1760 Ich Jobs - Page 4

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: BCom Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving customer id...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Document Management Systems (DMS) Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure project milestones are met, facilitating discussions to address challenges, and guiding your team through the development process...

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Sr Analyst Qualifications: Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes b...

About The Role Project Role : Business Analyst Project Role Description : Analyze an organization and design its processes and systems, assessing the business model and its integration with technology. Assess current state, identify customer requirements, and define the future state and/or business solution. Research, gather and synthesize information. Must have skills : Business Requirements Analysis, Pharmacovigilance & Drug Safety Surveillance, Life sciences Business Analyst Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Analyst, you will analyze an organization and design its processes a...

About The Role Project Role : Business Analyst Project Role Description : Analyze an organization and design its processes and systems, assessing the business model and its integration with technology. Assess current state, identify customer requirements, and define the future state and/or business solution. Research, gather and synthesize information. Must have skills : Business Requirements Analysis, Pharmacovigilance & Drug Safety Surveillance, Life sciences Business Analyst Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Analyst, you will analyze an organization and design its processes a...

About The Role Project Role : Business Analyst Project Role Description : Analyze an organization and design its processes and systems, assessing the business model and its integration with technology. Assess current state, identify customer requirements, and define the future state and/or business solution. Research, gather and synthesize information. Must have skills : Business Requirements Analysis, Pharmacovigilance & Drug Safety Surveillance, Life sciences Business Analyst Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Analyst, you will analyze an organization and design its processes a...

Skill required: KYC Corporate - Anti-Money Laundering (AML) Designation: Int Controls & Compliance Manager Qualifications: Any Graduation Years of Experience: 13 to 18 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeThe Anti Money Laundering team focuses on articulating the business requirements and implement the process and system controls required to prevent moving illegally acquired cash through an organization s financial systems. The role requires a good understandi...

About The Role Job Title Responsible AI Associate Manager Project Role : Responsible AI Advisor Management Level: 8 Project Role Description : Develop strategies to ensure the ethical and responsible use of artificial intelligence (AI) technologies. Shape the strategic direction of guidelines, policies, and practices implementation to mitigate AI-related risks. Promote transparency, accountability, and align AI initiatives with the organizations values and legal requirements. Must have skills : Responsible AI Good to have skills : NA Summary :As a Responsible AI Advisor, you will develop strategies to ensure the ethical and responsible use of artificial intelligence technologies. Your typica...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Analyst Qualifications: MSc/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 3 to 5 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our L...

About The Role Project Role : Application Support Engineer Project Role Description : Act as software detectives, provide a dynamic service identifying and solving issues within multiple components of critical business systems. Must have skills : SAP HCM Payroll Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Support Engineer, you will act as software detectives, providing a dynamic service that identifies and solves issues within multiple components of critical business systems. Your typical day will involve collaborating with various teams to troubleshoot software problems, ensuring tha...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to li...

About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : SAP HCM Payroll Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Engineer, you will engage in a variety of tasks that involve analyzing, designing, coding, and testing multiple components of application code across various clients. Your typical day will include collaborating with team members to perform maintenance and e...

***Greetings from You & I Consulting*** You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. Hirings for MNC: - Great Opportunity in Giant MNC . Grab the Opportunity to grow and explore. Statistical Programmer!!! We are hiring for: Statistical Programmer up to 20 lpa ctc Experience Level: 5 to 15 years Location- Mumbai, Pune, Noida, Bangalore Job Description: We are looking for a skilled Senior Statistical Programmer I / II to join our team at Icon Pharmaceuticals. The ideal candidate will have a strong background in statistical programming and analysis, with excellent problem-solving skills and attention to detail.. Key Responsibilities: Develop and...

1. Biosimilar Regulated market submissions - US / EU injectable market submission. 2. Biosimilar Product Development Strategy for CMC and Clinical. 3. Review of all Dosisier related Quality documents including coordination with Cross functional teams ( RD, QC/QA and Manufacturing). 4. Biosimilar Dossier Authoring, Review and Hands on experience in eCTD submissions. 5. MOH Query response. 6. Biosimilar Product Life Cycle Management. 7. RA support for Plant related QMS activities.

