Ensure required documentation is complete. There is an inherent risk associated with all travel, often as a result of extraordinary circumstances. Have at least two other people (preferably someone with superior grammar and spelling skills) to look it over. Download Pharmaceutical Resume Sample as Image file, Certified Pharmacy Technician Resume Sample, Pharmaceutical Sales Representative Resume Sample, Pharmaceutical Representative Resume Sample, Achieve contract performance goals and objectives for geographical assignment as established in the client agreement, Deliver product messages to prescribers and office personnel within established policies, procedures, standards, and workflows, Engage physicians in telephonic interactions and deliver product messages to prescribers within established policies, procedures, standards, and workflows, Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in telephonic dialogue, Foster ongoing trust with HCP/Physician, consumer or pharmacy as relationship develops to facilitate the decision making process, Develop superior product and disease state knowledge to effectively educate and engage healthcare professionals in two-way dialogue, Develop a daily/weekly call schedule to insure efficient and comprehensive coverage of territory, Provides back up to Account Manager in areas of reporting, coaching, mentoring and sharing of best practices, Candidate sourcing, recruiting and screening, Interview and assess internal & external candidates (phone screens and in-person) using behavioral, competency-based interviewing techniques, ‘Sell' candidates to hiring managers based on passive recruiting and/or phone interview results, Consistently consult and collaborate with hiring managers regarding expectations, challenges and strategies, Consistently consult with hiring managers regarding expectations, challenges and process improvements, Database Management; consistently reviewing pipeline for each requisition and dispositioning candidates accordingly, Maintain, clean and organize work area and participate in safety improvement projects, Maintain, clean, and organize work area and participate in safety improvement projects. This includes, Developing robust formulations and manufacturing processes for all pipeline products in PTDU portfolio, Develop new technologies & innovative drug delivery approaches enabling future products, such as ocular products, co-formulated products and sustained release products, Identify, prioritize & oversee DP processing technology development efforts in line with mid to long term business objectives, Oversee execution of drug product process characterization and validation programs in preparation for licensure, with a focus on continuous improvement and productivity, Oversee equipment development and qualification activities, Provide leadership direction for production of material in Genentech’s clinical & commercial manufacturing facilities, transferring formulation & technical knowledge and processes to commercial sites and providing ongoing support where appropriate, Ensure sufficient expertise is available to support all Drug Product programs, Provide senior level contributions to the development of the PTD business strategy, culture and capability, Take personal accountability to Sponsor PTD initiatives and projects as requested by PTD leadership, Implement CMC Productivity initiatives and cultivate an organizational culture that is agile, lean, innovative and encourages smart risk taking, Provide leadership and development of staff with strong focus on continuous improvement, performance management and career development, Foster teamwork among global and local colleagues, Evidence of strong established relationships with local endocrinology specialists, Understanding of the business drivers, dynamics, regulations and market access environment within the pharmaceutical industry, Skills at building and maintaining professional relationships with key customers, office staff and others in the customer influence network, Strong business analytics to analyze data as well as develop, execute and adjust business plans, Conduct and/or oversee laboratory research in process development for pharmaceutical sterile products, Evaluate, recommend, and oversee contract research and manufacturing organizations capable of providing the technical services required, Direct and coordinate process optimization of development formulations, Direct and participate in technology transfer and validation efforts at commercial manufacturing sites, Provide technical support of commercial products to ensure adequate supply at all times, Coordinate project activities with other internal functions through the Product Development Teams, Review of CMC documentation for US and ROW submissions, Build and maintain a strong working relationship with colleagues in Analytical Research, Project Management, Quality Assurance, and Regulatory Affairs, Prepare and review CMC submission documents, Interface with Regulatory Authorities pre and post submission as required to support global filings, Participate in due diligence activities as required, Ph.D. in a relevant discipline, with ten (10) years experience in sterile pharmaceutical dosage form technology/development, or M.S. Maintain and educate organization on industry trends, risks, and opportunities, Strategically partner with CIGNA Pharmacy Management Clinical Program Management to align contracting options to meet client requirements, coverage criteria and formulary strategy, Lead a