V S International (VSI) – Walk-Ins for QC / QA / Production / Packing / Formulation Development / Analytical Development on 9th April’ 2023

V S International (VSI) – Walk-Ins for QC / QA / Production / Packing / Formulation Development / Analytical Development on 9th April’ 2023

Walk-In Interviews @ V S International

Production Officer / Sr. Officer

Roles and Responsibilities

  • Responsible for all Production activities at Tablet Compression, Granulation, and Coating with respect to cGMP.
  • Maintain Weekly and Monthly Production Planning by Checking RM/PM availability and Production Equipment feasibility
  • Should have knowledge of documentation exposure of cGMP.
  • Completion of BMR (Batch Manufacturing Record), Equipment Log Book/ Shift & all cGMP Records.
  • Co-Ordinating with warehouse, QA, QC & Engg. Department, to run the shift activity Smoothly.
  • Maintaining documentation of the BMR requisitions in process.
  • Maintaining good housekeeping on the shop floor.
  • Manpower work allocation and Training.
  • Exposure in Regulatory Markets like EUGMP, USFDA, MHRA, TGA etc.

Desired Candidate Profile

  • Minimum B. Pharma
  • Ready to relocate Daman location
  • Experience: min. 2 – 5 Years
  • Industries: OSD (Tablet & Capsule), Pharma

Packing Officer / Sr. Officer / Executive

Roles and Responsibilities

  • Responsible for handling all primary and secondary packaging activities.
  • To coordinate with other departments like warehouse, Engineering, QC, QA
  • Planning for day-to-day activity in the packing department
  • Able to handle regulatory audits.

Desired Candidate Profile

  • Education: B.Sc / M.Sc. /B. Pharm / M. Pharm
  • Experience: 01 to 06 Years

QA Officer / Sr. Officer / Executive

Roles and Responsibilities

  • Vendor Management,
  • APQR Activity,
  • QMS (Change control, Handling Market Complaints, Audit Compliance)
  • IPQA

Desired Candidate Profile:

  • Education: M.Sc. /B. Pharm / M. Pharm
  • Experience: 01 to 06 Years

QC Officer / Sr. Officer / Executive

Roles and Responsibilities:

  • FP / Stability / RM / GLP section
  • Should have handled independently HPLC / GC
  • Calibration of QC Instruments

Education: B.Sc / M.Sc. /B. Pharm / M. Pharm

Experience: 01 to 06 Years

Formulation Development Research Scientist / Associate

Roles and Responsibilities:

  • Project development
  • QBD concept,
  • Scale-up, Technology Transfer

Desired Candidate Profile:

  • Education: M. Pharm
  • Experience: 01 to 06 Years

Analytical Development and Research Associate

Roles and Responsibilities:

  • Knowledge of AMV / AMT / MMD / Analysis & Calibration
  • Required knowledge of HPLC / GC / UV / Auto titrator / Disso.
  • Knowledge of GLP activity like SPC / STP / Calibration / Reference Std / Working Std. / Training

Desired Candidate Profile:

  • Qualification: M.Sc. / M.Pharm
  • Job Location: Daman

Interested candidates, please share your Updated CV, Notice period, and Expected CTC on career@vsinternational.co.in or WhatsApp at 9712914477.

Walk-In Date: 9th April, 2023
Time: 9.30 AM – 5.30 PM
Venue: V S International Pvt. Ltd, Plot No 11, 17&18 Golden Industrial Estate, Dabhel Road, DAMAN DIU, Daman & Diu, India
Job Category: pharma
Job Type: Full Time
Job Location: Daman.

Apply for this position

Allowed Type(s): .rtf

About Abha Maurya

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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