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<< Back to Employment Categoriescraigslist | science/biotech jobs in inland empireEstablished in 1987, our Company is a manufacturer of high-quality dietary supplements and functional foods. We are looking to hire a highly motivated QC Manager to head our Quality Control Department.
Regulatory Affairs & Compliance, Strong Technical Background and in-depth Chemistry Knowledge preferred. JOB RESPONSIBILITIES -Manage the QC / Compliance Department activities -Review formula and batch record for missing information and accuracy. -Review existing SOPs and update current procedures and documents. -Write standard operating procedures. -Perform internal GMP audits of production operations and compliance. -Perform supplier certification through supplier site audits. -Provide technical assistance to production and quality operations. -Provide continuous improvement (ISO 9001:2008) support. -Provide and train on current FDA GMP guidelines to all NHK employees and ensure compliance. -Find out non-conformances in operations, procedures and documents. -Write corrective actions requests and monitor implementation of corrections. -Adjust product formulae for production of good quality products. -Plans, coordinate, and direct quality control program designed to ensure continuous production of products consistent with established standards: -Develops and analyzes statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product. -Formulates and maintains quality control objectives and coordinates objectives with production procedures in cooperation with plant Manger and Production Supervisor o maximize product reliability and minimize costs. -Directs, through intermediate personnel, workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products. -Plans, promotes, and organizes training activities related to product quality and reliability. -May investigate and adjust customer complaints regarding quality. EDUCATION Bachelor degree in Science, Biology, Chemistry, Microbiology or Engineering We are located in Santa Fe Springs, California and we offer competitive pay and benefits. We do not discriminate on the basis of gender, age, religion, creed, color or national origin. We are an equal opportunity employer. Please email your resume to juan.gonzalez@nhklabs.com The Riverside Audiovisual Speech and Audition Laboratory at U.C. Riverside is looking for qualified individuals to participate in a speech perception study.
Qualified participants must: -be between the ages of 18 and 35 -have English as their first language -have normal hearing -have normal or corrected to normal vision The experiment takes about 30 minutes to complete and all participants will be compensated $10.00 for their time! If you meet the requirements and are interested in participating, please email James Dias at avspeechlab@gmail.com Position: Chemistry Technician/analyst
Duration: Full-time Permanent. Pay rate depends on experience (approx. $15 per hour). Typical hours: M-F 8:00am-5:00pm. DESCRIPTION: KC is a private-label pharmaceutical manufacturer. We have one current opening for a Chemistry Technician/Analyst. The ideal candidate will have some relevant experience using HPLC, GC, UV-VIS. Desirable qualifications: Research experience (graduate school, internship). REQUIREMENTS: *BS or BA in Chemistry (US institutions only; proof required before hiring). *Local candidates only. *Assist in testing of In-Process, Finished Product and stability samples, and raw chemical ingredients in accordance with written procedures. *Capable to apply and execute official procedures in USP, and/or EP or other methods and procedures. *Report activities to the Chemistry Supervisor. *Assist with other tasks for continuous quality improvement *Will be cross-trained to perform other routine tests as needed. *Computer literate, proficient in Microsoft Office applications. *Self-starter, detail-oriented, with cGMP and OSHA knowledge. *Desirable: be able to work at night and/or weekend occasionally. BENEFITS: *Paid sick days, holidays, and vacations. *Company helps to cover medical and dental insurance. *Free parking, and convenience access to major highways (10, 60, 57 freeways). Contact: ale@kc-ph.com Every day, those of us at Promethean Biofuels turn waste vegetable oil and inedible kitchen grease into renewable products that meet the demands required of a nation aspiring to energy independence. At our flagship plant located in scenic Temecula, California, we convert lipids and oil into products for animal feed, chemical and energy uses. For more information about our Cooperative and our products, visit www.newfuels.coop. We have a challenging opportunity as a Process Technician Trainee. Charged with learning our biofuel operations and will ultimately be responsible for biodiesel fuel production. We are seeking an individual with a unique background that includes chemical process and mechanical engineering experience. Reporting to the Plant Chemist, this person will have key role in critical process and manufacturing improvements. Responsible for the learning, implementation and maintenance of biofuel process methods Responds to related process problems and pursues and implements remedies to such problems Documents daily activities produce biodiesel from animal fats and vegetable oils. Performs tests and takes measurements throughout stages of production to determine degree of control over variables such as temperature, density, etc. Analyze operating procedures and equipment and machinery functions to reduce processing time and costs Evaluate emerging technology in the biodiesel industry and their worth to the company Review and analyze proposals submitted to determine if application and benefits derived justify expenditures Responsibilities: Maintain and improve the quality management system of an environmental laboratory, including developing and implementing new processes and procedures as needed. Lead the organizational effort to achieve ISO 17025 and/or NELAC certification. Support the organizations efforts in process improvement. Support managements improvement goals and ensure all work performed in the laboratory meets applicable regulatory and client requirements.
