235 Pharmaceutics Jobs - Page 4

Clinztech is looking for Pharmacovigilance Associate I to join our dynamic team and embark on a rewarding career journey. Monitor and assess the safety of pharmaceutical products through the collection and analysis of adverse event reports. Ensure compliance with regulatory requirements related to pharmacovigilance. Prepare and submit reports to regulatory authorities regarding product safety. Collaborate with internal teams to develop risk management strategies for pharmaceutical products. Provide training and guidance to staff on pharmacovigilance practices and policies. Maintain up - to - date knowledge of industry trends and regulatory changes.

Kalol Institute & Research Center is looking for Pharmaceutics Professor to join our dynamic team and embark on a rewarding career journey. Deliver lectures, seminars, and practical sessions on pharmaceutics to undergraduate and graduate students. Develop and update curriculum content to ensure alignment with industry standards and advancements. Conduct research in the field of pharmaceutics, publishing findings in reputable journals. Mentor and supervise students in their research projects, theses, and internships. Participate in academic committees, contributing to the development of the department and university.

Responsibilities: Dispense medications accurately and efficiently Collaborate with healthcare team on treatment plans Provide patient counseling and education Ensure compliance with regulatory standards

To ensure the quality of raw materials, packaging materials and finished products are compliant with the approved specifications and GMP/GLP. Maintains a controlled documentation system in the quality control department. ETC ETC

Formulation - Research & Development - Pellets exp is must , Comply with GMP’s, SOP’s,regulatory documentation.,Develop Robust formulations & Evaluate patents and develop non-infringement strategiesScale up and optimization of manufacturing process.

with We are Vasan Eye Care , a leading chain of eye hospitals in South India, headquartered in Chennai, Tamil Nadu. With over 25 years of excellence in the healthcare industry, we serve more than 6 million patients annually . Starting from our first hospital in Trichy, today we have a network of 100+ super-specialty eye care hospitals across India, and we continue to grow! We are currently hiring a Pharmacist for our Perambur & Tondiarpet Branch, Chennai location. Job Summary: We are seeking a dedicated and detail-oriented Pharmacist with 23 years of experience to manage the pharmacy operations at our ophthalmology hospital. The ideal candidate should have a sound understanding of ophthalmic medications, prescriptions, inventory management, and patient interaction in a hospital setting. Key Responsibilities: Dispense medications accurately based on prescriptions from ophthalmologists and other consultants. Provide clear instructions to patients regarding dosage, usage, and storage of medicines. Counsel patients on drug interactions, side effects, and precautions for ophthalmic medications (e.g., eye drops, ointments). Maintain and manage stock levels, placing orders for replenishment as required. Ensure that all medicines are stored according to prescribed standards. Maintain up-to-date pharmacy records, including purchase, sales, and stock registers. Ensure compliance with hospital policies, legal regulations, and drug control guidelines. Work closely with doctors, nurses, and other medical staff to support patient care. Handle billing and insurance documentation related to prescriptions. Conduct periodic stock audits and support inventory reconciliation. Key Skills & Qualifications: B.Pharm or D.Pharm from a recognized institution. Valid Pharmacy Council registration is mandatory. 25 years of pharmacy experience in a hospital or clinical setup (Ophthalmology experience preferred). Strong knowledge of ophthalmic medications and drug handling. Excellent communication and customer service skills. Attention to detail and strong documentation abilities. Proficient in pharmacy software and basic computer operations. Job Title: Pharmacist Department: Pharmacy (Immediate Joiners Required) Industry: Healthcare / Hospital Location: Perambur & Tondiarpet Branch Experience: 2–3 years (Preferably in Ophthalmology/Healthcare industry) Employment Type: Full-Time Salary: As per Industrial Standard Education: B.Pharm or D.Pharm from a recognized institution. Reporting To: Centre Head Contact Numbers: +91 7904204159 / +91 6384456712 Please share your updated resume to Email: hr.corp@vasaneye.com Website: www.vasaneye.com Feel free to share this opportunity with your friends!