team of contracting professionals in their daily work, Strong analytical background, business oriented, strategic thinking capabilities and attention to detail, while maintaining a "big picture" view.” Linking results to business performance drivers, generate alternatives, future options and drive positive change, Highly collaborative individual with ability to influence others and build strong professional relationships, especially in a highly matrixed organization, Understanding of the financial principles and operations of the business and able to drive profitability, A comprehensive understanding of contract negotiations, pricing models, network & strategy, products and claim operations, including reimbursement, Ability to integrate functional unit needs and competencies with those of other functional units in the organization in order to maximize overall service efficiency and response. Cover the given universe of companies, Make relative valuation comparisons and investment recommendations to portfolio managers, Participate in managing regional and global analyst funds, Work and communicate with a global network of JPMIM analysts, Strong understanding of financial markets and securities valuations, Ability to deliver clear/concise investment recommendations under significant uncertainty, Ability to distinguish between essential and nonessential information, Excellent oral and written skills. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. Operate under strict QSR and ISO compliance, Perform complex formulations, component and material evaluations, equipment calibrations and maintenance, Participate in product/process troubleshooting and validations, Formulate complex reagents and solutions as directed, following established guidelines and procedures, Under broad direction provides skilled level support for the product line(s), technical selling, key field product application, well prognosis, and/or completion product performance, Leads with new product market introductions and field trials, Investigates unusual or unsatisfactory product performance to determine root cause and preventative action, Leads special projects in region or area, as assigned, Conducts all business activities in accordance to Baker Hughes HSE policies, Legal Compliance requirements and Baker Hughes Core Values, University Degree in Engineering or Applied Science required, 3+ years’ experience and in-depth knowledge of specialty chemicals products and services, Able to identify the proper product and service for simple to complex applications, Ability to work and communicate well with internal and external customers, 5+ years’ experience in Oilfield operations environment, Thorough understanding of customer requirements as well as processes and procedures of the operating area, Specialized technical knowledge of company’s products and services, Recognise the responsibility to share knowledge and information by listening actively and communicating completely, Carry out process trouble shooting, to identify and solve process issues, involving and supporting the Team Leader as appropriate, Take ownership of and carry out production projects and perform associated quality tests, Encourage the use of Practical Process Improvement (PPI) tools, Value Stream Mapping (VSM), 5 Whys, Lean and 5S principle; be a promoter in the strive for excellence, To continue to acquire and develop the necessary skills and knowledge, to ensure continuing personal growth in the requirements of the job, Utilize thorough knowledge of the production processes to carry out effective and informative lab tours when required, Know, fully understand and champion compliance with health & safety regulations, COSHH requirements and ISO9001 quality procedures, Ensure that Risk Assessments are completed in a timely manner and are kept up to date and available for team members, Proven industrial or laboratory experience, Detailed knowledge and understanding of organic and inorganic chemistry in general, and chromatography in particular, Awareness of Health & Safety regulations, COSHH requirements, ISO9001 quality procedures, operational practices and relevant chemistry, PC skills, in particular Excel and knowledge of Statistical Processing, Ability and willingness to acquire new knowledge and skills, Ability to take responsibility, work on own initiative and meet deadlines, High level of communication and interpersonal skills, Plan, organise and perform simultaneous formulation of solutions such that products are supplied in the correct quantity and on time, Manufacture to defined specifications following defined procedures and completing all documentation accurately to produce products of high quality, Preparation of pilot solutions including raw material tittering, conformance and investigative samples to assist in the continued supply of products, To competently and safely operate, maintain, clean and calibrate equipment / machinery / areas used in the manufacturing process, Maintenance of stocks and stock records through timely computer transactions, Handling of hazardous biological and chemical materials safely, Use all company equipment supplied in a safe and efficient manner and keep the equipment in good order at all times, Communicate effectively both verbally and written within the team, departments and line management, Agree and deliver deadlines and quantities as required, Play an effective role in any projects in which you are involved and perform other duties consistent with your position as may be