GMP operational Quality, Senior Specialist (contract) 25421
GMP operational Quality, Senior Specialist (contract) 25421
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Job Description
Job Description
The Senior Quality Specialist will provide QA support for commissioning Qualification and Validation (CQV) and projectrelated 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 decisionmaking with a crossfunctional 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:
- Crossfunctional collaborator
- Results Driver
Key Knowledge/ Skills and Competencies:
- Strong leadership skills with the ability to thrive in a high throughput environment
- Critical Thinking / ProblemSolving
- Ability to evaluate quality matters and make decisions
- Strong oral and written communication skills required
- Good Interpersonal skills required
- Attention to detail
- Knowledge in the following areas:
- Knowledge of global GMP requirements governing oral drug products and knowledge of oral drug product manufacturing practices
- Ability to work under limited supervision
Oversight 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 crossfunctional teams.
- Collaborate effectively with crossfunctional 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 qualitydriven approach to all CQV activities.
- Facilitate productive discussions and collaborations with stakeholders to resolve qualityrelated issues and ensure project success.
Minimum Qualifications:
- M.S in life sciences (or equivalent degree) and 57 of relevant work experience or
- B.S in life sciences (or equivalent degree) and 810 years of relevant work experience
- Experience providing QA support and oversight of GMP manufacturing operation
- Experience with drug product (oral solid dosage forms preferred) development and manufacturing with proficient knowledge of the following in a pharmaceutical setting:
- cGMPs and associated CMC regulatory considerations
- experience with continuous manufacturing a plus
- Experience with equipment facilities and utility system qualifications activities in a cGMP setting
- Experience successfully leading change control event investigations Root Cause Analysis (RCA) and CAPA
- Experience with networkbased 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 skills
- Great attention to detail and high degree of accuracy in task execution and GMP documentation
- Ability to complete tasks autonomously providing updates to senior management and identifying potential issues
- Strong organizational skills including ability to follow assignments through to completion
- Knowledge of ASTM E2500 CSV/GAMP and other associated standards
Pay Range
$6070/hr
Requisition Disclaimer
This job posting is for a temporary role with a thirdparty 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 thirdparty 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 jobrelated factors permitted by law. In addition this role will be eligible for overtime pay in accordance with federal and state requirements
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No C2C or ThirdParty Vendors
Required Experience:
Director
Employment Type
Full-Time
