Senior Executive - Quality Assurance Piramal Pharma Ltd

5.0 - 9.0 years

0 Lacs

telangana

On-site

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...

Posted 2 weeks ago

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Specialist - Product Complaints Novartis

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

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...

Posted 1 month ago

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Manager - Corporate Quality Audit Sun Pharmaceutical Industries Ltd

10.0 - 15.0 years

0 Lacs

karnataka

On-site

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 ...

Posted 1 month ago

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Specialist - Product Complaints - QOP Novartis India

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

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 ...

Posted 1 month ago

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Senior Executive - Quality Assurance Piramal Finance

5.0 - 10.0 years

4 - 6 Lacs

Medak

Work from Office

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 ...

Posted 3 months ago

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Specialist - IT Quality Amgen Inc

7.0 - 12.0 years

9 - 14 Lacs

Hyderabad

Work from Office

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...

Posted 3 months ago

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