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Job Requirements of Scientist:
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Employment Type:
Contractor
-
Location:
Devens, MA (Onsite)
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Scientist
Careers Integrated Resources Inc
Devens, MA (Onsite)
Contractor
Job Title: Scientist (Global Capabilities MS&T – Materials and Cryogenics Science)
Location: Devens, MA (Hybrid: 50% onsite — Tuesday, Wednesday, Thursday; First month 100% onsite)
Duration: 12 Months+ (Possibility of Extension)
Work Hours: 40 hours/week, Core hours 9:00 AM – 4:00 PM
Pay Rate: $75.21/hr. on W2
Job Description:
As a Scientist in Manufacturing Sciences & Technology, you will support the Materials and Cryogenics Science group in managing the lifecycle of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing. You will collaborate cross-functionally with Manufacturing, Manufacturing Technology, Quality Assurance, Quality Control, Supply Chain, and Global Procurement teams.
Key Responsibilities:
Top Skills / Must-Haves:
Requirements:
Additional Info:
Location: Devens, MA (Hybrid: 50% onsite — Tuesday, Wednesday, Thursday; First month 100% onsite)
Duration: 12 Months+ (Possibility of Extension)
Work Hours: 40 hours/week, Core hours 9:00 AM – 4:00 PM
Pay Rate: $75.21/hr. on W2
Job Description:
As a Scientist in Manufacturing Sciences & Technology, you will support the Materials and Cryogenics Science group in managing the lifecycle of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing. You will collaborate cross-functionally with Manufacturing, Manufacturing Technology, Quality Assurance, Quality Control, Supply Chain, and Global Procurement teams.
Key Responsibilities:
- Qualify alternative raw material suppliers by working with procurement to identify and test new suppliers.
- Lead or contribute to technical equivalency assessments, specification comparisons, and material characterization reports.
- Support risk assessments and author change controls to maintain GMP compliance.
- Support investigations related to materials and consumables manufacturing.
- Manage supplier change notifications and evaluate material specifications.
Top Skills / Must-Haves:
- Proven technical writing skills.
- Experience working in cross-matrix teams.
- Project management in a fast-paced environment with the ability to manage multiple projects simultaneously.
- Ability to work independently and effectively with multiple stakeholders.
- Experience with change controls in GMP environments (preferred).
- Investigation experience.
- Biopharmaceutical industry experience (preferred).
Requirements:
- BS/MS degree with 2+ years of relevant industry experience OR PhD in Material Science, Engineering, Chemistry, or related scientific field.
- Awareness of cGMP compliance and regulatory agency requirements.
- Strong problem-solving skills; familiarity with root cause analysis and CAPA preferred.
- Excellent organizational, oral communication, and technical writing abilities.
- Effective team player and strong independent contributor.
- Familiarity with analytical techniques such as FTIR, SEM-EDS.
- Knowledge of data trending, tracking, and statistical analysis software is a plus.
Additional Info:
- No travel required.
- Lab environment without blood or animal exposure.
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