The successful candidate will: Possess strong organizational skills and the ability to work closely and effectively with a variety of personalities. Set an example of honesty and integrity. Leadership skills are also desirable. Requirements: Bachelors degree in chemistry or other science and 1 year applicable experience or Associates degree in laboratory technology or other science and 2 years applicable experience or Some college level science and 3 years applicable experience The desirable candidate will have a background in continuous improvement and possess at least one of the following: ASQ certification (CQA, CQE, CQIA, CQT etc) Experience in an ISO or NELAC certified organization Knowledge of and interest in TQM, Lean Manufacturing and/or Six Sigma principles Experience as an environmental analyst or microbiologist Recent graduates with no applicable experience will not be considered for this position. Local applicants only, relocation not offered. Synedgen, Inc is biotechnology company developing new biomaterials for use in anti-infective clinical and non-clinical pharmaceutical applications. We currently have an opening for a Senior Regulatory Affairs Manager.
Overall Responsibilities: Responsible for managing regulatory affairs for the development of drug FDA regulated products through CDER, managing regulatory compliance, evaluating regulatory issues and providing accurate and timely recommendations and alternatives, as needed, to management and functional business units. Serves as a team leader on the development and submission of IND and NDA applications, control and management of documents and binders, as well as providing oversight on clinical trials, toxicology requirements and CMC documentation. This individual interacts with FDA and must have a firm command of regulations and guidelines pursuant to federal, international and corporate regulatory requirements and standards. Experience with international product registration is beneficial. Act as the regulatory project manager for IND and NDA document preparation and compliance, amendments, binders, supplements, annual reports, control documents, etc., for FDA submissions to CDER. Interact effectively with functional business units in order to coordinate and facilitate documentation required for submissions, ensuring that timelines are met. Mentor other associates in proper documentation and regulatory compliance including review change requests and the preparation of FDA submissions. Participate and contribute to strategic planning for multiple submissions to CDER and leveraging of previous IND and NDA components Evaluate changes to regulatory documents, updates, FDA requests and formulates strategies to maintain submission goals. Assure timely submissions and expeditious approvals. Successful applicant will demonstrate: Strong critical and logical thinking. Thorough knowledge of all FDA requirements pertaining to the control and submission of regulatory documents for drug approval Excellent organization skills and the ability to multi-task; detail oriented. The ability to establish and maintain good working relationships at all levels of the company and with external contacts. Excellent verbal and written communication skills. Share concepts, ideas, information, and suggestions with management, peers and others. The ability to evaluate regulatory documents and determine appropriate action. The ability to provide regulatory assessment to other departments with little or no supervision. REQUIREMENTS: Minimum of a Masters degree or 5 years industry experience; PhD preferred A minimum of 4 years of full-time regulatory FDA drug experience Demonstrated experience in project management and FDA documentation A working knowledge of FDA and regulations and how to interpret and monitor updates with experience or knowledge in US Title 21 CFR Parts 300-314 Subchapter DDrugs for Human Use Domestic and international travel may be required. Must be willing to relocate. For consideration, submit FULL resume and contact information for three references. Specialty Enzymes and Biochemicals Company
Laboratory Manager Chino, California. Specialty Enzymes and Biochemicals Company, a rapidly growing enzyme manufacturer and distributor, is in need of an experienced Laboratory Manager. This position requires a successful history of supervising and training laboratory personnel. Other requirements include 5 years laboratory experience including a thorough knowledge of GMP procedures, QA/QC standards. A degree in chemistry, biochemistry, biology or microbiology is preferred. A background in food science, flavor science, enzymes, pharmaceuticals, nutraceuticals or a related field will be acceptable. Responsibilities include quality control, R&D, maintaining GMP standards and managing laboratory staff. Salary is commensurate with experience. EOE. Fax or email your resume and cover letter, MUST INCLUDE SALARY HISTORY to (909) 613-1663 or email to mike@specialtyenzymes.com. Please note, resumes without a salary history will not be considered. Mining Consultant in need of a certified geologist to work in a mine in Mexico. Must have vast knowledge and experience in exploration and mines. Please send resume to the above email. Serious Inquiries Only.
Spanish Speaking a Must Veolia Water North America is looking for an Operations Supervisor for its Rialto, CA Wastewater Treatment Plant. The Operations Supervisor supervises two or more full time employees and plans and coordinates activities of workers to operate and maintain wastewater treatment, processing, disposal and testing equipment in wastewater treatment facility to meet permit requirements and operational requirements.
