eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-39 of 39 ads in Fairfield

Job Title: Director of Environment, Health & Safety (EHS) Location: White Plains, NY Type: Full-time/Direct-hire Summary: The purpose of this position is twofold. It is to promote a safe and healthful workplace that protects the employees, community and environment by establishing and implementing environmentally sound business practices and complying with all state/federal and local regulations and applicable guidelines.  In addition it is to promote and coordinate (identify, establish, conduct and ...

Job Title: Associate DIr. Quality Assurance & Auditing # of Positions to Fill: 1 Location Country: United States State/Region: NY City: Tarrytown Compensation Base Salary: tbd Functions Quality Assurance / Safety Industries Pharmaceutical / Biotech Other factors Will Relocate Interview Travel Reimbursed Detailed Description Associate Director, Quality Assurance & Auditing If you are looking for an uncommon opportunity -- a chance to join an organization known for its scientific ...

Allied Search Partners, the only boutique laboratory staffing firm in the country is currently working to identify a qualified laboratory professional. Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Job Title: Cytopreparatory Technician (Cytoprep) Location: Port Chester, NY area Schedule: Monday-Friday 10pm-6am/Full ...

Title: Clinical Project Manager (Official title - Feasibility Analyst) Company: Pharmaceutical Location: Southwestern CT Duration: 12 months extendable Role: • Responsibilities include: data driven analyses/evaluation/recommendation of investigators/sites for future/on-going studies; internal/external communications; cross-functional collaboration and analysis; presentations to senior management, CTMS usage/analysis. • Responsible to recommend high-quality potential investigators to meet ...

Drug Safety Medical Doctor Ridgefield, CT  1 year contract Physician with internal medicine residency and some clinical practice. Also must have safety physician experience in PV department doing med review for single case processing. Assessing individual clinical trial and spontaneous case reports for determining regulatory reporting responsibilities; assessing seriousness, expectedness and comparing causality and querying for additional medical information needed to understand the event ...

Champion aspects of transgenic and knockout production at a major company including embryo production and recovery in transgenic and knockout mice by performing: *** Pronuclear and blastocyst injections *** Egg and blastocyst implantation into pseudo pregnant mice *** Hormone injection to induce super-ovulation *** Identify pseudo-pregnant recipients for embryo transfers *** Collect mouse eggs and blastocysts High visibility position with an international pharmaceutical company includes ...

Contact Kimberly at 815-756-1221 for more details. Qualifications: - PhD Chemistry, Chem-E, Materials Science - 5+ years formulating coatings for metal protection - Working knowledge of synthetic and colloidal chemistry and adhesion science - Excellent communication skills - US Citizen/Perm Resident Job Scope: - Will assist with design and promotion of new products to meet current market needs - Plan and execute projects - Responsible for products from concept to commercialization

Contact Kimberly at 815-756-1221 for more details. Qualifications: - BS+ Chemistry, Chem-E, Materials Science - 5-10 years of tech service and coatings formulation experience - Working knowledge of metal pre-treatment desired - Excellent communication and interpersonal skills - US Citizen/Perm Resident Duties: - Responsible for product promotion and development - Give input for new functional silicones that will add value to products - Customer interaction, troubleshooting, support, etc. - Travel ...

MECHANICAL/PRODUCTION TECHNICIANS NEEDED ASAP (ORANGEBURG AREA, NEW YORK) A leading manufacturer of spray pumps for pharmaceutical, cosmetic and food and beverage industries is looking for experienced career minded technicians to join our growing high tech manufacturing team as Mechanical and Production Technicians at our facility in Orangeburg area, NY. Positions are available on our (4 day) Monday - Thursday AM or PM shifts or our (3 day) Friday - Sunday AM shift. As a Mechanical/Production ...

QUALITY ASSURANCE MANAGER NEEDED ASAP! COMPETITIVE SALARY + BONUS & EXCELLENT BENEFITS!!~ Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA inspectors and Documentation Review Group. Reviews and approves ...

Mechanical/Production Technician About the Job A leading manufacturer of spray pumps for pharmaceutical, cosmetic and food and beverage industries is looking for experienced career minded technicians to join our growing high tech manufacturing team as Mechanical and Production Technicians.. Positions are available on our (4 day) Monday - Thursday AM or PM shifts or our (3 day) Friday - Sunday AM shift. As a Mechanical/Production Technician, you will provide full technical support to our production ...

QUALITY ASSURANCE MANAGER NEEDED ASAP!!! (Nyack) QUALITY ASSURANCE MANAGER NEEDED ASAP! COMPETITIVE SALARY + BONUS & EXCELLENT BENEFITS!!~ Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA ...

We are hiring a Medical Publications Manager to work with a major pharma located in Ridgefield, CT. The person must work onsite. Medical Publications Manager Degree / College Major:  PhD in life sciences. Number of Years Work Experience Required:        5+ Minimum Requirements: o PhD degree in biomedical discipline or equivalent o Knowledge of the drug development process o Excellent written and oral communication skills, manifested as the ability to express medical information accurately, clearly, ...

