23 Medical Healthcare Rd Pharmaceuticals Biotechnology Jobs

Dear Candidate, We're seeking a talented individual for a Medical - Non Clinical role. If you're interested, please share your updated biodata at carrers@prodocssolution.com Freshers are welcome to apply! Desired Candidate Profile: - HSC or Any Graduate with diploma in MLT/DMLT. - 0-3 years of experience in clinical or non-clinical setting. - Familiarity with pharmacy software systems an asset. - Fresher or Lab experience considered. - Rotational Shifts (Morning/Second/General) Interview Details: - Walk-in interviews from Monday to Saturday, 1:00 PM - 5:30 PM - Bring your updated CV/Biodata/Resume - Venue: Prodocs Solutions Ltd, 1st Floor, Plot No 6/19, Compound No 82, Marol Co-operative industrial estate, Near Marol Bhavan, Sir Mathuradas Vasanji Road, Andheri East, Mumbai 400059 Feel free to forward this opportunity to those who may be interested. Thanks & Regards, Gaurav Acharya Manager - HR Prodocs Solutions Ltd

A pediatrician's job description involves caring for infants, children, and adolescents, encompassing preventative care, diagnosis and treatment of illnesses, and monitoring growth and development

Role & responsibilities 40.1.1.1 Daily rounds in wards two times a day 40.1.1.2 To see presence of RMO on all floors and supervise their activity. In absence of RMO organizing a RMO in floors. 40.1.1.3 In busy time support RMO on the wards. 40.1.1.4 To attend patient and patients grievance. 40.1.1.5 To attend patient or relative with quires regarding treatment, nature of disease, his investigations or its results 40.1.1.6 To check completion of rounds by consultants 40.1.1.7 To check number of admission and completion of admission on time (completion of paper work, sending of investigation, starting of treatment and informing of consultant) 40.1.1.8 To check discharges and readiness of discharge cards 40.1.1.9 Completion of documents as per SOPS. 40.1.1.10 Check MLC cases. 40.1.1.11 To clear quires regarding investigations a. 40.1.1.12 Co-ordinate with patient, consultants and hospital administration if any investigations advised that is not available in our hospital like PET scan etc.

Role & responsibilities * Check prescriptions to ensure that there are no errors and that they are appropriate and safe for the individual patient. * Dispense the medicines as per the prescription. * Bill the medicines dispensed and collect cash. * Check the expiry date and batch number of the medicine and compare it with the bill entry. * Contacting referring physicians offices with questions over prescription. * Maintaining inventory of the medicines dispensed. * Keep records of patient history and of all activities regarding heavy medication. * Handle customer queries and resolve their issues or initiate appropriate steps such as complaint escalation to relevant departments for resolution. * Record all pharmacy transactions and keeping cash registers up to date. * Comply with all applicable legal rules, regulations, and procedures. * Maintain confidentiality with respect to customers medical details.

This vacancy is on contract basis for a period of 2 years. Role & responsibilities: Will be part of the Company Secretarial team and handle the following tasks; Data and record management which includes preparation of index of files. Filing of documents, minutes book or any other documents in the file and keeping the information updated from time to time in the index. Co-ordination with the Legatrix team and internal departments on the mapping / remapping / change of users / frequency of tasks in legasis compliance automation tool. Assisting the supervisor in ensuring compliance with the help of compliance automation tool. Providing administrative and secretarial support to the secretarial department from time to time. Preferred candidate profile: Preferably handled compliance automation tool. Fluency in English and Computer literate. Good typing speed. Basic working knowledge of word, excel and PPT. Job Location - Airoli West, Gigaplex.

