Halma - Associate - Regulatory Affairs

About Halma : Halma is a global group of life-saving technologies companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US. Our diverse group of nearly 50 global companies specialize in market leading technologies that push the...

About Halma : Halma is a global group of life-saving technology companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US. Our diverse group of nearly 50 global companies specialise in market leading technologies that push the...

Company Overview:At Inter IKEA Group, we value diverse backgrounds, perspectives, and skills. We are committed to providing coworkers with a work environment free of discrimination and harassment.Sectoral Expertise:Align Public Affairs and Regulatory Affairs priorities within assigned areas, communicate to relevant stakeholders.Lead and facilitate strategic...

Job SummaryRandstad is seeking a detail-oriented and organized Regulatory Affairs Coordinator to join our team. In this role, you will be responsible for assisting with label registration applications, tracking submissions and approvals, and maintaining the label artwork approval tool. You will also collaborate with design and marketing teams to ensure...

**Job Title - CMC RA Associate I Submission Excellence & Project Management.** **CAREER LEVEL: C** **ABOUT ASTRAZENECA** AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more...

About UsIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the healthcare and life science industries.Our team of experts is dedicated to helping our clients navigate complex regulatory landscapes and stay ahead of the competition.Job Title / Primary Skill:Regulatory Affair...

**Job Description** Regulatory Affairs BA Position Description Requirement Regulatory Affairs BA Recruiter Name Nikitha Njoyn ID J1122-2759 Primary Skills Regulatory Affairs BA Secondary Skills Pharma Domain Experience 3-6+yrs Notice Period 0-30days Location Bangalore/ Hyderabad Detailed Job Description Technical Skills: - Regulatory Affairs - 3+...

**Job Title: Regulatory Affairs Associate I (International Regulatory Affairs)** **Career Level - C** **Introduction to Role**: Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients in international markets. We work across the AZ pipeline and business to...

At Biocon, we seek an experienced Regulatory Affairs Specialist to lead our efforts in the US market. As a key member of our team, you will be responsible for ensuring the timely submission of ANDA applications and managing product life cycles.About this RoleThis is an exciting opportunity to join our dynamic team and contribute to the growth of our...

Job OverviewSyngene International Limited seeks a highly skilled Regulatory Affairs Leader to oversee the regulatory function across various facilities. The ideal candidate will ensure compliance with national regulations, foster strategic partnerships, and drive business growth.Key Responsibilities:Develop and execute a forward-looking, risk-based...

Job Description:The Senior Regulatory Affairs Specialist will play a key role in the coordination and preparation of regulatory plans and document packages for regulatory submissions to various agencies worldwide. This includes the FDA, Health Canada, EU, Asia, and other countries.This position requires strong knowledge of medical device regulations,...

About Syngene : Syngene ( ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared...

About Syngene : Syngene ( ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared...

**JOB TITLE: REGULATORY AFFAIRS ASSOCIATE II**: **CAREER LEVEL: C**: Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively take a strategic approach earlier in the product lifecycle to get involved in shaping...

Job DescriptionWe are seeking a Product Stewardship and Regulatory Affairs Specialist to join our team. As a key member of our Product Stewardship and Regulatory Affairs Department, you will play a crucial role in ensuring the compliance of our products with regulatory requirements.

As a Regulatory affairs leader, you will be leading regulatory development, internally and externally, to keep up a proactive approach to new and updated regulations. What you do in this role - Align Public Affairs and Regulatory Affairs priorities, within assigned area(s), and communicate to relevant stakeholders, - Lead and facilitate strategic...

Job Title / Primary Skill: Regulatory Affair SpecialistShift Timings : US EST timings (IST- 6.00 pm to 3.00 am)Job Location: Remote/HomebasedExperience: 5 to 10 YearsJob Overview:You will oversee all labelling activities for specified APIs and collaborates with our client and/orIQVIA stakeholders, such as Global Labeling, PV, GRLs and the LOCs (Local...

Job Title / Primary Skill: Regulatory Affair ManagerShift Timings : UK timings (2 PM to 11 PM)Job Location: Remote/HomebasedExperience:8 to 12 YearsSkills: Core labelling and EU labelling experience, Global labeling lead role, SMPC, CCDS, CDS, Authoring, Plasma derivativesJob Overview:You will oversee all labelling activities for specified APIs and...

**Internal Title**:Regulatory Affairs Professional **External Title**:Deputy General Manager **Position Summary** To perform regulatory tasks as applicable to SHPL products pertaining to regulating authorities like radiation safety related certification from Atomic Energy Regulatory Board (AERB) for Zone India (India, Bangladesh, Nepal, Sri Lanka &...

Supports worldwide product registrations by providing information and documents to Siemens Regional Unit (RU) in Asia-Pacific, Middle East Asia, South and Latin America and Europe. - o Provides answers to technical questions from Siemens Regional Unit (RU) and international regulatory authorities. - o Prepares and/or compiles technical documents for the...