40 Pharmaceuticals Jobs - Page 2

Description As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in 100 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Own and manage regulatory projects accounts and work towards achieving excellence in service delivery and exceeding Service Level Agreements through team of delivery manager and project managers. Lead the team of cross functional regulatory affairs specialist to support global specification management, raw material qualifications, change control, toxicology, analytical methods and stability reports, packaging material, labelling etc. for global product portfolio including cosmetics/consumers, pharmaceutical, medical devices and biologics. Set up matrix team of regulatory affairs professionals to manage the post approval life cycle maintenance. Lead and manage the regulatory affairs functions; manage delivery of regulatory affairs projects for global customers across all geographies including US, EU, APAC, MENA, LATAM, CIS etc. Participate in and/or lead business development activities e.g., RFI and RFP responses, lead bid defense efforts for potential new regulatory affairs project opportunities. Provide guidance/direction for regulatory affairs staff on development and training needs. Responsible for ensuring that staff are available for projects requiring regulatory submissions services. Responsible for defining RA strategies to meet submission timelines for post approval life cycle maintenance, for implementing these strategies and for the ongoing assessment of the appropriateness for continuing established regulatory strategies and for adjusting the strategies as appropriate. Interface with project management office to generate process productivity metrics and communicate them at appropriate forums. Interface with audit and compliance team to manage QA related issues/escalations within the account Ensure customer satisfaction targets are met and exceeded. Experience (Minimum Required): Minimum of 15 years experience in the pharmaceutical industry in Regulatory Affairs or Regulatory Operations, ideally at least 10 years international regulatory affairs/operations experience in approvals and post approval product life cycle maintenance. Expertise in project governance, escalation, issue resolution and other project management skills Experience of PL management Experience in transition of business processes to an offshore location Experience in budgeting, forecasting and pricing Excellent written and verbal communication and interpersonal skills Ability to manage relationships across diverse set of stakeholders Ability to produce quality materials within tight timeframes Good Negotiation skills Willingness to work in a flexible schedule.

Medical Representative Role Noida HQ Derma - Biosil Speciality Segment Experience - 1 to 4 years Required Candidate profile Preferably D. Pharm, B.Sc having 1-5 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors, effective in-clinic presentation to doctors, identifying & promoting right product for right doctors, retail chemist prescription audit, timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 1-5 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Key Responsibilities: Conduct thorough quality control reviews of PBRER/PSURs, DSURs, PADER/PAERs, and other aggregate safety reports to ensure content accuracy, data integrity, formatting consistency, and adherence to regulatory and internal requirements. Verify correct incorporation of safety data, narratives, tables, and appendices, ensuring alignment with source documents and databases. Collaborate with Periodic Report Specialists to address discrepancies and ensure timely resolution of quality issues. Maintain up-to-date knowledge of global regulatory requirements and industry standard methodologies for periodic safety reporting. Contribute to the development and refinement of QC checklists, templates, and SOPs to ensure consistent review practices. Track QC metrics and support continuous improvement initiatives related to safety report quality and delivery. Responsible for performing QC reviews of periodic safety reports to ensure compliance with the style guide, templates, and contributor inputs. Responsible for verifying content accuracy, data integrity, and consistency across all report components. Responsible for collaborating with Periodic Report Specialist to resolve QC findings and ensure timely delivery of high-quality reports. Inspection Readiness: Support inspection readiness efforts by ensuring all QC activities are well-documented, traceable, and compliant with applicable regulatory requirements. What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Masters degree and 1 to 3 years of pharmaceutical, biotech or regulatory authority experience in a research and development setting experience OR Bachelors degree and 3 to 5 years of pharmaceutical, biotech or regulatory authority experience in a research and development setting experience OR Diploma and 7 to 9 years of pharmaceutical, biotech or regulatory authority experience in a research and development setting experience Strong attention to detail with the ability to identify inconsistencies and errors in complex regulatory documents. Proven ability to operate effectively in a collaborative environment requiring coordination, communication, and analytical judgment. Solid understanding of pharmacovigilance principles and global regulatory requirements related to periodic aggregate reporting (e.g., PBRERs, DSURs, PADERs). Proficiency in scientific and technical writing/editing, with an emphasis on quality control and adherence to style guides and templates. Excellent written and verbal communication skills in English, with strong organizational and time management abilities. Demonstrated ability to manage competing priorities and strict deadlines while maintaining high-quality standards. Familiarity with the structure and content of safety reports and the ability to interpret and validate data inputs from multiple contributors. Proficient in Microsoft Office tools (Word, Excel, PowerPoint), Adobe Acrobat, and document management systems (e.g., Veeva Vault, SharePoint). Working knowledge of AI tools and prompt use is a plus, especially for enhancing QC efficiency. Team-oriented approach with the ability to work cross-functionally to support compliance and inspection readiness efforts.

