Dir, Engineering Technology & Qualif

Under administrative direction, oversees plans and directs the engineering for technology, facility, utility and equipment qualification functions of Watson Pharmaceuticals. Coordinates and directs the activities and functions of engineering projects and provides timely engineering support to Manufacturing, Packaging, Laboratories Administration and Research & Development, as required. Also provides qualification support to Distribution center and any other corporate entity on as-needed basis. Will travel 50%.• Provides guidance and direction to subordinate engineers in ensuring compliance with corporate business plans and objectives.• Evaluates, manages and provides consultation on manufacturing/packaging technology,equipment and support system issues.• Provides qualification support to corporate R&D, Distribution and third-party manufacturers. Approve and manage Qualification protocols and reports• Perform engineering evaluations for new R&D site selection.• Manages engineering document systems, capital project timelines, budgets and engineering staff for equipment procurement, installation and start-up.• Coordinates and directs the activities and functions of engineering projects ranging from several thousands to several millions of dollars.• Provides timely engineering support to Watson manufacturing sites in US, pilot plant equipment needs, and contract manufacturers of Watson products, when required.• Ensures compliance with all Company policies and procedures, including safety rules andregulations.• Carries out responsibilities in accordance with the organization’s policies, procedures;and state, federal and local laws.• Performs related duties as assigned.QualificationsTen (10) years related pharmaceutical facilities engineering experience, with at least two (2) years at a manager level; or equivalent combination of education and experience. Additional prior experience required includes:• Management, administration and training practices and methods.• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.• Responding to inquiries from management, employees and regulatory agencies.• Preparing, presenting and administering complex budgets and financial reports.• Managing multiple projects, duties and assignments.• Interpreting and applying Federal, state and local policies, procedures and regulations.• Directing, coordinating, and delegating assignments of assigned personnel.As part of Watson's mission, we dedicate ourselves to providing a respectful and rewarding work environment which includes competitive compensation and benefits.Watson Pharmaceuticals, Inc. is an Equal Opportunity Employer M/F/D/V. We value the benefits of diversity. As part of Watson's mission, we dedicate ourselves to providing a respectful and rewarding work environment which includes competitive compensation and benefits. Watson Pharmaceuticals, Inc. values the benefits of diversity. EOE M/F/D/V.