Umedica Laboratories- Walk-In Drive for QC-Micro/ Technology Transfer On 8th & 9th Aug’ 2022





Umedica Laboratories- Walk-In Drive for QC-Micro/ Technology Transfer On 8th & 9th Aug’ 2022

Job Description

Umedica  Laboratories is a manufacturer and exporter of Pharmaceutical Formulations invites dedicated passionate & Competent young professionals to be part of our USFDA, EU GMP & TGA Australia approved formulation manufacturing plat UMEDICA LABORATORIES at Vapi, Gujarat for following requirements.

Department: Quality Control (microbiologist)
Position: Officer to Sr. Officer
Education:  M.Sc (Micro)
Experience: 2 to 6 years

  • Skill Set: 
  • Media Preparation and growth promotion test.
  • Environment Monitoring of manufacturing area.
  • Biological assay, Microbial limit test, BET.
  • Culture maintenance
  • Water and bio burden testing
  • Microbial limit test validation
  • Calibration of laboratory equipment

Department: Technology Transfer
Position: Officer to Executive
Education:  M. Pharm/ B.Pharm
Experience: 2 to 6 years

  • Skill Set:
  • To co-ordinate between R & D / client (product transferring unit) and all applicable stake holder departments in the plant (receiving unit) so as to ensure the smooth and effective transfer of product.
  • To evaluate / review the necessary documentation provided from transferring party (from R & D, Client etc.) with respect to product and process criteria in terms of facility, available equipment’s etc.
  • To review of product development summary report from transferring site in order to gain /understand the products as well as product as well process knowledge and to ensure the smooth transfer of any new product to receiving site by organizing a proper and systematic meeting / discussion with involvement of all relevant stake holder from both transferring and receiving site.
  • Responsible to ensure the clarity, accurate information, adequate communication / feedback in order to improve the understanding and to maintain the transparency of new product which is to be transferred.
  • Responsible to prepare of batch documents like MFC, MPR, BMR, BPR, protocol, report and other technical documents (if any) with respect to R & D scale / pilot batch(s), scale-up batch(s), pre-exhibit / confirmatory batch(s), exhibit / submission batches.
  • To monitor and provide assistance during execution of submission / exhibit batch (s) and initial Commercial Validation batch (s) of any new product as R&D representative based on the minimum criticality / lower risk criteria towards the process / product.
  • To provide necessary assistance regarding challenges faced during execution scale-up, pre-exhibit / confirmatory, submission / exhibit batch(s) and also initial commercial validation batch (s) i.e., PPQ batch(s) in terms of deviation / incident investigations and to frame necessary Corrective Action and Preventive Action (CAPA) towards way forward activities. To participate in meetings, telecom etc. between inter/intra-departments and also with clients (if applicable) related to new product transfer, status update and filing / submission aspects.
  • Responsible to take care Sample registration work for different Regulatory/ Non-Regulatory market.
  • To ensure that the appropriate process validations of a product and calibration/qualification of equipment are performed and recorded and the reports made available.

Date : 8th & 9th Aug’ 2022
Time: 09:00 AM to 02:00 PM
Venue: Umedica Laboratories Pvt. Ltd , Plot No. 221, 2nd Phase, (Nr. Morarji Circle), Vapi, Gujarat-396195

  • CTC: As per Industrial Standard
  • Only Experience Candidates (Preferably from Formulation Pharma)
  • Interested Candidates are requested to bring Updated Resume , Passport Size Photograph, Degree Certificate (Original & Photo Copy), Salary Slip, Last CTC Proof (Original & Photo Copy).
  • Those who are not able to attend interview on schedule date , can send their updated resume on [email protected]
  • Candidates not permitted without face-mask.

Umedica Laboratories- Walk-In Drive for QC-Micro/ Technology Transfer On 8th & 9th Aug’ 2022






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Data feed by Quality Assurance desk and reviewed by pharmapathway team.


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