9 Clinical Supplies Jobs nearby Sonipat

Pathology Lab Technician is responsible for assisting pathologists and medical technologists in the preparation, testing, and analysis of tissue, blood, and other bodily samples. The technician ensures that all laboratory procedures comply with medical standards and safety regulations, contributing to accurate and timely diagnoses.  Key Responsibilities: Collect, label, and process tissue, blood, and fluid specimens for examination. Operate and maintain laboratory equipment such as microscopes, centrifuges, and analyzers. Prepare slides and specimens for microscopic analysis. Assist pathologists in performing gross and microscopic examinations. Record and maintain detailed and accurate data of all tests and procedures. Ensure samples are properly stored and disposed of according to protocols. Maintain a clean and sterile laboratory environment. Monitor quality control and safety compliance. Participate in inventory control of lab supplies and reagents. Assist in preparing diagnostic reports and documentation.

As a Clinical Research Monitor / CRA / Site Monitor, your role involves coordinating clinical studies and taking responsibility for study execution, monitoring, site training, and close-out. You will have the following key responsibilities: - Managing the execution of clinical trial projects from initiation to closeout across multiple projects, sites, and teams. - Managing site relationships to ensure compliance with regulations, budgets, and timelines. - Providing operational insights to ensure compliance with Protocol, SOPs, policies, and practices. - Collaborating with project teams and sponsors. - Handling site qualification, contract negotiation, IRB/EC submissions, study initiation, monitoring, and site close-out. - Providing training and oversight to site staff. - Conducting periodic reviews of site-level KRIs. - Early identification and escalation of site-level risks/issues during study conduct. - Maintaining the Trial Master File (TMF). - Coordinating study supplies, biospecimen management, and stakeholder coordination. - Resolving data queries. - Supporting audit readiness and preparations. - Preparing study progress and performance metrics. - Traveling to investigative sites (up to 25% of the time). Desired Candidate Profile: - Rich experience in clinical research operations and project management, preferably in global clinical trials. - A degree in medicine, pharmacy, or life sciences. - In-depth understanding of clinical research regulations, industry standards, and GCP. - Excellent verbal and written communication skills. - Proficiency in using MS Word & MS Excel. This is a full-time position with a day shift schedule. The work location is in person.,

As an Area Sales Manager (ASM) in the Medical Equipments / Healthcare industry located in Haryana, your primary role involves leading and managing sales operations within assigned cities or districts. You will be responsible for developing and maintaining relationships with dealers, hospitals, clinics, and healthcare professionals to drive revenue growth through strategic sales initiatives. Key Responsibilities: - Develop strong relationships with channel partners, hospitals, clinics, doctors, and procurement departments. - Achieve or exceed sales targets and KPIs set by the National Sales Manager. - Monitor and analyze sales performance metrics and market trends within the assigned territory. - Collect and report customer feedback, product usage trends, and competitor activities to marketing and product teams. - Support training and development of team members to ensure product knowledge and sales excellence. - Plan and conduct product demonstrations, clinical evaluations, and training sessions for healthcare professionals. - Coordinate with the logistics and supply chain teams to ensure timely product availability. - Maintain accurate sales records, reports, and forecasts. Qualifications & Skills: - Bachelor's degree in Life Sciences, Pharmacy, Business, or a related field. - 3-6 years of experience in medical device/pharma/healthcare sales, with at least 1 year in a supervisory role (for ASM). - Strong understanding of the healthcare ecosystem and buying behavior in hospitals and clinics. - Excellent communication, negotiation, and team management skills. - Ability to travel extensively within the assigned territory. - Proficiency in MS Office. In addition to the above responsibilities and qualifications, you can expect competitive base salary along with performance-based high incentives as part of the compensation package. This is a full-time position with day shift schedule and performance bonus opportunities. The work location is in person.,

Role Overview: As a Staff Nurse at Care Medical Hospital in Saudi Arabia, you will play a crucial role in providing high-quality patient care while adhering to hospital standards, clinical guidelines, and Saudi Ministry of Health regulations. Your compassionate nursing practice, strong clinical knowledge, and ability to work in a multidisciplinary medical environment will be essential in ensuring the well-being of patients under your care. Key Responsibilities: - Provide direct patient care by conducting assessments, performing nursing procedures, administering medications, and monitoring vital signs. - Assist doctors during examinations, treatments, and medical procedures. - Maintain accurate and timely patient records, charts, and reports. - Ensure proper infection control, hygiene, and safety standards are upheld. - Monitor patient condition closely and promptly report any changes to the physician. - Handle emergency cases and offer first-line care when necessary. - Prepare patients for diagnostic tests and assist in clinical procedures. - Manage medical equipment and ensure proper sterilization processes are followed. - Educate patients and their families on treatment plans, post-care instructions, and preventive health practices. - Offer compassionate emotional support to patients and their relatives. - Maintain patient confidentiality in accordance with hospital and regulatory guidelines. - Ensure nursing practices align with Saudi Ministry of Health standards. - Organize the nursing station and ensure the availability of necessary supplies. - Participate in hospital quality improvement programs and training sessions. Qualifications Required: - Bachelor's Degree or Diploma in Nursing. - Valid Nursing License. - Preference for Saudi Prometric & Dataflow certifications (or willingness to complete). - Minimum 3 years of clinical experience in a hospital or medical center. - Experience in ER, ICU, Ward, OPD, or any specialty is advantageous. - Strong clinical and patient care skills. - Proficient in English communication (Arabic is a plus). - Ability to thrive in a fast-paced hospital environment. - Team player with empathy and professional work ethics. Additional Company Details (if applicable): (Omit as no additional details provided in the Job Description),

