It is recommended that the resume should always be saved as a PDF file because it keeps the content intact. PSD. Strong knowledge of relevant SOP, GLP, GMP. This way, you can position yourself in the best way to get hired. You need to be respectful and should show gratitude towards the person you are conversing with. Support and assign associates in specific projects and/or networks. 2. ... View All No Experience Resume Samples. The next thing you should consider doing is choosing a layout. It is always a good practice double check your resume before you send it to pharma companies or CROs. Knowledge of automated Materials Requirement Planning (i.e. Regional VMRD projects and BD opportunities, Motivates and lead a group of technical support/project leaders, ensure the team has the appropriate skills, training, equipment and priorities to meet the needs of GMS and to be a valuable asset to Zoetis, Develop and maintain an effective organization; Implement continuous improvement of best practices and standard work (Co-Dev, Launches, Transfers) across projects and the organization to meet company vision and mission, Recognize development needs and create development opportunities within the team. Manufacturing experience, Actively participate in teams, projects, networks and/or platforms, Fulfill all related tasks and responsibilities related to own discipline, Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s), Design, plan, perform and monitor all assigned activities, Drive and implement innovations in the area of Pharmaceutical Equipment-Engineering at the interface to innovative Process Engineering Engineering, Ensure quality, quantity and timelines in all assigned projects, networks and/or platforms. Contribute to the development of organizational knowledge management processes, Establish and maintain an environment that encourages teamwork, motivation and commitment, Manage appropriate and timely communication on objectives and priorities within the project teams and to stakeholders, Ensuring key project decisions are taken on time to meet the commitments for transfers, new products and life cycle management initiatives, Develop innovative concepts, take appropriate risk to successfully complete projects and guide direct reports on acceptable level of risk taking, Support the development and maintenance of technical support agreements with stakeholders, May lead co-development and/or launch projects, May lead special projects as required by customer and group needs, Support the establishment of the GMT Pharma DP budget, track and ensure alignment, Make decisions on long term objectives, manage projects with cross functional representatives and lead team by influence, Minimum of Bachelors Degree in Management, Business Administration or related disciplines applicable to Supply Chain Management, Information Technology, or Vaccine and Pharmaceutical Manufacturing, Minimum 2 years of relevant experience in Supply Chain, Manufacturing, Materials Management, and/or Marketing. ), Good written and verbal communication skills in English, Demonstrated ability to work safely in a production environment, Demonstrated ability to read/interpret/follow instructions in regard to workplace documentation, such as SOP’s, Operator Manuals, Work Instructions, etc, Good PC Skills, including use of e-mail, attaching documents to e-mail required. answer questions, assist employees, etc. In that case, you need to acquire and show up your hard skills and then use soft skills to show how you will implement your ideas and what is your approach. Income Tax Compliance - Preparation of Corporate and Partnership return workpapers (federal and state) … Notifies immediately any accident or safety/environmental incident to the supervisor, Supplies materials to the manufacturing area as needed, Complies with all the training required to perform the tasks, including SOPs, forms, guidelines, Safety and Environmental training, Provides support in the auditing of the manufacturing batch records and related documentation, Keeps the areas cleaned and organized, including using the correct identification according to areas cleaning status. To get shortlisted, companies go through your resume first to call you for an interview. Work is expected to result in the development of new or refined products, processes or equipment, Selects techniques to solve complex problems and make sound design recommendations, Release and stability testing at internal and external laboratories, Write CMC sections to support IDE and PMA submissions for combination products, Participate in cross-functional product development teams and provide technical support to sterilization process selection, packaging specification requirements, clinical manufacturing, quality assurance, analytical R&D, and regulatory affairs, The selected candidate must have an ability to collaborate effectively with other scientists in a multidisciplinary team environment and possess excellent verbal and written communication skills, PhD in Pharmaceutical Sciences (Pharmaceutics), Chemistry (Physical, Organic, or Analytical), Biomedical Engineering or related technical field, 1-3 years of industry experience in pharmaceuticals under a research and development environment, Understanding and experience in pre-clinical model development, Previous experience with major analytical techniques such as HPLC, GC, LC/MS, GC/MS, and NMR, Experience in practical lab-based