Job Title: Research Scientist
Experience: 2 – 7 Years
Qualifications:
Exp:2-8yrs
Qualification-M.Pharm/Msc
Performing various analytical method development activities and provide analytical data support to regulatory deficiencies.
Job Responsibilities:
1. Responsible for all activities in Analytical Research and Development, including cGLP, documentation and implementation of departmental quality systems
2. To assist the Sr Research scientist / Team Leader / Group Leader in the day-to-day functioning of the Analytical Research and Development Laboratory.
3. To perform routine development analysis and method development activities.
4. Responsible for performing analytical activities as a part of response to Regulatory queries.
5. Responsible for performing analytical activities for Investigation, Justification, Compendial evaluation, Method development, Method validations.
6. Communicating the requirements for the Leaders and within the team members for affective cGLP procedures and departmental quality systems to achieve all outcomes.
7. Performing all the activities in support of Apotex Corporate Values of Pride, Accountability, Integrity and Diligence; Demonstrates strong and visible support of our values.
8. Performing the activities with established regulatory compliance and safety requirements.
9. All other duties as assigned.
Job Requirements:
1. Post graduate degree in Chemistry / Pharmacy from a recognized Institution.
2. Desired candidate should have a minimum of 2 years of experience as a Laboratory Analyst.
3. Should be proficient in MS office tools.
4. Should have competent verbal & written communication skills.
5. Experience of working on online modules / software would be an added advantage.
6. Hands on experience in stability Sample testing (Solid Oral Dosage form) and completion within stipulated timeline by following GLP.
7. Hands on experience in multimedia dissolution study analysis of test products and innovator products.
8. Hands on experience in calibration and qualification of instruments.
9. Knowledge on preparation of various documents like SOPs, Formats, Protocols, Reports, analytical data etc.
10. Should possess troubleshooting knowledge on Instruments and analysis.
11. Knowledge on Technology Transfers /Method validation.
12. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities.
Walk-In Details
- Date of Interview – 10th February
- Time of Interview – 9 AM onwards
- Venue of Interview -Apotex Research Private Limited, Gate 1 ,Plot No. 1&2,Bommasandra Industrial Area, 4th Phase, Jigani Link Road, Bangalore-560099