Junin Records Management & Document Control Job Listings

Corporate & Public Affairs Intern - Bogotá64520999165057120

Indeed

Corporate & Public Affairs Intern - Bogotá

**Additional Locations:** N/A **Diversity \- Innovation \- Caring \- Global Collaboration \- Winning Spirit \- High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high\-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. **About the role** We are looking for a committed, analytical student with a strong interest in public affairs, government, legal matters, and institutional relations, who wants to learn and contribute from the private sector to the transformation of healthcare systems. **Key Responsibilities** As a Corporate, Public, and Legal Affairs intern, you will support the following: * Research on regulatory, legal, and public policy issues in Colombia, and occasionally in Ecuador and Venezuela. * Analysis of regulatory and policy documents to support company strategies. * Preparation of internal and external communications (policy memos, information alerts, presentations, letters, etc.). * Participation in meetings with stakeholders in the sector, providing support in monitoring commitments and generating input. * Support in institutional relations initiatives and industry participation. * Support in administrative processes for the area. **Requirements** * Student in the final semesters of a degree program such as Law, Political Science, International Relations, Government and Public Affairs, Public Administration, Communication, or related fields. * Interest in public affairs, government relations, regulation, and the health sector. * Excellent analytical, synthesis, and research skills. * Excellent oral and written communication skills. * Ability to work in interdisciplinary teams and with external stakeholders. * English proficiency: Proficient (oral and written). **Requisition ID:** 618924 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem\-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

WXJC+53 Cajicá, Cundinamarca, Colombia

Negotiable Salary

Indeed

Warehouse Worker,2

Performs working level duties in receiving, stores, and/or shipping functions. Stocks material/commodities in a neat, orderly way; receives, inspects, and counts incoming material/commodities; rejects damaged items, records shortages, reviews, and interprets accompanying documentation; maintains records of stock received/shipped; and/or moves materials/commodities between locations. Operates material handling, forklift and packaging equipment. 35\-60% Performs general material handling/warehousing duties involving receiving, storing, inventory, shipping, and disbursing materials/commodities; pick orders and prepare pallets for shipment; process materials using postal manifest and meter equipment; load and unload trucks; operate various powered material handling equipment i.e., forklift and pallet jack; provide some lead direction to material handlers, warehouse workers and volunteer works as assigned. 10\-20% Review and interpret shipping documents, verify quantifies, inspect for damage, determine country of origin and specific language code for international materials, and prepared receiving and inventory records; record weight and dimension figures for new items in warehouse management system. 10\-60% May drive small or medium\-sized trucks to deliver and pick up materials/commodities from vendors; assist supervisor in ensuring vehicles are properly maintained, licensed and operating safely; complete and submit logs and reports on vehicles as required. 5\-10% Assists in maintaining equipment, building, grounds, and keeps appropriate records as assigned; assist in loading 40 foot trailers for shipment or prepare pallets of assorted materials for worldwide shipping, requiring special knowledge in order to balance the load to meet weight, space and distribution requirements. High school education or equivalent required; basic math and computer skills; experience operating motorized material handling equipment including forklifts preferred; must be able to become Church certified within 6 weeks of hire; excellent interpersonal and organizational skills; must be able to read and understand English; must be able to physically lift/move/push/pull items (up to 50 lbs alone or occasionally lift up to 100 lbs with two people), climb ladders, stairs, scaffolding, and ramps to store/retrieve items, and operate a pallet jack containing up to 2500 lbs.; excellent interpersonal, organizational, training and leadership skills.

