Takes a leading role in the effective functioning of the Infection Control Team. Assists the HICC in drawing up annual plans and policies for infection control. Ongoing contribution to the development and implementation of infection control policies and procedures, participation in audit, and monitoring tools related to infection control and infectious diseases. Supports Infection Prevention and Control Program as Continuous Quality Improvement initiatives To supervise infection prevention and control procedures carried out in the hospital. To ensure availability of appropriate resources, facilities and equipments for infection prevention and control activities. To provide specialist nursing inputs in the identification, prevention, monitoring and control of HAI within the hospital. To carry out regular surveillance activities of all high-risk areas in the hospital. To identify and investigate an outbreak and collecting and coordinates surveillance data for the same. To carry out surveillance of occupational exposure. To carry out surveillance of Antibiotic use in wards and critical areas. To coordinate isolation of an infected patient. To coordinate in providing information regarding notifiable diseases to medical record department for notifying government authorities. To supervise disinfection and sterilization procedures carried out in the hospital. To organize the training and awareness program for all health care providers related to infection prevention and control practice. To supervise on Biomedical Waste (BMW) management program in the hospital. To prepare the monthly reports of surveillance. To coordinate for Environmental Surveillance (air, swabs and water) culture results. Demonstrates loyalty, perform responsibility, and maintains work confidentiality Able and willing to seek out new methods, principles and incorporate them into existing practices by attending external / internal workshops, CNEs and other training programs. Any other duties, assignments or delegations assigned. Qualification - BSC/MSC Experience - 2 yrs to 10 yrs.

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Analyst Qualifications: Master of Pharmacy,BSc Years of Experience: 3 - 5 Years Language - Ability: English - Expert What would you do? Experience in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred. -Create reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation.-Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Master of Pharmacy,BSc

Skill required: Control Testing - Agile testing Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with SOX testing experience.Conduct testing tasks within Agile models and integration processes and manage development sprints. What are we looking for? Conduct testing tasks within Agile models and integration processes and manage development sprints.Conduct testing tasks within Agile models and integration processes and manage development sprints. Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? -Exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred.-Extensive experience in database design, edit check programming, custom function programming and unit testing.-Experienced in various modules such as IVRS/RWS integration and Lab administration.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy,Master of Pharmacy

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Analyst Qualifications: Any Graduation,BSc Years of Experience: 3 to 5 years Language - Ability: English - Expert What would you do? Exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred.-Extensive experience in database design, edit check programming, custom function programming and unit testing.-Experienced in various modules such as IVRS/RWS integration and Lab administration.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Any Graduation,BSc

