Virchow Biotech – Interview For Fresher and Experienced BSc, MSc (All Streams) B Pharma or M Pharma, Diploma or B Tech – Manufacturing on 12&13 Jan’2024

Virchow Biotech – Interview For Fresher and Experienced BSc, MSc (All Streams) B Pharma or M Pharma, Diploma or B Tech – Manufacturing on 12&13 Jan’2024

Interview

Requirement of Manpower for Manufacturing (Vial, Cartridge, PFS & BFS)

Designation: Trainee Executive to Sr Executive

Qualification: B. Sc, M. Sc (All Streams) B. Pharma or M. Pharma, Diploma or B. Tech(

Location: Hyderabad

Experience : 0 to 6 Years

No Of Positions: 16

Walk-ins on 12 & 13.01.2024

Salary Range: 1.5 lpa to 5.4 lac

Job Description:

1) Should be able handle line activities of Manufacturing of Injectable (Vial, Catridge, PFS

2) Should have basic idea on aseptic operations

3) Should have an idea on CIP & SIP

4) Control and adjust machine settings as needed to maintain desired line speed 5) Responsible for accurate production and packaging changeovers as per packaging scherare

6) Maintain a clean work area and clean equipment before and after shift.

7) Perform basic troubleshooting and minor repairs to ensure production equipment runs efficiently.

8) Remove damaged products or supplies, as needed.

Interested and Eligible candidates are requested to share the updated resume on the below mentioned mail-Id

Raghuvirchowbiotech.com or hr@virchowbiotech.com

Time: 9 am to 11 am On 12 & 13.01.2024(Friday & Saturday)

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

Land Mark:- Beside Granules India Limited

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

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ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits 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. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube