J&J Family of Companies
Senior Manager Quality Control
J&J Family of Companies, Greenville, North Carolina, United States, 27834
J&J Family of Companies - Senior Manager Quality Control
Location: Greenville, North CarolinaJob Code:
2406205418WDescriptionJohnson & Johnson is currently seeking a Senior Manager Quality Control to join our Innovative Medicine Supply Chain organization located in Wilson, North Carolina.This role will support site operations in Wilson, NC, and will require presence with design teams in the Greater Philadelphia region during the project design phase. Once the design phase is completed, this role will support the construction and operational start-up of the site, with expected travel to be less than 10%.J&J is expanding our manufacturing capacity with a $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients.Are you a seasoned professional with a passion for quality control in the biopharmaceutical industry? Do you thrive on ensuring strict compliance with regulatory standards and driving continuous improvement in laboratory operations? If so, we have an exciting opportunity for you!Essential Job Duties and Responsibilities:Manage all aspects of the Quality Control (QC) laboratories in compliance with established GMP and safety regulations.Oversee training of supervisors and associates within the department.Manage raw material, in-process, environmental/utility, microbiological, and biotherapeutic drug substance release testing.Investigate laboratory non-conformances and develop effective CAPAs.Maintain, calibrate, and qualify laboratory instruments and equipment.Review and approve quality documents, non-conformance investigations, CAPA, and change controls.Support internal and external audits.Analyze laboratory performance and quality data for quarterly site management and annual product reviews.Utilize statistical tools and data analysis techniques for continuous improvement initiatives.Collaborate with cross-functional teams to support business needs.Drive a culture of quality throughout the organization.QualificationsRequired:Bachelor's degree in Chemistry, Biochemistry, or a related field.8 years’ experience in the biological and/or pharmaceutical industry.5 years’ experience in QC supervisory/management roles.Deep understanding of global GMP regulatory requirements.Experience with health authorities and regulatory inspections.Excellent communication and interpersonal skills.Strong leadership and problem-solving skills.Detail-oriented mindset with a focus on process improvements.Preferred:Master's degree in Chemistry, Biochemistry, or a related field.Experience in a supporting functional area (e.g., Manufacturing, Technical Operations, Engineering & Maintenance, R&D, etc.).This job posting is anticipated to close on 10/20/2024. For more information on Company benefits, please visit
here .Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status.
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Location: Greenville, North CarolinaJob Code:
2406205418WDescriptionJohnson & Johnson is currently seeking a Senior Manager Quality Control to join our Innovative Medicine Supply Chain organization located in Wilson, North Carolina.This role will support site operations in Wilson, NC, and will require presence with design teams in the Greater Philadelphia region during the project design phase. Once the design phase is completed, this role will support the construction and operational start-up of the site, with expected travel to be less than 10%.J&J is expanding our manufacturing capacity with a $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients.Are you a seasoned professional with a passion for quality control in the biopharmaceutical industry? Do you thrive on ensuring strict compliance with regulatory standards and driving continuous improvement in laboratory operations? If so, we have an exciting opportunity for you!Essential Job Duties and Responsibilities:Manage all aspects of the Quality Control (QC) laboratories in compliance with established GMP and safety regulations.Oversee training of supervisors and associates within the department.Manage raw material, in-process, environmental/utility, microbiological, and biotherapeutic drug substance release testing.Investigate laboratory non-conformances and develop effective CAPAs.Maintain, calibrate, and qualify laboratory instruments and equipment.Review and approve quality documents, non-conformance investigations, CAPA, and change controls.Support internal and external audits.Analyze laboratory performance and quality data for quarterly site management and annual product reviews.Utilize statistical tools and data analysis techniques for continuous improvement initiatives.Collaborate with cross-functional teams to support business needs.Drive a culture of quality throughout the organization.QualificationsRequired:Bachelor's degree in Chemistry, Biochemistry, or a related field.8 years’ experience in the biological and/or pharmaceutical industry.5 years’ experience in QC supervisory/management roles.Deep understanding of global GMP regulatory requirements.Experience with health authorities and regulatory inspections.Excellent communication and interpersonal skills.Strong leadership and problem-solving skills.Detail-oriented mindset with a focus on process improvements.Preferred:Master's degree in Chemistry, Biochemistry, or a related field.Experience in a supporting functional area (e.g., Manufacturing, Technical Operations, Engineering & Maintenance, R&D, etc.).This job posting is anticipated to close on 10/20/2024. For more information on Company benefits, please visit
here .Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status.
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