Free, fast and easy way find Pharmaceutical industry jobs of 139.000+ current vacancies in Canada and abroad. Completes all required training on time. Feb 29, 2016 - Sample Resume For Pharmaceutical Industry Sample Resume For Pharmaceutical Industry sample resume for pharmaceutical sales sample resume for pharmacy pharmacy technician sample resume sample resume for pharmacy tech pharma resume for freshers pharmaceutical resume objective pharmaceutical resume samples for quality assurance resume format for pharma marketing For agents supplied by industry, forecast and monitor supply requirements, develop distribution plan (obtain and review proposals, review budgets, and integrate into overall budgetary plan), review labels and labeling requirements, develop plan for meeting shipping requirements (regulatory documentation) and develop protocol ordering instructions and forms. Conversely, facilitate evaluation, recommendations and decision-making on client accounts and opportunities of lower investment priority, Lead capture strategies for key pursuits and major projects within the regional market and ensure those strategies yield high capture rates, Lead market specific external affairs and branding activities that promote AECOM, Provide analysis and performance forecasts against business plans, and when necessary make timely adjustments of priorities to achieve plans, Ensure the proper staffing of Key Account positions, in coordination with the National Market Sector Director, Provide mentoring and coaching to Key Account Managers, Advanced degree in Environmental related studies, Direct activities and support supervision of contracted resources, Perform diagnostics of automation systems, Provide support and troubleshooting on a wide range of process, facility and utility automation systems, Identify and manage high value cost and time savings, Participate in new processes to improve efficiency and cost savings, Participate in continuous improvement program to maintain instrument support within a given budget, Identify problems and inefficiencies in processes and methods, with proposed solutions, Maintain accurate and complete records supporting GxP operations, Read blueprints, P&IDs and technical documents related to operations/facilities, Efficiently use CMMS to request and direct work flows, Prioritize, plan, provide for minor and major repair efforts, Make effective use of PdM, PM and predictive maintenance techniques, Provide data to assist with forecasting budgets, training needs, capital purchases and staffing needs, Maintain a positive, can-do attitude while seeking opportunities for cost savings both inside and outside of the immediate team, Maintain GMP compliance for all assigned work, Develop and follow SOPs on maintenance and repair of process equipment, instrumentation and controls, Assist in the execution of IQ/OQ/PQ protocols, Provide the Customer Relations Manager with recommended work priorities for CMMS generated work requests, Participate in planning sessions with the customer, maintenance manager, planners, schedulers, and technicians, Support system owners in performing reliability assessment, efficiency improvements, and strategic planning, Participate in “Management of Change” process for equipment modifications, Perform corrective action for abnormal events or system failures including issuance of incident reports, Maintain CMMS database for assigned assets and optimize spare and replacement parts inventories and purchase, Comply with and enforce AECOM and company policies and safety practices, procedures and guidelines such as job hazard analysis, lockout/tagout, and the use of PPE, Operate various measuring, diagnostic and testing tools, instruments and software to perform troubleshooting, work completion and to provide energy efficiency solutions, Maintain a strict schedule in order to be successful in the assignment and meet expected client service levels as established by the Company, Be flexible in the day-to-day activities and shift scheduling for the benefit of the customer’s mission, Comply with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP), Respond to emergency calls (by phone or in person) during off-hours and determine resources needed to mitigate problem (AECOM or subcontractor), Perform other duties as assigned by the AECOM Program Manager, Working knowledge of process instrumentation maintenance and/or calibrations, Bachelor’s degree in an Engineering or related technical field, Experience performing maintenance and calibrations on process instrumentation, Experience troubleshooting, programming, or working with DeltaV, Foxboro, Allen Bradley, OSI PI, and/or OPC interface, Experience with direct repair and/or maintenance of automation systems, Understanding of Service Level Agreements (SLA) and Key Performance Indicators (KPI), Understanding and alignment of recordable metrics to customer needs for Financial Management, Experience with GxP compliance in pharmaceutical environment, Specific knowledge of pharmaceutical manufacturing compression practices and hands on experience in the operation, setup, repair and modification of tablet presses such as Kilian & Korsch, Specific knowledge of pharmaceutical manufacturing encapsulation practices and hands on experience in the operation, setup, repair and modification of capsule filler machines such as Macofar & Bonapace, Responds to requests and calls from customers related to client specific programs and products, Identifies and responds to customer’s needs based on designated procedures of account/client, Makes attempts to resolve issues and deescalate issues of irate or dissatisfied clients, Tracks call related information of each call received for auditing and reporting purposes, Provides feedback reports on call issues related to downtime and/or training issues, High School Diploma or GED required; graduation from a college with an Associate’s degree preferred, Familiarity with Microsoft Windows, Word, and Excel applications, May require client specific bilingual language requirement, as necessary, To be the account manager for a number designated accounts acting as the principal contact between the client and RSSL operation teams in order to achieve sales growth, Optimise calls by ‘selling-on’ other services to the client, where appropriate, Monitor multi laboratory projects, ensuring that work is carried out in a timely manner and reports are sent out as per customer requirements, Assist the Customer Services team as required at periods of peak demand to ensure that clients are provided with a professional service and act as the liaison between RSSL lab staff and clients, Generally assist the Head of Sales (Senior Group Leader Sales) and wider commercial team as required, Represent RSSL at external events (conferences, exhibitions, seminars, industry meetings) in order to grow sales, Support the Commercial team with the co-ordination and collation of RFI’s proposals and tenders as required, Know the ethical and legal compliance responsibilities of the position; raise questions and concerns when faced with an ethical or compliance issue; apply integrity in all aspects of professional conduct, Have a proven scientific background with recognised qualification - HND or equivalent qualification, Have an understanding of laboratory work and its application to solving customer problems, The personality and technical credibility to develop excellent working relationships with both clients and laboratory staff, Outgoing proactive approach, energy, drive, enthusiasm