Cra 46 # 127-45, Suba, Bogotá, D.C., Bogotá, Bogotá, D.C., Colombia

Negotiable Salary

Nola Cluster Medical Director64329411160577122

Indeed

Nola Cluster Medical Director

PURPOSE The NOLA Cluster Medical Director Provides *leadership to all cross\-cluster and in\-country medical functions* and is the NOLA Cluster medical voice both *internally and externally* (acting as Pfizer CMAO in the local country environment). SCOPE The NOLA Cluster Medical Director role includes, but not limited to;* Role model of Pfizer’s values and behaviors, embracing the company’s purpose of breakthroughs that change patients’ lives * Strong record of scientific leadership, peer\-to\-peer external relations, academic and/or clinical work * Able to provide scientific guidance, insights and expertise across the broad and complex Pfizer portfolio, across different TAs * Embraces lightspeed mindset \- champions cutting the red tape, challenges the status quo, and empowers teams to do their best work * Track record of building non\-traditional, innovative medical affairs organizations at the cutting\-edge of science, medical mission, and evolving trends * Strong record of growing and maintaining high\-performing and \-functioning talent, able to build and transform low performance * Inspirational leader whom colleagues trust and look up to \- thrives on transformation and understand and articulates change Geographic area covered by the role: Colombia, Ecuador, Venezuela, Central America and the Caribbean REPORTING LINE: The NOLA Cluster Medical Director reports to EM LATAM Medical Lead ORGANIZATIONAL RELATIONSHIPS* Life science partnerships * IMI initiatives * Proactive media coverage * Serves on hospital and society boards, collaborates with industry boards MAIN REPONSIBILITIES / DUTIES* Directly leads medical affairs, ensuring operational excellence for customer\-facing medical and ensuring new and effective ways of working with global medical platforms for evidence generation, medical enablement functions, etc. * Partners with the NOLA Cluster Lead to ensure alignment with internal and external Cluster strategies and represents all medical and related functions at Cluster Leadership Team; * Represents the immediate point of reference to the NOLA Cluster Lead and One\-Medical face of Pfizer to external stakeholders, such as KOL’s, Industry Bodies, Regulatory Authorities, Government \& Payers (in partnership with appropriate functional lines) and during Business Development discussions. * Represents Pfizer medical through relationships with medical associations, societies, academic medical centres and industry associations * In partnership with Global Medical Affairs, ensures Scientific Leadership and TA expertise by rigorous training and a single global medical “truth” asset by asset * Flawlessly lead execution of g/local strategies, ensuring appropriate resource allocation to execute medical plans; Hyperfocus on priorities and activities, enabling focus on customer facing effort and impact * Collaborates with medical quality and governance teams with respect to inspections, corporate governance and related complaints * Attends, or delegates attendance to NOLA Cluster country medical leads, the respective NOLA Cluster Medical Councils (CMC) with the purpose of maintaining compliance and information flow as well as to facilitate the resolution of issues that arise within any medical teams and partner functions Education \& Experience* An M.D. (preferred) or equivalent doctoral degree * 10\+ years pharmaceutical background with team management experience * CMD experience is preferred * Teaching courses at university/academic appointments is a plus * Discussing innovation and pharma, change agile * Active member of pharmaceutical associations / patient groups * Strong business acumen with deep financial and accounting knowledge in life sciences * Budget management experience * Business decision\-making at hospitals and pharmaceutical companies * Financial impact forecasting for various stakeholder groups (patients, etc.) Location: Colombia (Hybrid office\-based position) Relocation assistance not available. EEO (Equal Employment Opportunity) \& Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability. Medical

Ac. 153 #9325, Bogotá, Colombia

Negotiable Salary

Document AI/IDP Specialist64146193347842123

Indeed

Document AI/IDP Specialist

**Document AI/IDP Specialist** We are looking for a motivated and goal\-oriented Document AI/IDP Specialist to join our team. Expert in Intelligent Document Processing who designs and implements solutions to extract, classify, and process information from unstructured documents using AI. Converts documents (invoices, contracts, forms) into structured, actionable data. ### **Key Responsibilities:** Implement Document Understanding solutions with AI Train ML models for document classification and extraction Configure and optimize OCR/ICR engines with AI Develop end\-to\-end document processing pipelines Implement intelligent validation and human\-in\-the\-loop workflows Integrate with ERP, CRM, and database systems Improve extraction accuracy through model fine\-tuning Handle multi\-language and multi\-format documents ### **Requirements:** UiPath Document Understanding, Automation Anywhere IQ Bot, or Blue Prism Decipher Azure Form Recognizer, Google Document AI, AWS Textract Computer Vision and NLP Python with OpenCV, Tesseract, spaCy and Machine learning (text classification, NER) Data annotation and labeling tools Regular expressions and data parsing JSON, XML data structures Applies to individuals located in Latin America 100% Remote Remuneration in dollars Stability and growth opportunities If you’re ready to **turn data into game\-changing insights,** we want to hear from you! Apply today.

