- Merck & Co. (Durham, NC)
- …and patients on time, every time, across the globe.Reporting to the Director of Quality Systems and Compliance, the Associate Director - Quality Systems ... Job Description Job Description: Our Quality Assurance group ensures every single material inside...and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …grows. Relationships Reports to the Sr. Director, Patient Support Solution Quality /Safety Associate Director. Interacts with colleagues within Patient Support ... to maximize your potential with us? The Position The Associate Director will be the lead who is responsible...responsible for ensuring that all aspects of our patient quality and safety operations meets standards. This position requires… more
- Aequor (West Greenwich, RI)
- …PHD. Ideally looking for candidates with at least 2 years of an associate degree combined with 2 years of General lab experience/lab background, GDP/GMP experience ... preferred.Basic Qualifications: Science related background, lab experience Bachelor's degree OR Associate 's degree and 4 years of experience OR High school diploma… more
- Aequor (West Greenwich, RI)
- …supervision, this position will perform routine procedures to support testing within Quality Control. Tasks may include but not limited to performing sample ... collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data… more
- Aequor (West Greenwich, RI)
- …supervision, this position will perform routine procedures to support testing within Quality Control. Tasks may include but not limited to performing sample ... collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data… more
- Aequor (West Greenwich, RI)
- …for this role? IE office based, lab based, manufacturing floor? This is plant quality assurance role, therefore the EW will spend 50-60% of their time in a ... making.Job Details: In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position… more
- Aequor (West Greenwich, RI)
- …Job Details: In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires ... bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. Responsibilities Include the Following: Provide… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description:Reporting to a Technology Director or Associate Director in Global Engineering Solutions (GES), the Associate Director will ... portfolio of Large Molecule, Small Molecule, and Animal Health work.The Associate Director participates in project activities ranging from business case development… more
- Merck & Co. (Millsboro, DE)
- …(USDA, DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThis Associate Director will report to the Site Quality Head/Director of ... Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall… more
- Aequor (Thousand Oaks, CA)
- …using. We are looking for a candidate with skills to support the quality control/review of nonclinical scientific reports. Title: Associate Research Operations, ... Bioanalytical Sciences organization (TS&BA), this vital role is responsible for the quality control (QC) of nonclinical reports generated by the scientific staff in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In BARDS (Biostatistics and Research Decision Sciences), a ... benefit of patients and global human health.This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small molecules ... scientific background, excellent communications skills, and project management skills to derive high- quality reference data to meet the diverse needs of the business… more
- Merck & Co. (Rahway, NJ)
- …for Life" Objective. The Global Engineering Solutions (GES) group is seeking an Associate Director of Engineering to manage a significant portion of a very large ... mitigationManaging/ implementing commissioning, qualification, contract administration and project close-out.The Associate Director, Engineering will strive to develop good relationships… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks related to final printed… more
- Merck & Co. (Rahway, NJ)
- …individual to join our Biologics Process Development Department as an Associate Principal Scientist.- Applicant must have effective organizational and multi-tasking ... integrated clinical and commercial process and manufacturing solutions that achieve quality by design targets with robust control strategies.Advancing the upstream… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director, Global Regulatory Affairs, Regulatory Strategy to be a part of ... capabilities and will be responsible for planning, coordinating, and executing timely and high- quality submissions to the FDA.This is a hybrid position based in our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing ... scientifically accurate, high- quality clinical regulatory documents while adhering to regulatory guidelines....and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge… more
- Aequor (Thousand Oaks, CA)
- …to join our Pivotal Drug Product Technologies Group as Process Development Senior Associate in Thousand Oaks, CA. This group is responsible for late-stage drug ... monoclonal antibodies, bispecific T-cell engagers (BiTEs), fusion proteins, etc.). The Senior Associate will work in a highly collaborative team focusing on high… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory advice on advertising and promotion… more
