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- 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....


Seeking an experienced Quality Assurance professional with proven leadership skills, a collaborative work style, a passion for learning, and one who is decisive and takes initiative. As QA Supervisor you will lead all facets of the Quality Assurance Department including Quality Programs, Food Safety, Sanitation Programs, Customer Programs, Data Management, Process Improvement and Laboratory Analyses. You will be a key member of the management team driving a culture that values progress but....

- 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....

- East Hanover, NJ

To be considered for this position you must have at least 7 or more years of regulatory affairs experience in the area of In Vitro Diagnostics (IVD) along with hands-on preparation of 510K submissions for IVD products. Strongly prefer someone form the medical device industry (not pharmaceutical mfg). Any experience dealing with face-2-face meetings with regulators (like Pre-Submission meetings) will be considered a valuable asset. Provide regulatory strategies for products, including....


Excellent oppt'y for a Medical Technologist to work for a medical lab manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. Area to be covered is approx 150 mile radius of San Jose (Sacramento - Stockton - San Jose), and maybe a bit south of San Jose. Can reside almost anywhere is this area. Will also be involved with direct problem solving covering reagents, kits,....

- 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....


We are seeking a Engineering and Manufacturing Systems Analyst to be located at the Chattanooga, TN manufacturing facility. This is a rare ground floor opportunity with a leading global manufacturer. This position is due to growth and is just one of the first of many to follow at this location and within the organization. The company is growing rapidly and the opportunities are developing daily for this and other positions here. Start now! The sky is the limit. This is an exciting opportunity....


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


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

- Any US State

Title: Sr Reg Affairs Mgr Regulatory compliance with relevant regulations managing submissions with regulatory authorities. Ensures compliance with relevant regulations. Manage regulatory documents, pre and post approval.. Education: BS Science Minimum 7+ yrs animal health regulatory experience, Previous relationship with FDA


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....


JOB SUMMARY As a technical leader, the successful candidate will oversee and execute analytical development, strategies related to pharmaceutical product development, e.g. project planning and timelines, experimental design, data evaluation, report writing and review and forming scientifically based conclusions, coordinate studies with other technical groups (Formulation, and Production). The successful candidate will be expected to maintain a high level of expertise within their field and....


Join a global leader as a Ph.D. Toxicologist responsible for conducting quantitative risk assessments for agrichemical and fertilizer products and traits in North America. You will provide technical advice on study designs for regulatory and research oriented studies as well as advice to support new and existing registrations of client products and traits. --- Work closely with regional/global regulatory and product safety teams as well as other functional teams to produce risk assessments for


Top Tier Global Pharmaceutical company is expanding and looking for two Study Medical Experts (for Clinical) must be Medical Doctor with MD degree Can have experience in oncology or even internal medicine + endocrinology/rheumatology/gastroenterology/etc and have experience with research. Competitive salary and benefits and bonus, 401k, long term incentives and short term incentives and more Provide medical support for the study team:Global primary contact person during the course of the....


Process Development Engineer – Solids Processing Location: Pilot plant near Beaumont TX with main office in NY close to North NJ & NYC Here's an opportunity to make a big impact with zero “corporate red tape”. Get in near the ground floor in this established and well-funded startup company. They are working to develop a “Green” source of traditional petrochemicals used to make plastics! Your success in this position is a key step in the overall company’s success. In this role, you will be....


Top Tier Global Pharmaceutical company expanding in their Boston HQ: TWO POSITIONS AVAILABLE- Snr Scientist II level is Snr Manager at the organization Competitive salary, bonus, benefits - including LTI and STI, Full relocation, bonus, stock, 401k and match and more... If interested send resume to hbr at clinicaldynamix dot come Senior Scientist II, Immuno Biologics - OBJECTIVES: The Immunobiologics group within Immunology Research at Company Boston is seeking an experienced Immunologist with


Minimum Requirements:Ph.D. or M.S. in Chemistry or Chemical Engineering with 8+ years of experienceMust have experience in a PSM-regulated manufacturing or lab facilityMust have experience with: batch reaction, scale up, and ability to adapt new chemicals to existing equipmentIntimate knowledge of organic chemistryPluses would be the following: supervision, experience with process optimization, design through installation of projects, sourcing of improved chemicals, distillation and....


Summary Description: This position will be tasked with leading regulatory support and expertise to business units regarding requirements for selling products and conducting business Internationally. This role leads the development, planning and execution of regulatory strategies for development, registration and post-authorization initiatives for company in International Markets with Europe being the main focus (including but not limited to: Europe, Asia, South American and the Middle East).....


Our client is in need of adding a Senior Formulation Chemist to its staff. They are a contract manufacturer of pharmaceutical products located in the Madison area. Our client is well established and tries to promote from within. Responsibilities:Accurately complete and comply with FDA filingsPlans and coordinates development, scale up and validation activities with minimal direction.Helps develop formulas for new products.Uses knowledge of processing equipment to develop and troubleshoot....

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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.