Trainee Associate / Officer
Job Description
Title: Trainee Associate / Officer
Company Name: Novartis (Bangladesh) Limited
Vacancy: --
Location: Anywhere in Bangladesh
Published: 30 May 2024
Education:
∎ Minimum bachelor’s degree from Pharmacy, Chemistry, Biochemistry or Applied Chemistry.
Requirements:
Additional Requirements:
∎ Freshers are encouraged to apply.
∎ Excellent interpersonal, communication, analytical, problem solving and decision-making skills, and adaptability
∎ Adequate proficiency in lab and relevant computer applications with investigational report writing.
∎ Physically fit to do analytical activities at chemical laboratory.
∎ Freshers are encouraged to apply.
∎ Excellent interpersonal, communication, analytical, problem solving and decision-making skills, and adaptability
∎ Adequate proficiency in lab and relevant computer applications with investigational report writing.
∎ Physically fit to do analytical activities at chemical laboratory.
Responsibilities & Context:
∎ Managing and executing analytical method development,
∎ Responsible for analytical method validation/verification, analytical technology transfer and to ensure pharmacopeial
∎ compliance.
∎ Supporting in the development of raw and packaging material sources.
∎ Ensuring compliance of all activities aligning with QM, QD, GOP, SOP and official regulations.
∎ Responsible for overall management of GMP Documents and Records including Central Archive
∎ Coordinating functional training program
∎ Preparation of Product Quality Review report
∎ Contributing to performing Quality Oversight
∎ Supporting batch record review
∎ Performing GxP Document Review/Approval
∎ Ensuring compliance of all activities aligning with Novartis QM, QD, GOP, SOP and official regulations.
∎ Responsible for effective shift management, management of raw material dispensing as per DOS, follow and maintain BMR, execute production plan.
∎ Manufacture pharmaceutical products by aligning with Production Manager in a cost effective and compliant way.
∎ Maintain relationships among stakeholders as applicable for overall Manufacturing operations.
∎ Qualification and Calibration of manufacturing equipment’s
∎ Enforce cGMP practice, follow HSE guideline, prepare and maintain different relevant documents.
∎ Join us to reimagine medicine to improve and extend people's lives
∎ Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!
∎ We are looking for suitable candidates for the role of Trainee Associate / Officer for Quality Assurance and Production department. These roles involve laboratory testing, analysing results, troubleshooting, manufacture pharmaceutical products, implementing improvements, managing documents, coordinating training, ensuring safety, reviewing batch records, overseeing quality, conducting product reviews, and reviewing/approving documents
∎ Major Responsibilities:
∎ Quality Control:
∎ Managing and executing analytical method development,
∎ Responsible for analytical method validation/verification, analytical technology transfer and to ensure pharmacopeial
∎ compliance.
∎ Supporting in the development of raw and packaging material sources.
∎ Ensuring compliance of all activities aligning with QM, QD, GOP, SOP and official regulations.
∎ Quality Operations:
∎ Responsible for overall management of GMP Documents and Records including Central Archive
∎ Coordinating functional training program
∎ Preparation of Product Quality Review report
∎ Contributing to performing Quality Oversight
∎ Supporting batch record review
∎ Performing GxP Document Review/Approval
∎ Ensuring compliance of all activities aligning with Novartis QM, QD, GOP, SOP and official regulations.
∎ Production:
∎ Responsible for effective shift management, management of raw material dispensing as per DOS, follow and maintain BMR, execute production plan.
∎ Manufacture pharmaceutical products by aligning with Production Manager in a cost effective and compliant way.
∎ Maintain relationships among stakeholders as applicable for overall Manufacturing operations.
∎ Qualification and Calibration of manufacturing equipment’s
∎ Enforce cGMP practice, follow HSE guideline, prepare and maintain different relevant documents.
Employment Status: Full Time
Job Location: Anywhere in Bangladesh
Read Before Apply:
*As equal employment company, Female candidates are encouraged to apply**
Company Information:
∎ Novartis (Bangladesh) Limited
∎ Tower One One Seven (5th Floor), Plot # 117/A, Tejgaon I/A, Dhaka 1208, Bangladesh
∎ https://www.novartis.com/bd-en/
∎ Pharmaceutical
Address::
∎ Tower One One Seven (5th Floor), Plot # 117/A, Tejgaon I/A, Dhaka 1208, Bangladesh
∎ https://www.novartis.com/bd-en/
∎ Pharmaceutical
Application Deadline: 15 Jun 2024
Category: Medical/Pharma
Deadline Expired on 15th Jun 2024
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