דרושים Microbiologist Iii ב-Boston Scientific ב-קוסטה ריקה

Costa Rica-Heredia

About the role:

Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.

Your Responsibilities Include:

• Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments.
• Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
• Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
• Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.
• Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor.
• Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.
• Acts independently to implement and follow through.
• Perform root cause analysis of failed product.
• Participates in project planning and scheduling.
• Optimize processes for yield improvements, cycle time improvements, and scrap reduction.
• Attends and contributes to product core team meetings.
• Performs responsibilities required by the Quality System and other duties as assigned or requested.

What we're looking for:

• Bachelor or Licenciature degree in Mechanical, Electromechanical, Electronic, Electrical Industrial Maintenance or related.
• Experience: At least 3 years
• English Level desired: 70-79%
• Technical Competencies: Problem Solving, Networking, Process Improvement, Lean manufacturing and Six Sigma knowledge, Process Validations.
• Knowledge of the Lab View programming
• Knowledge of automated vision systems
• Work Mode: Onsite.

Benefits • Life-Work Integration • Community • Career Growth

工作职责：

• 负责区域内客户的手术支持工作并培训相关医院技师，使其能独立配合客户开展手术。
• 与负责区域内的客户建立良好的合作关系，推动区域手术例数及相关产品的应用。
• 为客户提供专业的学术支持，培养并提升客户的手术技能。
• 在直属经理的指导下制定相应的区域管理计划，更好的推动区域手术例数及相关产品的应用。

岗位要求：

• 统招本科及以上学历，2年以上医疗器械工作经验，外企优先；
• 良好的自我驱动力及较强的学习能力
• 良好的沟通技巧、人际交往能力以及团队协作精神
• 诚信，有责任心，富有激情，有创造力，有良好的工作抗压能力
• 能接受高强度跟台，具有电生理相关行业经验者优先

Hybrid Roles:

About the Role:

Provide oversight of Microbiology Department for the sustaining operation, support projects requiring microbiology evaluation or testing. Under the direction of the Microbiology Manager, this position will serve as senior matter expert on microbiology, assuring the product meets documented requirements and that processes are controlled and providing support and guidance in the areas of cGMP, Regulatory, technical investigations.

Your Responsibilities Include:

· Strong knowledge of microbiology test methods, standards and regulations governing the quality system and microbiological topics.

· Review and assess from a microbiology context all changes that impact product or the cleanroom environment.

· Support new product development by participating as the microbiology functional team member and represent the Microbiology department on cross-functional project teams as required.

· Support Regulatory submissions by conducting review to ensure appropriate microbiology information is present in the submission.

· Review test reports from internal, external testing for compliance to BSC and external compliance requirements.

· Ensures that products are validated for bioburden and endotoxin testing and support the establishment of routine sampling plans.

· Support Internal/External Audits and ensures all non-conformances are adhered to in a timely manner.

· Provide technical guidance/troubleshooting in the event of Microbiology related issues.

· Act as Quality Engineer for Facilities related matters.

· Revise SOPs and support maintenance of product and environmental documentation.

· Support product bioburden alert limits and cleanroom air and surface alert and action limits periodical revision.

· Organizes and presents data/ information to influence decision making, primarily to internal audiences

What We’re Looking For:

• Degree in Microbiology, Biotecnology or related field.

• At least 3 years of experience in similar position.

• English Level desired: 80-89%.

Benefits • Life-Work Integration • Community • Career Growth

Our Graduate Programme is designed to accelerate your professional development and provide you with extensive experience within Boston Scientific Clonmel. Throughout the 23 month programme, you will be provided with dedicated mentors and will have professional development 1:1 meetings to provide you with a solid foundation for a successful career. Our Graduate Programme is created around hiring the most innovative and best individuals, while Boston Scientific Clonmel provides the means for you to continuously learn and enhance your skill set to drive your career growth.

Responsibilities

• Works as part of the Global Team to assist in creation and monitoring of project plans, communication and documentation of ways of working (standard processes).
• Works on the Global Implementation of a new Enterprise Resource Planning (ERP) tool SAP S4 HANA.
• Works in the JIRA system to update data on project progress
• Works using Agile & Waterfall project management tools
• Conducts her/ himself as a regular full-time member of the staff by accepting and adhering to Boston Scientific's rules and regulations and by engaging in professional and personable conduct at all times with staff and customers. The intern is also obligated to comply with any confidentiality and professional policies established by the Boston Scientific.
• Becomes knowledgeable about her or his own responsibilities and the business and operational issues inherent in them as well as about the Boston Scientific's management and particular issues relevant to the Company.
• Contributes to the preparation and production of proposals and reports by using word processing, spreadsheets, and other computer programs.

Required

• BSc degree (Honours) in relevant discipline essential.
• Must have graduated within the last two years or in final year of University
• Relevant work experience/ co-op programme completed.
• Eligible to work in IrelandCommunication Skills
• Project Management Skills

** 23 Month Contract ** Closing Date 27th November

Should you require a reasonable accommodation during the recruitment process or after if offered, please let us know.