Skill required: Contract Management - Contract management Designation: Compliance & Ethics Counsel Sr Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years What would you do? Accenture is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. Accenture will not tolerate discrimination or harassment based on any of these characteristics. Accenture encourages applicants of all ages.Global Legal Network (GLN) is a group of professionals operating globally from 10 countries. It provides a broad spectrum of differentiated services - focused on delivering value and innovation. We partner with Legal teams across Accenture to build efficiencies and centres of excellence related to Legal services; and through our size, geographic spread and language diversity, the Global Legal Network is able to drive quality, agility and speed in our services, aligned to Accentures relentless focus on maximum efficiency and operational effectiveness.CORE and Global Services (CGS) is a group of legal professionals working and supporting different legal areas such as Compliance, Regulatory Offerings, Ethics, Procurement, Corporate Matters and the Services Areas aligned with the new offerings and technologies such as Strategy & Consulting, Interactive, Technology, Security and Operations.Ethics & Compliance Role Summary- The objective of the role is to provide comprehensive support to legal and business teams in all the activities associated with Accentures Ethics & Compliance program. This includes all kinds of support in the areas of Anticorruption, Anti money laundering, Data privacy, Trade Compliance, Gov Compliance, and Competition law, etc. What are we looking for? Bachelors degree in LawWork Experience: Minimum of 3 to 5 years of experience at law firm or as in-house counsel and/or in legal outsourcing.Knowledge and Skill Requirements: Experience in generic legal in-house matters, including but not limited to risk identification and mitigation, compliances, contracts, legal research, etc. Exposure to E&C work, especially due diligence, screening, background checks would be a plus Basic awareness of Accenture offerings and function specific services performed, understands commercial agreements, legal and compliance fundamentals, general corporate business practices and contracting regulations Demonstrates promptness, accuracy and consistency with the activities supported, effectively manage priorities and stakeholder expectations, ability to work under pressure, with exposure to leadership Demonstrates keenness to learn and train on new processes and areas, able to assist with day-to-day support and to understand delivery requirements Detail-oriented, sound judgement, prioritization, organized, adaptable, team player who looks to build trust-based relationships, proactively helps new members Comfortable with technology and has experience in the use of tools & databases, good at using Microsoft Office applications (e.g. Excel, Word, PowerPoint, SharePoint)Behaviours and Attributes: Open to work with and understand cross-cultures and locations throughout Accenture global organization Understand the value of diversity and recognizes the strengths that different styles, innovative perspectives and experiences bring to Accenture Demonstrate inclusion and respect for all individuals regardless of gender, race, ethnicity, religion, belief, age, disability, culture, social status and/or sexuality Collaborative and persuasive; able to work well with executives and non-executives. Roles and Responsibilities: Key Responsibilities: Understand the CORE areas, relevant company policies, company s approval processes and ensures that all stakeholders are timely engaged and informed on the relevant process Understand and suggest process improvements in the support area, enhance knowledge in context of the support area Directly liaison with internal stakeholders on various issues, build credible and effective relationships with onshore counsels and within GLN team, recognize issues and provide timely escalation to Team Lead or appropriate stakeholders Assist team in drafting checklists, process documents and generic tracking reports Provide on the job training and support to the new joiners of the team, supervise resources, as required Support implementation of new initiatives in the support area or within GLN/Legal Support tech team in development of new tech tool or enhancement of existing ones Manage SharePoint and communication records Support the Team Lead manage and deliver services to global Ethics & Compliance Team as per direction from E&C team; Work on E&C advisory matters; Address questions by business and Leadership; Provide E&C tailored guidance including but not limited to Business, Delivery, and Finance Teams; Review contracts and other documents relevant to E&C area; Be PoC for E&C process issues; Recognize issues and provide timely escalation to E&C Leadership, Counsels, or appropriate stakeholders, in a precise and concise manner; Research and monitor global regulations related to E&C area Ensure compliance with E&C covenants, internal policies, and procedures; Build good working relationships with key stakeholders in applicable geographies (including, but not limited to:E&C, Country Legal, etc.); Deliver trainings inside the E&C Team and across Accenture to spread E&C related awareness amongst CM, Business, and regional stakeholders; Ensure general understanding of E&C process within/outside the team Qualifications Any Graduation

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy,Master of Pharmacy Years of Experience: 5-8years What would you do? Exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred.-Extensive experience in database design, edit check programming, custom function programming and unit testing.-Experienced in various modules such as IVRS/RWS integration and Lab administration.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy,Master of Pharmacy

B.Sc. or M.sc BOTANY Fresher Location :Surat / Navsari / Bharuch / Ahmedabad/ Vadodara Salary : 15000 to 35000 Living + Travel Available Chemical handling and disposal Analyze retrieved data and prepare reports for laboratory management Required Candidate profile Lab work to develop and improve both new and existing chemical product Assist with testing and calibrating lab equipment in preparation for specific tasks Maintaining lab and operating lab equipment

