About the company igc pharma sas, is based in bogota and is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young, ... ver más job description a sales development representative (sdr) is typically responsible for the early stages of the sales process, focusing on prospecting, lead generation, and qualifying potential clients for the sales team. also a strong focus on creating customer service strategy, customer follow-up and offering customer service solutions in white label, private label, etc. activities description identify and reach out to potential private label and white label clients in the u.s. market. develop the service strategy for the client in terms of holistic solutions in white label, private label, etc., together with the follow-up, advice and support to the client in order to obtain the solution required by the client. act as a salesperson by pitching the company’s manufacturing capabilities to prospective clients. have a deep understanding of the products being manufactured, including features, benefits, compliance, and customization options. educate clients on product options and manufacturing capabilities. develop tailored proposals that align with client needs, including moqs, quotes, packaging options, and timelines. negotiate contracts and terms to close deals effectively. build and maintain strong relationships with clients, ensuring repeat business and long-term partnerships. serve as the main point of contact for client...
Quality control analyst 1886444973 about the company: igc pharma sas, based in bogota, is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young company... job description: the quality control analyst will coordinate and oversee all quality control activities at igc pharma, working closely with our third-party laboratory to ensure that all raw materials, in-process samples, and finished pharmaceutical products meet the required internal specifications. the role involves reviewing analytical data, managing product release processes, and ensuring compliance with cgmp 211, regulatory requirements, and company quality standards. this position will report to the quality assurance (qa) lead and collaborate cross-functionally with manufacturing and regulatory teams. key responsibilities: coordinate third-party laboratory interactions, ensuring timely and accurate testing of raw materials, intermediates, and finished products. review and translate from english to spanish method validations /verifications/scopes/challenges. review and approve laboratory test results, certificates of analysis (coas), and investigations related to out-of-specification (oos) results or deviations. ensure compliance with gmp, regulatory guidelines (e.g., fda, ema), and internal quality policies by monitoring qc activities. coordinate product release processes by verifying all quality documentation and ensuring specifications are met before distribution. assist in stability s...
About the company igc pharma sas, is based in bogota and is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young, ... ver más job description a sales development representative (sdr) is typically responsible for the early stages of the sales process, focusing on prospecting, lead generation, and qualifying potential clients for the sales team. also a strong focus on creating customer service strategy, customer follow-up and offering customer service solutions in white label, private label, etc. activities description identify and reach out to potential private label and white label clients in the u.s. market. develop the service strategy for the client in terms of holistic solutions in white label, private label, etc., together with the follow-up, advice and support to the client in order to obtain the solution required by the client. act as a salesperson by pitching the company’s manufacturing capabilities to prospective clients. have a deep understanding of the products being manufactured, including features, benefits, compliance, and customization options. educate clients on product options and manufacturing capabilities. develop tailored proposals that align with client needs, including moqs, quotes, packaging options, and timelines. negotiate contracts and terms to close deals effectively. build and maintain strong relationships with clients, ensuring repeat business and long-term partnerships. serve as the main point of contact for cl...
Quality control analyst 1886444973 about the company: igc pharma sas, based in bogota, is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young company... job description: the quality control analyst will coordinate and oversee all quality control activities at igc pharma, working closely with our third-party laboratory to ensure that all raw materials, in-process samples, and finished pharmaceutical products meet the required internal specifications. the role involves reviewing analytical data, managing product release processes, and ensuring compliance with cgmp 211, regulatory requirements, and company quality standards. this position will report to the quality assurance (qa) lead and collaborate cross-functionally with manufacturing and regulatory teams. key responsibilities: coordinate third-party laboratory interactions, ensuring timely and accurate testing of raw materials, intermediates, and finished products. review and translate from english to spanish method validations /verifications/scopes/challenges. review and approve laboratory test results, certificates of analysis (coas), and investigations related to out-of-specification (oos) results or deviations. ensure compliance with gmp, regulatory guidelines (e.g., fda, ema), and internal quality policies by monitoring qc activities. coordinate product release processes by verifying all quality documentation and ensuring specifications are met before distribution. assist in stability...
About the company: igc pharma sas is based in bogota and is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young company dedicated to advancing innovative treatments to improve patient outcomes. as part of our commitment to advancing pharmaceutical innovation, we are currently seeking a motivated clinical operations associate to support our clinical trial operations team in bogotá, colombia. this is a great opportunity to start or advance your career in clinical trial operations in an exciting and impactful industry. job description: the clinical operations associate will play a key role in supporting the clinical trial process, ensuring smooth and compliant trial operations. working closely with senior clinical staff, including clinical trial managers, this position provides essential support in the day-to-day management of clinical trials. key responsibilities: trial support: assist with the preparation, execution, and oversight of clinical trials, ensuring adherence to trial protocols and regulatory guidelines. documentation and compliance: support the management of essential clinical trial documentation, ensuring completeness, accuracy, and compliance with regulatory requirements (e.g., gcp, ich). communication: serve as a liaison between the clinical trial team, external partners, and clinical trial sites to ensure smooth communication and prompt resolution of issues. logistical coordination: coordinate logistics related to clinical trials...
Information security manager about the company: igc pharma sas is based in bogota and is a subsidiary of an nyse-listed u.s. start-up clinical-stage pharmaceutical company that focuses on preventing and managing alzheimer’s and other cns diseases. we are an exciting, young, diverse workplace with excellent benefits. overview: we are seeking a highly experienced and strategic information security manager to lead our cybersecurity initiatives. the ism will be responsible for developing and implementing a comprehensive information security program, ensuring compliance with regulations, and managing risks across the organization. key responsibilities: develop and maintain the enterprise-wide security strategy. oversee security operations and incident response. ensure compliance with iso 27001, gdpr, fda, and other standards. lead the security awareness and training programs. manage risk assessments and vulnerability management. collaborate with senior leadership to integrate security into business operations. qualifications: bachelor’s in computer engineering, it, cybersecurity, or related field (master’s preferred). 10+ years of experience in information security, with 5+ years in leadership roles. certifications like cissp, cism, or cisa preferred. strong knowledge of security frameworks (iso 27001, nist, etc.). language required: english, b2 or above. why join us? if you are looking for a role that allows you to grow professionally in information security management, working with a dynamic team and having opportunities to learn and apply new skills, this is your opportunity....
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