Mylan Pharmaceuticals Inc.
Associate Manager, Quality Control, Weekend Shift 7:00 pm - 7:00 am
Mylan Inc. ranks among the leading generic and specialty pharmaceutical companies in the world and provides products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios supported by a robust product pipeline; operates one of the world’s largest active pharmaceutical ingredient manufacturers; and runs a specialty business focused on respiratory, allergy and psychiatric therapies. For more information, please visit
We are currently seeking an Associate Manager for the Quality Control laboratory for the weekend shift, 7:00 pm – 7:00 am. They will have a role in giving guidance and direction to fellow analysts and leadership for the laboratory teams. They will serves as a leader of Quality Control (QC) and be a representative for the functional area at the meetings.
The Associate Manager will enforce laboratory policies and resolve personnel issues. Coordinate with senior chemists and project management to schedule assignments and projects.
Represent functional area in QC management, operations, and organizational meetings.
Perform data analysis, audit data and analytical procedures, generate metrics, prepare protocols, and summary reports.
Prepare, review, and update laboratory analytical procedures, Standard Operating Procedures (SOPs) and guidelines.
Perform troubleshooting of functional area problems and issues.
Lead continuous improvement initiatives.
The successful candidate will have the minimum of a Bachelor's degree in a science related discipline (or equivalent) and 2-4 years of experience in analytical/quality/manufacturing environment . However, a combination of experience and/or education will be taken into consideration. Master’s Degree is a plus. Minimum of 1 to 2 years Supervisory experience is desired. Must possess knowledge of Company and departmental policies and procedures, US/European/Japan regulatory agencies, FDA regulations and guidelines, USP and SOP guidelines, and an overall understanding of the industry.
Working knowledge of pharmaceutical manufacturing and analytical testing is required.
Knowledge of SOPs, Mylan Laboratory Procedures, USP regulations, Analytical Testing Techniques, cGMP, and OSHA regulations/procedures for disposal of organic waste and procedures for the safe handling of chemicals.
Must possess excellent writing and communication skills and reading and interpretation skills. Must possess strong leadership and management skills. Necessary computer skills and knowledge include Microsoft Word, Excel, PowerPoint, SAP, LIMS,
’s TrackWise System, and Lotus Notes.
At Mylan, we are not satisfied with anything less than being the best. As one of the world's leading generics and specialty pharmaceutical companies, the key to our success starts with a relentless drive to set the highest industry standards in everything we do. It takes exceptional people working together to achieve excellence. As a team, we earn our customers’ trust and loyalty by placing a high premium on always doing the right things in the right way.
Mylan offers competitive salary, excellent benefits and an environment conducive to professional growth and advancement. Mylan is an Equal Opportunity Employer, M/F/D/V.
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