Job description
LOOKING FOR A SENIOR OPERATIONS MANAGER WITH CONSUMER GOODS EXPERIENCE. THIS COMPANY MAKES SENSUAL LUBRICATES AND MOUTH GERM SPRAYS THAT TREATS AND PREVENTS INFECTIONS.
SALARY: $130K-$180K
Work Schedule: Tues-Friday Mondays Off!!!
Local Candidates needed RIGHT now. No Relo:
MUST HAVE:
Looking for a Sr. Operations Manager with experience in MANUFACTURING CONSUMER GOODS OR Medical Device OR CONSUMER PRODUCTS.
B.S. DEGREE IN ENGINEERING (OR RELATED FIELD) OR 10 YRS OF EQUIVALENT EXPERIENCE.
Job Description: Sr. Operations Manager
Vista, CA
Alternative Work Week:
COMPANY works an alternative work schedule of four 9.5-hour days. You will be likely assigned to one of the following schedules, 6:00 am – 4:30 pm -or- 7:00 am – 5:30 pm, with one hour for lunch.
The Senior Operations Manager will oversee the day-to-day activities of the company, ensuring that the organization is managed and performing efficiently and effectively.
Company is Looking for a Sr. Operations Manager with experience in Production, Distribution, and Medical Device or CPG. If this is you, then send us your resume!
This role will oversee the day to day activities of the operations team, ensuring that the organization is managed and performing efficiently and effectively.
5 Key Roles of Accountability
1. LEAD, MANAGE, AND ACCOUNTABILITY
2. LEAD OPERATIONS ACTIVITIES INCLUDING MANUFACTURING (MIXING & PRODUCTION), ENGINEERING, FACILITIES, AND DISTRIBUTION DEPARTMENTS
3. ANALYZE, PROPOSE AND MANAGE BUDGETS, TECHNOLOGIES AND RESOURCES FOR PROJECTS
4. PROVIDE INPUT IN STRATEGIC TECHNICAL DECISIONS AND SOLUTION
5. COMMUNICATE AND COLLABORATE WITH OTHER MANAGERS, STAKEHOLDERS AND CONTRACTORS TO MEET AND EXCEED CORPORATE GOALS
Requirements
7+ YEARS OF EXPERIENCE IN FIELDS SUCH AS PRODUCTION OPERATIONS, MANUFACTURING ENGINEERING, DEVELOPMENT ENGINEERING, PRODUCTION ENGINEERING IN A REGULATED ENVIRONMENT
5+ YEARS OF INCREASING RESPONSIBILITY LEADING AND MANAGING ENGINEERING AND PROJECT TEAMS
STRONG TECHNICAL AND PROJECT MANAGEMENT CAPABILITIES
WORKING KNOWLEDGE OF CURRENT REGULATORY REQUIREMENTS SPECIFICALLY PERTAINING TO FDA, CGMP, ISO 13485 AND DESIGN CONTROL FOR MEDICAL DEVICES A PLUS
B.S. DEGREE IN ENGINEERING (OR RELATED FIELD) OR 10 YRS OF EQUIVALENT EXPERIENCE.
PROJECT MANAGEMENT PROFESSIONAL (PMP) CERTIFICATION PREFERRED
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