HAYWARD LABORATORIES, Inc. - East Stroudsburg
,
PA
The QC Microbiologist is responsible for performing all microbial testing in an accurate, consistent and precise manor. Job Functions Employee is to perform microbial content testing on raw materials, in process bulk and finished product samples Employee is to maintain documentation and records of the above testing in a computer to prepare report Employee is to analyze, interpret, and compile data in result report(s) for completed testing on raw materials, in-process bulk, and finished product samples. Employee is to prepare and maintain microorganism cultures in the microbiology lab Employee is to control lab supplies inventory. Employee is to endeavor to acquire new technology related to microbiology Employee is to perform other duties as assigned. Requirements B.S. degree in Microbiology or equivalent science courses is mandatory. Basic knowledge of aseptic techniques, media preparation and culture maintenance Knowledge of current FDA, USP, EU and ISO test procedures Be able to set
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Yoh, A Day & Zimmermann Company - Rockville
,
MD
Job Description Job Description QC Microbiologist needed for a contract opportunity with Yoh Scientific’s client located in Rockville, MD. This position is for a pharmaceutical company and is seeking an Expert Scientist in Quality Control Microbiology with experience or specialty in endotoxin detection methods. The ideal candidate would have 3 years or more experience in working in research and/or analytical development and/or quality control functions. Shift: Monday through Friday, standard day shift. 100% onsite. Key Responsibilities Design and execute method development and GMP validation for recombinant factor C endotoxin testing. Contribute to method development and method qualification. Perform laboratory operations to support and implementation of compliant, state of art methodology and instrumentation. Provide scientific understanding and analytical support for development of new test method, validation, and specifications. Support for scientific report writing and document rev
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The QC Microbiology Associate will be responsible for all aspects of microbiological issues, including but not limited to the following: writing and validating microbiological procedures, testing samples and interpretation of results. Responsible for obtaining samples and coordination the timing and testing of each sample as described in the SOP. **US Citizens or Greencard Holders only** Pay Rate: $25/hr Location: San Bernadino County Responsibilities: Perform microbiological testing of bulk samples, finished goods, raw materials and other samples as outlined in SOP’s. Perform preservative efficiency/challenge testing. Review, interpret and perform test protocols as directed. Develop and coordinate document control related to microbiological testing. Maintains and coordinates equipment calibration to support QC compliance in key aspects. Maintain various logbooks with departmental data. Support the department by typing memos, reports and spreadsheets with distribution and filing as req
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Anika Therapeutics - Bedford
,
MA
Position Scope: Responsible for microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.) Strategic Focus Area: Effectively collaborates with internal colleagues to meet corporate objectives and drive business results. Demonstrates business and regulatory knowledge. Specific Responsibilities: * Perform bioburden, sterility and endotoxin testing of raw materials, in-process samples, bulk and finished products and stability samples * Perform company's purified water and DI water bioburden, endotoxin and TOC testing as per USP requirements * Complete all required documentation according to SOP * Write validation protocols, perform validation and write validation reports * Update database for microbiological and validation data * Perform environmental monitoring investigations, out of specif
- 1 day ago
Planet Pharma - Memphis
,
TN
QC Microbiologist Needed ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability Participates with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.) Responsible for assisting with routine laboratory upkeep and organization Utilizes GMP systems such as MODA and other laboratory computer systems Reviews test results of other QC analysts for accuracy and precision and maintains and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates Perform all other related duties as assigned. QUALIFICATIONS: Bachelor's degree in
- 1 day ago
Noven Pharmaceuticals - Miami
,
FL
Overview: Performs professional, technical laboratory functions. Responsibilities: The QC Microbiologist I - is an entry-level role in the Microbiology Quality Control, responsible for performing Microbiological laboratory testing associated with Environmental Monitoring (EM), Purified Water (PW), and product specific Microbiological samples. Additionally, Microbiologist I, will be trained to perform Environmental Monitoring (EM) and Purified Water (PW) sampling in support of cGMP manufacturing activities associated with transdermal manufacturing. The Microbiologist is expected to follow all policies and procedures which include but are not limited to; Standard Operation Procedures (SOPs), Work Instructions (WI), current Good Manufacturing Practices (cGMPs), and current Good Laboratory Practices (cGLPs). Perform Microbial Limit Testing for finished products and raw materials to assess potential microbiological contaminants. Creates and maintains laboratory record documentation in compl
- 2 days ago