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		<title>Bausch and Lomb - Bausch &amp; Lomb cGMP Jobs</title>
		<link>http://bauschandlomb.jobs2web.com/go/Bausch-&amp;-Lomb-cGMP-Jobs/13322/</link>
		<description>View Bausch &amp; Lomb cGMP Jobs at Bausch and Lomb</description>
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			<title><![CDATA[Bausch and Lomb - Bausch & Lomb cGMP Jobs]]></title>
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		<title>Maintenance Associate III / Utility Operator Job (Tampa, FL, 33603, USA)</title>
		<description><![CDATA[<b>Job Title:</b><br> Maintenance Associate III / Utility Operator
<br><br><b>Req #:</b><br> 5175BR
<br><br><b>Job Description:</b><br> The Maintenance Mechanic performs limited or routine preventative maintenance duties and repairs of Utility and Facility equipment and systems as assigned, and assists skilled mechanics in performing maintenance duties.
Essential Job Functions:
. Performs preventative maintenance on all minor and major pieces of equipment related to Utilities and Facility.
. Performs daily testing of boiler water and soft water systems; troubleshoots and repairs steam and hot water equipment.
. Troubleshoots and repairs utility and facility equipment and/or systems including mechanical, electrical, pneumatic, or hydraulic circuits (motors, pump, compressors, boilers, chillers, and water system)
. Performs basic building and equipment repairs using hand tools, power tools and basic electric multi-meter skills
. Assembles basic components from supplied instructions or drawings
. Performs basic maintenance of non-critical equipment using lubrication utilizing oil or grease pumps/guns,replacing and adjusting drive belts, replacing filters, replacing lights, light pipe fitting and replacing mechanical parts supplied original manufacturer parts
. Picks-up ordered parts or suppliers and restocks parts or supplies
. Complies with all equipment, safety, cGMP, ISO, FDA, OSHA, and any other outside agencies rules and regulations
. Monitors and responds to computerized control systems for HVAC, Water, and Environments, including making routine rounds in utility area to log equipment data.
. Enters maintenance data into Computerized Maintenance MGMT (CMMS) system
. Performs cleaning and painting as needed in utility areas
. Covers the different shifts for operators vacations
Must possess a valid driver's license and acceptable driving history.
Knowledge of the following areas is required:
. cGMP, FDA, and other regulatory requirements
. Facility and equipment operations and maintenance practices
. Standard Operating Procedures for equipment operations including safety rules and regulations
. Basic electrical and mechanical control and/or operating systems.
. Mechanical aptitude and basic mathematics
. Basic computer skills, such as Windows, Microsoft excel and word
. Ability to read basic blue prints.
Primary 1st shift /Floating for vacation coverage.
Weekends/OT may be required
<br><br><b><u>Qualifications</b></u><br> <br><br><b>Education:</b><br> this role requires a high school diploma or equivalent, hands-on or vocational school training preferred.
Experience: minimum of 3 year of experience as a general Maintenance Mechanic and/or utility operator in a manufacturing environment or equal combination of training and experience is required.
<br><br><b>Special Skills:</b><br> Facility and equipment operations and maintenance practices
. Standard Operating Procedures for equipment operations including safety rules and regulations
. Basic electrical and mechanical control and/or operating systems.
. Mechanical aptitude and basic mathematics
<br><br>Work Location FL - Tampa
Relocation Available No
<br><br>Status Full-Time]]></description>
		<link>http://bauschandlomb.jobs2web.com/job/TAMPA-Maintenance-Associate-III-Utility-Operator-Job-FL-33603/563781/?utm_source=J2WRSS&amp;utm_medium=rss&amp;utm_campaign=J2W_RSS</link>
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		<title>Scientist I Job (Tampa, FL, 33603, USA)</title>
		<description><![CDATA[<b>Job Title:</b><br> Scientist I
<br><br><b>Req #:</b><br> 5316BR
<br><br><b>Job Description:</b><br> To provide analytical support to R&D analytical operations by executing methods development and validations, and methods transfer. Supporting site analytical and R&D investigations & process improvement projects. These include, but not limited to finished products and raw materials qualification, analytical method development and validations, testing of process and cleaning evaluations and validations samples; evaluating container and closure systems leachables and extractables. Providing technical support in the designing, specifying, commissioning, overseeing systems, testing and releasing of clinical trial materials. Complying with company cGMP and safety practices and procedures, including, participating in GMP training and FDA audits.
