- Repligen (Waltham, MA)
- …quality standards. This role is based in Waltham, MA, and will report to the Senior Manager of Supplier Quality.Responsibilities Supplier Performance Monitoring and ... ReportingCollect, analyze, and report on monthly supplier performance data, including quality, delivery, and service metrics.Prepare and distribute supplier … more
- Repligen (Clifton Park, NY)
- OverviewThe Molding Operator will report to the Molding Lead. This position will be located at our Clifton Park, NY location. The molding operator will be required ... execute assigned tasks Operate equipment following SOP's and training guidelines Report any equipment/mold issues to supervisor Responsible for following SOPs and… more
- Aequor (Houston, TX)
- …reader, translate simple to moderate scientific events into a brief and cohesive report as a finished product o Demonstrates ability to capture immediate actions and ... event, address comments from stakeholders on the compiled final report o Displays ability to gather data from various...to moderate scientific events into a brief and cohesive report as a finished product Displays ability to gather… more
- Merck & Co. (Rahway, NJ)
- …This role requires excellent analytical, negotiation and communication skills.This role will report directly to the Chief of Staff to the General Counsel & ... analytics tools (eg, MS Excel, Power BI, Tableau, Cognos) and report automation preferred.Project management experience leading large-scale projects, ideally in a… more
- Repligen (Hopkinton, IA)
- …to meet production targets.Inspect products for quality assurance and report defects or inconsistencies.Communicate effectively with supervisors and other ... quality, engineering).Assist with scheduling, timekeeping, and attendance tracking.Identify and report equipment issues or process inefficiencies.Maintain production records, logs,… more
- Aequor (Houston, TX)
- …translate difficult and complex scientific events into a brief and cohesive report as a finished product. Accurately capture immediate actions and containment of ... address comments from both internal and external clients on the compiled final report . Gathering Data from various sources across the site, performance of Root Cause… more
- Aequor (Tampa, FL)
- …3rd party laboratory testing and reporting of data and EM when necessary. Report on testing results, including CoA's. Maintain equipment, media, and sample logs as ... requirements and expectations are either unknown or unclear. Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents,… more
- Repligen (Waltham, MA)
- …of biologic drugs.This role will be based in Waltham, MA and will report to the Sr. Director, Quality - Quality Network Leader, Chromatography & ... to date with current trends in biopharmaceutical manufacturing.Supervise direct report (s) which includes setting objectives, monitoring performance and conducting… more
- Aequor (Pearl River, LA)
- …under moderate supervision with regular review. - Identify and report experimental problems, troubleshoot causative factors, implement necessary corrections after ... discussing with the supervisor, and train other analysts on established technologies. Qualifications BA/BS with at least 3 years of experience or MBA/MS with any years of experience. - Hands-on experience in cell culture and cell-based assays. - Experience in… more
- Novo Nordisk Inc. (Tyler, TX)
- …and other paramedical customers and current co-promotion partners. Internally, the DCS I report to the District Business Manager of the specific sales territory. The ... DCS I also interact and collaborates on a regular basis with other field-based employees covering the same geographic areas, particularly the territory partner. Essential Functions Demonstrates competencies on a consistent basis with territory level impact… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …audits including, but not limited to Common Technical Document (CTD), Clinical Study Report (CSR) and Nonclinical Study Report (NCR), electronic Trial Master ... File (eTMF) and other pivotal documents to be submitted to the regulatory authorities for application Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from… more
- Merck & Co. (Rahway, NJ)
- …integrity as needed.Share best practices across the company to enhance overall capabilities. Report to the SAS E2E Investigation Support lead.Bring a strong technical ... background combined with superior problem-solving skills and an innovative mindset.Exhibit exceptional leadership abilities and strong knowledge of cGMP and Data Integrity.Uphold strong values essential to fostering and contributing towards the company… more
- Repligen (Clifton Park, NY)
- OverviewThe Packaging Operator will report to the Packaging Lead. Responsibilitiesability to gown appropriately and operate in an ISO 7 environmentexecute assigned ... packaging floor tasks.responsible for following SOPs and safety proceduresresponsible for area cleanlinessread and understand quality and inspection documentsread/understand molding drawingsbasic math competencyunderstanding of measuring instrumentsinspection… more
- Merck & Co. (Boston, MA)
- …with key internal departments and external contactsAbility to collect, analyze, and report on meaningful resource usage metrics to drive value and communicate ... impactFamiliarity with copyright compliance and literature-related regulationsAbility to perform independent research to learn and master new systems and toolsAttention to detail, ability to problem-solve and work independently, escalating risks and issues as… more
- Repligen (Rancho Dominguez, CA)
- …supervisor. This role will be based in Rancho Dominguez and will report to the MFG Supervisor.Schedule: Monday - Friday, 7am to 3:30pmResponsibilitiesThe Assembler ... I will be responsible for:Perform packaging of assembled productsPerform assembly of packaging boxesClean, maintain, and operate automated production equipment per Sr Operator guidance and adherence to SOP's.Comply with Good Documentation Practices on all… more
- Tris Pharma (Monmouth Junction, NJ)
- …discrepanciesDocuments all testing details and results in laboratory notebooks and report sheets, compliant with current Good Documentation Practices (cGDPs), cGMPs ... and SOPs Evaluates compendial methods and procedures, as neededPrepares regulatory submissions; Executes studies and prepares technical protocols/reports in response to FDA Information Requests (IRs)/Complete Response Letters (CRLs)Cleans, maintains and… more
- Merck & Co. (South San Francisco, CA)
- …Clinical Research while developing and expanding your career.This role will report directly to the Immunology Therapeutic Area Lead in Translational Medicine.Primary ... responsibilities for the Senior Principal Scientist include the following:Key member of an early development team, providing leadership in designing and executing early clinical development strategyDevelopment and execution of early clinical strategy for novel… more
- Repligen (Hopkinton, IA)
- …by closely following the standard operating proceduresPerform inventory counts and report any inaccuracies on in a timely mannerComplete documentation according to ... Good Documentation Practices (GDP)Learn the Repligen Performance System and contribute to a culture of continuous improvementOther Duties:Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or… more
- Repligen (Hopkinton, IA)
- …in Hopkinton, MA for 2nd shift operations (M-F).The QC Inspector I will report directly to the QA/QC Director.This position is responsible to actively participate in ... the Repligen ISO 9001 Quality Management System. This role is responsible for inspecting, auditing and reporting on in-process and final inspection of single use assembly parts at the Hopkinton, MA production facility, using various visual techniques and… more
- Merck & Co. (North Wales, PA)
- …through the entire product lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and ... following departmental SOPs and good programming practices.Maintain and manage a project plan including resource forecasting.-Coordinate the activities of a global programming team that includes outsource provider staff.Membership on departmental strategic… more
