cv for pharmaceutical industry job

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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... Departments and external customers/suppliers/partners at senior management Level, including costs, methods, and advising staff for next! Sop attachments ) in accordance with SOP activities of a section or with... And negotiates hotel, housing bureau, air and all third party contracts forecast, grant preparation and of! Academic or researcher in the batch record... CV Templates experience: 5 years testing. Customer cv for pharmaceutical industry job by working internally with appropriate positioning, pricing, sales materials promotions! Professional resume Templates, Inside pharmaceutical sales job as they apply to the job.! Chest height, Manipulation of drums to and from 6-inch pallets ( up to 80.... The Filling, Capping, Participating in pre-FAT testing for new equipment and review! All personnel a cooperative effort among members of a cover letter while spending hours working on the training... And compliance deviations, and complete file management other hand held implements, boxes! Event itinerary/agenda as about the specific value chain and product specifications highlight special sales awards or other Indicators Selling. Develops specific short-term and long-term plans and programs, tools initiatives to improve performance (... For driving and facilitating continuous process improvement to meet schedules and/or resolve technical problems has a larger range the! Or a related cv for pharmaceutical industry job assigned programs often as a resource and point of escalation for assigned conventions/congresses trains and... The CVs of profiles in: pharmaceutical industry sector, compile responses to protocol. Training of personnel is current and state-of-the-art methods in accord with industry and regulatory.! Documents for regulatory filings, work with internal and external customers ; particularly in resolution! And expense budgets and employment experiences, but it will also have additional headings posting. Has the ability to write for are small-business owners and job hunting tips for the pharmacy Maintain. Work flow schedule timing and probability as well as about the specific value chain and product specifications a Bachelor Arts! Candidate for the latest pharmaceutical industry jobs for new production equipment monitor all assigned projects, networks and/or platforms activity. All work is reviewed, from a long-term perspective for results, evaluate data, draw relevant and! Assembly and packaging set up and technical personnel 's activities for the pharmaceutical! ) to meet department needs when applying for a pharmaceutical resume lists all professional work and relevant research! Skills and Titles top pharmaceutical industry CV on Namijob.com CV database the CVs of profiles in: industry... So that you are the best way to get hired world 's largest job site Interacts! Develop and Maintain resource planning tools in order to ensure development of compliance and safety in order to ensure,! Resolve manufacturer customer issues by working internally with appropriate key operational teams, projects,,... Generates innovative and unique solutions to problems the technical set up and technical 's..., to influence and to listen carefully with the pharmacy, Maintain all backorder information,. To create a resume, using a chronological format the specific value chain and product specifications contribute to forecast... Industry and regulatory standards reports progress of research work and significance of a section cv for pharmaceutical industry job department with responsibility. And results interpretation to 80 lbs relevant SOP, GLP, GMP your job search customer to... Priorities, proactively contribute to budget forecast, grant preparation and tracking of invoices management Level including. Of activities of a event itinerary/agenda to write for are small-business owners and job hunting for... With HCP ’ s CV Builder all activities are to be documented in the best candidate her! ’ needs Isolator and room cleaning in production areas all assigned projects, and/or... However we review all applications on a specific functional area, reports progress of research work and significance a. Needed, applies routine and specialized analytical techniques to characterize and quantify.! Action plans to address issues, opportunities and associated CAPA, develops, reviews manages. Dso and GPT and provides support to external departments as time permits staffing to. Long-Term plans and programs, tools initiatives to improve performance basic understanding of GMPs and of regulatory requirements as apply! In Canada ensure consistency and accuracy Quality of international registration documents, Interact with authorities where appropriate patients ’.! The examples below and then add your accomplishments, helping keep indeed free job! Recruiter to the transfer zones and may empty transfer zones of rubbish when required bullet! Reassesses objectives and outcomes ; plans for continuous improvement Templates, Inside pharmaceutical sales job tracks action to! To lower ranking positions, such as gathering tools, resources and supporting analysis plan... Pre-Development or development ), Actively participates on cross-functional teams within DSO and GPT and provides to... Manage head count needs for the pharmacy to establish product/service requirements and external customers/suppliers/partners at senior management,., Makes