Qureos Mentor

Grifols

<div></div><div><div><div><div><div><p>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.</p></div></div><div><br>
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</div></div><div><b>Full Time RN / Registered Nurse</b></div><br>
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Job Title:</b><b> </b>Center Medical Specialist - Registered Nurse / RN</div><br>
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<div><b>
What&rsquo;s In It for You</b></div>
<ul>
<li>Competitive Pay</li>
<li>Geographic mobility among our more than 300 donation centers</li>
<li>No Third Shift</li>
<li>Incredible Comprehensive Benefits Package Including: Medical, Dental, Vision, up to 6% 401K match, Tuition Reimbursement, PTO, Holiday Pay, Opportunity to participate in Company Bonus Program</li></ul><br>
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Are you looking for something different?</b><i> </i>Did you know that your skill set/experience makes you a valuable candidate for a Center Medical Specialist position in one of our plasma donation centers?</div><br>
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</div><div>For more information visit: www.grifolsplasma.com</div><br>
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</div><div><b>About the Job</b></div>
<ul>
<li>Perform physical examination and establish medical history to determine donor suitability</li>
<li>Build rapport with donors to ensure overall customer satisfaction</li>
<li>Ensure donor and staff confidentiality</li>
<li>Responsible for donor awareness to potential hazards</li>
<li>Provide donor education regarding general health and provide counseling regarding unacceptable test results</li>
<li>Evaluate &amp; manage donor injuries and adverse events</li>
<li>Perform evaluations of any history of illness or medications to ensure continued donor suitability</li>
<li>Assist in employee training</li>
<li>Administer employee Hepatitis Vaccine program</li></ul><br>
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Job Requirements
</b></div><ul><li>Educated and currently certified/licensed in the state of employment and according to state requirements as a Registered Nurse.</li>
<li>Current CPR certification required</li>
<li>Bilingual in Spanish</li></ul><br>
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Attributes:</b></div>
<ul><li>Work is performed both standing and sitting for up to 2 to 4 hours per day each.
</li></ul><ul><li>The position does require bending and twisting of neck up from 1 to 2 hours per day.
</li></ul><ul><li>Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists.
</li></ul><ul><li>Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects.</li></ul>
<ul><li>Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist.
</li></ul><ul><li>Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential.
</li></ul><ul><li>Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye.
</li></ul><ul><li>Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
</li></ul><ul><li>Works independently and within guidance of oral or written instructions.
</li></ul><ul><li>Performs a wide range of tasks as dictated by variable demands and changing conditions.
</li></ul><ul><li>Relates sensitive information to diverse groups. Work is performed in a plasma center.
</li></ul><ul><li>Exposure to biological fluids with potential exposure to infectious organisms.
</li></ul><ul><li>Exposure to electrical office and laboratory equipment.
</li></ul><ul><li>Exposure to extreme cold below 32 degrees F while performing functions in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear.</li></ul><br>
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Pay scale of $41.00 - 43.50 per hour, depending on training, education and experience. This position is eligible to participate in up to 4% of the company bonus pool. We offer benefits including medical, PTO, up to 6 % 401K match, and tuition reimbursement. We are committed to offering our employees opportunities for professional growth and career progression. Even though we are a global healthcare company with employees in 30 countries, Grifols prides itself on its family-like culture. Our company has more than tripled its workforce in the last 10 years - we&rsquo;re growing, and you can grow with us!</div><br>
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#biomatusa</div>
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#app</div><br>
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<p></p><p>Third Party Agency and Recruiter Notice:</p>
<p>
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</p><br>
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Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance.</b></p>
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California Personnel Privacy Policy and Notice at Collection</p>
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<p><b>Location: 355 E 3rd St Calexico CA 92231</b></p>
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Learn more about Grifols</p></div><p></p>