As a Senior Associate, Operations at our tech-enabled global provider network, your role is to support the stability, compliance, and efficiency of our provider network across global markets. You will be responsible for driving regular provider supply planning, regulatory & compliance readiness, and overall cost efficiency analysis to ensure the right providers are available at the right capacity and sustainable economics. **Key Responsibilities:** - Build regular provider supply and demand plans aligned with pipeline forecasts, service launches, and utilization trends. - Collaborate with the Engagement and Recruitment teams on hiring goals and backfill coverage. - Monitor capacity signals across markets and identify early risks with clear mitigation actions. - Review and refine cost assumptions, skill-mix planning, and hiring recommendations to enhance efficiency across markets. - Support regulatory and compliance operations by monitoring regulatory requirements and provider credential needs. - Work with Legal and Clinical teams to embed credentialing and regulatory checks correctly in workflows. - Assist in the rollout of new SOPs, compliance updates, or regulatory processes for clarity and adoption. - Maintain organized documentation, decision logs, compliance checklists, and operational references for audit readiness. - Analyze cost per session trends, utilization patterns, and incentive impacts to maintain overall cost efficiency. - Define clear operational standards and metrics for availability, supply planning, compliance, and cost efficiency. - Lead project management within the Ops team to ensure timelines, dependencies, risks, and requirements are on track, especially for new deal launches. - Assist in operational readiness for service expansions, new geographies, and high-priority commercial deployments. - Prepare monthly operational updates summarizing progress, risks, trends, and recommended improvements. - Utilize dashboards and raw data to uncover patterns, validate assumptions, and guide operational decisions. - Coordinate cross-functional investigations for availability, compliance, or capacity-related issues and ensure closed-loop resolutions. - Review and refine operational processes to stay aligned with best practices, regulatory changes, and evolving business needs. **Qualifications Required:** - Experience: 3-6 years in operations, regulatory/compliance ops, marketplace ops, or similar fields in a tech startup. - Regulatory Awareness: Basic understanding of credentialing or regulatory checks in healthcare or service delivery environments. - Analytical Skills: Ability to interpret data, build basic models & dashboards, and extract meaningful efficiency insights. - Technical Proficiency: Strong with Google Sheets; familiarity with compliance tools or data dashboards is a bonus. - Project Management: Experience coordinating cross-functional projects and ensuring successful, timely go-lives. - Organization & Planning: Strong ability to manage multiple workstreams and maintain clean documentation. - Problem-Solving: Comfortable breaking down operational or compliance issues and recommending practical solutions. - Communication Skills: Clear and structured communicator in both written and verbal formats. - Detail Orientation: High attention to detail in compliance checks, planning inputs, and documentation. - Adaptability: Thrives in dynamic environments and adjusts quickly to evolving operational needs. Please note: This is not a BPO role. It is an in-house operations position within a tech-enabled global provider network. **Additional Company Details:** - Global company with a diverse environment comprising individuals from nearly 20 countries. - Generous leave policy, including Christmas week off, birthday leave, and quarterly mental health days. - Flexible work arrangements and a culture that values work-life balance and long-term wellness. - Comprehensive medical coverage, performance bonuses, and a development budget for professional growth. - Mental health support with access to premium coaching and resources. - Regular non-work events/activities to foster social connections and fun within the team.,

