pharmaceutical analyst

Accenture

Skill required: Pharmacovigilance Services - Pharmacovigilance &amp; Drug Safety Surveillance 
Designation: Pharmacovigilance Services Analyst 
Qualifications:Any Graduation/Bachelor of Pharmacy/Master of Pharmacy
 
Years of Experience:2 to 5 years
 
Language - Ability:Japanese - Elementary
 
About Accenture 
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song&mdash; all powered by the world&rsquo;s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
 
What would you do? You will be aligned with our Life Sciences R&amp;D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance &amp; Regulatory, helping the world&acirc;&euro;&trade;s leading biopharma companies bring their vision to life &acirc;&euro;&ldquo; enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. 
What are we looking for? &bull;Ability to work well in a team &bull;Adaptable and flexible &bull;Agility for quick learning &bull;JLPT (N3 to N5)
 
Roles and Responsibilities: &bull;In this role you are required to do analysis and solving of lower-complexity problems &bull; Your day to day interaction is with peers within Accenture before updating supervisors &bull; In this role you may have limited exposure with clients and/or Accenture management &bull; You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments &bull; The decisions you make impact your own work and may impact the work of others &bull; You will be an individual contributor as a part of a team, with a focused scope of work &bull; Please note that this role may require you to work in rotational shifts
 
Any Graduation,Bachelor of Pharmacy,Master of Pharmacy

Pharmacovigilance Services Analyst

BKM Health Pvt Ltd

Education: B.Pharm / M.Pharm / M.Sc (Chemistry, Microbiology, or related field)Experience: 4-6 years of experience in pharmaceutical quality control. (OSD)Conduct HPLC, GC, UV Spectroscopy, FTIR, Dissolution, and other analytical tests as per standardoperating procedures (SOPs). Analysis of formulation, API, and stability. (In-process/Intermediate/BU/CU/Assay/Dissolution/RS) Ensure compliance with Good Laboratory Practices (GLP) and industry standards. Conduct stability studies as per ICH guidelines and prepare related reports. Maintain proper documentation of test results, certificates of analysis (CoA), batch records, andspecifications. Ensure compliance with GMP, WHO, USFDA, MHRA, EU-GMP, and other regulatory guidelines. Participate in internal and external audits and assist in audit preparations. Conduct periodic calibration and validation of laboratory instruments. Hands-on experience with analytical instruments (HPLC, GC, UV, FTIR, Dissolution). Knowledge of pharmacopoeial guidelines (USP, BP, EP).Job Types: Full-time, PermanentPay: ₹400,000.00 - ₹600,000.00 per yearBenefits:<ul><li>Paid sick time</li><li>Paid time off</li></ul>Education:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>pharmaceutical quality control. (OSD): 4 years (Preferred)</li></ul>Language:<ul><li>English (Preferred)</li></ul>Work Location: In person

QC Analyst – Executive

US Pharmacopeia

<div>
 
 Description
 
 
 
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 
 
 
 Brief Job Overview
 
 
 
 This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
 
 
 Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
 
 
 
 The Scientist-II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Executes all testing and analysis of data with excellence and essentially no errors.
 </li>
 <li>
 Supporting Verification, GPH, PQM, stability and other departmental teams in terms of testing whenever needed.
 </li>
 <li>
 Responsible for sample archival, sample tracking and chemical inventory tracking in the laboratory.
 </li>
 <li>
 Coordination with supervisor to ensure completion of the projects allotted to the team.
 </li>
 <li>
 Completing the project as per the timelines and troubleshoot the scientific aspects of the projects on need basis.
 </li>
 <li>
 Responsible for performing the calibration of the equipment as per the schedule.
 </li>
 <li>
 Responsible for preparing, executing, and completing IQ/OQ/PQ of new instruments.
 </li>
 <li>
 Ensuring that the chemicals and column etc. are available for the projects and forward the purchase requisitions.
 </li>
 <li>
 Taking up any additional responsibilities assigned by Supervisor from time to time.
 </li>
 <li>
 Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 The candidate must have strong analytical chemistry knowledge with the ability to analyze, interpret and report effectively on data from a variety of analytical instrumental tests (e.g., HPLC, GC, Wet analytical techniques, spectroscopic techniques). Well-developed organizational and interpersonal skills. Able to establish and nurture relationships with individuals of varying backgrounds, cultures and learning styles.
 
