Established in 2010 Stabicon specializes in managing product quality processes, upgrading and introducing advanced technology into products, laying the foundation for a prosperous future in the prevention and cure segment.

Stabicon is Offering Opportunities for Freshers & Experienced in various fields, The interview Process shall be through Skype or Telephone/Video Calls. Details are Given Below:


SKYPE/VIDEO CALL INTERVIEW FROM 28TH MAY TO 06TH JUNE 12:00 AM TO 04:00 PM

Join Us for Regular Vacancy Updates on – 

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Department: Quality Control

1. Trainee: M.Pharma/M.Sc – Passout 2018,2019,2020

No of Vacancies:3

2. Officer/Sr Officer – QC

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 02

Qualification: M.Sc/M.Pharma

Experience: 1-3 Years

3. Executive/Sr Executive – QC

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 03

Qualification: M.Sc/M.Pharma

Experience: 3-5 Years

4. Team Leader – QC

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 01

Qualification: M.Sc/M.Pharma

Experience: 5-8 Years


Department: A R&D

1. Trainee – Fresher (Passed out-2018, 2019, 2020)

Qualification: M.Sc/M.Pharma

Vacancies: 02

2. Officer/Sr Officer – A R&D

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 02

Qualification: M.Sc/M.Pharma

Experience: 1-3 Years

3. Executive/Sr Executive – A R&D

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 04

Qualification: M.Sc/M.Pharma

Experience: 3-5 Years

4. Team Leader – A R&D

  • Handling of Instruments – HPLC/UPLC/UV & GC, Analysis, Preparation, and Review of Project Docs.
  • Review of Validation Reports/Protocols.
  • Handling QMS Documents
  • Managing team, Planning & Monitoring.
  • Maintaining Lab in accordance with GLP.

Vacancies: 01

Qualification: M.Sc/M.Pharma

Experience: 5-8 Years


Department: Quality Assurance

1. Trainee – Fresher (Passed out-2018, 2019, 2020)

Qualification: M.Sc/M.Pharma

Vacancies: 02

2. Officer/Sr Officer – A R&D

  • Project Documents Review
  • Releasing COA, QMS Activity Monitoring.
  • Management of Team, Planning & Monitoring executions
  • Maintaining Lab in accordance with GLP.

Vacancies: 02

Qualification: M.Sc/M.Pharma

Experience: 1-3 Years

3. Executive/Sr Executive – A R&D

  • Project Documents Review
  • Releasing COA, QMS Activity Monitoring.
  • Management of Team, Planning & Monitoring executions
  • Maintaining Lab in accordance with GLP.

Vacancies: 02

Qualification: M.Sc/M.Pharma

Experience: 3-5 Years

4. Team Leader – A R&D

  • Project Documents Review
  • Releasing COA, QMS Activity Monitoring.
  • Management of Team, Planning & Monitoring executions
  • Maintaining Lab in accordance with GLP.
  • Managing team, Planning & Monitoring.

Vacancies: 01

Qualification: M.Sc/M.Pharma

Experience: 5-8 Years


Department: Formulation R&D

1. Trainee Scientist – F R&D Fresher (Passed out-2018, 2019, 2020)

Qualification: M.Pharma

Vacancies: 01

2. Jr Scientist – F R&D

  • The literature search for new projects.
  • Preparation of manufacturing trial, Sample Submission for Testing & Compilation of analytical results, stability Protocol Preparation and charging, prototype development, product development report & TT documents.
  • Co-ordinate with the CSC & AD department for analysis of trial& stability products.

Qualification: M.Pharma

Experience: 1-2 Years

3. Research Associate – F R&D

  • The literature search for new projects.
  • Preparation of manufacturing trial, Sample Submission for Testing & Compilation of analytical results, stability Protocol Preparation and charging, prototype development, product development report & TT documents.
  • Co-ordinate with the CSC & AD department for analysis of trial& stability products.

Qualification: M.Pharma

Experience: 2-3 Years

4. Executive – Sr Research Associate

  • The literature search for new projects.
  • Preparation of manufacturing trial, Sample Submission for Testing & Compilation of analytical results, stability Protocol Preparation and charging, prototype development, product development report & TT documents.
  • Co-ordinate with the CSC & AD department for analysis of trial& stability products.

Qualification: M.Pharma

Experience: 3-5 Years


Department: Information Technology

Post: Trainee – Freshers Pssout of 2018, 2019, 2020

  • Handling of day to day issues related to system hardware & networking.

Qualification: B.E/Diploma in IT/CS


Department: Engineering

Post: Technician

  • Handling of equipment and facility maintenance.

Qualification: Diploma/ITI – EEE

Experience: 2-3 Yrs


Department: Training

Position: Trainer

  • Handling of Training department – Training planning, execution, coordination and completion.

Qualification: M.Pharma/M.Sc

Experience: 5-8 Years in Academics or Industrial in QA/QC


Click for details of More Walk-Ins

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Contact Details: 

HR:  Mr. Jagadeesh Gowda

+91-7022281070

+91 80 27839259/27839260

hrd@stabicon.com

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