We are looking for a Quality Control Chemist at a pharmaceutical manufacturing company. This candidate will need to to 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. Quality Control Chemist's Responsibilities: * The Qualit
(Sorry only GC EAD or TN or USC please) (corp to corp ok). (note: Remote position 95%. Some travel for conferences, meetings. Prefer Midwest location) Career Opportunity for IT Professional with 3-5 years experience in Puppet, AWS, Linux, and github. Six month contract - to - HIRE. In-house full time role. Convert to direct employee at six months (or sooner). Work for a hi-tech, friendly, mid-size national automot
My client is expanding and looking to hire a Scientist with polymer and enzyme experience to help develop new products. The ideal candidate will take on the following tasks: * Work with global internal and external collaborators to create new and support existing products. * Liaise with multiple downstream groups, including marketing and commercial teams, to develop new products. * Plan + execute experiments, ove
Vice President, Product Development (CMC) Our client is a biopharmaceutical company located in the Princeton, NJ area. With strong financials, a marketed product and promising pipeline, over 50 patents, and proprietary, patented platform technology this company has a strong foundation to continue to build upon. The correct individual for this role will thrive in a fast paced culture where you are free to lead. Someo
Love your job! Due to the growth of the business, our Edison, NJ based client is seeking a top notch Senior Manager of Regulatory Affairs. Excellent salary, benefits and relocation package are all included! Job Summary: The primary responsibility for the position is to manage the Regulatory Affairs team members. Ensure that deliverables are being met based on planned submission timelines. Provide training f
: Our client is a leader in the chemicals, paints and coatings industry that has been in business for over 100 years. Their broad portfolio of material solutions helps advance their customers in many industry spaces like automotive, electronics, medical and food & beverage. While their Headquarters are based in Dallas, the company has over 7,500 employees working to serve their customer based worldwide from Amsterdam
GLP QA MANAGER, SR MANAGER- CONTRACT RESEARCH - FULL TIME Position Title: Quality Assurance Manager/Senior Quality Assurance Manager Department: Quality Assurance Summary: This position is responsible for overseeing the internal and external quality assurance audit program to ensure regulatory compliance for a preclinical contract research organization. This role requires the ability to work closely and effective
MEDICAL DEVICE STUDY DIRECTOR/ PRINCIPAL SCIENTIST SAN DIEGO, CA Medical Device Study Director/ Principal Scientist The Principal Scientist would participate in Medical Device & Therapeutic studies in the functional role of a Study Director to conduct and oversee pre-clinical studies (acute and chronic, GLP and non-GLP, rodents, rabbits, pigs, sheep) that evaluate implantable devices (blood glucose monitors, prosth
Medical Director for High Profile Pharmaceutical company Looking for an M.D. to work with the Head of Clinical Affairs with Oncology early and late phase VP would consider an individual from academia - provided they had a strong background in immunology/oncology/hematology or a seasoned Pharmaceutical Professional Director or Senior Director, Clinical Oncology Job Summary: Oversees one or more trials of medium to hi
Position Summary: The Clinical Researcht Manager is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). This one is a Global Phase 1b pivotal study. Reports directly to the Executive Director, Clinical (who reports to CMO). In concert with the ED, is accountable for achieving successful delivery of Company clinical team activities at the project level by meeting co
