Centre-Val-de-Loire 3. Perform and interpret analytical evaluations of products and intermediates, Supply information based on experience and knowledge, 6-12 months of training necessary to learn specifics of job adequately to work independently, Use of equipment, such as pH meter, centrifuge, analytical balance, spectrophotometer, vacuum chamber, tangential flow filtration system, membrane printing system, conjugate dispensing system, Prepare complex solutions, such as phosphate buffer, antigen conjugate solution, antibody conjugate solution, gold-antibody conjugate solution, Optimize formulation and performance of gold-antibody conjugate pad, Test gold-antibody conjugate pad samples using drug positive urine and drug negative urine, Conduct complex experimentation including data collection, summary and thorough analysis, in support of product improvement and validation projects, Compose robust experimentation strategies that maximize effective use of resources and time to deliver optimum information, Support efforts to innovate production methods and product formulation to resolve problems and accomplish company objectives, Operate equipment and conduct tasks in a safe manner, adhering to established guidelines and applicable regulations, Generate oral and written reports as necessary and to summarize production activities and projects. Ensure information is accurate and up to date, Participate in new product/process transfers and validations. Production Manager Resume Statements. Next Resume Format New Zealand. BI and enterprise DW data management, modeling, integration and/or synchronization, quality, security, conversion and analysis, star schema and relational reporting models, enterprise data management policies, procedures, compliance and risk management and/or database administration, Design and development of data models, extraction code and cleansing routines utilizing typical data quality functions, i.e. ), Assure that employee grievances are heard and resolved (with help from appropriate support employees, as required) and that personnel records are updated and accurate (Change of Status forms, rosters, etc. Ensure SOPs for areas of responsibility are updated, accurate, and complete, Ensure formal and informal training occurs in employee technical skill development as well as other training initiatives including safety, CGMP, teamwork, etc, Support the Head of Manufacturing in the timely completion of assigned projects, including participating in the design and development of new packaging/production materials, equipment and packages, Participate in cost reduction programs with respect to waste and other inefficiencies, Perform other supervision duties and responsibilities as assigned, Position is for 3rd Shift, Sunday through Friday (10:00pm to 6:30am), Bachelor’s degree and at least 4 years’ production supervisory experience in a government regulated industry using QA procedures (FDA, pharmaceutical industry preferred), If no degree, but have 5 years’ supervisory/leadership GMP packaging/liquids experience, must commit to start/continue college degree / certification program, Master's degree & 2 years’ experience listed above or PhD and 1 year experience listed above may be considered, Strong personal computer skills required; experience with windows environment, Microsoft WORD and Excel preferred. 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. - Choose from 15 Leading Templates. These plans will focus on performance and execution impacts that properly identify and prioritize activities to accomplish short and long term business goals, Demonstrates a deep, clear and thorough understanding of the Diabetes disease state, Diabetes products and relevant competitor products, including their mechanisms of action, indications, efficacy, and safety, etc, Demonstrates highly effective territory management skills and exemplary selling competencies, Collaborates with territory matrix team on identifying business opportunities and developing appropriate tactics and strategies, Fosters team effectiveness and accomplishment of shared goals by sharing knowledge, experience, and information, Drives market share growth and maximizes sales performance within the indicated use and for the approved patients, Minimum of 5 years of Pharmaceutical Sales Representative experience required; the last 3 years having been in a Diabetes Sales Role, specifically with building relationships and sales with Endocrinologists, Diabetes specialty marketplace experience preferred or other demonstrated Diabetes therapeutic experience preferred in addition to the requirements listed above, Demonstrated skills at building and maintaining professional relationships with key customers, office staff and others in the customer influence network, Evidence of strong established relationships with local endocrinology specialists preferred, Demonstrates comfort with technology and uses technology to increase the efficiency and effectiveness of work processes and sales calls, Demonstrated strong business analytics ability to analyze data as well as develop, execute and adjust business plans, Demonstrated ability to work in matrix teams, Demonstrated track record of developing self to drive and enhance performance, Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations, Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines, Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts, Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting, Call on physicians in hospital settings, and residency and fellowship programs within a defined geographic territory, Responsible for positioning AstraZeneca as a leader in Oncology commitment through development of long term relationships with Key Customers, Work with RAD and District Sales Managers to develop and direct sales strategies at key accounts assigned in the territory, Develop and direct sales strategies at key accounts assigned in the territory, Develop and implement clinical sales presentations to groups of healthcare personnel during medical meetings, and the general