ZipRecruiter

Log In

1

Grifols Jobs in Raleigh, NC (NOW HIRING)

GRIFOLS, S.A.

Instrumentation Technician

Clayton, NC · On-site

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 ...

GRIFOLS, S.A.

NFF Technician I (Night Shift)

Clayton, NC · On-site

$16.25 - $21.50/hr

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 ...

GRIFOLS, S.A.

Plant Maintenance Engineer

Clayton, NC · On-site

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 ...

previous pagenext page

Showing results 21-40

All JobsGrifols JobsGrifols Jobs in Raleigh, NC

Grifols information

See Raleigh, NC salary details

$13

$21

$28

How much do grifols jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for grifols in Raleigh, NC is $21.20, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $24.28 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Grifols employee?

To thrive at Grifols, you generally need a background in life sciences, pharmacy, or medical technology, with relevant degrees or certifications. Familiarity with laboratory equipment, Good Manufacturing Practice (GMP) standards, and specialized software systems such as LIMS or SAP is commonly required. Strong attention to detail, teamwork, and effective communication are essential soft skills in this environment. These competencies ensure product safety, regulatory compliance, and efficient collaboration in a highly regulated, patient-focused industry.

What is Grifols?

Grifols is a global healthcare company specializing in the development, production, and distribution of plasma-derived medicines and transfusion medicine solutions. The company operates plasma donation centers and manufactures products used to treat rare, chronic, and life-threatening conditions, such as immune deficiencies and bleeding disorders. Grifols is also involved in diagnostic systems and hospital equipment, with a strong focus on innovation and patient care. Its operations span over 30 countries, supporting both patients and healthcare professionals worldwide.

What is the typical work environment like for employees at Grifols?

At Grifols, employees often work in a highly regulated, team-oriented environment, especially within manufacturing, laboratory, and plasma center settings. Teams are composed of professionals from diverse backgrounds such as quality assurance, research and development, and operations, requiring frequent cross-functional collaboration to ensure compliance with industry and safety standards. Communication and teamwork are emphasized, with regular meetings and clear protocols in place to ensure efficiency and product quality. This collaborative atmosphere not only supports daily operations but also fosters opportunities for professional growth and internal mobility within the company.

What is the difference between Grifols vs Plasma Center Technician?

AspectGrifolsPlasma Center Technician
Required CredentialsHigh school diploma, phlebotomy certification often preferredHigh school diploma, phlebotomy certification usually required
Work EnvironmentBlood plasma donation centers, healthcare settingsBlood donation centers, healthcare facilities
Employer & IndustryMajor plasma donation company, biotech industryVarious plasma donation centers, healthcare industry
Common Search & ComparisonYesYes

Both roles involve working in blood/plasma donation centers and require similar certifications. While Grifols is a specific employer in the industry, Plasma Center Technicians work at various centers. The main differences are the employer and specific company protocols, but the job functions and credentials are quite comparable.

What are popular job titles related to Grifols jobs in Raleigh, NC? For Grifols jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Grifols jobs in Raleigh, NC look for? The top searched job categories for Grifols jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Grifols jobs? Cities near Raleigh, NC with the most Grifols job openings:
Grifols jobs near you
Infographic showing various Grifols job openings in Raleigh, NC as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, 1% Contract, and 2% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $44,102 per year, or $21.2 per hour.

Regulatory Documentation Specialist I

GRIFOLS, S.A.

Clayton, NC • On-site

Full-time

Posted 27 days ago

Job description

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.
Summary
Maintains regulatory documentation and filing systems in support of the Biopharma North America regulatory team. Maintains accurate files of health authority correspondence in paper and electronic formats as needed and word processing submission documents as needed. This position will support the product managers to meet business objectives for the overall regulatory team.
Primary Responsibilities
  • Perform updates, facilitate SME reviews, and ensure proper hard copy and electronic filing of Regulatory Submission Documents (RSDs) as needed.
  • Ensure that regulatory records are properly filed and accessible in the appropriate documentation system.
  • Assist in maintaining SOPs/IBPs that describe the Regulatory Affairs filing system and other RA SOPs/IBPs files and maintenance.
  • Manage requests for translations and legalizations with vendors.
  • Respond to requests for records by researching and reviewing internal documentation, including the retrieval of documents from off-site storage.
  • Communicate with regulatory personnel regarding regulatory records.
  • Process and track all invoices to ensure prompt payment.
  • Request Certificate of Foreign Governments (CFG) and Certificate of Pharmaceutical Products (CPP) from FDA
  • Serve as primary contact with Accounts Payable.

Note: 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. Manager and supervisors may assign other duties as needed.
Knowledge, Skills, and Abilities
  • Basic knowledge of applicable laws and regulations.
  • Ability to work with limited supervision and initiate contacts essential to submission preparation.
  • Ability to manage multiple and possibly conflicting priorities.
  • Ability to work as part of the regulatory team to meet group objectives.
  • Ability to review a document in detail to ensure accuracy based on regulatory requirements, and to ensure the use of the appropriate forms, format, content, and authorized signatures.
  • Ability to clearly communicate verbally and in writing.
  • Ability to effectively use Microsoft Office (particularly Word and Excel) to create, edit, and format documents.
  • Ability to work with other computer systems for filing supplements and reports.
  • Ability to meet statutory deadlines to ensure compliance, as well as business timelines to accomplish company objectives.

Education Requirements
Bachelor's degree in a relevant discipline, or equivalent work experience.
Experience Requirements
0 to 1 year of related technical and/or regulatory experience in pharmaceutical or blood industry or an equivalent combination of education and experience.
Equivalency
Depending on 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 requirement. Example: if a job level requires a Bachelors degree plus 4 years experience, an equivalency could include 8 years, an Associates degree with 6 years experience, or Master's or a Master's degree with 2 years experience.
Occupational Demands
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. Occasionally walks and stands. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues.
Third Party Agency and Recruiter Notice:
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.
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.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Learn more about Grifols

Apply