Responsibilities: * Dispense medications accurately and efficiently * Collaborate with healthcare team on patient care plans * Maintain confidentiality at all times * Adhere to regulatory compliance standards

Responsibilities: * Dispense medications accurately and efficiently * Collaborate with healthcare team on patient care plans * Provide expert advice on drug usage and safety * Manage pharmacy inventory and ordering process

Job Description Designation: Pharmacist Role: QC Pharmacist Department: Warehouse Operations Location: Bangalore/Chennai / Mumbai About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities And were just getting started. Leading the chart as one of the top consumer health platforms through ePharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M ePharmacy orders, 2M eDiagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs Brief about the Team The warehouse operations team is within the supply chain vertical of Tata 1mg. The team works closely with the org-wide leadership team, business, product, growth, and category teams to drive operational excellence and strategic initiatives. The team works on special projects and innovations that aim to deliver high impact. The projects span across business verticals including e-pharma, e- diagnostics, and retail. What will you do What will you do Customer Support Read & validate prescriptions (Rx) + OTC orders Contact customers for clarification or information required to process the order - Situational requirements Inventory Management & Order Processing management Responsible for physically performing order picking, quality checks, packing and handover to the riders Ensure all orders are processed within the defined cut-off TAT (Turnaround Time) Responsible for physically performing stock receiving and put away processes Conduct daily stock audits and ensure accountability for inventory shrinkage Follow up and ensure timely closure of pullout and purchase returns Ensure customer satisfaction through timely order fulfillment, issue resolution, and excellent service Compliance Ensure strong quality checks while packing/ dispensing medicines Ensure 100% compliance per the process guidelines What we are looking for 1 + years of relevant experience (pharmacist Diploma or Bachelor (D. Pharma or B. Pharma License for that state. Should be comfortable working in shifts and on weekends Why Join Us? Tata 1mg provides one of the most exciting and high-growth environments to work. You get the added benefit of working in a prestigious legacy brand like Tata and a highly dynamic and versatile startup like 1mg. Being an integral part of the Warehouse Operations will provide you to closely work with the Operations and Logistics team which is spread PAN India.

PRESCRIPTION HANDLING, STOCK MANAGEMENT, PURCHASE & SALES REPORT.

Kalol Institute & Research Center is looking for QA & Pharma. Chemist Faculty to join our dynamic team and embark on a rewarding career journey Developing and teaching plans Advising and mentoring students Conducting research and publishing findings in academic journals Participating in departmental and university-wide committees Engaging in professional development activities to stay current in the field Excellent communication and interpersonal skills

Alembic Group is looking for Senior Executive - Digi Labs to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

As a Research Associate/ Executive/ Analyst in the Small Molecule Bioanalytical Research Laboratory at Syngene International Ltd., you will be responsible for conducting BA/BE studies in the laboratory. Your role will involve critical method development and validation programs, ensuring technical and regulatory compliance in all studies. To excel in this position, you should have a strong background in pharmaceutics or related life sciences, along with extensive experience in the bioanalytical field, specifically in small molecule bioanalysis. Your commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis, will be essential for success in this role. Key responsibilities include performing bioanalytical work such as sample processing for method development, method validation, and study sample analysis in compliance with SOPs and STPs. You will be required to prepare STP, MV protocol, and study sample analysis protocol, as well as coordinate with the maintenance department for any equipment failures. Documenting data generated and ensuring adherence to regulatory guidelines set by GCP/GLP will also be part of your responsibilities. To qualify for this role, you should hold a Masters in Pharmaceutics or related life sciences from a reputed university, along with a minimum of 1 year of experience in regulated small molecule bioanalysis. Hands-on experience in small molecule regulated bioanalytical experiments is crucial for this position. Additionally, having experience working in a Bioanalytical CRO lab will be considered an advantage. Core competencies required for this role include scientific expertise, technical proficiency, and strong documentation skills. You should be able to bring a creative and innovative advantage to projects, think scientifically, and conduct experiments effectively. Syngene International Ltd. is an equal opportunity employer committed to fostering a diverse and inclusive workplace. If you are interested in joining our team and contributing to cutting-edge bioanalytical research, please visit our website at https://syngeneintl.com/ for more information about our company and the work we do.,