Urgent requirement for MBBS,BHMS,BDS,BAMS -Rajasthan(Jaipur) Freshers/candidate with clinical or TPA experience. Interested candidates can call on 9371762436 or share their updated resumes to career@mdindia.com Job Description: Scrutiny of medical documents and adjudication. Assess the eligibility of medical claims and determine financial outcomes. Identification of trigger factors of insurance related frauds and inform the concerned department. Determine accuracy of medical documents. Required Candidate profile: MBBS ,BHMS,BDS,BAMS graduate. Male candidate prefer. Good Medical & basic computer knowledge Should have completed internship (Permanent Registration number is mandatory) Freshers can also apply. Work from office. Venue details: MDIndia Health Insurance TPA Pvt. Ltd Naval Tower, J.L.N. Marg, 4 & 6th Floor, Near Fortis Hospital, Jaipur 302017 .

To offer consultation & patient diagnosis at Kaya Skin Clinics, perform/supervise all medical procedures to be carried out in clinic, ensuring efficacy, safety & high professional standards of medical procedures carried out under your supervision. Required Candidate profile Presentable & Good Communication Candidate must be MBBS with MD or DVD or DDV or DNB Must be committed to work for minimum 2 years 6days working (Week Off in weekday) Contact- 7022617038/8247551800 Perks and benefits Leaves & Incentives as per company policy

We are in search of a dedicated and skilled professional who will conduct TB diagnostics, including smear microscopy, staining, and NAAT for sputum, EPTB, and pediatric TB samples, following SOPs and NTEP guidelines. Responsibilities include maintaining lab records, ensuring timely reporting, coordinating sample testing, assisting in MDR-TB suspect identification, and overseeing sample collection and transport for DST. They will ensure biosafety compliance, support quality assurance, implement new diagnostic tools, and manage data using Nikshay. Reporting to the Cluster Coordinator, they will collaborate with the STLS to uphold lab standards. The ideal candidate will work from the respective district. Essential Qualification/ Requirements: Intermediate (10+2) and Diploma or certified course in Medical Laboratory Technology or equivalent. One year experience in NTEP sample testing using Sputum smear microscopy and NAAT Candidates with Higher qualification (for example Graduates) shall be preferred. Roles and Responsibilities Adhere to standard operating procedures (SOPs) for smear preparation, staining, microscopy, reporting, and M. tuberculosis detection using modern NAAT methods for sputum, EPTB, and Maintain laboratory registers and ensure timely reporting of results to the Medical Officer and Coordinate with staff to ensure prompt testing of pulmonary and extra-pulmonary samples following the National Tuberculosis Elimination Program (NTEP) diagnostic algorithm. Assist the Medical Officer in identifying MDR-TB suspects and ensure proper collection and transportation of sputum specimens for Culture and Drug Susceptibility Testing (DST) per Oversee and supervise the safe disposal of contaminated laboratory materials in compliance with Support the Senior TB Laboratory Supervisor (STLS) in implementing NTEP Laboratory Assist in the rollout and implementation of new TB diagnostic tools within NTEP. Facilitate the adoption and effective use of Nikshay tools for data entry, validation, and public health action. Note: The principal responsibilities listed above are an illustrative list and not an exhaustive list. Additional responsibilities may be added from time to time depending on Project requirements. Reporting: The Lab. Technician will be reporting to the State Coordinator. Remuneration: The compensation for the above-mentioned position/s will adhere to internal policies and market standards, determined by qualifications, relevant experience, budget availability, internal The above-mentioned position requires outstanding communication, analytical skills, documentations skills, interpersonal, and computer skills, as well as the willingness to travel. Preference will be given to candidates with work experience in the relevant field and local candidates who possess the necessary

