOP reviews, and assist in grievance handling. Document & review: Specifications, SOPs, Test Data Sheets, Analytical Test Reports, and Master documents. Review Method Validation Protocols & Reports. Monitor calibration and preventive maintenance schedules. Initiate procurement of impurity/reference standards, chemicals, reagents, columns, and laboratory glassware. Develop and implement site policies and procedures ensuring regulatory compliance. Supervise deviation and CAPA review, approval, and implementation. Create QC goals, objectives, and metrics to drive continuous improvement. Ensur...

Overview The Enterprise Operations and Quality team oversees the data, services, and applications within the Climate and Sustainability Engineering and MSCI's Data Technology verticals. Our primary responsibility is to manage and support end-to-end Quality Engineering by creating tools and tests that ensure continuous quality assessment of applications, services, and generated data. MSCI is renowned for its high-quality data, which is crucial for critical investment decisions, and our role is vital to this mission. Responsibilities Develop and implement engineering solutions to address complex data validation challenges. Develop code in Python and/or Java to maintain high-quality data integr...

We are looking for QC - Manager profile with 15-20 years' experience in Quality Control of API Pharma. Specifically looking for candidates from Vizag or nearby locations. Job Description Responsible for all QC activities at OWN manufacturing site located at Vizag. Ensure timely completion of vendor samples, RM, In-process, cleaning samples, stability samples, FP analysis and miscellaneous samples. Plan and perform QC work such that production-related activities continue uninterrupted Identify training needs of QC personnel and provide job-related training to meet the GLP needs and skill upgradation. Maintain analytical instruments with suitable calibrations, preventive maintenance and suppor...

Tracking of all orders from the CFA / Warehouse Monitoring shipments to outstation locations and updating ETD. Maintaining a tracker for PODs and uploading PODs on SAP> Maintaining a working relationship with all E Comm/MT warehouse personal and Supply Chain co-ordinators at HO. Ensuring sufficient fleet/manpower at CFA to ensure appointments are met. Flagging any concerns at the CFA well in advance. Monitor stocks and flag potential OOS situations well in advance. Ensure FIFO at CFA.

Job Description : Design and maintain database objects (indexes, triggers, functions, procedures). Set up and manage PostgreSQL streaming replication and backups. Monitor, analyze, and optimize database performance. Ensure data integrity, availability, and disaster recovery. Implement security protocols and manage user roles and permissions. Perform regular maintenance (vacuuming, health checks, etc.). Guide developers on best practices for queries and schema design. Troubleshoot production data issues promptly. Automate data processing and database administration tasks. Use PostgreSQL tools like pg_ctl, psql for admin activities. Optimize complex SQL queries and tune performance.

Position : Executive Engineering QMS Qualification : BE Mechanical/ Electrical/ Instrumentation or B pharma preferably BE Experience : 6-7 years experience in handling engineering department GMP documentation activities and supporting engineering function as SME in QMS documentation Responsibilities : 1.Implementation of quality assurance standards, processes, controls and cGMP in warehouse. 2. Preparation of SOPs and ensure effective implementation. 3. should be well versed with deviation management SOP 4. Should be well versed with change control and CAPA management related to engineering department 5. Should be familiar with documentation like DQ, IQ, OQ and PQ. 6. To ensure that training...

Required QC Analyst exp 4-5 year, Finish Good HPLC salary -Hike on current salary Male only Location - Baddi Call at -9818040604

Ipca Laboratories Ltd, Wardha is as API plant we are looking for Production Manager with below mentioned JD To ensure weekly / monthly production schedules as per plans. Monitor shift wise production and provide feedback to HOD on daily basis. To ensure smooth running of the plant, co-ordinate effective with maintenance department for any break down, utility, services etc. To co-ordinates with Q.C., Store, R&D, Inprocess lab for production related jobs. To ensure that production norms as per laid down procedure are achieved. Through optimum use of resources & report to HOD about the area requiring improvement. To prepare daily logbook containing functioning of the plant in all respects, cove...

Led the qualification and validation of HVAC systems to ensure compliance with regulatory standards and maintain optimal environmental conditions for pharmaceutical manufacturing. Required Candidate profile Monitor the qualification process for water systems (e.g., purified water, WFI). Conducted performance testing, system validation, and routine monitoring to ensure the water quality meets.

Role & responsibilities Analytical QA Review the analytical documents which are generated after analysis of Drug Products. Preparation and Review of all Departmental SOP's for cGMP Compliance. Compilation and Review of the Batch Records, Certificate of Analysis, Analytical Protocol, etc which are required for release of Batches. Review and Approve SOPs, Change Controls, Deviations, Annual Product Quality Reviews, Incident Reports, Out of Calibrations, Out of Specifications, Out of Trends, Approve the Investigation Reports. Market Compliant, & manage Stability Samples etc. Review of Regulatory Requirements and its Compliance. Periodic review of all Quality functions and Procedure for appropri...