Role & responsibilities Good understanding on Pharma Finance , month end processes , MIS reporting, data analysis , Variance analysis , Budget, Forecast in Pharma Industry. Ability to create financial models (cash flow, DCF, NPV, P/L , CAPM, payback, CBA, business valuation, equity analysis, Investor deck ,forecastand various models) Understanding of M&A and related documentations Helping to develop project plans and monitor their timely completion Market analysis , Industry analysis , Business plan , able to extract data from financials Good understanding and practical knowledge of Office 365, advance tools. Preparation of Presentations ,Investor dec, process models, specifications, diagrams, charts ,flowchart Analyzing an organization's large data sets to provide actionable insights Staying up-to-date on the latest industry trends , process and IT advancements to automate and modernize systems. Effectively communicating your insights and plans to cross-functional team members and management. Gathering critical information from meetings with various stakeholders and producing useful reports. Strong understanding of international trade regulations, finance principles, and risk management. Knowledge of trade finance products and instruments, including letters of credit, guarantees, and export credit insurance. Proficiency in financial analysis, due diligence, and risk assessment. Excellent communication and negotiation skills. Attention to detail and accuracy in trade documentation. Preferred candidate profile M.com with 15+ yrs experience in Pharma companies Good in Analytics numbers.

K.K. Patel Super Speciality Hospital is looking for Pharmacy (Assistant) to join our dynamic team and embark on a rewarding career journey Assist licensed pharmacists in preparing and dispensing medications. Maintain accurate patient records and medication inventories. Provide information to patients about their prescriptions. Ensure compliance with pharmacy laws and regulations. Assist in the management of pharmacy supplies and inventory. Support the overall operations of the pharmacy.

About Company ASG Eye Hospitals is a chain of super specialty eye hospitals in India. It offers a comprehensive range of eye care services including treatment and surgeries of Retina, Cataract, Squint, Oculoplasty, Cornea, Lasik, ICL, Glaucoma, and Paediatric Ophthalmology. Currently, the group has 165+ Eye Hospitals across 83+ cities in India. Role - Executive - Pharmacist Location - Jaipur Job Responsibilities Provide advice about health issues, symptoms and medications in response to customer enquiries. Process prescriptions and dispense correct medication. Ordering, selling and controlling medicines and other stock. Manage inventory to ensure an adequate supply of medications. Managing budgets Keeping statistical and financial records Preparing publicity materials and displays Counsel patients on proper medication and side effects. Desired Candidate Profile D.Pharm / B.Pharm Must be a registered Pharmacist from the State Pharmacy Council. Good Communication Skills. Must have Basic computer knowledge. Perks and Benefits + Performance Based Incentives Interested candidates mail your resume along with below details to simran.meena@asgeyehospital.com or WhatsApp the same on 88750 29935 Total Experience - Current CTC - Expected CTC - Notice Period -

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy Years of Experience: 1 to 2 year About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases. What are we looking for Looking for the candidate with Good Communication and written skills, Bachelor of Pharmacy,Bachelor of Physiotheraphy,BSc. Nursing Roles and Responsibilities: n this role you are required to solve routine problems, largely through precedent and referral to general guidelines,Your expected interactions are within your own team and direct supervisor. You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments Qualification Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy

Job Description Summary The Regulatory Affairs Senior Associate is responsible for the preparation, compilation, evaluation and submission of ANDAs & Amendments to USFDA and handling deficiencies with timely submission of responses to agency. Job Description Coordinate with cross functional team/stakeholders (R&D, Quality, manufacturing, SCM, IP, PM) and vendors as required and evaluation of documents in-line with the current regulatory requirements Review of Product Development Report, Executed and Intended Batch Records, Specifications, Analytical Procedures, Method Validation Protocols and Reports & Certificate of Analysis of API / Excipients / In-Process / Finished products/Packaging materials, stability protocols and reports. Review of vendor documents of API, Excipients and Packing materials Review of documents for adequacy (w.r.t content, requirements, legibility, PDF requirements, etc.) Preparation, review and compilation of ANDAs, Amendments and Supplements in eCTD format. Coordinate with Regulatory Operation team member for uploading the submission in e CTD software Review of exported submission shared by Regulatory Operation team for submission . Monitor the FDA website for any updation. Education & Experience :- Master of Pharmacy in Dept. of Pharmaceutics Total experience of 3-5 Years in Regulatory Affairs

Urgent hiring for Research Scientist / SRA Formulation R&D (OSD) for Roorkee & Gurgaon location Location: Roorkee Department: Formulation & Development (F&D) Industry: Pharmaceuticals OSD & Liquid Job Description: We are hiring a Research Scientist – Formulation R&D for its Roorkee facility . The candidate must have strong experience in formulation development, technology transfer , and scale-up activities for regulated and semi-regulated markets . Key Responsibilities: Execute and support formulation development and scale-up for OSD products Conduct technology transfer from R&D to production Prepare and review MFC, MFR, PDR , and tech transfer documentation Develop and optimize exhibit and validation batches Ensure compliance with regulatory standards for global markets Coordinate with cross-functional teams including QA, Production, and Regulatory Knowledge of bioequivalence/bio study is desirable (not mandatory) Requirements: M.Pharm with specialization in Pharmaceutics (mandatory) 3–6 years of experience in Formulation R&D (OSD) Must have experience working for regulated and semi-regulated markets Strong documentation and project execution Apply at: anupriya.1@walterbushnell.com WhatsApp CV to: 9650111639

We are seeking a knowledgeable and detail-oriented Corporate Pharmacist to join our team. In this role, you will be responsible for ensuring that the companys pharmaceutical products and services meet regulatory and safety standards. This role involves overseeing compliance with laws, regulations, and corporate policies while optimizing pharmaceutical operations across the organization. Key Responsibilities: 1. Oversee day-to-day pharmacy operations across multiple locations or divisions within the company. 2. Ensure compliance with all state and federal pharmaceutical regulations across operational units. 3. Streamline medication inventory and distribution processes to enhance efficiency. 4. Supervise pharmacy staff, providing training and development opportunities. 5. Collaborate with the logistics team to ensure on-time product delivery and stock levels. 6. Analyze operational data to improve workflow and reduce errors or inefficiencies Preferred candidate profile 1. Education: Doctor of Pharmacy (Pharm.D.) or equivalent degree. 2. Licensing: Active pharmacist license in the state of employment. 3. Experience: Fresher or 1-2 years of experience in a pharmacy setting, preferably in a corporate, regulatory 4. Strong understanding of pharmaceutical law, regulations, and quality assurance practices. 5. Expertise in medication therapy management and safety protocols. 6. Ability to interpret scientific data and product formulations. 7. Excellent written and verbal communication skills. 8. Ability to work collaboratively in cross-functional teams. Registration certification is compulsory

understand organizational structure, strengths & drivers Utilize diverse mix of sourcing channels (referrals, job boards, search firms, events) to build robust talent pipelines for various teams cultivate relationships with high-potential candidates Required Candidate profile 7+ yrs of exp in the Manufacturing, Oil & Gas, Pharma or Chemical sector. Strong communication & influencing skills Strong track record of exceeding hiring goals & filling open positions efficiently.

