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Cat Current
Centralized Recruiter- Randstad Sourceright integrated MSP - A Randstad Enterprise Business
Role Overview:
This position will perform in a cGMP environment following FDA and ICH guidelines. Duties include but are not limited to: method development; method and instrument validation; testing in accordance with cGMP regulations, regulatory filings, and approved procedures for products including, but not limited to: raw materials, drug substance, finished product
and stability.
Responsibilities:
(60%) Perform analytical testing
(15%) Prepare and maintain reagents and reference standards
(10%) Operate and maintain equipment
(10%) Record, report, and verify data
(5%) Participate in special projects, as necessary
Weekend work is possible but not expected
Education:
Bachelor of Science in Chemistry or related scientific discipline
License/certification: N/A
Competencies:
Ability to work and prioritize independently
Strong computer and organizational skills; excellent oral and written communication in English; self-motivated
Adaptable to changing priorities; positive attitude
Quick learner; familiar with Good Documentation Practices (GDP).
Experience:
0 – 3 years in a laboratory, GMP preferred
Employment type
Contract
Job function
Science, Research, and Analyst
Industries
Research Services and Medical Practices
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