Cl. 127b # 70D-4, Suba, Bogotá, D.C., Bogotá, Bogotá, D.C., Colombia

Negotiable Salary

RPA Developer with AI/ML64146193366019124

Indeed

RPA Developer with AI/ML

**RPA Developer with AI/ML** We are looking for a motivated and goal\-oriented RPA Developer with Artificial intelligence and Machine Learning to join our team. The RPA Developer creates and maintains robotic process automation (RPA) solutions integrated with artificial intelligence and machine learning capabilities. Designs intelligent bots that can learn, adapt, and make data\-driven decisions ### **Key Responsibilities:** Develop RPA bots using UiPath, Automation Anywhere, or Blue Prism Integrate ML models to improve automated decision\-making Implement OCR/ICR with AI capabilities for document processing Design intelligent workflows that combine rules and ML Maintain and optimize existing bots with cognitive capabilities ### **Requirements:** Proficiency in UiPath, Automation Anywhere, or Blue Prism (certification preferred) Python for scripting and ML integration Experience with REST APIs for connecting AI services Basic ML knowledge (classification, regression, NLP) Azure Cognitive Services, AWS AI Services, or Google Cloud AI SQL and database management Knowledge of Document Understanding/IQ Bot and Git for version control ### **Important** English level B2 or higher conversational (will be validated) Applies to individuals located in Latin America 100% Remote Remuneration in dollars Stability and growth opportunities If you’re ready to **turn data into game\-changing insights,** we want to hear from you! Apply today.

Cl. 127b # 70D-4, Suba, Bogotá, D.C., Bogotá, Bogotá, D.C., Colombia

Negotiable Salary

Health Outcomes Liaison (HOL) - Bogota64144776110466125

Indeed

Health Outcomes Liaison (HOL) - Bogota

**Additional Locations:** N/A **Diversity \- Innovation \- Caring \- Global Collaboration \- Winning Spirit \- High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high\-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. **About the Role:** As a Health Outcomes Liaison (HOL), you will be the interface between Boston Scientific and healthcare decision makers, ensuring our technologies are recognized for their clinical and economic value. You will translate health economics evidence into actionable insights that support reimbursement, access, and adoption of our portfolio. **Key Responsibilities:** Identify and prioritize health economics needs for BSC products in Colombia in alignment with Andean Region HEMA Strategy. Develop and execute reimbursement strategies, including coding, coverage, and health economic evaluations tailored to the Colombian system. Engage payers and hospital decision\-makers with clear, evidence\-based value messages (Clinical and Economic). Monitor and analyze health policy and reimbursement developments; provide strategic recommendations. Collaborate cross\-functionally (sales, marketing, clinical, regulatory, legal) to deliver compelling economic value communication tools. Provide internal training on health economics and market access concepts to strengthen business impact. **Qualifications:** Degree in Economics, Public Health, Epidemiology, or related field; Master’s in Health Economics preferred. 2\+ years of experience in Health Economics \& Market Access (MedTech or Pharma). Strong knowledge of the Colombian healthcare and reimbursement system. Analytical skills in economic modeling, budget impact, and policy assessment. Excellent communication skills; ability to influence diverse stakeholders. English proficiency: B2 or higher. Team\-oriented mindset; willingness to travel occasionally within Colombia. **Requisition ID:** 615213 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem\-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

