Field Clinical Rep Endo - Lima jobs at Boston Scientific in Peru, Lima

Requirements

• Experience: minimum of 2-5 years of experience in a clinical or medical field, preferably assisting with procedures, and providing technical product support.
• Business Knowledge: understanding of business and administration principles to track performance, identified business opportunities and optimize operational workflows.
• Communication Skills: Proven ability to deliver training and communicate complex technical details clearly to healthcare professionals.
• Problem-Solving: Ability to quickly assess issues during clinical procedures and provide effective solutions, also ability to work independently and collaboratively.
• Project Management: project management skills, especially in customer education programs, experience collaborating with multiple stakeholders across clinical and business units.
• Education: Bachelor’s degree in health-related discipline (life sciences, medical devices, nursing, or healthcare).
• Experience in multinational companies, with knowledge of their operational and multicultural dynamics.

Preferred Qualifications

• Business & Administrative Skills: understanding of business administration, including budgeting, scheduling, and report generation.
• Master's degree in Business Administration (MBA) or related fields
• English level (A2 or above)
• Technical Expertise: background in medical devices and clinical environments, with the ability to provide technical assistance and troubleshooting​.
• Experience in data analysis and reporting, particularly in optimizing clinical outcomes and improving efficiency.
• Familiarity with regulatory requirements and compliance in medical device use.

ABOUT THE ROLE

REQUIRED QUALIFICATIONS

• Bachelor’s degree in Life Sciences, Medicine, Nursing, Biomedical Engineering, or other health-related fields.
• 2 to 5 years of experience in the medical device industry, preferably in intragastric balloons or bariatric endoscopy.
• Proven ability to engage healthcare professionals and support product adoption through clinical evidence and technical knowledge.
• Knowledge of the endobariatric segment and experience working with bariatric surgeons, endoscopists, and gastroenterologists. Understanding of the patient journey, treatment pathways, and market dynamics for obesity interventions.
• Excellent interpersonal and communication skills with the ability to engage, influence, and build relationships with multidisciplinary clinical teams.
• Able to resolve clinical and commercial challenges in real-time, both independently and in team environments.
• Capability to understand key commercial metrics, support product positioning, and contribute to pricing and market development strategies.

PREFERRED QUALIFICATIONS

• Prior experience with intragastric balloon products or bariatric therapies.
• Background in launching new technologies or disruptive solutions in the endoscopy market.
• Strong clinical aptitude and ability to translate clinical data into commercial value.
• Familiarity with regulatory and reimbursement processes for obesity treatment devices.
• Experience in multinational companies, with knowledge of their operational and multicultural dynamics.
• Fluent in both English and Spanish (spoken and written).

About the Role:

Provide support with tasks related to the Microbiology department.

Responsibilities include:

• Coordinate and conduct Environmental Monitoring tests in Controlled Environment Rooms and accurately record data, draft and review reports, and communicate results precisely, promptly, and timely.
• Coordinate and conduct product tests such as bioburden and endotoxins, accurately record data, draft and review reports, and communicate results precisely, promptly, and timely.
• Competently use Microbiology laboratory equipment such as particle counters, incubators, and air samplers.
• Support process and laboratory equipment qualification activities , design test methods, perform intermediate-advanced statistical analyses, and correctly document and communicate results to teams. Also, define training requirements for these activities and execute the training.
• Coordinate audit activities and provide support roles during external audits: Document retriever, auditee.
• Lead failure analysis in Environmental Monitoring and product tests (i.e., significant support in CAPA activities, initiate and assist in the development and completion of NCEPs) and involve required assistance if necessary.
• Create, maintain, and update data files and forms , databases, spreadsheets, and forms, such as maintaining the laboratory records archive to ensure proper record flow, track and monitor department activities. If necessary, escalate concerns, trends, and emerging issues that need to be addressed.
• Use documentation systems to investigate information and generate document changes, as well as use scientific knowledge to read and interpret SOPs and Work Instructions to perform laboratory tests according to established laboratory requirements.
• Coordinate the receipt, acceptance, and disposal of laboratory materials and supplies.
• Identify, prioritize, and resolve quality issues identified by metrics.
• Coordinate preventive maintenance tasks on equipment and verify compliance with these tasks for the respective functional unit at the end of the week.
• Collect, preserve, analyze, and follow up on units/samples. Use good laboratory practices to ensure result accuracy. Seek appropriate help when necessary and create communication channels for required support.
• Identify and lead departmental initiatives related to best quality practices and continuous improvement.

Job Requirements:

• High School Diploma.
• Complete technical degree: Microbiology, Laboratory Technician, or otherwise, 50% of a university degree in related fields such as Biology, Biotechnology, Bioprocesses, Microbiology, Chemistry, or a related field.
• Availability to work Shift A (Monday to Friday 6:00 a.m to 3:30 p.m) at the Cartago plant.
• 5 years of experience in medical device manufacturing or pharmaceutical companies.

Technical Knowledge:

• Aseptic Technique
• Environmental Monitoring of Controlled Rooms (Viable and Non-viable)
• Product tests such as endotoxins and bioburden.
• Creation and analysis of trends in Excel and/or Power BI.
• Handling laboratory equipment for Environmental Monitoring, incubation, and product tests (Bioburden and endotoxins).

Required qualifications

• Education: University degree in Life Sciences, Nursing, Biomedical Engineering, or another health-related discipline.
• Experience: 2 to 5 years of experience in a clinical or medical settings, preferably with surgical room exposure. Proven track record in technical product support during medical or surgical procedures.
• Technical Expertise: Deep understanding of surgical clinical environments. Skilled in intraoperative support, troubleshooting, and use of advanced medical technologies.
• Communication Skills: Demonstrated ability to train, educate, and communicate effectively with healthcare professionals, translating technical information into clinical value.
• Problem-Solving: Ability to quickly assess issues during clinical procedures and provide effective and proactive solutions, also ability to work independently and collaboratively.
• Business curiosity: Commercially curious, able to identify clinical opportunities that translate into competitive advantages.
• Project Management: Strong organizational skills and ability to manage multiple clinical support and training initiatives across diverse stakeholders.

Preferred qualifications

• Experience analyzing clinical data and outcomes.
• Familiarity with healthcare regulations and compliance.
• Understanding of hospital systems, market access pathways, and local healthcare dynamics.
• Previous experience in multinational healthcare companies.