What you'll do...Provides pharmaceutical care to Customers, including processing and accurately dispensing prescription orders, counseling Customers regarding health care and prescription medication needs, maintaining confidential information, maintaining controlled medication and required documentation.Models, enforces, and provides direction and guidance to Associates on proper Customer service approaches and techniques to ensure Customer needs, complaints, and issues are successfully resolved within Company guidelines and standards.Ensures compliance with Company and legal policies, procedures, and regulations for assigned areas by analyzing and interpreting reports, implementing and monitoring loss prevention and safety controls, overseeing safety, operational, and quality assurance reviews, developing and implementing action plans, and providing direction and guidance on executing Company programs and strategic initiatives.Maintains confidential information, documentation, and assigned records as required by Company policies, and local, State, and Federal guidelines.Provides comprehensive patient care to customers by processing and accurately dispensing prescription orders; administering immunizations; counseling customers regarding health care and prescription medication needs; and maintaining confidential information, controlled medications and required documentation.Demonstrates up-to-date expertise and applies this to the development, execution, and improvement of action plans by providing expert advice and guidance to others in the application of information and best practices; supporting and aligning efforts to meet customer and business needs; and building commitment for perspectives and rationales.Provides and supports the implementation of business solutions by building relationships and partnerships with key stakeholders; identifying business needs; determining and carrying out necessary processes and practices; monitoring progress and results; recognizing and capitalizing on improvement opportunities; and adapting to competing demands, organizational changes, and new responsibilities.Models compliance with company policies and procedures and supports company standards of ethics and integrity by incorporating these into the development and implementation of business plans; using the Open Door Policy; and demonstrating and assisting others with how to apply these in executing business processes and practices.Minimum Qualifications:Bachelor's Degree in Pharmacy or PharmD degree, or equivalent FPGE (NABP). Pharmacy license (by job entry date). Completion of an ACPE Accredited Immunization training program (for example, APhA, Pharmacy School Curriculum, State Pharmacy Association sponsored).
Walmart • Washington, U.S.
A Pharmaceutical Company is seeking a Research Associate in Frederick, MD. Role Description This role will provide process engineering and analytical support for commercial manufacturing of cell therapy. Working cross functionally with quality, operations, material management, facility and engineering functions, the role is expected to provide technical input for product/process response and investigations, technology implementation, technology transfers, process validation and regulatory filings. • Execute scientific laboratory studies to support process/product understanding and continuous improvement projects • Execute analytical testing of cell therapy products – flow cytometry, ELISA and PCR assays. • Ability to follow laboratory procedures with attention to detail, and successfully execute experiments at the bench • Provide technical input to the execution of process validation and comparability campaigns. • Participate in evaluation of new technology and process automation for introduction into GMP manufacturing • Participate and support process FMEAs to understand process and product risks as a pre-requisite for process validation. • Participate and report to a cross-functional team to advance production activities. • Participate in Operational Excellence activities within Tier Structure. • Participate continuous improvement projects supporting commercial manufacturing site • Ensure systematic DMAIC based approach utilization for process/product related investigations to identify root cause and provide impact assessment to maintain routine manufacturing operations and determine process improvements for manufacturing. • Support technology transfers of launch and commercial cell therapy products • Effectively & efficiently communicate manufacturing process performance internally. • Support the implementation of automation and IT infrastructure projects • Assist in writing technical documentation (protocols & reports for equipment/instrument qualifications, comparability, and cell therapy manufacturing process validation) Skills & Requirements • Bachelors Degree in Biochemical Engineering, Tumor Immunology, Biotechnology or Life Sciences. • Basic understanding in Bioprocessing, Cell Culture and Biochemistry. • Knowledge of ELISA and/or PCR testing • Knowledge in flow cytometry and data analysis (FACSDiva, FlowJo, GraphPad Prism, Excel) is a plus • Ability to think critically, demonstrate troubleshooting and problem-solving skills • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment • Previous experience with other technologies is a plus • Experience with the use of Microsoft word, Excel, Power Point, Smartsheet, Prism, JMP, and other data analysis applications • Highly collaborative with excellent interpersonal, verbal and written communication skills • Ability to think critically with demonstrated problem-solving and troubleshooting skills • Comfortable working in a fast-paced company environment with minimal direction and able to adjust workload/assignments based upon changing priorities • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description
HAYS PLC • Frederick, U.S.
Seeking Entry Level candidates with a Bachelor's Degree in Biology, Chemistry, Microbiology, Biochemistry, or other scientific field, to work as QA Analyst / Consultants for a pharmaceutical client in Fort Worth, TX 76134. Recent graduates are fine.Technical Accountabilities:- Audit product lots- Pull analytical samples- Pull, log and inspect retention samples- Review MBR for release- Review and approve autoclave reports and logbooks- Update databasesEducation/Experience:- B.S. in Science (Chemistry, Biochemistry, Biology, Microbiology, Pharmacy) Demonstrated excellent written/verbal/interpersonal/communication and ability to perform effectively in a fast paced, team oriented environment. Skills:- Good computer skills- Good time management & communication skills- Attention to detail- Ability to multi-task- Fluent in English
Careerbuilder • Fort Worth, U.S.
Description:Positions in this function perform various duties related to the fulfillment of prescription orders. Dispense any or all of the following: unit doses, specialty pharmaceuticals, injectables, IV, enterals and related supplies following state and federal regulations and company policies and procedures. May compound medications using appropriate components, supplies and sterile/ventilated environment. Process, pack and ship outgoing pharmacy orders, ensuring drug, related supplies and patient collateral (education materials) are included. May also perform drug/supply ordering and inventory/warehouse duties, including proper storage of drugs and supplies and appropriate refrigeration of perishable product, monitor and adjust/calibrate pharmacy equipment, fill dispensing units. - Clerks, Techs and Pharmacists in regional and local pharmacies may also perform the following as permitted by state regulation: Prep and scan documents, verify member/patient data, submit prescription orders in computer system. Contact members/patients to validate data, resolve rejected claims, request payment information, establish priority of order or delivery details, consult on medication issues, and set up treatment in on-site facilities. Interpret provider prescription and create order, access, input and retrieve prescription and medical/lab information from computer system, verifies whether order/drug is reimbursable/covered.- Pharmacists monitor and verify all prescription orders upon creation and dispensing. Calibrate dosing pumps.- Pharmacists in this function may also act as the Pharmacist-in-Charge (PIC) which has additional duties to ensure Pharmacy is in compliance with federal and state regulations, professional standards and internal procedures. Note: (If duties are exclusively Rx order creation use Front Pharmacy job function for Clerks, Techs and Supervisors.) Navigate in and between internal and external computer systems quickly to respond to questions or find drug benefit or clinical information -Process prescriptions or prior authorization cases through on-line systems -Enter data (e.g., member or clinical) into computer systems that is used for making automated or clinical decisions -Utilize phone systems effectively to answer, make or transfer calls -Demonstrate proficiency in navigating basic computer systems (e.g., Microsoft Office software) -Review cases, orders, or prescriptions as they are received to determine urgency and accuracy -Review orders, prescriptions, or clinical information to make claim determinations, potential patient interventions, or prescription interpretations and approvals -Consult with members or others on medication use and appropriate interventions -Review claims processing status and reasons for rejections -Interpret and apply clinical guidelines or data to make judgments (e.g., approve prior authorizations, approve prescriptions, identify clinical interventions) -Make clinical decisions or recommendations (e.g., approvals/denials/incomplete for lack of information decisions)
Careerbuilder • Lenexa, U.S.
