9 Eu Market Jobs

Roles and Responsibilities Develop new business opportunities through market research, competitor analysis, and customer engagement. Manage existing client relationships to identify upsell/cross-sell opportunities and expand services offered. Collaborate with internal teams (e.g., sales, operations) to develop strategies for closing deals and delivering projects on time. Identify potential partnerships with other companies or organizations in the EU market. Analyze market trends, competitor activity, and customer needs to inform business development decisions. Desired Candidate Profile 2-5 years of experience in Business Development or a related field (BD). Strong understanding of advanced e...

Greetings of the day ! Our reputed MNC Client is hiring for: Designation: Regulatory Affairs- EU Market- Pre & Post Approval Location: Hyderabad Shift: General Work Mode: WFO (5 days working) Interview Mode: F2F interview NOTE: Looking for candidates from Generic Pharma and not from API as this is for formulation Role & responsibilities: 1. Component with EU-Filing requirements with respect to Module 2 & 3 ability to independently and correctly review technical documents related to Quality Module 2. Well versed with EU- Regulatory guidance and Processes (i.e. Ability to understand and interpret technical expectations as per applicable ICH & EMEA guidelines) 3. Clear Knowledge of basic aspect...

Develop & execute a market-entry &growth strategy for the EU private label tea business Identify, approach & onboard EU-based clients, retailers, ecommerce & Tea importer Coordinate sampling, quotations, pricing strategies & Lead contract negotiation Required Candidate profile Ensure compliance with EU regulations related to food safety Monitor EU tea market trends,consumer preferences &competitor activity Attend relevant trade shows, buyer meetings & B2B networking events

Hiring for a Well-Established MNC Pharma 2nd Largest in the Industry! Division : FORMULATIONS Department : Regulatory Affairs Qualification : M.Pharma-Pharmaceutics/Pharmaceutical Analysis/Regulatory Affairs/Quality Assurance/Pharmaceutical Technologies) Experience : 2 to 10 Years Work Location : Hyderabad No of Positions Vacant : 5 Key Responsibilities : PRE and POST APPROVALS : 1. Component with EU-Filing requirements with respect to Module 2 & 3 ability to independently and correctly review technical documents related to Quality Module 2. Well versed with EU- Regulatory guidance and Processes (i.e., Ability to understand and interpret technical expectations as per applicable ICH & EMEA gu...

Responsibilities: * Exp on procedure of application of new Drug * Manage COPPs, GMP, GLP compliance & SUGAM portal maintenance * Oversee license renewals, dossier reviews & NIB submissions * Trademark License & Coordinate with Drug Control Authority

• Business Development via out-licensing in Europe, Australia and NZ • Complete responsibility and accountability of the assigned countries • Structuring, negotiating and execution of commercial agreements • Maintain ongoing business relationship Required Candidate profile • Candidate should possess working knowledge of out-licensing business and regulatory requirements of EU (Formulation)- Territory: Europe, Australia and NZ Experience: 5 - 8 years

Working on UK IT RECRUITMENT Working with MSP/VMS clients Recruiting best talents using portals, professional sites, industry contacts within TAT Required Candidate profile Minimum 3 years of experience in UK/EU market in technical recruitment Proficiency in hiring through Ceipal, job boards & LinkedIn Excellent communication skill Knowledge on Beeline, SAP FieldGlass

Manage EMA registrations, liaise with authorities (EMA, BfArM, PEI), handle PI submissions, packaging, approvals. Review SmPC, PILs, labels, texts. Support RA team and associates, assist with data entry, invoicing, presales, and ensure EU compliance.

Opening for - Manager, Regulatory Affairs - CMC@ Mumbai , Pune and Hyderabad location. Experience : 5 to 10 Yrs relevant experience in RA CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network ...