Average salary: $142,723 /yearly
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- ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...SuggestedHourly payFull timePart timeReliefLocal areaFlexible hours
- ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...SuggestedLocal area
$30 - $50 per hour
...Description Position Objective: Performs screening and diagnostic mammographic procedures in accordance with established ACR and FDA safety and quality standards and the special needs of patients. Essential Job Duties: Reasonable accommodations may be made to...SuggestedFull timeLuminis Health
Bowie, MD2 days ago- ...internationally recognized as the GOLD STANDARD in post-surgical wound healing and scar therapies. All Stratpharma products are FDA-cleared and physician-dispensed, providing multiple options for patient care within the Veterans Affairs hospital system . This...SuggestedContract workFor contractors
Stratpharma
Hartford, CT2 days ago $200k - $250k
...used in over four million annual spine, orthopedics, trauma and interventional procedures world-wide. Cerapedics’ product, i-FACTOR, is FDA PMA approved for cervical use in the United States. Cerapedics’ next-generation product is currently being evaluated in lumbar...SuggestedWork at officeCerapedics Inc
Broomfield, CO26 days ago- ...who can fill in-house. Serving clients in 18 Countries Successful NDA and ANDA drug registrations In good standing with the FDA, PMDA, and MHRA NOTE: Afton Scientific does not sponsor work visas. No recruiters please. Essential Functions: Perform manufacturing...SuggestedContract workVisa sponsorshipWork visa
Afton Scientific
Charlottesville, VA19 days ago - ...specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and...SuggestedFull timeCurrently hiringLocal areaRelocation packageMonday to Friday
UPMC - Pittsburgh Medical Center
Carlisle, PA3 days ago $16.5 per hour
...finished production inspections, and primary packaging\n\t Ensuring product meets all acceptable criteria per SOPs\n\t Following all FDA/CGMP regulations regarding traceability and safety procedures\n\t Supporting, encouraging, and participating in team-related...SuggestedHourly payTemporary workWork experience placementLocal areaShift workNight shiftWeekend workKelly Services
Clearwater, FL26 days ago- ...trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at...SuggestedWork at office
MCKESSON
Nashville, TN7 days ago - ..., and provides training and support for all employees as needed. Ensures compliance with any applicable GDCH, CAP, CLIA, AABB, OSHA, FDA and TJC guidelines and other regulatory agencies. Interfaces with the lab manager to implement and monitor all internal and external...SuggestedFull timeShift work
- ...Alzheimer?s Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer?s Disease. Inglewood Clinical is hiring a clinician who is an NP or PA. The clinician will...SuggestedFull timeLocumWeekend work
Irvine Clinical Research
Inglewood, CA4 hours agonew - ...Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction. Shift:...SuggestedHourly payWork at officeLocal areaMonday to FridayShift work
Flourish Research
Leesburg, FL29 days ago - ...participants across Phase I, II, III, and IV clinical research trials. This role ensures adherence to Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols, while guiding a team dedicated to excellence in patient recruitment and engagement....SuggestedWork at officeMonday to FridayShift work
ClinLab Solutions Group
Winter Park, FL5 days ago - ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...SuggestedFull timeLocal area
Stellar Senior Living
Mack, CO1 day ago - ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...SuggestedLocal area
Ovation Hospice
Phoenix, AZ4 days ago - ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Full timePart timeWork at officeLocal areaFlexible hoursShift work
Stellar Senior Living
Elbert, CO5 days ago - ...of reusable medical instrumentation, and handling/storage of disposable sterile supplies and accurately documents in compliance with FDA, CDC, AAMI, and JCAHO. Operates large high vacuum steam sterilizers, Paracetic Acid sterililizers, and Hydorgen Peroxoide Plasma sterilizers...
Children's of Alabama
Birmingham, AL2 days ago - ...原因分析（RCA）与CAPA制定。 技术支持 为商业化生产提供工艺优化建议，参与复杂偏差调查及工艺验证（PPQ） 注册申报支持 撰写BLA/NDA申报资料（如CMC模块、工艺验证报告），支持全球监管机构问询。 参与工艺变更的法规影响评估，确保符合FDA/EMA/NMPA要求。 任职资格： 教育背景 ~ 生物工程、制药工程、分子生物学、药剂学等相关领域 博士学位 。 相关经验 研究方向与 生物药工艺开发 （如细胞培养、蛋白纯化、制剂稳定性）或 GMP生产 相关者优先。 发表...
Hengrui Pharma
Boston, MA2 days ago - ...systems, BMS/EMS) are maintained and operate to required standards. 2. Regulatory Compliance & Documentation Ensure compliance with FDA, cGMP, 21 CFR Part 11, OSHA, and related regulatory requirements. Maintain records including PM logs, calibration reports, service...
Biocon
Cranbury, NJ21 days ago - ...Job Description 主要职责： 1.参与药品全生命周期质量管理体系的维护与优化。 2.参与FDA/EMA等全球药监机构审计项目。 3.参与质量事件管理，包括偏差调查、变更控制及CAPA有效性评估。 4.处理药品放行检测与稳定性研究的整体质量合规工作。 5.监督QC实验室数据完整性体系运行，确保分析活动符合全球药典要求。 6.参与分析方法转移和验证的合规性审核。 7.协同生产、研发、采购等部门推动质量标准落地执行。 任职资格： 教育背景 ：药学相关专业，硕士及以上学历、博士优先 相关经验...Work at office
Hengrui Pharma
Princeton, NJa month ago $85k - $100k
...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA?approved COVID?19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Local areaOvation Hospice
Denver, CO4 days ago$18 - $25 per hour
...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Full timeReliefLocal areaImmediate startRelocation packageAll shiftsNight shiftLa Villa Grande Care Center
Grand Junction, CO1 day ago- ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...ReliefLocal areaFlexible hoursShift work
Forum at Desert Harbor
Peoria, AZ4 days ago - ...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Full timePart timeLocal areaFlexible hoursShift work
The Groves
Goodyear, AZ3 days ago - ...associated with Testosterone Deficiency through rational, practical, and innovative solutions. We are best known for KYZATREX®, an FDA-approved oral testosterone therapy, designed to redefine how Testosterone Deficiency is treated. As a company, we thrive at the edge...
Marius Pharmaceuticals
Raleigh, NC19 days ago - ...工艺攻关，负责药品关键工艺数据的收集、统计分析，为工艺和成本优化提供解决方案 3.监督GMP合规落实，负责工艺文件更新、验证管理、偏差管理及应对国内外认证核查 4.跟踪药品生产领域的技术发展(如AI)，负责制药新技术的探索、评估、试用及推广 5.跟进 FDA/EMA/WHO/ICH/NMPA 的法规动态，负责法规新政策的解读、翻译、培训及落地 6.深度学习成为药品生产一、两个专项领域的SME，引领工厂技术水平提升 7.深度参与卓越运营工作，提升工厂运营效率 任职资格： 教育背景 ： 有机化学、药学、药...
Hengrui Pharma
Princeton, NJ2 days ago - ...controls (CMC) documents for investigational new drugs (IND) and summary data for annual reports to the Food and Drug Administration (FDA). ROLES / RESPONSIBILITES Build and optimize a robust cGMP compliant platform for generation, expansion and cryopreservation...Contract workWeekend work
Astrix
Bethesda, MD3 days ago $35 - $44 per hour
...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Local areaLa Villa Grande Care Center
Grand Junction, CO3 days ago$38 - $44 per hour
...maintain a safe environment for all employees, residents, families, and visitors, Stellar strongly encourages its employees to receive an FDA-approved COVID-19 vaccination, as well as any subsequent booster doses, as recommended by the Centers for Disease Control and...Hourly payPart timeReliefLocal areaRelocation packageShift workNight shiftSkyline Ridge Nursing & Rehabilitation Center
Canon City, CO1 day ago- ...2.负责药品生产所用原辅料、中间体、成品的检测及放行，HPLC等分析仪器维保与校验 3.承担药品质量标准修订、方法优化，验证方案的起草、实施 4.跟进实验室异常情况，负责OOS、异常、偏差等的调查 5.监督实验室合规管理、数据完整性管理 6.参与FDA/EMA等全球药监机构审计项目 7.参与卓越运营管理，提升实验室运营效率 任职资格： 教育背景 ：药物分析相关专业，硕士及以上、博士优先 相关经验 ：熟悉USP美国药典 语言要求 ：英语听说读写流利 其他技能 ：熟练操作各 种分析系统软件...
Hengrui Pharma
Princeton, NJ1 day ago
