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>
<div></div>
</div><br>
</div></div><div>We&rsquo;re Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!</div><br>
<div></div>
<div>
If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a <b>QUALITY SYSTEMS MANAGER</b>! Please read on ...</div><br>
<div></div>
<div><b>
APPLICATION DEADLINE: </b>APRIL 12, 2026</div><br>
<div></div>
<div><b>
Job Title: </b>QUALITY SYSTEMS MANAGER</div>
<div><b>
Estimated Salary Range: </b><b>$62,500.00 - $93</b><b>,500.00</b> per year, depending on training, education, and experience. This position is eligible to participate in up to 20% of the company bonus pool.</div>
<div><b>
Relocation Assistance! </b>This position is eligible for relocation assistance of up to $20K!</div><br>
<div></div>
<div><b>
Summary:</b></div>
<div>
Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.</div><br>
<div></div>
<div><b>
Primary Responsibilities for Role:</b></div>
<ul>
<li>Maintains oversight of the center&rsquo;s quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties.</li>
<li>Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance.</li>
<li>Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained.</li>
<li>Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks.</li>
<li>Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required.</li>
<li>Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations.</li>
<li>Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.</li>
<li>Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness.</li>
<li>Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment.</li>
<li>Performs a review of the documentation of unsuitable test results and unit lookback information.</li>
<li>Performs a review of donor adverse event reports and the applicable related documents.</li>
<li>Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file.</li>
<li>Performs employee training observations to ensure staff competency prior to releasing employees to work independently.</li>
<li>Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance.</li>
<li>Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities.</li>
<li>Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues.
</li><li>Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented.
</li><li>Holds monthly Quality Meeting to communicate status updates and manage action outcomes.</li><br>
</ul>
<div></div><div><b>Other Responsibilities for Role:</b></div>
<ul>
<li>Leads projects and initiatives as requested.</li><br>
</ul>
<div></div><div>This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.</div><div><br>
</div><div><b>Job Requirements:</b></div>
<div><b>
EDUCATION:</b></div>
<ul>
<li>Bachelor of Science degree or equivalent.</li>
<li>Certified and proficient in quality and compliance.</li>
</ul>
<div><b>EXPERIENCE:
</b></div><ul><li>Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment.</li>
</ul><ul><li>Experience with plasma or whole blood.</li>
</ul>
<div><b>EQUIVALENCY:
</b></div><div>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.</div>
<div><b>
KNOWLEDGE, SKILLS &amp; ABILITIES:
</b></div><div>Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.</div><br>
<div></div>
<div><b>
Occupational Demands:</b></div>
<div>
Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32*, miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel 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. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.</div><br>
<div></div>
<div>
&ldquo;We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers.&rdquo;</div><br>
<div>
</div><div>#BiomatUSA
</div><div>#CB
</div><div>#GrifolsJobs
</div><div>#Plasma
</div><div>#app
</div><div>#LI-Onsite</div>
<div>
#Indeed</div><br>
<div></div>
<p><b>COMPENSATION AND BENEFITS:</b></p>
<p>
The estimated pay scale for the <b>QUALITY SYSTEMS MANAGER </b>role based in <b>Colorado Springs, CO</b> is <b>$62,400.00 - $93,500.00</b><b> per year</b>. Additionally, the position is eligible to participate in up to <b>20%</b> of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!</p>
<p><b>
THIRD PARTY AGENCY AND RECRUITER NOTICE:</b></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>
<p><b>
EEO:</b></p>
<p><b>
GRIFOLS </b><b>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>
<p></p>
<p><b>Location: NORTH AMERICA : USA : CO-Colorado Springs</b></p>
<div><b>
Center Address: </b>3776 Airport Rd, Colorado Springs, CO 80910</div>
<div><b>
Contact:</b> Alex S. Contreras, <i>Senior Talent Acquisition Partner </i>&ndash; (213) 219-5494 | acontreras@grifols.com</div><br>
<p></p>
<p>
Learn more about Grifols</p>
<ul>
<li>Follow us on<b> Facebook:</b> https://www.facebook.com/grifolsplasma1940/
</li><li>Follow us on<b> LinkedIn:</b> https://www.linkedin.com/company/grifols/
</li><li>Follow us on <b>Instagram:</b> https://instagram.com/grifolsplasma_us</li></ul><br>
<div>
</div><div>To find more jobs with<b> Grifols:</b> https://grifols.jobs</div>
<div>
Or Text GRIFOLS to<b> 833-233-7621</b></div></div>