 
 <ul>
 <li>
 Master&rsquo;s degree in chemistry or Pharmacy.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 3 to 6 years with relevant laboratory experience.
 </li>
 <li>
 Proven track record of consistently delivering projects on time and with high quality for API&rsquo;s.
 </li>
 <li>
 Expert in chromatographic analysis, particularly in HPLC.
 </li>
 <li>
 Proficient in other related analytical instrumentation such as Water determination, Loss on drying, Residue on Ignition, Titrations, Spectroscopic analysis (UV, IR etc.,).
 </li>
 <li>
 Knowledge of pharmaceutical testing requirements and test protocols involving compendial methods for reference materials (USP compendia, ICH guidelines, FDA regulations etc.).
 </li>
 <li>
 Must possess effective communication skills, both written and verbal.
 </li>
 <li>
 Expert in Empower software with knowledge on Audit trails and Custom fields.
 </li>
 <li>
 Must possess good technical and analytical skills to independently resolve or troubleshoot issues.
 </li>
 <li>
 Should have a strong understanding of GLP regulations and exposure to external regulatory audits.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Knowledge in other related analytical instruments (GC, Thermal, Elemental analysis, Mass analyzers etc.), Electronic Laboratory Notebook, ERP, QR coding system will be an added advantage.
 </li>
 <li>
 Understanding monograph procedures and participating in compendial methods for reference materials (USP, FCC, NF, etc.).
 </li>
 <li>
 Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&amp;D, or a contract pharmaceutical analytical laboratory testing organization is a plus.
 </li>
 <li>
 Awareness of GLP regulations, QMS, ISO/IEC 17025 and exposure to external regulatory audits is desirable.
 </li>
 <li>
 Ability to embrace and lead change. Extremely adaptable.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected..
 
 
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist II, RSL

Eurofins BioPharma Product Testing North America

<div>
 
 
 Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
 
 
 
 
 
 
 The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
 
 
 
 
 
 
 In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
 
 
 
 
 
 
 In 2024, Eurofins generated total revenues of EUR &euro; 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
 
 
 
 
 
 
 
 
 
 
 
 Job Description
 
 
 
 <ul>
 <li>
 Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products
 </li>
 <li>
 Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
 </li>
 <li>
 Executing method transfer protocols
 </li>
 <li>
 Performing monthly maintenance of laboratory equipment
 </li>
 <li>
 Working efficiently, documenting work clearly, and performing tests accurately
 </li>
 <li>
 Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
 </li>
 <li>
 Reads and understands analytical procedures (compendial and client supplied) and internal SOPs
 </li>
 <li>
 Processes data, generates reports, and evaluates data
 </li>
 <li>
 Trains others in laboratory procedures
 </li>
 <li>
 Performs laboratory maintenance
 </li>
 <li>
 Communicates with vendors and repair personnel
 </li>
 <li>
 Writes investigations
 </li>
 <li>
 Leads project/test areas and perform method transfers/feasibility studies
 </li>
 <li>
 Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 The Ideal Candidate would possess:
 
 
 
 
 <ul>
 <li>
 Good dexterity; positive attitude; solution driven
 </li>
 <li>
 Due to the size of the site, employees are required to flex into positions and activities outside their normally assigned duties as workload requires and as trained. These activities require working in all departments including QA, microbiology, chemistry, and general support for laboratory operations
 </li>
 <li>
 Conducts all activities in a safe and efficient manner
 </li>
 <li>
 Performs other duties as assigned
 </li>
 <li>
 Strong computer, scientific, and organizational skills
 </li>
 <li>
 Excellent communication (oral and written) and attention to detail
 </li>
 <li>
 Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
 </li>
 <li>
 Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
 </li>
 </ul>
 
 
 Minimum Qualifications:
 
 
 
 
 <ul>
 <li>
 Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
 </li>
 <li>
 1-2 years of previous laboratory experience
 </li>
 <li>
 Authorization to work in the United States indefinitely without restriction or sponsorship.
 
