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Manufacturing Supervisor - Filling Weekend Night Shift
full-timeClayton

Summary

Location

Clayton

Type

full-time

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About this role

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.

 

Hours:  Friday-Sunday 7pm-7am and every other Monday from 7pm-3am

 

Summary:

The Manufacturing Supervisor is responsible for a Manufacturing department’s day to day operations to ensure the manufacture of products are within cGMP, safety regulations and policies and procedures.  This is an entry level Supervisor role.  Provides routine technical support and makes decisions within a well defined area of responsibility.

 

Primary Responsibilities for role (level specific responsibilities should be included in the chart below):

  • Directs shift operations and ensures product integrity in accordance with the production schedule, cGMP, safety regulations and policies & procedures.
  • Maintains floor presence to minimize discrepancies and promote process compliance and accurate documentation.
  • Participates in process/product troubleshooting in order to correct/maintain desirable process parameter.
  • Acts as an initial point of contact for partner groups (i.e. Maintenance, Quality, Tech Doc Support, etc.) Research and address simple process deviations, documentation errors, etc.
  • Qualified to operate all equipment and lead processes to ensure the production schedule is met.
  • May recommend and with direction, implement measures to improve production methods, equipment performance, facility layout and quality of product.
  • Manage employees performance, coach and counsel for development.
  • Ensures required training for employee is achieved, effective and timely.
  • Makes decisions independently, but within a well-defined area.
  • Sought for counsel within field of expertise.

 

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/or supervisors may assign other duties as needed.

 

Knowledge, Skills and Abilities

  • Ability to communicate effectively at all levels of the organization.
  • Ability to lead teams and promote a positive and thriving team environment.
  • Ability to troubleshoot and provide sound solutions for complex process related matters.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                        

Education:

  • BA/BS degree + 2 years related experience.
  • Masters degree + 0 years 

 

Experience:

  • Previous leadership experience required.

 

*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’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate’s degree with 6 years of experience, or a Master’s degree with 2 years of experience.

 

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 4-6 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. Often performs duties standing. Frequently bends and twists neck and waist.  Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to other facilities.  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.  Frequently interacts with others, relates sensitive information to diverse groups.

 

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

 

Other facts

Tech stack
Communication,Leadership,Troubleshooting,Technical Support,Process Compliance,Documentation,Coaching,Decision Making,Team Environment,Production Methods,Quality Control,Safety Regulations,CGMP,Employee Training,Process Deviation,Equipment Operation

About GRIFOLS, S.A.

Grifols is a global healthcare company founded in Barcelona in 1909 committed to improving the health and well-being of people all over the world.

A leader in essential plasma-derived medicines and transfusion medicine, we develop, produce and provide innovative healthcare services and solutions in more than 110 countries.

Patient needs and our ever-growing knowledge of many chronic, rare and prevalent diseases, sometimes life-threatening, drive our innovation in plasma-based therapies and other biopharmaceuticals to enhance quality of life.

Grifols is focused on treating conditions across a broad range of therapeutic areas: immunology, hepatology and intensive care, pulmonology, hematology, neurology and infectious diseases.

With a workforce of over 23,000 employees in more than 30 countries and regions, we are committed to a sustainable business model that sets the standard for continuous innovation, quality, safety and ethical leadership in the industry. Our work has a positive social and economic impact in the countries where we operate, creating jobs and generating wealth.

People are at the heart of what we do, and we strive to create an inclusive, diverse, fair and equal society. Maintaining and promoting a workforce that reflects this reality leads to enhanced professional relationships and helps us to give our best to patients, donors and customers.

In 2024, Grifols was named one of TIME’s ‘World’s Best Companies’ for the second year in a row, reaffirming our commitment to excellence. We were also recognized by Forbes as one of the "Best Employers for Women 2023," reflecting our dedication to fostering an inclusive and supportive workplace for all.

To maintain a positive community and overall respectful communication, please keep our community guidelines in mind.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 1909

What you'll do

  • The Manufacturing Supervisor is responsible for overseeing day-to-day operations in the manufacturing department, ensuring compliance with cGMP and safety regulations. They direct shift operations, maintain product integrity, and manage employee performance.

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Frequently Asked Questions

What does a Manufacturing Supervisor - Filling Weekend Night Shift do at GRIFOLS, S.A.?

As a Manufacturing Supervisor - Filling Weekend Night Shift at GRIFOLS, S.A., you will: the Manufacturing Supervisor is responsible for overseeing day-to-day operations in the manufacturing department, ensuring compliance with cGMP and safety regulations. They direct shift operations, maintain product integrity, and manage employee performance..

Why join GRIFOLS, S.A. as a Manufacturing Supervisor - Filling Weekend Night Shift?

GRIFOLS, S.A. is a leading Pharmaceutical Manufacturing company.

Is the Manufacturing Supervisor - Filling Weekend Night Shift position at GRIFOLS, S.A. remote?

The Manufacturing Supervisor - Filling Weekend Night Shift position at GRIFOLS, S.A. is based in Clayton, North Carolina, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Manufacturing Supervisor - Filling Weekend Night Shift position at GRIFOLS, S.A.?

You can apply for the Manufacturing Supervisor - Filling Weekend Night Shift position at GRIFOLS, S.A. directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about GRIFOLS, S.A. on their website.