GxP Operations Support Specialist, Manufacturing Systems
Boston, MA - USA
Job Summary
Job Description
General Summary:
The GxP Operations Support Specialist will support the implementation maintenance and continuous improvement of digital manufacturing systems. Working under the guidance of more senior team members this role will partner with Manufacturing Quality Engineering and IT stakeholders to document business processes support system enhancements test system changes and help ensure reliable and compliant system operations.
Key Duties and Responsibilities:
- Help configure test and deploy MES and other system changes under the direction of senior team members system owners and technical teams.
- Participate in workshops and meetings with Manufacturing Quality Engineering Supply Chain and IT stakeholders.
- Support user acceptance testing (UAT) including preparing test cases documenting test results tracking defects and coordinating issue resolution.
- Assist with documentation including requirements test evidence and change-control records.
- Support manufacturing digital system operational activities including monitoring incidents documenting issues escalating concerns and coordinating with support teams.
- Help maintain system and business-process documentation including standard operating procedures work instructions training materials and process maps.
- Assist with end-user communications and training activities related to MES enhancements and system releases.
- Analyze basic system production and issue-management data to identify trends and support continuous improvement initiatives.
- Develop a working understanding of manufacturing operations electronic batch records GxP requirements and MES best practices.
- Perform other system-analysis and project-support activities as needed.
Knowledge and Skills:
- Strong attention to detail and ability to create accurate organized documentation.
- Demonstrated problem-solving analytical and communication skills.
- Ability to learn new technologies and business processes in a fast-paced collaborative environment.
- Ability to work effectively with cross-functional teams and manage assigned work with appropriate guidance.
- Familiarity with regulated environments and concepts such as Good Manufacturing Practices (GMP) GxP data integrity or computer system validation
Education and Experience:
- Bachelors degree or high school diploma with experience in a pharmaceutical or biotechnology manufacturing or the equivalent combination of education and experience in a related field.
- Typically requires 1 year of experience in a GMP pharmaceutical/biopharmaceutical industry or the equivalent combination of education and experience
At Vertex we embrace continuous learning and encourage employees to stay informed on advances in AI technology automation and industry trends. We seek talent who bring an external perspective demonstrate curiosity and sound judgment and thoughtfully adopt new capabilities that improve decision-making drive innovation increase efficiency and help deliver better outcomes for patients.
Pay Range:
$38 - $57Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors including skills competencies experience and other job-related factors permitted by law.
At Vertex our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career financial family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter) educational assistance programs including student loan repayment a generous commuting subsidy matching charitable donations 401(k) and so much more.
Flex Designation:
On-Site DesignatedFlex Eligibility Status:
In this On-Site designated role you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at
Required Experience:
IC
About Company
Vertex Pharmaceuticals invests in scientific innovation to create transformative medicines for people with serious diseases.