<br><br><b>Job Duties:</b><br>
- Analytical support for analytical method development and validation, and testing of sterile and non-sterile solutions, suspensions, and ointments, nasal and injectable products, and any other product type manufactured at the site, and as deemed necessary by the company.
- Develop and validate analytical test method procedures for new and existing products deemed necessary by the company.
- Qualify new raw material supplier chemical ingredients, and develop and validate analytical test method procedures for use in releasing them in commercial environment.
- Participate or lead analytical method transfer process to QC, other R&D, or CRO labs.
- Demonstrate effective technical skills in technical writing, data collection and analysis skills.
- Participate in project team environment, and maintain technical skills by keeping up with current analytical training.
- Conducting investigations to support R&D projects and commercial product testing.
- Other duties not included above, but are required to support the growth and viability of company.
<br><br><b><u>Qualifications</b></u><br> <br><br><b>Education:</b><br> BS, MS, or PhD in Chemistry, Biology, or related physical sciences.
Experience: Minimum of one year experience in analytical chemistry in pharmaceuticals with BS. Entry level for higher level degree.
<br><br><b>Special Skills:</b><br> Computer literate, and is able to use MicroSoft Office software (Word, XL, PowerPoint, Project, Vision, etc.)
Specialized Training: Empower, LIMS experience are positives.
<br><br>Work Location FL - Tampa
Relocation Available No
<br><br>Status Full-Time]]></description>
		<link>http://bauschandlomb.jobs2web.com/job/TAMPA-Scientist-I-Job-FL-33603/644696/?utm_source=J2WRSS&amp;utm_medium=rss&amp;utm_campaign=J2W_RSS</link>
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		<title>Sr. Microbiologist Job (Greenville, SC, 29603, USA)</title>
		<description><![CDATA[<b>Job Title:</b><br> Sr. Microbiologist
<br><br><b>Req #:</b><br> 5317BR
<br><br><b>Job Description:</b><br> The Senior Microbiologist is responsible for providing technical expertise/leadership as subject matter expert in the area of pharmaceutical microbiology. An emphasis will be placed in providing direct support for microbiology investigations, trend analysis metrics, LIMS Support, Validation, training, Environmental and Personnel Monitoring and technical studies for the Microbiology department. This position has no direct reports but at times where the microbiology management may be out of the office, can provide direct support to personnel, as needed. The Sr. Microbiologist provides analytical expertise and informational support to the Global Quality, Research and Development organizations, and other Bausch & Lomb sites on an as needed basis. This position is responsible for creating and executing against strategic goals, providing limited overall direction and oversight in the attainment, measurement and monitoring of established site level performance metrics.
Job Duties Include but are not limited to:
Responsible for completion of all Microbiology Investigations.
. Support implementation of LIMS system. Eventually, the position will administer the system for the laboratory.
. Support microbiology validations. Prepare protocols, final report, and technical studies as needed.
. Review and or approve sterility testing, bioburden testing, EM data, growth promotion, microbial ID, and other microbiological tests when necessary.
. Prepare and analyze trend analysis reports of EM, sterility and other microbiology test data as needed.
. Provide/coordinate training, re-<br><br><b><u>Qualifications</b></u><br> and certification as needed.
. Promote a culture a safety in the laboratory.
Qualifications <br><br><b>Education:</b><br> MS degree in Science, Microbiology, Biology or related discipline.
Experience: 4-8 years of microbiology experience in a biopharmaceutical/medical device industry.
<br><br><b>Special Skills:</b><br> Must have demonstrated expertise and knowledge in microbiological principles and application related to sterility testing, microbial identification, GMP laboratory practices and clean room technology.
Must have demonstrated computer literacy skills (e.g. Microsoft Office, Oracle, LOTUS Notes, etc.). Should have demonstrated proficiency in LIMS or other trending database applications. Demonstrated ability in statistical process control is a plus.
Specialized Training: Trained in cGMP for laboratory operations and compliance to regulatory guidelines with working knowledge of microbial ID systems, (VITEK 2, Biolog, ect), USP sterility and bioburden test methods to include use of Isolator technology).
<br><br>Work Location SC - Greenville
Relocation Available Yes
<br><br>Status Full-Time]]></description>
		<link>http://bauschandlomb.jobs2web.com/job/GREENVILLE-Sr_-Microbiologist-Job-SC-29603/644697/?utm_source=J2WRSS&amp;utm_medium=rss&amp;utm_campaign=J2W_RSS</link>
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