Role Overview: As a Sales Admin, your prime purpose is to participate in the day-to-day business operations to provide excellent customer service efficiently. Your role involves meeting the needs of both external and internal customers, as well as supporting business growth. This includes tasks ranging from order entry to invoicing, claim and return handling, providing information and support, processing orders within a timely manner, and offering prompt solutions to problems and queries. Key Responsibilities: - Provide prompt and accurate invoicing for customers, internal, and external partners - Process all orders received in the region through various channels like phone, fax, e-procurement, etc., including invoicing processes - Manage the outbound process while ensuring prioritization effectiveness and neutrality - Communicate with customers via phone, email, or fax as necessary - Maintain the accuracy of invoiced data and ensure compliance with SOPs, accounting rules, local regulations, and SOX requirements - Coordinate product returns within approval guidelines - Monitor and analyze backorder situations, taking appropriate actions as per SOP - Interface with local selling units and departments of the Pacific Region - Collaborate with departments such as FIN, IT, HR, and QA/RA - Possess knowledge of Customer Service, Order Processing, supply chain issues, logistics, and business administration - Comfortably handle ERP-based and web-based order processing - Understand the impact of applications on logistics, supply chain processes, and business administration/accounting with a customer-oriented focus Qualifications Required: - Graduation/Bachelor's degree in Business or Customer Service - Minimum of 1-2 years of experience in a similar customer service role - Working experience with SAP system and SFDC - Proficiency in standard MS Office and collaboration tools About the Company: Bio-Rad, a global leader in life science and healthcare products, has been advancing the discovery process for 70 years. They are committed to developing, manufacturing, and marketing high-quality research and clinical diagnostic products to help people live longer, healthier lives. Voted as a Best Place to Work, Bio-Rad offers a collaborative employee experience that empowers individuals to drive impactful change and build successful careers. (Note: Omitted the benefits and EEO statement sections as per the provided instructions.),

You will be part of a team at Clinikally that is dedicated to simplifying skin and hair care with effective products. Working closely with dermatologists, you will contribute to creating scientifically-backed products using high-quality ingredients. The aim is to boost confidence by bridging the gap between clinical dermatology and everyday skincare through data, science, and design-led innovation. In this role, your key responsibilities will include: - Managing vendor relationships, queries, discrepancies, and ensuring compliance and documentation accuracy. - Collaborating with procurement, warehouse, and finance teams to align processes and ensure smooth operations. - Identifying and leading process optimization initiatives to enhance P2P efficiency and minimize delays. We are seeking individuals who possess: - Previous experience with ERP / procurement systems such as Oracle, Business Central, etc. - Strong vendor management, coordination, communication, and problem-solving capabilities. - Exceptional attention to detail and a robust analytical mindset. - A Bachelor's degree in Finance, Commerce, Supply Chain, or a related field. If you join us, you can expect to work in a dynamic startup setting, where you will have the chance to influence the creative direction of a growing brand. You will collaborate with a team of passionate, ambitious, and creative individuals. Moreover, you will have the freedom to experiment, learn, and develop alongside us. For more information about Clinikally, you can visit our website at [https://www.clinikally.com/](https://www.clinikally.com/). Connect with us on Instagram at [www.instagram.com/clinikallyofficial/](www.instagram.com/clinikallyofficial/).,

Role Overview: You will be responsible for implementing and integrating ESG (Environmental, Social, and Governance) strategies aligned with business objectives and global standards in a healthcare setting. This role involves ESG strategy development, reporting, compliance, environmental management, social initiatives, stakeholder engagement, and data analytics. Key Responsibilities: - Implement ESG roadmap aligned with business objectives and healthcare-specific standards - Integrate ESG considerations into operational, clinical, and supply chain decision-making - Conduct ESG risk and opportunity assessments, including climate risk and social impact - Conduct employee induction programs as per approved training modules - Ensure ESG disclosures are in line with relevant standards - Prepare responses for ESG rating agencies - Track and improve performance on energy, water, waste, emissions, and biomedical waste management - Monitor employee well-being, occupational health, diversity & inclusion, patient safety, and community health initiatives - Engage with rating agencies, regulators, investors, and industry bodies - Collect, validate, and analyze ESG data across various facilities - Develop dashboards and KPIs for ESG monitoring Qualifications Required: - Masters in Environmental Science or Sustainability - Bachelors degree in Environmental Science, Sustainability, Engineering, Business Administration, or related field Additional Company Details: The company encourages applicants with 3-4 years of experience in ESG and Sustainability to share their resumes at shobha@maxhealthcare.com.,

As a Front Line Medical Sales Manager at Ruokamill based in Gurugram, your role will be crucial in leading the expansion of Ruokamills across Delhi NCR. Your main focus will be on achieving sales targets, driving product prescriptions, and building strong relationships with healthcare professionals to establish Ruokamill as a trusted name in advanced nutrition. **Key Responsibilities:** - Develop and implement territory-specific sales strategies to meet and exceed monthly and quarterly targets. - Build and nurture strong relationships with healthcare professionals and key opinion leaders. - Engage HCPs in detailed scientific discussions and offer nutrition-based patient solutions. - Organize and support clinical education programs and training workshops. - Analyze market dynamics, identify growth opportunities, and report actionable insights. - Collaborate with distribution and channel partners to ensure seamless supply and execution. - Drive new account acquisition and expand market presence in key hospital and clinic setups. **Qualifications Required:** - Proven experience in medical or healthcare sales (nutrition, pharma, or hospital accounts preferred). - Demonstrated ability to independently manage KOL relationships and drive results. - Strong analytical, communication, and territory management skills. - Bachelor's or Master's degree in Pharmacy, Nutrition, or Life Sciences. - 12 years of field experience in nutrition or healthcare product sales. - Experience launching new products or territories is an advantage. At Ruokamill, we are redefining everyday nutrition by bringing science, transparency, and taste together for better health outcomes. If you're passionate about healthcare, nutrition, and driving meaningful growth, this is your opportunity to be part of something transformative.,