Butcher – Competitive – Tracy, CAThe RoleDo you possess at least a year’s experience in a food processing environment? Do you have advanced knowledge of GMP’s and are you HACCP certified?American Custom Meats (ACM), a leading national meat supplier, has an immediate need for a Butcher. The successful candidate will prepare raw materials to specifications and transform the product into finished goods.The key responsibilities of a Butcher include, but are not limited to:Reads and follows instructions on Production Sheet.Safely handles knife or tools to perform tasks.Sharpens and adjusts cutting equipment.Performs cuts to ACM and/or NAMP standards.Operates assigned machinery to ACM standards and expectations.The CompanyAmerican Custom Meats is a state-of-the-art food processing company servicing the military, and regional and national institutional foodservice and retail channels.As a quality-driven company with 8-figure sales revenue, we are a well-established and financially sound organization driven by a fast-paced and entrepreneurial “can-do” team of professionals.The PersonThe key skills and qualities of a Butcher: Minimal High School or GED.1-year experience in a Food Processing environment.Advanced knowledge of GMP’s; HACCP Certified.Two to Five years’ experience in a manufacturing or distribution environment (Desirable).Previous experience working in meat processing environment USDA trained (Desirable).Bilingual in Spanish/English (Desirable).
Careerbuilder • Tracy, U.S.
A Pharmaceutical Company is seeking an Research Associate /Senior Research Associate – Translational Biology in Lexington, MA. Role Description • Play a role in guiding creative and rigorous biological research programs aimed at fully understanding the disease mechanism of our pipeline. • Conduct efficacy, pharmacokinetic, pharmacodynamics, structure-activity-relationship and mechanisms of action studies of drug candidates • Use appropriate in vivo models to understand the mechanisms by which our drug candidates may contribute to adverse events in patients • Present working progress to team members in group meeting • Work closely with members of our research team to develop in vivo strategies to quickly and effectively address key questions related to the safety and efficacy of our drugs. • Review literature and provide insights to research directions, while predominantly making hands-on contributions to the research Skills & Requirements • Bachelor’s or Master’s Degree in Biology, Pharmacology, or related field, with a minimum of 1-3 years of experience. • Proficient in animal handling, dosing and surgery. Proficient in techniques including but not limited to oral gavage, intravenous injection, subcutaneous injection, blood collection and basic surgery • In depth knowledge of, and hands-on experience with, in vitro and in vivo models used for mechanistic investigation with small molecule or RNAi therapeutics • Experience performing molecular and cellular biology techniques, including but not limited to RNA preparation, RT-qPCR, ELISA, immunohistochemistry, urine biomarker analysis, plasma biomarker analysis • Broad and deep understanding of signaling pathways and biological processes implicated in rare genetic liver diseases as well as the mechanism of action of RNAi therapies is desirable • Previous experience in drug discovery is preferred • Outstanding written and oral communication skills • A high level of motivation and demonstrated record of accomplishment throughout your career • The ability to work effectively as part of a team, in a fast-paced environment
HAYS PLC • Lexington, U.S.
Currently, we have several roles available depending on your knowledge and skill set including:� Oven Operator� Mixer Operator� Packaging Line Operator Summary:Reporting to the production supervisor, line operator will follow good manufacturing practices (GMP�s) and food safety standards by operating different types of equipment. The incumbent will prepare for the production line start-up, ordering the proper ingredients and materials to be used, check the quality of the product, and report any concerns that need to be addressed. Job responsibilities:� Safely operate assigned line equipment in accordance with the standards and specifications associated with each production area following all proper sops. This includes but is not limited to the mixer; make up line, proofer/retarder(s), oven and packaging. � operate the specific equipment efficiently and ensures product standards, specifications, and quality requirements are met� ensure ingredients and other raw material are stored safely and check for any cross-contamination� use and dispose of cleaning agents and chemicals in a safe and efficient manner� troubleshoot issues under pressure and perform root cause analysis with corrective actions to prevent the same issues in future� Participate in operator-based machine maintenance� practices and complies with all company policies and procedures including health & safety, work rules, etc.