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- Boston, MA

NO VISA's Our client is a rapidly growing company that is on a mission to reinvent the way scientific research is done. They are a SaaS company that bridges software, hardware, and innovation. You will be responsible for architecting, managing and scaling the entire IOT platform that is built on Rancher/Docker and AWS. The RoleTake ownership for health, scalability and availability of our cloud services and IOT platform.Automate the deployment pipeline between our pre-production to production....


Our client, a global manufacturer of specialty chemicals used in a variety of applications, requires an experienced professional to promote the company's raw materials to the Personal Care products and related industries. The successful candidate will work from a company office in either the Midwest or Northeast. Home office arrangements can be made for an exceptionally well qualified candidate. ResponsibilitiesUse understanding of North American market for personal care raw materials to....


Quality Supervisor - Food or Beverage Product Manufacturing - Day Shift - $65-75,000 plus 10% bonus target We are seeking a Quality Supervisor for a multi-site food product manufacturer. Opportunities for future career advancement abound with this prominent national manufacturer. This is a 50 person plant, 24x7 operation, day shift role. Supervises one lab tech currently. Relocation Assistance is provided! Big company Benefits! General Purpose of the Quality Supervisor position Ensure all....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....

- Hopkinsville, KY

Our Food Safety Manager is responsible for managing our in-house Micro-Lab and implementing and managing process control systems and preventative actions in the food safety area. You will manage all HACCP and Regulatory compliance issues at this processing site. Client company cannot sponsor or transfer Visa's at this time. Qualifications:Bachelor’s degree in Food Science, Microbiology, Chemistry, Biology. An advanced degree is preferred.A minimum of two years’ experience in Food Safety....


Reporting to the Executive Director of Early Development this physician will serve inside the medical sciences group as a leader in Hematology/Oncology early development. This Oncologist will lead early phase clinical development of oncology compounds from first-in-man studies through proof of concept. They will define, design, and execute early phase clinical and translational projects as the initial strategy for drug development. This physician should be trained in Oncology and have....


Responsibilities for 3rd Shift Sanitation Supervisor:Manage cleaning and sanitation employees in a food manufacturing facility on the 3rd shift;Train new sanitation employees in proper cleaning SSOPs, chemical use and safety procedures;Ensure uniform pre-operational standards through inspection and training;Solve concerns in regards to GMP, SSOP, SQF, SDS, and Process Control programs;Inspect plant, stored equipment, and environment for cleanliness;Establish and maintain a Master Sanitation....

- Cincinnati, OH

Job Description: Responsibilities include supporting daily compliance and systems activities. Performs audits (internal and vendor audits), supports change control program, complaints and any customer services related to Documentation Center. Also works with manufacturing to identify resolution to events while working with Quality Management. The candidate will perform general QA work, using their ability as a skilled contributor in completing tasks where judgment is required in resolving....


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....

- Buffalo, NY

Provides quality oversight to the Chemistry & microbiology laboratories and product transfer by supporting all work. Work in partnership with the aforementioned groups to produce quality work in compliance with all applicable regulations. - Review/approve deviations, OOS's, OOT's, EE's, and change controls. - Perform audits of the chem & micro labs. - Review/approve protocols, investigative studies, raw data and reports. - Establish and control quality programs to ensure conformance....


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....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


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....

- Greenville, NC

Excellent opportunity for Sr. Chemist to supervise and direct a staff of 6 Laboratory Technicians, conducting non-routine analyses and analyses on substances as part of research projects to evaluate chemical and physical properties. Will provide technical expertise for commissioning and support of all laboratory analytical systems/ instruments (ICP-OES, GC, XRF, N-TOC, IEC, Colorimetry, and Density Meters), promoting the accuracy of analytical data, optimum productivity. Responsibilities....

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