Vantive: A New Company Built on Our Legacy Since last year, Baxter has been on a journey to separate our Kidney Care segment into a standalone company. Vantivewill build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us are driven to help improve patients lives worldwide. Join us as we revolutionize kidney care and other vital organ support. Job Summary Job Title - Research Associate III (Testing Coordinator) Location - Whitefield, Bangalore Shift - General This position is responsible for The Testing Coordinator will utilize his/her scientific knowledge to own operational excellence and continuous improvement; This role involves streamline processes; coordinate business, management, and technical SMEs; identify risks; devise solutions, all to support the establishment of Operational excellence. Essential Duties and Responsibilities: Provide business and execution leadership for multiple analytical and stability-related projects and holding accountability for testing schedules, risks, and interacts with all functions and levels of management ensuring effective communications. Lead internal initiatives that enhance operational excellence. Interact with platform core team leaders and other key business stakeholders to be able to proactively anticipate business needs. Process inputs from Global Analytical, Stability Functional Leader and Analytical leads and Stability SMEs to determine schedules and forecast resource allocations to projects. Ensuring the availability of all prerequisites for scheduled laboratory analytical and stability testing. Master the planning of activities for testing and ensure on-time completion of all testing activities. Effectively coordinate testing with global teams and CROs as applicable to meet the KPIs on time. Interact with other testing groups (Particle, Sterility/BET, etc.) to determine schedules and alignment with business needs/function commitments. Ensure the maintenance of laboratory compliance as per regulatory requirements. Ensure import licenses are in place and manage laboratory samples inventory. Coordinate with procurement and technical teams for on-time procurement of chemicals and resolution of analytical instrument problems. Coordinate with external and internal sample shipment personnel s for receiving testing samples on time. Participate in handling of laboratory investigations that correspond to atypical or out-of-specification / out-of-trend test results and other nonconformance records and leverage critical thinking skills to drive the investigation to conclusions based on sound scientific principles and propose appropriate corrective and Preventive root causes. Author/Follow SOPs of relevant procedures. Qualifications: Proven experience in stability testing, analytical method validation and transfers, laboratory management, or a similar role. Strong leadership and project management skills. Excellent communication and interpersonal skills. In-depth knowledge of relevant QSRs, GxP, and other regulatory requirements. Handling of software like Trackwise. Proficiency in resource planning and inventory management. Critical thinking and problem-solving skills. Ability to work effectively in cross-functional and global teams. Proactive and able to anticipate business needs and challenges. Basic computer skills (MS Office Word, Excel, PowerPoint, etc.) Education: Master s in chemistry or Pharmaceuticals, with 6 to 10 years of experience. Education and/or Experience: Bachelor s degree with 8-14 years or Master s degree with 5 to 10 years of experience in relevant scientific discipline (Analytical chemistry/Pharmaceutical chemistry).

CORE JOB RESPONSIBILITIES REQUIRED Business generation & development: Achieve monthly, quarterly, half yearly and yearly sales target by promoting companys products ethically to customers as per the business plan, also ensure Doctor / Customer Call average as per the customer management plan of the division Organizing Camps (CME) as per the division strategy and customer needs Facilitate the process of successful new product launch. To create and update customer list as per the therapy and product of the division. Ensure Ipad adoption (if applicable) as per division norms and adherence to CLM calls Brand Management: Prescription audit for Abbott brands and other competitors brands Generate POBs for Abbott brands as per the business plan REQUIRED EXPERIENCE BSc/ B. Pharm or Any Graduate with minimum 2 years of prior experience as a Medical Representative PREFERRED EXPERIENCE Candidate with prior/current experience in the same therapy. Candidates from MNC and top Indian Pharma companies will have added advantages. Fluent and confident in communication

About Us :- Indira IVF centre is the pioneer in providing affordable yet creditable infertility curation to the common people for the first time in India. It is armed with the state-of-the-art infrastructure, advanced equipments and a pool of renowned physicians. We started with a two room clinic back in 1988 and today we stand tall as one of the most esteemed and prestigious IVF service providers in the country and beyond. Job Description :- Issue & Return of Material against Patient indents from Stores and against Departmental indents Direct Issue of drugs/ medical consumable to Patient Issue of Narcotics as per protocols Receiving the material at Receiving Bay & Processing of Invoices Emergency Cash Purchase Receipt of consignment goods & Processing their Invoices on Consumption Physical Stock Verification.

