|
Position: |
Location: |
|
International Regulatory Affairs and Quality Specialist
Our client is a sports medicine product distributor that focuses on innovative products that are changing the way companies view the sports medicine industry. Their long line of products include support wraps and braces for joint injuries, as well as mouth guards and other sports accessories. Our client values teamwork and creative thinking and rewards employees with a competitive compensation package. This is a challenging opportunity for the right candidate. |
Prairie du Sac, Wisconsin |
|
Vice President, Quality and Regulatory Affairs
Our client is a global leading developer and manufacturer of medical diagnostic instrument and reagent systems. They focus on providing leading-edge automation technology for use in slide-based diagnosis of cancer and infectious disease. With their 40-acre campus HQ based in Tuscan, AZ, our client boasts a financial and intellectual capital to partner successfully with the healthcare community. Their products are found in hospital-based histology laboratories, independent reference laboratories and the drug discovery laboratories of some of the world’s largest pharmaceutical and biotechnology companies, government labs and medical research centers. This is an exciting opportunity for the right person to join a world leader. |
Tuscon, Arizona |
|
Regulatory Product Manager
Our client is a biopharmaceutical company focused on the discovery, development and potential commercialization of fully human antibody-based therapeutics to treat life- threatening and debilitating diseases including cancer, inflammation, autoimmune and infectious diseases. |
Bloomsbury, New Jersey |
|
Compliance Audit Specialist
Our client is a biopharmaceutical company focused on the discovery, development and potential commercialization of fully human antibody-based therapeutics to treat life-threatening and debilitating diseases, including cancer, inflammation, autoimmune and infectious diseases. |
Bloomsbury, New Jersey |
|
CMC Manager, Regulatory Affairs
Our client is a publicly traded biotechnology company headquartered in Los Angeles that focuses on the development and commercialization of various oncology therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Los Angeles, California |
|
Director of Regulatory Affairs
Our client is a publicly traded biotechnology company headquartered in Los Angeles that focuses on the development and commercialization of various oncology therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Los Angeles, California |
|
Director of Regulatory Affairs
Our client is a dynamic and growing, independent contract drug development and consulting company. Employees at this company are experienced and highly qualified team players, essential to its success. |
New Jersey |
|
Vice President of Regulatory Affairs
Our client is a developer of products to treat artery disease, which can occur throughout the body including the heart, neck, torso, and legs. At the core of this company lies a team of experts and successful medical device veterans that have developed a multi-use, proprietary catheter technology that identifies, selects and reduces atherosclerotic disease. The unique technology addresses the unique dynamics of arteries, utilizes well-known device procedures and does not require an implant, such as a stent. The company is initially targeting Peripheral Artery Disease (PAD), “probably the most under-diagnosed and least aggressively managed" of the three vascular beds.” |
San Diego, CA |
|
Regulatory Affairs Specialist
Our client, based in Arizona, is a leading specialty pharmaceutical company focused on treating skin conditions. They are devoted to helping patients attain a healthy and youthful look and self-image. Our client has numerous leading branded prescription products in various therapeutic categories, like acne, fungal and skin infections. With a stable business in North America and an amazing track record of revenue, operating income growth and impressive gross profit margins, this is an exciting opportunity for someone to join a stable and profitable company. |
Scottsdale, Arizona |
|
Regulatory Affairs Manager/Associate
Our client is a rapidly expanding generic pharmaceutical company based in Minneapolis. They focus on the high-volume manufacturing of generic pharmaceuticals and OTC specialty products. Founded in 1977, they now have 250 employees, an 180,000 square feet facility and revenue of $120M this year alone. This is an excellent opportunity for the right person to join a stable, profitable and rapidly growing company! |
Minneapolis, Minnesota |
|
Director of Regulatory and Clinical Affairs
Our client is an leading diabetes management company based in Bedford MA. They focus on providing superior treatment options and lifelong health benefits for people with diabetes. Our client’s employees have extensive knowledge and experience in the diabetes and medical device industries. Their first marketable product is a new insulin blend. It brings together all of the functionality of a predictable insulin pump and blood glucose monitor into a system that features no tubing and automated cannula insertion. With a leading product on board and an experienced management team, this is an excellent opportunity for the right person to join a dynamic and rapidly growing company. |