Quality Systems Manager for Plasma Center

<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>
<div></div>
</div><br>
</div></div><div><div><p><b>Phlebotomist &ndash; We Train</b></p></div><div><br>
<p>
</p></div><div><p>You are a fit for us if you have:</p>
</div>
<div><ul><li><p>Superior customer service standards</p>
</li>
</ul></div></div><div><div><ul><li><p>A High School diploma or GED</p>
</li>
</ul></div><div><ul><li><p>Ability to work a flexible schedule</p>
</li>
</ul></div><div><ul><li><p>An interest in making a difference in the world</p>
</li>
</ul></div><div><ul><li><p>Obtains required state licensures or certifications where applicable</p></li></ul><br>
</div>
<p></p><div><p>Phlebotomist</p>
</div>
<div><p>Our ideal phlebotomist is patient, reliable, and really commits to keep our donors comfortable and happy.</p></div><div><br>
<p>
</p></div><div><p>Primary Responsibilities:</p>
</div>
<div><ul><li><p>Assist in determining the suitability of donors.</p>
</li>
</ul></div><div><ul><li><p>You establish rapport with donors to ensure overall customer happiness while ensuring donor confidentiality.</p>
</li>
</ul></div><div><ul><li><p>You respond to and assist with handling donor reactions.</p>
</li>
</ul></div><div><ul><li><p>Monitors donor and equipment to ensure health of donors and quality of product.</p>
</li>
</ul></div><div><ul><li><p>Sets up, disconnects, and operates the automated plasmapheresis machines.</p>
</li>
</ul></div><div><ul><li><p>Disconnects and disposes of all contaminated disposable equipment.</p></li></ul><br>
</div>
<p></p><div><p>We're Grifols, a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.</p></div><div><br>
<p><b>
</b></p></div><div><p><b>Occupational Demands Form </b><b># 74</b><b>:</b> Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while working in plasma freezer. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed standing for 6 to 8 hours per day. Bending and twisting neck and waist for 1-2 hours per day. 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. Frequent foot movement; may infrequently squat, crouch or sit on one's heels. May walk up to 6-8 hours per day. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. 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 comprehend and follow instructions to complete assigned tasks. must possess the ability to listen to and understand information and ideas presented through spoken words and sentences. must perform within the guidance of both oral or written instructions. Relates sensitive information to diverse groups.</p></div><div><br>
<p>
</p></div></div><div><p>#biomatusa</p></div><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>
<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: NORTH AMERICA : USA : ID-Pocatello:USPO - Pocatello ID-E Center St-BIO</b></p><br>
<p></p>
<p>
Learn more about Grifols</p></div><p></p>

Phlebotomist

<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>
<div></div>
</div><br>
</div></div><div><b>Phlebotomist &ndash; We Train</b></div><br>
<div></div>
<p><b>
You are a fit for us if you have:</b></p>
<ul>
<li>Superior customer service standards</li>
<li>A High School diploma or GED</li>
<li>Ability to work a flexible schedule
</li><li>An interest in making a difference in the world</li>
<li>Obtains required state licensures or certifications where applicable</li></ul><br>
<p></p>
<p><b>
Phlebotomist</b></p>
<p>
Our ideal phlebotomist is patient, reliable, and really commits to keep our donors comfortable and happy.</p><br>
<p></p>
<p><b>
Primary Responsibilities:</b></p>
<ul>
<li>Assist in determining the suitability of donors.</li>
<li>You establish rapport with donors to ensure overall customer happiness while ensuring donor confidentiality.</li>
<li>You respond to and assist with handling donor reactions.</li>
<li>Monitors donor and equipment to ensure health of donors and quality of product.</li>
<li>Sets up, disconnects, and operates the automated plasmapheresis machines.
</li><li>Disconnects and disposes of all contaminated disposable equipment.</li><br>
</ul>
<p></p><div>We're Grifols, a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.</div><br>
<div></div>
<div><b>
Occupational Demands Form # 74</b><b>: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while working in plasma freezer. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed standing for 6 to 8 hours per day. Bending and twisting neck and waist for 1-2 hours per day. 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. Frequent foot movement; may infrequently squat, crouch or sit on one's heels. May walk up to 6-8 hours per day. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. 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 comprehend and follow instructions to complete assigned tasks. must possess the ability to listen to and understand information and ideas presented through spoken words and sentences. must perform within the guidance of both oral or written instructions. Relates sensitive information to diverse groups.</b></div><br>
<div>
</div><div><b>#biomatusa</b></div><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>
<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: NORTH AMERICA : USA : FL-Jacksonville:USNC0415 - Jacksonville FL-Mayport-TPR</b></p><br>
<p></p>
<p>
Learn more about Grifols</p></div><p></p>