required by the Company, To comply with all Health and Safety policies and procedures at all times and to highlight any real or potential Health and Safety to Management in a timely manner, To comply with documented Quality and Environmental System requirements at all times. Formulation, manufacturing (including GMP pilot plant), analytical testing and clinical supply functions totaling more than 100 staff, report to this position. May require the use of hands and arms to lift and scoop, May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing, Seek opportunities to capture and share learning cross-functionally, Identify and bring forth areas for continual process improvement to team and function; identify methods to decrease drug development cycle times and cost, Participate in retrospective project/process review meetings (i.e. - Choose from 15 Leading Templates. Love this resume? and product registration packages for local regulatory agencies, Facilitating meetings and otherwise maintaining relevant communication with local regulatory agency staff throughout the product approval process, Establishing timely updates and maintenance of global product listings, facility registrations, licenses, approvals and annual registrations, Investigating regulatory history of similar products to assess approval or registration implications, Collaborating the local teams to identify key regulatory requirements for projects and business initiatives, Assisting with the preparation of routine reports and regulatory agency communications; development, updating and maintenance of paper/electronic regulatory document archival systems; and, reviews of promotional/advertising or educational items, Identifying and addressing clients’ or managers’ needs, including actively participating in client or management discussions and meetings; preparing concise, accurate project documents; and, communicating with clients in an organized and knowledgeable manner (e.g, Participating in practice development and thought leadership opportunities including, but not limited to client proposal development efforts, assisting with service/solution creation or enhancement, publishing industry whitepaper, and attendance at industry conferences, Minimum education BSc. Assist the call center management with customer issues and communications when drugs are out of stock, Up to 2 years of relevant work experience, Demonstrated ability to meet multiple deadlines and manage heavy workload, ABOUT THE DEPARTMENT Procurement is responsible for purchasing all goods and services through approved channels. Resume Details. Take action to safely reduce equipment setup and changeover times; Initiate and establish equipment operating parameters to maximize production, while meeting all product specifications, Accurately record on the appropriate documents the process/manufacturing steps, production results, equipment in-process checks, samplings, cleanings, ingredients used, and any other required cGMP information. To develop the manufacturing process using commonly employed unit processes, Support the GMP manufacturing of clinical supply drug product, Support the installation/qualification of new technology/equipment in the pilot plants, Available for 10-12 week internship beginning June 2017, Superior communication and interpersonal skills, Excellent academic achievement and analytical ability, Good team player and ability to work independently, Knowledge of commonly employed pharmaceutical unit operations to manufacture drug products is preferred, Operate and clean the following manufacturing equipment/systems, Minimum GCE ‘O’ level/SPM or NITEC/Higher NITEC/Diploma in Biotechnology/Biomedical/Electrical & Electronics/Mechanical/Mechatronics Engineering or relevant disciplines with 2 - 5 years of manufacturing experience in Pharmaceutical/Petrochemicals/Chemicals/Semiconductor or related industries, Fresh NITEC/Higher NITEC/Diploma graduates are welcome to apply, Good understanding of safe working practices and cGMP, A good team player with positive learning attitude, Must be willing to accept the following work condition, Support of direct knowledge transfer between the manufacturing sites, support of development of global key technology platforms, technical expertise and Manufacturing Division technology network, Facilitation of communication and interface for manufacturing sites to other global departments such as SCM, Regulatory Affairs, Pharma R&D, Strategic Procurement and CMO Organization, Support or lead investigation teams established to solve major quality issues occurring with our AH pharma products, Master or PhD degree in Science (Process technology, Pharmaceutical technology, Industrial Chemistry, Food technology,…) and at least 10 years of experience in technology or manufacturing position in a Pharmaceutical, Food manufacturing or Fine chemicals producing company or in extended experience in an academic environment of Pharmaceutical/Chemistry departments, Business Experience in projects as site to site and R&D to site transfers will be asset, Regulatory background incl. 141 Pharma Production Manager jobs available on Indeed.co.in. Maintains accurate records, system input, and complete file management. hypothesis testing, repeat test approvals e.t.c. Resume Format for Production. Resume Templates; Pharmacy Technician Resume Templates; We can commonly see pharmacists in drug stores. CAD drawings), Provide efficient and robust processes for the manufacture and/or specialized facilities e.g. Career