with twenty (20) years experience, Hands-on experience in sterile pharmaceutical dosage formulation and production, Expertise with sterile pharmaceutical processing equipment, including ability to set-up, operate, and trouble shoot equipment, Ability to work with multiple disciplines within the organization, including but not limited to Analytical Research, Marketing, Project Management, Quality Assurance, Regulatory Affairs, Thorough understanding of QC sampling, testing, and interpretation of analytical results, Time management and the ability to multitask, as multiple projects will be operational at the same time, Domestic and international travel will be required, Maintain a high level of product knowledge, policies, procedures, contacts, and the pharmaceutical industry; continual learning & training as required, Ensure timely and appropriate communication occurs with sales professionals in the field, Minimum of 2 years of sales experience in an office/call center environment required, Experience contacting or detailing Physicians or Healthcare Professionals strongly preferred, Demonstrated ability to learn, retain, and articulate technical and scientific-product related information, and provide unscripted responses on appropriate subject matter, Superior rapport and relationship building skills, Define the desired customer experience through customer and market insight, Identify and remedy billing and other performance issues that lead to customer dissatisfaction, Writing, communicating, facilitating, and presenting cogently to and/or for all levels of industry audiences, clients and internal staff and management, including utilizing MS PowerPoint and Adobe Creative Suite, Developing mobile applications for a payer or provider, Supervise multi-skilled personnel as assigned, to ensure that performance meets established safety, quality/Good Manufacturing Practices (cGMP), quantity and cost standards, Manage, coordinate and directly supervise employees including coaching, counseling, performance reviews and feedback/initiating corrective action as needed, in a timely fashion, Collaborate with other area supervision and Human Resources in ensuring consistency in situations requiring corrective action with employees, Provide leadership and support to production and non-exempt production personnel in solving technical problems or contacting other resources as appropriate to solve problems, Ensure compliance of local, state and federal regulations and guidelines (e.g., Good Manufacturing Practices (CGMP), Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), etc.). Criteria of strategic importance to the client are often included in the contract as well, and typically define additional commitments required of CH2M HILL to achieve delivery success (e.g. Under the Pollution Prevention Act of 1990 (PPA), TRI collects information to track industry progress in reducing waste generation and moving towards safer waste management alternatives. Evaluate total share of wallet to optimize investments and grow revenue. Strong leadership skills. In addition, 3+ years experience in the field of professional information analysis in life science industry using advanced analysis technologies using databases and controlled vocabularies/thesauri/ontologies, Scientific expertise on molecular targets, diseases, biological compounds, processes and technologies, Detailed knowledge about content, structure, and limitations of pharma related information sources, Good technical grasp, creativity and innovative mindset, High degree of reliability, confidentiality, and ability to work under pressure; flexibility and excellent communication, presentation and organizational skills, Develop, evaluate, and implement business critical retrieval and analysis technologies (text, data mining and visualization) with focus on pharmacology, biomedical, technical and business/competitor information, Development of new and augmentation of existing controlled vocabularies (thesauri) and ontologies reflecting all major areas of activity of global BHC, Identification and evaluate new information sources, databases, applications & techniques for information professionals as well as for BHC professionals, scientists, project leaders and senior management, Analysis of information retrieved from commercial text mining applications for BHC core Development interests and activities, Retrieval and analysis of high quality information from databases, literature and competitors for BHC R&D processes and projects, Provide in-depths analyses, reports, recommendations mandatory for strategic decisions (go/no-go decisions in R&D projects, licensing, etc.) As executives rethink and reimagine their business, they must reset cost structures and redeploy resources to support it and build new capabilities that can help enable them to adjust as conditions change. How can you maximize profits; Accentures Anshul Singhal explains how a cost-to-serve methodology With inflation hitting a 40-year high, CEOs need to transform costs with a zero-based approach. Pharmacy, Nursing, Physicians Assistant) is an advantage, Background in health sciences or human centered design is an advantage, Experience in developing pharmaceutical dose forms as a formulation scientist, process engineer, or design engineer, Strong knowledge of Design Principles with Focus on Human Centered Design, Human Factors Systems engineering, Experience