Allied Search Partners is currently looking for a qualified, NY Licensed, Grossing Technician or Technologist to work the day shift for a Grossing Histotech Job Opening. Know someone for this position? We pay you $$ for any of your referrals that we place in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Sign On Bonus: One of the benefits of working with Allied Search Partners is that we offer a ...

 Job Title: Director of Radiopharmaceuticals Manufacturing and Process Sciences Location: White Plains, NY Type: Full-time/Direct-hire     Summary This position will be responsible for process development of radiopharmaceutical therapeutic and imaging products. The position is also responsible for manufacture of radiopharmaceuticals and active pharmaceutical ingredients at external Contract Manufacturing Organizations (CMOs). As a key leadership role which reports to the Senior VP of Manufacturing, ...

East Coast-based Global pharmaceutical seeks Associate Director Medical Writing to join their team.  This is a highly successful company with a diverse product line.   The position can be 95% remote (work from home) for US-based candidates.  Excellent compensation, bonus, benefits.  Relocation also offered for candidates who prefer to work in-house. The Associate Director Medical Writing: ·         Executes medical writing activities for projects in accordance with applicable regulatory regulations ...

Contact Kristine at 815-756-1221 for more details. The Sensory Director will be responsible for the advancement of current products. They will also manage technical experts, provide direction and training to the sensory and consumer programs. Qualifications: - MS/PhD in Behavioral or Food Science - 10+ years of sensory and consumer science experience within the food and beverage industry - Working knowledge of sensory techniques, qualitative consumer techniques, data analyses, market-research ...

Assist with aspects of genetically modified mouse creation including embryo collection, DNA cell microinjection, embryo transfer, animal care, and detailed record keeping. Must possess at least 3 years experience performing DNA or ES cell microinjection experiments on a daily basis for the routine, predictable, and reproducible production of genetically modified mice. Work along side our industry recognized, Ivy League personnel in this highly visible position. Top base salary to $80,000 and ...

The Surgical Sales Representative would be responsible for selling surgical products in accordance with budgeted objectives and to obtain maximum profitability and volume in relation to pre-set standards Responsibilities include: - Educate and inform doctors, nurses, and appropriate staff personnel as to the proper use and maintenance of company products - May direct product evaluations in OR and office settings - May assist in the preparation and operation of trade shows, conventions, and/or ...

Allied Search Partners is currently looking for a qualified, NY Licensed, Grossing Technician or Technologist to work the night shift for a Grossing Histotech Job Opening. Know someone for this position? We pay you $$ for any of your referrals that we place in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Position Name: Grossing Technician (Histotech) Location: Port Chester, NY area Schedule: Full ...

Feasibility Analyst Study Feasibility and Site Selection Therapeutic Area  (1) Oncology (1) Immunology Responsible to recommend high-quality potential investigators to meet study requirements and timelines. Works pre-allocation through Initiation of a study.  The Feasibility Analyst will be the primary operational contact and project manager for the Site Selection activities in the U.S. Activities may be done in consultation with TCM, CML, CDMA, and other clinops functions Conduct Strategy ...

Associate DIr. Quality Assurance & Auditing Other factors Will Relocate Interview Travel Reimbursed Detailed Description Associate Director, Quality Assurance & Auditing B If you are looking for an uncommon opportunity -- a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals Founded on the principle that strong science would lead to important new medicines, We have become an integrated biopharmaceutical company that ...

Screens and evaluates any gynecologic and non-gynecologic specimen sent to the laboratory for the determination of possible malignant or related abnormal conditions. Administrative: Answer telephones, maintain logs/records, organizational skills, proficiency with numbers, research information, time management, train employees, use computerized databases, written and verbal communications. Speech clarity, utilization of fingers and hands, standing-remaining on one’s feet in an upright position, ...

Job Details: - Evaluates and makes best use of patient specimens. - Performs assigned functions in flow, to include specimen preparation, testing, and evaluation as needed. - Completes preventive and corrective maintenance on equipment as instructed by policies and procedures. Troubleshoots instrument malfunctions to ensure timely repair. - Complies with all standards and regulatory requirements. - Follows the policies and procedures of the organization. - Responsible for accuracy and ...

Overview: Reconciliation of cytology specimens. Process cytology specimens by opening, labeling, numbering, verifying patient identity and enter information from the test requisition. Gross and prepare smears, mono-layered cytospins and cell blocks. Stain, cover slip, collate and book all cases. Operation of and responsible for all clinical testing (urinalysis, breath test, proficiency tests) the documentation and quality assurance surrounding both cytology and clinical testing. Responsibilities ...

Key Responsibilities - Evaluates and makes best use of patient specimens. - Performs assigned functions in flow, to include specimen preparation, testing, and evaluation as needed. - Completes preventive and corrective maintenance on equipment as instructed by policies and procedures. Troubleshoots instrument malfunctions to ensure timely repair. - Complies with all standards and regulatory requirements. - Follows the policies and procedures of the organization. - Responsible for accuracy and ...

