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Job opportunities in Pharma field in US/India


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Posted
3 minutes ago, Amulya2020 said:

Cool, thank you. 

Check your PM

Posted

MS Medical device RA cheyyi...It is an emerging market...RA is a cool and composed job.....

  • Thanks 1
Posted
10 minutes ago, godfather03 said:

Check your PM

Tq so much, I appreciate your help!😊

Posted
13 minutes ago, AndhraPickles said:

MS Medical device RA cheyyi...It is an emerging market...RA is a cool and composed job.....

Ok, thank you. 

Posted
3 hours ago, Amulya2020 said:

Thank you, FDA regulations are usually covered in regulatory affairs(RA). So RA cheyadam better antunara?

And Medical devices manufacturing or validation?

nope ... rest of the world regulations and US FDA regulations rendu untaye. it should US FDA regulatory and dosieres not ROW

  • Like 1
Posted
3 hours ago, Amulya2020 said:

Thank you, FDA regulations are usually covered in regulatory affairs(RA). So RA cheyadam better antunara?

And Medical devices manufacturing or validation?

Pharma ki Medical devices ki em relation ??
biotech degree bio medical engg stream emanna chustunnava ??

Posted

You plan on going into IT side or Manufacturing side?

Manufacturing side aithey Regulatory affairs/Quality usually fall under same department. You need to have knowledge of regulations/guidelines (FDA,ICH,EUDRA,MHRA etc). Again, it depends if you are in API or final drug products or medical devices. Validation antey employers prefer someone with engineering background or atleast chemistry. medical device and pharma have different regulations just so you know. 

Pharmacovigilance and regulatory affairs go hand in hand but you need some phramacist knowledge there.

IT side validation ayithey all you need for the most part is 21cfrpart11 knowledgesSa_j@il

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Posted
49 minutes ago, keviinusa said:

Pharma ki Medical devices ki em relation ??
biotech degree bio medical engg stream emanna chustunnava ??

Pharma and medical devices are completely different things kani, nenu reply ichina comment context lo medical devices gurinchi unte dani refer chesthu malli mention chesa

and 21 CFR 820- cGMP and validation of medical devices related kabatti Vati gurinchi specific ga adiga

Posted
56 minutes ago, Panasa_pandu said:

You plan on going into IT side or Manufacturing side?

Manufacturing side aithey Regulatory affairs/Quality usually fall under same department. You need to have knowledge of regulations/guidelines (FDA,ICH,EUDRA,MHRA etc). Again, it depends if you are in API or final drug products or medical devices. Validation antey employers prefer someone with engineering background or atleast chemistry. medical device and pharma have different regulations just so you know. 

Pharmacovigilance and regulatory affairs go hand in hand but you need some phramacist knowledge there.

IT side validation ayithey all you need for the most part is 21cfrpart11 knowledgesSa_j@il

One with good opportunities (US/India) and obviously better pay. Yes, mostly IT. 
 

Thanks for the detailed explanation.👍


 

Posted
2 minutes ago, Amulya2020 said:

One with good opportunities (US/India) and obviously better pay. Yes, mostly IT. 
 

Thanks for the detailed explanation.👍


 

intaki meeru endulo degree chesav

 

Posted
4 minutes ago, Amulya2020 said:

One with good opportunities (US/India) and obviously better pay. Yes, mostly IT. 
 

Thanks for the detailed explanation.👍


 

IT ayithey you dont need a specific degree in regulatory field....As long as you have a bachelors in any field you should be fine!

sSa_j@il

  • Like 1
Posted
1 minute ago, Panasa_pandu said:

IT ayithey you dont need a specific degree in regulatory field....As long as you have a bachelors in any field you should be fine!

sSa_j@il

ameerpet ki poyi oka 4 certifications cheste saal antava

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