 
 </li>
 </ul>
 
 
 Additional Information
 
 
 
 
 
 Position is full-time position, Monday - Thursday 8:00am - 6:00pm, 4*10 schedule. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply.
 
 
 
 <ul>
 <li>
 Excellent full time benefits including comprehensive medical coverage, dental, and vision options
 </li>
 <li>
 Life and disability insurance
 </li>
 <li>
 401(k) with company match
 </li>
 <li>
 Paid vacation and holidays
 </li>
 </ul>
 
 
 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
 
 
 
 
</div>

Analytical Scientist

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking an experienced Analytical Specialist specializing in Mass Spectrometry to develop sensitive and robust methods for quantifying genotoxic impurities (Like: Nitrosamines) in drug substances and products. This role involves method development, validation, troubleshooting, and resolving method-related issues. Your expertise in Mass Spectrometry will be crucial in creating accurate impurity profiles through comprehensive analysis.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible for developing sensitive and robust methods to quantify genotoxic impurities in drug substance and products. This involves selecting appropriate quantitation modes, validating methods, and transferring them to QC sites. Your role includes troubleshooting and resolving method-related queries and issues, ensuring quality robust method development.
 </li>
 <li>
 You will be responsible for identifying impurities in stress and stability studies, correlating data based on Mass and fragmentation, and developing methods for screening leachables in Parental formulations. The goal is to create accurate impurity profiles through comprehensive analysis.
 </li>
 <li>
 You will respond to regulatory deficiencies related to Mass spec techniques, provide quantitation support for plant samples, and perform structure confirmation activities for working/reference standards and impurities. Anticipating potential queries from regulatory authorities/customers and proposing relevant measures for timely responses are crucial aspects of this role.
 </li>
 <li>
 You will be responsible for training new team members, preparing Standard operating procedure (SOPs) and guidelines, conducting incident/investigation analysis, identifying Corrective Action Preventive Action (CAPA) and root causes, and ensuring adherence to safe work practices. Maintaining Good Manufacturing practices (GMP) in laboratory and conducting preventive maintenance of instruments are essential for meeting minimum operating standards.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Post Graduation in Pharma/Physics
 
 
 
 
 
 Minimum work experience:
 
 8-10 years of experience
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Able to understand the mass spectrometry principles and Liquid chromatography principles.
 </li>
 <li>
 Good hands-on experience on Liquid chromatography-mass spectrometry (LC_MS), Tandem mass spectrometry (MS/MS) and High resolution mass spectrometry (HR-MS) techniques.
 </li>
 <li>
 Excellent skill set on method development, sample preparation, matrix interference removal and validation of quantitative methods in API and formulations.
 </li>
 <li>
 Experience on extractable and leachable, analytical method development, validations &amp; transfers.
 </li>
 <li>
 Good documentation practices and laboratory practices.
 </li>
 <li>
 Sound knowledge and understanding of FDA regulations governing pharmaceuticals.
 </li>
 </ul>
 
 
 Behavioral
 
 
 Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Ability to work with cross functional teams.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Leadership skills to motivate and mentor the team.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