• Ensure specimen integrity upon arrival and throughout the entire process. Dictate a gross description for each biopsy specimen, dissect and prepare tissue for cassettes. • Gross core needle biopsy and all anatomical pathology specimens (under the supervision of a Pathologist Assistant and /or pathologist). • Prepare dissected tissue specimens and place into cassettes. • Load prepared cassettes in Tissue Processors. • Operation of all tissue processors. • Familiar with safety procedures and standard ...

MUST HAVE NY STATE LICENSE!!! Candidate will serve as a technical specialist in IHC testing as well as receive, prepare and process pathology specimens, following approved standards, policies & procedures. • Ensures steady workflow and accurate testing information. • Diagnoses IHC instrument malfunctions, performs preventive & corrective maintenance and repairs & maintains records. • Candidate will provide coverage in histology operations as necessary • Analyze laboratory reports for ...

Job Responsibilities: 1. Provides oversight for routine histology functions inclusive of processing, embedding, microtomy, and staining. 2. Oversees daily routine laboratory operations on each shift to ensure that quality standards and turnaround time are met. 3. Maintains quality control standards within CAP and CLIA guidelines. 4. Performs personnel performance reviews and coaching. 5. Responsible for scheduling employees. 6. ...

Key accountabilities include: • Responsible for the day-to-day operations of the Histology laboratory and supervision of the technical and support staff. In conjunction with the Department Manager, ensures that all departmental policies and procedures meet the standards of current state and federal regulations. • Monitor and control expenses in line with department budget. Assist in the preparation of the budget and recommend capital equipment needs. • Maintain appropriate levels of supplies and ...

Contact Kristine at 815-756-1221 for more details Qualifications: - PhD Food Science, Nutrition, Sports Science, Physiology, Biomedical or related - 8+ years of R&D experience within a food and beverage company - Nutrient metabolism and intake knowledge - Excellent communication and interpersonal skills - Management experience - Able to travel 20% - US Citizen/Perm Resident Duties: - Support development of nutrition science and new product development - Partner with product development, marketing ...

QA MANAGER - MUST HAVE LEAN/SIX SIGMA EXPERIENCE (ORANGEBURG AREA, NEW YORK) Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA inspectors and Documentation Review Group. Reviews and approves all ...

MICROBIOLOGIST - MUST HAVE ATLEAST 1 YR MICRO LAB EXPERIENCE (ORANGEBURG AREA, NEW YORK) Microbiologist I ORANGEBURG AREA, NEW YORK (ROCKLAND COUNTY) Description: Responsible for the accurate analysis of incoming raw materials, bulk liquids and finished products utilizing Standard Operating Procedures (SOPs), Work Instructions (WIs) and Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs). Assures released raw materials, bulk liquids and finished products have met the required ...

Plan and conduct GCP audits, issue audit reports, recommend corrective action and conduct follow up to audits and corrective actions for a company currently involved in several clinical trials Shall assist in preparing investigational sites for FDA inspection, review and recommend compliance related policies and procedures and evaluate impending regulations, guidelines and industry standards and their impact on the clinical trials and the company. Must possess at least 5 years experience in ...

Seeking at least 5 years directing and coordinating quality assurance activities for good clinical practices, coordinate and oversee inspections to ensure compliance to FDA regulations, IRB and IEC regulations and guidelines, site SOPs, protocols, and industry standards. Shall: *** Direct and coordinate GCP quality assurance activities. *** Author GCP documentation: protocols, case report forms, tables, listings, reports, and investigational brochures. *** Plan and execute document audits and ...

Responsible for the accurate analysis of incoming raw materials, bulk liquids and finished products utilizing Standard Operating Procedures (SOPs), Work Instructions (WIs), and Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs). Assures released raw materials, bulk liquids and finished products have met the required specification criteria prior to release. Investigate failures to determine final disposition. Maintain accurate, complete and traceable documentation related to ...

Join team developing in vitro diagnostics from concept, through design, development, verification and validation, production scale-up and technical transfer. Must have experience with assay development platform developing oligos and protein coatings. Top base salary to $120,000 and added incentives including: a work environment that promotes creative thinking, state of the art technology at your disposal, multiple opportunities to attend annual scientific symposiums, and the ability to work along ...

all use Luminex and similar assay development platforms using microsphere reagents and developing applicable oligos and protein coatings. Required Experience: *** Developing custom protein assays *** Designing and creating primers for nucleic acid assays *** Track record commercializing in vitro diagnostic kits from concept, through design, development, verification and validation, production scale-up and technical transfer. Base salary to $120,000 as well as attractive employment packages, ...

Seeking a strategic leader for analytical method development team with expertise in characterization of proteins and drug products to lead a team developing, qualifying and transferring analytical methods for in-process, lot release and stability testing in early, late and commercial phase and oversee the creation and review of documents such as: method development reports, SOPs, validation protocols-reports, CMC regulatory filings (IND, IMPD, BLA, etc.), and scientific journal publications. Well ...