Job Title: Sr. Executive Job Grade: G11B Function: GLOBAL BUSINESS DEVELOPMENT AND PORTFOLIO MANAGEMENT Sub-function: IP Litigations Manager s Job Title: Sr. Manager Skip Level Manager s Title: Sr. General Manager Function Head Title: Vice President Location: Sun House, Mumbai No. of Direct Reports (if any) NA Date of Joining: Job Summary Executive role in IP litigations - FTO searches & evaluation reports, identifying IP risks pre-PIF assessment, providing IP litigation support to various internal stakeholders. Areas Of Responsibility FTO searches & preparing evaluation reports Pre-PIF assessments Timely support to Portfolio, Business Development, R & D, PMO, and Regulatory teams New Product Opportunity Identification - based on IP scenarios Monitoring of IP updates, Competitive Intelligence and regulatory developments Travel Estimate Up to -- % Job Scope Internal Interactions (within the organization) Yes - with R &D, BD, PMO, RA, and Portfolio teams External Interactions (outside the organization) No Geographical Scope Global stakeholders Financial Accountability (cost/revenue with exclusive authority) NA Job Requirements Educational Qualification Master of Pharmacy or M. S. or M. Tech. (Pharmaceutics or Chemistry preferred) Specific Certification P. G. Diploma in Patents Law (preferred) Skills Sound understanding of IP dynamics, technical skills, Good communication skills, Team player, Agility & adaptability Experience Around 4-5 years of relevant experience in Formulation- IP domain

We are seeking a Regulatory Affairs Executive with 1 to 3 years of experience in the pharmaceutical industry. The ideal candidate should have hands-on experience in compiling and reviewing ACTD and CTD dossiers for various regulatory submissions. Required Candidate profile B.Pharm & M.Pharm With Knowledge of Regulatory Affairs CTD ECTD DMF and Regulatory Guidelines are Eligible to Apply

Akshara Consultancy - Laboratory Items Distribution Company Qualifications: Bachelors degree,or masters preferably Pharmaceutics, or Pharmacology 2-3 years of sales experience, preferably in pharmaceutical laboratory items. Key Responsibilities: Sell laboratory items, including microbiology and chromatography products (HPLC/GC vials and columns). Develop and expand client relationships. Conduct regular field visits to follow up with clients and secure orders. Maintain and enhance sales performance for both existing and new business. Travel across Telangana to meet clients and ensure customer satisfaction. Desired Skills and Attributes: Strong interpersonal and communication skills. Ability to work independently and manage time effectively. Self-motivated with a proactive sales approach. Willingness to travel extensively within the region.

Qualification B.Pharm and M.Pharm with at least 55% or equivalent grade with NET/SLET/PhD Eligibility Criteria Assistant Professor : Fresher or 2 years of Teaching experience Associate Professor : Minimum of 8 years of Teaching with at least 5 years at the Assistant Professor level. Minimum 7 Research publication Guided students for research projects Professor : At least 10 years of Teaching with at least 5 years at the Associate Professor level. Minimum 10 Research publication Leadership roles in academic or research institutions Roles and Responsibility 1 ) Provide case studies, group discussions, laboratory experiments, pharmaceutical formulations, practical exercises, and field visits to create an engaging learning experience for students. 2) Publish research papers in national and international pharmacy journals, and present findings at pharmaceutical conferences and seminars. 3) Teach a variety of pharmacy subjects such as Pharmacology, Pharmaceutical Chemistry, Medicinal Chemistry, Clinical Pharmacy, Pharmaceutical Analysis and Pharmacognosy. 4) Participate in departmental meetings, curriculum review processes, and assist with the development of new programs or courses in the pharmacy department. 5) Serve on university or faculty-level committees for academic and administrative purposes, including research committees, examination boards, or curriculum committees within the pharmacy department. Skills Guiding and Advising Learners Participatory Instructional Methods Evaluation and Constructive Guidance Optimal Time Management and Scheduling Research Approaches and Techniques