About Us :- Indira IVF centre is the pioneer in providing affordable yet creditable infertility curation to the common people for the first time in India. It is armed with the state-of-the-art infrastructure, advanced equipments and a pool of renowned physicians. We started with a two room clinic back in 1988 and today we stand tall as one of the most esteemed and prestigious IVF service providers in the country and beyond. Job Description :- Issue & Return of Material against Patient indents from Stores and against Departmental indents Direct Issue of drugs/ medical consumable to Patient Issue of Narcotics as per protocols Receiving the material at Receiving Bay & Processing of Invoices Emergency Cash Purchase Receipt of consignment goods & Processing their Invoices on Consumption Physical Stock Verification.

Nutritionists must handle 2 OPDs/day. It's a target-based role involving product recommendations and diet counselling. Strong communication, local language skills, and nutrition knowledge are essential for effective patient engagement.

Job Title: Clinical Research Lead Location: Bangalore Company: Janitri Innovations Pvt. Ltd. About Janitri Innovations Pvt. Ltd.: Janitri is a social enterprise with a vision to create a world where no mother or newborn dies during pregnancy, birth, or post-delivery. We innovate and develop medical devices and technologies to improve maternal and newborn health. Our focus is on bringing impactful solutions to healthcare through continuous research and clinical studies on maternal-fetal health monitoring technology. Job Summary: The Clinical Research Lead will take charge of leading clinical studies from initiation to completion. This role involves overseeing clinical trials, coordinating with hospitals and stakeholders, ensuring the quality of data collection and analysis, and leading research initiatives. The ideal candidate will have experience in clinical research, especially within the medical device sector, and be skilled in designing studies, managing execution, and ensuring scientific rigor. Key Responsibilities: Leadership in Clinical Studies: Lead the execution and coordination of ongoing and new clinical studies in collaboration with hospitals, PIs (Principal Investigators), and research teams. Oversee all phases of clinical studies from concept development, protocol design, and sample size calculation to execution, ethics approval, and data analysis. Study Design & Execution: Design clinical research protocols in accordance with scientific guidelines and regulatory standards. Work closely with the study team to ensure smooth execution of clinical trials, including participant recruitment, data collection, and study monitoring. Data Analysis & Reporting: Lead data analysis and generate reports using statistical tools (e.g., SPSS, SAS, Excel, Matlab, Python). Provide insights through data interpretation, ensuring data integrity, and maintaining detailed records of study findings. Stakeholder Management: Regularly engage with key stakeholders such as hospital teams, public health experts, and internal staff to track progress, resolve issues, and drive study success. Facilitate meetings and discussions with stakeholders to ensure alignment on study objectives and timelines. Regulatory & Ethics Coordination: Ensure all studies comply with regulatory guidelines and secure necessary ethics approvals. Liaise with ethics boards, hospitals, and government authorities for study submissions and compliance requirements. Manuscript Writing & Publications: Lead the writing and publication of scientific papers and reports based on research findings. Collaborate with the public health team on research publications and ensure high-quality submissions to relevant journals. Team Collaboration & Mentorship: Mentor junior clinical research staff and provide guidance on study design, execution, and data analysis. Collaborate with cross-functional teams (product, public health, and regulatory) to align clinical study outcomes with company goals. Skills, Knowledge, and Experience: Minimum 4 years of experience in clinical research, with at least 2 years in a leadership role within the medical device or healthcare industry. Strong understanding of clinical research methodologies and statistical analysis. Proficiency in statistical analysis software (SPSS, Matlab, Python, SAS, Excel) and other relevant tools. Experience in study design, protocol writing, sample size calculation, and data management for clinical trials. Strong project management skills with a focus on delivering quality results on time. Proven experience in coordinating with ethics boards and securing regulatory approvals. Excellent communication, interpersonal, and leadership skills with proficiency in English. Experience in writing and publishing research papers in scientific journals. Why Join Us? This role offers the opportunity to lead impactful research that will directly contribute to improving maternal and newborn health outcomes. If you are passionate about clinical research and want to be part of an innovative team making a difference, we encourage you to apply.

