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Jodas Expoim Pvt. Ltd

Website Jodas Expoim Pvt Ltd

About Jodas Expoim Pvt Ltd

Jodas Expoim Pvt Ltd (JEPL) is a global, innovation-driven biopharmaceutical company, committed to delivering high-quality specialty and generic products. With EU GMP certifications for Oncology (orals), Contrast Media (SVP and LVP), and Cephalosporins, JEPL is a leader in the production of Anti-Cancer and Antibiotic products.

Join our growing team and contribute to transforming lives through science and innovation!


Open Positions

1. Formulation Research & Development (FR&D) – Injectables

Designation: RA I / RA II
Experience: 3–8 years
Qualification: B. Pharma / M. Pharma
Number of Positions: 05
Location: Karakapatla, Hyderabad

Key Responsibilities:

  • Conduct literature and patent reviews to devise pre-product development strategies.
  • Execute experimental work and document observations meticulously.
  • Compile pre-formulation data for drugs and excipients in formulations.
  • Prepare tentative and final input specifications, master formula records, and product development reports.
  • Perform process evaluation, optimization, scale-up, and exhibit batches for new or amended products.

2. Injectables QA Validation Specialist

Designation: Executive / Sr Executive / Assistant Manager
Experience: 3–10 years
Qualification: B. Pharma / M. Pharma
Number of Positions: 05

Job Summary:
Seeking experienced professionals to ensure the quality and compliance of injectable drug products during validation processes.

Key Responsibilities:

  • Plan, execute, and document validation activities for injectables.
  • Oversee the qualification of equipment, facilities, and systems.
  • Develop and review validation protocols (IQ, OQ, PQ).
  • Ensure compliance with GMP, FDA, EMA, and other regulatory standards.
  • Identify risks, propose corrective actions, and resolve quality issues in collaboration with cross-functional teams.

Preferred Skills:

  • Strong knowledge of GMP, FDA, EMA, and ICH standards.
  • Hands-on experience with process validation and equipment qualification.
  • Excellent attention to detail, communication, and problem-solving skills.

3. Regulatory Affairs – EU/ROW Market (Parenteral Dosage Forms)

Designation: Executive / Sr Executive
Experience: 2–7 years (Experience with EU/ROW regulatory affairs preferred)
Qualification: B. Pharma / M. Pharma
Number of Positions: 05

Key Responsibilities:

  • Prepare high-quality EU/ROW dossiers for Parenteral Dosage Forms (Modules 2 & 3).
  • Ensure adherence to EU/ROW regulatory guidelines, ICH/EMEA standards, and compliance throughout the product lifecycle.
  • Manage post-approval variations and assess the impact of change controls.
  • Collaborate with cross-functional teams to ensure timely regulatory filings and approvals.

Basic Skills:

  • Strong understanding of Parenteral Dosage Formulations and analytical aspects.
  • Proficiency in MS Office and regulatory software tools.
  • Excellent time-management, adaptability, and communication skills.

Location:
Plot No S-1, Sy No: 1043 & 1048, 3rd Floor, NSL Centrum, KPHB Phase 3, Kukatpally, Hyderabad, Telangana – 500072

Interested candidates can share their updated resumes at recruitment3@jodasexpoim.in.

Be part of a team shaping the future of healthcare! Apply today!

To apply for this job email your details to recruitment3@jodasexpoim.in