Virchow Biotech – Interview For Quality Control Dept on 14 & 15th june 2024

Virchow Biotech – Interview For Quality Control Dept on 14 & 15th june 2024

Virchow Biotech - Interview

We have an urgent requirement (VIRCHOW BIOTECH PVT LTD) for the fallowing position with below mentioned details.

Designation: Jr Executive or Sr Executive

Department: Quality Control

No of Vacancies: 20

Qualification: M. Pharmacy, B. Pharmacy or M. Sc or B. Sc (Life Sciences)

Experience: 2 to 6 years

Budget- 2.6 to 5.4 lac

Preferably Males As per below mentioned Job Description.

1) Responsible for inspecting and/or testing products.

2) Should have worked on Aseptic (Injectable) products and QC Instrumentation(HPLC).

3) Responsible for testing & sampling finished products.

4) Should have basic communication.

5) Should be able to validate the collected sample .

6) Perform tasks as required GLP/ GMP according to allocation of QC manager and report monthly on their tasks.

7) To audit all laboratory worksheets, calibration protocols/reports and raw data archives to ensure the validity and accuracy of the data

8) To prepare and check Certificates of Analysis for all lots of raw materials and packaging materials tested in the QC Department

9) Checking the tidiness, orderliness and cleanliness of their working area

Venue: Virchow Biotech Pvt Ltd Survey no.172 part, Gagillapur, Quthbullapur, Hyderabad Telangana -500043

Time : 9 am to 11 am On Walkins on 14 & 15.06.2024

(Friday & Saturday )

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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