Bedford, Massachusetts |
|
Vice President of Scientific and Clinical Affairs
Our client is a leading provider of contracted drug development services to the pharmaceutical industry. Their services span from pre-clinical through manufacturing, clinical, regulatory and commercial phases of drug development. Our client’s executive team are accomplished leaders in the full spectrum of drug development and have extensive experience working in and with pharmaceutical, biotech and contract services organizations. |
Cincinnati, Ohio |
|
Director and Subject Matter Expert
Our client is a leading provider of contracted drug development services to the pharmaceutical industry. Their services span from pre-clinical through manufacturing, clinical, regulatory and commercial phases of drug development. Our client’s executive team are accomplished leaders in the full spectrum of drug development and have extensive experience working in and with pharmaceutical, biotech and contract services organizations. |
Cincinnati, Ohio |
|
Regulatory Affairs Manager
Our client is a publicly traded pharmaceutical company headquartered in Pennsylvania. The company develops generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies and an experienced management team. |
Pennsylvania |
|
Director of Compliance
Our client is a New York-based cGMP facility with a strong pipeline. The company has an opportunity for growth. |
Long Island, New York |
|
Director of Regulatory Affairs
Our client is a dynamic and growing, independent contract drug development and consulting company. Employees at this company are experienced and highly qualified team players, essential to its success. |
Texas |
|
Director of Regulatory Affairs
Our client is a young venture-backed biotechnology company with several locations on the East Coast that focuses on the development and commercialization of devices for the orthopedic industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
East Coast, USA |
|
Clinical Affairs Manager
Our client is a leading medical device company. They have a leadership position in their targeted markets and an established reputation as a leading innovator in the field. The company has premier investors and a strong pipeline. This is a great opportunity for the right candidate. |
New Jersey |
|
Regulatory Affairs Manager
Our client is a life science company focused on the development of products that eliminate contagious pathogens. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term development of it's employees. |
Malvern, Pennsylvania |
|
Director of Regulatory Affairs
Our client is a pharmaceutical company that develops, manufactures and markets pharmaceutical therapeutics for medical conditions requiring specialized treatment. The company’s prescription drugs are marketed both nationally and internationally. |
Pennsylvania |
|
Regulatory Affairs Manager
Our client is a medical device company located in Naples, Florida. They focus on providing the finest quality engineered products and educational services for orthopedic surgeons. With over 3,000 products for arthroscopic and orthopedic surgical procedures (shoulder, knee/hip and small joint), our client has built up a strong customer base across the USA and in 60 countries worldwide. This is a great opportunity for the right candidate! |
Naples, Florida |
|
Coordinator of CMC Services, Analytical
Our client is a leading provider of contracted drug development services to the pharmaceutical industry. Their services span from pre-clinical through manufacturing, clinical, regulatory and commercial phases of drug development. Our client’s executive team are accomplished leaders in the full spectrum of drug development and have extensive experience working in and with pharmaceutical, biotech and contract services organizations. |
Cincinnati, Ohio |
|
Regulatory Affairs Manager
Our client is a young venture-backed pharmaceutical company headquartered in Massachusetts that is using a science-driven approach to develop novel therapeutics to treat a number of large, poorly served dermatological disorders. The company has premier investors and an experienced management team that is committed to the highest standards of integrity and to improving the lives of patients and their families. This is a strong opportunity for someone that wants to put their drive and initiative to work! |
Massachusetts |
|
Director of Regulatory Affairs and Compliance
Our client is a leading global producer of active pharmaceutical ingredients. The company has demonstrated strong growth and profitability in recent years and brings a lengthy history of innovation to each of its products. With a profit sharing program and best-in-class benefits this is a great situation for a candidate that is pursuing a challenging and visible leadership opportunity. |
Connecticut |
|
Senior Director, CMC Regulatory Affairs
