Senior QA Auditor Salary at Clario BETA

DIRECT HIRE MUST HAVES: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) 4+ years of experience in a cell/gene therapy GMP environment or the pharmaceutical industry within a Quality Control Sterility Assurance role or Microbiology role Hand on experience running or validating at least 2 of the following microbiology rapid safety methods: endotoxin, mycoplasma, and sterility Overview We are seeking a highly motivated Quality Control Specialist II, Sterility Assurance. The incumbent is responsible for assisting in the development and implementation of all microbial contamination control processes/procedures for the company’s clinical and commercial programs at two manufacturing sites in Philadelphia. This role will effectively collaborate with multiple stakeholders to ensure the harmonized execution of contamination control policies across the two manufacturing sites in Philadelphia. This role will also support new product transfers related to contamination

**Senior Manager, Global Process Owner, Order to Cash** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier live. **This is a full-time,** **remote** **, salaried position: Monday Friday, 1st shift.** Our Somerset location is the corporate headquarters for Catalent Pharma Solutions. This location houses our state-of-the-art laboratory, clinical, commercial manufacturing plant for oral dose forms in addition to being the Center of Excellence for Highly Potent Active Pharmaceutical Ingredients (https://www.catalent.com/oral-dose/highly-potent-active-pharmaceutical-ingredients/) . The **Senior Manager, Global Process Owner, Order to Cash** is the Global subject matter expert on the process for which they are responsible. The **Senior Manag

**Senior Manager, Global Process Owner, Order to Cash** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier live. **This is a full-time,** **remote** **, salaried position: Monday Friday, 1st shift.** Our Somerset location is the corporate headquarters for Catalent Pharma Solutions. This location houses our state-of-the-art laboratory, clinical, commercial manufacturing plant for oral dose forms in addition to being the Center of Excellence for Highly Potent Active Pharmaceutical Ingredients (https://www.catalent.com/oral-dose/highly-potent-active-pharmaceutical-ingredients/) . The **Senior Manager, Global Process Owner, Order to Cash** is the Global subject matter expert on the process for which they are responsible. The **Senior Manag

About Acadia Pharmaceuticals Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and commercialized the first and only FDA-approved drug to treat hallucinations and delusions associated with Parkinson's disease psychosis and the first and only approved drug in the United States and Canada for the treatment of Rett syndrome. Our clinical-stage development efforts are focused on Prader-Willi syndrome, Alzheimer's disease psychosis, and multiple other programs targeting neuro-psychiatric and neuro-rare diseases. For more information, visit us at Acadia.com and follow us on LinkedIn and X. Please note that this position is based in Princeton, NJ or San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary: The Senior Manager, Quality Control, is responsible for Quality

Job Description Job Description As the Commercial Property and Casualty Quality Assurance Analyst, you will be is responsible for the quality review strategy focusing on portfolio analysis in Non Profit Human Services, Religious Organizations and Programs. The team works together reviewing targeted and random underwriting files identifying strengths and opportunities. You will assist underwriting leaders in the identification and implementation of training strategies to address the personal job improvement and performance of underwriters and underwriting activities. You will also work closely with both underwriters and underwriting management to identify process and performance opportunities, and may assist with project initiatives for the department as needed. The changing business climate and marketplace requires nimble decision making and you will be a part of that process and decision making. You will rely on experience and judgment to plan and accomplish goals. To be successful in

**_What Quality Assurance contributes to Cardinal Health_** Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Assurance develops and implements a compliant and cost effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented. **_Job Summary_** Position will oversee and enhance through continuous improvement the quality systems that support the repackaging of drug products, achieved through collaboration with contract repackagers. The position includes ensuring that the repackaged products meet the highest standards of quality and compliance. Closely moni

Quality Control Specialist needed! The Quality Control Specialist II, Sterility Assurance will have substantial experience leading QC sterility assurance program(s) in a Pharmaceutical or Biotechnology environment. The Quality Control Specialist II, Sterility Assurance is a key support role and reports to the Manager, QC Sterility Assurance. Essential Functions and Responsibilities: Assist with the development of sterility assurance principles at the site in the areas of aseptic processing, and contamination control. Support the site compliance to the global microbial control standards/procedures on environmental monitoring, critical utilities, contamination control strategy, clean-room management, microbiological methods and validations, sterilization and aseptic processing controls, disinfectant efficacy studies and microbial risk assessments. Assist with the design of the contamination control strategy. Develop microbial contamination/Cross contamination risk assessments (HACCP/FMEA

About Orchestra BioMed Orchestra BioMed is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s vision is to accelerate medical innovation to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s partnership-enabled business model focuses on forging strategic collaborations with leading medical device companies to drive successful global commercialization of products it develops. Orchestra BioMed is led by a highly accomplished, multidisciplinary management team and a board of directors with extensive experience in all phases of therapeutic device development. Orchestra’s business was formed in 2018 by assembling a pipeline of multiple late-stage clinical product candidates originally developed by its founding team. Its flagship product candidates are BackBeat CNT for the treatment of hypertension, the lead