Officer, Quality Department (Quality Control)

Job Description

Title: Officer, Quality Department (Quality Control)

Company Name: Nuvista Pharma Limited

Vacancy: --

Location: Gazipur (Tongi)

Experience:
∎ 1 to 3 years
∎ Freshers are also encouraged to apply.

Published: 27 Jul 2024

Education:
∎ M. Pharm or M.Sc. in Chemistry / Biochemistry from any reputed University.
∎ M. Pharm or M.Sc. in Chemistry / Biochemistry from any reputed University.

Requirements:

Additional Requirements:
∎ At least 1 to 3 years working experience in a well-known pharmaceutical Quality Control laboratory is preferred.
∎ Knowledge of cGMP regulations like USP/BP, WHO, TGA, MHRA, US-FDA related to manufacturing of sterile and non- sterile pharmaceutical products is a plus.
∎ At least 1 to 3 years working experience in a well-known pharmaceutical Quality Control laboratory is preferred.
∎ Knowledge of cGMP regulations like USP/BP, WHO, TGA, MHRA, US-FDA related to manufacturing of sterile and non- sterile pharmaceutical products is a plus.

Responsibilities & Context:
∎ Analytical work (i.e. raw material, intermediate, bulk, packing material, finished product and stability studies) of products according to the specified method and routine chemical analysis of PW, WFI and PS.
∎ Preparation of RM and finished product specification, COA, testing method, SOPs and register.
∎ Perform analysis of cleaning validation, process validation & method validation of products.
∎ Monitoring of calibration, qualication & maintenance of QC equipment and their proper documentation.
∎ Ensuring that raw materials, components, products, or monitoring results that do not meet specications or expectations are promptly investigated, risk assessed and necessary CAPAs are implemented.
∎ Analytical work (i.e. raw material, intermediate, bulk, packing material, finished product and stability studies) of products according to the specified method and routine chemical analysis of PW, WFI and PS.
∎ Preparation of RM and finished product specification, COA, testing method, SOPs and register.
∎ Perform analysis of cleaning validation, process validation & method validation of products.
∎ Monitoring of calibration, qualication & maintenance of QC equipment and their proper documentation.
∎ Ensuring that raw materials, components, products, or monitoring results that do not meet specications or expectations are promptly investigated, risk assessed and necessary CAPAs are implemented.

Employment Status: Full Time

Job Location: Gazipur (Tongi)

Read Before Apply:

If you believe that you are the right person for the winning team, apply online or email your resume to: [email protected] with the position applied for clearly mentioned in the subject line

Only short listed candidates will be invited for further selection process

Nuvista Pharma Limited is an equal opportunities employer. Female candidates are highly encouraged to apply.

Apply Procedure:

Email your CV:
∎ Send your CV to the given email [email protected] or Email your CV from My Bdjobs account

Company Information:
∎ Nuvista Pharma Limited
∎ Mirpur DOHS Cultural Centre (6th floor), Road-9, Mirpur DOHS, Pallabi, Dhaka-1216, Bangladesh

Address::
∎ Mirpur DOHS Cultural Centre (6th floor), Road-9, Mirpur DOHS, Pallabi, Dhaka-1216, Bangladesh

Application Deadline: 10 Aug 2024

Category: Medical/Pharma