Our client is a biopharmaceutical company based in San Diego. They focus on in-licensing, developing and commercializing therapeutics for the treatment of cancer and infectious disease. Coupled with these is an experienced management team with significant product development, clinical, regulatory, finance and business management expertise. This is a great opportunity for the right individual to join a dynamic company! |
San Diego, California |
|
Senior Director of Global Regulatory Affairs
Our client is an emerging biopharmaceutical company that is focused on the development and commercialization of next generation therapeutics for infectious diseases and cancer. With an experienced CEO and a strong, diverse pipeline, they present a great opportunity for the right candidate! |
Vermont, New Jersey, New Hampshire, New York, California |
|
Senior Director of Regulatory Affairs
Our client is an ophthalmic biopharmaceutical company based in Florida. They focus on the discovery, development and commercialization of products to meet the medical needs for the preservation of eyesight. Their corporate headquarters are based in Tampa and they boast a state-of-the-art R&D center in San Diego. With an experienced management team, a robust pipeline and a ‘can do attitude’, this is a great opportunity for the right person to join a rapidly growing company! |
Tampa, Florida |
|
Director of Regulatory Affairs
Our client specializes in clinical research and is an expert in a variety of areas including trial design, quality of life and health economics. |
California |
|
Associate Director of Regulatory Affairs
Our client is a biopharmaceutical company based in Westminster, Colorado. They focus on the development and commercialization of small molecule therapeutics for the treatment of cancer. Their team is dedicated to patients and the customers they serve. They want to attract, develop and retain world-class talent to build a high-performance organization. This is a great opportunity for the right candidate! |
Westminster, Colorado |
|
Senior Regulatory Affairs Manager
Our client is a privately held biopharmaceutical company focused on the treatment of vascular disease. |
Pennsylvania |
|
Director of Regulatory Affairs
Our client is a rapidly growing development-stage pharmaceutical company that is focused on the commercialization of therapeutics for patients with unmet needs that are suffering from chronic kidney disease. With offices in Canada and the US the company boasts a world class management team with unparalleled expertise in this area, a varied selection of cutting edge protocols and an empowering corporate culture that is focused on the long-term professional development of it's employees. |
Chicago, Illinois |
|
Vice President of Regulatory Affairs
Our client is small private company that specializes in developing therapeutics for endocrinology, bone loss and neuromuscular disease. They have a strong pipeline as well as great leadership and culture. This opportunity is great for someone who is hands-on and is looking for a sense of ownership and accomplishment. |
Cambridge, Massachusetts |
|
Regulatory Affairs Manager/Associate
Our client is a privately owned medical device company that is focused on the treatment of vascular disease. The company has an experienced CEO and board, an exciting product candidate and a team that is committed to the highest standards of integrity and to improving the lives of patients and their families. |
Kirkland, Washington |
|
Director of Regulatory Affairs
Our client is a successful division of a world-leading medical device company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. The company has some of the strongest financial indicators in the industry, an experienced management team and a robust pipeline. This is a strong opportunity for someone that wants to put their drive and initiative to work! |
San Jose, California |
|
Division Statistical Leader
Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. |
Michigan |
|
Manager, ELISA Technology Lab
Our client is a fast growing Contract Research Organization (CRO) located in Central New York State that focuses on conducting research and providing GLP/cGMP compliant analytical testing services for the development of various therapeutics for the Biotech/Pharmaceutical industry. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
New York |
|
Regulatory Affairs Manager/Associate
Our client is a leading medical device company based in the Northeast. They specialize in developing technologies for the treatment of cardiovascular diseases, such as coronary stents and state-of-the-art hernia repair. The company has offices in Australia and The Netherlands and boasts a demand of over 2 million sterile medical products to over 60 countries every year. With emphasis placed on personal development of employees, this is a great opportunity for the right candidate! |
Hudson, New Hampshire |
|
Regulatory Submissions Manager
Our client is a rapidly growing biopharmaceutical company based in The Woodlands, Texas. Using their state of the art technology, they have discovered the physiological and behavioral functions of nearly 5,000 genes. They have an exciting goal of advancing 10 drug candidates into human clinical trials by the year 2010. This is a great opportunity for someone looking for personal growth and a challenge! |
