Friday 25 November 2016

JODAS EXPOIM WALK IN ON 29/11/16 @ HYDERABAD


REFERENCE
Srinivasulu Tirumalasetty
Global pharma News

WALK IN INTERVIEW DRIVE at Jodas Expoim Hyderabad 

Date:- 29th November ,2016

Timings:10 AM to 4 PM

Venue: - Plot No:45, Biotech Park, Phase 3,  Karkapatla (vil), Siddipet (Dist).

1) Filling Operators(Injectable) : 3-8 years of experience require, preferable working on Auto line of Tofflon, NKP , Bosch.
2) Autoclave Operators :3-8 years of experience require,
Preferable Operate to terminal sterilizer and equipment sterilizer.
3) Manufacturing Operators (Liquid Injectables): 3-8 Years of experience require preferable should know the Autoline operation of manufacturing, CIP & SIP.

Contact number: 9100953911

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QC VACANCY IN BRUCKE PHARMA PVT.LTD @ DAMAN


REFERENCE
Srinivasulu Tirumalasetty
Global pharma News

Hiring: Looking for people ready to relocate to Daman (India). 

Required experience: 2-6 years in Quality Control Formulations. 

Person should have good experience in Instrumentation, Method validations, CGMP and Documentation. 

About Company: Brucke pharma pvt. ltd is manufacturer and exporter of Sterile oncology products of Injections, Tablets and Capsules to US and Europe markets. 

If interested please send resumes to vamsi@brucke.co.in.

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Thursday 24 November 2016

APOTEX WALK IN DRIVE "R&D Stability" ON 25/11/2016 @ Bangalore

    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.

    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.

    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.

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-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Doctorate Not Required
Company Profile:
Apotex Research Pvt. Ltd.


Apotex Inc., founded in 1974, is the largest Canadian-owned pharmaceutical company. We employ over 6,000 people worldwide in research, development, manufacturing and distribution. We produce more than 300 generic pharmaceuticals in approximately 4000 dosages and formats and export to over 115 countries around the globe.

APOTEX RESEARCH PRIVATE LIMITED (ARPL) based at Bangalore is a 100% owned subsidiary of Apotex Inc., and is engaged in the development, bio-clinical evaluation, manufacturing and distribution of safe and efficacious generic pharmaceutical formulations for the global market.

As a part of this dynamic team, you will get to work in our state-of-the-art facilities, which include sophisticated equipments', high standard processes and the opportunity to work alongside some of the world's top professionals.

Apotex encourages the new technological developments in the field of research, manufaturing and distribution and embraces all the new techniques and technologies available in our area of concentration, our new manufaturing facility has been inaugurated in June 2012 and uses some of the most sophisticated technologies and machines available today.

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