Join us as a BA4-Research" at Barclays, where youll spearhead the evolution of our digital landscape, driving innovation and excellence. We are diversified by business, by different types of customers and clients, and by geography. Our businesses include consumer banking and payments operations around the world, as well as a top-tier, full service, global corporate and investment bank, all of which are supported by our service company which provides technology, operations and functional services across the Group. To be successful as a BA4-Research , you should have experience with: administrative tasks like booking travel, processing expenses, etc Basic/ Essential Qualifications: Booking business related travel and arranging the necessary logistics Managing complex travel/meeting schedules Ensuring all travel adheres to the T&E policy Arranging visa s and licences where necessary Expense processing Processing of all expenses within the T&E guidelines and deadlines Reconciling corporate credit cards - proactively managing all outstanding payments Ensuring compliance with company expense policies. Processing and auditing expense reports for accuracy and adherence to guidelines. Maintaining accurate records or audit trail of expense processing done Resolving any expense-related issues or emergencies promptly. Staying updated on policies and best practices Raising new Subscriptions, Market Data, IT requests on behalf of the team(s), troubleshooting and following through to resolution Helping with other administrative tasks as required Help to ensure there is reciprocal cover across the expense processing support group during times of absence. Working closely with the Business Management team and Compliance to help ensure that all team activities are undertaken in accordance with firm guidelines and filtered through the correct channels for consultation and approval Helping with other administrative tasks as required Desirable skillsets/ good to have: Excellent communication skills both verbally and written Highly organised Ownership of tasks Ability to work quickly, accurately and effectively during times of increase work flow Proactive & solution orientated Exceptional attention to detail Effective time management skills Discretion and confidentiality Flexible and resilient Team player Prior experience with Coupa, Concur strongly preferred This role will be based out of NKP Mumbai. Purpose of the role To support Research Analysts in the production and delivery of Research with differentiated market insights and actionable ideas to Barclays Clients. Accountabilities Compilation and analysis of data to help Analysts develop investment theses for their coverage areas. Presentation of Research views to Barclays Clients by helping to prepare materials or responses to client questions. Collaboration with the Analyst, Supervisory Analyst, Compliance and other stakeholders to help ensure Research is produced and delivered to Clients and internal stakeholders in a compliant manner. Analyst Expectations To perform prescribed activities in a timely manner and to a high standard consistently driving continuous improvement. Requires in-depth technical knowledge and experience in their assigned area of expertise Thorough understanding of the underlying principles and concepts within the area of expertise They lead and supervise a team, guiding and supporting professional development, allocating work requirements and coordinating team resources. If the position has leadership responsibilities, People Leaders are expected to demonstrate a clear set of leadership behaviours to create an environment for colleagues to thrive and deliver to a consistently excellent standard. The four LEAD behaviours are: L - Listen and be authentic, E - Energise and inspire, A - Align across the enterprise, D - Develop others. OR for an individual contributor, they develop technical expertise in work area, acting as an advisor where appropriate. Will have an impact on the work of related teams within the area. Partner with other functions and business areas. Takes responsibility for end results of a team s operational processing and activities. Escalate breaches of policies / procedure appropriately. Take responsibility for embedding new policies/ procedures adopted due to risk mitigation. Advise and influence decision making within own area of expertise. Take ownership for managing risk and strengthening controls in relation to the work you own or contribute to. Deliver your work and areas of responsibility in line with relevant rules, regulation and codes of conduct. Maintain and continually build an understanding of how own sub-function integrates with function, alongside knowledge of the organisations products, services and processes within the function. Demonstrate understanding of how areas coordinate and contribute to the achievement of the objectives of the organisation sub-function. Make evaluative judgements based on the analysis of factual information, paying attention to detail. Resolve problems by identifying and selecting solutions through the application of acquired technical experience and will be guided by precedents. Guide and persuade team members and communicate complex / sensitive information. Act as contact point for stakeholders outside of the immediate function, while building a network of contacts outside team and external to the organisation.

Job description What you'll do : To develop as complete skin and hair Counselor and provide consultations to clients for their skin and hair-related problems. Suggesting and performing treatments on patients based upon the diagnosis of skin and hair-related concerns. Must have knowledge of Hair Loss Control and Hair Growth Treatments, Hair Growth Laser treatment, Mesotherapy, treatment with Derma roller, and PRP treatments. Must have knowledge of Skin Treatments like peels, pigmentation treatment, removal of moles, warts & tags; Facial PRP; Q-switched laser treatment, and CIT Treatments. Must have knowledge of Laser Hair reduction treatments and consultation thereof. Consultation of Surgical hair transplant procedure. Consultation for Hair Replacement procedure. Follow-ups with the Patients about the treatments and their results. Managing overall consultation and treatment process and converting the clients for the business. What makes you a great fit : Fluent in English, Positive Attitude, Self-driven, Self-Motivated, A Background of Skin, Hair, and Laser will be preferred, Must be having on In-house Sales & Business Development., Will be preparing the Reports & analyzing the sales reports of the center., Fair to do Sales and forte in Service is a must. Female Candidate preferred. EXPERIENCE 1+ Experience in any hair and skin clinic. Experience in taking consultations of all the aesthetic treatments related to hair and skin. REMUNERATION Between 3.60 LPA to 7.00 LPA (depending upon relevant experience and capabilities) PLUS Assured incentive. Provident Fund (optional) Gratuity payable as per law TDS deductible as per law JOB TYPE Full-Time/Permanent OFFICE TIMINGS 6 days working in a week and there will be no weekly off on Friday, Saturday, and Sunday. Office hours:- 10:00 to 19:30 (Flexible 9 Hours )