Pharmacokinetics/Pharmacodynamics data analysis, Good understanding of cell biology, pharmacology, and biochemistry is highly desirable, Good understanding of controlled drug delivery systems, Deep understanding of pharmaceutics and physical chemistry is a must, Substantial knowledge in assay method development and validation and familiarity with release and stability testing are desirable, Responsible for running all monthly pharmaceutical procurement reports and serve as primary point of contact for questions related to these monthly reports, Maintain all electronic product catalogs with national drug distributors that link to FMS Pharmaceutical Formulary, Update and maintain all catalogs to ensure accurate pricing in all systems, Update all systems including SAP to ensure that FMS facilities have access to purchase the most cost effective Formulary products that are linked to contracted pharmaceutical suppliers, Support Corporate Medical and Clinical Services departments to drive FMS clinics compliance to the FMS drug formulary, Assist Pharma Procurement leaders in review of all available direct and Group Purchasing Contracts to determine the best pricing available by generic drug class for any multi source medications listed on FMS Pharmaceutical Formulary, Conduct daily oversight of the daily SAP Pharma distributor interface, Assist FMS Corporate and Division Finance Centers in resolving any problems encountered with the interface. Seeking a … Experience in supervising and scheduling responsibilities and managing processes, planning and tracking of budget. However, don’t forget to tweak it as per your requirement. Financial management throughout the life cycle of an event, Planning, coordination, and execution of group air travel including any applicable transfers, Use resource efficiently and maximize productivity by utilizing the relevant technology. Pharmacist @ CVS Health. Never prioritize or brag about your soft skills as they are important but not sufficient. Contact no. Design, plan, perform and monitor all assigned activities. Follow up with all impacted groups, Serve as a liaison between FMS Finance offices and Corporate SAP IT Team to address any technical issues with the SAP Pharma distributor interface program, Maintain all pharmaceutical contract reporting and provide updates to FMS Finance and other key stakeholders to provide critical senior management reports to track the usage of all ESA and other key medications in use in the NA facilities, Work in collaboration with FMS Supply Chain to maintain and update all pharmaceutical purchase forecast models, Work in collaboration with FMS Corporate Accounting to monitor any pharmaceutical contract rebates earned to ensure accuracy and timeliness of all rebates paid by all contracted suppliers, Validate pharmaceutical sales reports released by national drug distributor against chargeback reports received by all FMCNA contract pharmaceutical supplier. Create and implement optimized processes and procedures for activities within the own area of responsibilities, Actively contribute to engineering related innovations / improvement of tools and equipment in lab and pilot plant)Lead risk analyses and/or peer review and process challenge meetings, Generate and select most appropriate scientific documents to hand over to internal and/or external partners (TechOps, authorities, other companies). Function head within a Life Sciences Research organization preferrred, Minimum 10 years leadership experience managing teams; proven ability to build, manage and foster a team-oriented environment, Deep understanding in one or more of the following: pharmacology, biologics, genomics, cheminformatics, translational science, Expertise in research / laboratory processes and methods, assay workflows, data management and data curation, Experience in one or more of the following: knowledge mining, scientific data curation, target profiling, drug repositioning, Significant client impact and value creation, On time and on budget high quality project delivery, Significant experience with research informatics software and solutions, including research platforms, workflow systems, and data aggregtation, management and curations solutions in the Research / Early Discovery spaces, Experience working with executives in Life Sciences R&D, with network of existing clients, Significant responsibility leading teams and exceptional team building/ mentoring skills, Excellent leadership, client-facing communication (written and oral) and interpersonal skills, Follow-on project sales and ability to sell work to new clients, Technically savvy and/or interest in working with technology as part of identifying and delivering solutions to clients, Experience with scientific software/ knowledge management solutions, Orchestrating and bringing together expertise from across the entire organization—strategy, consulting, digital, technology and operations—to deliver value to clients, Selling the full breadth of Accenture’s services, 4+ years of experience with regulatory information management tools in a consulting, implementation or support capacity, with exposure to all phases of a regulatory information management tool implementation including requirements gathering, development, deployment and support preferred, 4+ years of experience managing a team of multiple direct reports, clients and vendors, Typically we work at client sites. 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