Open Drive for Analytical Research & Development 18,19 and 20 Oct, 16 at Apotex, Bangalore Corporate Office.
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 given position:
Analytical Research & Development / Analytical Operations (Research Scientist/Sr. Research Scientist): M. Pharm/M.Sc. with 2-7 years of experience, with exposure to product development activities for regulated markets, exposure to solids orals / semi solids will be added advantage. Exposure to USFDA, MHRA, Health Canada, TGA Markets.
Interview Venue: Apotex Research Private Limited, Plot No. 1&S, Bommasandra Industrial Area, 4th Phase, Jigani Link Road, Bangalore-560099
Time: 9.00 AM to 4.00 PM
Job Location: Bangalore
Note: Experience in a Pharmaceutical manufacturing unit with exposure to Solid oral dosage forms (tablets and capsules) is a must.
Candidates from Quality Control Department can apply to the above open position.
Required Documents: Candidates are requested to carry 2 copies of resume, passport photo, pay slips, Education certificates, salary annexure and previous experience certificates.
Desired Candidate Profile
Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Ph.D - Advertising/Mass Communication
Desired Candidate Profile
Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Ph.D - Advertising/Mass Communication
Job Summary:- Performing and reporting of analytical method validations, analytical method transfers, archival of analytical method validation documents. Review of validation documents and preparation of validation protocol and reports wherever applicable.
Job Responsibilities:-
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.
Job 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.
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.
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.
FOR MORE DETAILS
CONTACT : SRINIVAS (RECRUITMENT MANAGER)
LOCAL PHARMA JOBS,
8499928928,
EMAIL : localpharmajobs@gmail.com
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