Costa Rica-Heredia

Your Responsibilities Include:

• Responsible for Manufacturing Engineering of a given area.
• Works with Value Stream and Quality Engineering Manager to deliver business objectives – lean manufacturing metrics, VIP, cycle time, scarp as %VOP etc.
• Responsible for developing a world class-manufacturing group that is proficient in problem solving manufacturing issues using Six-Sigma tools.
• Drives IBP (Integrated Business Plan) contract deliverables by providing input on process technology selection.
• Develops and executes departmental budgets and capital spending.
• Leads or represents function in periodic business metric reviews.
• Initiates cross-functional partnerships to identify and resolve production/engineering issues.
• Prioritizes and drives execution of multiple complex department projects. Sponsors and supports Operations Value Improvement Process (VIP) or Strategic Activity Review (STAR) projects.
• Responsible for the departmental basics including budgeting, hiring, day-to-day management, project resourcing, etc.
• Establishes and supports a work environment of continuous improvement that supports BSC’s Quality policy, Quality System & the appropriate regulations for the area.
• Ensures employees are trained to do their work and their training is documented.
• Maintain compliance metrics around adherence to preventative maintenance schedule and calibration schedule.
• Ensure relevant documentation is prepared and updated in line with all Quality and Regulatory guidelines and promotes full compliance to all GMP & ESQ requirements.
• Keep abreast of all relevant technological advancements.
• Maintain and develop the team’s technical and trouble shooting skills.
• Sustain an environment of continuous improvement.
• Develop and maintain relationships with technical management in sister sites and R&D.
• Develop new equipment/processes as necessary.
• Develop and implement the appropriate maintenance procedures and protocols to ensure processes always remain in control.
• Oversee the specification and purchase of capital equipment ensuring balance between optimizing technological capabilities and return on investment.
• Manage the planning and execution of equipment validations per ESQ requirements.
• Providing technical leadership on maintenance and equipment issues.
• Provide effective and responsive Calibration support to Operations to meet their area’s objectives of quality, cost and output.

What We’re Looking For:

• Bachelor’s degree in Mechanical, Electromechanical, Electronic, Electrical Industrial Maintenance or related field.
• English Level: B2 (70% - 79%).

• Desired knowledge: Equipment Maintenance, Process Validations, Execution, Decision-making, Planning, Communication, Quality Oriented, Relationship Building, Innovation
• At least 3 years of experience in similar position.
• 1 year or more in current position.
• Annual Performance evaluation rating "Meets Expectations" or "Exceeds Expectations".

Costa Rica-Heredia

Hybrid Roles:

About the role:

To develop, implement, and ensure continuous improvement of the Environment, Health and Safety (EH&S) systems. The primary purposes of these systems are: 1) maintaining compliance with the requirements of Boston Scientifics’ corporate EH&S policies and requirements and all applicable national, state, and local regulations, 2) driving EH&S performance improvements across the site, and 3) capturing and communicating information describing EH&S roles, responsibilities and contribution. 4) Lead the direct reports under him/her. This position will report directly to the EH&S Supervisor

Your Responsibilities Include:

• Main responsible for Safety, Emergency Response and Occupational Health programs implementation and programs health for the Business/Facility assigned.
• Local Safety/ER/OH regulations compliance.
• Definition and documentation of Safety/IH & OH indicators.
• Incidents & Injuries Investigations support.
• EHS Engineer will be the main responsible of several Safety/ER & OH Programs as requested (program owner).
• Develop and implement new EH&S programs, policies, procedures, and training related to field of expertise.
• Maintain and report site EH&S metrics, statistics and records to maintain compliance with regulatory requirements, systems and fulfill Corporate reporting and information needs.
• Support management to reduce work place injury frequency and severity rates.
• Advocate for EH&S as a core value of Boston Scientific, and provide regular communications within the EH&S team regarding EH&S activities and performance.
• Chair or serve on EH&S-related committees, task forces and/or cross functional teams as applicable.
• Conduct EH&S compliance audits, self-assessments, and inspections throughout the facilities.
• Conduct and/or coordinate periodic industrial hygiene, safety, and environmental sampling/testing.
• Conduct chemical and MSDS risk assessments, as well as operations risk assessments to specify engineering controls, and other regulatory requirements as applicable.
• Identify hazardous workplace conditions and establishes guidelines for compliance, risk and injury reduction.
• Takes effective steps to ensure that workplace conditions comply with applicable local, national and state regulations.
• Provide regulatory guidance and recommendations for equipment specifications/installations, and facilities modifications.
• Participate in regulatory inspections and serve as liaison with regulatory agencies.
• Specify requirements and develop systems to ensure on-going operational permits compliance.
• Serve as EH&S representation in cross functional operation projects for new process/chemical introduction, capacity expansion, facility changes, new equipment introduction, etc.
• May be responsible for the implementation of the Environmental, Health and Safety Management System. (ISO 14001 and ISO 45001).
• May be main responsible for Carbon Neutral System for the Business/Facility assigned.
• According to the academic profile may be main responsible for the Chemical Regency.
• True Zero Waste

What We’re Looking For:

• Bachelor’s degree in Occupational Safety, Health or Environmental Engineering or related.
• Experience: At least 3 years.
• English Level desired: 80%.
• Desired knowledge: Problem Solving, Knowledge of OSHA, EPA, NFPA, DOT, ANSI regulations/guidelines required.

Benefits • Life-Work Integration • Community • Career Growth