US – Vendor Quality Partner/Lead

Please note: in line with *** policy, this role is VDI only. *** will not be providing a laptop or equipment.
Preferably hybrid, but for great candidate can be remote
Some travel
Primary Purpose / Regulatory Responsibilities:
This position will provide leadership and in-depth QA expertise in driving strategic and operational Quality Assurance activities associated with complex Global Vendors (Contract Manufacturing Organizations) engaged in GMP manufacturing activities for *** Products.
This will be achieved through close partnering with QA management within *** and at interfaces with Product CClient Quality Leads, Vendor Quality Leads for other vendor sites, and in collaboration with *** Technical Operations and other *** teams (Vendor Team, Extended Vendor Team).
The incumbent takes responsibility for above summarized Product of activities in relation to the assigned Manufacturing sites
Vendor Quality Lead (VQL) related accountabilities:
Be the central QA point of contact for the organization for investigations / deviations / out-of-specifications / audit observations associated with the assigned vendors. Perform the QA review of deviation notifications and investigations, retrieve and collect supportive information from involved stakeholders (*** Vendor Team, CClient Quality Leads, ILA, ALO, Business) to allow assessment.
Manage the key performance indicators (metrics) for key operational QA activities and services associated with the vendors in the defined described tracking tools and track the vendor s performance
Ensure all Quality agreements are in place and take ownership of agreements for the vendors. Maintain Quality Agreement with the vendors up to date and perform periodic reviews and update of the agreement in close collaboration with the vendors.
When applicable, be sure that the Annual Product Stability Program is rolled-out and executed at the vendor in accordance with the *** Stability Program
Ensure the Product Quality Reviews (PQR) are completed by the vendors in a timely manner and as needed and are reviewed within the established leadtimes. Ensure that this review is documented and made available in the *** EDMS.
Participate as QA representative to the recurrent vendor meetings, present issues and resolutions, and drive vendor quality performance through these meetings
Quality Complaints: be the contact person for the follow-up with vendors for the manufacturing investigation part. When applicable, ensure that initial receipt, logging of quality complaints into the *** Complaint System and provision of responses to the complainant are professionally coordinated and managed.
If needed work with the Vendor team and CClient Quality Lead to determine the Root cause of issues which may lead to a Corporate Technical Review (CTR) meeting. Coordinate vendor quality related investigations
Participate on ad-hoc basis to the *** Product/Global Change Control Committees for activities related to the vendors
Provide in-depth expert QA advice, support and management for technical operational QA and general QA strategic matters associated with the vendors
Work closely with Corporate QA teams, Technical Operation Teams, Business stakeholders and Affiliates in an effective and efficient way
Cover the entire product life cycle from initial commercialisation including Technology Transfer/Knowledge transfer, commercial (key raw materials to distribution), product improvements to phase out for the assigned vendors
Developer and owner of the QA plans and product resource and capacity overview for activities associated with the assigned vendors
Ensure all relevant documentation are provided to the vendors and implemented (Methods, Specs, Master Batch record)
Ensure review of relevant RA dossier section related to the assigned vendors
Have the overview of *** audit and HA inspections related to the vendors. Track and follow-up on Audit observation and CAPA plan implementation at the vendor.
Be the QA stakeholder for Vendor Risk management.
Manage and control quality documents related to the vendors in the *** EDMS
Support on customer audits and Health Authority inspections at the vendors, as needed
Receipt, coordinate review and authorize product reworks and repackaging
Drive resolution for complex quality issues related to the vendors in Product . Be the point of contact for critical post-release vendor issues (supply chain, distribution, etc.). Challenge current practices for issue resolution and incorporate new perspectives into existing problems.
As required provide Operational QA support to other vendors
Act as substitute for other Vendor Quality Leads in times of absenteeism (e.g. vacation, illness)
Work in accordance with *** HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development.
Acts as a Best Practice ambassador, leads best practices steams and uses knowledge of internal/external business environment to improve existing processCompetencies
Must have Masters
Must be knowledgeable in several areas of the global pharmaceutical industry, including the interpretation and practical application of applicable regulations. Has good background knowledge of the pharmaceutical industry from a business and technical perspective.
Must be able to work independently and handle complex / difficult situations. Output from actions will most likely impact activities across several departments.
Possess good auditing capabilities and skills.
Must be able to effectively interact with and influence senior internal and external personnel on many aspects of project and product related matters.
Must have the ability to manage projects / activities across global geographies within the area of expertise. Be capable of leading and motivating teams and demonstrate professional maturity in difficult situations. Set challenging objectives for self and others and drive for results.
Must possess excellent interpersonal, verbal, and written communication skills at all levels internally and externally especially at senior management levels.
Generate commitment from within teams, encourage and support new ideas and act as a role model for others in driving the departmental / company vision.
Must be skilled and experienced in operating across cultures and in a multi-cultural environment.
Root cause and risk management/assessment skills.
Problem solving (Describe the level of self-starting thinking required in the for recognizing, analyzing and solving problems)
Must have the ability to independently analyze data and information to draw conclusions and make effective decisions.
Must have ability to identify risks and propose corrective actions within areas of expertise. Also demonstrates initiative and the ability to help others solve problems in a creative and practical way.
Must be able to coach staff and colleagues through effective complex problem solving to ensure the best resolution is obtained. Challenges existing solutions for pertinence.
Must be able to develop innovative solutions through judgment and reasoning. leveraged from extensive quality experience.

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Job Overview

Work Mode

Hybrid

Job ID

26-13433

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Integrated Resources Inc.

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Join leading healthcare organizations hiring radiologists, technologists, and imaging professionals across the country.

Complete your application in under 2 minutes.

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Remote, hybrid & onsite roles available

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Average recruiter response within 48 hours

Trusted Network

Connected with top hospitals nationwide

US – Vendor Quality Partner/Lead
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Integrated Resources Inc.

Build Your Career With Confidence

Join leading healthcare organizations hiring radiologists, technologists, and imaging professionals across the country.

Complete your application in under 2 minutes.

Flexible Opportunities

Remote, hybrid & onsite roles available

Fast Hiring Process

Average recruiter response within 48 hours

Trusted Network

Connected with top hospitals nationwide

US – Vendor Quality Partner/Lead
Upload Your Resume
Your information is protected and securely processed.