2X22+22 Zipaquirá, Cundinamarca, Colombia

Negotiable Salary

Indeed

Safety Officer

Use Your Power for Purpose At Pfizer, our Worldwide Medical and Safety colleagues are essential in bridging evidence\-based medical decision support with colleagues and stakeholders to achieve better health and treatment outcomes. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically necessary expertise, or investigating ways to close data gaps, our mission remains clear. We aim to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. What You Will Achieve In this role, you will:* Monitor and manage the company's drug, biologics, and medical devices surveillance program, including adverse report intake, evaluation, and processing. * Support clinical trials and post\-marketing activities, ensuring compliance and safety. * Guide operational teams in project management, forecasting resource needs, and identifying improvement areas in products, processes, or services. * Lead or co\-lead moderately complex projects, managing time and resources effectively, and provide guidance to teams. * Apply discipline knowledge to contribute to departmental work, making decisions to resolve moderately complex problems and developing new options. * Work independently on assignments, seeking guidance on unusual or complex problems, and review your own work and that of colleagues in a mentor role. * Oversee the development and maintenance of the Country Quality Plan and guide colleagues on adverse event report processing. * Collaborate with internal and external stakeholders to support local safety activities and act as a Business Management Subject Matter Expert for Safety Evaluation and Reporting (SER). * Manage safety team resources, ensure the completion of safety\-related reports, and support audits, regulatory inspections, and related requests. * Develop and maintain expertise in assigned products, corporate policies, local regulations, and safety database functions, applying judgment and leadership to ensure continuous inspection readiness. Here Is What You Need (Minimum Requirements)* BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high School Diploma (or Equivalent) with at least 10 years of relevant experience * Experience in pharmacovigilance, data management, clinical care, or scientific research * Deep understanding of the pharmaceutical business, including drug development and regulatory aspects * Familiarity with international regulations and worldwide reporting requirements * Strong organizational and time management skills to meet strict regulatory compliance goals * Ability to solve problems and make decisions in complex situations * Proficiency in computer literacy, especially in managing relational databases * Fluency in spoken and written English Bonus Points If You Have (Preferred Requirements):* Master's degree * Relevant pharmaceutical industry experience * Managerial experience in hospital or pharmacy and familiarity with clinical assessment * Knowledge of training design and tools and experience in applying training methodology * Ability to work collaboratively with cross\-functional teams * Strong analytical and problem\-solving skills EEO (Equal Employment Opportunity) \& Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability. Medical

Ac. 153 #9325, Bogotá, Colombia

Negotiable Salary

Therapy Development Specialist | Bogotá63839665452417127

Indeed

Therapy Development Specialist | Bogotá

**Additional Locations:** N/A **Diversity \- Innovation \- Caring \- Global Collaboration \- Winning Spirit \- High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high\-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. **About the role:** The Veins (Thrombectomy and Endovascular) therapy development specialist is a clinically oriented business ambassador for a proven procedure to treat peripheral vascular disease. This role will execute thrombectomy therapy adoption initiatives. This individual is a trusted clinical partner and thrombectomy specialist to drive safe adoption, superior outcomes, and achieve sales revenue for this therapy. The Veins (Thrombectomy and Endovascular) Therapy Development Specialist practices excellent clinical/case acumen and relationship management with medical and healthcare professional clients and serves as a clinical role model across the FCS team. The position is responsible for increasing the number of patients treated and/or market share of Thrombectomy and Endovascular franchises products in Colombia, while developing and leveraging relationships with key opinion leaders/management of hospitals and medical societies. In addition to marketing initiatives, this role will be responsible for developing education and training programs for physicians and hospital staff in the thrombectomy and endovascular portfolio, including patient identification, and follow\-up procedures. **Your responsibilities will include:** * Participate in medical training, product development programs and maintain high standards of personal and professional conduct * Develop and maintain comprehensive clinical and technical knowledge of the product. Understand current events Published (thrombectomy and endovascular) and relevant literature. * Recognize and understand competitive products, industry thrombectomy and endovascular portfolio trends and portfolio. * Maintain communication with leadership and sales of the thrombectomy and endovascular portfolio by providing market intelligence and potential sales leads * Plan and implement effective clinical/product presentations to clients. * Maintains knowledge of industry, competition, healthcare and economic trends and their impact on short\- and long\-term Thrombectomy and endovascular business plans, adjusting plans and strategies as necessary to reflect market conditions. * Identify new business opportunities and accounts by developing and leveraging relationships with academic and research institutions and key opinion leaders * Works in close cooperation with the clinical specialist, and sales teams to develop and maintain working relationships with the economic buyer on key accounts in their region * Case assistance and clinical support in the operating room to ensure the correct use of technology **What We Are Looking for in You** Required qualifications: * Professional in Life sciences, Biomedical Engineering or Business Administration * Previous experience in commercial and/or clinical medical device or related experience in a hospital environment role with proven record of sales growth (\+4 years) * English Level: advanced. Minimum requirement B1/B2 * Availability for local, regional, and international travels **Skills:** * Strategic Thinking * Communication \& Negotiation Skills * Excellent verbal and written communication skills to effectively convey product information, articulate value propositions, and build rapport with healthcare professionals * Ability to comprehend complex medical device technologies and explain them in a clear and concise manner to diverse audiences * Strong interpersonal skills to establish and maintain relationships with healthcare providers, key opinion leaders, and decision\-makers * Flexibility to navigate a dynamic sales environment, adapt to changing market conditions, and overcome challenges * Self\-motivated \& enthusiastic * Data forecasting and analysis * Planning and execution to achieve objectives **Requisition ID:** 611765 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem\-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

