Microbiology Study Director | Regulated Lab Expert
Sgs
SGS, the world's leading testing, inspection and certification company, is seeking a Microbiologist II to join our New Jersey team to conduct a variety of microbiology analyses and ensure studies comply with GMP/GLP/ISO and client specifications. The candidate will train staff and participate in SOP approvals. Responsibilities include media prep, analyses per USP/EP/ASTM/AOAC/FDA, scheduling to meet deadlines, maintaining notebooks and LIMS, and upholding cGMP standards while mentoring junior #J-18808-Ljbffr Sgs
- Associate Director/Director-Global Clinical Pharmacology 1 week ago Be among the first 25... ...facets of Clinical Pharmacology, including study design, PK and PK/PD analyses, and... ...Good Clinical Practice and internal SOPs, regulations for specific projects to which assigned,...SuggestedWorldwide
$182k - $242k
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...planning and input on TA strategies, real world evidence (RWE) study designs, real world database (RWD) research, scientific presentations... ...of drug development and life-cycle management in the regulated environment Learn fast, grasp the 'essence' and can change the...Local area- ...independently in tools like Jira, Confluence, or equivalent for planning, documentation, and tracking.Bonus for hands-on experience in regulated domains like payroll, tax, HR, fintech, healthcare, where compliance, accuracy, and user trust are table stakes.Bonus points if...Full timeDay shift
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$103.6k - $192.4k
...Chemistry (AD-Chem) team, the successful candidate will independently design, execute, interpret, and communicate complex analytical studies supporting gene therapy product development. The individual will apply scientific expertise to characterize product quality...Full timeRelocation package- ...Gilead Sciences seeks an Associate Director of Biostatistics to provide strategic statistical... ...Represent biostatistics on study management and development teams, providing... ...development phases Familiarity with FDA, EMA regulations, ICH guidelines, and GCP standards...
$194.6k - $361.4k
...Level 6 Job Description Summary The Director Senior Legal Counsel R&D Legal will be... ...support for clinical development and study operation activities in the Americas as... ...~ Significant knowledge of FDA law and regulation including drug research and development...Full time- Novartis is seeking an Associate Director of Product Innovation to lead CRM Labs with rapid experimentation, prototyping, and evidence-based decision making. You will partner with Product Owners, IT, architecture, UX, analytics, privacy, legal, and compliance to translate...
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Overview The Associate Director, GCP Quality Assurance provides senior... ...and advisor to assigned study teams, this role evaluates processes... ..., vendors, phase I units, labs. Follow up on audits, ensure... ...knowledge of global GCP regulations and guidelines (ICH, FDA, EMA...Full timeWork at officeLocal area2 days per week3 days per week- ...our satellite locations to draw blood, collect specimens, and ensure accurate labeling and documentation. You will support the main lab by processing samples and communicating critical findings to clinicians. The ideal candidate has 2+ years of phlebotomy experience, basic...
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$136.6k - $257.4k
Job Description SummaryAs the Associate Director, Clinical Supply Management, you will lead... ...). Ensures alignment with all required regulations and guidelines in order to ensure... ...packaging and distribution strategies for studies (as applicable). Leverages AI-enabled insights...Full timeWork experience placementLocal areaRemote workRelocation- ...conduct, and cross-functional teams for clinical pharmacology studies of increasing complexity Design study protocols, data analysis... ...teams and matrix management Thorough knowledge of FDA, EMA regulations, ICH guidelines, and Good Clinical Practice Experience...
$144.64k - $216.96k
...real difference, there’s only one choice. Director, HR Operational Excellence and... ...Business Administration, Finance, Legal Studies, Public Policy, Risk Management, Organizational... ...subject to compliance with local rule and regulations as they may vary from time to time and...Local area$275k - $300k
...grow your career, this is where you belong.The OpportunitySenior Director - Infrastructure Debt, Renewable Structured Finance, Tax... ...lessees, partners, sponsors, asset and O&M managers, counsels, regulators and governmental entities.Oversee and ensure ongoing monitoring...Full timeTemporary workWork at officeLocal areaWorldwideRelocation package3 days per week- Job DescriptionADP is hiring a Director, Privileged Access ManagementLocations: Roseland NJ, Alpharetta GA, Pasadena CA, Orlando FL, Miami FL, Norfolk VAAre you empathetic to client needs and inspired by transformation and impacting the lives of millions of people every...Remote work
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...is your profile, we want to hear from you.Director, Translational Science (Neurology)... ...translational components of programs from study design through data analysis and interpretationInterpret... ...with academic and industry experts to stay at the forefront of emerging science...Full time$193.84k - $242.3k
...better health worldwide, together.Our Team, Your ImpactThe Senior Director, Supplier Relationship Management (SRM) is a senior leader... ...pharmaceutical, biopharmaceutical, medical device or another highly regulated manufacturing environment. Significant experience in external...Contract workLocal areaWorldwideFlexible hours$165k - $242k
...confidence. Trusted by leading AI labs, startups, and global... ...Learn more at .What You’ll Do:As Director of Field Enablement, you will... ...and successYou are an expert in go-to-market strategies for... ...conform to U.S. Government export regulations applicable to that information...Permanent employmentFull timeTemporary workCasual workWork at officeFlexible hours
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