in Clinical Trial Coordination or support, Outstanding Organizational and Communication (written and verbal) Skills, Evaluating the physical and chemical characteristics of raw materials, intermediates, APIs, and drug products utilizing approved laboratory methods or developing new methods, Executing analytical methods and test procedures in accordance with written processes. Ensure the efficient and 3 million job seekers receive fresh jobs from Jora daily! Today, technology consultants assist organizations in using new technology across all parts of a business, which requires great, Management consulting vs. technology consulting, Management consultants help organizations develop business strategies powered by insights from data and, Digital Engineering and Manufacturing Jobs. Fulfill all related tasks and responsibilities related to own discipline. and product registration packages for local regulatory agencies, Facilitating and leading meetings and maintaining relevant communication with affiliates and 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, Collaborating with local teams to identify key regulatory requirements for projects and business initiatives, Overseeing/preparing routine reports and regulatory agency communications, Building, updating, and maintaining paper/electronic regulatory document archival systems. This notebook is numbered, signed out, and is part of Corporate record retention guidelines, Formalizes analytical methods to be utilized in the evaluation of raw materials, intermediate, APIs, and drug products and creates protocols and test procedures to be followed in future testing, Performs peer review of other analytical research associates methods, results, and documentation, Assists with instrument qualification, metrology, and maintenance, Creates, reviews, and/or revises laboratory SOPs when appropriate, Experience developing, revising executing analytical methods, Knowledge and understanding of a variety of analytical techniques including UPLC, GC, UV-Vis Spectrophotometry, and Karl Fischer titration, Experience performing qualitative and quantitative analytical tests, Minimum of 3 years analytical laboratory experience, Familiarity with cGMP regulations and FDA and ICH guidelines, Contribute to the overall evolution of SLFs Drug Benefits strategy and the products roadmap, Present the Drug Benefits vision at client presentations and industry conferences, Develop strong relations with the various level of governments, as needed, to represent our customers best interests (e.g. We integrate other solutions, such as pipe and tubing installations, conveyors, curing, spray booth, drying ovens and more. Our Technology Strategy & Advisory practice helps architect and realize exceptional business value from technology. Today, technology consultants assist organizations in using new technology across all parts of a business, which requires great agility and also makes their day-to-day role incredibly versatile. Microsoft takes the gloves off as it battles Sony for its Activision Communicates between Information Technology support and clients with respect to web requirements on assigned programs. Technology is a critical component to a business success. Both help companies better connect with customers, improve resilience, and drive sustainable growth. Townhall is the leading source for conservative news, political cartoons, breaking stories, election analysis and commentary on politics and the media culture. Coach on target dates and priorities. Tape specializes in supplying paint, powder and sealant/adhesive applications and fluid management equipment. A Microsoft 365 subscription offers an ad-free interface, custom domains, enhanced security options, the full desktop version of Office, and 1 Notifies immediately any accident or safety/environmental incident to the supervisor, Supplies materials to the manufacturing area as needed, Complies with all the training required to perform the tasks, including SOPs, forms, guidelines, Safety and Environmental training, Provides support in the auditing of the manufacturing batch records and related documentation, Keeps the areas cleaned and organized, including using the correct identification according to areas cleaning status. We extend our technology and business capabilities through a powerful ecosystem of market leaders and innovators, from the largest platform companies to startups and niche players. This includes removal of equipment, room sanitization and disposal of waste according to established safety requirements, Responsible for performing filling operations and assisting in visual inspection operations, Ensures components, materials and supplies are stocked prior to the start of the filling operations, A minimum of 5 years direct experience in a heavily regulated (e.g. 5 years of experience Preferred, Strong knowledge and practical experience of production, inventory and planning systems currently deployed in Zoetis including but not confined to SAP, Strong knowledge and practical experience in utilizing analytical tools, spreadsheets and databases to develop reports for strategic planning and communication, Proven ability to lead, synchronize and motivate colleagues to meet short and long term objectives, Ability to conceptualize, analyze and implement new methodologies in support of improving customer service, inventory management, and business