Director of Quality Management - PCAM Penn MedicineDirector of Quality Management - PCAMPhiladelphia, PAPenn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. 6+ years Minimum of 6 years of quality assurance and process improvement/management experience, preferably in a healthcare related field.
Quality R&D Operations Drug Substance Director GSK plcQuality R&D Operations Drug Substance DirectorKing of Prussia, PAWe need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people.
Associate Director, Risk Based Quality Management Lead Summit Therapeutics plcAssociate Director, Risk Based Quality Management LeadPrinceton, NJServing as the primary RBQM subject matter expert within study teams, this role implements and maintains study-level risk management, centralized monitoring, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), targeted monitoring strategies, and risk review processes. Working closely with Clinical Operations, Clinical Science, Data Management, Biostatistics, Medical Monitoring, and CRO partners, the RBQM Lead proactively identifies, evaluates, escalates, and mitigates risks throughout the clinical trial lifecycle to support participant safety, data reliability, and regulatory compliance.
Director_Manufacturing Quality Consultant_ Life Sciences PricewaterhouseCoopers LLPDirector_Manufacturing Quality Consultant_ Life SciencesPhiladelphia, PA$155,000–$410,000 / yearDemonstrates some proven abilities to collaborate and work with a diverse team including: Basic problem solving and analysis skills; Financial modeling skills; Basic spreadsheet, presentation and document development skills; Demonstrates the ability to build, maintain, and utilize networks of client relationships; Interpersonal skills and proactive communication; and, Collaborative and "can-do" mindset eager to take on challenges. Functional Experience: Demonstrates knowledge and a proven record of success in or a desire to deliver advisory services in the following capability areas: Experience in the pharmaceutical or medical device industry and/or top consulting firms with a focus on Pharma/Life Sciences.
Medical Director Hospital Quality Capital HealthMedical Director Hospital QualityHopewell, New JerseyWhen determining base salary and/or rate, several factors may be considered including, but not limited to location, years of relevant experience, education, credentials, negotiated contracts, budget, market data, and internal equity. Capital Health is a dynamic health care resource accredited by the DNV that includes two hospitals, an outpatient center, satellite ED, and an expansive network of primary and specialty care.
Associate QA Director IQVIA Holdings IncAssociate QA DirectorWayne, PA$88,600–$246,600 / yearInfluence quality outcomes across multiple functional areas, business units, and customer engagements through expert guidance, risk-based decision making, and oversight of quality systems and compliance programs. Provide strategic quality leadership and oversight across assigned Quality Assurance (QA) programs, with a strong focus on clinical research, clinical operations, pharmaceutical development, and GxP-regulated activities.
Director, Quality Globus Medical Inc.Director, QualityAudubon, PAPosition Summary: The Director of Quality provides strategic leadership and oversight of the company's global quality systems, with direct responsibility for Quality Engineering at the Audubon (HQ) site, International Operations Quality, and Sterile Manufacturing Quality. The Director will collaborate cross-functionally with Manufacturing, Supply Chain, R&D, and Regulatory teams to maintain a culture of quality excellence and operational efficiency across all facilities and international markets.
Senior Director for Operations, Quality, and Compliance (SDOQC) Temple UniversitySenior Director for Operations, Quality, and Compliance (SDOQC)Philadelphia, Pennsylvania$124,630–$150,000As the institutional lead for accreditation, the Senior Director oversees all aspects of LCME preparation and ongoing compliance, including directing the Institutional Self-Study process, coordinating cross-functional committees, managing timelines, and ensuring the accuracy and completeness of all required submissions. The Senior Director for Operations, Quality, and Compliance (SDOQC) serves as the school wide administrative and strategic leader for quality, regulatory compliance, and accreditation across all LKSOM campuses, including the primary North Philadelphia campus and all regional and affiliate sites.
