- Merck & Co. (Durham, NC)
- …required to successfully support the QC laboratory Team to include the following: Quality Manager overseeing analytical testing and personnelLead the ... responsible for using principles of our Company Production Systems, Lean Laboratories, and cGMP requirements in the laboratory.- The Manager will manage the team… more
- Merck & Co. (Durham, NC)
- …bulk active ingredient, finished product, and laboratory testing for the BCG vaccine.The Quality Operations Laboratory Manager leads a team of analysts in the ... cGMP /GLP, Compendial, and other applicable regulatory requirements toward analytical testingCapability to function effectively within an automated/electronic laboratory… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Manager as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe CAR-T Operations Manager is an exempt level position working within Technical Operations. This individual will be responsible for overseeing the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Senior Project Manager , PMO as part of the Technical Operations team based in Raritan, ... responsible for providing operational excellence project management support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …& Beverage or Automotive production, leadership skills, and a commitment to excellence in quality and safety. The Plant Manager will be responsible for ensuring ... Position Summary We are seeking a dynamic and experienced Plant Manager to oversee our manufacturing operations. The ideal candidate will have a strong background in… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position SummaryThe Technical Data Reviewer reports to the Data Review Supervisor or quality management (ie, Manager or Director). The reviewer will be ... that all activities are performed in compliance with cGDP, cGLP and cGMP requirements.Job ResponsibilitiesReview logbooks for daily, monthly, quarterly, and final … more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position SummaryThe QC Chemistry Finished Product Supervisor will report directly to quality upper management, (QC Senior Manager ), and will provide both ... of his/her group.Job ResponsibilitiesWrite and Implement Standard Operating Procedures according to cGMP and cGLP.Assist in validation of new test methods for raw… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... with relocation assistance eligible for selected candidate. Relationships Reports to: Manager of cLEAN & Training Number of subordinates with direct/indirect… more
- ECLARO (Warren, NJ)
- …methods for the assigned product. Must have strong understanding of global cGMP , quality systems (especially change management), and guidance documents. Must ... NJ. ECLARO's client is a leader in the Biopharmaceutical Industry, providing quality , innovative, and affordable medicines that make a difference in the lives… more
- Fujifilm (Thousand Oaks, CA)
- …a culture that will fuel your passion, energy and drive - what we call Genki. The Manager Quality Control Analytical will manage a group of Quality ... product release testing of cell therapy product.** **Job Description** ** Manager , Quality Control, Analytical ** **The...+ Support cGMP manufacture and supply of high- quality cell therapy products. + Assess analytical … more
- Amgen (Holly Springs, NC)
- …documenting the qualification, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities at Amgen North Carolina. ... and resolution of protocol discrepancies as required. + Alerting Quality Control Management if equipment fails to meet calibration...High school diploma / GED and 10 years of cGMP laboratory, analytical instrument validation, and/or Process… more
- PCI Pharma Services (Bedford, NH)
- …To support our rapid growth, we are seeking a highly talented and motivated Manager , Quality Control (QC) Analytical Development to join our organization. ... The Manager , QC Analytical Development will be responsible for the oversight and...candidate will be an innovative leader with experience in Analytical Development and Quality Control environments. **Essential… more
- Catalent Pharma Solutions (Harmans, MD)
- The ** Manager , QC** is responsible for leading analytical method transfers and method qualifications between the Pre-Clinical and Process Development group and ... Quality Control (QC). The Manager , QC must...to day operations in assigned area of the QC Analytical department. + Ensure staff are fully trained on… more
- Amgen (Holly Springs, NC)
- …documenting the qualification, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities at Amgen North Carolina. ... and resolution of protocol discrepancies as required. + Alerting Quality Control Management if equipment fails to meet calibration...High school diploma / GED and 8 years of cGMP laboratory, analytical instrument validation, and/or Process… more
- Merck (Durham, NC)
- …required to successfully support the QC laboratory Team to include the following: + Quality Manager overseeing analytical testing and personnel + Lead the ... principles of our Company Production Systems, Lean Laboratories, and cGMP requirements in the laboratory. The Manager ...within own area of responsibility. **IMPACT:** **Influence** + Represents Quality in the laboratory to influence cGMP … more
- ThermoFisher Scientific (Plainville, MA)
- …operational skills to join our growing Process Development team. **Job Title: Manager , Analytical Development** **Location/Division Specific Information** : US - ... our clients deliver lifesaving therapies to patients. As the Manager of Analytical Development (AD), You will...Process Development. You will be supporting assay transfer to Quality Control (QC) for cGMP testing. This… more
- System One (Mahwah, NJ)
- …to Thursday ( 6:00 am to 2:30 pm) Type: Contract to Hire Responsibilities: The Quality Control Analytical Associate III serves as a support role to clinical and ... will assist with process check point, stability, and release analytical testing to ensure that quality standards...produced at the facility. Under the direction of the Manager , QC Analytical , responsibilities of the QC… more
- System One (Mahwah, NJ)
- …Sunday to Thursday 6 AM- 2:30 PM Type: Contract to Hire Responsibilities: The Quality Control Analytical Associate II serves as a support role to clinical ... will assist with process check point, stability, and release analytical testing to ensure that quality standards...produced at the facility. Under the direction of the Manager , QC Analytical , responsibilities of the QC… more
- Bristol Myers Squibb (Warren, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Title: Manager , QA Engineering ( Analytical Lead)** **Location: Warren, NJ** This ... education and experience acceptable. + Must have strong understanding of global cGMP , quality systems (especially change management), and guidance documents. +… more
- System One (Mahwah, NJ)
- Title: Quality Control Analytical Associate I Location: Mahwah, NJ area Schedule: 1st Shift 6 AM- 2:30 PM Tues to Saturday OR Sunday to Thursday Type: Contract ... to Hire Responsibilities: The Quality Control Analytical Associate serves as a...at the facility. + Under the direction of the Manager , QC Analytical , responsibilities of the QC… more
