- Salary
- $34 – $36/hr
- Location
- Marietta, Pennsylvania
- Workplace
- Hybrid, Onsite
- Type
- Contract
- Department
- IT
- Education
- Bachelor
- Visa
- Not sponsored
- Source
- BetterTeam
Description
🔬 Now Hiring | MSAT Product & Process Validation Specialist
📍 Location: Marietta, PA | Hybrid - 3 Days Onsite
💰 Pay Rate: $34.00-$36.00/hour W2
📅 Contract: 10 Months (Potential Extension)
🏭 Industry: Pharmaceutical / Vaccine Manufacturing
💼 Employment: W2 Only - No Sponsorship or Third-Party Submissions
💰 Pay Rate: $34.00-$36.00/hour W2
📅 Contract: 10 Months (Potential Extension)
🏭 Industry: Pharmaceutical / Vaccine Manufacturing
💼 Employment: W2 Only - No Sponsorship or Third-Party Submissions
We are seeking an experienced MSAT Product & Process Validation Specialist to support vaccine manufacturing operations at a leading global pharmaceutical organization in Marietta, PA.
This role focuses on process validation, incoming material qualification, technical transfers, and continuous improvement within a highly regulated GMP manufacturing environment.
Key Responsibilities:
- Support technical transfer and qualification of incoming materials, including chemicals and Single-Use Systems (SUS).
- Execute manufacturing process validation, cleaning validation, and incoming material qualification activities.
- Support Continued Process Verification (CPV) and Cleaning Verification (CV).
- Monitor critical process parameters, analyze manufacturing data, and identify opportunities for process improvement.
- Support manufacturing investigations, deviations, troubleshooting, and change controls.
- Collaborate with MSAT, Manufacturing, Quality, and Engineering teams to maintain GMP compliance.
Qualifications:
- Bachelor's degree in Chemical Engineering, Biological Engineering, Pharmaceutical Sciences, or a related scientific discipline.
- 2-5 years of pharmaceutical or vaccine manufacturing process and/or validation experience.
- Experience with process validation, cleaning validation, technical transfers, or incoming material qualification.
- Familiarity with chemicals, Single-Use Systems (SUS), and GMP manufacturing environments.
- Strong technical writing, data analysis, and problem-solving skills.
Preferred Experience:
- Vaccine manufacturing, formulation, filtration, or aseptic processing.
- Process optimization, Quality by Design (QbD), and validation lifecycle management.
- Statistical analysis tools such as JMP, Statistica, or Power BI.
Work Authorization & Employment Requirements:
Candidates must be authorized to work in the United States on a W2 basis without requiring employer sponsorship now or at any time in the future.
No C2C arrangements, third-party agency submissions, or third-party applicants will be considered. Direct W2 candidates only.
Why Join Alphanumeric?
At Alphanumeric, we connect talented professionals with opportunities to make a meaningful impact. Join us in supporting initiatives that advance patient engagement, communications, and collaboration within the life sciences industry.
Apply today to learn more about this opportunity!
Skills
Power BIGMPComplianceTechnical Writing