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Job Requirements of Associate Scientist:
-
Employment Type:
Contractor
-
Location:
High Point, NC (Onsite)
Do you meet the requirements for this job?
Associate Scientist
Careers Integrated Resources Inc
High Point, NC (Onsite)
Contractor
Job Title: Associate Scientist
Location: High Point, NC
Duration: 10 Months (Contract)
Shift: Days, 8:00 AM – 5:00 PM
Position Summary:
The Associate Scientist will support the Quality Control (QC) Chemistry and Microbiology laboratories by performing a wide range of activities including sample testing, environmental monitoring, equipment calibrations, and documentation. This role ensures all laboratory work is conducted in compliance with current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), and data integrity guidelines.
Key Responsibilities:
Environmental Monitoring, Water Testing, and Lab Preparation (Up to 50%)
Qualifications:
Education & Experience:
Location: High Point, NC
Duration: 10 Months (Contract)
Shift: Days, 8:00 AM – 5:00 PM
Position Summary:
The Associate Scientist will support the Quality Control (QC) Chemistry and Microbiology laboratories by performing a wide range of activities including sample testing, environmental monitoring, equipment calibrations, and documentation. This role ensures all laboratory work is conducted in compliance with current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), and data integrity guidelines.
Key Responsibilities:
Environmental Monitoring, Water Testing, and Lab Preparation (Up to 50%)
- Conduct environmental monitoring and water testing.
- Perform routine calibrations and standardizations of lab equipment (e.g., balances, pH meters).
- Assist with inventory management: receiving, storing, and stocking lab supplies, media, and solutions.
- Prepare and stage solutions for testing by senior analysts.
- Follow proper documentation practices and data integrity protocols.
- Independently conduct testing of raw materials, finished products, in-process samples, and stability samples.
- Execute complex testing methods requiring high precision.
- Ensure critical lab equipment is calibrated prior to use.
- Document results accurately and in compliance with laboratory standards.
- Maintain cleanliness and organization of lab spaces including benches, storage areas, fume hoods, refrigerators, and glassware.
- Properly dispose of lab waste and replace consumables as needed.
- Ensure lab areas remain audit-ready at all times.
- Engage in training to develop technical and compliance skills.
- Train junior analysts in specialized techniques and documentation standards.
- Participate in or lead lab projects, offering technical solutions where needed.
Qualifications:
Education & Experience:
- Bachelor’s degree in Chemistry, Microbiology, Biology, Biochemistry, or a related scientific discipline.
- Prior experience in a GMP-regulated Quality Control Laboratory within a pharmaceutical environment is preferred.
- Strong understanding of laboratory techniques and instrumentation.
- Detail-oriented with a commitment to accuracy and compliance.
- Able to work both independently and as part of a collaborative team.
- Strong documentation and communication skills.
- Commitment to maintaining confidentiality and upholding professional standards.
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