Horizon Biolabs Pvt Ltd

Job DescriptionHorizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries .We are looking for :Candidate with Msc/Bsc/Bpharm/Mpharm having minimum 03-05 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry as a Sr.QC Analyst.About the jobThe Quality Control Analyst will report to the Manager of Quality.Experience<ul><li>3+ years of QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li><li>Must have hands on experience on HPLC/GC (Gas Chromatography)</li><li>Method Development/validation experience desirable.</li></ul>Education<ul><li>Bachelor&rsquo;s /Masters degree in Science related field required.</li></ul>Job Type: Full-timeSchedule:<ul><li>Day shift</li></ul>Education:<ul><li>Msc/M Phrama/B Pharma/Bsc(Chemistry)</li></ul>Experience:<ul><li>total work: 03-05 years (Required)</li><li>Candidates from QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li></ul>Job Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Location:<ul><li>Hyderabad, Telangana (Preferred)</li></ul>Work Location: In personJob Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Application Question(s):<ul><li>Are you currently staying in Hyderabad?</li><li>Are you having QC lab experience in CRO/pharmaceutical industry in a cGMP environment?</li><li>are you ready to join immediately?(within 7 days)</li></ul>Work Location: In personJob Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

QC Analyst-HPLC,GC

VCU Health System

**This position allows for Remote work to allow a flexible work environment**
 
**To be considered for the role, you must permanently reside in one of the following states: Alabama, Arkansas, Florida, Georgia, Kentucky, Kansas, Maryland, Michigan, Missouri, North Carolina, Ohio, South Carolina, Tennessee, Texas, Virginia, or West Virginia**
 
Job Description Summary
 
The Willow Analyst-Pharmacist partners with the application team while working collaboratively with our customers to bring cutting-edge technology and automated solutions to the department.
 
The Analyst implements and maintains EHR systems and databases to ensure optimum performance and exceptional outcomes for employees and patients.
 
The Analyst manages or performs work associated with the analysis, design, implementation, operation, deployment, and support of the organization’s information technology resources in application specialty.
 
Also, the Analyst will interface with all areas of Information Technology Services to ensure project success from development to implementation with the ultimate outcome of customer satisfaction.
 
Licensure, Certification, or Registration Requirements for Hire: Current licensure with the Virginia State Board of Pharmacy Licensure, Certification, or Registration Requirements for continued employment: Current licensure with the Virginia State Board of Pharmacy Certification in job relevant Epic module(s). Successful Epic certification(s) completion required within 60 days of final training. Experience REQUIRED: Three years to six years hospital pharmacy experience Possesses thorough knowledge of the inpatient environment and clinic based operations, procedures/functions and the relationships between them and the hospital Understand the integration of applications and their impact on business processes and operations Demonstrate innovative forward thinking, able to meet project deadlines, delivers to commitments, possess high level of energy and professional acumen, and be client service oriented. Knowledge of physician practice/healthcare professional services, billing requirements, hospital administration and/or processes Ability to communicate on a professional level with physicians, nurses and other professional staff when discussing drugs and drug related problems Ability to work at a high technical level on all phases of application systems analysis, workflow analysis, build, design, testing, interface knowledge and programming activities Experience PREFERRED: Previous Epic experience in the training, build, and/or support of the Epic systems electronic health record suite Education/training REQUIRED: Graduate of an accredited School of Pharmacy with a B.S. in Pharmacy or Pharm.D. Degree Education/training PREFERRED: Doctor of Pharmacy (Pharm.D.) from an accredited academic program Independent action(s) required: Determines and develops approaches to solutions with work subject to general input by manager or senior team members Open to change and acts with high ethical standards Focused on excellent customer service Exhibits a dedication to quality, reliability and resourcefulness work environment Able to handle pressure due to multiple demands and tight timelines Subject to fast paced work setting with competing priorities Supervisory responsibilities (if applicable): N/A Additional position requirements: N/A Age Specific groups served: N/A Physical Requirements (includes use of assistance devices as appropriate): Physical Lifting less than 20 lbs. Activities: Prolonged sitting Mental/Sensory: Strong recall, Reasoning, Problem solving, Hearing, Speak clearly, Write legibly, Reading, Logical thinking Emotional: Fast pace environment, Able to handle multiple priorities, Frequent and intense customer interactions, Able to adapt to frequent, change
 
EEO Employer/Disabled/Protected Veteran/41 CFR 60-1.4.

Epic Analyst, Pharmacist

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2856 pharmaceutical analyst jobs NEAR_ME

Pharmacovigilance Services Analyst

QC Analyst – Executive

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