Maithri Drugs is one of India’s fast-growing pharmaceutical companies. Maithri’s strategic focus is on active pharma ingredients (APIs). The company is widely recognized for its excellent research & development and aggressive growth strategies. Our 35 US DMFs and 10 CEPs in a short span attest to our R&D excellence. Maithri’s manufacturing facility is located in Hyderabad. This facility is audited and approved by the US FDA.
Job Description
VACANCIES: Executive’s, Senior Executive’s
QUALIFICATION: MSc(Chemistry)/M Pharmacy
ELIGIBILITY CRITERIA: 02 -05 yrs. of work experience
JOB SPECIFICATIONS:
- DMF Compilation and submission to respective regulatory authorities.
- Complie and submit the deficiency responses to Authorities within the time frame.
- Conduct the cross functional team (CFT) meetings for deficiency related activities.
- Respond the customer queries in timely manner.
- Evaluate the changes and assess the Changes controls as per Regulatory variation guidelines.
- Lifecycle management for Regulatory submissions
- Maintaining the databases for Regulatory submission.
- Good knowledge on eCTD submission software.
DOCUMENTS TO BE CARRIED: Candidates are requested to carry updated resume, photocopies of educational certificates, All employment documents, last 3 months’ pay slips, last 6 months salary bank account statement, latest increment letter, photocopy of updated Aadhar and pan card.
TIMINGS: Interested candidates may walk-in from 09:00 AM to 01:00 PM
INTERVIEW MODE: Face to Face interview
Interview Location : SY.NO 810/PART,820/PART,821/PART,GUMMADIDALA(V)&(M),NARASAPUR ROAD,SANGAREDDY(D), TELANGANA, INDIA-502313.
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