� performs other job-related duties as requiredQualifications and Requirements� high school diploma or equivalent combination of education and experience� prior experience or training in manufacturing environment is preferred� ability to operate and work with mechanical and electrical machines� ability to understand and follow both written and verbal instructions, warnings, labels, and postings in English effectively and with a high level of detail� ability to work and communicate effectively in a fast-paced environment � ability to learn and abide by the gmp-s and health & safety standards� computer literacy Work and Physical requirements� ability to lift, pull, and push up to 50 lbs� ability to stand or walk for prolonged periods of time� perform repetitive motions, and work in an environment with varying temperatures� willing to work in shifts from Monday to Friday and Saturdays (subject to orders)� Overtime may be needed Shift available: � morning (7am to 3pm), � afternoon (3pm to 11pm), � night (11pm to 7am)
Alliance Employment Services • Toronto, Canada
QA Specialist – Contract or CTP – Morris Plains, NJRole DescriptionThe Quality Assurance delivers on the client's commitment to bring life-changing therapies to patients through the robust QA processes and systems. Our approach is agile, innovative and collaborative and our teams are genuinely committed to the rapid delivery of safe life changing therapies. As part of the broader Pharmaceutical Development & Manufacturing (PDM) team you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. The Quality Assurance on the floor is responsible for coordinating, managing on the floor Quality Oversight within commercial Drug Product operations to ensure sustained compliance with GMPs and regulatory readiness. • Provides Quality oversight to operations on the shop floor. Supports manufacturing operations (upstream and downstream) at real time. • Assists and advises on pertinent quality issues as they arise during plant operations. • Troubleshoot and elevate noncompliance issues and events observed. • Demonstrates knowledge of investigation, CAPA, and corrective action processes. • Demonstrates ability to effectively prioritize and manage multiple project workloads • Ensures compliance to policies and procedures • Maintains and supports material inventory, status and transfers. • Performs and supports changeovers in production area as required. • Participates in audits and other projects as appropriate. • Supports manufacturing operations (upstream and downstream) and staff as needed to identify and address product quality and compliance issues as they arise. • Reviews documentation associated with production operations. Ensures adequate levels of documentation are acceptable and compliant to existing procedures. • Participates in process improvement initiatives targeting for Right First Time (RFT) on documentation. • Participates in activities associated with event resolution and CAPAs, with a focus on organizing and attending cross-functional meetings. • Implements and ensures adherence of appropriate regulations and quality standards. • Supports operations to encourage a Quality Culture and ensure a safe working environment. • Completes job-related training as required. Skills & Requirements • 2+ years of relevant experience in a GMP environment related field and a BS OR 3+ years of relevant experience and an AA degree. • Prior experience in pharmaceutical industry is preferred.
HAYS PLC • Morris Plains, U.S.
We are seeking Butchers for our meat processing facility. Individuals must be willing to work in a cold environment. Positions are Temp to hire for entry level butchers. Job duties include, but not limited to:• Debone, cut and trim meat to specification while maintaining yield, throughput, and quality standards. Product includes but not limited to beef navels, beef briskets, pork picnics, pork hams, pork loins and poultry product.• Further trimming of specific cuts of beef and pork after bones have been removed maintaining the same standards.• Make cost effective cutting decisions.• Perform all duties as required by production supervisor.Capabilities• Butcher experience required.• Required to work overtime• Dependable.• Required to wear all personal protective equipment.• Strong attention to detail.• Excellent communication skills.• Ability to lift up to 50 pounds and push up to 50 pounds depending on specific function being performed.• Ability to crouch and bend repeatedly.• Meat processing and/or refrigerated manufacturing experience preferred.• Worked at least one year in each of the previous 3 jobs preferred.• Ability to work with cold materials in a cold, humid environment.• Follow Good Manufacturing Practices (GMPs).• Follow all safety regulations and support others in working safely.
Careerbuilder • Forest Park, U.S.
