Schedule Drive "R&D Stability" - 23rd/24th & 25th November, Bangalore
Apotex Research Private Limited (ARPL) based at Bangalore is engaged in in the development, bio-clinical evaluation, manufacturing, and distribution of safe and efficacious generic pharmaceutical formulations for the global market.
Inviting applications for the following positions:
Research Scientist/Sr. Research Scientist - R&D Stability
Interview Venue :- Apotex Research Pvt Ltd, Gate No. 1 BEC, Plot No. 1 & 2, Bommasandra Industrial Area, 4th Phase, Jigani Link Road.
Time:- 9.00 AM to 12.00 PM
Job Location: Bangalore
Note: Experience in a Pharmaceutical manufacturing unit with exposure to Solid oral dosage forms (tablets and capsules) is a must.
Job Location: Bangalore
Note: Experience in a Pharmaceutical manufacturing unit with exposure to Solid oral dosage forms (tablets and capsules) is a must.
People with Quality Control experience can also apply.
Job Summary :-
Performing and reporting of development, formulation development support, development stability and exhibit stability sample analysis and archival of analytical documents.
Performing and reporting of development, formulation development support, development stability and exhibit stability sample analysis and archival of analytical documents.
Job Description :-
1. Responsible for initiation, execution and completing of exhibit stability sample analysis.
2. Responsible for all activities in analytical research and development including cGLP, documentation, and implementation of departmental quality systems.
3. To assist the Sr. Research scientist/Team Leader/Group Leader in the day to day functioning of the analytical research and development laboratory.
4. Maintenance and management of stability samples and inventory.
5. Works as a member of a team to achieve all outcomes.
6. Communicating the requirements for the leaders and within the team members for effective CGLP procedures and departmental quality systems to achieve all outcomes.
7. Performing the activities with established regulatory compliance and safety requirements.
2. Responsible for all activities in analytical research and development including cGLP, documentation, and implementation of departmental quality systems.
3. To assist the Sr. Research scientist/Team Leader/Group Leader in the day to day functioning of the analytical research and development laboratory.
4. Maintenance and management of stability samples and inventory.
5. Works as a member of a team to achieve all outcomes.
6. Communicating the requirements for the leaders and within the team members for effective CGLP procedures and departmental quality systems to achieve all outcomes.
7. Performing the activities with established regulatory compliance and safety requirements.
Desired Candidate Profile
- Job requirements
1. A post graduate degree in pharmacy/chemistry from a recognized college.
2. Desired candidate should have a minimum of 2years of experience as a laboratory Analyst.
3. Should have competent verbal and written communication skills.
4. Experience of working on online modules/software would be an added advantage.
5. Hands on experience in stability samples testing (Solid oral dosage form) and completion within stipulated timeline by following GLP.
6. Hands on experience in multimedia dissolution study analysis of test products and innovator products.
7. Hands on experience in calibration and qualification of instruments.
8. Knowledge on preparation of various documents like SOPs, formats, protocols, reports, analytical data etc.
9. Knowledge on technology transfers/method validation.
10. Should have well versed knowledge on regulatory guidelines and thorough knowledge on CGMP activities.
Education-
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