Hi, We are hiring for ITES Company for Spotfire Programmer Role. Job description: Minimum 3 years of experience as a Spotfire Programmer and Clinical experience is Mandatory Working on Refreshes requests for SRT & CSTV Building Oncology & Standard Visuals for Clinical Study Team Visualization (CSTV) Setting up standard and Study Specific Spotfire requests for Safety Review Team (SRT) Knowledge of Spotfire, Study configuration tool and On Demand Tool. Creating SAS Codes as per the requirement Setup and customization of visuals for Medical Reviewers Validation of visuals as per the specifications Optimize data models and queries for improved performance and scalability. Monitor and troubleshoot issues related to the Spotfire platform and coordinate with vendors for advanced support. Seeking opportunities to leverage expertise in Spotfire development and data visualization to contribute to the success of a data-driven organization. Integrate and prepare data, create visualizations and reports, optimize performance, and collaborate with stakeholders. Possesses a strong understanding of data exploration, ETL processes, and programming in R. Adept at collaborating with clients and stakeholders to translate complex data into clear and actionable insights. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Bangalore Search : Spotfire Programmer Bangalore (Job Code # 80) b) For Position in Ahmedabad Search : Spotfire Programmer Ahmedabad (Job Code # 82)

1- 2yr of Clinical Data Management Experience . Perform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient, quality management products. Support coordinate with other departments, sites and sponsors as and when necessary Essential Functions Perform/Assist regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor. Serve in the role of back-up to a Sr. Data Coordinator or Data Team Lead. Manage the allocated tasks with minimum oversight. Ensure that all the deliverables are of expected quality standards and meet customer expectations with support of Senior Data Manager. Interact with Data Management team leaders to report on the quality of data collection and tasks done. Attend internal study meetings and internal/ sponsor audits. Assist in tracking and managing the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL. Be compliant to trainings and eSOP reading. Communication with Data Team Lead and other team members across functions should be collaborative. Qualifications Bachelors Degree Graduate Science/Bachelor Pharmacy or equivalent Pref English Fluency Spoken and English Basic computer applications like Microsoft excel, word, Inbox etc Should have basic understanding of Drug development lifecycle and Overall Clinical research process

Core Responsibility: Ability to clinically evaluate the patient independently Ensure service excellence with high standard of patient care Plans and administers standard diagnostic and prognostic examination of muscles, nerves, joints and functional abilities. Plans treatment objectives and programs according to the results of evaluation. Taking decision and administer the modalities & treatment procedures with high skill of performance Explains treatment objectives and methods to patients and their families, Designs and constructs, or directs construction of specialized splints and prosthesis Directs and aids patients in exercises and functional training using appropriate devises and equipment. Records initial assessments, treatments given and other updates appropriately in Patient Records/ CPRS. 10.Records patients progress and document on timely manner 11.Re-evaluates and document reassessment procedures timely. 12, Evaluates patient response and progress, and discusses with appropriate physician as and when required. Report daily progress of patients to assigned supervisor. Maintain good & healthy relations with other professionals, including physicians, patients, patients relatives Directs and supervises the activities of the physiotherapy aids, assistants, interns, and GDAs. To ensure that ethical professional practice is followed. Follows proper/daily handover of the patients between the shifts in the department. Knowledge of safe and proper operations of all equipment. To Comply with the clinical quality & policies of the respective area To comply with service quality Process, environmental & occupational issues Follows team work in the department and consults seniors in any required situation. To Comply with patient safety policy To ensure safe utilization of equipments and proper waste disposal system 24. To go for home visits as and when required

The Core Analytics & Science Team (CAS) is Ubers primary science organisation, covering both our main lines of business as we'll as the underlying platform technologies on which those businesses are built. We are a key part of Ubers cross-functional product development teams, helping to drive every stage of product development through data analytic, statistical, and algorithmic expertise. CAS owns the experience and algorithms powering Ubers global Mobility and Delivery products. We optimise and personalise the rider experience, target incentives and introduce customizations for routing and matching for products and use cases that go beyond the core Uber capabilities. 1. Refine ambiguous questions and generate new hypotheses about the product through a deep understanding of the data, our customers, and our business 2. Design experiments and interpret the results to draw detailed and impactful conclusions. 3. Define how our teams measure success, by developing Key Performance Indicators and other users/business metrics, in close partnership with Product and other subject areas such as engineering, operations and marketing 4. Collaborate with applied scientists and engineers to build and improve on the availability, integrity, accuracy, and reliability of data logging and data pipelines. 5. Develop data-driven business insights and work with cross-functional partners to find opportunities and recommend prioritisation of product, growth, and optimisation initiatives.

