Quality Assurance Specialist - Global MES projects
Job Description
Job Descriptionjob summary:
Seeking an enthusiastic, results-oriented, and experienced Quality Assurance (QA) Specialist to join the Quality Assurance (QA) team within the Worldwide Operations Manufacturing department.
As a Quality Assurance Specialist, you will be responsible for supporting the global Manufacturing Execution System (MES) projects and initiatives to ensure compliance, quality assurance, and operational excellence in a GMP-regulated environment.
Work Schedule: Strong preference for candidates located in Eastern Standard Time (EST) to align with global teams
location: Telecommute
job type: Contract
salary: $33.86 - 39.84 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Ensure quality oversight and compliance for MES and PT project activities.
- Support validation and qualification efforts for computerized systems in alignment with GMP requirements.
- Review and approve documentation related to MES workflows, change controls, and deviations.
- Collaborate with cross-functional teams to ensure quality standards are met during system implementation.
- Participate in risk assessments and support mitigation strategies for quality-related issues.
- Ensure that quality processes and procedures are updated and aligned with project deliverables.
- Provide training and guidance on quality practices and regulatory compliance.
- Support audits and inspections by providing documentation and subject matter expertise.
- Monitor and report on quality metrics and continuous improvement initiatives.
- Ensure alignment with global quality standards and local regulatory requirements.
qualifications:
- Bachelor's (BS) or Masters (MS) degree in Life Sciences, Engineering, or related field.
- Four (4) to five (5) years of experience in a pharmaceutical quality assurance or related function.
- Minimim of one (1) to two (2) years of experience working with the MES platform.
- Proven experience in quality assurance within a GMP-regulated manufacturing environment.
- Experience supporting MES and process transformation initiatives.
- Strong understanding of validation principles and regulatory compliance.
- Excellent documentation and communication skills.
- Ability to work collaboratively in cross-functional teams.
- Detail-oriented with strong analytical and problem-solving skills.
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skills: Risk Assessment and Mitigation, IT Systems Validation, Good Manufacturing Practices (GMP), Quality Assurance (QA), Food and Drug Administration (FDA)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
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