The Woodlands, Texas |
|
Process Equipment Engineer
Our client is an acute care specialty pharma company based in San Diego. They specialize in a technology that provides sustained-release delivery of medications for post-surgical pain. Our client has two marketed products that are used by professionals in the healthcare industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
San Diego, Southern California |
|
Toxicologist
Our client is a global specialty pharma and medical device company located just outside of Chicago, IL. They focus on the design, development, and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. |
Lake Forest, Illinois |
|
Director of Pre-clinical Development/Toxicology
Our client is a global specialty pharma and medical device company located just outside of Chicago, IL. They focus on the design, development, and manufacturing of solutions to improve the safety, delivery and effectiveness of patient healthcare. |
Lake Forest, Illinois |
|
Regulatory Affairs Project Manager
Our client is a top 10 pharmaceutical company that has established a reputation as one of the most desirable companies to work for in Canada. With operations around the globe and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! |
Toronto, Ontario |
|
Medical Products Manager
Our client is a rapidly growing company headquartered in Honolulu that is focused on tissue generation for people with illness. The company has an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. |
Honolulu, Hawaii |
|
Toxicologist
Our client is a publicly traded provider of personal care products that has established a reputation as one of the best managed companies in North America. With operations in over 120 countries, over $1B in revenue, and an empowering corporate culture that is focused on the professional development of its employees, this is a strong opportunity for the right candidate! |
Illinois |
|
Director of Regulatory Affairs
Our client is a dynamic and growing, independent contract drug development and consulting company. Employees at this company are experienced and highly qualified team players, essential to its success. |
West Coast |
|
Senior Manager, Regulatory Affairs
Our client is a well established biologics (allergy extract) located in beautiful Western North Carolina. The company, founded in 1904, is a leader in developing and providing allergy immunotherapy products/services for treatment of human beings and animals. In addition to their current product line, they have clinical trials also in process. |
North Carolina |
|
Senior Regulatory Affairs Specialist
Our client is a diagnostics company based in California, with their head office in New York. They offer products and services used by the industry to assist with the diagnosis, treatment and management of infectious diseases. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
South California |
|
Associate Director of Regulatory Affairs
Our client is a publicly traded pharmaceutical company headquartered in NJ with over 10 years of success in the development and commercialization of OTC therapeutics. The company has some of the strongest financial indicators in the industry, an experienced management team and a robust pipeline. They also offer an empowering corporate culture that is focused on the professional development and advancement of clinical team members. |
New Jersey |
|
Scientist, Regulatory Affairs
Our client is a leading drug company with close to $10B in sales and over 10,000 employees worldwide. The company has strong financials, an experienced management team and a loyal customer base. They have developed an industry-wide reputation for a positive work environment and an aggressive training program that ensures employees are up-to-date on current trends and best practices. This is a strong opportunity for someone that wants to put their drive and initiative to work! |
San Francisco, California |
|
Director, Regulatory Affairs
Our client is a leading medical device company specialized in ophthalmology and eye care products. They have over 13,000 employees globally and a reputation as a leading innovator in the field. With operations in 36 countries and a 150-year track record of success, this is a great situation for a candidate that is pursuing a challenging opportunity with a world-class employer. |
New York |
|
Regulatory Affairs Manager
Our client is a leading medical device company headquartered in Pennsylvania, which is focused on the development and commercialization of various fluid collection devices. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term development of its employees. |
Pennsylvania |
|
Manager Regulatory Affairs
Our client is a rapidly growing biotech company headquartered in the NE that is focused on the development and commercialization of various therapeutic for Cardiology. |
North East, USA |
|
Regulatory Affairs Supervisor
Our client is a leading pharmaceutical company specialized in pain therapy. They have close to 5,000 employees globally and have a developed a reputation as a leading innovator in the field. With operations in approximately 30 countries and a 70-year track record of success, this is a great situation for a candidate that is pursuing a challenging opportunity with a world-class employer. |
