Pfizer Job Opening For 0-4 Years Exp Candidates, Apply Online For Associate Role

Pfizer Job Openings For 0-4 Years Exp Candidates, Apply Online For Associate Role

Pfizer Job Openings For 0-4 Years Exp Candidates, Apply Online For Associate Role. Pfizer is hiring candidates for an Associate -Microbiology vacancy. Interested and eligible applicants can check out all of the details on the same below –

Possible Interview Questions for the role of Associate at Pfizer are posted below

Job Title – Associate -Microbiology

Job ID – 4885616

Location of Pfizer Vacancy – India – Vizag

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, biological or microbiological products will help us manage our quality. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility 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, retain management, 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 to

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

• Assist in preparation of media, maintenance of dehydrated and prepared media stocks, and sterilization of media accessories by autoclave cycles.
• Assist in the maintenance of Master cultures Isolates and preparation of Cryovials.
• Manage receipt, storage and handling of Bio ball cultures.
• Perform water analysis, Microbial Limit tests, Sterility tests, Bacterial Endotoxin Test and Assays, CCIT and micro challenge studies.
• Ensure training records are updated and correctly filed to reflect current testing capabilities.
• Perform sampling and labelling 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 documentation and quality records are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance with 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

• Master’s Degree in Microbiology with 0-4 years experience
• Demonstrated technical skills in EM sampling and Product testing
• Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
• Knowledge of Good Manufacturing Practices and their 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 EM sampling techniques
• Experience leading continuous improvement projects
• Knowledge of lean manufacturing, six sigma methodologies, and statistics

APPLY ONLINE

Possible Interview Questions for the Role of Associate at Pfizer:

1. Can you explain your experience and knowledge in microbiological product testing and quality control? Answer: Certainly. I have completed my Master’s Degree in Microbiology and have acquired 0-4 years of experience in this field. During my experience, I have developed expertise in EM sampling and product testing, adhering to applicable compendial methods, Standard Operating Procedures, and governmental regulations.
2. How familiar are you with Good Manufacturing Practices (GMP) and their application in quality control? Can you provide examples of how you have applied these standards in your previous work? Answer: I have a strong understanding of Good Manufacturing Practices and their application in maintaining quality control. For instance, I ensure that all documentation and quality records are conducted in accordance with GMP and Good Laboratory Practices (GLP) requirements. I also review and revise Standard Operating Procedures and analytical methods to ensure compliance and keep them up to date.
3. In your experience, how have you contributed to complex projects and managed your time effectively to meet targets? Can you provide an example of a project you successfully completed? Answer: Throughout my career, I have actively contributed to complex projects, managing my time efficiently to achieve agreed targets. One notable project involved [describe the project briefly]. I effectively coordinated with the team, developed a plan for work activities, and successfully delivered the project within the set timeline, meeting all objectives and quality standards.
4. Can you share your experience with microbial identification, sterility testing, and other microbiological protocols? How have you ensured accuracy and precision in these testing procedures? Answer: I have hands-on experience in microbial identification, sterility testing, and conducting various microbiological protocols. To ensure accuracy and precision, I carefully follow standardized procedures, interpret and evaluate data for trends and potential impacts on Good Manufacturing Practices (GMP). If any discrepancies are observed, I recommend appropriate corrective actions to maintain the highest quality standards.
5. Have you been involved in any continuous improvement projects or demonstrated knowledge of lean manufacturing and six sigma methodologies? How have you applied these methodologies to enhance quality control processes? Answer: While I haven’t specifically led continuous improvement projects, I have actively participated in process improvement initiatives. I possess knowledge of lean manufacturing principles, six sigma methodologies, and statistics. I have utilized these methodologies to analyze data, identify areas for improvement, and propose effective solutions to optimize quality control processes, ensuring efficiency and adherence to quality standards.

Remember to personalize your answers based on your own experiences and achievements to make them more impactful during the interview.

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