Objective / Profile Summary: View this as the introduction to your resume and include 1-3 sentences giving a broad overview of your background, years of industry experience and the industry sectors of interest. Support TMO 4I Values of Integrity, Intensity, Innovation, and Involvement while Making Connections, Creating Value, and Being Determined. Highly organized, team oriented, dependable, a self-starter, Knowledge of protein biochemistry is required, Ability to conduct process characterization and validation experiments, design-of-experiment robustness studies, as well as assay qualification studies, Basic to advance analytical knowledge in characterizing proteins with HPLC-based chromatographic techniques, electrophoresis methods, spectroscopy, and other biophysical characterization techniques, Clinical lab experience and GMP/GLP knowledge a plus, Ability to work independently and as part of a team, self-motivated, adaptable and with a positive attitude, Ability to learn new techniques, perform multiple tasks simultaneously, attention to detail, keep accurate records, follow instructions, and comply with company policies, Bachelor's or Master’s degree in biochemistry, chemistry, analytical chemistry, chemical engineering, or other related degree concentration, 1-2 years of industrial experience or 1-2 years of academic research experience, Partner with outside Bio/Pharmaceutical Business Development colleagues to prospect and grow assigned territories, Develop new business revenue for the Bio/Pharmaceutical Division by qualifying and responding to in-coming calls, e-mails, and website inquiries from prospect accounts, Utilize CRM software to manage assigned territory sales funnels. better ) in Life Science related field, Working experience in Pharmaceutical Industry, 5+ years of Writing and Editing experience, Bachelor's Degree in English or Communications, Comfortable marking up edits digitally via Adobe PDF, Agency or CME (continuing medical education) experience, Previous experience within the Pharmaceutical industry, Engage physicians and office personnel in live video detail and/or telephonic interactions, Able to influence prescribers in an effort to significantly grow market share, Adhere to regulated guidelines for communications via all channels, Maintain a high level of product knowledge, policies, procedures, contacts, and the medical device industry; continual learning & training as required, Ability to build strong relationships with key staff members and establish relationships with the appropriate personnel in the physician’s office, Ensure timely and appropriate communication occurs with client’s sales and marketing team, Display flexibility and willingness to accept constantly changing project/program updates, Demonstrate corporate values on a consistent basis, Extensive self-study, training and testing are required; eligibility to proceed through training and selling certifications are dependent upon passing required exams, Adhere to all company policies and guidelines, Superior rapport and relationship building skills with the gatekeeper and office personnel, Demonstrated ability to learn, retain, and articulate technical/scientific-product related information and provide unscripted responses on appropriate subject matter, Planning efforts are well thought out and result in directly influencing a strategic selling approach, Responsible for selecting external Shire contractors as well as leading the team managing the day-to-day contractor activities, Responsible for providing strategic guidance regarding drug substance and drug formulation development to Shire project teams, Leads the development of drug formulation with Shire contractors, Leads the manufacturing of drug substances and drug products with Shire contractors, Reviews protocols for manufacturing drug substances and drug products, Writes and/or reviews analytical method development and stability protocols and reviews resulting data, Ensures development of robust chemical and finished product processes through the use of operational excellence tools such as DOE and QbD, Responsible for managing and developing reporting staff, Participates and contributes to Due Diligence assessment of potential product licensing or company acquisition opportunities as required, Delivers CMC Quality Documents (Module 3 and relevant part of Module 2) and supports the QA department by providing regulatory annual updates, ensuring full compliance with relevant regulatory authority quality standards, Leads or contributes to R&D Process improvement initiatives, Participates in Shire Product Strategy and Project Teams. 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. Analyzes results according to established SOPs. Ensure information is accurate and up to date, Participate in new product/process transfers and validations. Find Top pharma production talent resumes and profiles, contact them directly for Freelancing, Jobs and Internships free Ensure that projects receive necessary resources and scientific support. All events are to be recorded in the batch record and brought to the attention of the production supervisor for further action, Assists with room cleaning in production areas. 