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)

Contact – HR ( 9398326257 )
SWARNALATHA B

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