Omrix Biopharmaceuticals is seeking a Production Team Leader, for our SD and Gamma lines in Tel-HaShomer site.
This position is open for INTERNAL MOVE ONLY
Reports to Production line Supervisor
Responsible for managing production personnel to maximize quality and output in a manufacturing operation. Accountable for achieving production targets while maintaining cost controls.
DUTIES & RESPONSIBILITIES
Under limited supervision and/or general directions and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Supervises production operation and work to meet production goals. Establishes personnel schedules and product lines based on business needs. Provides input to production flow and identifies potential manufacturing issues. Tracks production orders and schedules. Compiles and submits data for production and operating reports. Trains staff in the areas of safety and quality. Reviews work to ensure compliance with the standards. Schedules or performs training for all employees. Recommends changes to standard operational and working practices. Educates employees and observes to ensure understanding and compliance. Provides input to operational budget. Manages costs to improve business' financial results. Administers equipment maintenance and repair. Maintains records and notifies management of reoccurring issues that may require equipment replacement.
Responsible for communicating business related issues or opportunities to next management level. In case supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable. Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures, performs other duties assigned as needed.
High School Diploma
1-2 years of related experience or equivalent-is preferred.
Previous experience in a pharmaceutical manufacturing environment-is preferred.
Knowledge of and compliance with CGMP (Current Good Manufacturing Practices) regulations, preferred but not required.
Basic Computer skills.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS.
•Able to read and understand English procedures and instructions.
•Demonstrate knowledge of manufacturing principles and practices.
•Ability of meeting tight schedules and achieving tasks due dates according to plan.
•Ability to perform review of batch records and data spread sheets in high accuracy and ensure compliance with protocols and standards.
•Verbal and written communication skills.
•Organizational and leadership abilities.
•Presentation, guidance and training skills.
•Ability to work cooperatively with coworkers and other departments and interface.
•Ability to motivate employee under his/her responsibility and Promotes positive employee relation.
•Ability to maintain and motivate operators for 100% compliance maintenance in all SOP, cGMP, EHS and other training curriculum as assigned.
•committed to implement high standards of health, Environment and safety
•Ability to perform duties in accordance with policies and procedures, follow cGMP and comply with Industry and regulations requirements
•All other duties may be assigned as required.
ADDITIONAL POSITION REQUIREMENTS
•The job schedule requires work in 3 shifts, weekend and overtime as needed.
•Operate and monitor operation of specialized pieces of equipment.
•Required for checking and verification of all operations and activities performed by department operators and junior staff during a shift.
•Informing line Supervisor of any nonconformance', safety or quality events which occurred or reported during the shift.
•Opens new department nonconformance's in the company quality system as require, Participates in investigations when applicable.
•Reporting to Department manager supervisor.
•Direct managing various employees including shift coordinators and operators.
RESPONSIBILITY FOR OTHERS & INTERNAL INTERACTIONS
•This position will directly report to main line Supervisor of the relevant department.
•Works with other departments and functions as relevant.
PHYSICAL WORKING CONDITIONS / REQUIREMENTS
•This position will be partially performed in a clean room production environment which requires certain preparation and gowning practices
•Ability to work in a special environment such as a clean room
•Ability to wear protective garb such as clean room gowns
•Must be able to stand for long periods of time
•Must be able to move short distances quickly and frequently
•Must be able to perform lifting, pulling and pushing movements.
•Must be able to complete repetitive movements for extensive periods of time