Polish Machining Team Lead
PharmaMedTechQuality Assurancegmpsasfdaiso 13485croinform
Job description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Supply Chain Manufacturing Job Sub Function: Manufacturing Assembly Job Category: Business Enablement/Support All Job Posting Locations: Raynham, Massachusetts, United States of America Job Description: About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Polish Machining Team Lead. Purpose : Operates diverse types of machinery in an assigned cell, to produce various types of Medical Devices, including implants. Equipment used depends on product being manufactured or operation being performed and may vary from cell to cell. Under direction of the supervisor and/or cell lead, works to ensure production requirements are met, product quality is maintained, machine maintenance schedules are adhered to and safety rules are followed. You will be responsible for: Operates diverse types of equipment used to manufacture various types of Medical Devices established within the manufacturing processes and quality requirements. Completes tasks using technology systems such as PLM, MES, Microsoft Office, ERP systems, etc. Operations being performed depend on cell assignment and product being manufactured but may include and are not limited to, cutting raw material, drilling, milling, bending, deburring, buffing, laser etching, wax injection, dipping, dewax, pour, assembly or packaging/labeling. Equipment used may be but not limited to CNC, Hydraulic, Pneumatic, CMM, Grinding, Drags, Manual, or automatic and includes, but is not limited to, various types of lathes, mills, grinders, vibratory machines, drill presses, bead blaster, grinding wheels, buffer, bench presses, laser etch machines, assembly equipment, pack/labeling equipment, etc. Equipment used depends on product being manufactured or operation being performed. Operator will inspect finished and in-process product for dimensional and cosmetic attributes according to defined specifications. Operator will also assemble, package, and label various orthopedic medical devices following specific procedures, and operate various manual and semi-automatic packaging equipment All operators use various types of measuring instruments including, numerous types of gauges, micrometers, calipers, comparators, pH meters, go/ no-go gages, conductivity meters, visual inspectional, and digital titrators for chemical analysis. All operators use diverse types of hand tools but not limited to wrenches, screwdrivers, deburr knifes etc. Operator Asset Care on a regular basis such as, but not limited to, process machine maintenance. Completes rework or reprocessing, as necessary, on products rejected by process in the specification. Works with other production areas and cell leaders, as necessary, to resolve quality problems. Works following appropriate safety practices and/or JSAs to prevent accidents to self or co-workers. Know and follow all policies that apply to one's job, and maintain the highest levels of professionalism, ethics, and compliance always. Ensures that in process quality checks are completed following established quality specifications. Interface with quality and other production employees to resolve problems. Works in accordance with all requirements for manufacturing medical devices (e.g. FDA QSR, ISO 9000, ISO 13485). Completes required documentation as required by process, and inspection sheets, work instructions, and the document traceability. Lift up to 25 pounds may be required on a regular basis. Ability to learn and adhere to specific procedures according to the department training plan. Sets the standard for production performance, effective communication, promoting positive morale and supporting employee involvement programs. Works with the PP&L group to ensure completion of production schedule Partners with area supervisor on ensuring that production seats are adequately covered based on the production scheduled and that attendance events (i.e. PTO) is managed and the floor accommodated to compensate accordingly Develops and regularly reports on department metrics, including OEE, production output, equipment downtime, continuous improvement activities, safety improvements, and other departmental tracking as defined by the Business Unit. Monitors machine downtime and escalates repairs through Maximo. Monitors and maintains operating supply inventories, as assigned by supervisor Knows and follows all laws and policies that apply to one's job, and maintains the highest levels of professionalism, ethics, and compliance at all times. Partners with engineering team to ensure completion of expansion & validation activities in a timely manner, acting as subject matter expert where applicable or providing correct point of contact to operator subject matter expert. Follow all applicable EHS&S policies and procedures which includes PPE, work practices, and control measures. Promptly report EHS&S Incidents and Good Saves Complete EHS&S training and CAPAs on-time. Ensure department waste is segregated for proper disposal (recycle vs trash). Responsible for communicating business related issues or opportunities to next management level Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable. For those who 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
Stand out for this role
NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Mechanical Assembler
Thermo Fisher Scientific — Eindhoven, Netherlands
CRA (Level II)
Thermo Fisher Scientific — 2 Locations
Application Scientist
Thermo Fisher Scientific — Shanghai, China
Biostatistician II
Thermo Fisher Scientific — Beijing, China
Sr Project Mgr
Thermo Fisher Scientific — Beijing, China
Programmer Analyst
Thermo Fisher Scientific — Guangdong, China