
Regulatory Affairs Officer
3 days ago
Responsibilities
In the context of a project for one of our top Pharma client, we’re looking for 2 talented Regulatory Affairs Officer to lead the following missions, and much moreCompile, or supervise the compilation of regulatory dossiers
Provide on-going regulatory advice to project teams to ensure regulatory concerns are planned and accounted for and the relevant data are generated to meet project objectives
Provide regulatory support to clients and associate companies
Provide format and contents review of packaging texts, Summary of Product Characteristics, Patient Information Leaflets and labelling
Review tasks for, support and mentor Regulatory Affairs Associates
Profile
UK and IE lifecycle maintenance experience
Providing support during external and unannounced audits.
Responding to internal requests for technical and/or regulatory information.
Preparation and submission of Technical/Site Transfer Applications
Assisting with the preparation of UK and IE Marketing Authorisation Applications
Monitor and maintain up-to-date knowledge of national and European guidelines/legislation.
Ensuring compliance with all regulatory processes, in readiness for both internal and external audits.
Ensuring compliance with the regulations of the MHRA and HPRA
Use a variety of software packages to produce correspondence and documents, maintain spreadsheets and databases, and locate information and data eg Microsoft Office Suite, Veeva (or comparable EDMS), LorenZ, Trackwise etc
A proven ability to consistently deliver to tight timelines, without negatively impacting on quality or departmental budget
General regulatory administration duties and compliance requirements
Experience of promotional/non-promotional activities would be an advantage
Experience of operating within the post-Brexit regulatory landscape in UK and IE
Good IT skills/knowledge
Good organisational skills
Good communication skills
Pro-active attitude and able to work on own initiative as well as part of a team
Ability to prioritise different workloads/multi-task
**Salary**: ₹145,587.64 - ₹711,603.98 per year
Schedule:
- Evening shift
**Experience**:
- Regulatory Affairs: 6 years (preferred)
**Speak with the employer**
+91
+918851863930
-
Drug Regulatory Affairs Officer
3 days ago
Dwarka, Delhi, Delhi, India Career Strategy Solutions Full timeUrgent Hiring for Drug Regulatory Affairs for Delhi Location Should have relevant expeirence in 3 to 8 years in DRA DRUG REGULATORY AFFAIRS (DRA) **Job Description**: Knowledge of Dossier Compilation as per the Country Guideline (CTD, ACTD, and Country Specific Format) Knowledge of COPP, FSC, Product Permission, and Summary of Product...
-
Executive - Regulatory Affairs
3 days ago
Delhi, Delhi, India Domnic Lewis Pvt. Ltd Full time**Executive - Regulatory Affairs - Delhi**: **Domnic Lewis has been mandated to hire for Executive - Regulatory Affairs - Delhi** **Position Title**: Executive - Regulatory Affairs **Grade**: C **Reports to**: Lead/Manager - Regulatory Affairs **Position Purpose**: - Monitor and report the status of all product licenses in a timely and accurate manner -...
-
Regulatory Affairs Executive
3 days ago
Delhi, Delhi, India SAVVI SALES AND SERVICE PVT.LTD. Full timeJob Title: Regulatory Affairs Executive Location: Rohini, Delhi Industry: Pharmaceuticals / Nutraceuticals Salary Package: ₹25,000 - ₹50,000 per month Gender Preference: Male Experience Required: 2-3 years in Pharma or Nutra Industry (Regulatory Affairs) Key Responsibilities: - Prepare and submit regulatory dossiers such as INDs, NDAs, ANDAs,...
-
Regulatory Affairs
10 hours ago
Delhi, India First Choice Consultant Service Full timeProfile: Regulatory Affairs (CDSCO) Location: Paschim Vihar, New Delhi **Salary**: Up to 50,000 5 Days Working Exp: 1 to 2 Years Yearly Bonus Office Timing: 9:30 to 5:30 **Job Descriptions**: - Proficient in English. - Must understand the regulatory requirements for medical devices in India. - Significant experience within the legislative and...
-
Regulatory Affairs Executive
3 days ago
Delhi, Delhi, India Ample Leap Cognition & Technologies Pvt Ltd Full timeDESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...
-
Regulatory Affairs Specialist
2 days ago
Delhi, Delhi, India beBeeEODB Full time ₹ 8,00,000 - ₹ 12,00,000Regulatory Affairs SpecialistThis role involves collaborating with industry members to gather inputs on regulatory challenges and leading the development of policy notes and white papers to improve the business environment in India.The position requires identifying cross-cutting industry-wide regulatory bottlenecks through analysis of member inputs,...
-
Senior Regulatory Affairs Specialist
4 days ago
Delhi, Delhi, India beBeeRegulatory Full time ₹ 20,00,000 - ₹ 24,50,000Job Title:Senior Regulatory Affairs Specialist
-
Regulatory Affairs Executive Cdsco
2 days ago
Nehru Place, Delhi, Delhi, India PU Professional Utilities Pvt. Ltd Full timeWe are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...
-
Vacancy for Regulatory Affairs at Delhi Ncr
2 weeks ago
Delhi, India RIGHT STAFF Full timeGreetings from Right Staff One of our client who are into Medical Devices Are looking for a Regulatory Affairs person at Delhi NCR Job Description - **Experience minimum 5 Years and above compulsory** Designation - Regulatory Affairs/QA Affairs Time - Day Shift Location - Delhi NCR **Responsibilities**: - 1. Identify regulatory and post market...
-
Officer - Regulatory Affairs
3 days ago
Dwarka, Delhi, Delhi, India Harasha Pharma Pvt ltd Full timeØ Preparation and reviewing of administrative documents. Ø Preparation and Review of Dossier in CTD, ACTD and ECTD Format. Ø Preparing the SPC/ Leaflet/ SMPC as per country guidelines. Ø Preparation of Dossier for CIS, Africa countries, ASEAN, EU, LATAM, ROW and Gulf Countries,. Ø Review and Making of Stability Data, Analytical Method Validation,...