23 Director, Quality Oprations Jobs in Philadelphia, PA
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Haven Behavioral Hospital of Philadelphia
Philadelphia, PA | Full Time
$114k-144k (estimate)
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Greater Philadelphia Community Alliance
Philadelphia, PA | Full Time
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IntePros is Hiring a Director, Quality Oprations Near Philadelphia, PA
Compensation Range:$170,000 to $180,000
Welcome to IntePros, a certified woman-owned company specializing in innovative and results-oriented recruiting and staffing solutions. We take immense pride in genuinely understanding what drives and inspires exceptional individuals like you. Your success is our priority, and we are dedicated to actively shaping your long-term career journey. At IntePros, we believe in comprehensive well-being. You have access to our medical, dental, vision, and mental health programs, ensuring your health and wellness are taken care of. To support your continuous growth, we also provide a $1,500 per year education and professional certification fund. Diversity and inclusion are cornerstones of our company ethos. IntePros is proud to be an equal opportunity employer. We do not discriminate in employment on the basis of race, color, religion, sex, pregnancy, gender identity, national origin, sexual orientation, disability, age, veteran or military status, retaliation, or any other characteristic protected by law. We celebrate the rich tapestry of backgrounds and perspectives that make us stronger as a team. Please note that only qualified individuals being considered will be contacted. We appreciate your interest and look forward to potentially embarking on a transformative journey together.
IntePros is currently looking for a Director, Quality Operations to join one of our growing Medical Device clients in Philadelphia, PA. The Director, Quality Operations is an important part of our clients Leadership Team and is a partner to our business and customers. Overall scope includes having the experience to balance product and process quality requirements, with respect to the demands of a broad portfolio of clients customers and customer products. The position is responsible for the Quality Operations function supporting device assembly and packaging activities at the Philadelphia site.
Director, Quality Operations Responsibilities:
Welcome to IntePros, a certified woman-owned company specializing in innovative and results-oriented recruiting and staffing solutions. We take immense pride in genuinely understanding what drives and inspires exceptional individuals like you. Your success is our priority, and we are dedicated to actively shaping your long-term career journey. At IntePros, we believe in comprehensive well-being. You have access to our medical, dental, vision, and mental health programs, ensuring your health and wellness are taken care of. To support your continuous growth, we also provide a $1,500 per year education and professional certification fund. Diversity and inclusion are cornerstones of our company ethos. IntePros is proud to be an equal opportunity employer. We do not discriminate in employment on the basis of race, color, religion, sex, pregnancy, gender identity, national origin, sexual orientation, disability, age, veteran or military status, retaliation, or any other characteristic protected by law. We celebrate the rich tapestry of backgrounds and perspectives that make us stronger as a team. Please note that only qualified individuals being considered will be contacted. We appreciate your interest and look forward to potentially embarking on a transformative journey together.
IntePros is currently looking for a Director, Quality Operations to join one of our growing Medical Device clients in Philadelphia, PA. The Director, Quality Operations is an important part of our clients Leadership Team and is a partner to our business and customers. Overall scope includes having the experience to balance product and process quality requirements, with respect to the demands of a broad portfolio of clients customers and customer products. The position is responsible for the Quality Operations function supporting device assembly and packaging activities at the Philadelphia site.
Director, Quality Operations Responsibilities:
- Develops, establishes and maintains quality assurance programs and systems, policies, processes, procedures and controls.
- Engages directly with customers on quality related issues to ensure client is meeting regulatory and customer requirements.
- Provides leadership over the Quality Operations teams that are involved in batch record creation, batch record review, product release, deviation management, change controls, and customer interactions.
- Supports key customer-facing meetings and venues such as business reviews, audits, risk - escalations, business development, and like activities.
- Establishes and ensures the Quality Operations team achieves the appropriate levels of compliance and develops actions to ensure ongoing performance is achieved and maintained through metrics and other forms of KPI's.
- Provide Quality leadership within internal teams (Operations, Engineering, Business Unit) to drive organizational unit objectives and achieve company goals.
- Establishes and ensures policy throughout the commercial manufacturing enterprise for the adherence to FDA, EMA, ANVISA and all other government agencies in which business is conducted.
- Responsible for the product quality lifecycle of respective products within drug delivery (e.g. Change Control, Deviations, Complaints, CAPA.)
- Drives continual improvement within the quality teams and operation to foster a culture of quality that permeates all levels of the organization.
- Ensures compliance and regulatory readiness of the operation at all times.
- Assists in the preparation for and participation in external regulatory inspections and audits that occur at the Philadelphia site.
- Leads a group of approximately 2-3 direct reports (10-15 indirect reports)
- BA or BS degree and a minimum of 10 years of experience with a minimum of 5 years in medical device/combo products. Operational quality and manufacturing experience required.
- An advanced degree in science or business administration is a plus.
- Prior leadership experience in managing Quality teams with product release responsibilities.
- Strong understanding of device requirements, standards, and regulations, focusing on auto injectors and ISO 13485 standards.
- Process Excellence (lean, six sigma) experience across diversified business areas or equivalent quality standards programs preferred.
- Experience in managing contract service providers or working in a contract manufacturing or contract packaging environment.
- Must be able to develop and improve advanced concepts, techniques, and standards and new applications based on quality principles and theories.
- Must be able to develop solutions to problems of unusual complexity, which require a high degree of ingenuity, creativity and innovativeness. Challenges are frequently unique and solutions may serve as precedent for future decisions which effect the entire organization.
- Must be able to interpret, execute, and recommend modifications to company-wide policies to achieve corporate goals and objectives.
- Experience in Root Cause Analysis and technical investigation writing
- Must have effective communication skills and the ability to deal across several multi-national agencies and organizations.
- Communication skills are required in effectively communicating and partnering between internal and external parties.
- Establishes and communicates vision, focus and direction to align organizational and individual action and achieve results. Creates a "learning" culture that enables individuals to reach their maximum potential and builds the capability of the organization. Effectively manages talent to strengthen client. Creates an exceptional working environment that motivates high performance. Communicates a clear vision and expectations that create energy, enthusiasm and commitment from others.
- Microsoft Office is a requirement. Prior experience in usage of an eQMS system is a must.
Job Summary
JOB TYPE
Full Time
SALARY
$168k-206k (estimate)
POST DATE
06/27/2024
EXPIRATION DATE
07/25/2024
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