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. Post your CV - Let employers find you. Interact/collaborate with Research and/or other functions in Development to facilitate transfer of knowledge and deliveries of DS and DP, Initiate and lead new scientific/development programs. 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), Design, plan, perform/supervise, monitor and contribute to projects related to complex scientific/technical engineering activities and design, plan and supervise scientific experiments, Create and implement efficient and robust engineering solutions and procedures/processes for the design, manufacture and/or analysis of Equipment Prototypes and final Equipment designs, Coordinate with team members and external partners assigned to multiple or complex engineering development activities, Drive appropriate planning of workload and resources internally and externally, controlling costs and timescale of projects or respective project tasks, Evaluate and implement new engineering technologies, Address complex research issues within own discipline and lead and supervise new engineering development activities, Report and present scientific/technical work at internal/external meetings/conferences including patents. Ability to identify gaps in PS technology/trends and influence change/improvements to affected areas/processes, Communication– ability to expresses one’s self clearly and concisely to key stakeholders and functional management; documents issues and/or concerns concisely and comprehensively; adjusts style, language and/or terminology appropriate for the audience. Operational excellence, including operations strategy development, implementation, and due diligence, Identifying and addressing client needs: building, maintaining, and utilizing networks of client relationships and community involvement; communicating value propositions; managing resource requirements, project workflow, budgets, billing and collections; and preparing and/or coordinating complex written and verbal materials, Performing as a team leader: supervising teams to create an atmosphere of trust, leverage diverse views, coach staff, and encourage improvement and innovation, Minimum of 5 years experience in project, event or meeting management, at least 2 of which are in procurement required, Knowledge of domestic hotels and destinations required, international a plus, Knowledge of travel supplier operations, overall capabilities/range of services, Program management system experience preferred, especially with an online sourcing tool, Understanding of and ability to effect win/win solutions, Operations experience in hospitality industry or equivalent a plus, Prior successful experience in developing and maintaining key client and supplier relationships, Prior experience in effectively handle multiple projects/demands, Strong knowledge of program/event management and budget maintenance, Ability to travel by airplane, boat, rail and/or car, Contribute to research experiments to 1.) Assures that all safety information such as MSDSs are available for all lab personnel, The incumbent may be called upon to perform other tasks to support the attainment of business objectives, The incumbent is responsible for mentoring less experience lab personnel in good documentation practices (notebook, investigative and other technical report writing, annotating and archiving supporting data, maintaining procedural formats, etc. Performs environmental inspections to the waste area as required, Evaluates process data and performs product sampling and inspections as part of the manufacturing process and quality monitoring, Documents manufacturing and cleaning steps as per SOPs, batch records and batch official forms, including inspection, sampling and process monitoring, Assists technical personnel in equipment and process validation, including performing the required sampling according to approved instructions, Documents shift events and status in logs, as needed, Technical, associate or bachelor’s degree from an accredited institute is preferred, Operate filling and packaging production unit for FDA and EPA regulated and less regulated pharmaceutical products, Organize and perform equipment set-ups for production processes, Perform unit and equipment cleaning procedures, Record information throughout the process into the batch record and/or log books to ensure compliance, Follow proper trouble shooting procedures when malfunctions occur, Follow GMP’s and SOP’s and plant safety guidelines, Must be able to work any shift (1st, 2nd, or 3rd), Talking/listening to others to convey/understand information effectively, Ability to read, understand and execute operating instructions, guidelines, SOPs, and batch records, Prior working experience with FDA, EP & EU regulated products required, Good math skills: adding, subtracting, multiplication, percentages, conversions, Demonstrate ability to work in teams and lead by example, Silver Level WorkKey Assessment required or an Associates or higher degree in lieu of the WorkKey Assessment, Ability to operate equipment in accordance with established safety guidelines and operating parameters, Ability to palletize shippers based on pallet configuration drawings, For the advanced analysis of proteins and their modifications you develop LC-MS methods, You author/review compiled analytical results and provide comprehensive result presentations to project teams, Regarding stakeholders and interfaces (e. g. project teams, line management) you ensure excellent communication, interaction and collaboration, You consult on analytical strategies for samples originating from upstream, downstream and formulation development, Project Management of Pharmaceutical projects through all project phases: planning; preconstruction, construction, commissioning & validation, Cost Forecasting and financial reporting on projects assigned, Management of Change Orders and procurement process, Project Management with high levels of customer satisfaction, Manage projects to completion on-time, within budget and within the scope of work, Manage Client