WX88+MM Cajicá, Cundinamarca, Colombia

Negotiable Salary

Indeed

EHS Coordinator

Date Posted: 2025\-05\-19 Country: Colombia Location: LOC42001: Otis Colombia \- Bogotá Calle 140 No 12b \- 25, Bogotá Job Summary Would you like to join a truly international company, driven by talent, that values Safety, Ethics, Quality, Innovation and Employee Opportunities? Otis is growing and looking for an EHS Coordinator, who will be responsible for supporting the promotion of occupational safety and health among direct and subcontracted personnel by preventing potential accidents and/or work-related illnesses, as well as identifying factors and conditions that could endanger the physical integrity of everyone involved. Initial contract for 3 months On a typical day, your responsibilities will include:* Safety oversight during NE Installation, Modernization, or Service activities. * Supervision of compliance with safety measures by direct or subcontracted operational personnel. * Verification and approval of ART documentation prior to starting field work. * Support EHS department requirements during field activities. \* Provide support and guidance regarding customer-issued safety requests * Assist in safety inspections during field activities * Conduct site visits and follow-up according to company EH\&S guidelines * Provide documentary support for entry requirements of personnel assigned to elevator and escalator installation projects. What you'll need to succeed!* Education: Technical, technological, or professional degree in Occupational Health and Safety or related field, required for signing and approving field risk analysis documents. * License to provide services in Occupational Health and Safety. \*50-hour course in SG\-SST or 20-hour SG\-SST refresher course * Course in Safe Work at Heights Coordinator. * Advanced level course or authorized person for work at heights and/or retraining in safe work at heights * Preferably experienced in construction or civil works projects. Apply today to join us and help build the future together. \#BuildWhatsNext. If you live in a city, chances are we will give you a lift or play a role in keeping you moving every day. Otis is the world’s leading elevator and escalator manufacturing, installation, and service company. We move 2 billion people every day and maintain approximately 2\.2 million customer units worldwide, the industry's largest Service portfolio. You may recognize our products in some of the world’s most famous landmarks including the Eiffel Tower, Empire State Building, Burj Khalifa and the Petronas Twin Towers! We are 69,000 people strong, including engineers, digital technology experts, sales, and functional specialists, as well as factory and field technicians, all committed to meeting the diverse needs of our customers and passengers in more than 200 countries and territories worldwide. We are proud to be a diverse, global team with a proven legacy of innovation that continues to be the bedrock of a fast\-moving, high\-performance company. When you join Otis, you become part of an innovative global industry leader with a resilient business model. You’ll belong to a diverse, trusted, and caring community where your contributions, and the skills and capabilities you’ll gain working alongside the best and brightest, keep us connected and on the cutting edge. We provide opportunities, training, and resources, that build leadership and capabilities in Sales, Field, Engineering and Major Projects and our Employee Scholar Program is a notable point of pride, through which Otis sponsors colleagues to pursue degrees or certification programs. Today, our focus more than ever is on people. As a global, people\-powered company, we put people – passengers, customers, and colleagues – at the center of everything we do. We are guided by our values that we call our Three Absolutes – prioritizing Safety, Ethics, Quality in all that we do. If you would like to learn more about environmental, social and governance (ESG) at Otis click here. Become a part of the Otis team and help us \#Buildwhatsnext!*Otis is An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other protected class according to applicable law. To request an accommodation in completing an employment application due to a special need or a disability, please contact us at careers@otis.com.*

Cl. 140 # 12B-21, Usaquén, Bogotá, D.C., Bogotá, Bogotá, D.C., Colombia

Negotiable Salary

Indeed

METROLOGY ASSISTANT

Carry out activities related to the verification, calibration, and metrological control of measuring instruments in inspection and quality assurance processes. Interpret technical drawings, perform conversions within the International System of Units, and support related document management. Requirements: Industrial technician in Quality Control areas, preferably in Metrology, with 2 years of experience performing duties related to the position and basic knowledge in: * Basic fundamentals of metrology * Verification and calibration of instruments * Interpretation of technical drawings * Handling of manual and digital measuring instruments * Conversion in the International System of Units (SI) * Microsoft Office (basic to intermediate level) Conditions: * Schedule: Monday to Friday * Type of contract: Fixed-term directly with the company. Job type: Full-time

232M+28 Tocancipá, Cundinamarca, Colombia

Negotiable Salary