ResponsibilitiesChecking and verification of Dispensing of materials and label generations as per approved procedures including Cross check of material identity and quantity Supervise dispensing activity to ensure compliance with Good Dispensing Practices and cross-contamination prevention measures. Coordinate with production and QA for line clearance and material reconciliation. Ensure all transactions are documented in e-logs and other software systems Ensure all transactions are done under controlled environment conditions including monitoring of daily environment records Ensure the cleaning of the area along with preparation of sanitation solutions and maintain proper records. Conduct calibration/daily verification of Weighing balances and other equipment as per SOP and schedule. Perform the dispensing of solvent materials. Perform QMS activity related to warehouse.Qualification & ExpeirenceQualification: -BSC /B. Pharm /D. Pharm or equivalent Experience of NLT 2 years Should have exposure to handling of SAP systems.

ResponsibilitiesMarket identification within ANZ & entry strategy Prospecting for new partners in the chosen marketsShowcase Rubicon’s Capabilities & Products To Potential PartnersEvaluation of short-listed opportunities, negotiate for deal terms, prepare business case presentations.Negotiation of term sheets / definitive agreementsAlliance ManagementInfluence the cross functional team to drive the BD endeavors at organizational level Qualification & ExpeirenceMust have 10+ years of international BD experience in Finished Products Must have proven success in regulated marketsMust have travelled to assigned territories for customer meetings (not only CPhI)

Responsibilities Execute assigned tasks as per planned production activity to meet production targets for a shift  Regulate usage of consumables in the production process at optimum levels to save costs  Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality  Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance  Ensure equipment, facility and block premises are maintained as per regulatory compliance  Maintain system integrity by updating documentations and deviations on CipDox while performing operations  Perform validation, qualification and calibration as per schedule and update output of all activities in the systems  Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (3/6) Prepare manufacturing records and update online documentation to meet production and cGMP requirements  Maintain online documentation and timely entries in BMR and supporting documents  Prepare new documents and update existing documents as per GMP requirement  Operate software such as SAP, CipDox and QMS Qualification & ExperienceBachelor in Pharmacy Relevant Work Experience  3-4 years of experience with 2 years of experience in pharmaceutical manufacturing  Knowledge of cGMP practices, equipment operations required for Formulation Production

ResponsibilitiesAnalyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLAReport errors, abnormal observations, non-compliances related to procedures, equipment and instruments, and deliver results promptly to facilitate timely action and avoid delay in releasesInitiate investigations and take necessary corrective and preventive actions Investigate incidence & lab error on priority basis so that batch release timely and issues are not recurring Key Accountabilities (3/6)Document entries, raw data and findings concomitantly in relevant test data sheets so as to facilitate the lab QA to review the reports and avoid missed entries Review reports as per cGMP & GDP for compliance to GLP Ensure no GMP / regulatory concern are raised by adhering to SOPs and following proceduresKey Accountabilities (4/6)Evaluate & document Instrument / equipment break down and suggest mechanisms to avoid the sameMaintain equipment and instruments optimally to ensure no incidences or non-compliances occur due to malfunctioning of equipment/ instrumentsQualification & ExperienceM. Sc (Microbiology) Relevant Work Experience 1-5 years’ experience for analyst and 3-7 years for reviewer in Microbiology Good knowledge of Microbiology, skill to perform assigned task, communication in English

Responsibilities. Prevent incidences across Unit to ensure employees and stakeholder¢�s safety Assess and Improve emergency preparedness across Unit to reduce impact of Incidences to human and propertyExecution of the planned Activity, promotional Activity and improvement and Statutory complianceQualification & ExperienceScience graduate in chemistry/ Diploma or Degree with Diploma in Advance industrial safety 2 years of safety experience in Pharma or chemical industries

