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- Hackensack, NJ

Analytical Chemist Northern New Jersey (Hackensack, NJ - Full Relocation Offered) Competitive Base Salary, 15% target Bonus We have an immediate need for an experienced Analytical Chemist for our New Jersey facility (petro / chemical / industrial manufacturing environment). They have developed some of the petrochemical industry’s most significant process technologies, which are used today to produce millions of tons of petrochemical intermediates in numerous licensed process plants worldwide.....

- Lancaster, SC

Analytical Chemist responsibilities include, but are not limited to, the following :Execute experiments utilizing analytical methods to support preclinical pharmaceutical product development activitiesUse analytical techniques and instrumentation, such HPLC and spectroscopyPrepare test solutions, compounds, and reagentsMaintain laboratory instruments to ensure proper working order and troubleshoot malfunctions when neededBe the owner of technical data you generateRead, write, and prepare....


Reporting to the Director of Regulatory Affairs, this key role is to function as global lead on device teams. Ensure that submission content meets regulatory requirements. Strategize to identify risk areas and develop alternative courses of action. Manage scenario planning and development of regulators responses. Manage medical device Regulatory Affairs activities for developing global CMC medical device and IVD strategies across product life cycles & execution in North America. Support....

- Lancaster, SC

Summary of the Position: The Batch Record Reviewer is responsible for the review and release of batch records, Certificates of Analysis and other pertinent document and relaying this information to the appropriate departments. Roles and Responsibilities:Communicating accurate and up-to-date status reviews to appropriate personnel and updating the Finished Product Release spreadsheet. Additionally on a daily basis, the Batch Record Reviewer will assist in the correction of deficiencies found....


Description of Work: This position is required to support the budget activities related to the various entities Responsibilities: Responsible for managing the preparation, maintenance and reporting of the annual budget for the various entities. Assist operating divisions and departments with developing their annual operating budgets.Assist other departments in developing and maintaining budgets for special projects.Monitor actual results to budgeted results on a periodic basis (i.e., monthly).


Job Description: Reports directly to Vice President of Research & Development for investigation of ingredients and product sourcing. Provide scientific assessment of new or existing active ingredients. Investigate formulations and assist formulators with ingredient sources and dosing. Roles and Responsibilities:Assist in the development of new products for the Veterinary Division, including rationale, project timeline, and budget.Assist and support V/P R&D in development of product....


Salary Range: $160,000 to $175,000 base salary, bonus eligible Location: Danbury, CT Minimum Requirements: B.S. Chemistry, B.S. Biology, or related degree (advanced degree preferred) with 8+ years of experience in commercializing products from onsite labs to an outside end user. For example: companies who sell products such as bug spray, facial creams, foods, fertilizers, and flavors. Candidates could come out of any of the products listed (or similar) and prior FDA/GMP experience is not....

- Lancaster, SC

Roles and Responsibilities:The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices.The QCC will assist in evaluating new testing applications and instrumentation, either developing methods or adopting compendial methods.....


Global Pharmaceutical Company out of Madison, NJ and Irvine, CA Position Summary: (Irvine, CA or Madison, NJ) Responsible for leading internal and outsourced Clinical Programming activities in support of Clinical Research studies and managing the design, development, validation, implementation, and oversees ongoing support to electronic case report form (eCRF) systems (e.g. InForm, etc.), external data acquisitions, reporting/business intelligence tools (e.g. SpotFire, J-Review), and other....

- Dallas, TX
new job!

A leading producer of composite materials near Dallas, TX is looking for a Chemical Engineer or Chemist to develop products and processes for the aerospace, automotive and consumer products industries. The products contain layers of plastics, textiles and polymer coatings. This is an individual contributor position reporting to the General Manager and much time will be spent in a new laboratory and testing facility. This is a small company with excellent growth potential. An Engineering or....


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....


Top Tier Pharmaceutical company is growing and needs a Strong Clinical Research Associate for the East Coast (must be located in the Danbury, CT area to be in house, Headquarters when needed) leading developer, manufacturer and supplier of premium molecular diagnostic products and services that are used to diagnose human diseases, screen donated human blood and to aid in biomedical research. Our business is dedicated to impacting the lives of people across the globe through the early detection


DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....


Director Health, Safety and Environmental (HS&E)Description The individual in this position is accountable for championing Health, Safety and Environment (HS&E) for the plant. Additionally, the Director of HS&E ensures HS&E systems at the facility are aligned with the companies Operational Integrity Management System (OIMS) and are compliant with regulatory standards and statutes. This position fosters a continuous improvement culture focused on process and occupational safety,

- Gaithersburg, MD

Director of Lab Operations - CRO Highly regarded contract research organization seeks a Director of Lab Operations to lead P&L business operations for the research group. The Director of Lab operations will:Support implementation of new service linesPlan and direct operational activities leading growth and profitsMaintain exceptional bioanalytical lab operations, focusing on customer satisfaction and successful outcomesEstablish and drive operational management and development....


New contract role (opportunity to convert to perm in future if desired) with Global Pharmaceutical company located in Cambridge, MA BACKGROUND: This Drug Product is an ALK Inhibitor for the treatment of patients with anaplastic lymphoma kinase-positive (ALK+) metastatic NSCLC. It was recently approved by the FDA under Accelerated Approval in April 2017, based on tumor response rate and duration of response, for previously treated anaplastic lymphoma kinase-positive (ALK+) metastatic....


Director, Drug Discovery, Proteomics, Neurodegenerative DiseaseIf you are an accomplished drug discovery leader who would like the freedom of a smaller research institute where your input and opinion really matters and would like to engage in translational research aimed at treating and someday curing a debilitating neurological disease this may be the opportunity for you. My central New Jersey client, a recognized leader in neurodegenerative disease research, seeks a Ph.D. researcher with....

- Bridgewater or Cambridge, NJ

Global Pharmaceutical company with high profile trials is expanding and looking for a Director, Regulatory Affairs for their Global Management Team Competitive base salary and bonus, full relocation and benefits, Long Term Incentives and more Position can be located in either the Bridgewater, NJ or Cambridge, MA location The Rare Disease Global Regulatory Team Lead (GRTL) is part of the Global Regulatory Affairs (GRA) team based in the US. He/she is responsible for developing long and....

- San Francisco Bay Area, CA

Director, Research - Immuno-OncologyOur pre-clinical stage client is working on exciting technology in the field of Immuno-Oncology.This newly created critical leadership has 4 direct reports currently. Ideal candidate will be a Ph.D with strong industry experience in a pre-clinical setting in Immuno-Oncology. This person will outline, implement, and lead the company research strategy and growth towards commercialization. Every day, they will make decisions that matter. Qualifications:Define....


Responsibilities:Develop new methodology techniques, develop fabrication processes for new products, and make improvements to processes for existing productsThoroughly understand all aspects of the cutting, shaping, grinding, and polishing processes for current and new materialsDevelop a thorough understanding of the current metrology techniques as well as creating new measurement techniques Transition new metrology techniques to a manufacturing environmentParticipate in developing new....

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