Key Responsibilities : Teaching & Learning : Deliver high-quality lectures, seminars, and laboratory sessions in pharmaceutical sciences. Develop and update course materials, including syllabi, lectures, and learning resources. Assess and grade student assignments, exams, and practical work. Provide support for students learning, offering office hours and additional academic support where necessary. Curriculum Development : Contribute to the design and development of new courses and programs within the pharmaceutical sciences discipline. Stay updated with advancements in pharmaceutical sciences to ensure the curriculum remains relevant and aligned with industry standards. Research : Engage in research activities within the field of pharmaceutical sciences, focusing on areas such as drug development, pharmacology, pharmaceutics, or clinical pharmacy. Publish research findings in academic journals and present at conferences. Supervise postgraduate students in research projects and thesis work. Academic Advising : Provide guidance and mentorship to students in their academic journey. Support student engagement and retention efforts through proactive advising and counseling. Administrative Duties : Participate in departmental meetings and contribute to the overall academic strategy of the institution. Assist with the coordination of exams, grading, and other academic processes. Professional Development : Participate in ongoing professional development activities, including attending workshops, conferences, and training relevant to pharmaceutical sciences and teaching. Collaboration & Networking : Collaborate with colleagues within the department and across other disciplines. Develop partnerships with external pharmaceutical organizations, research institutions, and industry experts.

Will implement marketing strategies&campaigns for product promotion to doctors, effective in-clinic presentation to doctors, identifying & promoting right product for right doctors, retail chemist prescription audit, timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 1-5 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors, effective in-clinic presentation to doctors, identifying & promoting right product for right doctors, retail chemist prescription audit, timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 0-2 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors, effective in-clinic presentation to doctors, identifying & promoting right product for right doctors, retail chemist prescription audit, timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 0-2 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

ASTER DM HEALTHCARE LIMITED is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Sales & BD of Excipients for PAN India for Pharma, Lifesciences & Biopharmaceutical Companies Handling existing accounts, obtain orders & develop new accounts Market info on pricing & products & new products Handle rejections & customer complaints Required Candidate profile Min 10 yrs of relevant exp with familiarity about Pharmaceutical product development & manufacturing operations commitment to excellence Self motivated & passionate to value selling Good team player

Develop and implement supply chain and logistics strategies, policies, and procedures for the organization. Coordinate and follow up for the supplies from the CMOs and logistics activities from service providers. Strong skills in order management, planning, organizing, and managing supply chain and logistics activities and processes. Supplier and Vendor Management - Liaise with suppliers, freight forwarders, and logistics service providers on day to day basis, monitor performance, and resolve any issues or discrepancies. interested candidates can share cv to hr3@sarthee.com or call @9033033650

Will implement marketing strategies&campaigns for product promotion to doctors,effective in-clinic presentation to doctors,identifying&promoting right product for right doctors,retail chemist prescription audit,timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 0-3 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors,effective in-clinic presentation to doctors,identifying&promoting right product for right doctors,retail chemist prescription audit,timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 0-3 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors,effective in-clinic presentation to doctors,identifying&promoting right product for right doctors,retail chemist prescription audit,timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 1-3 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements

Will implement marketing strategies&campaigns for product promotion to doctors,effective in-clinic presentation to doctors,identifying&promoting right product for right doctors,retail chemist prescription audit,timely reporting&achieve targets Required Candidate profile Preferably D. Pharm, B.Sc having 0.6-3 year exp. in pharma ethical selling having high energy level, effective communication / presentation / convincing skills and proven track record of achievements