Pharmacists Required "A"

Application in plain paper is hereby invited for filling up the following posts on contractual basis at a fixed pay as shown against each for District Health & Family Welfare Society, South Tripura. It will be purely contract basis for a period of 11 (Eleven) months likely to be extended based on performance of employees till the project period only.

Post : Pharmacist (Alio.)

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Career opportunity for Safety Associate II at inVentiv Health "A"

Job Description:


- Process adverse event reports received from sites/reporters.
- Perform QC review of completed individual and periodic safety reports.
- Complete data entry including writing of adverse event narrative and provide preliminary assessment of event seriousness and expectedness/listedness as per applicable Reference Safety Information.
- Generate adverse event queries, liaise with the medical reviewers/client to agree upon the queries, and send request for additional information to the sites/reporter.
- Engage with the Site Monitors to ensure follow up information is obtained from site effectively.
- Foster constructive and professional working relationships with all project team members, internal and external.
- File documents according to project specific requirements (electronically or in hard copy as applicable).
- Ensure case files are compliant with SOPs.

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Novartis hiring for Sr. Auditor "A"

Job Description
• Conducts GMP and Quality system audits primarily at Third party contractors or suppliers as lead or supportive auditor to monitor that all aspects of the operational business comply with GMP legal and regulatory requirements and the Novartis Group Quality Manual and Policies
• Monitors that Corrective and Preventive Actions which are necessary due the audit findings are implemented appropriately and as per schedule
• Evaluates and trend audit and inspection findings
• Maintains audit data in a related data system (incl. reports and follow-up of audits)
• Supports of training sessions, audit planning and risk assessments (e.g. for supplier qualification)
• Participate sin Due Diligence as deemed necessary
• Participates in Global/ Regional Audit Team continuous improvement initiatives.
• Conducts audits in accordance with company standard operating procedures and quality policies
• Interprets policies, standards, and regulations, and evaluates potentially critical problems not covered by policies, standards, and regulations
• Exercises judgment in ensuring that written procedures are followed and in evaluating quality systems, processes, procedures, and protocols for compliance
• Appropriately escalates any compliance issues
• Communicates audit results to management and auditees through written audit reports
• May manage post-audit activities and follow-up on any necessary corrective and preventive actions; resolves any conflicts



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Biocon hiring Executive Regulatory Affairs "A"

Job Description

*Regulatory filings and compliance of regulatory documents:.
*Authoring of CE marking Technical File, 510(k), CTD sections, registration dossiers, with device information as appropriate, Design History Files, deficiency response and post approval changes etc.
*Communicate/Interact with cross functional teams and ensure timely submission of dossier.
*Technical documents review:
*Review of Quality control, Quality Assurance, Production, RND documents like specifications, analytical procedures, reference to vendor documentation and batch packaging records.
*Review of all technical documents (documents related to development, manufacturing, verification, validation and control of device design including human factors design evaluation and risk management).
*Ensuring Good Documentation practice with in the team.
*Review of deviations, change controls and SOPs
*Review of deviations, change controls, SOPs and other documents.
*Active participation in Audit

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Improve your interview performance: Tips "A"

Practice good nonverbal communication

Dress for the job or company

Listen

Don't talk too much

Don't be too familiar

Use appropriate language

Don't be cocky

Take care to answer the questions

Ask questions

Don't appear desperate

source:http://www.monster.com/career-advice/article/boost-your-interview-iq 

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Walkins for CLINICAL DATA MANAGEMENT @ COGNIZANT "A"

Job Description

Hi!!


We have a Walk in drive for Clinical Data Management for Mumbai location.


Qualification: Graduate/Post Graduate in Science/Life Sciences/B.Pharm/M.Pharm


Experience : 2 to 4 years in Clinical Data Management.


Location: Powai - Mumbai


Walk in Drive: Saturday 8th Oct 2016



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Work in Regulatory Affairs Domain "A"

Reckitt Benckiser, RB is the world’s leading consumer health and hygiene company. Every day, across 60 countries, we work with the best people to challenge conventional thinking and strive to find even better ways to give people innovative solutions for healthier lives and happier homes. That’s how we generate the game-changing ideas that built 19 iconic Powerbrands around the world – well-loved names such as Nurofen, Strepsils, Mucinex, Dettol, Lysol Finish and Vanish.
Job Title : Asst Manager – Regulatory Affairs (GUR0001R)



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Govt Job:Drug Inspector "A"

The KPSC is a body created by the Constitution of India. The Commission advise the Government on all matters relating to civil services referred to it under Article 320 (3) of the Constitution and publish notifications inviting applications for selection to various posts as per the requisitions of the appointing authorities, conduct written test and/or practical tests, physical efficiency test and interview, prepare ranked list based on the performance of the candidates and advise candidates for appointment strictly based on their merit and observing the rules of reservation as and when vacancies are reported.

Applications are invited Online only from qualified candidates for appointment in  the undermentioned post in Kerala Government Service. Before applying for the post the candidates should register as per the One Time Registration through the official website of KPSC.

Post: Drugs Inspector

Last date for submission of application:- 05.10.2016 Wednesday up to 12 midnight.

Name of Website to which applications are to be submitted : www.keralapsc.gov.in

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Career for Research Scientist "A"

Job Description
The principal responsibility of the Research Scientist is the analysis by multiple procedures of intermediates and target compounds.  The Research Scientist is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry.  A major component in the scientist's performance rating will be based on productivity. In general, technical, organizational and compliance support for 170+ ongoing stability studies.





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Recruitment at DRDO "A"

DRDO, India’s premier R&D organization employs bright, qualified and competent scientists in Group ‘A’ (Gazetted) technical service known as Defence Research & Development Service (DRDS). DRDO offers exciting and challenging career opportunities in very broad spectrum of R&D at its more than 50 laboratories/establishments throughout the country. For further information about DRDO please visit DRDO website.

Recruitment & Assessment Centre (RAC) Invites online Recruitment Applications through RAC website rac.gov.in  for the post of Scientist 'B' in DRDO.

Post: Scientist 'B' (Chemistry & Pharmacy)

How to Apply:
Online registration on RAC website rac.gov.in/) is mandatory.
i) Candidates are required to submit their applications online alongwith legible and lighter file containing scanned copies of certificates for essential and higher educational qualification, if any, alongwith percentage of marks (duly supported by the mark-sheets), date of birth certificate, experience claimed if any in the column pertaining to employment history of online application, a recent passport size colour photograph (size not exceeding 30 KB; resolution of 110 x 140 pixels) and the details of required application fees through RAC website. The maximum file size of each attachment should not exceed 500 KB and it must be legible when a printout is taken.
ii) All candidates, whether in Govt. service or in Govt. owned organisations, should also submit their applications online directly to the Recruitment and Assessment Centre (RAC) and such candidates are required to upload a signed declaration (as per the proforma available at RAC website) that they have informed their Cadre Controlling Authority (CCA) in writing, that they have applied for the post in DRDO. However, such candidates, if in regular service whether in permanent or temporary capacity, are required to produce a “No Objection Certificate”(NOC) from their CCA as per the proforma available at RAC  website at the time of interview, in addition to the aforesaid declaration. If CCA considers withholding the NOC, the candidate should inform RAC within 30 days of the closing date.
iii) Candidates are advised to retain a copy of the online recruitment application (pdf) alongwith acknowledge slip generated after locking of online application form.
iv) Application completed in all respect will only be considered as locked application and only such applications shall be considered for further processing.

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