Chemist II

Katalyst Healthcares & Life Sciences; Worcester (MA); On-site; USD 60,000 - 90,000; Full time

Job summary

Join a forward-thinking company as a Chemist II in Quality Control, where you'll perform critical laboratory testing in a cGMP environment. This role offers the opportunity to validate test methods for both clinical and commercial projects, ensuring the highest standards of quality and compliance. You will collaborate with a dedicated team, maintain meticulous documentation, and support laboratory investigations. If you have a passion for science and a commitment to excellence, this role is perfect for you to make a meaningful impact in the healthcare sector.

Qualifications

• 2+ years of experience in a Quality Control laboratory setting.
• Strong knowledge of laboratory testing techniques and documentation.

Responsibilities

• Perform laboratory testing in a cGMP environment and validate test methods.
• Author validation protocols and support laboratory investigations.

Skills

Laboratory Testing

cGMP Standards

Documentation Skills

Troubleshooting

Education

BA/BS in Chemistry

BA/BS in Biochemistry

BA/BS in Medical Technology

BA/BS in Biology

Tools

CE-SDS

HPLC

ELISA

Empower Software

Softmax / PLA Software

Job description

Job Description

Position: Chemist II in Quality Control

Responsibilities:

• Perform laboratory testing within a cGMP environment, including validation of test methods for clinical and commercial projects.
• Maintain a safe work environment, adhering to procedural requirements.
• Implement and uphold cGMP standards related to laboratory records, procedures, and systems.
• Execute various laboratory techniques as trained.
• Complete assigned tasks within specified timelines and collaborate with team members to meet business objectives.
• Author validation protocols, reports, and test methods.
• Support laboratory investigations promptly.
• Perform a variety of testing techniques after training completion.

Requirements:

• BA/BS in Chemistry, Biochemistry, Medical Technology, Biology, or a related science field with at least 2 years of relevant experience.
• Experience with CE-SDS, HPLC, or ELISA, including troubleshooting skills.
• Familiarity with Empower or Softmax / PLA software.
• Experience with spectrophotometric concentration determination.
• Background in Quality Control testing of phase III and commercial products.
• Knowledge of empower audit trail.
• Strong documentation skills.

Additional Information

All your information will be kept confidential according to EEO guidelines.