- Catalent (Philadelphia, PA)
- Quality Assurance Document Control Supervisor Position Summary Catalent Pharma Solutions in Philadelphia, PA is hiring a Quality Assurance Document Control (QADC) ... Supervisor . The QADC Supervisor will supervise the...decisions for QADC collectively with the QADC team.Act as site subject matter expert for "Good Manufacturing Practices" and… more
- Catalent (Philadelphia, PA)
- QA Supervisor Position Summary Catalent Pharma Solutions in Philadelphia, PA is hiring a QA Supervisor . The QA Supervisor will p rovide Quality Assurance ... partner to support the Supply Chain and Operations department. Act as site subject matter expert for "Good Manufacturing Practices" and "Good Distribution… more
- Novo Nordisk Inc. (West Lebanon, IN)
- About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... as our next generation of cutting-edge medications. It's not your average production site - it's a tight-knit, supportive community working together to contribute to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QA Shop Floor Supervisor as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Shop Floor Supervisor is an exempt level position with responsibilities for providing quality oversight over the production of personalized cell therapy to… more
- Novo Nordisk Inc. (West Lebanon, IN)
- About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... as our next generation of cutting-edge medications. It's not your average production site - it's a tight-knit, supportive community working together to contribute to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QA Investigations Supervisor (2nd shift) as part of the Quality team based in Raritan, NJ. ... Role Overview The QA Investigations Supervisor has the responsibilities for providing quality oversight over the production of a personalized cell therapy to support… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … metrics reports to identify potential areas of concern and bring to supervisor 's attention.Track study metrics such as site start-up, Investigator/ site ... (eg.clinicaltrials.gov).Under supervision, review and document CRO-generated reports, such as site monitoring trip reports and protocol deviation reports and elevate… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …work in collaboration with Outsourcing Procurement Management.Lead trial feasibility and site identification activities in collaboration with the CRO and the study ... team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics...direction of daily activities in support of goals, the supervisor will:Manage all employee-related activities throughout the year, including… more
- Merck & Co. (Durham, NC)
- …(7pm - 7am) on a rotating 2-2-3 schedule.AccountabilityFirst line operations supervisor with a team of individual contributor production direct reports including ... Skills:Demonstrated ability to lead a team (ie experience leading directly as a supervisor /coach or indirectly as part of a project or through routine process… more
- Merck & Co. (West Palm Beach, FL)
- …and long-term account plans in collaboration with the account team and supervisor (known as the Oncology Customer Team Leader).Share learnings and best practices ... working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday...or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working… more
- Merck & Co. (Durham, NC)
- …Skills:Demonstrated ability to lead a team (ie experience leading directly as a supervisor /coach or indirectly as part of a project or through routine process ... working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday...or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working… more
- Merck & Co. (New Orleans, LA)
- …and long-term account plans in collaboration with the account team and supervisor (known as the Oncology Customer Team Leader).Share learnings and best practices ... working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday...or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working… more
- Novo Nordisk Inc. (West Lebanon, IN)
- About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... Support in-process activities and product development when instructed by supervisor Incorporate pre-planned process improvements/cost reduction program into manufacturing… more
- Novo Nordisk Inc. (West Lebanon, IN)
- About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... as our next generation of cutting-edge medications. It's not your average production site - it's a tight-knit, supportive community working together to contribute to… more
- UT Health Quitman (Quitman, TX)
- …radiation and treatment of disease. Functions under the general supervision of the site supervisor and in cooperation with the cardiovascular team. This position ... stroke center, surgical suites, advanced diagnostics, swing bed care, cardiopulmonary rehab, on- site physician clinics, and a sleep lab. We believe healthcare is a… more
- Novo Nordisk Inc. (West Lebanon, IN)
- About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility ... for this position. Relationships & Schedule Reports to: QC Supervisor (Microbiology) Schedule: Sunday-Thursday (8AM-5PM) Essential Functions Independently performs… more
- Catalent (San Diego, CA)
- …Lead discussions with clients on technical topics relating to their project. Supervisor will not need to attend most client meetings.Exercise technical discretion ... design, execution and interpretation of experiments independently with minimal supervisor assistance. Data interpretation should be conducted independently.Assist in… more
- Insmed Incorporated (San Diego, CA)
- …the following: Mastery and execution of ddPCR assays developed in partnership with supervisor Following protocols and SOPs related to ddPCR lab work with in vitro ... for analysis Documentation of results in appropriate formats provided by supervisor Qualifications Bachelors' degree in biology, chemistry, or related field.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …processes. Key Responsibilities Lead the CAPA program for the CAR-T manufacturing site . Oversee metrics, trending, and reporting of relevant quality systems records. ... Implement and lead CAPA site governance program. Drive continuous improvement of quality systems...and information from established internal contacts, and consult with supervisor for decisions outside established processes Requirements A minimum… more
- Catalent (Manassas, VA)
- …weekendsManassas provides expanded capabilities in soft chews and lozenges. The site has the capability to manufacture cold-processed soft chews for nutritional ... ensure they are meeting quality standards; Report any deviations to QA Supervisor in complete appropriate details; Report any housekeeping issues that need… more
