Grifols
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Director, Product Release
role at
Grifols
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Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well‑being of people all over the world. Our four divisions – Bioscience, Diagnostic, Hospital, and Bio Supplies – develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.
Summary
Responsible for the final release of plasma to Grifols Manufacturing and all 3rd‑party customers requesting plasma from the US Plasma Logistic Centers.
Primary Responsibilities
Ensure the release of plasma for the further manufacturing of medicinal products is in accordance with all US and European regulations.
Review and ensure compliance with all Quality Agreements established between Grifols Worldwide and manufacturing customers.
Oversee activities and provide leadership to the team responsible for management of supplier quality to ensure suppliers meet the standards set forth by procedures and regulations.
Lead a team that manages supply and supplier qualifications, deviations, defective soft goods, investigations, quality agreements and general interactions with 3rd‑party suppliers and vendors.
Review and ensure compliance with all Quality Agreements established between Grifols Worldwide and plasma suppliers.
Responsible for managing the Grifols Plasma Quality Database (PQD) used to manage the plasma donor centers, plasma testing laboratories, plasma storage locations, and plasma refrigerated carriers.
Oversee the quality operations of the US Grifols Plasma Logistic Centers.
Develop, author, review, and approve standard operating procedures used by the US Grifols Plasma Logistic Centers.
Assess skills, knowledge, and abilities of candidates to make effective hiring decisions and identify developmental needs of staff members, including training, disciplinary action and performance management processes.
Regularly examine quality systems, processes and procedures as it relates to the US Plasma Logistic Centers for increased efficiency and/or increased quality assurance as necessary.
Act as liaison with quality/regulatory counterparts in international and domestic corporate positions, ensuring programs, systems, software are symbiotic in nature and in compliance with product release requirements for the US Plasma Logistic Centers.
Oversee internal and external audits of quality systems within US Plasma Logistic Centers. Act as liaison with external domestic and international auditors.
Acts as Subject Matter Expert in projects involving US Plasma Logistics Centers and product release.
Knowledge, Skills, And Abilities
Knowledge of quality systems preferably in a biopharmaceutical setting or in a regulated industry.
Must have good oral and written communication skills with experience writing and establishing procedures for quality systems.
Must have good working skills with MS Office suite.
Ability to examine existing processes and procedures for efficiency and increased quality assurance.
Education And Experience
A Bachelor's Degree in a medical or biological science; Master’s degree is preferred.
A minimum of 10 years’ practical post‑graduate experience in collecting and/or testing, preparing, storage and distribution of human blood and blood components. Experience managing employees strongly preferred with demonstrated experience in analyzing data to make individual and/or large‑scale decisions. Experience with initiating and implementing change.
Occupational Demands
The employee is frequently required to stand, walk, sit, use hands and arms, talk and hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance, color, peripheral vision, depth perception, and the ability to adjust focus. Extended periods of sitting, using keyboard, mouse and viewing computer monitor screen. The noise level in the work environment is usually moderate.
Employee must have the ability to apply common sense understanding to carry out detailed written and oral instructions.
Employee must perform a variety of tasks, influence others, and use judgement to plan and accomplish goals.
Employee may be exposed to toxic and caustic chemicals and frequently to biological hazards in the donor center.
Employee may be required to travel 35% of the time. Travel will include driving and both domestic and international flights.
This position is eligible to participate in up to 30% of the company bonus pool. We offer benefits including medical, PTO, up to 5% 401(k) 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’re growing, and you can grow with us!
Location : NORTH AMERICA : USA : NC-RTP
Seniority level
Director
Employment type
Full‑time
Job function
Product Management and Marketing
Industries
Pharmaceutical Manufacturing and Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Grifols by 2x
Get notified about new Director of Product Management jobs in
North Carolina, United States .
Learn more about Grifols
#J-18808-Ljbffr
Director, Product Release
role at
Grifols
Get AI-powered advice on this job and more exclusive features.
Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well‑being of people all over the world. Our four divisions – Bioscience, Diagnostic, Hospital, and Bio Supplies – develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.
Summary
Responsible for the final release of plasma to Grifols Manufacturing and all 3rd‑party customers requesting plasma from the US Plasma Logistic Centers.
Primary Responsibilities
Ensure the release of plasma for the further manufacturing of medicinal products is in accordance with all US and European regulations.
Review and ensure compliance with all Quality Agreements established between Grifols Worldwide and manufacturing customers.
Oversee activities and provide leadership to the team responsible for management of supplier quality to ensure suppliers meet the standards set forth by procedures and regulations.
Lead a team that manages supply and supplier qualifications, deviations, defective soft goods, investigations, quality agreements and general interactions with 3rd‑party suppliers and vendors.
Review and ensure compliance with all Quality Agreements established between Grifols Worldwide and plasma suppliers.
Responsible for managing the Grifols Plasma Quality Database (PQD) used to manage the plasma donor centers, plasma testing laboratories, plasma storage locations, and plasma refrigerated carriers.
Oversee the quality operations of the US Grifols Plasma Logistic Centers.
Develop, author, review, and approve standard operating procedures used by the US Grifols Plasma Logistic Centers.
Assess skills, knowledge, and abilities of candidates to make effective hiring decisions and identify developmental needs of staff members, including training, disciplinary action and performance management processes.
Regularly examine quality systems, processes and procedures as it relates to the US Plasma Logistic Centers for increased efficiency and/or increased quality assurance as necessary.
Act as liaison with quality/regulatory counterparts in international and domestic corporate positions, ensuring programs, systems, software are symbiotic in nature and in compliance with product release requirements for the US Plasma Logistic Centers.
Oversee internal and external audits of quality systems within US Plasma Logistic Centers. Act as liaison with external domestic and international auditors.
Acts as Subject Matter Expert in projects involving US Plasma Logistics Centers and product release.
Knowledge, Skills, And Abilities
Knowledge of quality systems preferably in a biopharmaceutical setting or in a regulated industry.
Must have good oral and written communication skills with experience writing and establishing procedures for quality systems.
Must have good working skills with MS Office suite.
Ability to examine existing processes and procedures for efficiency and increased quality assurance.
Education And Experience
A Bachelor's Degree in a medical or biological science; Master’s degree is preferred.
A minimum of 10 years’ practical post‑graduate experience in collecting and/or testing, preparing, storage and distribution of human blood and blood components. Experience managing employees strongly preferred with demonstrated experience in analyzing data to make individual and/or large‑scale decisions. Experience with initiating and implementing change.
Occupational Demands
The employee is frequently required to stand, walk, sit, use hands and arms, talk and hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance, color, peripheral vision, depth perception, and the ability to adjust focus. Extended periods of sitting, using keyboard, mouse and viewing computer monitor screen. The noise level in the work environment is usually moderate.
Employee must have the ability to apply common sense understanding to carry out detailed written and oral instructions.
Employee must perform a variety of tasks, influence others, and use judgement to plan and accomplish goals.
Employee may be exposed to toxic and caustic chemicals and frequently to biological hazards in the donor center.
Employee may be required to travel 35% of the time. Travel will include driving and both domestic and international flights.
This position is eligible to participate in up to 30% of the company bonus pool. We offer benefits including medical, PTO, up to 5% 401(k) 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’re growing, and you can grow with us!
Location : NORTH AMERICA : USA : NC-RTP
Seniority level
Director
Employment type
Full‑time
Job function
Product Management and Marketing
Industries
Pharmaceutical Manufacturing and Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Grifols by 2x
Get notified about new Director of Product Management jobs in
North Carolina, United States .
Learn more about Grifols
#J-18808-Ljbffr