Clinical Supplies Project Manager (Hiring Our Heroes Corporate Fellow)
Part-time
Merck
Job Requirements We are excited to be a sponsor of Hiring our Heroes and proud to offer transitioning service members a unique opportunity to gain valuable professional experience through our 12-week fellowship program.
- The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full portfolio of clinical trials. GCS supports more than 300 Phase I-IV clinical trials run in-house, 400+ outsourced or run by partners, and 300+ clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than 60+ countries, in accordance with US and Global regulations, company policies, and Standard Operating Procedures. - The GCS Clinical Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business. Clinical Supplies Project Managers (CSPMs) are responsible for the translation of global clinical study demand into supply plans and are accountable for all delivery of clinical finished goods materials to initiate trials on time and maintain patient continuity of supply. - Working independently, the CSPM designs strategic and operational plans for all activities associated with their assigned clinical studies within a given development program (CSPM Protocol Manager) and/or all clinical supplies across an entire compound program (CSPM Program Manager). The incumbent is expected to have a strong understanding of drug development, clinical research, and/or clinical supply chain, as well as interpersonal skills with a demonstrated ability to negotiate with key stakeholder groups and drive/influence results in a dynamic environment. - The CSPM Protocol Manager serves as the primary protocol-level GCS point of contact for given protocols to customers both internal and external to GCS and serves as the GCS spokesperson at clinical development related meetings (i.e., Clinical Trial Teams) and product development related meetings. - The CSPM Program Manager serves as the primary program-level GCS point of contact representing the GCS Planning Team to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical development related meetings that impact the clinical program (i.e. Clinical Supply Program Team, Clinical Development Sub-Team) as well as product development related meetings. - Primary activities include, but are not limited to: General Activities: - ----Interacts with various organizations, as a lead GCS Planning program representative, such as Clinical Sciences and Study Management (CSSM), Regulatory, CMC, Pharmaceutical Sciences, Formulation Development, and Global Development Quality as necessary to address drug supply related topics. ----Works directly in the SAP system to establish a consolidated, visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods). ----Responsible and accountable for utilizing key tools in the planning and managing of clinical supplies for assigned program(s). This may include Microsoft Project Plans, Actions, Issues and Risk (ADI) Logs, forecasting tools (SAP), etc. ----Support the collection of clinical supply chain metrics to describe business health and the identification of areas for operational improvement. ----Responsible for initiating non-Merck marketed drug product planning activities for new protocols ----Serves in a support or lead role for clinical supply issue escalation to GCS Leadership (as issue owner or in support of other CSPMs that support assigned programs) ----Mentors new team members and supports staff development, as needed ----Participates as a lead business process owner or SME in a particular area of expertise. ----Champions and drives identified business process improvement initiatives, as needed. - CSPM Protocol Manager Specific: - ----Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies. ----Responsible and accountable for establishing the timelines for clinical supply needs per protocol and providing the signal for sourcing, manufacturing, packaging, and distribution for development products and non-Merck marketed products. ----Analyzes and anticipates project risks as they relate to clinical supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. ----Responsible for authoring the Clinical Supplies section of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. ----Participate in Interactive Voice Response (IVR) System development and User Acceptance Testing (UAT) for assigned studies. - - CSPM Program Manager Specific: - ----Oversees all bulk drug supply management and ensures proper allocation of drug product as needed across assigned program(s) ----Responsible and accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s) ----Responsible for identifying significant supply risks associated with clinical bulk requirements. ----Responsible for the clinical supply budget for respective program(s) and for supporting all protocol and program cost estimates requested by Product Development Teams ----Chairs the Clinical Supply Program Team (CSPT) and works closely with Clinical Team Leads, Project Management (PM), CMC, Regulatory and other functional area representatives to negotiate timelines and strategy for clinical supplies across all assigned program(s) ----Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities. ----Ensures GCS Planning Leadership is aware of program pipeline forecast to ensure proper resourcing of all levels of planning support - Minimum education required: - ----Bachelor's degree in a scientific, business, or related discipline required, MS/MBA preferred. - Required Experience and Skills: - ----At least 8 years of experience in project management ----At least 3 years of experience in planning, scheduling, coordination and processing of clinical supply activities, or the equivalent ----Understanding of MRP systems and demand planning principles ----Strong organizational, time management and problem solving skills ----Results oriented with the proven ability to execute on collaborative projects and develop subject matter expertise Exceptional written and verbal communication and relationship skills along with high personal integrity, credibility, and energy. ----Ability to prioritize tasks and initiatives appropriately to mitigate supply risks. ----Advanced proficiency in Microsoft Excel, PowerPoint, and Word. ----Experience with change management and leading process improvement initiatives. - Preferred Experience and Skills: - ----Demonstrates ability to negotiate, resolve conflicts and engage in decision making as well as partner and influence across functional areas and organizations. ----Strong knowledge of the principles of project management and clinical customer relationship management. ----Knowledge of drug development, production, distribution, shipping, destruction, and reconciliation processes and procedures. ----Knowledge of order management, supply chain operations and document control. ----Experience leading teams and developing direct reports ----Familiarity with data analytics/visualization software. ----Familiarity with SAP as an ERP/MRP system. ----Familiarity with GMP requirements, quality procedures, and SOP execution.
