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<![CDATA[FDA registered Manufacturing plant has immediate opening for HPLC (High Performance Liquid Chromatography) Operator. 2+ years experience required. Must possess own methods and processes. Experience with Ketoconosole, Chlorhexidine, Miconazole, Triclosan etc. a plus.]]>

<![CDATA[<center><img src="http://www.rrmonstergraphics.com/landrys/rfc_animal_logo.jpg"> Rainforest Cafe - Sawgrass Mills Is Now Interviewing an: EXPERIENCED CURATOR to join the Landry’s Restaurants, Inc. family, one of America’s largest casual dining & entertainment companies. This individual will lead our Habitat Department in caring for a variety of tropical fish from all over the world. The job includes extensive educational interfaces with our guests via educational tours and outreach programs. Extensive knowledge and experience in maintaining and operating a complex aquarium system is an absolute requirement. </center> Position Requirements: - Must be SCUBA certified; First-Aid + CPR certifications a plus - Must be able to lift 50 lbs. and work in small spaces - Must be comfortable speaking to groups of various ages, especially children - Must have a flexible schedule and be willing to work weekends Education: - Degree in biology or closely-related field desirable but not required Experience: - Two or more years maintaining marine aquaria or familiarity with aquatic animal husbandry; Public aquarium experience preferred - Knowledge of tropical marine fish interaction, nutrition, and disease essential - Laboratory experience desired and must be able to work in a sterile environment with toxic reagents used to monitor water quality Responsibilities: - Maintenance of exhibits and behind-the-scenes quarantine and holding systems - Food preparation and feeding - Water quality monitoring and testing - Animal observation - Disease identification and treatment - Animal collection and transport - Diving in exhibits with surface-supplied air at least twice weekly - Provide enthusiastic educational tours for groups of various ages Compensation: - Commensurate with experience; We offer competitive salaries, excellent health and dental benefits. <center>To apply, please forward resume to: Email: sawgm@ldry.com and rfccareers@ldry.com Landry's Restaurants, Inc, a growing company, has over 180 units and is traded on the New York Stock Exchange under LNY. From coast to coast you'll find our innovative restaurant concepts - Landry's Seafood House, The Crab House, Rainforest Cafe, Cadillac Bar and Grill, Willie G's Steak and Seafood, The Aquarium, Muer Seafood Restaurants(Charley's Crab/Big Fish), Chart House and Saltgrass Steak House. We hire experienced and motivated individuals; train them in our systems, style and culture to prepare them for continued growth and leadership opportunities. Check out our website at www.LandrysRestaurants.com. EOE</center> ]]>

<![CDATA[Assisting in the manufacturing and production of skin care products. Ability to weigh products, basic weight and mass conversion knowledge, ability to follow procedures and directions, Bilingual in English and Spanish.]]>

<![CDATA[Job description Astellas is the bright spot in the pharmaceutical industry � not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. A high standard of ethics is mandatory. Quality is our pledge. Diversity is valued. Individual initiative is rewarded. Astellas offers an environment where our employees can make a real difference. Come, shine with us!This Medical Director plays a leadership role in the strategic creation and implementation of drug development programs for novel and existing compounds . The Medical Director will work closely with the Clinical and Drug Development Project Teams, as well as Sales and Marketing groups in order to facilitate this process. The Medical Director plays a key role in the design, conduct, analysis, and reporting of clinical trials including protocol development, evaluation of safety information from ongoing studies, data analysis and interpretation, and report writing. The Medical Director also has a primary role in interacting with regulatory authorities, both in helping direct strategy, preparation of key regulatory documents, and representing Astellas in meetings ]]>

<![CDATA[Rapidly growing pharmaceutical company in Palm Beach County seeks an experienced Quality Assurance/Quality Control Inspector. The Quality Assurance/Quality Control Inspector position performs in-line inspections and tests for quality control of the manufacture of pharmaceutical products as outlined in appropriate procedures. Essential Duties and Responsibilities: Ã¢Â€Â¢ Performs in-line inspections, ches, and tests for quality control batch records â€¢ Control product labels â€¢ Utilize and review batch records â€¢ Assist in validations and engineering studies as directed by the QA Supervisor Job Knowledge, Skills & Abilities: â€¢ Excellent verbal and written skills â€¢ Excellent mathematical and organizational skills â€¢ Ability to perform with minimal to moderate supervision Education and Experience: â€¢ THIS IS AN ENTRY LEVEL POSITION â€¢ Minimum HS diploma is preferred â€¢ Experience with pharmaceutical inspections preferred â€¢ Familiar with standard concepts and practices with generation of procedures and processes This company is an Equal Opportunity Employer dedicated to providing equal opportunity to all employees and applicants regardless of race, color, age, gender, sexual orientatioital or veteran status, disability or any other basis protected by federal, state or local law. The company is committed to providing equal employment opportunity with respect to recruitment, selection and all terms and conditions of employment. ]]>

