Cronus Pharma Pvt Ltd Walk-in On 18th oct 2025 for Multiple Positions

Cronus Pharma Pvt Ltd Walk-in Interview 2025.Cronus Pharma Pvt Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.

Vacancy details:

• Department: Executive / Sr. Executive / Asst Manager (Regulatory Affairs)/Purchase Executive – Formulations 

Important Details :

• Work Location: Hyderabad
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description: Greeting from Cronus Pharma Pvt Ltd !!!

Role & responsibilities

Job description

• Ensure that a company’s products comply with the regulations of the regions.
• Keep up to date with national and international legislation, guidelines and customer practices
• Respond to queries from Centre for Veterinary Medicines (CVM).
• Collect, collate and evaluate scientific data from FR&D, AR&D and DQA.
• Develop and write clear arguments and explanations for new product licences and licence renewals at R&D site.
• Prepare submissions of licence variations and renewals to strict deadlines as per CVM.
• Monitor and set timelines for licence variations and renewal approvals
• Advise scientists (AR&D, FR&D, Pkg.-R&D) on regulatory requirements.
• Provide strategic advice to senior management throughout the development of a new product
• Review company practices and provide advice on changes to systems if any.
• Liaise with manager, and make presentations to, regulatory authorities, if any.
• Negotiate with regulatory authorities for marketing authorisation
• Take part in the development of marketing concepts and approve packaging and advertising before a product’s release.
• Prepare the CTD sections of the dossier and ensure timely filing as informed by the functional head and Head -R&D.
• Review the data and check for its alignment and compliance from regulatory point of view as per CVM.
• Ensure the regulatory filing grid as shared by Functional head and Head-R&D is met on timely way and in complete regulatory compliance.
• Collaborate with FR&D, AR&D, Pkg-R&D on regular basis and together ensure the timely filing of products.

Role & responsibilities

1. Procurement & Sourcing:
   • Source APIs from qualified US Market suppliers.
   • Maintain relationships with existing vendors and identify new suppliers.
   • Evaluate supplier credentials and ensure regulatory compliance (e.g., GMP, USFDA, EUGMP).
2. Negotiation & Cost Management:
   • Negotiate prices, payment terms, delivery schedules, and contracts.
   • Work with finance and production departments to manage cost-effectiveness.
3. Inventory & Planning:
   • Monitor stock levels and forecast needs based on production plans.
   • Coordinate with production and warehouse teams for timely delivery.
4. Compliance & Documentation:
   • Ensure all procurement activities comply with regulatory and quality standards.
   • Maintain accurate records for audits, including COAs, DMFs, and vendor certifications.
5. Market Intelligence:
   • Stay updated on global market trends, pricing, and supply-demand changes.
   • Track geopolitical or regulatory changes that may impact sourcing.

Required Skills & Qualifications:

• Education: B.Pharm / B.Sc / M.Sc / MBA (Supply Chain or Pharma Management preferred).
• Experience: 28 years in pharmaceutical API procurement or supply chain.
• Knowledge:
  • Understanding of APIs and pharma regulations (e.g., USFDA, EDQM, WHO).
  • Familiarity with sourcing tools, ERP systems (SAP, Oracle, etc.).
• Skills:
  • Strong negotiation and communication skills.
  • Analytical thinking and attention to detail.
  • Vendor management and relationship building.

Walkin Interview Details:

Walkin Date: 18th October , 

Time: 9.30 AM – 5.30 PM

Venue:Level 18, 30/C, Orbit, Knowledge City Rd, Panmaktha, Hyderabad, Rai Durg, Telangana 500032 (View on map)

ABAC