As a Supplier and Contract Management professional at Piramal Pharma Solutions (PPS), you will play a crucial role in ensuring the success of critical engineering projects by effectively managing key suppliers and contracts. Your responsibilities will include: - Identifying, evaluating, and managing key suppliers to establish strong partnerships, maintain quality standards, and ensure on-time delivery for engineering projects. - Overseeing contract negotiations, including terms, pricing, service levels, and risk management provisions. - Establishing risk management frameworks for supplier relationships to ensure contingency planning and risk mitigation. You will work closely with legal and procurement teams on contract development, review, and execution to ensure compliance with corporate policies and regulatory standards. Additionally, you will collaborate with engineering, project management, finance, and legal teams to support project timelines, budget constraints, and compliance requirements. In your role, you will drive cost savings and value creation through strategic sourcing, supplier negotiations, and process improvements. You will also be responsible for overseeing the budget for procurement-related expenses and tracking performance metrics to report to executive leadership. As a part of the Piramal Pharma Solutions team, you will champion sustainable and ethical sourcing practices to align with the company's environmental, social, and governance (ESG) goals. Moreover, you will ensure compliance with all relevant legal, regulatory, and corporate policies across procurement activities. Qualifications: - Bachelor's degree in engineering (Civil / Mechanical / Production / Electrical etc.) - Preferably a Master's in Business Administration (MBA) or a Master's in Supply Chain Management Relevant Experience: - 15+ years in engineering & projects procurement within Pharma / Healthcare sector - Experience in managing sourcing efforts across multiple sites or international geographies About Us: In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. The Piramal Group is committed to inclusive growth and ethical practices. Equal Employment Opportunity: Piramal Group is an equal opportunity employer that makes employment decisions based on merit, qualifications, skills, and achievements. We ensure equal opportunity in all personnel matters, including recruitment, selection, training, promotion, compensation, and working conditions. About The Team: Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end solutions across the drug life cycle. PPS serves customers globally through a network of facilities in North America, Europe, and Asia, providing a comprehensive range of services in drug discovery, process development, clinical trial supplies, API commercial supply, and more. With a track record of excellence, PPS is a trusted partner for innovators and generic companies worldwide.,

As a Full Stack Developer with minimum 2 years of experience in Angular and .NET Core, you will be responsible for revolutionizing clinical trials through configured Interactive Response Technology (IRT) platform at ClinRT Global Services. Your mission will be to accelerate drug development by enhancing clinical trials efficiency, accuracy, and compliance. Your role will involve streamlining patient interaction, randomization, drug supply management, and data management to make the whole process seamless. **Key Responsibilities:** - Develop Quality Management System (QMS) for Clinical IRT Platform/System including SOPs, CSV, Deviation, Change Control, CAPA, Validation & Qualification, Training, etc. - Drive continuous improvement of Quality Management Systems (QMS) and processes. - Implement Clinical QA plans for IRT platform to meet GCP quality standards, policies, and procedures. - Serve as the QA Subject Matter Expert for cross-functional team meetings regarding quality matters. - Lead non-compliance event investigations related to IRT platform and CAPA implementation. - Prepare for regulatory/customer/sponsor inspections and act as a subject matter expert for inspectors. - Support and provide leadership in clinical audit activities for internal and external parties. - Coordinate and participate in the evaluation and selection of external vendors for clinical trials. **Qualifications Required:** - Bachelor's degree in a scientific area with 5-7 years of clinical quality assurance experience. - Minimum of 3 years of clinical auditing/oversight experience in the regulatory compliance environment. - Knowledge of CSV. - Excellent communication and negotiation skills. - Strong attention to detail and respect for accuracy of information. - Thorough understanding of applicable US and international GCP regulations/guidelines. - Intermediate to advanced software skills (e.g., Microsoft Excel, PowerPoint, Microsoft Project). - Ability to work effectively in a cross-functional team environment. If you are passionate about building cutting-edge web applications and meet the qualifications mentioned above, we encourage you to apply for the position of Clinical QA Manager at ClinRT Global Services by sending your resume and cover letter to swati@clinrtglobal.com with the subject line: "Clinical QA Manager Application - [Your Name]." As a Full Stack Developer with minimum 2 years of experience in Angular and .NET Core, you will be responsible for revolutionizing clinical trials through configured Interactive Response Technology (IRT) platform at ClinRT Global Services. Your mission will be to accelerate drug development by enhancing clinical trials efficiency, accuracy, and compliance. Your role will involve streamlining patient interaction, randomization, drug supply management, and data management to make the whole process seamless. **Key Responsibilities:** - Develop Quality Management System (QMS) for Clinical IRT Platform/System including SOPs, CSV, Deviation, Change Control, CAPA, Validation & Qualification, Training, etc. - Drive continuous improvement of Quality Management Systems (QMS) and processes. - Implement Clinical QA plans for IRT platform to meet GCP quality standards, policies, and procedures. - Serve as the QA Subject Matter Expert for cross-functional team meetings regarding quality matters. - Lead non-compliance event investigations related to IRT platform and CAPA implementation. - Prepare for regulatory/customer/sponsor inspections and act as a subject matter expert for inspectors. - Support and provide leadership in clinical audit activities for internal and external parties. - Coordinate and participate in the evaluation and selection of external vendors for clinical trials. **Qualifications Required:** - Bachelor's degree in a scientific area with 5-7 years of clinical quality assurance experience. - Minimum of 3 years of clinical auditing/oversight experience in the regulatory compliance environment. - Knowledge of CSV. - Excellent communication and negotiation skills. - Strong attention to detail and respect for accuracy of information. - Thorough understanding of applicable US and international GCP regulations/guidelines. - Intermediate to advanced software skills (e.g., Microsoft Excel, PowerPoint, Microsoft Project). - Ability to work effectively in a cross-functional team environment. If you are passionate about building cutting-edge web applications and meet the qualifications mentioned above, we encourage you to apply for the position of Clinical QA Manager at ClinRT Global Services by sending your resume and cover letter to swati@clinrtglobal.com with the subject line: "Clinical QA Manager Application - [Your Name]."

