- Full Time
- Kukatpally, Hyderabad, Telangana

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