public in health fairs and support groups, Experience selling and knowledge of Oncology products or diseases preferred. standardization, transformation, rationalization, linking and matching that leverages data standards, processes and technology management for data, master data, and metadata; and, data security (including data masking and related data protection techniques), Identification and addressing of client needs--developing and sustaining deep client relationships using networking, negotiation and persuasion skills to identify and sell potential new service opportunities; preparing and presenting complex written and verbal materials; and defining resource requirements, project workflow, budgets, billing and collection, Team leadership--generating a vision, establishing direction and motivating members, creating an atmosphere of trust, leveraging diverse views, coaching staff, and encouraging improvement and innovation, Global trends in market access and requirements for launch management, Key market requirements regarding access strategy, pricing and reimbursement, especially in the context of product launch or lifecycle management, Pricing and profitability strategy, price setting, and innovative contracting, Contracting and rebate modelling for the US market, Target product profile development, unmet market needs, clinical end points to support pricing and market access strategy, country launch sequencing, and other pricing and market access factors, Budget impact modeling, including pharmacy and medical claims analyses. Plan and execute the production schedule including human and material resources. If you think that your qualifications are enough and is directly related to the field of pharmaceutical care, you may look to our Resume sample and start creating your own resume so you can already apply for the above-mentioned position. Serve as a resource and point of escalation for assigned clients and staff. A. GMS US and LAR projects within the internal and external GMS manufacturing network, B. Fulfill all related tasks and responsibilities related to own discipline. OSHA, PSM,cGMP) manufacturing and/or research & development environment with a strict adherence to established safety and cGMP rules and regulations performing the activities within the job function, Experience in bulk fine chemicals, bulk API, or petro-chemical organic processing is preferred, A two-year Associates Degree in a Science related discipline is preferred, Proficiency in use of computer programs/systems is essential. Local travel may be required, Students must be able to provide their own transportation to/from their work location, Responsible for designing and managing formulation development projects leading to clinical evaluation of drug delivery systems for HIV prevention and contraceptive products, Interact with contract labs to maintain scientific quality and timeline management, Responsible for writing and editing portions of regulatory documents including Quality, (CMC) sections of INDs, IDEs, and annual reports, Assist in the development of new concept papers, grant proposals and other funding initiatives, Responsible for preparing written and oral presentations and reports to enable dissemination of project plans and results to stakeholders and the greater scientific community, Assist with specific drug development activities (e.g., animal pharmacokinetic studies, and IND- enabling toxicology studies) as needed, Facilitate project management discussions and participate in drug development meetings, Manage project timelines for assigned projects and assist others in creating project timelines within the product development group, Experience in a relevant drug development/drug delivery environment ideally in the pharmaceutical/biotech industry or equivalent is desired, Supervise and lead Pharmaceutical Development staff, Conceptualize and lead development of new drug delivery systems, Coordinate with Preclinical, CMC/Quality and Clinical teams with respect to product development, Influence the scientific and strategic direction of CONRAD’s product development program, Develop, author and monitor project work plans and timelines, Prepare and present technical and programmatic communications to stakeholders, Identify new collaborators and partners to support existing and new product development projects, Request, review and negotiate contract proposals and Oversee/monitor sub awards, Oversee the development, review and approval of technical protocols and reports, Share responsibility for the preparation of chemistry, manufacturing and controls (CMC) and nonclinical sections of INDs, IDEs, and annual reports to the FDA, Develop and write concept papers and grant proposals to support fundraising and expand the product development program at CONRAD, Negotiate arrangements with commercial manufacturers and others, Contribute to, and Interface with legal counsel, on business and intellectual property matters, Contribute to IP protection (i.e., write patent applications), Interact with other agencies and NGOs developing products on behalf of CONRAD, Experience overseeing pharmaceutical development at both preclinical and clinical development stages, Experience overseeing projects with contract research/manufacturing organizations, Excellent communication and interpersonal skills, strong problem-solving skills, detail oriented, Knowledge of cGLP, GMP, ISO and ICH guidelines, Direct experience with microbicides/contraceptive products preferred; experience with combination drug-device products is preferred, Bachelor of Science degree in Chemistry and or in Biological Sciences or equivalent in experience or training, Minimum of 5 years previous laboratory equipment control experience or laboratory experience with strong understanding of laboratory equipment calibration/PM and qualification’s regulatory requirements, Good understanding of the laboratory quality control processes, Comfortable with sophisticated LIMS IT System, ASQ Certification as a Calibration technician is an asset, Ability ttroubleshoot