As a Clinical Supply Chain Support Specialist at Capgemini, your role involves providing operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases (set-up, follow-up, closure). You will work independently and collaborate with cross-functional teams to ensure smooth supply chain operations and compliance with regulatory standards. Your responsibilities will include: - Prepare and track transfer orders. - Manage stock reconciliation and monitor destruction needs. - Perform quality checks and maintain inspection readiness. - Prepare documentation for labeling and shipments. - Archive documents in the electronic Trial Master File. - Communicate effectively with supply chain leaders, operational teams, and outsourcing partners. - Adapt to changing priorities in a fast-paced environment. Your profile should meet the following criteria: - Education: Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD). - Experience in clinical supply support or logistics for clinical trials (Phase IIV). - Knowledge of regulatory standards (quality, safety, documentation). Technical Skills: - Proficiency with tools: IRT (e.g., Endpoint, Suvoda), Smart Supplies, Veeva Vault. - Strong documentation and quality check skills. - Language: Fluent English for communication with stakeholders. Key Competencies that are essential for this role include: - Attention to detail and organizational skills. - Ability to manage multiple priorities and work collaboratively in a multicultural environment. - Strong problem-solving and adaptability skills. - Comfort with digital tools and documentation processes. At Capgemini, we value flexibility and support our employees with remote work options and adaptable schedules to maintain a healthy work-life balance. Our inclusive culture brings together diverse professionals committed to growth, innovation, and excellence. You will have access to continuous learning opportunities and certifications in emerging technologies and methodologies. Capgemini is a global business and technology transformation partner, helping organizations accelerate their dual transformation to address the evolving needs of customers and citizens. With a strong 55-year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needsfrom strategy and design to operations. The organization is responsible and diverse with market-leading capabilities in digital, cloud, and data, driven by the purpose of unleashing human energy through technology for an inclusive and sustainable future.,

As the Head of Supply Chain at Medanta's upcoming Noida unit, your role is crucial in leading, developing, and managing all supply chain functions to ensure uninterrupted availability of medical and non-medical supplies while optimizing costs, ensuring compliance, and supporting patient care delivery through efficient and resilient supply chain operations. **Responsibilities:** - Develop and implement the hospital's supply chain strategy aligned with organization goals - Lead and mentor a team of professionals across procurement, logistics, and inventory functions - Establish and manage contracts with suppliers and central purchase team - Ensure timely and cost-effective procurement of pharmaceuticals, medical equipment, consumables, and general supplies - Monitor supplier performance, negotiate terms, and resolve supply issues - Oversee end-to-end inventory lifecycle, including demand forecasting, stock rotation, and obsolescence reduction - Implement systems for real-time inventory tracking (e.g., ERP or hospital inventory systems) - Ensure accurate and timely distribution of supplies across hospital departments and units - Ensure all supply chain activities comply with healthcare regulations (e.g., local health authorities) - Maintain documentation and traceability for medical supplies and pharmaceuticals - Mitigate risks related to supply disruption and ensure disaster preparedness - Develop and manage the supply chain budget and cost control initiatives - Analyze spend data to identify cost-saving opportunities and efficiency gains - Collaborate with finance to align procurement strategies with budgeting and forecasting - Work closely with clinical and administrative departments to understand supply needs and improve service levels - Participate in hospital committees related to operations, patient safety, and procurement **Education:** - Bachelor's degree in supply chain management, Logistics, Business Administration, or related field - MBA or Masters in Healthcare Administration (MHA) preferred **Experience:** - 18+ years of progressive experience in supply chain or logistics, preferably within healthcare - 5+ years in a leadership role managing large teams **Skills:** - Deep understanding of hospital supply chain dynamics and healthcare regulations - Strong negotiation, analytical, and project management skills,

