Key Responsibilities1. Dossier Preparation & SubmissionPrepare, compile, review, and submit EU CTD/eCTD dossiers (Modules 15) for pharmaceutical finished formulations.Ensure accuracy, completeness, and compliance of dossi...

About The Role Skill required: Control Testing - Agile testing Designation: Regulatory Compliance Senior Analyst Qualifications:BE Years of Experience:5 to 8 years What would you do? This role is responsible for eva...

About The Role Skill required: Control Testing - Agile testing Designation: Regulatory Compliance Senior Analyst Qualifications:BE Years of Experience:5 to 8 years What would you do? This role is responsible for eva...

Dear All,Greetings from Titan Laboratories Pvt Ltd !!We are looking for Deputy Manager / Manager - Regulatory Affairs, where we are seeking a proactive and detail-oriented Regulatory Affairs professional to join our dynamic t...

The Regulatory Reporting Lead is responsible for the processing and submission of daily EMIR, MiFID, SFTR and SIX Swiss reporting ("Trade & Transaction Reporting") to regulators. In addition to BAU reporting the Analyst i...

Educational Requirements Bachelor of Engineering,Bachelor Of Technology,Bachelor Of Comp. Applications,Bachelor of Pharmacy,Master of Pharmacy,Master Of Technology,Master Of Comp. Applications Service Line Applicati...

As a Manager / Deputy Manager Regulatory Affairs in Vadodara, your role will involve developing and implementing regulatory strategies, ensuring compliance with regulatory requirements, preparing and submitting regulatory doc...

Walk-In Drive For Regulatory Affairs - FML Department in FML Division - MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 18-10-2025. Regulatory Affairs FML Department in FML Division , ...

Job Summary: Expert in bird and mammal ecotoxicology reporting to the Group Leader of Environmental Toxicology. Knowledgeable in all disciplines of ecotoxicology, including aquatic, plants, pollinator, and terrestrial. Conduc...

Responsibilities:Analyze and document complex healthcare business requirements, translating them into actionable technical specifications and user storiesCollaborate with cross-functional teams including product managers, dev...

Manage daily operations of regulatory function of the assigned categoryLiaise with a range of colleagues from Marketing, R&D, supply, and global/regional regulatory teams.Maintain Regulatory DatabasesReview, interpr...

Role & responsibilities Preferred candidate profile Job ClassificationIndustry: BPM / BPOFunctional Area / Department: Risk Management & ComplianceRole Category: Risk Management & Compliance - OtherRole: Risk Mana...

Roles & Responsibilities:Preparation and timely update of Technical Files Regular updating of the Quality Manual Review and update of all relevant Standard Operating Procedures (SOPs) Review and revision of Work Instructi...

Role & responsibilities:Outline the day-to-day responsibilities for this role.Preferred candidate profile:Specify required role expertise, previous job experience, or relevant certifications.Job ClassificationIndustry: BP...

Job DetailsRole: Regulatory Reporting Analyst Offshore role Location: Gurugram, Haryana (must be local) Experience Required: 5+ years Industry: Banking & Financial Services (experience required) Note: Must have an ...

Immediate Joiners Only -We need Model N with Pharma Commercial Domain or Regulatory Domain,Please go through the below jds and apply asap.JD 1 Model N Consultant (Pharma Commercial Domain)Job Title: Model N Consultant Pha...

Job summaryWe are looking for an individual to carry out core regulatory activities, including dossier finalization, filing regulatory applications, internal liaison for regulatory information compilation, coordination with Q...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...

Now, more than ever, the Toast team is committed to our customers. We re taking steps to help restaurants navigate these unprecedented times with technology, resources, and community. Our focus is on building the restaurant ...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specific...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifica...