External Manufacturing Quality Lead Job Openings by Johnson & Johnson Family of Companies in Markham

Job Title External Manufacturing Quality Lead Job Openings Markham Johnson & Johnson Family of Companies
Pub Date 4 days ago
Company Johnson & Johnson Family of Companies
Location Markham

Johnson & Johnson Family of Companies Careers 2020 - Johnson & Johnson Family of Companies calls a new official to fill External Manufacturing Quality Lead, that will be placed in Markham. You will receive a better prospect as well as safer dwell sometime soon. Becoming a member of this firm makes anyone able to reach the purpose less complicated and make current aspiration come true.

To help the corporation perspective along with mission come on legitimate Johnson & Johnson Family of Companies can be started on brand-new place seeing that December 2020. All people who are interested answering this specific vacant, make sure you take part in this kind of External Manufacturing Quality Lead recruitment. If you will be one which can certainly fill up qualifications, you can try to see further info about External Manufacturing Quality Lead Job Openings below.

Johnson & Johnson Family of Companies Recruitment 2020

External Manufacturing Quality Lead Job Opening in Markham

Johnson & Johnson Consumer Health, a member of Johnson & Johnson's Family of Companies, is recruiting for a External Manufacturing Quality Lead.

Johnson & Johnson Consumer Inc., based in Skillman, N.J., is one of the world's largest consumer health and personal care products company. Our consumer companies produce many of the world's most trusted brands, among them JOHNSON'S® Baby, BAND-AID®, NEUTROGENA®, TYLENOL®, MOTRIN®, and LISTERINE®. Each one of our consumer businesses embraces innovative science to create products that anticipate consumer needs and create experiences that help them live healthy, vibrant lives.

The External Manufacturing (EM) Quality Lead position provides overall Quality Assurance leadership in the management of contract manufacturing sites engaged in the production of oral ingestible and topical OTC drugs, medical devices, combination products, nutritionals, NDA’s and/or cosmetic formulations for the J&J Consumer Sector. The EM Quality Lead is responsible for supporting Contract Manufacturing sites, driving compliance & quality improvement initiatives, assisting resolution of process/product non-conformance events, monitoring/resolving complaints, reviewing Annual Drug Product Review reports, reporting Contract Manufacturer performance metrics, working with J&J business partners and providing batch release when required. This job position may represent QA on project and improvement teams by guiding setting quality/compliance requirements, development of SOPs & specifications, and providing technical transfer/validation support.

Key Responsibilities Include:

Serve as Subject Matter Expert (SME) for quality assurance processes, procedures, and activities.

Remain current on assigned quality system training and seek out training and knowledge in adjacent areas. A mentor to junior staff.

Provides detailed or summary communication to senior cross-functional leadership on status of key initiatives and issues.

Document rationales which are technically accurate and regulatory compliance focused for product disposition, risk assessment/mitigation, non-conformances, corrective actions, and audit observation responses. Hold business partners accountable for delivering documentation of similar quality.

Conduct, execute and document thorough investigations and CAPAs for high risk/high complexity issues.

Ensure timeliness of results through independent, proactive intervention. May act as a CAPA owner or be assigned as QA lead resource for a CAPA

Troubleshoot high risk/high complexity quality/compliance issues, using experience, resourcefulness, and creativity to provide solutions to a wide range of root causes.

Design and implement quality and compliance improvement programs and initiatives. Innovate solutions to significant quality system gaps and lead continuous improvement projects.

Represent NA Source Quality on multiple, simultaneous, high-impact/ high-value projects as the “Voice of Quality”, including active team engagement, proactively ensuring quality and compliance inputs are integrated into the project objectives, and act as a QA “go-to” resource for cross-functional business partners.

Independently lead and prioritize highly complex and diverse workload ensuring results are on-time, accurate, and meet their intended objective.

Independent decision-making authority and accountability for product disposition and compliance decisions with significant potential impact to customer service

Review and approve compliance records, specifications, development plans, procedures, and other documents, as required by procedure.

Leads the development and introduction of new processes and procedures which may impact multiple functions or regions. Brings forward innovative process improvements to drive compliance and/or efficiency

Drive closure of MAPs, through holistic and comprehensive engagement and negotiation with EM.

are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.


Qualifications
  • A minimum of a bachelor’s degree is required, with a preferred focus of Biology or Chemistry.
  • A minimum of 5 years (or an Advanced degree/MBA in related discipline and a minimum of 4 years) of GMP experience in Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements
  • Detailed working knowledge of cGMP requirements and current FDA OR Health Canada enforcement issues.
  • Experience in MS Word, Excel, and Power Point applications is REQUIRED along with knowledge of SAP, TRu and EtQ.
  • Demonstrated ability to lead cross-functional teams and collaborate with internal/external partners to enhance relationships and interactions, including interfacing with senior levels of management to inform, drive change, and provide direct feedback.
  • Demonstrated ability to work on complex or ambiguous issues autonomously, with little/no daily direction.
  • Proven ability to lead and influence others within product teams with excellent communication and presentation skills
  • Experience and demonstrated skills in navigating in a matrix environment, managing complexity, collaborating

across boundaries and influencing without authority required.

  • Detail-oriented, with the ability to work in a fast-paced environment with multiple, concurrent priorities many needing immediate resolution.
  • Strong communication (verbal & written) and interpersonal skills, self-awareness and adaptability required.
  • Prior experience working in a manufacturing plant

Primary Location
United States-New Jersey-Skillman-199 Grandview Road
Other Locations
Canada-Ontario-Guelph, United States-California-Los Angeles, United States-Pennsylvania-Fort Washington, United States-Pennsylvania-Fort Washington, United States-Pennsylvania-Lititz, Canada-Ontario-Markham
Organization
Johnson & Johnson Consumer Inc. (6101)
Job Function
Quality
Requisition ID
2005866089W

As one of the leading companies in Canada, Johnson & Johnson Family of Companies offers variety of opportunities for employees to grow and make them as future leaders of the professional and disciplined. Johnson & Johnson Family of Companies also gives a dynamic work environment in order to encourage employees to give optimally, and at the same time, you are able to learn new skills and knowledge through the company programs.

If You are fascinated to send an application for External Manufacturing Quality Lead Jobs Markham December 2020 by Johnson & Johnson Family of Companies, please prepare requirements files and documents as soon as possible. To apply by online, please click the "Apply" button below. If you still do not satisfy with a job above, you can try to read more jobs list in Markham region from another company below.


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