<![CDATA[Rapidly growing pharmaceutical company in Palm Beach County seeks an experienced Quality Assurance Supervisor. The QA Supervisor position is responsible for the supervision of the Quality Assurance Department and assisting in maintaining the quality systems by ensuring compliance with regulatory requirements. Essential Duties and Responsibilities: Ã‚Â· Train and supervise quality control inspectors Ã‚Â· Generate and perform final review of batch records Ã‚Â· Track validation projects (media fill/SIP/Equipment IQ/OQ/PQ) Ã‚Â· Track and maintain Preventive Maintenance and Equipment files Ã‚Â· Assist in internal audits Ã‚Â· Perform employee performance reviews Ã‚Â· Analyze data and documentation for accuracy Ã‚Â· Develop, execute and summarize validation documents Job Knowledge, Skills & Abilities: Ã‚Â· Excellent communication and supervision skills Ã‚Â· Excellent verbal and written skills Ã‚Â· Knowledge of MS Office (Word, Excel, Outlook, Access) Ã‚Â· Professional appearance and conduct Ã‚Â· Ability to handle multiple tasks and deadlines Education and Experience: Ã‚Â· BachelorÃ¢â‚¬â„¢s Degree in Chemistry or Laboratory Science is preferred Ã‚Â· Minimum 2 years at supervisory level in small to mid-size company This company is an Equal Opportunity Employer dedicated to providing equal opportunity to all employees and applica race, color, age, gender, sexual orientation, national origin, marital or veteran status, disability or any other basis protected by federal, state or local law. The companmployment opportunity with respect to recruitment, selection and all terms and conditions of employment. ]]>

<![CDATA[With at least 2 years experience. English/Spanish preferred. To coordinate administrative and clinical aspects of multiple research protocols. Responsible for the initial submission, continued review and reporting of regulatory documents to the Sponsor and the assigned IRB. To deal directly with the Sponsor concerning all monitoring procedures and Internal Audits. To assure that the regulatory binders are kept up to date and that all guidelines of IRB, FDA and the Sponsor be adhered to. GCP knowledge. HIPPA compliance. Windows, Excel a must. RESUME: Diabetes@bellsouth.net]]>

<![CDATA[ • MD or DO (Physician) • Minimum of 1 year of work experience in clinical trials for pharmaceutical research • Accredited residency program in Internal Medicine and Specialties • Board certified a must. • . Excellent interpersonal skills; detail oriented, with ability to work in a Developing Environment. • Excellent English/ Spanish written and verbal communication skills. • Demonstrated ability to work independently and as part of a team, with minimal supervision • Preferred: Endocrinologist, Cardiologist, Internist, Hospitalist, Family Practitioner . Please Provide Updated CV . Able To Travel Once a Month. ]]>

