QC Analyst 3

Job Summary Join a cutting-edge biotech leader in Portsmouth, NH, as a QC Analyst 3. This 8-month, 100% on-site contract role offers the chance to support critical cGMP manufacturing by executing technical transfer activities, method/software validations, and data integrity initiatives in a fast-paced laboratory setting. Location Portsmouth, New Hampshire Job Type Contract Salary $62.00 - 64.75 per hour Work Hours 9 to 5 Education Bachelors Responsibilities Lead method and software validations, including writing GMP procedures, executing test scripts, and authoring validation documents. Serve as a Subject Matter Expert (SME) for key laboratory software platforms. Execute root-cause analyses to troubleshoot complex technical software errors. Collaborate across cross-functional teams to translate operational needs into actionable priorities. Enforce rigorous Data Integrity principles across all laboratory workflows in strict compliance with GMP guidelines. Qualifications Bachelor's degree in a science-related discipline. Proven experience with specialized analytical software: SoftmaxPro, Empower, or SoloVPE. Direct GMP experience within the pharmaceutical or biotechnology industry. Proficiency with laboratory computer systems and data interpretation. Preferred Prior experience with GMP Quality Systems such as TrackWise or LIMS. Skills Laboratory Information Management Systems (LIMS), Quality Control (QC) 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. 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. Required: Bachelor's degree in a science-related discipline. Proven experience with specialized analytical software: SoftmaxPro, Empower, or SoloVPE. Direct GMP experience within the pharmaceutical or biotechnology industry. Proficiency with laboratory computer systems and data interpretation. Preferred: Prior experience with GMP Quality Systems such as TrackWise or LIMS.

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#J-18808-Ljbffr Randstad USA