alignment, Demonstrated ability to function and influence in a team matrix environment and have excellent interpersonal and communication skills, Demonstrated understanding of Right First Time and Lean Manufacturing concepts and principles preferred, Proactively demonstrate and promote client's products to targeted and non- targeted physicians and healthcare professionals in territory and develop an appropriate territory business plan to influence their prescribing decisions for the appropriate patient, Develop programs to enhance customer engagement and assist in business plans and goals. Provides direction to meet department objectives, Reports progress of research work and significance of results. The manager will work with internal and external staffing recruiters to manage head count needs for the shift team. Get the latest science news and technology news, read tech reviews and more at ABC News. Informs any deviation or potential deviation to the supervisor Takes action as per procedures to avoid or minimize impact to the process or operations, Segregates waste (dangerous, non-dangerous) according to procedures and guidelines. Very good communication skills, Works with R&D team to establish studies needed to support CMC, Provides review, interpretation and reporting of study data needed to support CMC, Actively participates in issuing protocols, generating and evaluating data, and producing reports to support CMC, Acts as a technical resource in generating information in support of CMC, Collaborates with Regulatory Affairs to establish plan(s) for building CMC sections, BS in Chemistry, Engineering, or related science, 10 years experience in chemistry-related field, Demonstrated experience in project management or PMP Certification, Excellent organizational skills and attention to detail, Deep understanding of FDA-regulated practices, Leads project initiation and planning activities to structure the project, including facilitating the definition of project goals, objectives, and scope. Handle full set accounting using an approved accounting system Possess knowledge of MYOB will be an advantage. Recommends strategy, validating and justifying business needs, conducting feasibility studies, producing high-level and detailed business models, preparing business cases, overseeing development and implementation of solutions, Actively shares emerging industry standards/trends with customers and peers within area of responsibility, Assures projects and project team members follow all company and departmental policies, procedures and standards, Ensures delivered solutions are compliant with associated federal regulations (SOX, OFCCP, labor laws, GMP, GxP, GCP, etc), Proactively identifies and assists in prioritizing opportunities to streamline business and/or system processes, Act as an IT business partner responsible for program planning and project management for the Pharmaceutical Sciences Strategy and Operations area, with a focus on Pharmaceutical Sciences CMC Program Management, Clinical Supply Chain Strategy, and Alliance Management, Lead change management activities and technical assessments of software platforms environments, Lead program area success and system rationalization and alignment with business priorities during periods of transformation and change, Manage selection and support of externalization capabilities for working with Contract Research Organizations (CROs) and Contract Manufacturing Organizations (CMOs), Lead teams that deliver and maintain FDA 21CFRpart11 compliant solutions to Pharmaceutical Sciences departments in a cost efficient and high quality manner, Interact with vendors and Takeda IT Infrastructure/Architecture to understand system requirements and ensure optimal system architecture for global deployments, Ensure high quality documentation including Configuration and Design documents, Installation and Operational Qualifications, SOPs and execution of validation test scripts, Proactively identify and assist in prioritizing opportunities to streamline business and/or system processes, Bachelors Degree or high school degree and 12 years of work experience in any business related field, Extensive experience supporting functional processes and technical design, Extensive experience implementing applications, Excellent user knowledge of relevant systems solutions, Excellent oral and written communications skills, business acumen with problem solving and analytical skills, Ability to write and speak the English language, Bachelors degree with 8+ years experience or Masters with 6+ years experience in Engineering/Computer Science/Life Science, 5+ years' experience in a scientific or biotech/pharma environment and familiar with drug development processes, 5 years+ IT Business Analysis and Project Management experience in a large pharmaceutical environment with validated systems, 5 years + experience with deployment of supply chain and pharmaceutical sciences systems, Ability to work collaboratively and comfortable working in a dynamic, cross-functional, and fast-paced global environment, Experience in an FDA regulated environment required, Knowledge of System Development Life Cycle (SDLC) Processes, Knowledge of Clinical Supply Chain and Pharmaceutical Product Development domain, Experience with information systems for lab data including LIMS, and inventory systems a plus, Demonstrated successful management of IT