5 Investigation Reports Jobs

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3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

In this role as a Specialist for Global Product Quality Complaint Triage at Bristol Myers Squibb, you will play a crucial part in the accurate and timely review, evaluation, and assignment of incoming Product Quality Complaints (PQCs) within a dynamic and high-volume environment. Your responsibilities will involve collaborating with various stakeholders to ensure compliant and efficient management of PQCs. By maintaining a thorough understanding of procedures, intake routes, and product portfolio, you will contribute to delivering high-quality, comprehensive investigation reports and supporting continuous improvement initiatives. Your critical thinking skills will be essential in expediting ...

Posted 3 weeks ago

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9.0 - 11.0 years

0 Lacs

vadodara, gujarat, india

On-site

Job Title Manager-2 - FR &D Non-Orals (Compliance group) Business Unit R&D1 Regulatory Affairs Job Grade G11A Location : Baroda 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. Job Description Review documents required for reg...

Posted 3 weeks ago

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5.0 - 13.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: As a Formulations Scientist in Hyderabad, India, you will be responsible for the development of oral solid dosage forms of Non-DEA and DEA substances. Your key functions will include conducting Literature Search, Pre-Formulation, Formulation Design, and Development of stable, Bioequivalent, and Manufacturable generic solid oral formulations. Key Responsibilities: - Act as a mentor and motivator to the team. - Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms. - Evaluate patents and develop non-infringement strategies, including the capability of developing Paragraph IV products. - Scale-up and optimize manufact...

Posted 1 month ago

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5.0 - 9.0 years

0 Lacs

halol, gujarat

On-site

Role Overview: As a Manager-II in the MSTG department at Dadra, your primary responsibility will be to provide support in the execution and monitoring of trial, scale up, and exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheets, master formula cards, bill of materials, risk assessment reports, sampling protocols, reports, exhibit batch manufacturing records, and exhibit protocols. Sharing process knowledge with cross-functional departments through presentations to facilitate smooth technology transfer will also be a key aspect of your role. Key Responsibilities: - Review and evaluate product history a...

Posted 1 month ago

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5.0 - 9.0 years

0 Lacs

karnataka

On-site

Hands on experience in using SolidWorks CAD tool is required for this role. You should have expertise in various manufacturing methodologies, especially in sheet metal and/or plastics injection molding. It is essential to have experience in designing mechanical and electro-mechanical assemblies, particularly working on complex assemblies in SolidWorks. You should possess excellent drafting and detailing skills, as well as be proficient in GD&T and Tolerance stack up analysis. Experience in manual design calculation and exposure to FEA analysis are important aspects of this role. Supplier interaction and cross-functional coordination for project execution and closure are also key responsibili...

Posted 3 months ago

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