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DAILY QUIZ -38

DAILY QUIZ -38




Daily GPAT QUIZ 38 is another update to our series of MCQ GPAT QUIZ. The aim is to make life easier for aspirants looking for GPAT exam 2017 paper practice. Our each quiz consist of 1o MCQs based on complete B.Pharm syllabus. At times there could be one subject or topic dominant in a quiz but we make sure the other subjects/topics get their due in upcoming quizzes. The answers to these questions is given at the end.

Q1. Anomocytic stomata are present in

a) Senna

b) clove
c) Spearmint

d) Coca

 

Q2. Insulin is synthesized by

a) α-cells of pancreas   

b) β-cells of pancreas

c) Acinar cells of pancreas              

d) δ-cells of pancreas

Q3. Maximum bioavailability of drug is produced by

a) Subcutaneous route                 

b) Intramuscular route

c) Oral route        

d) Intravenous route

 




 

Q4. Ocimum sanctum plant belongs to the family
a) Labiatae
b) Leguminosae
c) Polygalaceace
d) Rubiaceae

Q5. Carboxyheamoglobin is formed by binding of heamoglobin with
a)
CO
b) CO2
c) CHO
d) COOH

Q6.  Complete drug elimination takes about
a)
1-2 half lives
b) 2-3 half lives
c) 3-4 half lives
d) 4-5 half lives

Q7. All acids are disinfectant except, one
a) Salicylic acid
b) Benzoic acid
c) Boric acid
d) Sulphuric acid

 




 

Q8.One of the phospholipids possesses antigenic properties

a) Lecithin

b) Cephaline

c) Cardiolipin

d) Plasminogens

Q9. The drug which cannot be given orally

a) Phenobarbitone       

b) Theophylline

c) Isoprenaline

d) Pindolol

Q10. Hydrogen peroxide is not used for

a) Cleansing the wound               

b) Deodorant         

c) Removing ear wax                  

d) Anaesthesia


1-;B  2-B;    3-D;    4-A;   5-A;   6-D;    7-D;   8-C;   9-C;    10-D


Bookmark this page as more GPAT MCQ quizzes are on the way.

 

Posted by anurag in PHARMA MCQ, 0 comments
Stabicon Life Sciences Pvt. Ltd – Walk-in Interviews for QC / AR&D on 10th -12th November, 2016 @ Bangalore

Stabicon Life Sciences Pvt. Ltd – Walk-in Interviews for QC / AR&D on 10th -12th November, 2016 @ Bangalore

Company: Stabicon Life Sciences Pvt. Ltd

Department: QC / AR&D

Job Title: Executive

Experience: 2 – 5 years

Location: Bengaluru

Walk In date: 10 November-12th November
Job Description:

-Having knowledge in current GLP requirements. -Having adequate knowledge in handling of analytical instruments like HPLC, UPLC, GC and Dissolution testers.

-Having technical exposure on testing of various dosage forms for Assay, Related substances/compounds, Dissolution, Content Uniformity & etc as per Good Documentation practices

-Experience in method validations, method verification and method transfer for analytical methods of drug products for Assay, Related substances/compounds, Dissolution, Content Uniformity and residual solvents by using HPLC, GC and UV-Visible Spectrophotometer as per current ICH guidelines and Pharmacopoeia.

-Experience in calibration / Qualification of analytical instruments like HPLC, UPLC, GC, Dissolution tester, UV-Visible Spectrophotometer, etc.

-Having adequate knowledge in Preparation and review of analytical method validation/ method verification protocols, Method transfer/Routine/Stability documents for drug products for Assay, Related compounds, Dissolution, Content Uniformity & residual solvents.

-Having adequate knowledge in review of analytical raw data & trends of stability samples.
-Ability to work in a multi-task environment. -Ability to produce high quality outputs.

Venue Details:

Stabicon Life Sdences Pvt. Ltd.

Plot No. 28,

Bommasandra Industrial Area,

4th Phase, Jigani hobli, Anekal Taluk,

Bangalore 560 100
Interested candidate can send confirmation either by mail to hrd@stabicon.com or call at 91 80 27839259/9260 between 9.00 AM to 5.00 PM.

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Walk in Interview for freshers in Pharmacovigilance at Synowledge (Bioclinica)

Walk in Interview for freshers in Pharmacovigilance at Synowledge (Bioclinica)

No of Posts : 40

Job Description :

We have an walk ins for freshers for Pharmacovigilance role

Candidate Profile :
M Pharmacy, Pharm D, BDS, BSc (Nursing).