and the ability to motivate others, Team player, plus ability to work on own initiative, Excellent inter-personal skills, with the ability to interact effectively by telephone, written communication and face-to-face, An organised approach, capable of working on several projects at any one time, Experience within the pharmaceutical industry, 1 + years pharmaceutical sales experience, Successful completion of all sales training requirements, Ability to perform the duties of a pharmaceutical representatives, 80% travel - weekly overnight travel may be expected, Ensure a safe work environment by following all safety and ergonomic rules, including any special personal protective equipment (PPE) and standard operating procedures (SOP's) applying to a particular process or area, Ensure product quality by performing in-process checks, complying with current good manufacturing practices (cGMP’s), being alert for unacceptable quality of incoming and outgoing materials, initiating quality improvements and participating on quality improvement projects, Communicate quality and other problems to supervision in a timely manner, Dispense components, operate, clean, set-up, change and maintain equipment and rooms to manufacture products, Clean and maintain process equipment which may include, but not limited to tanks, filler pumps, blenders, mills, presses, coating pans, etc, Operate electric or manual hand trucks for most stocking operations as well as forklift operation as needed, Accurately record on the appropriate documents, the process / manufacturing steps, production results, equipment in-process checks, samplings, cleanings, ingredients used, and any other relevant information, Maintain daily production sheets and time sheets for team, Take ownership of personal training and learning to develop skills to continuously improve processes, Help build team-oriented culture by motivating and supporting team members by sharing knowledge with all members of the factory to continuously improve the process, Properly dispose of waste product and containers, Inform department administrative assistant when to order supplies as needed, At least 6 months experience using motorized and non-motorized material handling equipment, At least 6 months experience using automated inventory system or equivalent computer systems (i.e., SAP, MES, Microsoft Software, etc. 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. 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. Job email alerts. ), The incumbent may perform such metrology functions as instrument/system calibration and qualifications, 3-5 years of experience in the pharmaceutical industry, The incumbent must demonstrate excellent verbal, written and interpersonal communications skills, In that there are stringent requirements associated with the pharmaceutical industry a high degree of accuracy, commitment and integrity is required, The incumbent should exhibit proficiency in software such as Microsoft Word and Microsoft Excel, Please submit resume directly to the posting, Writes technical documents such as methods, specifications, validation protocols and reports, transfer protocols and reports based on corporate policies and SOPs, compendial, ICH and FDA regulatory guidance, Ensures that the integrity and accuracy of all laboratory documents are maintained, Assess overall document compliance with protocols, SOPs, company policies, and applicable regulations, Evaluates compendial documents and reviews procedures for analytical development and validation, Reviews Drug Master Files (DMFs) of active ingredients and provides essential information to laboratory personnel, Reviews analytical data for accuracy, completeness and compliance to cGMPs and established laboratory documentation standards, Generates change requests required for analytical documents and routes documents for review and approval. This typically includes client relationship development, program-specific positioning activities, teaming arrangements, proposal preparation, orals presentation, and contract negotiation consistent with established business development processes, Bachelor’s degree in applicable discipline or equivalent experience, 12 - 20+ years progressively responsible Project Management experience, Minimum 15 years of experience in the design of both Pharmaceutical and Biopharmaceutical facilities, Must have excellent communication skills in a Business Development (BD) “support” role, Present the Pharma vision at client presentations, industry conferences, Meet with clients to review drug plan design and performance, Develop strong relations with the various provincial governments to represent our customers best interests (e.g. Provide raw data documentation, evaluation and results interpretation. Companies in Namibia check on Namijob.com CV database the CVs of profiles in: Pharmaceutical Industry sector. Meet the production schedules outlined by team and/or Supervision, Ensure product quality by performing in-process checks, complying with cGMPs, being alert for unacceptable quality of incoming and outgoing materials, initiating quality improvements, and participating on quality improvement projects; Communicate quality and other non-compliance issues to supervision in a timely manner, Review and approve work output for team members by using validated methods, Perform work, on personal computer (i.e., Business Operating Systems, read and respond to electronic mail in a timely manner, Microsoft Software, etc); Complete, maintain, and update production documentation (both electronic and paper) to perform material movements, material take-outs and yield determinations by following SOPs and utilizing systems as required such as Systems/Applications/Products (SAP), Manufacturing Execution Systems (MES), Electronic Batch Records (EBRs), etc, Operate motorized and non-motorized material handling equipment for assigned stocking operations as well as stand up and sit down forktrucks as needed, Inform department Administrative Assistant when to order supplies as needed, Coordinate the utilization of outside contractors and vendors as needed, Ensure safe work environment by following all safety procedures, workplace standards and company guidelines, and ergonomic rules, including proper use of personal protective equipment (PPE), standard operating procedures (SOPs) applying to a particular process or area, Current Good Manufacturing Practices (cGMPs), Occupational Safety and Health Administration requirements (OSHA), Lockout Tagout, Dispense components, operate, clean, set-up, changeover and maintain equipment and rooms to manufacture products. ResumeZest. Defines the Process Validation (PPQ/CPV) requirements resulting from such equipment changes, Leads and executes projects for evaluation and qualification of new sources of excipients and primary packaging components for new and marketed products, Works cross-functionally with Regulatory, Quality, and other departments, as well as internally with Process Technology API colleagues, to implement new API suppliers, Leads or participates in data analysis and interpretation using relevant statistical tools to evaluate experimental results generated as well as production data to improve process control and process robustness, Provides information to support establishing overall budgets, schedules and performance standardsas related to Sterile Drug Product processing operations. Indicators ( KPI ) in order to project staffing needs and manage cost the... 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