Quality Assurance Senior Specialist, Engineering/Validation (Contract) 858

Senior Quality SpecialistThe Senior Quality Specialist will provide QA support for commissioning, Qualification and Validation (CQV), and project-related QA activities at Vertex Manufacturing Center (VMC), Boston, MA.As a key member of our Quality Assurance team, this person will be responsible for ensuring the quality and compliance of our facilities, equipment, and utilities through meticulous review, guidance, and collaboration with stakeholders. This person will leverage their project management expertise and deep understanding of quality systems to facilitate successful CQV projects and maintain the integrity of our manufacturing processes. The Senior Quality Specialist supports or executes daily activities related to equipment or instrumentation supporting Facilities, Utilities, Manufacturing, and Labs.The position will support multiple production functions (from Quality operations to Quality Engineering) to achieve site goals while providing Quality oversight and ensuring compliance. Supporting resolution of potential nonconformance events by applying the deviation and CAPA management procedure, in conjunction with other procedures as applicable, to facilitate decision-making with a cross-functional team, as needed. Advising Production on proper documentation as needed and performing other duties as assigned.This role will require local presence at the VMC, Boston site.Key Leadership Skills:Cross-functional collaboratorResults DriverKey Knowledge/ Skills and Competencies:Strong leadership skills with the ability to thrive in a high throughput environmentCritical Thinking / Problem-Solving Ability to evaluate quality matters and make decisionsStrong oral and written communication skills requiredGood Interpersonal skills requiredAttention to detailKnowledge in the following areas: Knowledge of global GMP requirements governing oral drug products and knowledge of oral drug product manufacturing practicesAbility to work under limited supervisionOversight of Internal Operations – Quality Engineering:Provide QA oversight and support for Commissioning, Qualification, and Validation projects for facilities, equipment, and utilities, ensuring alignment with project timelines and quality standards.Review and approve comprehensive qualification and validation strategies and plans developed by stakeholders.Critically review and approve qualification protocols (IQ, OQ, PQ) and validation protocols (e.g., process validation) for accuracy, completeness, and compliance.Analyze qualification and validation data presented by stakeholders, review reports for accuracy and completeness, and provide QA input on findings.Independently author and manage quality system records, including deviations, change controls, and Corrective and Preventative Actions (CAPAs) related to qualification and validation activities, often initiated by or in collaboration with stakeholders.Provide expert QA guidance and support during the execution of qualification and validation protocols by cross-functional teams.Collaborate effectively with cross-functional teams, including Engineering, Manufacturing, and Quality Control, to ensure a productive and compliant approach to CQV.Participate in risk assessments related to facilities, equipment, and utilities, providing a QA perspective and critical evaluation.Contribute to the development and improvement of quality assurance procedures and policies related to validation, facility, and engineering standards through insightful review and recommendations.Critically review and assess CQV documentation and activities, providing constructive feedback and guidance to stakeholders.Provide Quality oversight and review of calibrations, PMs, eCRs, work orders and laboratory operations via instrument qualifications.Review and approval of qualification activities, and periodic assessments, and trending programs (equipment, facility, utilities, etc.)Support EM and UM programs and control programs (Veriteq, pest control)Provide support for facilities and engineering projects, including capital projects, annual plant shutdowns, and various improvement projects as assigned.Ensure that all CQV activities are performed in accordance with Good Manufacturing Practices (GMP) and other applicable regulatory requirements through effective review and guidance.Support regulatory inspections and internal audits related to qualification and validation by providing QA expertise and documentation.Maintain a strong understanding of current industry best practices and regulatory expectations for CQV to provide informed guidance and ensure compliance.Proactively work with stakeholders to ensure a quality-driven approach to all CQV activities.Facilitate productive discussions and collaborations with stakeholders to resolve quality-related issues and ensure project success.Minimum Qualifications:M.S in life sciences (or equivalent degree) and 5-7 of relevant work experience, orB.S in life sciences (or equivalent degree) and 8-10 years of relevant work experienceExperience providing QA support and oversight of GMP manufacturing operationExperience with drug product (oral solid dosage forms preferred) development and manufacturing with proficient knowledge of the following in a pharmaceutical setting:cGMP's and associated CMC regulatory considerationsexperience with continuous manufacturing a plusExperience with equipment, facilities and utility system qualifications activities in a cGMP settingExperience successfully leading change control, event investigations, Root Cause Analysis (RCA), and CAPAExperience with network-based applications such as Oracle and Trackwise preferred.Ability to thrive in a high throughput environment.Preferred Qualifications:Affinity with digital innovation, data sciences, and Quality engineering.Experience with Cleaning validation and practices.Experience with Temperature Control unit qualifications.Highly effective verbal and written communication skills, strong interpersonal skillsGreat attention to detail and high degree of accuracy in task execution and GMP documentationAbility to complete tasks autonomously, providing updates to senior management, and identifying potential issuesStrong organizational skills, including ability to follow assignments through to completionKnowledge of ASTM E2500, CSV/GAMP, and other associated standardsPay Range$57-$65/hrRequisition DisclaimerThis 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 law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. 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