1. Biosimilar Regulated market submissions - US / EU market submission. Preferred US FDA .Alternatively candidates having exp in Small molecules and injectables for US. 2. Should Have dossier authoring for CMC for EU market. 3. Should have authoring of pre approval dossiers and query responses for US and EU. 4. Biosimilar Product Development Strategy for CMC and Clinical trials 5. Review of all Dossier related Quality documents including coordination with Cross functional teams ( RD, QC/QA and Manufacturing) . 6. Biosimilar Dossier Authoring, Review and Hands on experience in eCTD submissions 7. MOH Query response. 8. Biosimilar Product Life cycle Management. 9. RA support for Plant related ...

LTFinance is looking for TEAM MEMBER - QUALITY ASSURANCE to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to identify and mitigate risks, ensuring compliance with regulatory requirements. Develop and implement effective quality control processes to ensure high standards of service delivery. Conduct regular audits and reviews to identify areas for improvement and provide recommendations for enhancement. Analyze data and metrics to measure performance and identify trends for improvement. Provide training and coaching to team members on quality procedures and best practices. Foster a culture of continuous improvement, encouraging team mem...

Site Name: Bengaluru Luxor North Tower Posted Date: Nov 28 2025 Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. We're uniting science, technology, and talent to get...

We are looking for a highly skilled and experienced Informed Consent Specialist II to join our team at Icon Pharmaceuticals. The ideal candidate will have a strong background in informed consent and excellent communication skills. Roles and Responsibility Develop and implement effective informed consent strategies to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to design and deliver high-quality informed consent forms and materials. Conduct thorough reviews of informed consent documents to identify areas for improvement. Provide training and support to internal stakeholders on informed consent best practices. Stay up-to-date with changing regulation...

Roles and Responsibility Accurately code patient data using various coding systems. Review medical records to ensure accurate coding compliance with regulations. Collaborate with healthcare professionals to clarify coding discrepancies. Develop and implement efficient coding processes to enhance productivity. Stay updated with changes in coding regulations and guidelines. Maintain confidentiality and adhere to HIPAA policies. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Roles and Responsibility Assist in the development of clinical trial protocols and study designs. Coordinate with cross-functional teams to ensure timely and successful study execution. Conduct site feasibility assessments and coordinate with investigators. Review and approve clinical study reports and other regulatory documents. Collaborate with data management teams to ensure accurate and timely data submission. Provide support for quality control and compliance activities. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer...

Roles and Responsibility Conduct thorough reviews of clinical trial data to identify potential safety concerns. Develop and implement effective pharmacovigilance strategies to mitigate risks. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze complex data sets to identify trends and patterns that may impact patient safety. Prepare detailed reports and presentations to communicate findings to stakeholders. Stay up-to-date with changing regulations and industry standards in pharmacovigilance. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encoura...

Job Title: Executive / Senior Executive - Regulatory Affairs (Formulation) Location: Pune, Maharashtra Department: Regulatory Affairs Company: SAVA Healthcare Limited Job Purpose: To manage the preparation, compilation, and submission of regulatory dossiers in compliance with international guidelines, with a focus on Europe (eCTD format) and Rest of the World (ROW) markets. The role ensures timely approvals and lifecycle management of pharmaceutical products. Key Responsibilities: Preparation and compilation of dossiers in eCTD format for European submissions (hands-on experience in eCTD is a must). Sound understanding and working knowledge of EU DCP/MRP procedures . Preparation and review o...

Prepare, Review and Approval of COA. Review and Approval of stability protocols, reports, and summary reports. Prepare justification for reduction of tests for Input material testing such as raw and packaging material; In-process testing; Finished product testing; Stability testing; Microbial testing. Prepare and review of specification/Method of analysis. Initiation, evaluation of Change control. Review of vendor qualification documents. Handling of item codification. Technical Skill Required Analytical documentation : Advanced ICH Guidelines : Advanced Stability Management : Advanced QMS Automation System : Intermediate US Guidelines : Advanced

Review and approve change control requests raised by cross-functional teams. Assess GMP, regulatory, and quality impact for process, equipment, documents, and systems. Perform/verify risk assessments and ensure adequate mitigation. Review and approve revised documents (SOPs, BMR/BPR, validation protocols/reports). Ensure validation/qualification requirements are identified and completed. Verify training, implementation readiness, and completeness of supporting data. Approve and close change controls within defined QMS timelines. Ensure compliance with cGMP, data integrity, and regulatory guidelines. Skills Required Analytical problem-solving skills : Advanced cGMP, GDP ICH Q10 knowledge : Ad...

. Job Title: Manager 2/1 - RD Biotechnology Business Unit: RD1 Regulatory Affairs Job Grade G11A/G10 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 SunshineAs 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. Key Responsibilities: Develop and implement phase-appropriate...