RN / Registered Nurse - Bilingual in Spanish

<p></p><div><div><div><div><div><p>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.</p><br>
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</div></div><p></p><p>The incumbent will provide technical or scientific expertise to the development, scale-up, transfer, and/or support of production processes for plasma derived or recombinant proteins. Activities are centered on unit operations such as filtration methods, chromatography, precipitation, and process trouble shooting.</p>
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The candidate must have the ability to set and meet deadlines, multitask, and prioritize personal tasks based on project needs.</p>
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The candidate will also have a large role in maintaining the laboratory facilities in accordance with procedure.</p><br>
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</p><p><b>Primary responsibilities for role:
</b></p><ul><li>With supervision, develops actions plans in support of departmental goals.
</li></ul><ul><li>Identifies and collects data on critical process attributes.</li></ul>
<ul><li>Executes action plans independently or as part of a team.</li></ul>
<ul><li>Assists in the design of scientifically rigorous experiments. Executes and interprets results independently.</li></ul>
<ul><li>May conduct laboratory or clinical production work, as required, using standard processing and analytical equipment.
</li></ul><ul><li>Independently prepares procedures or technical reports, including data interpretation.</li></ul>
<ul><li>With supervision, prepares and effectively communicates technical results in cross-functional settings.</li></ul>
<ul><li>Develops solutions to complex technical problems within area of expertise.</li></ul><br>
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</p><p><b>Knowledge, Skills, and Abilities</b></p>
<ul><li>Ability to set and meet deadlines, multitask, and prioritize tasks based on project needs.</li></ul>
<ul><li>Experience performing and analyzing results from protein assays relevant to process or formulation development: SDS-PAGE, HPLC, ELISA and UV/Vis spectroscopy.</li></ul>
<ul><li>Applies scientific or engineering principles in problem solving.</li></ul>
<ul><li>Has ability to apply scientific or engineering principles and company&rsquo;s policies and procedures in completion of job tasks.
</li></ul><ul><li>Takes initiative in keeping current in area of specialization (e.g., protein purification, chromatography, filtration) and expanding knowledge base in professional area.</li></ul>
<ul><li>Experience with laboratory notebooks</li></ul>
<ul><li>Must have excellent written communication and strong oral communication skills.</li></ul>
<ul><li>Must be proficient in use MS Office Suite.</li></ul><br>
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Education</b> Biochemistry, Chemistry, or relevant life science field.</p><br>
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</p><p><b>Experience</b> 6+ years of relevant experience</p><br>
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</p><p><b>Occupational demands:</b></p>
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Work is performed in a clinical and/or a laboratory environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to chemicals. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits and bends neck for 4-6 hours per day. May stand and twist neck for 2-4 hours per day. Occasionally walks, bends and twists waist and squats. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Moderate lifting of 15-30lbs. with a maximum lift of 35 lbs. May reach above and below shoulder height. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Frequently works with diverse groups to obtain consensus on complex issues. Ability to apply abstract principles to solve complex conceptual issues. Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence.</p><br>
<p></p><p>Third Party Agency and Recruiter Notice:</p>
<p>Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</p><br>
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<p><b>Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws.</b></p><br>
<p></p><p><b>Location: </b><b>NORTH AMERICA : USA : NC-RTP</b><b>:</b><b>[[cust_building]]</b></p><br>
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<p>Learn more about Grifols</p></div><p></p>

Senior Associate Process Development Scientist II

<p></p><div><div><div><div><div><p>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.</p><br>
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</div></div><div></div><p>Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols' activities focus on fulfilling the needs of its patients as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 75 years, Grifols has developed, manufactured and marketed product designed to improve human health. Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. For more information, please visit our website: http://www.grifols.com</p><br>
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<p><b>
Summary</b></p>
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Reporting to the Global Director of Indirect Procurement the Global Category Manager - Indirect Procurement Facilities and/or Engineering is a global category manager and a key leader role working with the markets and global procurement teams to deliver best value across the indirect spend portfolio for the Facilities and/or Engineering Categories .</p><br>
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Primary responsibilities for role:</b></p>
<ul>
<li><p>Act as trusted adviser to business partners in the vendor sourcing process, communicating strategic approach for vendor negotiations and/or ongoing projects.</p>
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<li><p>Lead full range of projects from transactional to complex, spanning all types of third-party services. Identify data and research resources in the industry.</p>
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<li><p>Develop programs and projects to enable delivery of the short- and long-term objectives</p>
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<li><p>Influences and shapes category strategies, tactics and plans developed in conjunction with the Business and the global procurement team</p>
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<li><p>Partner with internal organizations to: define requirements; assist with identifying vendors; lead RFx process and evaluations; provide vendor evaluation framework and make recommendations on vendor selection.</p>
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<li><p>Conduct analysis, coordinate key partner participation (Legal, Engineering, Facilities , Finance, etc.) and complete supporting administrative processes.</p>
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<li><p>Facilitate efforts across multiple products/brands as well as multiple geographies in developing solutions to problems.</p>
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<li><p>Build, communicate, and initiate sourcing project work plan and timeline. Identify supporting efforts, dependencies or barriers. Identify and track any sourcing issues, supervise and report progress
</p></li><li><p>Coaches team in the use of sophisticated commercial models, reports and forecasts to challenge and strengthen decision making processes across the business area</p>
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<li><p>Optimizes key relationships across GRIFOLS to take full advantage of efficiencies and leverage best practice</p>
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<li><p>Networks externally to ensure awareness of current world class thinking</p>
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<li><p>Coaches and identifies development opportunities for indirect reports, ensuring appropriate succession planning and creation of a strong development culture</p></li></ul><br>
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</p><p><b>Skills/Qualifications/Education Requirements:</b> (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).</p><br>
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<li><p>Bachelor's Degree in a related field and 8+ years procurement/supply chain experience with extensive and significant track-record in strategic procurement OR Master&rsquo;s Degree and 6+ years procurement/supply chain experience with extensive and significant track-record in strategic procurement</p>
</li>
<li><p>Has the mindset and behaviors that are aligned to working in a global pharmaceutical company where compliance, reputation management and the highest ethical standards are at the heart of our values</p>
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<li><p>Strong leadership skills, including demonstrated ability to spot and develop talent, build procurement teams and empower others to accomplish individual and organizational objectives</p>
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<li><p>Deep experience with a Facilities and/or Engineering spend portfolio is required</p>
</li>
<li><p>Deep understanding of category management development, contracting, RFX processes</p>
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<li><p>Strong influential skills to partner with internal and external stakeholders</p>
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<li><p>Willingness to travel domestically and internationally</p>
</li>
<li><p>Demonstrates successful track-record of driving performance across a complex matrix within a global enterprise and can influence and optimize operating models for his/her functional area</p>
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<li><p>Ability to influence strategically, solve problems using conceptual and analytical thinking and constructively work through conflict</p>
</li>
<li><p>Familiarity with the latest research and market trends
</p></li><li><p>Multilingual is a plus</p></li></ul><br>
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</p><ul><li>Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor&rsquo;s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate&rsquo;s degree with 6 years of experience, or a Master&rsquo;s degree with 2 years of experience.</li></ul><br>
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Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Frequently walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations and frequently travels within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Frequently interacts with others, relates sensitive information to diverse groups. Ability to apply abstract principles to solve complex conceptual issues. Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence.</p><br>
<p></p>
<p></p><p>Third Party Agency and Recruiter Notice:</p>
<p>Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</p><br>
<p></p>
<p><b>Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.</b></p><br>
<p></p>
<p></p><p><b>Location: </b><b>NORTH AMERICA : USA : NC-Clayton</b><b>:</b><b>[[cust_building]]</b></p><br>
<p></p>
<p>Learn more about Grifols</p></div><p></p>