Project Management Information System (PMIS), including monthly updates of project data, Produce reports and briefings using Microsoft Word, Excel and PowerPoint, Bachelor of Science Degree in Engineering, Architecture, Construction Management or Quantity Surveying, Project Management experience in manufacturing or research & development process and/or building projects, 3 to 5 years Cost Management experience in Healthcare/Pharmaceutical process and/or Healthcare/Pharmaceutical building projects, Proficient in Microsoft Word, Excel, PowerPoint, and Outlook, Experience of PMIS systems used to manage capital projects program, Pharmaceutical Facilities/Engineering experience to include office, R&D laboratories, mechanical / electrical infrastructure, central plant, site work, building expansions, BAS, and process controls, Experience in Pharmaceutical building projects ranging up to $10 million in value, Maintain and verify drug inventory controls are at a level to meet customer demand. Leveraging industry contacts to make introductions and connect the firm to potiential clients (short term or long term). Register your CV on and search for jobs in: Pharmaceutical Industry sector in Namibia. Help bridge the gap between MDM/DuPont/ SPM, Managing contact strategies for sales, marketing, technical, application development and leadership, Organize conferences and professional events in cooperation with industry partners, Support market research activities, open doors for customer interviews, administrate VOC and Promoter feedback to enforce continuous product and service improvements, Represent DuPont at Tradeshows, review and develop sales tools, Responsible for the customer data base accuracy, work on continuous improvements of the related software tools, Strong Technical and/or Regulatory background in the Medical or Pharmaceutical Industry ideally related to Packaging or Product protection. Very good communication skills, Works with R&D team to establish studies needed to support CMC, Provides review, interpretation and reporting of study data needed to support CMC, Actively participates in issuing protocols, generating and evaluating data, and producing reports to support CMC, Acts as a technical resource in generating information in support of CMC, Collaborates with Regulatory Affairs to establish plan(s) for building CMC sections, BS in Chemistry, Engineering, or related science, 10 years experience in chemistry-related field, Demonstrated experience in project management or PMP Certification, Excellent organizational skills and attention to detail, Deep understanding of FDA-regulated practices, Leads project initiation and planning activities to structure the project, including facilitating the definition of project goals, objectives, and scope. Deliver accurate and timely follow-up discussions with HCP’s and office staff. Pharmacy, Manufactures, Wholesalers) to manage current and develop new partnering opportunities, Generate innovative / creative ideas that align to our strategic objectives, Identify and prioritize opportunities for feasibility studies and concepts, evaluating the overall value they can deliver as a basis for prioritization of future product development projects, Accountable for the success of the Drug Benefits offering, Build and influence effective two-way communication with key internal business partners, specifically Business Development, IT, Finance, Legal, Claims/Operations, incorporating their view into the strategy and the product development, Licensed pharmacist (practicing pharmacist is preferable), 6 - 8 years in a variety of marketing, product development functions, Pharmacy Benefits Management, or other relevant experience, Organizes and provides guidance in the business planning process as well as monitoring progress towards individual and district level goals, Identifies opportunities using sales data, insights, and customer needs to effectively, Previous industry management experience (2-3 years), Previous Hospital/LTC experience preferred, Strong leadership, interpersonal skills and communication agility with various stakeholders, Strong business acumen and project management skills, At least 1 year of work experience in a GMP (Good Manufacturing Practice) facility is preferred, At least 1 year work experience in oral solid dosage manufacturing (blending, compression, pan coating, fluid bed or encapsulation manufacturing processes) is preferred, Flexibility to work a non-traditional shift is required, Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required, Knowledge, practical application, and understanding of analytical chemistry is necessary to perform the functions of this position, Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision, Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required, Must demonstrate initiative and a willingness to learn, Good working knowledge of advanced laboratory instrumentation and personal computer skills are required, Experience in wet analytical methods and instrumentation techniques preferred; HPLC, UV, GC, IR, AA, TOC, and Dissolution preferred, A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is desirable, A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP’s), quality control methods and procedures preferred, Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills, At least 1 year of lab experience preferred, Assigned within the lab: bench chemistry or lab experience preferred, Assistant/Associate Quality Control Lab Analyst provides Quality support to the Incoming Material Supplies Inspection processing and laboratory areas, Will perform activities that support and ensure process quality and data integrity with incoming sampling of raw materials and inspection of primary packing components, The Contractor Quality Analyst will become knowledgeable in Federal and other regulatory agency requirements and cGMPs to assure that all areas in compliance, and will train on and gain competency in activities to support incoming sampling in Classified D and C processing areas and component inspection. 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