SUMMARY Job Summary: Exciting job opportunity as a Staff Nurse in Germany! Key Responsibilities: Providing comprehensive patient care, including personal care and medical attention. Adhering to the medical instructions and orders prescribed by doctors. Maintaining accurate and organized patient case records. Administering medications as per doctor's prescriptions. Ensuring patient comfort and safety by repositioning them regularly. Timeline for Migration: Application to Selection: Not more than 5 days German Language Training: 9-10 months Visa Processing & Departure: 2-3 months Start working in Germany within 12 months! Requirements: Educational Qualification: Bachelor's Degree in Nursing or GNM Experience: Minimum 6 months working experience as a Nurse Citizenship: Indian Age limit: 18 to 35 years Certification: registration Certification from Nursing Council Language: Basic English proficiency required, German knowledge is a plus (we provide German language training!). Clinical Skills: Bed side nursing, patient care, patient assessment and monitoring Even if you don’t meet all requirements, apply now and let our experts assess your eligibility! Benefits: High Salary & Perks: Trainee Nurse Salary: 2,100 to 2,700/month (1,97,000 to 2,54,000 INR/month) Staff Nurse Salary: 2,700/month to 3,500/month (2,54,000 to 3,29,000 INR/month) Career Growth: Advanced Nursing career in Germany with competitive salaries, opportunity to work in the best healthcare system in the world Relocation Support: Visa assistance, accommodation guidance, and on-boarding support provided. German language training to boost your employability International Work Experience: Boost your resume with experience in the most advanced healthcare facilities and International healthcare expertise. Comprehensive Health Insurance: Full medical coverage for under Germany’s healthcare system. Permanent Work Contracts: Long-term stability with retirement benefits and social security. Family Reunification: Bring your spouse and children to Germany once you receive full recognition. Housing Assistance: Support in finding accommodation with potential eligibility for German housing benefits to lower rental costs. Tax Benefits for Families: Receive 255 / INR 24,213 per child as a government child benefit while working in Germany. Path to Citizenship: Become eligible for German permanent residency in 3 years and citizenship in 5 years for long-term security. Limited slots available! Apply now to secure your place in the next batch of skilled Nurses migrating to Germany!

A BAMS doctor, also known as an Ayurvedic doctor, works by diagnosing and treating patients using Ayurvedic principles. This involves assessing a patient's health condition, determining the underlying imbalances,

Medical oncologists explain cancer development stages to patients, discuss treatment options and assist in pain management. -They care for patients throughout the entire course of cancer treatment, from diagnosis to recovery or death.

A Compliance Auditor ensures adherence to laws, regulations, and internal guidelines. They enforce standards, review compliance, and conduct labor law audits.

Role & responsibilities To effectively conduct and communicate nursing assessments effectively with HCL patients and their families. To effectively conduct and communicate routine and urgent nursing assessments effectively with HCL Healthcare clinical providers, including doctors, other nurses, and ancillary provider staff. To effectively coordinate patient care and referrals for doctors and other care providers from multiple health care departments and clinics. To conduct the following procedures accurately and consistently. • Measure and assess every patients vital signs. Lab sample collection including phlebotomy as needed. Administers immunizations, other injections, medications, and other treatments. Job Type OPD / OHC job only for corporate employees. Qualification Essential: Diploma in GNM or B,Sc(Nursing) from a recognized nursing training program. Experience 3+ years. Job Details Location- WhiteField, ITPL Tech Park, Bangalore Shifts- Rotational Shifts (Morning/Evening/Night)