Document Controller jobs in Rajasthan

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Urgently required candidates for reputed Company 🔍Profile: QC Documentation Specialist 👨‍🎓Qualification: B.Pharma,M.Pharma 💵Salary: Up to ₹40,000 per month Experience -5-6(Should have good experience in a GMP- regulated QC laboratory. Reports to -Quality Control Manager /QA Lead. Industry : Pharmaceutical. 🛠️ Key Responsibility - 1. Data Integrity & GDP Oversight Audit Trail Review:...

About Dover: Dover is a diversified global manufacturer with annual revenue of over $7 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Fueling Solutions, Imaging & Identification, Pumps & Process Solutions and Refrigeration & Food Equipment....

Company Description Bioscan Research is a company based in Ahmedabad, dedicated to improving patient outcomes for traumatic brain injury through the use of a machine learning-powered NIRS device, CEREBO. The company aims to achieve early detection of brain injuries at a pre-symptomatic phase, ultimately enhancing patient care and treatment outcomes. Role Summary The Regulatory Affairs Engineer...

Company Description Moxie Beauty is shaping the future of beauty — with products built on science, sustainability, and authenticity. We’re solving for Indian hair types and building the styling category in India from the ground up, creating products tailored for local needs but benchmarked to global standards. We’re a Series A, digital-first consumer brand backed by leading investors including...

Company Description Moxie Beauty is shaping the future of beauty — with products built on science, sustainability, and authenticity. We’re solving for Indian hair types and building the styling category in India from the ground up, creating products tailored for local needs but benchmarked to global standards. We’re a Series A, digital-first consumer brand backed by leading investors including...

About Dover: Dover is a diversified global manufacturer with annual revenue of over $7 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Fueling Solutions, Imaging & Identification, Pumps & Process Solutions and Refrigeration & Food Equipment....

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Company Description Bioscan Research is a company based in Ahmedabad, dedicated to improving patient outcomes for traumatic brain injury through the use of a machine learning-powered NIRS device, CEREBO. The company aims to achieve early detection of brain injuries at a pre-symptomatic phase, ultimately enhancing patient care and treatment outcomes. Role Summary The Regulatory Affairs Engineer...

About Dover: Dover is a diversified global manufacturer with annual revenue of over $7 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Fueling Solutions, Imaging & Identification, Pumps & Process Solutions and Refrigeration & Food Equipment....

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

About Dover: Dover is a diversified global manufacturer with annual revenue of over $7 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products, Fueling Solutions, Imaging & Identification, Pumps & Process Solutions and Refrigeration & Food Equipment....

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...

Role & responsibilities Department: R&D Experience: Minimum 2 Years Qualification: B.Tech / B.Pharma Key Responsibilities: - Prepare, maintain, and update documentation related to Design Input, Design Output, and Technical Files. - Ensure documentation compliance with ISO standards applicable to medical devices. - Support in preparation and maintenance of documents required for regulatory...