New Jersey |
|
Regulatory Affairs Supervisor
Our client is a leading producer of medical device products with approximately 4,000 employees globally. The company has exceeded all growth expectations over the past few years and has demonstrated a stable history, recently celebrating their 50th anniversary! This is a great situation for a candidate that is pursuing a challenging and visible opportunity with a world-class employer. |
Minneapolis, Minnesota |
|
Regulatory Toxicologist
Our client is a world-leading specialty chemical and materials’ company that has developed a reputation for successfully bringing impacting products to market. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! |
East Coast, USA |
|
Director/Senior Director of Regulatory Affairs
Our client is a global biopharmaceutical company headquartered in MA that is dedicated to the development and commercialization of therapeutics for the treatment of anti infective diseases.The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! |
Lexington, Massachusetts |
|
Associate Director of Regulatory Affairs
Our client is a rapidly growing contract drug development and manufacturing company that provides complete solutions for API, prototype and final product, clinical supplies, as well as commercial production and distribution. The company has an experienced management team, a strong track record with its clients and an empowering corporate culture that is focused on the long-term professional development of its employees. |
Southern California |
|
Regulatory Affairs Operations Specialist IV
Our client is a leading pharmaceutical company headquartered in California that is focused on the development and commercialization of various ophthalmology diseases therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! |
Irvine, California |
|
Regulatory Affairs Operations Specialist I
Our client is a leading pharmaceutical company headquartered in California that is focused on the development and commercialization of various ophthalmology disease therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! |
Irvine, California |
|
Regulatory Affairs Specialist IV
Our client is a leading pharmaceutical company headquartered in California that is focused on the development and commercialization of various ophthalmology diseases therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! |
Irvine, California |
|
Senior Regulatory Affairs Representative
Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company, which offers a great corporate culture and is focused on the long-term development of its employees. |
North California |
|
Regulatory Affairs Representative
Our client is one of the world's leading medical device providers. They are a highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company, which offers a great corporate culture and is focused on the long-term development of its employees. |
North California |
|
Senior Regulatory Affairs Specialist
Our client is a leading medical device company, which is focused in the development and commercialization of less invasive medical devices and procedures. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
Massachusetts |
|
Principle Specialist, Corporate Regulatory Affairs
Our client is a leading medical device company, which is focused in the development and commercialization of less invasive medical devices and procedures. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
Massachusetts |
|
Regulatory Affairs Manager (Endoscopy)
Our client is a leading medical device company, which is focused in the development and commercialization of less invasive medical devices and procedures. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
Massachusetts |
|
Regulatory Affairs Manager
Our client is a publicly traded pharmaceutical company headquartered in Southern California that is dedicated to the development and commercialization of generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees. |
Irvine, California |
|
Associate Director, Regulatory Affairs (Oncology)
Our client is a human health care company seeking innovative solutions in disease prevention, cure and care for the health and well being of people worldwide. |
New Jersey |
|
Director Regulatory Affairs
Our client is a rapidly growing pharmaceutical company headquartered in the Midwest that is focused on the development and commercialization of therapeutic radio-pharmaceuticals for the US nuclear medicine market. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Midwest, USA |
|
Director of Monitoring Services (Home-Based)
Our client, a niche CRO with focus on oncology studies, has an opportunity for home-based Director of Monitoring Services. |
East Coast, USA |
|
Regulatory Affairs Manager
Our client is a reputable R&D company based in PA. They focus on assisting pharmaceutical companies across the globe in product development. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Pennsylvania |
|
Director (Scientific and Regulatory Affairs)
