Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

MSAT Scientist III

Job

Spectraforce

Portsmouth, NH (In Person)

Full-Time

Posted 1 week ago (Updated 6 days ago) • Actively hiring

Expires 6/29/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
52
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Position Title:
MSAT Scientist/ Data Entry Work Location:
Portsmouth
NH 03801
Assignment Duration:
12
Months Work Schedule:
Sunday through Thursday required
Work Arrangement:
Onsite Position Summary:
Process Data Collection Specialist to support critical manufacturing data collection activities at our organization's Portsmouth site.
Key Responsibilities:
  • Be a contributing team member to a larger team of Data Scientists, Business Analysts and other Data Process Specialists.
  • Collect, transcribe, and verify manufacturing process data from paper batch records
  • Ensure data accuracy, completeness, and compliance with GMP standards
  • Resolve data discrepancies with manufacturing and support teams
  • Manage assigned workload independently to meet demanding timelines
  • Perform hands-on work in cleanroom and controlled manufacturing environments
Qualification & Experience:
  • Bachelor's degree is desirable for this role, preferably in a laboratory science.
  • Data science or computer science background is not essential for this role
  • Should demonstrate the potential to be a strong long-term fit for our organization as an organization, even though this role is a fixed-term contract
  • Early-career professionals seeking hands-on experience in a regulated GMP manufacturing environment
  • High attention to detail and strong documentation discipline
  • Ability to work independently with limited day-to-day supervision, once onboarded and properly trained.
  • Comfortable executing repetitive, accuracy-critical tasks under timeline pressure.
  • Willingness to spend significant time on their feet and working in cleanroom environments
  • Demonstrated reliability, accountability, and quality first mindset
  • Interest in long-term growth within our organization as an organization, even though this role itself is time-limited Working Conditions & Physical Demands (If Applicable): Willingness to spend significant time on their feet and working in cleanroom environments