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

Qualifications: 4+ years of Siebel Administration. Coordinate, Lead and Deliver Change Management throughout environments along with Release planning. Good communication skills and leading the team Interacting with the client regularly through the conferences Extremely motivated with good Inter-personal Skills, have ability to work under strict deadlines 3+ years of DevOps Automation Experience in DevOps and Agile culture. Experience Linux Shell scripting, Python Experience Windows batch jobs, PowerShell Experience Git version control system Automated build and integration experience with tools like Jenkins 3+ years of hands on experience in large and complex Oracle CPQ engagements Able to w...

Job Title:- KMIL- Wholesale Banking- Risk Monitoring Analyst Grade:- M4/M5 Location:- Mumbai Track financial and project performance covenant: Monitoring financial and project performance against predefined convenants. Identify deviations and promptly communicate findings to relevant stakeholders. Project performance analysis: Conduct through analysis of project performance metrics. Provide insights and recommendations to mitigate risks. Track Compliances to sanctions conditions: Moniotor compliance with sanctions conditions imposed on credit facilities. Take proactive measures to address any non- compliance issue Site Visit: Conduct on site visit to assess the progress and status of project...

The Apex Group was established in Bermuda in 2003 and is now one of the worlds largest fund administration and middle office solutions providers. Our business is unique in its ability to reach globally, service locally and provide cross-jurisdictional services. With our clients at the heart of everything we do, our hard-working team has successfully delivered on an unprecedented growth and transformation journey, and we are now represented by over circa 13,000 employees across 112 offices worldwide.Your career with us should reflect your energy and passion. Thats why, at Apex Group, we will do more than simply empower you. We will work to supercharge your unique skills and experience. Take t...

Title: QA Manager Business Unit: CQC (Complaints) Job Grade: G11A / Manager 2 Location : Tandalja, Vadodara Educational Qualification: B.Pharma / M.Sc (Life Sciences) Experience: 10 to 14 Years Position Summary Review of Product Quality Complaint Investigation Reports (Drug Products). Coordinate with other stakeholders involved in the complaint handling process. Monitor the progress of Filed Alert Reports, Recalls & Product Quality Complaint closure etc. Logging of Product Quality Complaints (PQC) in the database (TrackWise). Acknowledge the complaints to the complainants. Providing the response letter to the complainant. Reconciliation of received Product Quality Complaint. Note: 1) Candida...

Role Description The Group Audit (GA) function comprises c. 880 staff who take a proactive, risk based and independent approach to assist the Bank's business and infrastructure functions to identify key control weaknesses. GA prides itself in ensuring the highest standard in professional delivery. Being DB's 'third line of defense GA have a high internal profile, acting as an independent and forward-looking challenger and adviser to Senior Management. We are strongly rem/lied upon by the Regulators. We are a diverse and inclusive global division where culture is at the core of our team dynamic; GA is inextricably linked to promoting strong corporate and ethical governance, a philosophy that ...

Designation - Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 8yrs. and above share with your friends Required Candidate profile company will provide transportation facility from Bharuch. Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

Enhance images by correcting resolution and composition, cropping images and adjusting tone, color, saturation and brightness. Adding or removing objects from an image or inserting text. Smoothen skin, remove big creases, general tidy up, clean up floor, sharpen clothing better where it looks too big, remove flyaway/loose hair strands Have an eye for art and composition as they relate to whats typically desirable in a photographic image. To present your designs and ideas when required to all levels up to and including managers & clients. To constantly review competitor sites and make recommendations to maintain client s position as market leader, ensure client s on-line content continues to ...

Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

Key Responsibilities Develop and maintain supply chain analytics to monitor operational performance and trends. Lead and participate in Six Sigma and supply chain improvement initiatives. Ensure data integrity and consistency across all analytics and reporting platforms. Design and implement reporting solutions for key supply chain KPIs. Analyze KPIs to identify improvement opportunities and develop actionable insights. Build and maintain repeatable, scalable analytics using business systems and BI tools. Conduct scenario modeling and internal/external benchmarking. Provide financial analysis to support supply chain decisions. Collaborate with global stakeholders to understand requirements a...

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.

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

As a part of this role in the pharmaceutical industry, you will be responsible for handling CAPA (Corrective and Preventive Actions), OOS (Out of Specification) incidents, and deviations effectively. Your duties will also include the generation of Standard Operating Procedures (SOPs) to ensure smooth operations within the organization. Additionally, you will be involved in validation processes and maintaining compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year in a similar role within the pharmaceutical sector. The work location for ...

The primary purpose of this position is to ensure compliance with Herbalife requirements and adherence to HLF's global procedures in Quality assurance and control during the manufacturing and storage of Herbalife products at the Contract manufacturing location in India. As the Site QA lead at the CM (Indore) for Herbalife, you will be responsible for various QA activities on-site, including but not limited to: - Monitoring processes on set frequencies to ascertain compliance with Herbalife Quality procedure requirements - Conducting periodic audits of the facility and operations associated with Herbalife to help CM meet and improve quality and hygiene standards - Communicating with CM regula...