6 jobs found in de soto

Walgreens Overview Our pharmacy technician positions have undergone an exciting transformation, moving from a transaction-based environment to a much more patient-centric one. As a Walgreens pharmacy technician, you'll be front and center - interacting with our customers and developing strong patient relationships. Pharmacy is the core of our business, and our pharmacy technicians enjoy all the tools and support - including the latest technology - to grow their careers and reach their goals. Responsibilities In accordance with state and federal regulations, assists the pharmacist, under direct supervision, in the practice of pharmacy. Assists the pharmacist in the performance of other Pharmacy Department duties in accordance with Company policies and procedures. Responsible for using pharmacy systems to obtain patient and drug information and process prescriptions. If PTCB certified, assists with and coaches pharmacy technicians in the operation of pharmacy systems and cashiers in the operation of the pharmacy cash registers. Models and delivers a distinctive and delightful customer experience. Customer Experience Engages customers and patients by greeting them and offering assistance with products and services. Resolves customer issues and answers questions to ensure a positive customer experience. Models and shares customer service best practices with all team members to deliver a distinctive and delightful customer experience, including interpersonal habits (e.g., greeting, eye contact, courtesy, etc.) and Walgreens service traits (e.g., offering help proactively, identifying needs, servicing until satisfied, etc.). Develops strong relationships with most valuable customers. Operations Under the supervision by the pharmacist, assist in the practice of pharmacy, in accordance with state, federal, and company policy. Reviews and complies with the Walgreen Co. Pharmacy Code of Conduct. Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions. Assists pharmacists in scheduling and maintaining work flow. Reports, immediately, prescription errors to pharmacist on duty and adheres to Company policies and procedures in relation to pharmacy errors and the Quality Improvement Program. Strictly adheres to the Walgreen Co. policy regarding Good Faith Dispensing during all applicable prescription dispensing activities. Responsible and accountable for registering all related sales on assigned cash register, collects and handles cash as required. Takes customer to OTC aisle when possible to assist in locating products. Handles telephone calls that do not require personal attention of the pharmacist, including those to physicians. Processes (corrects and resubmits) manual claims for third party program prescription services in a timely and efficient manner, and performs other clerical duties, as assigned by the Pharmacy Manager. Assists and supports Pharmacy Department on inventory management activities, such as, ordering, unpacking, checking and storing shipment of pharmaceuticals. Maintains knowledge of Company asset protection techniques, and files claims for warehouse overages (merchandise received, but not billed), shortages (merchandise billed, but not received), order errors or damaged goods involving Rx drugs. May assist pharmacist in administering clinical services including the collection and proper labeling of blood/urine samples from patients and other clinical services as required; assists pharmacy staff in coordination of clinical services, Walgreens healthcare clinics and external providers. Assists Pharmacy Manager and Staff Pharmacist in developing and maintaining good relationships with the local medical community, including physicians, nurses, and other health care providers, by medical provider detailing and outreach to health groups, retirement homes, nursing homes, and other forums for enhancing growth opportunities. Assists with exterior and interior maintenance by ensuring the Pharmacy Department is stocked with adequate supplies, clean, neat and orderly in condition and appearance. Complies with all company policies and procedures; maintains respectful relationships with coworkers. Completes special assignments and other tasks as assigned. Training & Personal Development Earns and maintains PTCB certification through the designated PTCB training program and/or state required certification/registration. Otherwise, earns PTCB certification as condition of promotion to senior technician. Attends training and completes PPLs requested by Manager and acquires continuing education credits. Maintains knowledge and skill in healthcare and pharmacy, including latest news and developments.

