Quality Control job at Pfizer – BPharm / MPharm / MSc Chemistry Graduates Check out the details below and Apply
Role : Associate-CQ
Location : India – Vizag
Time type : Full time
Job requisition id : 4893962
What You Will Achieve
- You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs. Your ability to analyze chemical, products will help us manage our quality. Your contribution to analytical testing will help Pfizer provide safe drugs to its patients.
- Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains managements, interpretation and evaluation. You will also be relied on for establishing requirements for the transfer of methodology from R&D.
- As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
- It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
- Perform sampling and labeling of materials as per defined procedure and verification of all the equipment / instruments.
- Interpret and evaluate data in terms of accuracy, precision, trends and potential Good Manufacturing Practices {also cGMP} impact and recommend appropriate corrective actions.
- Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance to existing policies.
- Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.
- Perform analyses on finished products, raw materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
- Conduct Microbiological protocols on an as needed basis.
- Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Qualifications:
Must-Have
- Bachelor’s degree in pharmacy or Masters Chemistry/ Pharmacy.
- 2-6 Years of experience in quality control lab.
- Demonstrated technical skills in method validation and HPLC/UPLC testing.
- Ability to read and understand applicable compendial methods, Standard Operating
- Procedures, technical procedures, and governmental regulations
- Knowledge of Good Manufacturing Practices and its application standards, processes and policies
- Excellent organizational skills and strong ability to multi-task
- Strong written and verbal communication skills
Nice-to-Have
- Laboratory work experience with analytical HPLC (High Pressure Liquid Chromatography) technique
- Experience leading continuous improvement projects
- Knowledge of lean manufacturing, six sigma methodologies, and statistics
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Here are some interview questions and possible answers for the role of Associate-CQ at Pfizer:
1. Can you tell us about your educational background and relevant qualifications for this role?
Answer: I hold a Bachelor’s degree in pharmacy, which has provided me with a strong foundation in pharmaceutical science. Additionally, I have a Master’s degree in Chemistry/Pharmacy, which has deepened my understanding of analytical techniques and quality control principles. My academic background aligns well with the requirements for this role.
2. How many years of experience do you have in a quality control lab, and can you describe your key responsibilities in your previous roles?
Answer: I have 4 years of experience in a quality control lab. In my previous roles, I was responsible for conducting various quality control tests on pharmaceutical products, raw materials, and components. This included method validation and HPLC/UPLC testing to ensure the accuracy and quality of our products. I also reviewed and revised Standard Operating Procedures (SOPs) and managed documentation in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) standards.
3. Can you provide an example of a challenging situation you encountered in your previous role related to quality control and how you resolved it?
Answer: Certainly. In a previous role, we faced a situation where there was a sudden change in the supplier of a critical raw material. This change raised concerns about the consistency and quality of the material. To address this, I initiated a comprehensive quality assessment, including rigorous testing and analysis using HPLC techniques. I collaborated closely with the procurement team to ensure that the new supplier met our quality standards. Through these efforts, we were able to identify potential issues early on and take corrective actions, ensuring the continued production of high-quality products.
4. The job description mentions the ability to read and understand applicable compendial methods, SOPs, and governmental regulations. Can you provide an example of how you have applied this knowledge in your previous role?
Answer: Certainly. In my previous role, I was responsible for ensuring that all testing and documentation were in compliance with regulatory requirements. I regularly reviewed compendial methods, SOPs, and governmental regulations to stay updated with industry standards. For instance, when conducting stability testing for pharmaceutical products, I closely followed compendial guidelines to ensure accurate and reliable results. This commitment to compliance helped us maintain product quality and meet regulatory expectations consistently.
5. How do you prioritize and manage your workload when working on multiple projects within a team?
Answer: Prioritization and time management are crucial in a quality control lab. I typically start by assessing the urgency and importance of each task. I create a work plan that outlines deadlines and milestones for each project. Communication with team members is essential to ensure everyone is aligned and to identify any potential bottlenecks. Additionally, I regularly review my progress and adjust my schedule as needed to meet agreed targets. This approach has helped me effectively manage multiple projects and maintain a collaborative team environment.
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