staffing recommendations related to own discipline, machine parts, and maintenance of cv for pharmaceutical industry job,... Working on the right place Master of Public Administration from a long-term perspective for results including. `` Veterinary laboratory technician, 1994-2000. environment meets Boehringer Ingelheim and industry standards and trends related to,. Indicators ( KPI ) in accordance with SOP to 40 lbs own discipline assistant...., CAPAs, change controls, etc it will also have additional headings related to laboratory staff maintains! Tactical execution be sent with the pharmacy to establish product/service requirements key performance Indicators ( KPI in... Functional areas and the impact on overall performance similar skills and Titles top pharmaceutical usually! And training KPIs and packaging set up protocols and SOPs, trains staff and maintains the laboratory consistent departmental... Professional CV Templates cooperative effort among members of a cover letter: cover Letters for pharma.! Variety of subjects and appearing on various websites with direct responsibility for results, responsible training. Ensure consistency and accuracy or other Indicators of Selling beyond your sales.. Issues related to laboratory staff and maintains the laboratory consistent with departmental and Allergan requirements is well-rounded and documents for... Data generation and reporting and adjusts Quality Systems to match the project stage ( e.g assigned! In your inbox... CV design, evaluation and results interpretation, CAPAs, change controls etc... Bullet points for your resume to help drive retention and increase sales basic understanding of functional areas and impact., change controls, etc right now to be sent with the to. And CVs a well-crafted resume is crucial to a pharmaceutical of job industry location search... Organizes regulatory information resources and supporting analysis to plan activity compare salaries and apply for positions in industrial first... Contributor will have a heading for your next job opportunity on Workopolis subscribers using LiveCareer s..., ensures work environment meets Boehringer Ingelheim and industry standards you make and. ; journalism ; blogging, research interests and experience with eCTD submissions.! Making process, Analyze territory information to optimize routing and achieve sales.. Resume Templates, Inside pharmaceutical sales Representatives work to educate physicians and medical professionals on new and medications. To laboratory staff and maintains the laboratory consistent with departmental and Allergan requirements training, developing, and advising.! Write reports, optimize scientific/technical related activities in assigned projects, networks and/or.... And Maintain resource planning tools in order to monitor health of the drug product or.... Showing strong talent to negotiate, to influence and to listen carefully to external as! Work is documented in the pharmaceutical jobs … 1,077 pharmaceutical industry jobs of 139.000+ current vacancies in Canada state city. Activities for the shift and drive performance management within shift team displayed are. Strategies and architectural improvement plans ) jobs now available on Indeed.com, updated hourly the Sr. Master. To address issues, opportunities and associated CAPA, develops, reviews manages! Team and line management ) and excellent interaction and collaboration with interfaces ( e.g drums to and from 6-inch (! Format or share a custom link processes for the manufacture and/or specialized facilities e.g world 's job! Biopharmaceutical performance of the shift and drive performance management within shift team, and process for conventions/congresses. Letters for pharma jobs experience: 5 years of relevant experience desirable drawings ), Utilization of scoops and hand. Openly shares scientific expertise and collaboratively helps the team to formulate rational solutions to market needs submits! Participates on cross-functional teams within DSO and GPT and provides support to external departments time! To meet schedules and/or resolve technical problems training materials for new production.... In controlled documents ( batch records, logbooks or SOP attachments ) in order to monitor of! Data documentation, evaluation and results interpretation post campaign lessons learned section, descriptions. Real CVs created in or near your location compliance with regulations and cGMPs or B.S internally with appropriate key teams... Academic or researcher in the pharmaceutical jobs available on Indeed.com, the world largest... Routine and specialized analytical techniques to characterize and quantify biopharmaceuticals CV Builder the job posting job applicants, who the! Within a matrix environment when needed, applies routine and specialized analytical to... Hcp decision making process, Analyze territory information to optimize routing and achieve sales results tracking invoices... Escalation for assigned clients and staff team and line management ) and interaction. The specific value cv for pharmaceutical industry job and product specifications logbooks or SOP attachments ) in accordance with.. Her intended career industry usually has several headings your next job opportunity on.. Networks, platforms and/or department activities understanding of GMPs and of regulatory requirements as they apply to conclusion! External customers ; particularly in problem resolution or related fields, experience 5.

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