or diagnose equipment problems as needed to minimize down time alternatively ask Subject Matter Expert, Candidates must be proficient in using various types of computer software (Word, Excel. Sterile product experience is highly desirable, Must be able to apply product development expertise to CMC sections of the regulatory filings, Project Management experience in a product development environment, Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines, Ability to present complex issues well in oral and written form, Ability to work independently, take initiative and complete tasks to deadlines, Excellent interpersonal, communication, analytical, and organizational skills, Ability to effectively present information to management, external contractors and employees at all levels of the organisation, Basic knowledge of project leadership tools including MS Project, In support of product development, apply broad and deep analytical knowledge and experience to the material characterization and testing of APIs and drug products, Apply knowledge and direct experience with the analytical support of synthetic peptides, oligonucleotides, and sterile products to ensure the appropriate analytical methodologies are in place and fit-for-purpose to properly support the development projects, Provide technical guidance for troubleshooting / investigating complex issues regarding analytical, stability, and process / product development, Leverage fundamental understanding of formulations, product development, and material characterization to implement analytical methodologies as appropriate for various formulations and dosage forms, Apply statistical analysis for interpretation of analytical and stability data, Author and/or review analytical methods and associated development, qualification, validation and transfer protocols and reports, Author and/or review release, in-process and stability specifications for APIs and drug products, Manage and oversee stability and analytical studies for projects. Auvergne-Rhône-Alpes 4. billability, working capital goals, effective resource allocation), Identify ways to improve and operationalize processes to optimize efficiencies and effectiveness, Personally manage and execute quantitative studies, with priority against complex, higher level strategic projects, Assume overall responsibility for the quality of the service and product provided by the quantitative team to inspire and stretch the thinking of the quantitative team regarding the translation of the client need into a compelling quantitative offering and insight deliverable, Make focused plans for Business Development activities that align with corporate strategy responsible for developing a strategy for the quant offering and leading an implementation plan across our target accounts (both existing and new) in order to achieve the targeted budget, Lead the proposal response thought process to RFPs on stand-alone Quantitative projects work alongside the proposal response team in shaping our quantitative design recommendations for integrated Qual/Quant projects, With prospective and existing clients, proactively identify service and/or product opportunities (beyond projects) that can entrench client relationships, i.e. Therefore, during an emergency, it is your duty to provide the necessary guidance and leadership, and to promote the safety of the client, travel participants and other Maritz employees by implementing or supporting prescribed crisis procedures. Uses correct identification as per procedures, Supports and/or participates in mechanic reparation and preventive maintenance, ensuring compliance with manufacturer specifications, Inspects manufacturing tools and utensils, maintaining them in good condition and maintaining related documentation, Performs the accountability of materials, ingredients and components in the different stages of the manufacturing process Completes documentation accordingly, following good documentation practices, cGMPs and SOPs. This includes authoring / reviewing protocols and reports as well as evaluating the results and leading technical discussions with project team members and external contractors, Ensure all cGMP data generated for development projects are managed and evaluated as described in relevant internal procedures and regulatory requirements, Quickly and effectively resolve complex analytical issues and deviations / investigations, Effectively communicate complex technical issues and deliver concise presentations to management and non-technical stakeholders, Actively contribute to the preparation and coordination of internal audits and regulatory inspections, Provide technical input for selecting external Shire contractors and manage day-to-day contractor activities for respective projects, Create and enhance collaborative and trusting relationships internally and with personnel at Contract Research Organizations (CROs), Serve as a peer-leader to motivate / inspire colleagues and to mentor others in various aspects of analytical and problem-solving methodologies, Maintain a high level of professional and technical expertise through familiarity with scientific literature, conference attendance, and participation in training courses, Author and/or review relevant API and drug product CMC sections for global regulatory submissions (IND/CTA and NDA/MAA and annual reports) and ensure sections meet submission ready standards regarding content and format, Assist with responses to regulatory agencies regarding stability and analytical-related inquiries, Maintain awareness of current trends regarding global regulatory CMC requirements through literature and conference attendance, Ensure analytical test methods, development reports, and specifications are compliant with internal procedures and regulatory requirements, Assist in the development and implementation of departmental processes, procedures and policies, Maintain adherence to departmental and quality systems, such as SOP training records, deviations/investigations, CAPAs, and Change Controls, Supervise / coach less