Payer Quality Consultant, Director PwCPayer Quality Consultant, DirectorPhiladelphia, PA$155,000–$410,000 / yearPreference for at least one of the following fields of study: Accounting, Actuarial Science, Analytics/Data Science, Business Administration/Management, Computer Science/Information Systems, Economics, Engineering, Finance, Government/Public Policy, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk Management/Insurance. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Associate Director, GxP Quality Auditor Cabaletta Bio IncAssociate Director, GxP Quality AuditorPhiladelphia, PAThis individual will also act as a Subject Matter Expert (SME) for GxP auditing, quality projects and will be responsible for supporting implementation and management of the Quality Management Auditing system. Utilize root cause analysis tools, critical thinking, and interviewing techniques to determine the root and contributing causal factors of noted findings.
Director, Business Operations, Global Quality Bristol-Myers Squibb CoDirector, Business Operations, Global QualityPrinceton, NJ$190,060–$230,308 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Additionally, the role is accountable for developing and implementing portfolio resource management strategies, driving financial accountability, and fostering a culture of quality, agility, and operational excellence across the organization.
Associate Director, Quality Assurance Merck & Co IncAssociate Director, Quality AssuranceWest Point, PA$142,400–$224,100 / yearThe DDQ Associate Director will be responsible for all quality aspects of assigned GMP computerized systems and supporting infrastructure utilized by our Manufacturing Division to ensure compliance with company policies, procedures and regulatory expectations, this includes involvement in all quality-related activities for computerized systems used in support of GMP processes and which are required by our Manufacturing Division's Quality Manual or with potential for impact on product quality, patient safety or data integrity. As part of the global DDQ leadership team and reporting to the Director of DDQ, the Associate Director DDQ will be responsible for: Collaborating with stakeholders (e.g., System Owners, Process Owners, Data Owners, and Technical Unit) to assess and select computerized systems which enable GMP business processes.
Associate Director Quality Assurance Catalent Pharma Solutions, Inc.Associate Director Quality AssurancePhiladelphia, PADemonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Quality/Performance Director Amentum Services IncQuality/Performance DirectorPhiladelphia, PA$150,000–$180,000 / yearLead and oversee the development and implementation of robust processes for the enterprise and regional aspects of the system, including internal audit, corrective action, document control, business continuity, risk management, tool management, and performance management. Establish a systematic approach for corrective action, ensuring that identified issues and non-conformities are addressed in a timely manner, root causes are identified, and appropriate corrective/preventive measures are implemented to prevent reoccurrence.
Director, Clinical Quality Assurance Jazz Pharmaceuticals PlcDirector, Clinical Quality AssurancePhiladelphia, PARemote$184,000–$276,000 / yearThe successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. Is personally committed and actively works to continuously improve him/herself; understands that different situation and levels may call for different skills and approaches; works to deploy strengths; works on compensating for weakness and limits.
Quality/Performance Director AmentumQuality/Performance DirectorPhiladelphia, Pennsylvania$150,000–$180,000 / yearLead and oversee the development and implementation of robust processes for the enterprise and regional aspects of the system, including internal audit, corrective action, document control, business continuity, risk management, tool management, and performance management. Establish a systematic approach for corrective action, ensuring that identified issues and non-conformities are addressed in a timely manner, root causes are identified, and appropriate corrective/preventive measures are implemented to prevent reoccurrence.
Associate Director - Program Management - Quality & Compliance Programs (Hybrid) Cabaletta Bio IncAssociate Director - Program Management - Quality & Compliance Programs (Hybrid)Philadelphia, PASmartSheet Management: Utilize SmartSheet for project planning, tracking, and reporting both within a singular project and across multiple projects/programs creating one unified portfolio summary/report Create, maintain, and publish SmartSheet dashboards and reports for project status updates. Work with Quality & Compliance Leadership Team to provide scenario planning and project reporting for all Quality & Compliance project management activities, aligning them with company goals and regulatory requirements, including the development and maintenance of charters, dashboards, trackers, schedules and other PM documentation.
