Senior Manager, GMP Operational Quality (Contract)

General Summary:

The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects. The Sr. Quality Manager manages and develops personnel to support department and functional activities.

This is a 6 month contract.

Onsite at Leiden Center

Sun-Wed 7am-5:30pm

Key Duties and Responsibilities:
Collaborate with internally and external business partners to resolve complex quality issues to ensure compliant solutions
Participates in cross-functional teams as an experienced Quality technical resource
Drafts and enforces Quality Agreements between CMOs/Suppliers and Vertex as needed
Assists Change Control owners with ensuring compliance to change procedure requirements
Assesses and approves change controls
Conducts quality investigations /deviations and reviews corrective action plans for adequacy and compliance. This includes root cause
analysis and product impact assessments for investigations resulting from deviations and OOS.
Ensures appropriate CAPA actions are identified and addressed.
Approves investigations/CAPAs.
Identify facilitate and/or lead continuous improvement efforts
Maintains Quality Metrics to support process improvement activities
Provides tactics to address compliance gaps or determines enhancements to cross-functional quality systems
Conducts GMP document review including procedures work instructions specifications methods protocols and method reports
Responsible for coordinating facilitating and follow up on any QLT action items assigned.
Identify and communicate risks and assist with risk mitigation plans as necessary
Supports internal audit or external audit programs
Assists in preparation of audit responses

Manages audit CAPAs & metrics
Provides technical advice for partner and regulatory agency audits
Provides information to assist in budgeting and scheduling
Responsible for the following activities related to people management responsibilities
Talent Acquisition/ Recruiting/Interviewing/ Selection/Onboarding
Performance Management (goals monitoring reviews)
Monitoring /Supporting Employee Engagement and Retention
Succession Planning
Accomplishing staff results by communicating job expectations planning coaching training and developing personal growth
opportunities through IDPs.
Accountable to provide oversight of day to day operations
Assists with workforce planning/resource modeling and to update through forecasting activities

Knowledge and Skills:
In-depth knowledge of both the conceptual and practical application of cGMPs in a pharmaceutical setting; in-depth knowledge of global
GMP requirements and support of GMP manufacturing
Strong team leadership skills with the ability to work in a fast-paced environment and meet quality accuracy and timeliness objectives
In-depth experience leading complex projects/teams and continuous improvement initiatives within stated objectives and timelines;
effectively applies project management processes / tools to lead meetings assist with project planning and facilitate completion of tasks
Ability to independently lead cross-functional teams and represent the Quality unit
Ability to mentor and guide staff skilled at transferring technical knowledge and teaching quality management skills
Ability to communicate cross-functionally to a wide variety of audiences; exchanges complex and sensitive information and is able to
influence others to understand a point of view and gain alignment around a proposed action
Demonstrated ability to manage teams and to develop personnel
Demonstrated ability to work independently to provide QA advice for large multifaceted projects
Demonstrated ability to evaluate quality matters and make complex decisions leveraging technical experience advanced judgement and
the analysis/synthesis of a a variety of information; able to work outside of precedent and takes a new perspective on existing solutions
Strong experience successfully leading event investigations Root Cause Analysis (RCA) and CAPA
Strong experience with electronic document management systems (e.g. QDoccs Trackwise Veeva)

Education and Experience:
Bachelors degree in a scientific or allied health field (or equivalent degree)
Typically requires 6 years of experience or the equivalent combination of education and experience

$75-$85/HR

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements

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No C2C or Third-Party Vendors