Skill required: Marketing Operations - Medical Affairs Designation: Copywriting Senior Analyst Qualifications: MBBS/Master of Pharmacy/MD Years of Experience: 5 to 8 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designIn Medical Affairs, you will have to design, develop and deliver business solutions related to the medical affairs group of pharmaceutical companies, including thought leadership development, medical publications, education and information, medical grants, advisory boards and advocacy, regulatory review and approval of pharmaceutical drugs and perform publishing and quality control tasks on submission components. What are we looking for? Clinical & Regulatory Writing Life Sciences Regulatory Operations Life Sciences Regulatory Affairs Medical Review Medical Affairs Written and verbal communication Strong analytical skills Results orientation Experience in research and development Collaboration and interpersonal skills Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualification MBBS,Master of Pharmacy,MD

Skill required: Marketing Operations - Medical Affairs Designation: Copywriting Senior Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? Able to develop content and perform medical review for various clinical and regulatory documents following regulatory guidelines. Use scientific expertise to develop high-quality medical/scientific content outlines and guide the team in content development for assigned modules/projects in line with client expectations. Experience in writing white papers, manuscripts, point of view, etc. Write scientific content for projects if the nature of the project is extremely complex and it requires expertise or based on business need. Communicate the clinical data in a clear and concise manner. Follow department best practices for processes, communication, project management, documentation, and technical requirements. Converts relevant data and information into a form that meets regional regulatory requirements. Understands and complies with appropriate conventions and other governing bodies following applicable divisional guidelines, templates, and SOPs to comply with regulatory requirements. Completes assignments independently or for more complex documents, under the guidance of a mentor. Ensure compliance with client and Accenture internal SOPs for all materials. Collaborate with technology and creative teams to develop innovative digital solutions. Participate in client pitches and business development meetings. Train and mentor scientific writers, contributing to skill development. Ensure quality delivery and client engagement for organic growth.In Medical Affairs, you will have to design, develop and deliver business solutions related to the medical affairs group of pharmaceutical companies, including thought leadership development, medical publications, education and information, medical grants, advisory boards and advocacy, regulatory review and approval of pharmaceutical drugs and perform publishing and quality control tasks on submission components. What are we looking for? Clinical & Regulatory Writing Life Sciences Regulatory Operations Medical Affairs Strong analytical skills Problem-solving skills Results orientation Written and verbal communication Experience in research and development Ability to define medical communication strategy and development of new content for communication. Medical Review Life Sciences Regulatory Affairs Experience from the pharmaceutical/life sciences industry Experience in creating medical communications content for medical affairs/promo medical communication and education, preferably within an agency or pharma environment. Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy,Master of Pharmacy

Responsibilities: * Manage OPD * Perform day-care activities * Blood collection * Operate instruments/machines * Provide assistance to sonologist & specialist doctors/consultants * Provide nursing care in accordance with health-centre policies. Retention bonus Over time allowance

TBM AIL Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries. 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

Skill required: Control Testing - Agile testing Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with SOX testing experience.Conduct testing tasks within Agile models and integration processes and manage development sprints. What are we looking for? Conduct testing tasks within Agile models and integration processes and manage development sprints.Conduct testing tasks within Agile models and integration processes and manage development sprints. Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

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

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

MAIN PURPOSE OF ROLE Responsible for all business development activities . Perform projects of complex scope . MAIN RESPONSIBILITIES Involved in developing new processes to meet project needs , and for designing projects to suit the financial , operating , legal , regulatory and operating criteria elements of a project . Serve as a technical expert in economic modeling and discounted cash flow analysis . Demonstrate in-depth technical knowledge on all aspects of financial analysis and a good understanding of financial , tax , and legal issues . Utilize independent judgment within general practices and policies in selecting methods and techniques for creating solutions . Maintain in-depth knowledge of principles and concepts . Direct and coach lower level professionals . QUALIFICATIONS Education Associates Degree ( 13 years) Experience/Background Minimum 4 years