Requirements - NOTE: preference will be giving to candidates local to the jobsite address. - Must have an understanding of wastewater treatment process engineering, wastewater quality assurance, maintenance strategy, and laboratory procedures. - Highest level of Wastewater Certification with knowledge of current and pending wastewater treatment standards, regulations and federal, state and local laws and codes. - Lead experience in various positions within a wastewater treatment environment with knowledge of methods, principles and practices of operating, maintaining and repairing wastewater treatment plant equipment, instrumentation and associated systems. - Five to seven years experience or supervisory training required with understanding of human relations, training, performance evaluation and health and safety. - Demonstrated ability to prepare accurate, timely, effective, complete, and easily understood written communications and reports. - PC skills and knowledge of word processing, spreadsheet and presentation software for preparing work related reports, charts, graphs and data submittal requirements. Ability to use computer systems for preparing work orders and purchasing requisitions. - Must be able to respond to emergency calls as needed and work extended hours to accommodate site needs. - Must be able to pass a drug screen and criminal background check. - Must possess a valid driver license and safe driving history. We do not list compensation in our job advertisements; however, we have a competitive salary plan and benefits package. To apply, please visit our website at www.veoliawaterna.com/careers and apply to position 04999. Regional CRA for immediate need. As key team members supporting new drug applications, the Regional CRA is accountable for on-site clinical monitoring activities from study start-up through close-out. As specified in the monitoring plans, the RCRA will perform source document verification review of Case Report Forms, oversee drug accountability, as well as manage investigational site to ensure compliance with FDA regulations, ICH/GCP guidelines, and company SOPs.
Requirements: Travel These positions are home-based and require over 50% travel Experience: For you to be the successful candidate we are looking for in these roles you must have a proven track record of monitoring clinical trials in a variety of Therapeutic Areas through the CRO or Pharmaceutical industry Education: For consideration, you must hold a Bachelor's degree, preferably in a scientific or nursing discipline Due to the precise requirements of these positions, we will only be contacting candidates that meet all of the listed criteria. If you are qualified and interested in the excellent career opportunities we have for you, please reply to this ad immediately with your CV and availability. Join SEG and our rapidly growing southern California-based environmental consulting firm that's helping to find and solve indoor air quality problem. We are looking for a talented, passionate, and experienced professional to help us maintain and calibrate the existing equipments, and also design new devices for taking environmental samples. This is a technical position and the candidate should be able to work independently with minimum supervision. You should have experience in calibrating, maintaining, and trouble-shooting indoor air quality equipments and have the ability to consistently come up with new ideas for developing devices that can be used in IAQ industries. We offer a competitive compensation and benefits package. You should have a mechanical engineering degree or equivalent and able to perform the following duties:
- Daily calibration and maintenance of equipments such as low and high volume pumps, RH and temperature meter, cell flow indicators, rotameter, high flow defender calibrator, IH canisters, air quality meter, moisture meter, AC/DC charger, HVAC filters, negative air machines, fans, dryer, and thermal imaging and infrared cameras. - Supervise technicians, train them how to operate, prevent, and control accidents or hazards. - Product verification and hardware design. - Responsible for testing, compliance and standards. - Provide product support for field service operations and manufacturing. - Work closely with other testing laboratories, record data and test results, order material and equipments, maintain and update technical documents and inventories in a large computer database. - Prefer bilingual (Japanese or Chinese) candidate since this job will require frequent travel to Asia. Looking for experienced Exterminator!
Must have Pest Control License 2 Years Experience Clean Driving Record No D.U.I.'s or Felonies Come in to Apply! Monday thru Thursday 1pm-4pm ONLY! 26205 Jefferson Ave. Suite 103 Murrieta, CA 92562 Phone: 951.677.0600 Fax: 951.677.0366 You may also Apply online at: www.ResumesPlusTempService.com Requires a Bachelors degree or higher in botany, plant ecology, hydrology, soil science, geography, or related environmental or earth science field with three years experience in spatial data analysis or equivalent post-graduate study beyond Bachelors level. Inyo County offers an an excellent benefit package, including employer-paid CalPERS retirement (2% @ 55), employer-paid medical, dental, vision, and life insurance. Live and work in an area that offers an excellent quality of life and endless recreational opportunities including fishing, skiing, hiking, climbing, camping, and more! To obtain a complete job description and an Inyo County application form, contact the Personnel Office, P.O. Box 249, Independence, CA 93526, (760) 878-0407, or the County of Inyo website: www.inyocounty.us. Deadline for application: 5:00 p.m., September 1, 2010 (postmarks not accepted). Must apply on Inyo County application form. EOE/ADA. Looking for experienced Exterminator!
Must have Pest Control License 2 Years Experience Clean Driving Record No D.U.I.'s or Felonies Come in to Apply! Monday thru Friday 1pm-4pm ONLY! 26205 Jefferson Ave. Suite 103 Murrieta, CA 92562 Phone: 951.677.0600 Fax: 951.677.0366 You may also Apply online at: www.ResumesPlusTempService.com R&D Intern
Part time- 20 hours per week for 3-6 months (contract assignment) $8.25 per hour (negotiable) Functions: Requires: Candidates are encouraged to apply in person as we are looking to fill this position right away. Application hours are from Monday-Friday, 8am to 11am only. Personnel Plus, Inc. 15648 Arrow Hwy. Irwindale CA 91706 (626) 856-2722 |
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