<![CDATA[JOB DESCRIPTION Job Title: Chemical Laboratory Batching Manager Reports To: Director of Operations Department: Laboratory & Batching Full-Time Position TECHNICAL & FUNCTIONAL RESPONSIBILITIES: • The Chemical Laboratory & Batching Manager is responsible for developing, improving and batching/ mass producing chemical based products including liquids, powders, lotion, gels and creams. • The Chemist will test composition of substances by introducing heat, light, energy and chemical catalysts for quantitative & qualitative analysis. The Chemist is also responsible for maintaining reports and retains; and will prepare standards and specifications for processes, facilities, equipment, tools, products and tests. • Research new components • Develop, formulate and implement of the new products • Test completed formulation for package, chemical, and physical stability • Support transition of completed products from R&D to Manufacturing • Develop alternate formulations to reduce cost and improve performance • Prepare Certificate of Analysis, MSDS, Estimated Guarantee of Analysis • Perform raw material testing according to USP monograph including Specific Gravity, pH, Viscosity, Appearance, Loss on Drying and color comparison • Receive manufacturers' COA and MSDS for raw materials to establish in house specification • Adjust production batch products to meet finish products specification (acid/base demand, salt curve, dye solutions) • Collect and test samples of finished products to verify conformity to specification • Train batch supervisor in proper mixing procedures and resolve mixing problems • Ensure that work area and other relevant areas are kept in a tidy and orderly fashion • Organize COA, MSDS and other technical papers • Hold meetings with sales managers from different supplier companies • Keep clean shelves, sink, scales, mixers, other lab equipment and retain room • Find replacements for broken parts for lab equipment • Purchase new lab glassware • Help customer service with technical assistance • Provide technical support to Design department • Check new labels for ingredients accuracy • Half of time spent in the lab, while the other half will be on the manufacturing floor managing both workflow & other batching employees. • The Chemical Laboratory & Batching Manager must use appropriate tools to weigh chemical materials. The materials must be blended using an appropriately chosen vessel and the chemical materials must be introduced to the batching vessel while adhering to written mixing procedures. • Samples of all mixed material are tested in the laboratory for quality control. All batching team members must follow strict quality control procedures. • Attention to detail and perfection is an absolute must – as the Laboratory & Batching Manager is responsible for monitoring product quality to ensure compliance to the Company’s high standards and specifications. • Candidates must have professional experience with lab testing, chemistry, physics, pH testing, surfactants and numerous other globally sourced raw materials. SUPERVISORY RESPONSIBILITIES: 1. Plans, schedules and distributes incoming work to appropriate individuals. 2. Develops and maintains an effective organization through the selection, training, compensation, motivation, termination and review of direct staff. 3. Provides guidance and direction to batching staff to assist them in their professional development. 4. Communicates departmental & team members’ successes and failures with senior management. OTHER NECESSARY SKILLS: • Knowledge of Inorganic, Organic, Physical, Colloidal, Pharmaceutical chemistries and Biochemistry • Ability to analyze projects • Interest in research work • ability to organize and carry out multiple projects • Ability to work well within a team setting • Ability to work independently • Be detail oriented • Problem solving • Using scientific rules and methods to solve problems. • Using mathematics to solve problems, calculate efficiencies and batch as much product in a day as possible. • Watching gauges, dials or other indicators to make sure a machine is working properly. • Giving full attention to what other people are saying, taking time to understand the points being made, and asking questions as appropriate. • Using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. • Managing one’s own time and the time of others. • Understanding the implications of new information & new products for both current and future problem solving and decision making. • Recognizing problems and being open and willing to voice his/her opinion when something is wrong. REQUIREMENTS: • Candidates’ for the Chemical Laboratory & Batching Manager position MUST have a background working in a chemically based industry or manufacturing facility. • Must have an undergraduate degree in chemistry, biology or forensic science. • A background in mathematics is also preferred. • Must be able to communicate effectively in written and spoken English. • Must have 2+ years of management experience and 2+ years of experience working in a chemical lab. Must be able to operate HPLC, mass-spectrometry, autoclaves, dishwashers, drying ovens, top-loading balances, pH meters, viscometer, centrifuges TO APPLY: Please send a cover letter and resume to ctwomey@synergylabs.com with salary requirements and references. ]]>

<![CDATA[Scope of Function: 1. Primarily responsible for the development of new protein purification, protein modification and bio-conjugation manufacturing processes. 2. The characterization of intermediates and final products. 3. Responsible for the analyses of process step efficiency (e.g. purity, step loss, step yield, etc.). 4. The transfer of new or existing processes and procedures to manufacturing. 5. The resolution of technical problems and the monitoring of ongoing manufacturing campaigns. Specific Duties: 1. Downstream Process Development activities (cGLP and cGMP). Including chromatography (e.g. IEC, HIC, affinity and size exclusion chromatography, etc.) TFF sterile filtration and nanofiltration as applied to the purification and modification of antibodies and other proteins. 2. Addressing scale-up issues of process steps. 3. The development of filtration processes including Sterile Filtration, Ultrafiltration, Diafiltration, Microfiltration, and viral (Nano) Filtration. 4. Develop and perform in-process and final product testing as required (e.g. SDS-PAGE, western blots IEF, ELISA, activity/potency assays, protein concentration assays, HPLC and other assays). 5. The development and manufacturing of Bio-Conjugation and protein modification processes. 6. The implementation and transfer to production of processes (new and existing) defined during development. 7. Develop, plan and execute pre-GMP scaled process runs, establish Bill Of Materials list for process 8. The writing and execution of design input protocols and design output reports. 9. The writing of SOPs and batch records for newly implemented manufacturing processes. 10. Communicate and coordinate activities with other project team members to ensure the smooth transition and efficient transfer of project to manufacturing. 11. Implementation of new technologies as appropriate or as needed. 12. Assurance of process compliance with cGMPs and/or ICH guidelines as appropriate 13. Assurance of process compliance with and completion of all deliverables contained within the SOWs. 14. Maintain laboratory inventories and equipment. 15. Oversee and Train Process Development Associate Scientists as needed 16. Communicate the project status with clients and Project Management as needed 17. Manage Laboratory schedules to account for priority changes and project status 18. Multi-task multiple projects 19. Estimate Technical aspects of processes for Sales and marketing Education, Experience and Skills Required: Education: BS, MS, or PhD, in chemical, biological or biochemical sciences. Experience: BS 6+ years (or MS with 4+ years or Ph.D with 2+ years) of relevant process development and manufacturing experience in the Biotech industry with proven track record of accomplishments in the areas of protein purification, bio-conjugation and protein characterization). Experience with monoclonal antibody process development, manufacturing and characterization is a plus. Skills: Must be able to work semi-independently with minimum direction. Must be able to develop and implement to completion experimental protocols as they pertain to the duties listed above. Good communication and computer skills. Experience with process//product validation is a plus. ]]>