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. Assigns document numbers. Responsibilities may include strategy and process design in the following areas, Work in close collaboration with the DC-based program team, service delivery advisors in field offices, and local ministries and NGOs as appropriate to assure effective and efficient program strategic design, work planning, and implementation, Provide strategic technical leadership and expertise to MTaPS technical staff on the implementation of high-quality pharmaceutical service delivery, including prioritizing interventions and adapting best practices to local context, Build on existing tools and develop or adapt approaches to ensure the efficiency, acceptability, and impact of services, With other program staff, review, develop, and prepare project training and communications activities in the area of pharmaceutical service delivery, Remain current with the latest international technical developments in pharmaceutical service delivery, including best practices developed by implementing partners, international organizations, and the private sector, Build and maintain technical support network between program technical teams to ensure strategies and tools are appropriately applied in strategic intervention areas and challenges are shared to achieve program goals and objectives, Represent the program at international and local technical meetings and fora, as deemed appropriate by the program director, related to areas of responsibility, and relay lessons learned to program leadership and appropriate technical staff in field offices, Actively participate in operations research and monitoring and evaluation activities, dynamically seeking out and using available data to inform strategic and implementation decisions, Contribute systematically to program communications activities, including informing relevant international and national organization about project approaches, achievements, and challenges through face-to-face communications; contributing to the development of success stories; drafting, editing, and finalizing regular project reports as required by USAID; contributing to project blogs and other electronic communications; and any other communications activities as requested, Assist in the identification of short term technical assistance needs to support program activities and help to identify local and international consultants as necessary, Foster and demonstrate a workplace inclusive of creating opportunity, serving others, building trust, innovation and exceeding expectations, Perform other duties and responsibilities as required, Advanced degree in pharmacy, public health, health policy, or related field, At least 5-8 years’ project management experience in senior-level positions of large, complex international health sector development programs, Minimum 4 years of experience working in developing countries on pharmaceutical systems strengthening, with specific experience in improving and informing service delivery, Demonstrated outstanding leadership, strategic thinking, organizational, team-building and representational skills, Proven success as a decision-maker and respected supervisor overseeing professional and support staff, especially those in remote locations, Demonstrated experience in capacity-building and in working effectively with local NGOs, governments, and the private sector, Proven ability to function effectively with U.S. Government-funded cooperating agencies and contractors, host-country counterparts and government officials, USAID Mission staff, and representatives from other key stakeholders such as NGOs and other donors, Experience working with USAID, Global Fund, or other donors supplying healthcare commodities highly preferred, Demonstrated leadership, versatility, and integrity, Excellent verbal and written English communication and presentation skills are required; fluency in a second language is highly desirable, Associate Director or Senior Manager in a manufacturing or supply chain function within the life sciences industry, and, Prior consulting roles, including a Manager or Senior Manager at a consulting firm in a supply chain function with prior roles within the pharmaceutical life sciences industry. Immediately inform EMP Service Manager if you cannot resolve customer requests and ensure all requests are followed through, Maintain and have available at all times a daily EMP Service Diary/Log, Maintain the EMP Service Product File with all relevant bodies, Obtain and maintain the EMP Service Database of SPC's, PIL's and COA's, Control and process suppliers paper work and collate all relevant data, Ensure that all necessary manufacturing information is recorded in accordance with IMB Regulatory Reporting, Document and Report ADR's (Adverse Drug Reactions) to the EMP Service's Manager and the company's Responsible Person, Document and Report Product Recalls to the EMP Service's Manager and the company's Responsible Person, Comply with all GDP processes and procedures and in particular comply with regulations in force relating to supply of EMPs, Ensure that the EMP Service complies at all times to SOP's and Policies, Assisting in the coordination, implementation and follow up of regulatory agencies, internal audits and customer audits, Provide procurement support for other procured goods as required, To assist with all aspects of administration associated with the commercial team to include sales reports when required, Any other related activities as indicated by the EMP Service Manager, Required: Deep understanding of all issues specific to the supply of EMPs and must have, Previous experience with SAP is a distinct advantage, Flexibility: It is essential that the candidate be able to provide flexibility to the function. 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