Wednesday, August 18, 2021

Zenzi Pharmaceutical Industries Ltd QA Executive QC Microbiologist Openings

 Zenzi Pharmaceutical Industries Recruitment 2021. Zenzi Pharmaceutical Industries Private Limited is a Private incorporated on 20 December 2005. It is classified as Non-govt company and is registered at Registrar of Companies, Mumbai. Its authorized share capital is Rs. 1,050,000,000 and its paid up capital is Rs. 1,050,000,000. It is inolved in Manufacture of other chemical products.


  • Important Vacancy details:
  • Post Name: QC Microbiologist,QA Executive
  • Experienced:01+years
  • Location: Kalyan, Maharashtra
  • Salary :1,00,000 – ₹4,00,000 a year
  • Openings :NA
  • Contact number: 9867767435

 Job Description: We have requirement for the post of QC Microbiologist,QA Executive in Sitec Labs Pvt. Ltd !

QC Microbiologist

1) Media preparation, media stock, Media consumption record & Related Documentation.

2) Growth promotion test of rehydrated culture media.

3) Daily record of lab and equipment & instrument.

4) Daily PH Meter & balance calibration

5) Preparation / Review of SOP, validation protocol & Report.

6) Environmental monitoring of clean room and other controlled area / Trending.

7) Water sampling and testing / trending.

8) MLT Test of RM, FP, Bulk, Packing material as per pharmacopeia

9) Sterility test, BET Test, media Fill, BIs test.

10) Master sub culturing and Identification by VITEC System.

11) Validation of lab equipment & instrument.

12) Area validation and qualification / HVAC.

13) Validation of autoclave, Incubators & Dry heat sterilizer.

14) Online Documentation with respect to GLP, GDP, GMP.

15) Taking initiative of Change control, OOS, Deviation.

16) Injectable Experience preferred

QA Executive

1. Preparation, review, issuance, retrieval of SOPs.

2. Preparation and review of BMR, BPR as per the approved MFR received from customer.

3. Review of change control deviation, OOS, CAPA.

4. Release or rejection of batches of raw materials (API, excipients and packaging material) and finished products.

5. Review of executed BMR, BPR, Quality control documents like Inprocess, raw material, finished product and packing material analysis report.

6. Conducting training on new or revision of documents like SOP,BMR, BPR, validation, qualification protocol etc.

7. Imparting Training

  • To any new employee joining the department
  • Regular cGMP training to staff and workmen
  • SOP training.

8. Responsible for coordination to carry out the qualification activities of instrument, equipment at site.

9. Responsible for conducting the vendor evaluation.

10. Timely reporting of any incidences / failures / non-conformances observed.

11. Adherence to companys laid down code of conduct and discipline.

12. Providing assistance and execution of any task allocated by HOD as and when required.

Selection ProcessThe selection will be on the basis of Interview.

Apply online

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