Role Overview: You will be a Supply Chain Intern at Medisequence (Pvt) Ltd in Chennai, responsible for coordinating logistics operations and utilizing analytical skills to optimize the company's supply chain processes. Key Responsibilities: - Coordinate supply chain operations - Utilize analytical skills to optimize supply chain processes - Coordinate logistics operations - Maintain import and export inventory levels - Ensure warehouse maintenance - Knowledge of Shipping and Logistics processes and documentation for Domestic and International shipments - Understanding of Supply Chain Operations Qualifications: - Relevant educational background in Supply Chain Management or related field - Ability to work effectively in a fast-paced environment - Strong communication skills for collaboration and coordination - Strong analytical and problem-solving skills - Excellent communication and organizational abilities - Attention to detail and accuracy in work Company Description: Credence Genomics is among the world's leaders in clinical genomics and diagnostics, striving to provide cutting-edge genetic testing services and innovative solutions in the field of genomics. Medisequence (Pvt) Ltd. is a genomics and diagnostics facility located in Chennai, India, and a leading provider of clinical genomics services utilizing next generation sequencing technology to provide diagnostics and analytical support.,

As the Head of CAPEX Procurement at Piramal Pharma Solutions (PPS) in the SCM department located in Kurla, your role involves managing capital procurement activities independently. **Key Responsibilities:** - **Strategic Sourcing and Execution**: - Align procurement plans with business objectives for effective capital expenditure management. - **Supplier and Contractor Selection**: - Identify, evaluate, and select suppliers and contractors for major capital projects, ensuring they meet project requirements and standards. - **Relationship Management**: - Build and maintain strong relationships with key suppliers, contractors, and service providers to foster collaboration and ensure project success. - **Performance Monitoring**: - Monitor supplier performance to ensure quality, cost, and delivery timeline adherence, addressing issues promptly. - **Risk Assessment and Mitigation**: - Implement supplier risk assessment and mitigation strategies to minimize disruptions and ensure project continuity. - **Supplier Development**: - Drive initiatives for continuous improvement and innovation among suppliers. - **Cross-functional Collaboration**: - Collaborate with various teams to ensure seamless execution of CAPEX projects. - **Budget Management**: - Manage procurement budgets, report on cost savings, spend analytics, and project timelines to meet financial objectives. - **Compliance Assurance**: - Ensure procurement compliance with company policies, industry regulations, and sustainability goals. - **Best Practices Implementation**: - Implement best-in-class procurement practices for transparency, efficiency, and ethical sourcing. - **Regulatory Compliance**: - Ensure compliance with legal, contractual, and regulatory requirements related to CAPEX investments. - **Market Analysis**: - Monitor market trends and industry developments to mitigate risks and identify strategic advantages. **Qualifications Required:** - Bachelor of Engineering degree in Mechanical, Civil, Chemical, or Electrical from a reputed institute. - MBA/PGDBM or any post-graduation would be an added advantage. - 15-20 years of experience in industries such as Pharma, FMCG, or Chemicals, with a track record of handling CAPEX procurement. Piramal Group has pursued a strategy of both organic and inorganic growth, driven by core values promoting inclusive growth and ethical practices. As an equal opportunity employer, Piramal Group ensures that all applicants and employees receive fair treatment in personnel matters. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end solutions across the drug life cycle. With a global network of facilities, PPS provides a comprehensive range of services, including drug discovery, process development, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as highly potent APIs, biologics, and sterile fill/finish make PPS a trusted partner for innovators and generic companies worldwide.,