ResponsibilitiesLiterature Management Process Perform review of literature results retrieved and imported into literature citation management system on a weekly basis and determine if minimum criteria for ICSR is met for marketed products Perform review of literature results to determine if article contains new aggregate safety information in support of the periodic report and/or signal detection Determine whether full text article needs to be ordered and order them if further information is needed to confirm if citation meets criteria for ICSR or for signal detection Flag articles containing new aggregate safety information for TA Safety to perform secondary review Request Local Safety Officer to provide English translation if the article is not in English Notify business partner of articles received, if applicable Support audits and inspections Knowledge And Skills Ability to identify literature articles containing ICSR criteria or aggregate safety findings supporting signal detection Ability to order full text articles where needed Ability to receive feedback from Case Management and TA Safety and optimize quality of literature review Demonstrate knowledge of global aspects of pharmacovigilance Strong knowledge of processes and global regulations for pharmacovigilance and literature surveillance Ability to effectively manage competing priorities and timelines Strong knowledge of literature citation management systems and platform used to configure search strategies Experience in use of AI and prompts would be usefulQualification & ExperienceMaster’s degree and 1 year of pharmaceutical, biotech or regulatory authority experience in a research and development setting OR Bachelor’s degree and 1- 2 years of Literature screening/Review or relevant Safety experience

ResponsibilitiesLead and develop team of 7 Senior Associates across Clinical Customer Service, Logistics Vendor Management and Development Supply Chain Technologies. Define goals, manage performance, and support career development. Ensure appropriate staffing, cross-training, and succession planning. Foster a culture of accountability, compliance, and customer focus Drive adoption of new technologies and AI to increase team productivity and enhance performance Clinical Supply Chain Execution OversightEnsure efficient and compliant execution of assigned clinical supply chain processes with patient-centric mindset Closely coordinate issue triage and workload prioritization with global peers Monitor KPIs and overall team performance and drive corrective actions and learning when needed Provide guidance on complex operational matters. Ensure adherence to GMP, GDP, and regulatory requirements.Performance & Process ManagementEnsure procedures are current, compliant and inspection-ready Drive root cause analysis and continuous improvement. Represent the team during audits and inspections.Cross-Functional & Global CollaborationPartner with Global Clinical Supply Chain, Clinical Study Teams, Quality, Finance, and DTI. Translate global priorities into actionable local plans.Qualification & ExperienceBachelor’s Degree and 8+ years of supply chain, logistics, planning, or operations experience

ResponsibilitiesAuthor or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, Pediatric Investigation Plans, and other regulatory documents; Conduct the formal review and approval of authored documents, following applicable standard operating procedures; With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications; Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)  Provide functional area input for Global Regulatory Plan and team goals  oversee the work of contract and freelance writers train, mentor, or supervise more junior medical writers, as assigned  lead departmental and cross-departmental initiatives, as appropriate Generate document timeline and keep abreast of relevant professional information and technologyQualification & ExperienceDoctorate degree and 2 years of directly related experience OR Master’s degree and 6 years of directly related experience

ResponsibilitiesLead end-to-end supplier quality processes such as Vendor Change Notifications (VCNs), Supplier Quality Agreements (QAAs), and supplier complaints to ensure timely and compliant handling Evaluate supplier changes and requests using risk-based and analytical decision-making to protect product quality and supply continuity Review and approve supply chain records (VSCI) governing the use of materials, services, and equipment across the Lonza network Collaborate with cross-functional teams (Manufacturing, QC, Procurement, MSAT, Planning) to assess impact and manage risks effectively Maintain accurate supplier documentation, ensuring compliance with quality management systems, regulatory requirements, and data integrity standards Monitor and report key performance indicators (KPIs) related to supplier quality processes, identifying risks and driving continuous improvement Act as a global point of contact for supplier quality topics, supporting audits, inspections, and alignment across internal and external stakeholders

ResponsibilitiesMajor Tasks Job Description Summary Presents pharmaceutical products to prescribing healthcare professionals, including generalist practitioners, specialists and hospital professionals. Delivers therapeutic information in compliancewith ethical rules and according to the marketing and sales strategies defined for the product line. May use various e-detailing platforms such as web-based or video conferencing/training, data specific web sites, physician portals and blogs.