It's A Mission At Mylan, we mean it when we say we work every day to provide access to high quality medicines to the world's 7 billion people.
If you are unconventional, relentless and passionate. If you believe in doing what's right, not what's easy. If you are a doer and have a passion for serving others, we want to talk to you.
Make a Difference At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role.
Here's how this role will help :
To provide technical support to the Manufacturing or Packaging areas
To address any Technical issues and protect and maintain the quality and safety of the products being manufactured
Lead investigations to root cause any process issues which occur and to provide and implement suitable CAPAs to completion as per agreed timelines
Lead and support improvement projects in Manufacturing
To assist in any Product Transfer Manufacturing activities taking into consideration any EH&S and Technical concerns
To work closely with the Manufacturing Team for key data gathering activities and using that data to drive improvements and for tracking and trending
To participate in troubleshooting problem formulations, suggest and implement suitable improvements and work closely with TD to validate where necessary
To troubleshoot technical issues, investigate and write deviations, working closely with Supervisors, Operators, Managers, QA and TD to close out immediate and longer term CAPAs as per agreed timelines
To raise and critically review Change Controls and ultimately close as per agreed timelines
To critically review and approve BMRs for appropriate and suitable content such that errors are minimised and details are compliant
To write, review and approve Investigation reports
Determine the manufacturing requirements for new products
Make Our Values Your Values
Mylan hires only the best. People who thrive in a culture of innovation and empowerment. People who are active learners and have a positive attitude.
People who are leaders and know that by working together we can run faster, reach higher and achieve more. By doing so, we will continue to set new standards in health care.
Here are the minimum qualifications and essential functions for this position :
At least 3+ years’ experience in Pharmaceutical Industry in a GMP environment. Some knowledge of OSD processes would be ideal.
Process development and tablet formulation experience would be a distinct advantage
Technical report writing and Statistical Analysis knowledge through course content or hands on experience would be a distinct advantage
Science / pharmaceuticals / engineering related degree qualification
Proven problem-solving capabilities
Proficiency in speaking, comprehending, reading and writing English is preferred