projects, including scope, financial, and schedule goals, Experience working with solutions delivery teams such as corporate IT infrastructure/architecture, applications development & integration, and support, Access to transportation to attend meetings, Ability to fly to meetings regionally and globally, Pharmaceutical industry and/or drug development business experience, The successful candidate will have design experience of Biotechnology, Small Molecule API Synthesis , Fill Finish, Oral Dosage Facility Design and Operation mainly gained within an engineering design office, Active membership in a professional body, such as the IChemE, ISPE, PDA, EI, etc. (e.g. However, a combination of experience and/or education will be taken into consideration, Must possess knowledge of the FDA review process concerning accepted manufacturing policies and procedures, sound administrative management skills, strong teamwork orientation and effective communication skill sets, Proven ability to recruit, train, and motivate personnel in order to balance staffing strength with profitability and growth, Must possess strong analytical, numerical, and reasoning abilities. The PDTL should take a proactive role in identifying the right questions and providing the appropriate experimental design using relevant preclinical studies and formulation concepts, In case of unsatisfactory developability properties of a lead candidate, provide input into potential development issues and risk factors and recommend the strategy on how to move forward, Proactively connect and interact with key stakeholders within therapeutic areas, Pharmacokinetics, Toxicology, and PDMS, Responsible for the integrated Developability assessment in close collaboration with the PK representatives and PharmSci Representatives, Provide a complete developability assessment package at the time of Development candidate declaration in order to ensure smooth transition of a small molecule from Discovery into the Early Development portfolio, in terms of formulations suitable for (GLP) toxicology studies, and guidance for the formulation strategy for clinical phase-1 studies, Represent Discovery Sciences at review committees, Keep informed on and invest in innovative screening tools and formulation options to meet the needs of the Discovery and early Development programs, in collaboration with experts within PDMS, academic groups and contract labs, Provide strategic and scientific guidance to a team of scientists (developability representatives, formulators) and lab technicians, Take the scientific and strategic lead in shaping the global Pharmaceutical Developability team to fit with the requirements of the organization, to foster collaboration and synergy across multiple teams, and enhance the scientific expertise, A PhD degree in Pharmaceutical Sciences or Chemistry or proven equal experience, with a strong understanding of Pharmaceutical Development, ADME and Preclinical Safety evaluation, A minimum of 7-10 years of experience as a Pharmaceutical Scientist, with demonstrated experience in developability and formulation strategies, is required, Experience in interpretation of pharmaceutical properties in relation to exposure and toxicology data in drug discovery & development, Organizational, planning, problem solving skills and the leadership skills needed in the completion of deliverables to the discovery Teams, Excellent partnering and decision-making skills, Master the balance between nice-to-have and need-to-have, apply fit-for-purpose approaches to provide scientifically valid assessments, Negotiate and influence decision-making processes, think and manage through issues into resolution, lead scientific discussions, Make fast decisions if needed, but at the same time inclusive and excellent team player, Excellent oral and written communication skills and ability to clearly and concisely present and communicate developability assessment and its impact to various audiences, including medicinal chemists, biologists, preclinical leaders (for both Tox and ADME), and internal boards, Ability to connect and empower people, discover and develop potential and challenge in a positive manner where necessary, Experience or interest in Multichannel approach, Ability to plan strategically and logically, Knowledge of the drivers surrounding Community Pharmacy, High level of ability and experience in planning, preparation, and presentation, High-level numeric skills and demonstrates initiative, Full EU Driving licence (no more than 6 points), 1) Have the relevant tertiary qualifications from recognized SA institutions i.e. Modifies plans and procedures to suit business demand based on production results, Coaches and develops complex operations and skilled technical staff through talent and performance management of all direct reports. 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 customers 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, Bachelors 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 customers 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 Associates 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 RFIs 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 (cGMPs), 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. Wallet to optimize investments and grow revenue technology news, read tech reviews and more jobs! 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