11 Track Wise Jobs

• Site analytical testing, evaluation, and Development • Implementation of Pharmacopeial Updates and Source Change Document. • Managing master data operations within the LIMS and SAP system. • Developing, Optimizing, Validating, Verifying and Method transfer of analytical methods. • Ensuring discipline in Track Wise by monitoring pending tasks and facilitating the closure of quality events. • Ensuring adherence to regulations and maintaining the completeness of relevant logbooks or registers.

Date: 8 Oct 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Description Job Title: QC Analyst Job Location: Bangalore 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 Mandatory expectation for all roles as per Syngene safety guidel...

Sun Pharma Corporate Quality Department Position: Manager (G10) Effective Date: Department: Corporate Quality Location: Bengaluru, Reporting Manager Title: GM - Corporate Quality Classification: Manager Corporate Quality (Gamma Irradiation) Job Summary Manager Corporate Quality Individual Performer Role Responsible for oversight of Gamma Irradiation of Sun Pharma products at third party gamma irradiation sterilization. Essential Job Functions Should possess sound knowledge of pharmaceutical manufacturing process (Non-sterile & Sterile formulations) & quality assurance regulations and auditing technique. Responsible for the overall supervision of Gamma sterilization site (Third party) used fo...

As an experienced SAP BASIS Consultant at our company, your role will involve implementing and supporting SAP BASIS operations, ensuring optimal performance of our systems, handling system upgrades, and providing support for SAP applications. Your deep understanding of SAP architecture, database management, and strong troubleshooting skills will be essential in this role. Key Responsibilities: - Perform day-to-day Basis activities including: - Transport Requests management. - File transfers and support for peripheral systems. - Organize system restarts & outages. - Daily health checks. - Work as an independent team member, applying judgment to plan and execute tasks effectively. - Coordinate...

Role Overview: As a Specialist - Product Complaints - QOP at Novartis in Hyderabad, you will be responsible for handling market complaints received from across the globe. You will review investigation reports from Novartis sites and Contract Manufacturing Organizations and collaborate with external Supply organization, Novartis sites, and Country pharma organizations for continuous improvement. Key Responsibilities: - Perform day-to-day activities of processing market complaints assigned as per relevant SOPs, business matrix, and SLA timelines. - Assist in data collection and reporting of KPIs. - Assist in continuous improvement initiatives. - Manage ad-hoc projects assigned in the area of w...

More than 5 years of experience in Quality Management Systems (QMS), including handling of change control, deviations, OOS, and Audit readiness. Proficient in electronic systems such as Trackwise and SAP. Qualifications: - MSc in Chemistry or BTech in Chemical Engineering Piramal Group, with three decades of existence, has strategically grown through both organic and inorganic means. Committed to inclusive growth and ethical practices, the group values equal employment opportunities. Employment decisions are merit-based, considering qualifications, skills, performance, and achievements. The group ensures equal opportunities for all applicants and employees in recruitment, training, promotion...

Handle market complaints received from across the globe. You will be responsible for reviewing the investigation reports received from Novartis sites and Contract Manufacturing Organizations. Collaboration with external Supply organization, Novartis sites, and Country pharma organizations for continuous improvement is essential for this role. As a Specialist - Product Complaints - QOP based in Hyderabad, your key responsibilities will include performing day-to-day activities of processing market complaints assigned as per the relevant SOPs, business matrix, and SLA timelines. You will assist in data collection and reporting of KPIs, support continuous improvement initiatives, manage ad-hoc p...

As a Manager - Corporate Quality Audit at Sun Pharmaceutical Industries Ltd, you will be responsible for overseeing the Gamma Irradiation of Sun Pharma products at third-party gamma irradiation sterilization sites. Your primary role will involve supervising the sterilization process, monitoring the irradiation of batches, and ensuring compliance with quality assurance regulations and auditing techniques. Key responsibilities include: - Demonstrating a sound understanding of pharmaceutical manufacturing processes for both non-sterile and sterile formulations. - Supervising the Gamma sterilization site used for sterilizing drug products and components. - Monitoring the receipt and dispatch of ...

Handle market complaints received from across the globe. You will be responsible for reviewing the investigation reports received from the Novartis sites and Contract Manufacturing Organizations. You will collaborate with external Supply organization, Novartis sites, Country pharma organizations for continuous improvement. As a Specialist - Product Complaints - QOP based in Hyderabad, your key responsibilities will include performing day-to-day activities of processing market complaints assigned as per the relevant SOPs, business matrix, and SLA timelines. You will assist in data collection and reporting of KPIs, participate in continuous improvement initiatives, manage ad-hoc projects, and ...

We are looking for a highly experienced and skilled Senior Executive - Quality Assurance to join our team at PIRAMAL ENTERPRISES LTD. The ideal candidate will have between 5-10 years of experience in QMS, with expertise in handling change control, deviation, OOS, and audit properness. Roles and Responsibility Manage and implement quality management systems to ensure compliance with regulatory requirements. Handle change control, deviation, and OOS issues, ensuring timely resolution and corrective action. Conduct audits to ensure compliance with industry standards and regulations. Develop and maintain electronic systems, including Trackwise and SAP. Collaborate with cross-functional teams to ...

What you will do In this vital role you will lead the execution of complex or novel assignments requiring strategic planning and development of new and/or improved validation techniques, deviations, and procedures. In this position you will supervise validation activities through internal audits and conduct risk assessments to identify the need for requalification and establish policies for computer system re-validation. This individual will actively participate during all phases of qualification/validation of computerized systems: evaluate projects; provide guidance and technical information to others (lead qualification/validation activities); determine and establish requirements for quali...