NOC for Pharmaceutical Quality Assurance

[jazzu]

Hi everyone,
I have done M.Pharmacy and have joined as quality associate in a pharmaceutical company, section R&D Quality.
Total work experience is about three years.
Please help me to identify my NOC !!
Many days have passed..but I couldn't find relevant NOC for FSW purpose.
Hoping for a prompt reply...

 

[Stanlee]

Hi everyone,
I have done M.Pharmacy and have joined as quality associate in a pharmaceutical company, section R&D Quality.
Total work experience is about three years.
Please help me to identify my NOC !!
Many days have passed..but I couldn't find relevant NOC for FSW purpose.
Hoping for a prompt reply...

While selecting the NOC, the duties and responsibilities mentioned in the NOC should be a close match with the actual duties and responsibilities carried out by you at the respective job. You need not match the duties and responsibilities word by word, but the idea is to have the closest match in terms of the spirit of the duties and responsibilities (at least 60%-70% match).

Also, NOC should be selected on the basis of the match of actual duties and responsibilities carried out by you rather than the designation match in the NOC list. However, still if you need an expert opinion, I would suggest that you write to noc@workingincanada.gc.ca with your duties and responsibilities, they will help you find the closest fit.

 

[kvandhanapu]

Hi everyone,
I have done M.Pharmacy and have joined as quality associate in a pharmaceutical company, section R&D Quality.
Total work experience is about three years.
Please help me to identify my NOC !!
Many days have passed..but I couldn't find relevant NOC for FSW purpose.
Hoping for a prompt reply...

Hello,
I have the same situation.
I am working for a pharmaceutical company as a Quality Assurance Specialist and am unable to find the similar or nearly similar NOC.
could you help me in finding the NOC.

My job role includes.........
Company: Manufacturing of Pharmaceutical Products and Natural Health Products.

Position: Quality Assurance Specialist
Roles and Responsibilities:

· As required, participate in examining the results, change controls requests when necessary, generate deviation reports, investigate root cause determination, and provide recommendation for corrective actions.

· Ensure Good Manufacturing practices (GMP) are carried out by all employees.

· Provide administrative support when required and ensuring compliance with all aspects of GMP regulations as required by Health Canada and the US FDA.

· Investigate, prepare reports on Customer complaints and respond in a timely manner.

· Review Certificate of analysis, Calibration reports, Batch manufacturing records, Batch Packaging records for any discrepancies, or errors, deviations and investigations (etc.) that could or may have the potential to impact the efficacy of the product.

· As required, contact customers and internal departments to respond to their inquiries and resolve QA issues.

· Prepare reports of Annual Product Review as per the clients request and respond to clients in a timely manner.

· Ensure to perform Risk Assessment using FMEA in every stage throughout the process when required.

· As required check all reports, records and data for completeness and accuracy as well as to confirm compliance with internal procedures and regulations.

· Check the New formulations that meet the specifications of customers and file related documents.

· Review of SOP’s, Bill of materials, customer signed PFSS documents and mange them in the ERP system.


your time and reply will be helpful for me.

Thank you

 

[Nisha James]

Hello,
I have the same situation.
I am working for a pharmaceutical company as a Quality Assurance Specialist and am unable to find the similar or nearly similar NOC.
could you help me in finding the NOC.

My job role includes.........
Company: Manufacturing of Pharmaceutical Products and Natural Health Products.

Position: Quality Assurance Specialist
Roles and Responsibilities:

· As required, participate in examining the results, change controls requests when necessary, generate deviation reports, investigate root cause determination, and provide recommendation for corrective actions.

· Ensure Good Manufacturing practices (GMP) are carried out by all employees.

· Provide administrative support when required and ensuring compliance with all aspects of GMP regulations as required by Health Canada and the US FDA.

· Investigate, prepare reports on Customer complaints and respond in a timely manner.

· Review Certificate of analysis, Calibration reports, Batch manufacturing records, Batch Packaging records for any discrepancies, or errors, deviations and investigations (etc.) that could or may have the potential to impact the efficacy of the product.

· As required, contact customers and internal departments to respond to their inquiries and resolve QA issues.

· Prepare reports of Annual Product Review as per the clients request and respond to clients in a timely manner.

· Ensure to perform Risk Assessment using FMEA in every stage throughout the process when required.

· As required check all reports, records and data for completeness and accuracy as well as to confirm compliance with internal procedures and regulations.

· Check the New formulations that meet the specifications of customers and file related documents.

· Review of SOP’s, Bill of materials, customer signed PFSS documents and mange them in the ERP system.


your time and reply will be helpful for me.

Thank you

Hi,
I too have worked in Pharmaceutical industry as Quality Assurance Expert and am unable to find a relevant NOC code. Could you please suggest me the most appropriate one?

Thanks,
Nisha

 

[Nisha James]

Hi everyone,
I have done M.Pharmacy and have joined as quality associate in a pharmaceutical company, section R&D Quality.
Total work experience is about three years.
Please help me to identify my NOC !!
Many days have passed..but I couldn't find relevant NOC for FSW purpose.
Hoping for a prompt reply...

