QA Documentation Specialist III
$15.69 per hourjob summary:
Join a biopharmaceutical leader in Portsmouth, NH, as a QA Documentation Specialist. This 100% on-site, 6-month contract offers an incredible opportunity to support critical Quality System Management and document control processes within a highly collaborative, compliance-driven environment. location: Portsmouth, New Hampshire
job type: Contract
salary: $15.69 - 26.14 per hour
work hours: 9 to 5
education: Associate responsibilities:
qualifications:
Required:
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 View email address on 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.
Join a biopharmaceutical leader in Portsmouth, NH, as a QA Documentation Specialist. This 100% on-site, 6-month contract offers an incredible opportunity to support critical Quality System Management and document control processes within a highly collaborative, compliance-driven environment. location: Portsmouth, New Hampshire
job type: Contract
salary: $15.69 - 26.14 per hour
work hours: 9 to 5
education: Associate responsibilities:
- Support the implementation, execution, and maintenance of PQS integration and Quality Documents in Veeva.
- Coordinate elements of the document change process, completing workflows and document gating to ensure minimal operational disruption.
- Initiate, format, edit, and manage controlled documents within the Veeva Quality Docs system.
- Track and log requests for source documents accurately.
- Ensure all daily activities comply strictly with cGMP, global regulatory requirements, and internal standards to maintain constant inspection readiness.
qualifications:
Required:
- 1-3 years of Quality experience within the pharmaceutical or biopharmaceutical industry.
- Proven ability to effectively collaborate within a diverse, cross-functional team.
- Ability to work 100% on-site in Portsmouth, NH (Monday-Friday, 8:00 AM - 5:00 PM).
- Direct experience with the Veeva Quality Document Management System and Microsoft Teams.
- Technical writing experience.
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 View email address on 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.
Vacancy posted 4 days ago
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