Job Information
Cirtec Medical General Manager in Sturtevant, Wisconsin
General Manager
Department: Site SG&A
Location: Sturtevant, WI
START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req_id=3130326&source=3130326-CJB-0)
JOB SUMMARY
The GM has significant outside facing responsibilities and should be known as a go-to person for medical device contract design, development, and manufacturing services. The GM is responsible to ensure that the facility meets the commitments made to clients and makes amends for commitments missed and has overall responsibility for managing the revenue and cost elements for the assigned facility. The GM is responsible for planning, delegating, coordinating, staffing, organizing, and decision making to meet the above two objectives. This successful market-focused leader is a Corporate Officer and a member of the Leadership Team. The GM provides leadership and vision to the organization by supporting the CEO with the development of long range and annual plans and assisting with the evaluation and reporting of progress on plans as well as communicating strategic objectives to the facility.
ESSENTIAL RESPONSIBILITIES
Focuses resources to drive customer success and takes responsibility for commitments made to clients and makes amends for commitments missed.
Provide tactical direction for projects and client interactions to meet client objectives for client success.
Provide input to the budget process and manage revenue and cost elements to achieve profitability goals for the facility.
Assists business development to secure new opportunities.
Increases site management's effectiveness by recruiting, selecting, orienting, training, coaching, counseling, and disciplining managers; assigning accountabilities; developing a climate for offering information and opinions.
Assists in developing strategic plan by studying technological and financial opportunities; presenting assumptions; recommending objectives. Plays a major role in communicating values, strategies, and objectives to facility.
Work effectively in a collaborative fashion with site management team on all matters pertaining to ongoing operations in the facility and to long-term growth and objectives.
Maintains quality services and products by enforcing and improving organization and quality standards. Collaborates with corporate staff to provide continuous improvements to policies and procedures.
Responsible for reviewing the Quality Management System for adequacy, effectiveness and suitability through attending, participating and assigning action items at Management Review meetings.
Builds company image by collaborating with customers, government, community organizations, and employees.
Provide an effective voice for the company in the target community focusing on building relationships with current and potential clients, collaborators, industry organization, and technological community.
Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; benchmarking state-of-the-art practices; participating in professional societies.
Contributes to team effort by accomplishing related results as needed
Complies with company, quality and safety standards, policies and procedures
Other duties as assigned.
This is not a remote position.
An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
QUALIFICATIONS
A Bachelors- degree in an engineering discipline or equivalent.
Minimum 5 years medical device industry experience.
Minimum 10 years- experience in a multidisciplinary engineering and manufacturing environment with thorough knowledge of manufacturing and continuous improvement.
Proven organizational leadership ability and accountability for overseeing and managing a team, working cross-functionally, and delivering projects on schedule and within budget.
Strong collaboration, mentoring, team building, and development skills.
FDA and ISO regulations for design control and manufacture of medical devices.
Project management tools and methodologies
Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or governmental regulations.
Must be able to read, write and speak fluent English
Ability to write reports, specifications, business correspondence and procedure manuals.
Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
Evidence of outstanding personal values.
Six sigma certified black belt preferred
WORKING ENVIRONMENT
Work is performed in an office environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
EEO STATEMENT
Cirtec Medical Corporation is an Equal Opportunity Minority/Female/Individuals with Disabilities/Protected Veteran and Affirmative Action Employer
Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process
START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req_id=3130326&source=3130326-CJB-0)
