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
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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
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Contact Details:
HR: Mr. Jagadeesh Gowda
+91-7022281070
+91 80 27839259/27839260