Our client is a privately owned specialty pharmaceutical company focused on the design, development and commercial manufacture of sterile, injectable, sustained release pharmaceuticals. Products of this class have extremely high commercial potential. Our client concentrates exclusively in this drug delivery space. They are advancing their lead products, and building successful partnerships with major and specialty pharmaceutical companies worldwide. |
Ohio |
|
Regulatory Affairs Manager
Our client is a leading medical device company based in Bohemia, New York. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate! |
Bohemia, NY |
|
Senior Director of Regulatory Affairs
Our client, a clinical site dedicated to oncology patients, has an immediate need of two experienced clinical research nurses. |
Los Angeles, CA |
|
Senior Regulatory Affairs Specialist
Our client is one of the world's leading medical device providers. They are highly profitable, publicly traded company whose products are currently being sold in over 120 countries worldwide. This is a great opportunity for someone to join a company that offers a great corporate culture and is focused on the long-term development of its employees. |
Michigan |
|
Reimbursement Manager
Excellent opportunity to join a growing medical device company focused in the treatment of pulmonary diseases. |
Redwood City, CA |
|
Medical Writer
Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
Houston, TX |
|
CMC Manager, Regulatory Affairs
Our client is a publicly traded biopharmaceutical company that is dedicated to the development and commercialization of trans-dermal therapies. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees; this is a great opportunity for the right candidate! |
Southeast USA |
|
Regulatory Affairs Manager
Our client is the biotech division of a world leading healthcare company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! |
Southern California |
|
Senior Regulatory Affairs Associate
Our client is dedicated to improving and preserving human life by developing innovative pharmaceutical products. The company’s premier product has been developed for delaying/preventing renal flares. Treatment for various other autoimmune and inflammatory conditions have also been developed by the company. |
California |
|
Associate Director, Regulatory Affairs
Our client is a biopharmaceutical company dedicated to discovering, developing and commercializing orally active drugs that address significant unmet medical needs. Primarily focused on the treatment of cancer and inflammatory disease, their proprietary drug development pipeline includes several small molecule drug candidates designed to regulate targets in therapeutically important biologic pathways. This company aims to be the most efficient inventor of therapeutic products in the pharmaceutical industry. |
Colorado |
|
Regulatory Affairs Associate
Our client is a rapidly growing medical device company headquartered in San Diego that is known for innovative strides in the development and commercialization of minimally invasive therapies. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
San Diego, CA |
|
Regulatory Affairs Manager
Our client is a specialty generic pharmaceutical company engaged in the formulation and commercialization of both controlled release (CR) and immediate release (IR) products utilizing their proprietary drug delivery technologies. By applying the technologies to selected generic prescription pharmaceuticals, they seek to duplicate the release characteristics of these drugs in order to manufacture and market versions that can be substituted for branded products. The company intends to develop and use their drug delivery technologies to commercialize a portfolio of generic pharmaceutical products. In the near future, they also plan to apply their drug delivery technologies to the development of proprietary branded drugs. |
Florida |
|
Regulatory Affairs Analyst
Our client supplies incorporated services in product development, manufacturing, packaging and logistics. The company is synergistic, focused and has a leading edge. It offers challenging opportunities by empowering people to their full potential. |
Michigan |
|
Director of Regulatory Affairs
Our client is amongst the top servers of science and serves up to 35,000 customers in varied fields such as pharmaceutical and biotech companies, hospitals and clinical diagnostics labs, industrial process control settings, environmental settings, government agencies and also to universities and research institutes. The company has over 30,000 employees working for it in across 150 countries worldwide. They provide a complete range of high-end equipments, analytical instruments, reagents and consumables. They also provide software and services for research, analysis, discovery and diagnostics. |
Northern California |
|
Regulatory Affairs Manager
Our client is amongst the top servers of science and serves up to 35,000 customers in varied fields such as pharmaceutical and biotech companies, hospitals and clinical diagnostics labs, industrial process control settings, environmental settings, government agencies and also to universities and research institutes. The company employs over 30,000 people across 150 countries worldwide and provides a total range of high-end equipments, analytical instruments, reagents and consumables. They also provide software and services for research, analysis, discovery and diagnostics. |
