Drug Safety Jobs

We are looking for a Chemist to join our team at our Paonta Sahib location. This role is ideal for candidates with 0 to 3 years of experience and who hold a B.Pharma degree. The Chemist will work on various tasks that contribute to the development and quality assurance of pharmaceutical products.**Key Responsibilities:**- **Conducting Experiments:** Perform laboratory experiments to formulate and test new chemical products, ensuring they meet necessary standards.- **Data Analysis:** Analyze experimental data using appropriate methods and tools to draw relevant conclusions and report findings.- **Quality Control:** Monitor and test the quality of raw materials and finished products to ensure they comply with industry standards and regulations.- **Documentation:** Maintain detailed and accurate records of experiments, methods, and results to support compliance and regulatory requirements.- **Collaboration:** Work closely with team members and other departments to contribute to project goals and share knowledge effectively.**Required Skills and Expectations:**- A Bachelors degree in Pharmacy (B.Pharma) is essential for this role.- Candidates should be able to work independently and as part of a team, demonstrating good communication skills.- A strong attention to detail is required to ensure the accuracy of testing and reporting results.- Ability to follow protocols and safety guidelines in the laboratory is crucial to ensure a safe working environment.- Candidates should be motivated, eager to learn, and ready to take on new challenges in the field of chemistry.

As a Pharmacist at Lotus Polyclinic, you will:- Dispense prescribed medications accurately and safely- Counsel patients on dosage, side effects, and drug interactions- Maintain pharmacy inventory, stock levels, and expiry management- Coordinate with doctors and clinical staff regarding prescriptions- Ensure compliance with Drug Control and Pharmacy Council regulations- Manage billing, records, and pharmacy documentation- Provide OTC medication guidance and basic health advice- Maintain hygiene, storage standards, and cold-chain protocols- Support patient-centric service and ethical pharmacy practiceRequirements:- B.Pharm / D.Pharm with valid Pharmacy Council Registration- Minimum 1 year experience in retail or hospital pharmacy (freshers may apply)- Strong knowledge of prescription handling and drug safety- Good communication skills in Tamil & English- Basic computer and billing software knowledge- Ability to work in shifts and weekends- Professional attitude and patient-care mindsetPreferred Skills:- Experience with clinic or hospital pharmacy setup- Knowledge of inventory management systems- Familiarity with generic medicines and brand alternatives- Customer service & counselling skills- Immediate joiners preferredWhy Join Lotus Polyclinic?- Friendly and ethical work environment- Career growth in a multi-specialty clinic- Competitive salary + incentives- Learning exposure with doctors and specialists- Stable, long-term opportunity

JOIN US !!!Currently I am looking for few Register Pharmacist for HospitalLocation : Bhowanipore Kolkata Qualification : B. Pharma or D. Pharma Experience : Min 3-5 Years continue working experience Skill strong knowledge in medicine and handle a store or hospital pharmacy and a leadership quality and knowledge of inventory and supply managing knowledge in pharmacy.Dispense medications, provide patient counseling, and ensure proper dosages. Monitor inventory, order supplies, and maintain compliance with medical regulations. Collaborate with healthcare providers for optimal patient care.

Experience in hospital pharmacy preferred

Position: Research And Development ApprenticeshipEligibility: LGBT Applicants Only + B.Pharm/M.Pharm (2022, 2023 or 2024 pass outs) + Bangalore City candidate***The above 3 parameters in Eligibility will be considered ONLY***Qualification: (2022, 2023 & 2024 Pass Outs) B. Pharm / M. PharmStipend: INR 25,000 per month (in hand)Duration: 12 monthsCTA: Depending on performance maybe be converted into full time resources at the end of the internship periodWork Timing, General Shift: 9AM to 5 PMLocation: Bengaluru OnlyWho Can Apply - LGBT+ (Lesbian, Gay, Bisexual, Transgender+) Pharma Job Seekers who are based in and around Bengaluru only Role Requirements-Good English language skills written and verbal particularly in scientific/medical terminologyAbility to evaluate data and draw conclusions with appropriate guidance from senior team members or managerGood attention to detailGood interpersonal, presentation and communication skillsService-oriented attitude and ability to be a team player and interact effectively with all levels of personnel in an interdisciplinary and matrix environmentComputer proficiency, IT skills, the expertise and ability to work with web-based applicationsGood level of flexibility and ability to prioritize workIf you belong from LGBT Community then please send CVs at pamela@thepridecircle.com

1398169136 6-5 06:37:12Recruitment of part-time cross-border e-commerce export country purchasing managers (pharmaceuticals; also drug registration and listing): Qualifications, experience, responsibilities and salary system:The following items include the candidate's experience and future responsibilities:1. The cross-border e-commerce platform is generic drugs from India and Bangladesh, which are mainly exported to mainland China, followed by Europe and the United States, and supplemented by Southeast Asia, the Middle East, and Latin America.Job seekers' responsibilities and work experience include: Indian online international pharmacy cross-border e-commerce platform, cross-border e-commerce exports include active pharmaceutical ingredients (API), OTC, targeted drugs, prescription drugs, vaccines, biologics and biosimilars, Ayurveda is recruiting for pharmaceutical factory e-commerce platform check-in, cross-border e-commerce platform decoration and maintenance, sales maintenance, international express logistics and export customs declaration;3.Organize and participate in industry conferences and exhibitions, and use various social software (WA WS FB TG LINE Tiktok Ins Linkedin Twitter Viber) to accurately attract traffic;In the first half year, an average of 300 generic drug manufacturers can be organized to join the cross-border e-commerce platform every month;Cross-border e-commerce sales-side EPR management daily inventory and reconciliation with each settled pharmaceutical factory, express delivery logistics and customs declaration companyUnderstand and supplement the payment tools and payment gateways used by each purchasing country on the e-commerce platform (the company includes but is not limited to the cross-border e-commerce platform for generic drugs), and assists in the gateway API interface with the payment acceptance gateway of India and Bangladesh. enter;2. The job seekers responsibilities and work experience also include:

Role & Responsibilities:1. To own IRL Vision, Values, and Mission.2. The candidate should have excellent knowledge of Biochemical pathways, Cell-based, and Biochemical assays. Good knowledge of platforms like NanoBret, HTRF, AlphaLISA, LCMS-MS-based assays & in-life studies.3. Develop, validate, miniaturize and troubleshoot in-vitro biochemical and cell-based assays 4. A demonstrated record of delivering DMPK and PK/PD expertise, including dose-ranging, formulation, and stability studies for drugs, with the ability to successfully troubleshoot technical challenges5. S(he) should have the ability to manage diverse teams like cell biology and ADME teams. 6. Candidate should have good persuasive speaking skills. The candidate will be responsible for presenting regular scientific updates to clients. 7. The candidate should be curious and willing to do the work client requires8. Responsibility for managing timelines and deliverables 9. A good team player with strong interpersonal skills who shows a willingness to assist other laboratory personnel when required10. An inquisitive and fast learner who keeps abreast with the latest scientific developments in his/her areas of work and related fields.11. Seamlessly connect with the team to review the data carefully. Statistical analysis knowledge, creating data visualizations, and writing reports.Qualifications and Educational Requirements: 1. Ph.D. with a specialization in Pharmacology/ Biotechnology/Biochemistry with 12-15 years of experience in a Drug Discovery CRO space. 2. Experienced in working in and driving a cross-functional matrix. 3. Age will not be a constraint in deserving cases. 4. We are gender neutral.

Job Description: Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract, Review articles and Medico-marketing inputs) Should be able to develop LBL, Poster, News-letters, KOL cases, booklets, atlas, guideline booklet, product monographs, calendars, compendium, customized journals, handbooks, conference abstract booklets, yearbooks, KOL opinion booklets, case studies, CMES, etc. Should have hands on experience in literature search and systematic review Should be accountable for medical writing deliverable and should ensure work on assigned projects adheres to industry/international standards Should be able to draft article on Health Economic Outcome Research and understanding on subject will be added advantage Should be responsible for continual improvement of in-house medical writing capabilities Should have an excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards. Should liaise with internal team, clients, authors and KOLsExperience: Min 4 - 7 years experienceQualification: Bachelors degree / Masters Degree in any Pharma / Lifesciences/ Science related field. Excellent verbal and written skills (English). Good organizational, interpersonal, and team skills. Ability to deliver results under pressure. Goal oriented, self-motivated; able to work independently but within a team environmentDesired Skills/Experience: A good understanding of the healthcare market, challenges, growth prospects and healthcare delivery operations Strong customer and contact network in healthcare domain A minimum of three five years medical writing experience within the pharmaceutical industry or a contract research organisation. Able to work independently, initiate their own projects as needed to streamline their wo

Collections Specialists are generally responsible for managing and collection all the outstanding accounts receivables form clients and customers. In addition, they may be responsible for other aspects of collections, resolve customer billing problems and reducing the amount of accounts receivables.

Quality review of ICSRs, surveillance of known or emerging safety issues, participation in an escalation process, risk evaluation, and analysis of safety data. Apply safety concepts and regulations contained within FDA CFR, ICH, and EU GVP to management of Safety data across the development life cycle. Analyze aggregate safety data within a clinical program towards tracking and trending of risk assessments and additional mitigation measures. Contributes to safety sections of the investigational new drug and new drug applications, investigator or regulator communications, Investigator brochure, and other reports (DSUR) Participates in the set-up and maintenance of adverse event processes in global clinical trials Ensure Quality of the Individual Case Safety Report, including data and a concise, medically relevant narrative.

Position Clinical Research CoordinatorQualification B.PharmExperience - Above 1YearsTiming - General ShiftSalary Based upon PerformanceLocation ChennaiLicence: Pharmacy Lice(Only B. Pharm is eligible for this Job)Job Description Clinical Research Coordinator: To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist the Site Head in the managing the Site to ensure ethical conduct of research activities. Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. Provide guidance to CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Assist the pharmacist in drug accountability and temperature maintaining logs. Monitoring Sr. CRC and CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report to the Site Head daily and take advice for further action. Delegate the work to Senior/Junior/Trainee CRCs as per the requirement.Job Types: Full-time, PermanentSalary: ?10,000.00 - ?15,000.00 per month

Currently I'm looking for some Hospital PharmacistLocation : Bhowanipore Kolkata Qualification : B. Pharma / D. Pharma Experience : Min 3-5 years of experience in retail or hospital Contact : rajib801733@gmail.com 8017334906 Skills : Dispense Medications, provide patient counseling, and ensure proper dosages. Monitor inventory, order supplies, and maintain compliance with medical regulations. Collaborate with healthcare with healthcare providers for patient care.For more details call me @8017334906