Director, Quality Microbiology Integra LifeSciences Holdings CorpDirector, Quality MicrobiologyPrinceton, NJ$166,750–$228,850 / yearThe candidate must be an experienced team leader who leverages the talent of their team to increase performance, generate results, and maintain robust quality of manufacturing site microbiology programs. The Director, Quality Microbiology, is responsible for leading Integra LifeSciences operational microbiology teams across the Tissue Technologies and Codman Surgical Specialties businesses.
Director, Quality Data Analytics Integra LifeSciences Holdings Corp.Director, Quality Data AnalyticsPrinceton, NJ$166,750–$228,850 / yearThis role is responsible for establishing and scaling advanced analytics capabilities while leading complex, cross-functional programs that enable proactive Quality Compliance, regulatory readiness, and enterprise risk management across the medical device lifecycle. The Director, Quality Program Management, Quality Data Analytics leads managers and/or advanced individual contributors and partners with senior leadership to embed data‑driven decision‑making across the organization.
Director, Post Market Quality Integra LifeSciencesDirector, Post Market QualityPrinceton, NJ$166,750–$228,850 / yearThis leader will oversee process improvements for the end-to-end processes of complaint intake, investigation quality, medical device reportability (vigilance), complaint closure, health hazard evaluations, post-market surveillance, and signal detection across two businesses consisting of a diverse portfolio of leading medical devices. + Partner with Regulatory, Clinical, Medical Safety, R&D, and Supply Chain to ensure embedding of complaint signals into CAPA, risk management (ISO 14971), design controls , and production controls (e.g., ISO 13485 / 21 CFR Part 820 / Part 4 for combination products as applicable).
Director - Design Quality Assurance - Tissue Technologies Integra LifeSciencesDirector - Design Quality Assurance - Tissue TechnologiesPrinceton, NJ$166,750–$228,850 / yearThese activities include the development, implementation, and monitoring of quality programs and policies that ensure the development, manufacture, and distribution of medical devices in compliance with corporate policies, U.S. Food and Drug Administration regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable global regulatory agencies. The Director, Design Quality Assurance (DQA) - Tissue Technologies division has the primary responsibility to ensure the delivery of high-quality design history files (DHF) and Risk management files (RMF) that are compliant with applicable global regulations.
Associate Director Quality Assurance CatalentAssociate Director Quality AssurancePhiladelphia, PennsylvaniaDemonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Associate Director, Quality Assurance-Home Health/Hospice Bayada Home Health Care, Inc.Associate Director, Quality Assurance-Home Health/HospicePennsauken, NJ$110,000–$114,000 / yearCompetent to write reports, business correspondence and procedure manuals and the ability to effectively present information and respond to questions from groups of employees, managers, directors and clients. POSITION SUMMARY: Responsible for the development, communication, execution, reporting and analysis of quality assurance activities related to operational, contractual, or compliance audit activities.
Director, Data Quality and Process, External Data Clinical Data Management Genmab ASDirector, Data Quality and Process, External Data Clinical Data ManagementPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. As a member of the External Data Management Leadership Team, this role partners closely with Clinical Data Management, Clinical Operations, Biomarker Operations, Medical, Biostatistics, Clinical Programming, Regulatory, and external partners to ensure efficient acquisition, integration, quality, and governance of external clinical data throughout the study lifecycle.
Associate Director, Risk Based Quality Management Lead Summit Therapeutics IncAssociate Director, Risk Based Quality Management LeadPrinceton, NJ$174,000–$204,000 / yearServing as the primary RBQM subject matter expert within study teams, this role implements and maintains study-level risk management, centralized monitoring, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), targeted monitoring strategies, and risk review processes. Working closely with Clinical Operations, Clinical Science, Data Management, Biostatistics, Medical Monitoring, and CRO partners, the RBQM Lead proactively identifies, evaluates, escalates, and mitigates risks throughout the clinical trial lifecycle to support participant safety, data reliability, and regulatory compliance.