Requisition ID: PRO019070 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.  This 1st shift Technician position is available at the Merck Animal Health facility in De Soto, Kansas, located near Kansas City metropolitan area. The DeSoto facility is expanding operations to manufacturing vaccines and biologics for large and companion animals. Leveraging an experienced and innovative team environment, the key technologies at the site are biologics production using fermentation and cell culture platforms, filling and packaging. The De Soto facility is part of the global Merck Animal Health Manufacturing Division (MMD) network and is a key contributor to the manufacturing of animal health products. Initially working within the Fermentation/Downstream processing team you will learn the manufacturing processes associated with the large scale manufacture of M.Hyo antigen as well as be expected to be able to contribute to the daily completion and schedule adherance of other production activities within the team. Upon completion of the new production suite you will transfer to the new department. The antigen manufacturing operation is made up of teams that carry out the production activities for the preparation and sterilization of equipment, preparation and sterilization of media components, fermentation of bacterial antigens, downstream processing of bacterial antigens and serial batching of antigens to blend the final vaccines prior to sterile filling. The M.Hyo Department will be responsible for the end to end production of M.Hyo antigen at De Soto, which is a key component of swine vaccines manufactured at the site. Primary tasks for the team will include fermentation activities from breakout to large scale fermentation, set up and operation of single use bioreactors (SUBs) and single use mixing vessels (SUMs) and downstream processing of M.Hyo antigen using ultrafiltration methods. The position requires requires someone who can demonstrate a good attention to detail and achieve a consistent error-free execution of daily job responsibilities, be able to complete documentation using Good Documentation Practices and be able to identify opportunities for process improvement and employ basic problem solving skills. Qualifications Education Minimum Requirement: High School Diploma. Preferred Education Requirement: Associates degree or equivalent in a Science or engineering discipline. Required Experience and Skills: Proficient oral and written communication skills. Able to follow/comply with Manufacturing Directions, Standard Operating Procedures, Company/Corporate/Regulatory Policies.  Can demonstrate basic skills in effective time management to meet given deadlines. Can demonstrate ability to perform basic laboratory procedures. Can demonstrate ability to work effectively with team members and show initiative to support others on the team when needed. Proficient computer skills including MS Word and MS Excel. Successful completion of Physical Abilities Test Preferred Experience and Skills: Experience working in a manufacturing environment. Experience working with  fermentation and/or set up and operation of single use bioreactors (SUBs) preferred A good understanding of aseptic processes used in manufacturing. Experience using quality improvement tools and continuous improvement processes and site quality metrics. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.    If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to  staffingaadar@merck.com .    Search Firm Representatives Please Read Carefully:  Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.   Visa sponsorship is not available for this position.   For more information about personal rights under Equal Employment Opportunity, visit:                EEOC Poster              EEOC GINA Supplement            OFCCP EEO Supplement  Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations. Job: Production / Operator Other Locations: Employee Status: Regular Travel: Yes, 5 % of the Time Number of Openings: 2 Shift (if applicable): 1st Hazardous Materials: Acids, NaOH, BEI, BEA, Thiomersal, Formalin, steam, IPA, cleaning detergents. Company Trade Name: Merck

Requisition ID: PRO019072 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.  This 1st shift Technician position is available at the Merck Animal Health facility in De Soto, Kansas, located near Kansas City metropolitan area. The DeSoto facility is expanding operations to manufacturing vaccines and biologics for large and companion animals. Leveraging an experienced and innovative team environment, the key technologies at the site are biologics production using fermentation and cell culture platforms, filling and packaging. The De Soto facility is part of the global Merck Animal Health Manufacturing Division (MMD) network and is a key contributor to the manufacturing of animal health products. Initially working within the Downstream processing (DSP) team you will learn the manufacturing processes associated with the large scale manufacture of clostridia and M.Hyo antigen and be expected to contribute to the daily completion and schedule adherance of other production activities within the team. The antigen manufacturing operation is made up of teams that carry out the production activities for the preparation and sterilization of equipment, preparation and sterilization of media components, fermentation of bacterial antigens, downstream processing of bacterial antigens and serial batching of antigens to blend the final vaccines prior to sterile filling. The Fermentation & DSP Department are responsible for the end to end production of key antigens manufactured at the De Soto site, that are then used in the formulation of final vaccines. Primary tasks for the team will include fermentation activities from breakout to large scale fermentation, clean down, set up and operation of vessels and equipment and contribution to the site safety and continuous improvement activities. The position requires requires someone who can demonstrate a good attention to detail and achieve a consistent error-free execution of daily job responsibilities, be able to complete documentation using Good Documentation Practices and be able to identify opportunities for process improvement and employ basic problem solving skills. Qualifications Education Minimum Requirement: High School Diploma. Preferred Education Requirement: Associates degree or equivalent in a Science or engineering discipline. Required Experience and Skills: Proficient oral and written communication skills. Able to follow/comply with Manufacturing Directions, Standard Operating Procedures, Company/Corporate/Regulatory Policies.  