Northern California |
|
Regulatory Affairs Manager
Our client is a publicly traded pharmaceutical company headquartered in Southern California that is dedicated to the development and commercialization of generic therapeutics for the treatment of various diseases. The company has an excellent track record with regulatory agencies, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. |
California |
|
Senior Manager/Associate Director of Regulatory Affairs
Our client is a privately owned biopharmaceutical company headquartered in Los Angeles that is dedicated to the development and commercialization of protein and antibody-based therapeutics for the treatment of various diseases. They have an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Los Angeles, California |
|
Regulatory Affairs Associate
Our client is a company dealing in the biopharmaceutical sector, developing novel gene-based therapeutic drugs and vaccines. These products help in the production of proteins directly at the site of disease by the genes it delivers. All gene-based therapies use the same patent protected technology. |
Maryland |
|
Regulatory Affairs Specialist – I
Our client is in the field of human bone and connective tissue processing for transplants and is a world leader in their field. They are also an innovator in the development, manufacturing, and marketing of biological, biometrical, and device systems for musculoskeletal surgery. The company’s present and development-stage technologies address the needs within many musculoskeletal disciplines. |
New Jersey |
|
Senior Regulatory Affairs Specialist
Our client is in the field of human bone and connective tissue processing for transplants and is a world leader in their field. They are also an innovator in the development, manufacturing, and marketing of biological, biometrical, and device systems for musculoskeletal surgery. The company’s present and development-stage technologies address the needs within many musculoskeletal disciplines. |
New Jersey |
|
Senior Manager of Regulatory Affairs
Our client is an innovative drug development company. The firm develops pain reliever and acne treatment formulas. It uses advanced drug delivery technologies to create novel molecule formulations, which can be commercialized and are currently marketed by the company. They currently have three late-stage drugs in their clinical expansion channel. |
Ontario |
|
Director of Regulatory Affairs
Our client is a pharmaceutical company and works to develop, manufacture and market pharmaceutical therapies indicated for diseases/medical conditions requiring specialized treatment. The company’s prescription drugs are marketed both nationally and internationally. It caters to therapeutic categories of antiviral and anti-fungal agents. |
Pennsylvania |
|
Associate Director of Regulatory Affairs
Our client, a biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life threatening diseases. The programmes of the company are intended for gastroenterology as well as treating HIV infection and cancer. The company has many products in the development and pre-clinical development stage. |
New York |
|
Regulatory Affairs Manager
Our client, a biopharmaceutical company, focuses on developing therapeutic products, for the medical needs of patients with debilitating conditions and life threatening diseases. The programmes of the company are intended for gastroenterology as well as treating HIV infection and cancer. The company has many products in the development and pre-clinical development stage. |
New York |
|
Director of Regulatory Affairs
Our client is a leading privately held pharmaceutical company with operations in over 40 countries. With marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! |
New Jersey |
|
Regulatory Affairs Specialist
Our client is a biotechnology company focused on developing new treatments for under-served markets in oncology and infectious diseases. |
Montreal, Quebec |
|
Associate/Director of Regulatory Affairs
Our client is a rapidly growing biotech company headquartered in Maryland that is focused on the development and commercialization of various therapeutics for disorders of the nervous system. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Maryland |
|
Director of Regulatory Affairs
Our client is into brand and generic pharmaceutical products. It develops, manufactures, markets and distributes such products. The Corona-based specialty pharmaceutical company has one of the broadest product offerings in the US generics industry and a track record of service excellence. It is well known as a reliable and low-cost provider of quality pharmaceutical products. |
California |
|
Regulatory Affairs Manager
Our client is into brand and generic pharmaceutical products. It develops, manufactures, markets and distributes such products. The Corona-based specialty pharmaceutical company has one of the broadest product offerings in the U.S. generics industry and a track record of service excellence. It is well known as a reliable and low-cost provider of quality pharmaceutical products. |