Senior Director, Product Quality Lead (Post-Marketing and Pharmacovigilance Madrigal Pharmaceuticals IncSenior Director, Product Quality Lead (Post-Marketing and PharmacovigilancePA$244,000–$299,000 / yearAs a key member of the Quality leadership team, you will partner closely with Pharmacovigilance, Regulatory Affairs, Manufacturing, and Commercial teams to embed quality across the full product lifecycle, with particular focus on post-marketing safety surveillance, literature monitoring, and Product Quality Complaints (PQC). Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality.
Senior Director, Global Quality & Regulatory - Exton, PA DSM Nutritional Products Asia Pacific Pte LtdSenior Director, Global Quality & Regulatory - Exton, PAExton, PA$157,200–$225,000 / yearDeep knowledge of quality management systems and regulatory frameworks applicable to medical devices and related products for a Class III medical device operation (21CFR 820, ISO 9001, 13485, 14001, 45000); experience with clean room theory and operation is a plus. This member of the Global Leadership Team serves as the global head of Quality & Regulatory for Biomedical and is accountable for setting strategy, driving execution, and fostering a culture of compliance, continuous improvement, and operational excellence across all sites and functions.
Associate Director, Clinical R&D QA US Incyte CorpAssociate Director, Clinical R&D QA USWilmington, DEAssist with the maintenance of the clinical Quality Management System including QA support for change control deviations reviewrevision of SOPs with ensuring continuous process improvement Stay abreast of clinical trial requirements ICH GCP and guidelines from other regulatory agencies for the management of clinical trials as appropriate. Be thoroughly familiar with assigned Incyte Compounds and protocol REQUIREMENTS Bachelors degree in a science or healthcare related discipline or similarly conferred degree from a university 5 to 7 years experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
Associate Director, Clinical Quality Management Kyowa KirinAssociate Director, Clinical Quality ManagementPrinceton, NJ$175,000–$190,000 / yearThis role owns the end-to-end RBQM framework, including risk identification, assessment, mitigation, centralized monitoring, lessons learned, and maintenance of a clinical risk library, ensuring risks are managed consistently and intelligently across studies, programs, vendors, and regions. Summary: The Associate Director, Clinical Quality Management serves as the central Risk-Based Quality Management (RBQM) Lead for Clinical Operations, responsible for enterprise-wide, proactive risk management across clinical trials.
Associate Director, Quality Risk Specialist (GCP) Bristol-Myers Squibb CoAssociate Director, Quality Risk Specialist (GCP)Princeton, NJ$163,850–$198,543 / yearProject Management: Must be able to manage complex assignments/projects and effectively deliver all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines. The Associate Director, RBQM will mainly be responsible for developing the Quality Narrative at the study and/or ASSET and TA levels to document end-to-end RBQM for critical to quality (CtQ) data, processes, and vendors, demonstrating effective risk and issue management.
Associate Director, HRBP, Site Quality Global Business Unit Bristol Myers SquibbAssociate Director, HRBP, Site Quality Global Business UnitPrinceton, NJ$161,840–$196,112 / yearThis role helps to shape and execute the people strategy required to deliver a high-performing, compliant, and engaged workforce within a complex manufacturing and quality environment, under supervision of the Executive Director, HRBP, Global Business Unit and the Executive Director, HRBP Global Quality ‑performing, compliant, and engaged workforce within a complex manufacturing and quality environment. The HRBP serves as a critical connector across multiple GPDS functions, collaborating closely with Manufacturing Operations, Site Quality, and global Centers of Expertise (CoEs) to enable organizational effectiveness, workforce planning, talent management, and culture transformation.
