Pfizer Recruitment 2021 | Intern | B.A/ B.Sc/ B.Com/ BBA/ BCA | 2018 to 2020 Batch | Chennai, Tamil Nadu

Company: Pfizer Inc
Pfizer Recruitment 2021: Pfizer Inc is an American pharmaceutical corporation headquartered in New York City, with its research headquarters in Groton, Connecticut. It is one of the world’s largest pharmaceutical companies.

The company develops and produces medicines and vaccines for a wide range of medical disciplines, including immunology, oncology, cardiology, endocrinology, and neurology.

Company Website: www.pfizer.com

Positions: Intern

Job Location: Chennai

Salary: Best In Industry

Experience: Experienced

Qualification: Bachelor’s degree

Job Description:

• As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will perform qualitative and quantitative analyses of organic, inorganic compounds, or biologics. This will help you determine chemical and physical properties during chemical syntheses, fermentation or drug product development process by verifying their identity, purity, and homogeneity.
• Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.
• It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

Job Responsibilities:-

• Exercise and build basic team effectiveness skills {e.g., commitment, feedback, consensus management) within the work group.
• Prepare and review technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.
• Direct interaction with project team members, including presentation of data.
• Complete all Good Laboratory Practice {part of GxP}and safety training in compliance with departmental requirements and follow appropriate safety practices in the workplace.
• Perform various experiments for analytical method development/qualification/validation and characterization for biological therapeutics.
• Perform and document drug substance or drug product related Microbiological activities.
• Conduct all work according to appropriate Standard Operating Procedures’ following Good Manufacturing Practices/Good Laboratory Practices (GMP/GLP) requirements and ensure integrity of all data generated and documented.
• Independently analyze and provide conclusions regarding experimental data generated.
• Plan and prioritize related recovery and purification activities.
• Present problems and propose solutions in discussions with group members.

Requirements:

• Bachelor’s Degree
• Experience with Quality Systems in a Good Manufacturing Practices {also cGMP} environment
• Experience with laboratory data systems
• Hands on experience or working knowledge in Pharmaceutical industry in handling of analytical instruments
• Knowledge of drug development process for progression of biological incumbents
• Good documentation skills with high attention to detail, strong organizational skills, team oriented, effective interpersonal and communication skills

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