<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>
<div></div>
</div><br>
</div></div><div>Grifols Diagnostic Solutions Inc is seeking a Customer Service and Logistics Representative I. Responsible for developing and maintaining world-class relationships with both External and Internal Diagnostics Customers including the Commercial Operations and Technical Support departments. Assists with ensuring on-time and complete delivery of goods to Diagnostics Customers in the Americas region by developing and maintaining key relationships with all Logistics providers (manufacturers, warehouses and freight carriers). Key member of the America&rsquo;s Supply Chain Organization responsible for process development to improve efficiency and contribute to Cost Savings Initiatives.</div><br>
<div></div>
<div>
This position is a hybrid role (3 days onsite, 2 days remote).</div>
<div>
Hours are Monday through Friday, 8am to 5pm.</div><br>
<div></div>
<ul>
<li>This role also delivers quality products and services on time to all customers, internal and external. Where applicable, assist with providing employees with training and resources to meet or exceed customer requirements. Monitor processes and products to identify opportunities for continuous improvement. In some cases, minimal domestic and international travel may be required</li>
<li>Maintenance of sales order entry into SAP</li>
<li>Coordination and Management of outbound shipments to Customers, this includes but is not limited to facilitating import permits, meeting logistic requirements and other related process.</li>
<li>Manage the Track and Trace process to ensure meeting the validated shipping requirements</li>
<li>Customer invoicing and SOX compliance</li>
<li>Assist with the management of Logistics Providers, including 3PL warehouses and Freight Carrier</li>
<li>Maintenance of SAP transactions to ensure data integrity and traceability of products</li>
<li>Contribute to Supply Chain strategic/special projects</li>
<li>Collaborating with Planning/Procurement group for ongoing analysis of the required levels of inventory to meet customer requirements.</li>
<li>Performing Ongoing analysis of Supply Chain Key Performance Indicators (KPIs) including Customers On-time Delivery Performance</li>
<li>Other duties which may be assigned by the department manager</li>
<li>Seeks to understand customer&rsquo;s needs, educates customers, builds collaborative relationships with customers, takes actions to meet customer needs and concerns, sets up customer feedback systems.</li></ul><br>
<div></div>
<div>
Knowledge, Skills, and Abilities
</div><div>Demonstrated knowledge of SAP (preferably MM/SD modules)</div>
<div>
Working knowledge of MS office components, especially Excel, Word and PowerPoint</div>
<div>
Prior experience in air transportation, customs clearance processes and international logistics desirable</div>
<div>
Proven ability to work under pressure and with ambiguity</div>
<div>
Demonstrated analytical and problem solving skills</div>
<div>
Demonstrated ability to focus on key customer needs</div>
<div>
APICS certification/ Six Sigma or equivalent is desirable.</div>
<div>
Excellent communication and interpersonal skills</div><br>
<div></div>
<div>
Education</div>
<div>
Associates Degree, advanced training or equivalent experience required.</div><br>
<div></div>
<div>
Experience</div>
<div>
2-3 years of experience in supply chain/logistics roles</div><br>
<div></div>
<div>
Equivalency</div>
<div>
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.</div><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>
<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: NORTH AMERICA : USA : NC-RTP:USNC0001 - RTP NC-Headquarters</b></p><br>
<p></p>
<p>
Learn more about Grifols</p></div><p></p>

Supply Chain Customer Service Representative I

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

Quality Systems Manager for Plasma Center

Phlebotomist

Phlebotomist

Supply Chain Customer Service Representative I