Are you Covidien?
As a global, $11+ billion healthcare products leader, we deliver outstanding results and innovative solutions for challenging problems. Through progressive thinking and cutting-edge technologies, Covidien is well positioned to lead the way in today’s rapidly changing healthcare industry. Whatever your specialty or ambitions, you can make a difference at Covidien – both in the lives of others and your career.
At Covidien, we strive to fully understand our marketplace, customers, communities and employees, and we enter into relationships with a sense of honesty, fairness and trust.
We are an affirmative action/equal opportunity employer.
SUMMARY OF POSITION :
Responsible for assisting the Process Coordinator in the assembly and completion of required documentation and data entry in support of production.
ESSENTIAL FUNCTIONS :
Request and update all SOP's used in production area while maintaining new effective dates & revisions Complete, fill out & assemble paperwork for each batch/lot for production area Process disposition and paperwork regarding in-process samples Perform startup checks and data entry for each production lot Complete product accountability for each batch/lot Review production start-up and in-process batch records Enter production data into BPCS manufacturing execution system Complete daily production reports & logs 10. Complete other duties as assigned by the Production Supervisor
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS :
Work safely in accordance with regulations, standards, and procedures and in a manner that eliminates unreasonable risk to health and the environment. Notify management of unsafe conditions or practices, unlawful activities and activities which present unreasonable health and/or environmental risk. Report all safety and/or environmental incidents to management immediately. Help maintain production supplies and resources. Assist supervisor/superintendent with gathering data associated with variations. Other duties as assigned with or without accommodation.
MINIMUM REQUIREMENTS :
Education required/ preferred:
High school diploma, GED, or equivalent
3-5 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar) preferred
Proficient PC skills including working with spreadsheets and word processing Demonstrated ability to use the Microsoft Office package Skills/Competencies:
Working knowledge of BPCS Demonstrated basic math skills Good verbal and written communication skills Other Skills:
ORGANIZATIONAL RELATIONSHIPS/SCOPE :
Reports to Production Supervisor Works daily with other operators, set-ups, mechanics and Production Supervisors. Occasional interaction with cross-functional team members on project teams
Work in areas where special gowning and safety equipment is required. Standing is for extended periods of time. Requires ability to work flexible hours and overtime (occasionally on short notice) Requires a high degree of manual dexterity, under conditions in areas with limited space.
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
As a global healthcare leader, we drive advances in medical devices and medical supplies. Thanks to our scale, scope and pioneering spirit,...