Alembic Pharmaceuticals Hiring Freshers & Experience

Alembic Pharmaceuticals Hiring: Logistics Executive-0 – 6 years

  • Education UG: Any Graduate PG: Any Postgraduate

We are looking for a Logistics Executive to join our team in Vadodara.

Key Responsibilities:

  • Handling Shipping Bills and export documentation.
  • Checklist verification and approval.
  • Coordination with CHA, freight forwarders, and shipping lines.
  • Customs clearance and shipment documentation.
  • Internal coordination with Sales, Production, Warehouse, and Finance teams.
  • Maintaining shipment records and timely updates.

Requirements:

  • Graduate in Commerce, Logistics, Supply Chain, or related field.
  • 2-5 years of experience in export logistics/documentation.
  • Knowledge of shipping bills, customs procedures, and export documentation.
  • SAP experience.
  • Good communication, coordination, and MS Excel skills.

Interested candidates can share their CV at: creyesha.macwan@alembic.co.in

Assistant Manager / Deputy Manager – Regulatory Affairs (US Market, Non-Oral)

Location: Vadodara, Gujarat

Job Summary

We are seeking a highly motivated Regulatory Affairs professional to support US regulatory activities for Non-Oral dosage forms, particularly Sterile products. The incumbent will be responsible for post-approval regulatory submissions, lifecycle management, and coordination with cross-functional teams to ensure compliance with USFDA requirements.

Required Experience

  • 7 to 12 years of Regulatory Affairs experience in the pharmaceutical industry.
  • Hands-on experience in US Market Regulatory Affairs.
  • Strong experience in Post-Approval/Life Cycle Management activities.
  • Experience with Sterile/Injectable/Ophthalmic/Non-Oral dosage forms is mandatory.
  • Experience in preparation and submission of PAS, CBE-30, CBE-0, Annual Reports, and other post-approval filings.
  • Working knowledge of USFDA regulations, CFR requirements, and guidance documents.

Technical Skills

  • Experience in Electronic Submission Management.
  • Knowledge of eCTD publishing and submission processes.
  • Hands-on experience with regulatory software/tools.

Qualification :B.Pharm / M.Pharm / M.Sc. or equivalent qualification.

Interested candidate can share cv on creyesha.macwan@alembic.co.in

SWARNALATHA B

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