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The positions serves as the site’s Oral Solid Dosage (OSD) platform leader and reports directly to the Sr. Director of Process Development. Responsibilities include management and oversight of multiple early and late stage development projects and support personnel. Job Functions: Demonstrates technical expertise in OSD technology and methodologies. Lead site related process development, scale-up, commercialization and tech transfer responsibilities Collaboratively develop project strategies....


Company is seeking a Principal Engineer to lead projects in the Biologics process development and clinical manufacturing projects. The individual will design, develop, scale-up and optimize drug substance and drug product unit operations for protein therapeutics. Experience managing projects from Discovery integration through GMP manufacturing, with both internal and external partners are required. The candidate should have strong technical, communication and interpersonal skills, be able to....


Senior Regulatory Affairs Specialist (Medical Device) Newark, DE (Relocation Assistance Provided) Competitive Base Salary, Bonus 10%, 6 401K Match, Full Benefits, 4 weeks PTO We have a newly created opening for a Senior Regulatory Affairs Specialist position with a longstanding client; multi-billion global medical 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....


Job DescriptionThis position is responsible for providing technical support consisting of drafting “Ask a Vet” Forum responses for the Technical veterinarian to finalize until the new website is completely in place, overseeing Adverse Event Reports (AERs) by being the first contact for the Customer Service Representatives for any issues, questions or concerns, being responsible for the accuracy of the information contained in the reports, and responding to technical calls and e-mails as....


Job DescriptionRoles and Responsibilities:Serve as key contact to equine sales team to assist with 40+/yr national tradeshows.Serve as key contact to consumer sales team to assist with 25+/yr regional and national tradeshows.May serve as key contact or assist veterinary sales team with 13+/yr national veterinary tradeshows.May serve as key contact or assist with OTC sales team with 2+/yr national tradeshows.May provide booth graphic assistance to veterinary sales team with....


The Brand Protection Assistant will work with the business unit, in-house counsel and outside legal counsel to set up a network of authorized dealers and distributors and administer a unilateral policy. The Brand Protection Assistant will work to identify unauthorized dealers selling and advertising company products and assist the company in taking action against such sites. The Brand Protection Assistant will also conduct extensive online searches for parties misusing and/or infringing....

- San Francisco Bay Area, CA

SENIOR DIRECTOR, REGULATORY AFFAIRS – CMCSan Francisco Bay Area 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....


Vice President, Regulatory Affairs San Francisco Bay Area Our client is seeking a Vice President, Regulatory Affairs who will be responsible for regulatory strategy, oversight, and guidance drug development program. The successful candidate will bring strong leadership abilities to oversee the Regulatory Affairs team, a successful history of effectively leading IND and NDA filings through approval, and interacting effectively with the FDA and other foreign regulatory bodies. This position....


My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....


My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....


RESPONSIBILITIES - Plans, organizes, directs and coordinates daily technical laboratory activities for a quick response technical team. - Maximizes utilization of equipment, materials and personnel necessary to achieve safety, cost, cycle time, and product development goals. - Manages laboratory activities to meet business objectives and leads the team to meet KPI/business goals. - Develops team members and addresses day-to-day supervisory responsibilities. - Proven ability to solve problems....

- San Francisco, CA

Our client in the San Francisco Bay area, has a new opportunity for Medical Director with expertise in Oncology NGS. This is a full-time, onsite position, with the opportunity to make an impact, company is seeking a driver to lead change. Medical Director, Oncology NGS San Francisco Bay AreaServes as company’s internal and external oncology / medical expert collaborating with several departments / business units including marketing, market access, salesRespond to questions from physicians and....


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. Senior....


Unique Opportunity!This position intersects Coatings / Formulations / Process Engineering / New Application Development / Manufacturing.Looking for a SME Principal Engineer in Oral Solid Dose, preferably an Organic Chemist that has moved from the bench to a coatings manufacturing environment but still involved in formulations, troubleshooting. Company offers cutting edge technology, a leadership role, an opportunity to interface with executive management and provide manufacturing solutions to....

- Any US State

Game Mathematician provides detailed mathematical game concepts. Design game specifications and math models and calculates payback percentage, odds and other regulated parameters to ensure accurate payouts and compliance with gaming regulations. Develops mathematical models of games to test the pay table math for functionality and adherence to specifications. Applies programming principles to create game simulations and calculation programs and other duties as assigned. (Ability/willingness to


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....

- Danbury, CT

Our client - a growing Pharmaceutical company located in the Danbury, CT area - is looking for a Validation Associate. The Validation Associate will be responsible for supporting all aspects of equipment qualification (IQ/OQ/PQ) as well as supporting process validation programs. The Validation Associate will be involved with creating and implementing various protocols as well as Final Reports. The qualified candidate will have 1-5 years of Pharmaceutical Industry experience - as well as some....


5-7 years of Class II device experience. MUST have global experience MUST have experience authoring 510K's POSITION SUMMARY: Working with minimal supervision, manage complex projects/products, including responsibility for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies. Applies regulatory expertise to the evaluation and solution of product development issues. SPECIFIC....


Head of Product Labeling / Technical Communication Elmsford, NY - Full relocation provided Competitive Pay, Bonus, 4 weeks PTO, 6% 401K, Great benefits We have a new opening for a Head of Product Labeling / Technical Communication with a longstanding client; a multi-billion ($8B+) global medical 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....

- Los Angeles, CA

Salary Range: $110,000 – $130,000/yr. base salary (bonus eligible role) Minimum Requirements:B.S. Chemical Engineering, Chemistry or Mechanical Engineering required7+ years of overall experience with at least 3 years of supervision experienceMust have a background in chemicals manufacturing, ideally compoundingBig pluses would be: lean six-sigma certification Job Description: This person will work in a 100-person manufacturing plant; one side of the plant does catalyst recycling and the....

41-60 of 91 results