Northern California |
|
Director of Regulatory Affairs
Our client is a medical device company that designs, develops and markets products for restoring blood flow in patients who have suffered ischemic strokes, resulting from blood clots in the vessels of the brain. |
California |
|
Manager, Regulatory Affairs
Our client is a bio pharmaceutical company with four licensed products, two manufacturing sites and a strong program in research and development. |
New Jersey |
|
Regulatory Affairs Manager
Our client is a leading biopharmaceutical company based in San Francisco. The company focuses on the discovery, development and marketing of cardiovascular and anti-cancer therapies. Founded by cell biology pioneers working to create a unique and powerful approach to drug discovery, their mission is to translate cell biology into novel pharmaceuticals and technologies. The company’s exceptional approach has created two cancer drug candidates, one heart failure drug candidate and numerous other research programs addressing a variety of disease areas. Its development programs are based on a mechanistic understanding of the biology underlying their interests in cell cycle control and contractility. |
California |
|
Regulatory Affairs Manager
Our client is a biopharmaceutical company dedicated to the development and commercialization of therapeutics to treat patients with cancer and other life-threatening diseases. The company has an experienced management team, a strong pipeline and multiple products currently on the market. |
New Jersey |
|
Regulatory Affairs Manager
Our client is a biopharmaceutical company based in San Diego. The company focuses on in-licensing, developing and commercializing products pharmaceuticals to meet the needs of hospitalized patients and their care givers. Since their inception in 2004, they have in-licensed rights to two Phase III products, both of which have been studied in previous Phase III clinical trials conducted by their licensors. |
San Diego, California |
|
Regulatory Affairs Manager
Our client is a biopharmaceutical company. From treating life-threatening and incapacitating diseases (including cancer, autoimmune and infectious diseases), the company is focused on the discovery, development and potential commercialization of therapeutics. These are fully human antibody-based therapeutics. |
East Coast, USA |
|
Director of Regulatory Affairs
Our client is committed to developing, acquiring, and commercializing innovative treatments for cancer. The company pursues making cancer more treatable. They are developing a diversified portfolio of oncology products focused on identifying new, less toxic and more effective cancer therapies. |
Washington |
|
Director of Regulatory Affairs
Our client is a premier biopharmaceutical company. The company is focused on the discovery, development, and commercialization of novel small molecule drugs. |
Kansas |
|
Director of Regulatory Affairs
Our client is located in Kirkland Lake, Washington, and was founded in late ’80s. The company is into designing, developing and manufacturing innovative medical devices intended for the treatment of arterial disease. The company's primary focus is on peripheral artery disease (PAD). |
Washington |
|
Manager Regulatory Affairs and Compliance
Our client is a rising biopharmaceutical company engaged in the research and development of therapeutic products for transdermal delivery. The company’s task is to use their own technology to develop and commercialize products to overcome therapeutic barriers, and raise the standard of care for certain chronic conditions. |
Virginia |
|
Regulatory Affairs Manager
Our client is a manufacturer of dietary supplements and personal care products. The company follows Good Manufacturing Practices (GMPs), product formulation standards and product labeling standards of the countries that it does business with. |
Dallas, Texas |
|
Regulatory Affairs Manager
Our client is a leading biomedical company focused on enhancing patient care. |
Saskatchewan |
|
Regulatory Affairs Manager
Our client is a leading biomedical company focused on enhancing patient care. |
Arkansas |
|
Clinical Trial Manager
Our client is a publicly traded biotechnology company. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. |
Newfoundland and Labrador |
|
Clinical Trial Manager
Our client is a biopharmaceutical company focused on development and commercialization of therapeutic products. |
Delaware |
|
Clinical Trial Manager
Our client is a biopharmaceutical company focused on development and commercialization of therapeutic products. |
Michigan |
|
Clinical Operations Manager
Our client is a leading drug discovery company dedicated to the discovery and development of therapeutics across various therapy areas. |
New Brunswick |
|
Senior Regulatory Affairs Manager
Our client represents one of the most significant market opportunities in the medical device industry today. Their aim is to develop, manufacture, and market advance |