Can demonstrate basic skills in effective time management to meet given deadlines. Can demonstrate ability to perform basic laboratory procedures. Can demonstrate ability to work effectively with team members and show initiative to support others on the team when needed. Proficient computer skills including MS Word and MS Excel. Successful completion of a Physical Abilities Test. Preferred Experience and Skills: Experience working in a manufacturing environment. Experience using large scale centrifugation, ultrafiltration or similar separation techniques. A good understanding of aseptic processes used in manufacturing. Experience using quality improvement tools and continuous improvement processes and site quality metrics. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.    If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to  staffingaadar@merck.com .    Search Firm Representatives Please Read Carefully:  Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.   Visa sponsorship is not available for this position.   For more information about personal rights under Equal Employment Opportunity, visit:                EEOC Poster              EEOC GINA Supplement            OFCCP EEO Supplement  Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations. Job: Production / Operator Other Locations: Employee Status: Regular Travel: Yes, 5 % of the Time Number of Openings: 1 Shift (if applicable): 1st Hazardous Materials: Acids, NaOH, BEI, BEA, Thiomersal, Formalin, steam, IPA, cleaning detergents Company Trade Name: Merck

Requisition ID: QUA008671 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.  The Specialist, Quality Control position is available at the Merck Animal Health facility in De Soto, Kansas,located near Kansas City metropolitan area.  The DeSoto facility isexpanding operations to manufacturing vaccines and biologics for large andcompanion animals.  Leveraging an experienced and innovative team environment,the key technologies at the site are biologics production using fermentationand cell culture platforms, filling and packaging. Responsibilities may include: Independently plan and perform quality control procedures. Review records for compliance. This position requires a thorough understanding of the principles underlying the testing procedures used in the areas of assignment. In addition, a thorough understanding of the material being evaluated (virus, bacteria, cell line) is also required. The ability to use experience and/or education to optimize testing activities is expected. Perform in QC lead role as assigned for performance of annual Outline of Production/Special Outline reviews and participation in annual review meetings. Troubleshooting established testing methods and evaluating new testing methods. Take lead role in QC testing OOS (Out of Specification) and deviation investigations to determine root causes and develop effective corrective and preventive actions. Coordinate QC representation in working group meetings to resolve production and testing issues. Maintain and evaluate the sequential analysis of the testing standards used in the area of assignment. Prepare and qualify test reagents/supplies. Perform in lead role for tracking QC reagent inventories for all tests performed by DeSoto QC and lead and/or coordinate reagent replenishment projects with applicable Biological Technical Support (BTS), Analytical Technical Support (ATS), Research and Development (R+D), and QC personnel. Create and revise Standard Operating Procedures (SOPs)/test methods/test worksheets for testing performed in the area(s) of assignment. Perform in QC lead role for protocol and report preparation. Perform in QC lead role for applicable assay transfers from R&D or other sites; work closely with the assay transfer coordinator to assure timely and compliant transfers. Perform in change manager role for QC-related change controls. Ensure Adequate Tier 2 and Tier 4 Representation in absence of QC manager and provide leadership in QC Tier 1 meetings as assigned.  Enter test results in the appropriate tracking system. Cross-check wet records with information in the tracking system and evaluate test dispositions (satisfactory, unsatisfactory, inconclusive, no test). Responsible for closing QC inspection results and performing batch usage decisions in SAP for batches tested by QC. Report to QC Manager all unusual, non-routine occurrences when performing tasks.  Participate in project teams and/or complete/design special projects. Special Projects / Stretch Assignments and other lead roles as assigned. Qualifications Education Minimum Requirement: Minimum Bachelors degree in science or a related field Required Experience and Skills: A minimum of five years related experience including a thorough knowledge of procedures, paperwork, and specific laboratory testing experience.  Excellent oral and written communication skills and ability to interface with all levels of the organization.  Excellent computer skills (i.e. Word, Excel, Power Point, Microsoft Office, SAP, etc.). Ability to work on a team with people from both inside Quality Control as well as other departments such as Research and Development and Manufacturing.  