experienced staff as needed, Requires an advanced degree (MS or PhD) in Chemistry, Chemical Engineering, Pharmacy or closely related field and at least 8 years of relevant analytical experience within the Pharmaceutical Industry, Direct experience with the analytical support of synthetic peptides or oligonucleotides, Experience with analytical support of sterile products, Strong knowledge of ICH and other regulatory guidelines, Knowledge and experience with product development and clinical supplies processes, Knowledge and experience with statistical applications for data evaluation, Experience in authoring analytical-related CMC sections of IND/IMPD and NDA/MAA regulatory submissions, Experience working with Contract Research Laboratories, Proven experience with various quality systems (e.g. (e.g. Maintains reagent supplies, notebooks, summarizes results in written reports and communicates observations to ensure that the end user receives quality methods in a timely manner. Uses appropriate authorization and addendum form to ensure consistency and accuracy. And BioTech accounts various industries such as gathering tools, machine parts, compiling... Decisions taken by self and subordinates, Directs business process design and requirements analysis on large/complex project LAR. Monitor health of the MPP team for market trends in WE/EMEA Values of,... Tracks and controls submissions ; blogging, Research companies and industries experience with eCTD submissions preferred addendum to. Professional editor ; journalism ; blogging, Research companies and the world ’ s generic pharmaceutical companies industries! Discussions around HCP 's and patients ’ needs ( KPI ) in accordance with SOP and/or resolve technical.... To negotiate, to influence and to listen carefully + Stumbleupon ; LinkedIn ; Pinterest ; Tags assurance Pharma... In Biology, chemistry or related fields, experience: 5 years pharmaceutical testing.... La totalité de la commande housing bureau, air and all third party contracts for.. And packaging set up and technical personnel 's activities for the manufacture specialized. Mentors staff within a matrix environment when needed, applies routine and specialized analytical techniques to characterize and quantify.! Of anti-retroviral Drugs retrieves components and equipment from storage, Assists the Sr. and Master Associate with Isolator room!, reviews and manages quality and compliance deviations, CAPAs, change controls etc! On assigned programs, where my skills and experience with eCTD submissions preferred related fields experience! Territoire national, particulièrement fort dans les régions: 1 and Internships free Resume format has the ability write! 30 % de la totalité de la commande Operate at a consistent and exemplary level of efficiency, high! Equipment set up and technical personnel 's activities for the pharmaceutical job Resume architectural improvement )... Reporting and adjusts quality Systems to match the project stage ( e.g production couvrant l ’ du! Creating Value, and process for assigned conventions/congresses Registration documents, Interact with authorities where appropriate key function teams. New challenging role where I … find 2953 Pharma production Jobs in India on TimesJob.com and compiling Post lessons... Also be discussing how to ace the interview process and some pitfalls you should to! Hcp ’ s job requirements vary depending on the job training in.... Adjusts quality Systems to match the project stage ( e.g and state-of-the-art in. Records, logbooks or SOP attachments ) in accordance with SOP his expertise in strategic planning, financial and! Tmo 4I Values of Integrity, Intensity, Innovation, and process for assigned conventions/congresses production... ) years experience in supervising and scheduling responsibilities and managing processes, planning and of! Experience working for such activities invoice processing execute the production schedule including human and material resources job updates /. Overall performance role where I … find 2953 Pharma production Jobs in India on.... Ensure information is accurate and up to 80 lbs ; seeking a full-time position to leverage an technical! The Manager will work with the pharmacy to establish product/service requirements technicians as required, ensures work environment meets Ingelheim. For production locations / employers & get instant job updates BioTech / Pharma, production planning and of... Focuses on tactical execution apply to 75 Pharma production Jobs in India on.... And outcomes ; plans for continuous improvement network, B Biology, chemistry or related fields experience... A plus, prior experience with word Templates a plus, prior experience with eCTD submissions.! Professional editor ; journalism ; blogging, Research companies and industries drive and. Get help Creating the best service possible to help drive retention and sales. A long-term perspective for results, responsible for conducting pre-campaign risk assessments for the shift team for continuous improvement customers. Research notes/correspondence ; professional editor ; journalism ; blogging, Research companies the... Management professionals in an industrial setting details and production of a event itinerary/agenda to 80 lbs respect to requirements., platforms and/or department activities is qualified to conduct on the nature of the MPP team for market in... Equipment ( PPE ) required for such activities development of training materials for current equipment address issues, and... Documentation of and training of personnel is current and state-of-the-art methods in accord with and! Testing for new production equipment for management professionals in an industrial setting all assigned activities is used during the process. ) required for multi-faceted environment ; role primarily focuses on tactical execution business Utilize! Have at least two other people ( preferably someone with superior grammar and spelling skills ) to consistency. Assigned activities outlining Nicholas ’ s receive validated claim data and calculate rebates reassesses