Dear Doctors Greetings from Ohm Jobs! We are currently looking for a Radiologist for Bangalore Location Roles and Responsibilities Conduct diagnostic imaging procedures such as CT scans, MRI, ultrasound, and X-rays to aid in patient diagnosis. Interpret radiology images and reports to provide accurate diagnoses and recommendations for treatment. Collaborate with other healthcare professionals to develop effective treatment plans for patients. Stay up-to-date with latest advancements in radiology technology and techniques to improve patient care. Participate in quality improvement initiatives to enhance departmental efficiency. Share CV @ hr.ohmjobs@gmail.com Thanks & Regards; Ohmjobs Placement & Medical Staffing Solutions, Pune (Maharashtra ) Address: Vasant Sakha Plaza, 303, Sinhgad Road, near Navale Bridge, Phase 2, Narhe, Pune, Maharashtra 411041 We bring to you the best talent in Healthcare and Medicine Industry, With the Motto "You grow, we grow" kindly connect with us - 9853518080

Oliva clinics is looking for Consultant Dermatologist in Bangalore, Kochi & Chennai. Excellent scope for both (Fresher & Experienced Dermatologist) to offer client consultation, supervise and execute advanced skin & hair cosmetic procedures at the clinic. Responsibilities & Duties: Consult with and treat patients at the designated clinic, perform all dermatology-led medical procedures, and supervise non-dermatology-led procedures. Ensure the efficacy, safety, and adherence to high professional standards for all medical procedures performed under your supervision. Deliver treatments of the highest quality, following established SOPs and company guidelines. Strive for high client satisfaction in all consultations and treatments, as reflected by client feedback and evaluations from the Area Medical Head (AMH) and Area Operations Manager (AOM). Required Candidate profile: MBBS and Masters (MDDVL), Diploma (DDVL, DVD) or Doctorate (DNB) in Dermatology. Strong knowledge and experience in medicine and dermatology. Excellent communication skills and Energy Levels. Ability to connect well with clients. For more details contact 8886690138/9515343007 or careers@olivaclinic.com

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Analyst Qualifications: Master of Pharmacy Years of Experience: 3 to 5 years Language - Ability: English - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The incumbent will perform the regulatory affairs tasks of building regulatory dossiers of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components.You will be expected to collect, collate and evaluate the scientific data gathered as part of R & D. Advise on legal and scientific restraints and requirements. Ensure the organization`s products comply with current regulations. Example; Build regulatory submission strategy, author CMC documents, and health authority packages etc. What are we looking for? Life Sciences Regulatory Services Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Agility for quick learning Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Master of Pharmacy

Overview As a Packaging Specification Writer, this role is responsible for ensuring that packaging specifications meet all required criteria and standards. Initially, you will lead the migration of legacy specifications to the new specification management system. Additionally, you will provide ongoing support to PepsiCo Packaging Engineers across various projects, including Innovation, TBS, Sustainability, and Productivity, ensuring that all packaging specifications are written in compliance with industry standards and requirements. Responsibilities Understand the PepsiCo PLM and SW ways of working in Global Pkg documentation and become proficient in the specification management system and IT Applications associated. Create and Update Packaging Specification Database by taking incoming packaging spec information and ensuring accurate documentation by collaborating with regional pckg teams and vendors and digitize the information into the specification system (SAP/PV).Audit incoming spec information for any omissions of required fields, errors, or needs in linking specifications to associated Finished Good Eaches and Finished Good Case Specifications. Collaborate with Regional ING/Non-ING Spec Writing teams or Coordinators to handle routing of specification in spec system from intitiation to final packaging approval. For Foods Pckg : Convert attachments to report to TIFF file format when files are requested to print on spec. report (mostly PDF to TIFF). For Bev Pckg : Convert pdf technical drawings to jpeg to letter size jpegs to upload in PV Upload required reports from specification systems to local systems as needed. Work with Spec Mgmt. Team Lead OR Spec Mgmt. Foods Packaging Spec Coordinator to resolve issues that may arise with regard to risks/challenges (timing, acquiring information from Pkg. Engineers requesting specifications, or system problems) in meeting specification timelines. Qualifications Experience within the Packaging CPG space (min 1-2 years) and familiar with Packaging Engineering terms and test methods. Bachelors degree in Packaging Engineering is desired. Well versed in MS Office 365 Effective communication skills, both verbal (Conf Calls) and written (reports, e-mail) in English Learning agility, self-motivation and desire for continuous self-improvement. Team player and works well with cross-functional, cross-regional and cross-cultural teams.