Excellent mathematics and writing skills.  Ability to independently prepare written reports for submission to United States Department of Agriculture (USDA) and other agencies.  Individual must be highly organized and possess good planning skills to handle multiple projects. Preferred Experience and Skills:  Proficiency with advanced laboratory techniques and procedures relating to USDA 9 Code of Federal Regulations (CFR) testing of veterinary biologicals preferred.  Cell culture, ELISA (Enzyme-linked Immunosorbent Assay), UP-SEC (Ultra-performance Size Exclusion Chromatography), and viral titration experience. Effective leadership skills. Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.    If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to  staffingaadar@merck.com .    Search Firm Representatives Please Read Carefully:  Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.   Visa sponsorship is not available for this position.   For more information about personal rights under Equal Employment Opportunity, visit:                EEOC Poster              EEOC GINA Supplement            OFCCP EEO Supplement  Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations. Job: Quality Lab Related Other Locations: Employee Status: Regular Travel: Yes, 5 % of the Time Number of Openings: 1 Shift (if applicable): 1st Hazardous Materials: Biohazard Level 1 and 2 organisms and toxins and thimerosal-containing vaccines and other chemicals Company Trade Name: Merck

Requisition ID: ADM010592 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. The U.S. Communications Co-op will support the Global Communications Team via internal communications for the U.S. commercial business. The ideal candidate will be a self-starter with strong written and verbal communication skills, as well as editing abilities. Must be organized and possess the ability to multi-task. Knowledge of AP Style is a plus. The co-op will have responsibilities including but not limited to: writing content for and managing the distribution of a weekly internal newsletter, maintaining an intranet site, managing town halls, supporting leadership communications, aiding in the management of an ongoing video series and maintaining a company directory.   Qualifications Education Minimum Requirement:  Must have completed at least 3 years towards a Bachelor’s Degree in Communications, Journalism, Animal Health or related degree program by May 2019 Required Experience and Skills:  Must possess strong project management skills Must be able to work collaboratively with an array of internal stakeholders  Must have strong oral and written communication skills  Must be organized / proficient in multi-tasking  Must be familiar with Microsoft Office Suite  Preferred Experience and Skills: Strong writing and editing abilities Knowledge of AP style Design skills are a plus Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.  If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com .   Search Firm Representatives Please Read Carefully:  Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position.  For more information about personal rights under Equal Employment Opportunity, visit:              EEOC Poster             EEOC GINA Supplement              OFCCP EEO Supplement  Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations. MAH2019 FTP2019 MANRRS2019 Job: Administrative Svcs Generic Other Locations: Employee Status: Temporary Travel: Yes, 10 % of the Time Number of Openings: 1 Shift (if applicable): 1st Hazardous Materials: Company Trade Name: Merck

Requisition ID: RES002223 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. The Senior Specialist, BTS responsibilities consist of but not limited to: Develops virus, cell culture and bacterial processes that are robust, scalable and economical for bioreactor, roller bottle and fermentation platforms in the production of veterinary vaccines. Represents Manufacturing departments on interdisciplinary teams and demonstrates working knowledge of current USDA regulatory guidelines and advanced technical knowledge.  Designs and performs simple to complex experimental studies to identify and optimize critical process parameters for the development of robust manufacturing processes for new and existing veterinary biological products. Develops creative approaches and solutions and applies these to assigned projects as well as to develop new platform technologies and improve existing processes. Facilitate and lead product transfers from R&D and site to site. Orders supplies and reagents, prepares reagents and provides support for overall laboratory operations. Responsible for daily and regularly scheduled preventative maintenance of Product Development department equipment. Documents and prepares comprehensive, accurate and well written project summaries and reports. Interacts routinely and effectively with Manufacturing, Quality and Research. #LI-PG1 Qualifications Education: BS in relevant field of study Required: Bachelors or Masters degree plus a minimum of eight (8) years of industrial experience in Animal Health or other Biological field required OR PhD plus 5 years of industrial experience in Animal Health or other Biological field required. Experience in Research and Development, Process Development and/or Biological manufacturing or closely related field Highly developed communication, leadership and teamwork skills Excellent project management, documentation and writing skills Preferred: Working knowledge of USDA regulatory requirements for manufacture and testing of Veterinary products. Knowledge or experience of bioprocess scale-up Experience in virology, cell culture and fermentation Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations. Job: Research Support Generic Other Locations: Employee Status: Regular Travel: Yes, 10 % of the Time Number of Openings: 1 Shift (if applicable): 1st Hazardous Materials: Yes Formalin, BEI and thimerosal Company Trade Name: Merck