Microbiologist
Job
Hill Dermaceuticals, Inc.
Sanford, FL (In Person)
Full-Time
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Job Description
Microbiologist Sanford, FL Job Details Full-time 22 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Qualifications Stability testing CGMP Document review (document control) Microbiology GLP 5 years Pharmaceutical regulatory compliance Bachelor of Science English GMP Mid-level Microbiology Bachelor's degree Attention to detail Laboratory compliance Laboratory quality control Laboratory techniques Organizational skills Microbiological analysis Bachelor's degree in microbiology Bachelor of Arts Full Job Description Hill Dermaceuticals, Inc. is a privately-owned pharmaceutical company dedicated to developing and manufacturing innovative dermatology products for children and adults. We specialize in solutions for challenging skin conditions such as scalp psoriasis, eczema, melasma, and actinic keratosis. Join a team committed to improving patients' lives with science-backed skin therapies. The QC Microbiologist is responsible for performing microbiological testing for incoming raw materials, in-process samples, finished drug products, stability samples, consumer complaint samples, environmental monitoring samples, and other general testing in support of production activities. The QC Microbiologist has the responsibility to ensure current test procedures are followed, test materials are suitable for the intended use, and to allocate time for the timely completion of assigned tasks. The QC Microbiologist must review and approve assigned documents and assist in investigations as necessary to make quality decisions regarding acceptability of microbiological test results. Perform all microbiological testing and equipment set-up/operation as per procedures, while testing the following: Raw Materials In-process Samples Finished Drug Products Stability Samples Consumer Complaints with Samples Environmental Monitoring Samples Cleaning Verification Other special testing as required for validation, qualification, and protocol studies. Maintaining all laboratory documentation requirements with respect to content, completeness, accuracy, and timeliness of completion. Assist in laboratory investigations as required. Report any unexpected or anomalous findings to supervisor or manager. Additional assignments may be given by management. Qualifications and Education Requirements Bachelor's degree (BS or BA) in microbiology or equivalent. At least 5 years' experience in a cGMP pharmaceutical laboratory setting preferred.
Skills / Experience
Requirements Excellent organizational skills with high attention to detail. Strong ability be able to operate in an independent manner. Knowledge of Good Laboratory Practices (GLPs), Current Good Manufacturing Practices (cGMPs), and federal regulatory requirements.Benefits:
401(k) Dental insurance Health insurance Paid time offEducation:
Bachelor's (Preferred)Language:
English (Preferred)Work Location:
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