Associate Clinical Director, Integrated Care Quality (NP/MD) - Remote Included HealthAssociate Clinical Director, Integrated Care Quality (NP/MD) - RemotePhiladelphia, PARemoteAt Included Health, the Associate Clinical Director, Integrated Care Quality (NP/MD) is responsible for the strategy, external representation, and program leadership needed to ensure our clinical services perform credibly in high-stakes client, consultant, and audit-facing settings. The Director will represent Included Health in consequential meetings with clients, consultants, health plans, and internal leaders; shape the vision for external-facing clinical quality work; build trusted relationships; and translate audit and quality findings into durable operational improvement strategies.
Associate Director, Quality Change Management Madrigal Pharmaceuticals IncAssociate Director, Quality Change ManagementConshohocken, PA$164,000–$200,750 / yearPlease know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality.
Director, Quality (GCP/GCLP/GVP) Larimar Therapeutics IncDirector, Quality (GCP/GCLP/GVP)Bala Cynwyd, PAThe Director, Quality (GCP/GCLP/GVP) works with all members of the Quality team, including relevant internal contractors, to ensure quality compliance internally and among the company's contractors, CROs, service providers, etc. to enable development, regulatory approval, and commercialization of the company's products. The Company: Larimar Therapeutics Inc. is a publicly held clinical-stage biotechnology company focused on developing treatments for patients suffering from complex rare diseases using its novel cell penetrating peptide technology platform.
Senior Director, Supplier & External Manufacturing Quality Integra LifeSciences Holdings Corp.Senior Director, Supplier & External Manufacturing QualityPrinceton, NJ$192,050–$263,350 / yearThis role ensures that external manufacturing partners, critical suppliers, and service providers consistently meet regulatory, quality, and business requirements while enabling operational excellence, scalability, and risk‑based decision making. The Senior Director, Supplier & External Manufacturing Quality is responsible for providing global strategic leadership and governance for supplier quality management and contract manufacturing quality across the enterprise.
Director, Corporate Quality Management System (QMS) Integra LifeSciences Holdings CorpDirector, Corporate Quality Management System (QMS)Princeton, NJ$166,750–$228,850 / yearLead, execute, and provide expert guidance on enterprise Quality initiatives with significant regulatory complexity, including FDA Warning Letter responses, Form 483 observations, Recall/field action activities, enterprise-wide QMS change programs, manufacturing site remediation efforts involving complex CAPAs, and high-risk Quality remediation initiatives. The role leads global teams responsible for document control, training administration, management controls, technical writing, and regulatory response management, and acts as a key advisor to executive leadership on Quality strategy, compliance risk, and business performance.
Director, Corporate Quality Management System (Qms) Integra LifeSciences Holdings Corp.Director, Corporate Quality Management System (Qms)Princeton, NJ$166,750–$228,850 / yearLead, execute, and provide expert guidance on enterprise Quality initiatives with significant regulatory complexity, including FDA Warning Letter responses, Form 483 observations, Recall/field action activities, enterprise-wide QMS change programs, manufacturing site remediation efforts involving complex CAPAs, and high-risk Quality remediation initiatives. The role leads global teams responsible for document control, training administration, management controls, technical writing, and regulatory response management, and acts as a key advisor to executive leadership on Quality strategy, compliance risk, and business performance.
Senior Director, Global Quality & Regulatory - Exton, PA DSMSenior Director, Global Quality & Regulatory - Exton, PAExton, PA$157,200–$225,000 / yearDeep knowledge of quality management systems and regulatory frameworks applicable to medical devices and related products for a Class III medical device operation (21CFR 820, ISO 9001, 13485, 14001, 45000); experience with clean room theory and operation is a plus. This member of the Global Leadership Team serves as the global head of Quality & Regulatory for Biomedical and is accountable for setting strategy, driving execution, and fostering a culture of compliance, continuous improvement, and operational excellence across all sites and functions.
Associate Director PV QA Genmab ASAssociate Director PV QAPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.