As a Clinical Trial Associate (CTA) at our company, you will play a crucial role in supporting the planning, execution, and management of clinical trials while ensuring compliance with regulatory guidelines and company protocols. Your strong organizational skills, excellent communication abilities, and effective collaboration with cross-functional teams will be key to success in this role. **Key Responsibilities:** - Assist in coordinating and managing clinical trials from initiation to completion. - Maintain and update trial documentation, such as investigator brochures, protocols, and informed consent forms. - Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies. - Support the preparation and submission of regulatory documents to relevant authorities and ethics committees. - Track and manage trial-related materials, including investigational products and supplies. - Assist with site selection, activation, and ongoing monitoring activities. - Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations. - Organize and participate in clinical team meetings, taking minutes and following up on action items. - Assist in processing and tracking study invoices, contracts, and budgets. - Maintain trial master files (TMF) and ensure proper documentation for audits and inspections. **Qualifications & Requirements:** - Bachelor's degree in life sciences, healthcare, or a related field. - 1-3 years of experience in clinical research, preferably in a CTA or similar role. - Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards. - Strong attention to detail and organizational skills. - Excellent communication and interpersonal skills. - Proficiency in Microsoft Office (Word, Excel, PowerPoint) and G Suite. - Ability to multitask, prioritize, and work independently in a fast-paced environment. **Preferred Qualifications:** - Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting. - Certification in clinical research (e.g., ACRP, SOCRA) is advantageous. Please submit your CV and any relevant portfolio materials to Divjyot.kaur@sova.health. This job offers a competitive salary and benefits package, opportunities for professional growth and development, and a collaborative and inclusive work environment. As a Clinical Trial Associate (CTA) at our company, you will play a crucial role in supporting the planning, execution, and management of clinical trials while ensuring compliance with regulatory guidelines and company protocols. Your strong organizational skills, excellent communication abilities, and effective collaboration with cross-functional teams will be key to success in this role. **Key Responsibilities:** - Assist in coordinating and managing clinical trials from initiation to completion. - Maintain and update trial documentation, such as investigator brochures, protocols, and informed consent forms. - Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies. - Support the preparation and submission of regulatory documents to relevant authorities and ethics committees. - Track and manage trial-related materials, including investigational products and supplies. - Assist with site selection, activation, and ongoing monitoring activities. - Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations. - Organize and participate in clinical team meetings, taking minutes and following up on action items. - Assist in processing and tracking study invoices, contracts, and budgets. - Maintain trial master files (TMF) and ensure proper documentation for audits and inspections. **Qualifications & Requirements:** - Bachelor's degree in life sciences, healthcare, or a related field. - 1-3 years of experience in clinical research, preferably in a CTA or similar role. - Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards. - Strong attention to detail and organizational skills. - Excellent communication and interpersonal skills. - Proficiency in Microsoft Office (Word, Excel, PowerPoint) and G Suite. - Ability to multitask, prioritize, and work independently in a fast-paced environment. **Preferred Qualifications:** - Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting. - Certification in clinical research (e.g., ACRP, SOCRA) is advantageous. Please submit your CV and any relevant portfolio materials to Divjyot.kaur@sova.health. This job offers a competitive salary and benefits package, opportunities for professional growth and development, and a collaborative and inclusive work environment.

As a Clinical Research Associate (CRA), you will play a key role in conducting Phase I-IV clinical BA/BE studies. Your primary responsibilities will involve monitoring and managing activities at clinical sites to ensure that project timelines and deliverables are achieved. Building strong relationships with clinical sites and investigators will be essential, along with assessing protocol and regulatory compliance based on local and federal requirements, ICH GCP guidelines, and PSI SOPs. Your focus will be on safeguarding subjects" rights, safety, and well-being, as well as maintaining data quality. - Prepare, conduct, and report on various activities such as site selection, initiation, routine monitoring, and close-out visits - Monitor patient enrollment to meet recruitment targets and project timelines at both site and country levels - Verify source data, resolve data queries, and conduct ongoing reviews to ensure data quality and compliance with Risk Based Monitoring practices - Report and follow-up on Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations in a timely manner - Serve as the main communication channel between the Sponsor and the site, acting as a point of contact for in-house support services and vendors - Supervise the handling, accountability, and reconciliation of Investigational Product(s) and study supplies - Review essential documents at the site level and ensure the reconciliation of study OSF/TMF at the site and/or country level,

As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, this role as a Medical Device CRA II could be a great fit for you. As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, thi

