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Top Tier Global Pharmaceutical company is expanding and looking for a new AD, Biostatitics Must have heavy statistics experience (ideally in a pharmaceutical or biotech environment. PhD preferred. Salary 130-145k plus bonus , FULL RELOCATION to Irvine, CA Additional financial incentives- Short term incentives, Long Term incentives and stock, tuition reimbursement The Associate Director, Biostatistics position can independently lead one or more projects ensuring the proper design, analysis, and


Have you ever wanted to truly make a difference? Here's your chance... Our client - a premier Pharmaceutical company located in NJ is looking for a Principal Scientist - Analytical R&D. In this role - you will provide Analytical support in the development of cutting edge pharmaceuticals that saves people's lives. The Principal Scientist with perform Method Development/Method Validation for both Drug Substance and Drug Product. This role will provide analytical support for projects from....


Here's another excellent expansion opportunity with a multi-site company! Looking for a high quality individual, groom-able for future advancement. Apply for immediate, confidential consideration. Sr. Quality Manager -- $100-140k plus bonus -- food or dairy product experience -- relocation assistance to Dallas TX area from anyplace USA GENERAL DESCRIPTION: This position reports to the Plant Manager and will direct 3 professional quality positions as well as 12 staff laboratory technicians.....

- South Region, MD

Choose a hospital-based career opportunity within our newly renovated laboratory, equipped with the latest technologies! During the consideration and selection process both your interests, skills and our immediate needs will assist in placement within our Core Lab. Hiring Med Lab Technicians and Medical Technologist. Must be able to run chemistry, hematology, coagulation, and urine analysis in accordance with written policies and procedures. Properly ascertain results, make necessary....


Title: Pharmaceutical CMC Manager Oversees research efforts of the CMC team within the Pharmaceutical Development Group. Evaluates needed resources to meet the project expectations for CMC support and anticipates gaps to avoid project delays. Formulates a plan for building the CMC section of each project. Coordinates with key players inside and outside Research & Development to ensure CMC needs are met BS in Chemistry, Engineering, or related science10 years experience in chemistry-related


Requirements BS or higher, life or health sciences 7-10 years of relevant pharmaceutical /biotech industry experience RESPONSIBILITIESStudy Planning & Management Site Start-upPatient Enrollment and MaintenanceStudy ClosureCross-functional Representation Train and mentor junior regional team members such as CRAs and CTAsPrepare regional standard metrics (KPIs, SQMs)Ensure compliance with regional regulations, GCP, and SOPs during the execution of the studyContribute expertise to....


REQUIREMENTS: Looking for advancement opportunities in a small industry leader organization where you can wear lots of hats, make an impact and still maintain work life balance? Do you have the following?Minimum of a BS in Chemistry or Chemical Engineering, advanced degree preferredAt least 5 years of related experience in direct glazing, adhesives, sound damping or polymer/water-based coatingsExperience must include either: 1) Waterbased coating chemist for liquid applied sound dampening.....


Why is This a Great Opportunity?Our client is looking for a senior data scientist for our first-of-its-kind sales analytics platform, which combines a proprietary, active-learning network with applications that are ready to use, data backed, and built on predictive analyses.Job DescriptionOur client is looking for a senior data scientist for our first-of-its-kind sales analytics platform, which combines a proprietary, active-learning network with applications that are ready to use, data....

- Boston, MA

Highly successful technology company seeks a skilled Applied Scientist to join their specialized Search engineering team. This team helps build and power the engine that responds to tens of billions of queries per day, searching through terabytes of data in milliseconds. This team designs, builds, and deploys high performance, fault-tolerant distributed search systems used by millions of people every day.The search team is also responsible for building a platform that will enhance the customer


The Quality Control manager (QCM) reports to the Director of Quality Compliance. The QCM will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Analytical & Microbiology Laboratories and the Incoming Inspection departments are complaint in the areas of applications, release specifications, and documentation practices. It will be necessary for the QCM to execute and understand all in-house test methods. This person will be....