Lab Quality & MLS Program Director with ASCP-BOC/ASCP-BOC(MLS/MT) ResiliencyLab Quality & MLS Program Director with ASCP-BOC/ASCP-BOC(MLS/MT)Philadelphia, PennsylvaniaQualifications: Education Requirements • Master's Degree Experience • Relevant Experience Certification and Licensure • ASCP-BOC or ASCP-BOC generalist certification as Medical Laboratory Scientist/Medical Technologist Required Skills • Analytical Skills • Collaborative Skills • Computer Skills to include use and navigation • Customer Service Skills • Delegation Skills • Detail Oriented • Excellent Communications Skills • Excellent Interpersonal Skills • Good Reasoning Skills • Leadership Skills • Listening Skills • Medical Terminology • Microsoft Office Applications • Multitasking • Organizational Skills • Prepare & Give Presentations • Service Orientation • Strategic Thinking • Strong Team Player Appoints faculty, coordinates review of the program and all updates, receives and processes all applications for admission, acts as a liaison between the program and academic and clinical affiliates, oversees program faculty, instructors, and students, grants the certificates documenting program completion, and retains final transcripts and certificates indefinitely.
Executive Director, Quality Systems & Operational Excellence Lead Madrigal Pharmaceuticals IncExecutive Director, Quality Systems & Operational Excellence LeadPA$276,000–$337,000 / yearLeads quality event trending and signal detection across the product lifecycle, ensuring meaningful insight generation and management review from Development QA through Commercial QA in support of lifecycle management, continuous improvement, and risk-based decision making within a virtual biotech operating model. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.
NewSr. Director, eCompliance – Global Quality Technical Operations PCI Pharma ServicesSr. Director, eCompliance – Global Quality Technical OperationsPhiladelphia, PennsylvaniaMasterControl Implementation: Provide technical compliance oversight for the enterprise-wide rollout of MasterControl QMS and eBatch Record (eBR), ensuring that global templates and site-specific configurations maintain a high level of regulatory rigor. Data Mapping & Risk Assessment: Lead comprehensive data mapping exercises across global sites to identify high-risk data flows and implement technical controls (e.g., electronic signatures, restricted permissions) to mitigate risks.
Sr. Director, eCompliance - Global Quality Technical Operations PCI Pharma ServicesSr. Director, eCompliance - Global Quality Technical OperationsPhiladelphia, PAMasterControl Implementation: Provide technical compliance oversight for the enterprise-wide rollout of MasterControl QMS and eBatch Record (eBR), ensuring that global templates and site-specific configurations maintain a high level of regulatory rigor. Data Mapping & Risk Assessment: Lead comprehensive data mapping exercises across global sites to identify high-risk data flows and implement technical controls (e.g., electronic signatures, restricted permissions) to mitigate risks.
NewSr. Director, Ecompliance - Global Quality Technical Operations PCI ServicesSr. Director, Ecompliance - Global Quality Technical OperationsPhiladelphia, PAMasterControl Implementation: Provide technical compliance oversight for the enterprise-wide rollout of MasterControl QMS and eBatch Record (eBR), ensuring that global templates and site-specific configurations maintain a high level of regulatory rigor. Data Mapping & Risk Assessment: Lead comprehensive data mapping exercises across global sites to identify high-risk data flows and implement technical controls (e.g., electronic signatures, restricted permissions) to mitigate risks.
Sr. Director, Sterility Assurance – Global Quality Technical Operations PCI Pharma ServicesSr. Director, Sterility Assurance – Global Quality Technical OperationsPhiladelphia, PennsylvaniaHighest Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems and deal with nonverbal symbolism in its most difficult phases while dealing with concrete/abstract variables. Capital Project Support: Provide expert technical consultation for new builds and retrofits, ensuring facility design, airflow patterns (Grade A/ISO 5), and equipment sterilization (SIP/Autoclave) meet global regulatory expectations.