As the Director, Head of Global Product Supplies Capability Center at Bristol Myers Squibb in Hyderabad, your role is crucial in ensuring the sustained health, growth, and continuous improvement of the Global Product Supplies Capability Center in India. Your responsibilities include: - Managing oversight for the GPS CC Team (150+) in Hyderabad, ensuring day-to-day operations align with corporate goals and standards. - Advising the GPS Leadership Team on emerging trends in capabilities, people, technologies, and innovations to drive organizational sustainability. - Acting as a liaison between the Hyderabad team and global teams, facilitating communication and information flow. - Driving operational performance and excellence within the GPS CC organization by aligning to the GPS culture. - Supporting recruitment efforts and reinforcing leadership development through training and coaching. - Promoting a culture of innovation, excellence, and continuous improvement within the center. - Providing regular administrative reports to global teams and facilitating local initiatives for employee well-being and engagement. - Managing data enablement team(s) to ensure effective data insights for strategic decision-making. Qualifications & Experience required for this role: - Minimum Graduate degree. - Minimum of 16 years of experience in global product supply with a preference for managing global capability centers. - Minimum 8 years of experience in managing people and growing teams. - Knowledge of global supply chain processes in the Pharma industry preferred. - Demonstrated ability to operate and lead in a matrix organization with effective stakeholder management. - Excellent verbal and written communication skills. If this role intrigues you and aligns with your career aspirations, Bristol Myers Squibb encourages you to apply. Embrace the opportunity to be part of work that goes beyond the ordinary and transforms lives. At Bristol Myers Squibb, every employee contributes to the vision of transforming patients' lives through science. The inclusive culture values diversity, promoting inclusivity in clinical trials, with shared values of passion, innovation, urgency, accountability, inclusion, and integrity, unlocking the highest potential in each colleague. Please note that physical presence at the BMS worksite is a critical job function to enhance collaboration, innovation, and employee engagement, reflecting the company's culture. As the Director, Head of Global Product Supplies Capability Center at Bristol Myers Squibb in Hyderabad, your role is crucial in ensuring the sustained health, growth, and continuous improvement of the Global Product Supplies Capability Center in India. Your responsibilities include: - Managing oversight for the GPS CC Team (150+) in Hyderabad, ensuring day-to-day operations align with corporate goals and standards. - Advising the GPS Leadership Team on emerging trends in capabilities, people, technologies, and innovations to drive organizational sustainability. - Acting as a liaison between the Hyderabad team and global teams, facilitating communication and information flow. - Driving operational performance and excellence within the GPS CC organization by aligning to the GPS culture. - Supporting recruitment efforts and reinforcing leadership development through training and coaching. - Promoting a culture of innovation, excellence, and continuous improvement within the center. - Providing regular administrative reports to global teams and facilitating local initiatives for employee well-being and engagement. - Managing data enablement team(s) to ensure effective data insights for strategic decision-making. Qualifications & Experience required for this role: - Minimum Graduate degree. - Minimum of 16 years of experience in global product supply with a preference for managing global capability centers. - Minimum 8 years of experience in managing people and growing teams. - Knowledge of global supply chain processes in the Pharma industry preferred. - Demonstrated ability to operate and lead in a matrix organization with effective stakeholder management. - Excellent verbal and written communication skills. If this role intrigues you and aligns with your career aspirations, Bristol Myers Squibb encourages you to apply. Embrace the opportunity to be part of work that goes beyond the ordinary and transforms lives. At Bristol Myers Squibb, every employee contributes to the vision of transforming patients' lives through science. The inclusive culture values diversity, promoting inclusivity in clinical trials, with shared values of passion, innovation, urgency, accountability, inclusion, and integrity, unlocking the highest potential in each colleague. Please note that physical presence at the BMS worksite is a critical job function to enhance collaboration, innovation, and employee engagement, reflecting the company's culture.

Role Overview: At Signant Health, you will lead the logistics project service team to ensure seamless supply chain operations for global projects. As the Associate Director, you will provide strategic direction, oversee vendor management, and coordinate with internal teams to optimize supply chain performance throughout project lifecycles. Key Responsibilities: - **Operational Leadership & Team Management** - Provide strategic direction, performance management, and professional development for the logistics project service team - Optimize team resource allocation, manage workload distribution, and ensure adequate staffing levels - Lead continuous improvement initiatives to streamline logistics processes and implement best practices - Facilitate collaboration between logistics team and other business functions for on-time project delivery - **Comprehensive Vendor Oversight & Management** - Oversee third-party logistics providers and outsourced supply chain operations vendors - Establish and monitor Key Performance Indicators for service quality, delivery performance, cost efficiency, and compliance - Negotiate and manage service level agreements with outsourced partners - Develop risk management strategies and contingency plans for business continuity - **Import & Export Operations & Compliance Management** - Ensure compliance with customs regulations, import/export requirements, and documentation management - Manage cross-border logistics for electronic devices, ensuring smooth customs clearance - Monitor changing international trade regulations and implement necessary process adjustments - **Forecasting & Planning Leadership** - Lead demand forecasting processes and supply chain planning initiatives - Develop contingency plans for demand scenarios, supply disruptions, and market changes - Collaborate with stakeholders to align supply chain plans with business objectives - Continuously improve forecasting accuracy and planning processes Qualifications Required: - **Knowledge, Skills & Attributes** - Experience leading global teams and collaborating across organizational levels - Customer service excellence with prioritization skills and a customer advocacy mindset - Proficiency in process optimization, data analysis, and organizational prioritization - Expertise in demand forecasting, supply chain planning, and analytical interpretation Additional Company Details: At Signant Health, you will be part of a global team dedicated to transforming clinical research and improving patient lives. You'll work with cutting-edge digital health solutions, partner with leading life sciences organizations, and grow your career in a collaborative, innovative, and integrity-driven culture.,