Senior Clinical Research Manager Elmsford, NY or Glasgow, DE (Relocation Provided) Competitive Pay, Bonus, 4 weeks PTO, 6% 401K, Great benefits We have a new opening for a Senior Clinical Research Manager with a longstanding client; a multi-billion ($8B+) global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that impact people's lives. A lot of....

- Parsippany, NJ

Our client - a growing Pharmaceutical company in Northern NJ - is looking for a Sr. Regulatory Affairs Associate. The Regulatory Affairs Associate will helps to put together and submit regulatory submissions to the FDA. These submissions will include: ANDAs, Amendments, Supplements, Annual Reports etc. (There may be additional work involving 505 (b)(2) submissions as well.) This position will also involve effective interaction with other departments with regards to the information required for


Refinery Analytical Chemist Near Philadelphia PA Assists with Lab Technical activities related to all of the refinery processes and products including test methodology, equipment purchases, and equipment calibration and repair. Assists in managing daily laboratory operations insuring: quality of test results, efficient inventory management, and the proper storage/ handling of samples for regulatory compliance purposes.Perform technical work in analytical or physical chemistry involving a....


Job DescriptionSummary of the Position:Keeps Regulatory Affairs Director appraised weekly of all tasks and projects. Gather documentation and compile materials required for international product registrations. Coordinate with International Product Manager and the International Business Unit a viable timeline for registration approvals with the Regulatory Affairs Supervisor or Director of Regulatory Affairs & Technical ServicesRoles and Responsibilities:Maintains all (electronic/hard) files

- Charlotte, NC

Job DescriptionThe IT Service Desk is the central point of contact for all IT related incidents and service requests. The role of the Desktop Support Technician is to provide 1st level support for all company employees. The Desktop Support Technician is responsible for resolving support requests as well as meeting customer satisfaction and continuous service delivery demands. The position requires one to be able to work in a fast-paced environment which provides services via the phone, e-mail....

- Any US State

Title: Formulation Chemist Develop new pharmaceutical products. Pilot scale batches, test a variety of product dosage forms including tablets, liquids, powders, soft chews, sustained release products and ointments. Document laboratory and pilot scale batches to meet GMP requirements. Performs routine and non routine testing on new product formulations using established analytical procedures. B.S. Chemistry Degree 5 yrs experience in a chemistry or pharmaceutical related field Previous....

- Newark/Princeton Area, NJ

Our client, a Fortune 150 Medical Diagnostics Equipment Manufacturer, is looking for a Senior QA Auditor to join Division Team in Central New Jersey area and independently conduct assigned audits to assess compliance to applicable business/division requirements, external standards/regulations and Corporate Quality System requirements across multiple Plants within Division. Participate in audits of manufacturing and commercial affiliate sites.in US and CanadaManage and/or participate in....


The R&D Formulation Scientist will be responsible for all aspects of product development for topical cosmetic and OTC products, such as formulation development, sourcing raw materials, and oversee the process from scale-up through launch. Working on multiple projects simultaneously, this individual is responsible for designing experiments to support product development in a team based environment, and will conduct hands-on laboratory and bench work, while participating in multi-functional....


Title: Director Regulatory Affairs Oversee Regulatory Affairs (Animal Health) – USA & Canada (SME) FDA audits – Point Player with FDA Regulatory strategy, labeling, and promotional material Facilitate product transfers Degree – Scientific 10+ yrs Reg Affairs Experience


The successful candidate will be responsible for the development and validation of physicochemical characterization methods for topical drug products and raw materials with primary emphasis on particle size distribution (PSD) methods. In addition to the activities above, the successful candidate will conduct particle size method transfers and verifications, develop product specifications, troubleshoot process problems, lead physicochemical characterization outsourcing activities, evaluate....

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Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.