Senior Manager Quality Training
DescriptionJanssen Pharmaceuticals, Inc.
, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Manager Quality Training! This position will be located in Raritan, NJ.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease.
Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Learn more at and follow us @JanssenGlobal.
The Senior Quality Manager role is accountable for managing the training quality system to support all GMP operations.
In this role, you will lead all aspects of training design including site training governance program, curricular design and management, training system business owner, train the trainer program to ensure the best in class training system implementation at Raritan.
You will set quality standards with respect to manufacturing and quality systems and ensure compliance with those standards.
Key
Responsibilities:
Primary person accountable for the training quality system.
Develops and cultivates an interpersonal culture that promotes behaviors that lead to outstanding business performance and interpersonal excellence.
Encourages and supports initiatives and programs that support improved quality and compliance.
Leads and guides staff and those involved in quality activities to achieve the best results.
Mentors and coaches staff, as well as develops and implements training programs, to ensure professional and personal development of quality personnel.
Connects professionally with other Janssen departments, as well as staff from other affiliates, contractors and Johnson & Johnson to fulfill their responsibilities.
Ensures all employees align with all applicable and governmental (HPRA, FDA, etc.
) regulations, policies, and guidelines.
Establish a training program that coordinates onboarding of new employees, technical training governance for both CAR-T operations and Lentivirus operations and promotes a behavior of continuous learning through curricula design and management.
QualificationsEducation:
A Minimum of a Bachelor's or equivalent University degree is required with a focus in a scientific or engineering field preferred.
Advanced or Master s degree preferred.
Experience and Skills:
Required:
A minimum of 8 years experience in a leadership position within the biological, Quality and/or pharmaceutical industry.
Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics, advanced therapies, or pharmaceuticals.
Ability to apply GMP regulations and other FDA and international guidelines to the position.
Demonstrated success in leading in a global organizationExperience with internal and external regulatory auditsPreferred:
5 years supporting functional areas (e.
g.
R&D, Manufacturing, Engineering)Experience with Quality oversight of manufacturing processes (GxP).
Proven strategic and business plan development.
Other:
This position may require up to 10% domestic travel.
This position has an estimated annual salary of 118,000- 236,000 USD$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 and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit.
Job Field:
Quality TrainingOrganization:
JANSSEN SUPPLY GROUP, LLC (6046)Travel:
Yes, 10 % of the Time.
Estimated Salary: $20 to $28 per hour based on qualifications.
, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Manager Quality Training! This position will be located in Raritan, NJ.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease.
Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Learn more at and follow us @JanssenGlobal.
The Senior Quality Manager role is accountable for managing the training quality system to support all GMP operations.
In this role, you will lead all aspects of training design including site training governance program, curricular design and management, training system business owner, train the trainer program to ensure the best in class training system implementation at Raritan.
You will set quality standards with respect to manufacturing and quality systems and ensure compliance with those standards.
Key
Responsibilities:
Primary person accountable for the training quality system.
Develops and cultivates an interpersonal culture that promotes behaviors that lead to outstanding business performance and interpersonal excellence.
Encourages and supports initiatives and programs that support improved quality and compliance.
Leads and guides staff and those involved in quality activities to achieve the best results.
Mentors and coaches staff, as well as develops and implements training programs, to ensure professional and personal development of quality personnel.
Connects professionally with other Janssen departments, as well as staff from other affiliates, contractors and Johnson & Johnson to fulfill their responsibilities.
Ensures all employees align with all applicable and governmental (HPRA, FDA, etc.
) regulations, policies, and guidelines.
Establish a training program that coordinates onboarding of new employees, technical training governance for both CAR-T operations and Lentivirus operations and promotes a behavior of continuous learning through curricula design and management.
QualificationsEducation:
A Minimum of a Bachelor's or equivalent University degree is required with a focus in a scientific or engineering field preferred.
Advanced or Master s degree preferred.
Experience and Skills:
Required:
A minimum of 8 years experience in a leadership position within the biological, Quality and/or pharmaceutical industry.
Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics, advanced therapies, or pharmaceuticals.
Ability to apply GMP regulations and other FDA and international guidelines to the position.
Demonstrated success in leading in a global organizationExperience with internal and external regulatory auditsPreferred:
5 years supporting functional areas (e.
g.
R&D, Manufacturing, Engineering)Experience with Quality oversight of manufacturing processes (GxP).
Proven strategic and business plan development.
Other:
This position may require up to 10% domestic travel.
This position has an estimated annual salary of 118,000- 236,000 USD$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 and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit.
Job Field:
Quality TrainingOrganization:
JANSSEN SUPPLY GROUP, LLC (6046)Travel:
Yes, 10 % of the Time.
Estimated Salary: $20 to $28 per hour based on qualifications.
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