Pfizer walk-in interview for Quality Control department on 28th Apr 2024

Pfizer utilizes scientific knowledge and worldwide assets to deliver treatments that enhance and greatly enhance the lives of individuals. We aim to establish the benchmark for excellence, safety, and worth in the exploration, creation, and production of healthcare goods. Our international collection consists of medications, vaccines, and numerous well-known consumer healthcare items. Each day, Pfizer employees collaborate in developed and developing markets to promote well-being, prevention, therapies, and remedies that combat the most dreaded illnesses of our era.

Pfizer is hiring for Quality Control department. Bachelor’s Degree/ master’s degree with 1 – 5 years of experience candidates can attend the interview on 28th April 2024 at Visakhapatnam, Andhra Pradesh.

Job Title: QC Analyst roles.

Walk in interview on Sunday, 28th April 2024 at 8:00 AM

Interview Venue: GINGER HOTEL – GAJUWAKA- VIZAG | 27-8-308/1/1 |Sri Ram Nagar|Srinagar|Near Vadlapudi Railway Gate|Vadlapudi|Gajuwaka |Visakhapatnam 530046.

Job description:

• Equipment handling experience:
• Waters HPLC with EMPOWER, GC, IC, UV, IR, Potentiometer, KF, LBPC
• Preferably: Experience on Analytical method validations, method transfers handling of
• Stability testing for injectable products.
• Ensure training records are updated and correctly filed to reflect current testing capabilities.
• 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/ master’s degree
• 1 to 5 Years of relevant Experience.
• Demonstrated technical skills in method validation and 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 Chromotography) technique
• Experience leading continuous improvement projects
• Knowledge of lean manufacturing, six sigma methodologies, and statistics