Bimbo Bakeries USA currently has an opening for Production Associates at the Escondido, CA Bakery. The Production Associate will be responsible for several bakery manufacturing activities. Candidates must be willing and able to work in a fast paced manufacturing environment. Candidates must be able to safely and accurately operate bakery equipment as assigned by management. The Bakery operates 24 hours, 7 days a week.Responsibilities include the consistent production of a high quality product in a Bread baking facility while incorporating safety and sanitation standards.Will need to be a team player and have solid interpersonal skills, and a strong commitment to ensuring the best quality products are produced. Excellent customer service by maintaining regular quality audits (AIB), good manufacturing practices, compliance with federal/state/local regulations (FDA, OSHA, Department of Agriculture, Department of Health, etc.), HACCP, meet or exceed Global Food Safety Standards (BRC) and environmental compliance.Qualifications• High school diploma or GED preferred but NOT required.• 1 year of experience in a food manufacturing environment, a plus.• Must be able to perform basic computer skills.• Must be able to work any day and/or shift including weekends and holidays.• Must have physical ability and strength to perform assigned tasks.• Must be able to lift 50 pounds, carry and/or stack pans, ingredient containers, etc.• Must be able to work in elevated areas and enter confined spaces.• Must be able to stand while working and walking for the duration of the working shift, except for breaks and meal period.• Must be able to work in a fast-paced environment and adapt to frequent changes that occur on the production line.
Careerbuilder • Escondido, U.S.
An American Company is seeking an Sr CRA – Ophthalmology in Rockville, MD. Role Description he Senior Clinical Research Associate (Sr. CRA) will work closely with the Clinical Project manager and is responsible for assisting in the planning and execution of clinical trials which includes assistance in vendor and site management, coordinating or leading data review and cleaning. Will support the CPM with oversight of the clinical study while ensuring the trial is conducted in compliance with the protocol, ICG/GCP, applicable regulatory requirements and applicable SOPs/Work instructions. Candidates must have the ability to prioritize multiple tasks based on workload, work in a fast-paced environment, have strong computer skills (Word Document, Excel and Power Point), maintain completion of required corporate training on standards, policies, work instructions due date. • May act as primary point of contact for specific vendors investigational sites as needed • Create, implement, and maintain systems to track study metrics and general information relating to study execution. Provides the updates to the team on metrics as needed • Prepare trial-related documents including but not limited to Informed Consent Forms (ICF), source documents, patient instruction guides, lab manuals and Case Report Forms (CRFs) • Reviews site-specific study documents (site-specific ICF and study tools/worksheets), , and site payments • Works closely with enablement group and clinical project manager to track study metrics including CRO and other vendor activities • Conduct periodic review of metrics for completion of study files in the eTMF. Escalates appropriately to the CPM and study team of updates and timelines regarding file completion. • Participates in team meetings and may lead small operational teams and/or participates in collaborative efforts (e.g. Standard Operating Procedure (SOP) development, operational task forces, etc.) • Supports Clinical Project Manager in site and vendor selection process, training and evaluation of study personnel (contractors and CRO). • May participate in site visits as needed or accompany experienced clinical monitor for co-monitoring or training purposes • Collaborated with internal cross functional teams to ensure effective delivery of the assigned project milestones • Organizes internal team meetings, investigator, meeting and other trial specific meetings as required • Support the clinical project manager in the planning and organization of investigator meetings and other meetings as necessary • Provides support to the Clinical Project Manager in the management of vendor scope(s) of work, budget updates & reconciliation, as agreed upon with prospectively established milestones and timelines • Maintain completion of required corporate training on standard, policies and work instructions by due date • Generate purchase orders, process vendor invoices and assist in tracking spend approved in the budget • Performs other work-related duties as assigned Skills & Requirements • BS/BA degree in scientific discipline or related healthcare field is preferred but not required; however, the combination of experience and training will be taken under consideration • Minimum 5 years clinical research experience (e.g. pharmaceutical, biotechnology, CRO healthcare setting [including 2 +years monitoring experience is preferred]) • Ability to work on complex or multiple projects and exercise critical thinking • Knowledgeable in clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines, as required • Solid organizational skills, interpersonal skills and communication skills (both written and oral) • Demonstrates problem solving skills, self-motivated and adaptable to a dynamic environment • Strong computer skills (Word Document, Smart Sheet, Excel and Power Point) • Experience in global trials preferred\ • Experience in interactions with vendors (e.g CROs, central laboratories, and other vendors preferred) • Ability to work in a dynamic, fast paced environment • Ability to deal with ambiguity
HAYS PLC • Rockville, U.S.
Nom de famille