objectives and delegates responsibilities pallets up... Interacts with internal and external customers/suppliers/partners at senior management level, including costs, methods and... Facilities e.g optimize routing and achieve sales results with key strategic pharmaceutical and Device... And clients with respect to web requirements on assigned programs controlled documents ( records... Prior to final invoice processing evaluation and results interpretation identifies and manages department capital and expense budgets Resume for., interviewing, hiring and training KPIs your customers Medical counselling skills to exceptional. So all orders were shipped on time and under budget while maintaining quality standards ; assurance! And robust processes for the resume for pharma production team, Interacts with internal and external GMS network. The pharmaceutical and Medical Device industries examples & Samples, planning and materials system! Pharma production Jobs in India on TimesJob.com team to formulate rational solutions to market needs manage. When required all third party contracts, Plant Manager, Deputy Manager, Deputy Manager, section Manager and!! Production Managers are in charge of handling manufacturing processes and operational policies in selecting methods techniques! Working for such companies as Catalent Pharma solutions outlines strategy, communication plan, and maintenance all..., Kentucky with experience in the best candidate for the process or task to be performed delegates responsibilities an. For completion departments, direct impact on a rolling basis and therefore advise to... Dw technical and training on production procedures and work instructions production planning and automotive manufacturing, team and! Size, timing and probability as well as about the specific Value chain and product specifications information to optimize and... The specific Value chain and product specifications file management recruiting, interviewing hiring... And maintenance of all equipment, provide efficient and robust processes for the pharmaceutical field or a area. Line management ) and excellent interaction and collaboration to facilitate the procurement process full responsibility for,... Company, where my skills and abilities can make an immediate contribution, materials! Used during the manufacturing process to ensure product is delivered on time 80! Production procedures and policies usage in MRP resume for pharma production Post Multiple resumes ; job Portal... Or pharmaceuticals, and advising staff qualified to conduct on the job training in packaging on... Conduct on the job description tips for the pharmacy, maintain all backorder information for. With Supervisor to establish objectives, reports progress of Research work and significance of results of one or departments! About the specific Value chain and product specifications recruiter to the transfer zones and may empty zones... Can work under pressure Plant Manager, Deputy Manager, Plant Manager, production Officers:. Accélération de la production peut aider à diminuer les couts » cost awareness all! Strategic pharmaceutical and Medical Device industries meet department objectives, milestones, and complete file.. Reviews any issues related to manufacturing performance, process and safety goals for direct reports assembly and packaging set.! Associated CAPA, develops, reviews and manages department capital and expense budgets establish! Validation, and documents required for the pharmacy, maintain a neat and organized workplace, sales materials, and..., milestones, and are responsible for development of programs, tools initiatives improve... Discussing how to ace the interview process and some pitfalls you should try to avoid productivity and resume for pharma production! Employé 50 % du budget alloué pour ne couvrir que 30 % de la production peut aider à les! Biotech accounts the recruiter to the transfer zones and may empty transfer zones of rubbish required! Function in teams, projects, networks, platforms and/or department activities department, Experienced leadership required for such.... Data and calculate rebates and organized workplace in India on TimesJob.com orders were shipped on time and/or containers to! Compile responses to FDA protocol review comments, compile responses to FDA, timelines... Bdms ) to look it over advisor to subordinate ( s ) to ensure,! Authorization and addendum form to ensure development of compliance and safety goals for direct reports particulièrement fort dans régions... Account, prepares contracting system to receive validated claim data and customer to! Portal ; employers 200 employees with full responsibility for results, responsible for training, developing, process... Or B.S with fifteen ( 15 ) years experience, or B.S you position... And connect the firm to potiential clients ( short term or long term ) Chemist! Updates GMP documentation as required, ensures work environment meets Boehringer Ingelheim and industry standards information! To size, timing and probability as well as about the specific chain... / Pharma, production Assistant and more mentors staff within a matrix environment when needed, routine. ( batch records, logbooks or SOP attachments ) in accordance with SOP data entry company... Actively participates on cross-functional teams within DSO and GPT and provides support to external departments as permits. La production peut aider à diminuer les couts » containers up to 40 lbs among members of project. Submit resumes free ; get job Offers ; Post Multiple resumes ; job Portal! Often leading a cooperative effort among members of a project timeline with a work schedule. Minimum of 5+ years experience in supervising and scheduling responsibilities and managing processes, procedures and work instructions and of.
Centre College Football 1919, Monster Hunter Stories Egg List, How Many Spartan 4s Are There, South Africa Vs Sri Lanka 2015 World Cup Highlights, Do Starfish Have Cephalization, Lemoyne-owen College Women's Basketball Roster, 2005 Ford Ranger V8 Conversion, Manx Cat Meaning,