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Jodas Expoim - Walk-In Interviews on 06th Feb 2024

Jodas Expoim Pvt. Ltd is a Global, specialty, innovation driven, emerging, generic bio- pharmaceutical company that is asserting itself among the world’s foremost pharmaceutical companies. JEPL is having EU GMP certification of Oncology (orals), Contrast Media (SVP & LVP) and facility for Cephalosporin’s (DPI) currently delivering the products like Anti-Cancer and Antibiotics, Contrast media. We began our journey of growth in the year 2006 in India, and today Jodas is a modern, research driven organization that has quality and affordability at the heart of its activities.

Greetings from JODAS!!!

Please find the vacancy details below

1) Department: QA

• Experience: 04-08+ yrs

• Location: Telangana, India-Hyderabad

Time and Venue

Tuesday 06th February 2024, 9.30 AM – 2.00 PM

Jodas Expoim Pvt. Ltd., Plot No:55, Biotech Park, Phase III, Karkapatla (V), Markook (M), Siddipet (D). Telangana-502279, India.

Job description:

Department: Quality Assurance

Qualification– M.Pharmacy/ M Sc

1) QMS (Change control)

Experience: 4-6 Years Executive

Should have knowledge on QMS related to manufacturing and analytical and capable of review of change controls, CAPA and incidents.

2) QA (Regulatory support) – Experience: 5-8 Years – Sr Executive/AM

Should have knowledge on analytical/ Regulatory experience and capable of handling review and collection of analytical, formulation and manufacturing related documents and submit to RA team.

3) QA (vendor Management) – Experience: 5-8 Years – AM

Candidates should hands on experience in formulation and capable of review and maintain of all vendor related documents

(Questionnaires, Audits tracking and able to perform vendor audits)

4) AQA (formulations) – Experience: 6-8 Years Sr Executive

Person should have formulation experience in quality control and capable of review of all analytical documents like RM, PM. FP and stability documents.

5) IPQA (OSD) – Experience: 4-6 Years – Executive

Person should have oral solid dosage experience (Tablets &Capsules) and shopfloor activities including manufacturing & packing.

6) QMS (Laboratory incidents & OOS) Experience- 5-7 Years

Should have experience in analytical testing and capable of review all documents related to laboratory incident and OOS

7) Validation (PV & CV) Experience- 6-8 Years

Should have knowledge on process and cleaning validation for injectable formulations and capable of preparing protocols and reports related to process & cleaning validation.

Please carry copies of all required documents like- Aadharcard, 3 Months payslips, CTC Letter