• United States Of America, Usa
  • Save Job
  • 0 - 3 Years
  • Posted : above 1 month

Job Description:

At AstraZeneca we turn ideas into life changing medicines Working here means being entrepreneurial, thinking big and working together to make the impossible a reality Were focused on the potential of science to address the unmet needs of patients around the world We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life As a Quality Control Analyst III in Philadelphia, PA, youll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients lives Operations at AstraZeneca is a truly world-class business unit It offers one of the most exciting, fast paced, challenging and rewarding work environments in the world of operations, supply chain and manufacturing

Global Operations is fundamental to our purpose of delivering life-changing medicines to patients, touching every aspect of our business and providing a platform for everything that we do We harness the specialist talents of 13,000 people around the world 20 PERCENT of our global workforce With 30 production facilities in 18 countries were focused on supplying our medicines with care, quality and efficiency, reducing the time from lab to patient Keen to bridge the gap between science and patients Turn research into reality And forge a global career thats full of possibilities, as part of a world-class team Come and thrive in our vibrant, energizing, connected and supportive culture and make a real difference to patients Hear from our Senior Leaders about why they know AstraZeneca is a great place to work https//lnkdin/g8APibK

The Quality Control Analyst III is responsible for conducting routine and non-routine analysis of environmental samples, raw materials and in process samples according to standard operating procedures Completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms

Job responsibilities include but are not limited to

Calibrates and maintains laboratory equipment according to standard operating procedures
Reviews data obtained for compliance to specifications and reports abnormalities
Executes validation protocols, laboratory test plans, and reports results to management
Prepares documentation for presentation to Regulatory Agencies
Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis
Prepares validation protocols, executes experiments, and prepares validation reports
Responsible for writing new standard operating procedures or revising existing documentation
Applies critical thought to solving problems of complex scope

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
Functional Area : Production/Manufacturing/Maintenance/Packaging
Role : Production/Manufacturi ng/Maintenance
Salary : As per Industry Standards
Deadline : 14th Mar 2020

Key Skills:

Company Profile:


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