Are you a business? Hire fda candidates in Union City, NJ
Additionally, our Analytical Chemist will have experience working with the FDA on future submissions and serve as our liaison working with 3rd Party testing facilities. 7-10 years' experience with ...
... the FDA label to assigned customers, using approved messages and resources. • Build, lead, and manage a diverse team of high performing sales professionals to attain division sales goals. • ...
Pharmaceutical Environment/Compliance - Ability to apply knowledge of pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and procedures and FDA ...
FDA, EMA etc.) Key Responsibilities: Responsible for the planning and execution of clinical studies in order to successfully move programs though the clinical research process in a timely manner, in ...
Serve as a primary liaison between the plant and regulators (USDA, FDA, auditors, etc.)* Create and implement inspection criteria and procedures.* Design Quality training programs and ensure proper ...
Understanding of GxPs and FDA Compliance requirements. * Excellent communication skills, including spoken and written English. * Ability to travel International and Domestic up to 30%. Preferred ...
Possess a working knowledge of FDA guidelines and processes * Able to convert scientific market research information into compelling copy * Solutions oriented, skilled at recognizing problems and ...
... the FDA) is administered with psychological support. We are currently in phase 3 study for treatment-resistant depression (TRD), and phase 2 for both post-traumatic stress disorder and anorexia ...
Initiate new egg donor and gestational carrier consultations; complete full work up IAW FDA regulations. * Develop and implement patient management plans and collaborate with the physician team to ...
Knowledge of QC/QA program as mandated by MQSA/FDA guidelines * Participates in QA projects and program meetings as assigned. * Maintains the cleanliness of all work areas, equipment and accessories
S * Required to be fully vaccinated with an FDA approved COVID-19 vaccine prior first day of employment. * Spanish/English bilingual required; * Ability to work flexible days and hours including ...
... to fda approved cleaning chemicals. * exposure to temperatures: 90 degrees fahrenheit. * ability to work in wet and dry conditions. * ability to work a flexible schedule including nights, weekends ...
Strong knowledge of FDA regulatory and fraud and abuse law. * Ability to learn quickly and operate in a fast paced, matrixed environment * Able to participate on key teams and/or be involved in key ...
Familiarity with a GMP manufacturing environment and working with FDA and FDA cGMP regulations required. Knowledge of molecular imaging techniques and pharmaceutical study design and execution ...
Our exclusive LightSense® laser system is the most advanced tattoo removal technology available, FDA Cleared, and only found at NAAMA. With over 30,000 treatments under our belt and glowing reviews ...
Proficient in FDA approved cosmetic neurotoxins and all FDA approved Allergan dermal fillers * Must be able to work a flexible schedule including evenings and Saturdays * Up-to-date PA license
Familiar with client MRL and/or FDA requirements, and has experience blending social media best practice to lead brief development, efficiently execute projects, and develop case studies * Ability to ...
Administer neurotoxin (Botox®, Xeomin®, Jeuveau®, and Dysport®) in the 3 FDA on-label locations for facial wrinkles * Complete and maintain accurate charting and clinical documentation for every ...
Individuals selected for employment cannot begin working until they provide verification that they are fully vaccinated against COVID-19 (with an FDA-authorized vaccine). JOB SUMMARY: Under the ...
Sampling for food and food-related products at various regional locations, commonly warehouses, for reasons such as FDA Detention, import/export needs, production inspection, specification ...
Improving processes to ensure compliance to FDA 21 CFR 820, MDD/MDR, ISO 13485,ISO 1497, IEC 62304 and Butterfly's procedures * Collaborating with Quality Systems and cross-functional teams to ...
Interpret and navigate regulatory requirements, guidelines, and standards (e.g., FDA, EMA) to ensure compliance throughout drug development, manufacturing, and distribution processes. * Conduct ...
... FDA regulations/guidelines, 21 CFR Part 11, EU Annex 11, GAMP5, ICH Q10 and latest industry practices. The incumbent will also be responsible for QA oversight of all GxP computerized system ...
Ensure compliance with global GMP guidelines and regulatory requirements, defined by FDA, EMA, and other global health authorities, for CMC activities. Provide CDMO oversight through batch record ...