Category Manager - Facilities and Engineering Manager

<p>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and wellbeing of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce, and market innovative medicines, solutions, and services in more than 110 countries and regions.</p><p>We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.</p> Role Mission <p>As a <b>Regulatory Affairs and Quality Specialist</b>, you will act as a link between the company and regulatory authorities, ensuring that products are manufactured and distributed in compliance with applicable regulations and planned timelines.</p> What your responsibilities will be <ol><li>You will <b>support the Scientific Office Manager (SOM)</b> in obtaining timely approvals for product registration, reregistration, and variations with the Saudi FDA.</li><li>You will <b>actively follow up on submissions</b> to resolve any regulatory issues efficiently.</li><li>You will <b>anticipate and respond</b> to regulatory and technical queries from competent authorities.</li><li>You will <b>assist in closing deficiencies or observations</b> raised by regulatory bodies.</li><li>You will <b>monitor regulatory updates</b> and ensure compliance with new legislation to develop effective regulatory strategies.</li><li>You will <b>manage regulatory correspondence</b> between the company and competent authorities.</li><li>You will <b>review product artwork and promotional materials</b> to ensure compliance with regulations.</li><li>You will <b>liaise with the local Qualified Person for Pharmacovigilance</b>, supporting safety reporting compliance with local legislation, audits, and inspections.</li><li>You will <b>support the renewal of office licenses</b> and ensure compliance with scientific office requirements.</li></ol> Who you are <p>To perform this job successfully, you must meet the following requirements:</p><ol><li><b>Education</b>: Bachelor's degree in Pharmaceutical Sciences.</li><li><b>Experience</b>: 2-4 years in Regulatory Affairs or a related field.</li><li><b>Skills</b>:<ul><li>Strong knowledge of regulatory requirements and compliance.</li><li>Excellent communication and stakeholder management skills.</li><li>Ability to work in a fast-paced international environment.</li><li>Detail-oriented with strong problem-solving abilities.</li></ul></li></ol> What we offer <p>This is a <b>great opportunity</b> for someone with the right skills and mindset. You will be part of an international environment with opportunities to grow professionally in a critical function.</p><p>Information about Grifols is available at . If you're interested in joining our company and you have what it takes, then don't hesitate to apply.</p><p>We look forward to receiving your application.</p><p>Grifols is an equal opportunity employer.</p><p>Location: <b>Riyadh, KSA</b></p><p>For regulatory reasons, <b>you must strictly be a Saudi national.</b></p><p><b></b></p><p></p><p><b>Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic or status protected by law. We will consider for employment all qualified applicants in a manner consistent with the requirements of applicable state and local laws.</b></p><p><b>Location: EMEA: United Arab Emirates: Dubai: Dubai</b></p><p>Learn more about Grifols.</p><img src="https://www.jobg8.com/Tracking.aspx?n5tSDoUM%2b4aEkh11VHCiSZUkPrIFvC8rj" width="0" height="0" />

Regulatory Affairs and Quality Specialist 524731

Join Grifols and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Grifols

ABOUT_COMPANY

RN / Registered Nurse - Bilingual in Spanish

Senior Associate Process Development Scientist II

Category Manager - Facilities and Engineering Manager

Regulatory Affairs and Quality Specialist 524731