Sr. Director, Sterility Assurance - Global Quality Technical Operations PCI Pharma ServicesSr. Director, Sterility Assurance - Global Quality Technical OperationsPhiladelphia, PAHighest Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems and deal with nonverbal symbolism in its most difficult phases while dealing with concrete/abstract variables. Capital Project Support: Provide expert technical consultation for new builds and retrofits, ensuring facility design, airflow patterns (Grade A/ISO 5), and equipment sterilization (SIP/Autoclave) meet global regulatory expectations.
Associate Director, Quality (Validation And Data Integrity) Larimar TherapeuticsAssociate Director, Quality (Validation And Data Integrity)Bala Cynwyd, PAJob Responsibilities: The responsibilities for the Associate Director/Director, Quality, Validation and Data Integrity may include, but are not limited to the following activities: Provide Quality oversight of Computer System Validation (CSV)/Computer Software Assurance (CSA) activities related to initial implementations, changes, periodic review, maintenance, and decommissioning of GxP systems. The management team, employees, and consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs, commercialization, and the development of manufacturing processes utilizing good manufacturing practices (GMPs).
NewDirector of Nursing (DON) Christ's HomeDirector of Nursing (DON)Warminster, PAFull timeRequired Attributes:Active Registered Nurse (RN) license (Pennsylvania or eligible)Proven leadership experience in skilled nursing or long‑term careStrong knowledge of CMS regulations and survey processExcellent communication, leadership, and team‑building skillsCommitment to faith‑based, nonprofit values and compassionate careWhat We OfferCompetitive salary based on experienceComprehensive benefits packageSupportive, collegial leadership environmentOpportunity to lead within a high‑performing 5‑Star facilityA leadership role where your work has real impact-every day CMS 5‑Star Rated Skilled Nursing FacilityIntentionally small 48‑bed community allowing for meaningful leadership and personal connectionFaith‑based, nonprofit mission focused on dignity, compassion, and serviceCollaborative, stable leadership teamStrong culture of quality, integrity, and continuous improvementAt Christ's Home, we believe excellence in care begins with strong leadership and a supportive environment for both residents and staff.
Future Leaders Director of Nursing in Training - RN Crestview Center - PAFuture Leaders Director of Nursing in Training - RNLanghorne, Pennsylvania$75,000–$90,000 / yearFull timeStrengthen Leadership Skills: Attend leadership meetings, coaching sessions, and development workshops focused on communication, accountability, culture-building, and leading high-performing clinical teams. Gain Hands-On Leadership Experience: Rotate through key clinical and operational areas to understand how nursing leadership impacts quality outcomes, staffing, resident experience, compliance, and overall center success.
Director of Nursing, Children's Services BancroftDirector of Nursing, Children's ServicesMount Laurel, New Jersey$125,000–$139,000 / yearFull timeManages the ongoing job performance of direct reports; develops and communicates performance goals, completes performance evaluations within established timeframes; provides feedback, develops and takes action on performance improvement plans, and determines and implements disciplinary action as needed in the area of nursing function; Provides ongoing leadership, advice, training, and guidance to direct reports regarding the overall nursing care, instruction, and safety of persons served, and as outlined in the Individual Program Plan for each person served; Ensures proper staffing levels and work distribution for programs, to ensure the provision of high-quality care for all persons served; Conducts regular staff meetings and attends various management meetings to promote a constant flow of information, open discussions, knowledge sharing, and to keep staff well-informed; Attends various internal management meetings, external conferences, Interdisciplinary (IDT) and/or Trans-Disciplinary (TDT) meetings, and family conferences as needed. Conduit leader and liaison with discipline-specific clinical directors, managers and staff, Sr Director of Nursing, external case workers, state and federal regulatory agencies, family members, etc., to attain and maintain the provision of quality care for persons served and assist in the removal or modification of reported health-related barriers; Operating within personal license constraints in strict accordance with regulations and guidelines defined by the Nurse Practices Act in New Jersey, N.J.