Hi,
With what code did you go ahead?

 

[Chigsang2604]

Respected sir,

I am Chirag from India, have completed Master of Pharmacy in Quality Assurance Department in 2012.

Since now I am working in different pharmaceutical industries and having below mentioned job description.

Kindly suggest relevant NOC

Responsible to perform line clearance, in process check, sampling of intermediate and finished pharmaceutical products including solid as well as parenteral dosage forms during its manufacturing and packaging.

2) To carry out the in-process quality control audits during manufacturing of all the products in the plants.

3) To check the batch manufacturing records according to the in house guideline and all local and international regulatory requirements.

4) To bring to the notice the abnormalities and deviations to the notice of IPQA in charge/ manager and quality control manager.

5) To check and visit the area for IN-PROCESS QUALITY ASSURANCE starting from material receipt to pre-dispatch inspections, and reporting the abnormalities to the respective heads of IPQA manager.

6) To rectify all such process during manufacturing where the compliance of standard operating procedures are not there.

7) To help out IPQA in-charge to carry out investigation case of any product complaints.

8) To carry out in process quality check inspection during manufacturing process.

9) To ensure CGMP compliance in oncology block.

10) To review executed BATCH PRODUCTION CONTROL RECORD and other relevant documents prior to batch release.



So kindly request you to evaluate and suggest relevant NOC for the same.



Thanks

 

[kkaur3]

Hi,
I too have worked in Pharmaceutical industry as Quality Assurance Expert and am unable to find a relevant NOC code. Could you please suggest me the most appropriate one?

Thanks,
Nisha

You may check 1122 also. You may manipulate wording however, so many searches rigourous searchig, this is the only code mentioning Qulaity assurance as key word,

 

[kkaur3]

Respected sir,

I am Chirag from India, have completed Master of Pharmacy in Quality Assurance Department in 2012.

Since now I am working in different pharmaceutical industries and having below mentioned job description.

Kindly suggest relevant NOC

Responsible to perform line clearance, in process check, sampling of intermediate and finished pharmaceutical products including solid as well as parenteral dosage forms during its manufacturing and packaging.

2) To carry out the in-process quality control audits during manufacturing of all the products in the plants.

3) To check the batch manufacturing records according to the in house guideline and all local and international regulatory requirements.

4) To bring to the notice the abnormalities and deviations to the notice of IPQA in charge/ manager and quality control manager.

5) To check and visit the area for IN-PROCESS QUALITY ASSURANCE starting from material receipt to pre-dispatch inspections, and reporting the abnormalities to the respective heads of IPQA manager.

6) To rectify all such process during manufacturing where the compliance of standard operating procedures are not there.

7) To help out IPQA in-charge to carry out investigation case of any product complaints.

8) To carry out in process quality check inspection during manufacturing process.

9) To ensure CGMP compliance in oncology block.

10) To review executed BATCH PRODUCTION CONTROL RECORD and other relevant documents prior to batch release.



So kindly request you to evaluate and suggest relevant NOC for the same.



Thanks

Check 1122 also, else 3131

 

[Wajeeha05]

hello everyone, i am also working in quality assurance department in pharmaceutical company....please someone tell me which noc code to be used, i have been trying searching for the noc since last month but was unable to find the relevant noc.....
experts please guide

 

[kvandhanapu]

I have applied under 2233.
But 2211 is also an option

 

[Wajeeha05]

Did u get ur PR?

 

[Yogesh Kenjale]

Did you get PR? If yes through express entry or PNP (which?)

I have applied under 2233.
But 2211 is also an option

n

 

[Naturgrl]

Did you get PR? If yes through express entry or PNP (which?)

n

You will see from the posts that the person received AOR through CEC so he had Canadian experience. Invitation is based on your CRS score and for PNP, you determine what province your are eligible.

 

[Yogesh Kenjale]

You will see from the posts that the person received AOR through CEC so he had Canadian experience. Invitation is based on your CRS score and for PNP, you determine what province your are eligible.

Thank you for your response. Ihav 11 years experience in Pharmaceutical Quality Assurance and responsibilities matches with 3131. Can I submit express entry profile with this NOC code for purpose of getting PNP nomination. Is 3131 has license pre-requisite as Industrial Pharmacist and what are chances for PNP nominations?
Any alternative suitable NOC code for Pharmaceutical Quality Assurance professional.
Thank you in advance

 

[Naturgrl]

Thank you for your response. Ihav 11 years experience in Pharmaceutical Quality Assurance and responsibilities matches with 3131. Can I submit express entry profile with this NOC code for purpose of getting PNP nomination. Is 3131 has license pre-requisite as Industrial Pharmacist and what are chances for PNP nominations?
Any alternative suitable NOC code for Pharmaceutical Quality Assurance professional.
Thank you in advance

You need ECA and IELTS to submit profile? Are you eligible for Express Entry. NOC 3131 is a licensed profession so what does your ECA state? NOC 3131 is not eligible for PNPs.