Walk in Interview Details
Date : 9th & 10th of November
Venue:  #120/A, Elephant Rock Road, Jayanagar 3rd Block, Bangalore – 560011.
Timings : 09:00 AM
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Geltec Pvt. Ltd – Walk-In Interview on 05/11/2016 @ Bangalore

Geltec Pvt. Ltd – Walk-In Interview on 05/11/2016 @ Bangalore

Recruitment for below positions:

1. Executive- Quality Control-( QC )

Qualification & Experience:

M.Sc/M.Pharm with 1-5 years experience with Knowledge of handling Lab instruments (Like GC, HPLC, UV, AAS & KF), Stability Analysis and Finished goods Analysis preferably in Pharmaceutical Industry.

 

2. Executive -Analytical R&D

Qualification & Experience:

M.Sc/M.F harm with 2-5 years experience preferably worked in regulated markets like in US, EU able to handle all instruments like HPLC, GC, and AAS…etc, conduct stability studies.

 

3. Executive -Packing:

Qualification & Experience:

Any graduate with 2 years experience in Pharmaceutical Industry.

 

Walk-In Date: 05/11/2016 Time: 9am to 3pm

Venue:

Geltec Pvt. Ltd,

Yadavanahalli Bus stop,

Attibele, Bangalore-Hosur Road,

Bangalore- 562 107

Land mark: Near LA-CLASSIC HOTEL
Those who are unable to attend the interview contact at srinivas.hr@geltec.in

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Opening for M.Pharm as Trainee Scientific Writing in Indegene

Opening for M.Pharm as Trainee Scientific Writing in Indegene

Job Description:
The roles and responsibilities of the Trainee Scientific Writing include the following:
· Following the specifications for documentation, both client or company provided
· Maintaining records for all assigned projects, including archiving
· Ensuring getting feedback from customers and supporting implementation of customer management tactics
· Controlling/reducing the cost of content development, cycle time, and error rates in projects
· Adhering to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards, requirements, and policies

Job Summary:
A Trainee Scientific Writing needs to write, edit, reconcile, and manage high-quality medical and scientific communications, including abstracts, literature slide sets, and manuscripts, using data from various sources such as clinical study reports, patient profiles, and protocols. He or she also needs to develop abstracts for submission to regulatory authorities and/or clinical teams.

Candidate Profile
· Education—M.Pharm
· Experience—0-1 year of experience as a technical writer
· Flair for medical services/medico-marketing/healthcare/creative/ technology domain
· Excellent communication and articulation skills
· Excellent command of English
· Excellent writing and communication skills
· Ability to learn technical information quickly
· Should be proactive in seeking information

Additional Information:
Experience: 0-1 years
Education: M.Pharm
Location: bangalore
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Medical Writing
End date: 25th December, 2016

To apply online, Click here.

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Walk-In Interview for Experienced B.Pharm/M.Pharm/M.Sc Candidates in AR&D FR&D at Medreich

Walk-In Interview for Experienced B.Pharm/M.Pharm/M.Sc Candidates in AR&D FR&D at Medreich

Officer / Executive – Formulation Development:
Development of Solids (Tablets: IR, DR & ER dosage forms & Capsules: Powder and Pellets filled).
– Should independently carry out the Formulation R&D and scale up activities.
– Experience in handling equipments like RMG, Fluid bed driers & Granulators, size reduction mills, Blenders, compression, coating & capsule filling machines.
–    Preparation and review of Stability, Scale up, Process validation protocols and reports, Specifications (Raw material, Packaging material & product) etc. (EU, US & Emerging Markets) and requirements, Good Documentation Practices.
Qualification: M Pharma (Pharmaceutics) / PhD.

Officer / Executive – Analytical Development:
-Candidate should have experience in Method development, Method validation of different pharmaceutical dosage forms.
–  Hands on experience/ knowledge in handling Analytical work related to DS and DPs in different phases with a proven track record (having worked with Global partners/ International exposure).
– Hands on experience in Chromatography (HPLC, UPLC, HSGC), Spectroscopy (FTIR, UV), dissolution apparatus and Particle size measurements. Well versed with 21CFR Part 11 and other global laboratory compliances requirements.
Qualification: M Pharm (Analysis), M.Sc Chemistry.

Walk in Interview
Date: 05-11-2016
Time: 9 A.M to 1.00 P.M.
Venue: Medreich Limited (R&D-Genovo) Plot No. 36, Bommasandra Industrial Area, Anekal Taluk, Bommasandra, Bangalore-560099 Land Mark – Karnataka Bank, Jigani Road

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Opening for Executive-sr. Executive Regulatory Affairs Medical Devices @ Biocon

Opening for Executive-sr. Executive Regulatory Affairs Medical Devices @ Biocon

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
*Provide support for internal and external audit for ISO 13485, 21 CFR 820, CE certification and GMP audit team for device development, design control and manufacturing facility for global markets.
*Good knowledge of registration of combination products (drug & device), CE marking, MDD 93/42/EEC, 21 CFR Part 820, 510(k) submission, IMDRF/GHTF guidelines etc

Location: Banglore

Experience: 1 to 6 years
Openings: 1
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