As a power electronics engineer with at least 5 years of design experience, you will be responsible for: Manage PEP (Product Evolution Process) topics, considering our design rules Managing product maintenance and evolution topics (Quality, Obsolescence, Adaptation, QVE) Investigating to identify the root causes of design issue, then to find a solution to deal with it. Selection and dimensioning of active and passive components, and justification of the design. Creating electrical schematics and overseeing PCBA design in collaboration with the PCB team. Conducting design tests on prototypes, debugging for compliance. Performing verification tests and debugging the boards. Supporting the validation team during the testing phase. Providing internal advice and knowledge sharing, helping with decision-making in technical topics Mastering technical specifications, ensuring knowledge and know-how capitalization, staying updated on technological developments. Accelerating our digital transformation with 3D simulation tools. Equipment Management: Maintain and manage lab equipment, ensuring all hardware is functioning correctly and safely. Troubleshooting: Diagnose and resolve hardware issues with computers, servers, printers, and other peripherals. Documentation: Generate and revise engineering documentation, including test methods and procedures. Preventative Maintenance: Coordinate and execute daily preventative maintenance activities. Network Support: Provide network connectivity and support, including cabling and power management. Testing: Perform functional analysis and testing of hardware components and systems. Solid and proven knowledge in electronics (Power, Analog and digital) Solid and proven knowledge in power conversion and static converter topologies. Ability to work independently on t

Job description Urgent Opportunity for PICU-Pediatric Nurse/Neonatal Nurse(NICU) for Reputed Global Health Care !!! JOB DESCRIPTION Job Role : Junior PICU Nurse/NICU Nurse Job Location : Bangalore Experience: 2-4 Years KEY RESPONSIBILITIES Caring for neonates at the remote NICUs/PICU's from a centralized care center Manage these patients and document their progress, troubleshoot ICU issues, coordinate bedside nursing care in accordance with global standards, and escalate issues to the neonatal intensivist, who also will be at the command center 24/7 Should be aware of ICU patients monitoring parameters like SpO2, cardiorespiratory, NIBP, Invasive BP, CVP, ventilation parameters, non-invasive ventilation parameters, CPAP/HFNC settings and others Assisting or hands-on experience in procedures like CPAP/HFNC, intubation, initiating ventilation, securing central lines, and ABG sampling. Conducting tele rounds involving patient review, daily rounds, review of labs and radiology, drug charts, and protocol compliance. Liaising with the bedside team actively and providing critical care expertise in real time to augment the delivery of critical care to the NICUs Check-ins with regular intermittent tele rounds on sick patients and initiating appropriate actions with the help of the tele NICU nursing team in collaboration with the bedside team Documenting patient-level data and communication in our smartICU platform, RADAR keeping records of their health in NICU, diagnoses and documenting patients' symptoms and medical history. Identifying changes in the infant's symptoms and intervening in emergencies. Following appropriate guidelines and schedules. Keeping and tracking records for vital signs like temperature, pulse, breathing, oxygenation and blood pressure and any signs of distress due to birth asphyxia and trauma, respiratory distress, apnea, aspiration, sepsis, shock etc., in critically ill infants. PREFERRED QUALIFICATIONS NRP certification and BLS How to apply If you are interested. Interested candidates can share their resume to padmini.m@in.experis.com

Check the medical admissibility of claim by confirming diagnosis and treatment details Verify the required documents for processing claims and raise an information request in case of an insufficiency Approve or deny claims as per T&C within TAT If candidates are interested please drop your update resume/CV on my WhatsApp no - 9632777628 Thanks & Regards Dona Antony Email - dona.antony@mediassist.in