Requirement:
This posting is for the Hiring Our Heroes, Corporate Fellowship 2026 - Cohort 3. Candidates must be transitioning service member fellows who will complete the program within the last 180 days of transition from military service. The fellowship will be 12 weeks long.
- US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-For more information about personal rights under the U.S. Equal Opportunity
Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement•
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts
This is an unpaid, 12-week training fellowship hosted by our company, aligned with DoD SkillBridge guidelines. This is not an offer of employment. Participants are ineligible to receive employment benefits. This opportunity is exclusively for active participants in the Hiring Our Heroes (HOH) Corporate Fellowship Program.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
- The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full portfolio of clinical trials. GCS supports more than 300 Phase I-IV clinical trials run in-house, 400+ outsourced or run by partners, and 300+ clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than 60+ countries, in accordance with US and Global regulations, company policies, and Standard Operating Procedures. - The GCS Clinical Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business. Clinical Supplies Project Managers (CSPMs) are responsible for the translation of global clinical study demand into supply plans and are accountable for all delivery of clinical finished goods materials to initiate trials on time and maintain patient continuity of supply. - Working independently, the CSPM designs strategic and operational plans for all activities associated with their assigned clinical studies within a given development program (CSPM Protocol Manager) and/or all clinical supplies across an entire compound program (CSPM Program Manager). The incumbent is expected to have a strong understanding of drug development, clinical research, and/or clinical supply chain, as well as interpersonal skills with a demonstrated ability to negotiate with key stakeholder groups and drive/influence results in a dynamic environment. - The CSPM Protocol Manager serves as the primary protocol-level GCS point of contact for given protocols to customers both internal and external to GCS and serves as the GCS spokesperson at clinical development related meetings (i.e., Clinical Trial Teams) and product development related meetings. - The CSPM Program Manager serves as the primary program-level GCS point of contact representing the GCS Planning Team to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical development related meetings that impact the clinical program (i.e. Clinical Supply Program Team, Clinical Development Sub-Team) as well as product development related meetings. - Primary activities include, but are not limited to: General Activities: - ----Interacts with various organizations, as a lead GCS Planning program representative, such as Clinical Sciences and Study Management (CSSM), Regulatory, CMC, Pharmaceutical Sciences, Formulation Development, and Global Development Quality as necessary to address drug supply related topics. ----Works directly in the SAP system to establish a consolidated, visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods). ----Responsible and accountable for utilizing key tools in the planning and managing of clinical supplies for assigned program(s). This may include Microsoft Project Plans, Actions, Issues and Risk (ADI) Logs, forecasting tools (SAP), etc. ----Support the collection of clinical supply chain metrics to describe business health and the identification of areas for operational improvement. ----Responsible for initiating non-Merck marketed drug product planning activities for new protocols ----Serves in a support or lead role for clinical supply issue escalation to GCS Leadership (as issue owner or in support of other CSPMs that support assigned programs) ----Mentors new team members and supports staff development, as needed ----Participates as a lead business process owner or SME in a particular area of expertise. ----Champions and drives identified business process improvement initiatives, as needed. - CSPM Protocol Manager Specific: - ----Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies. ----Responsible and accountable for establishing the timelines for clinical supply needs per protocol and providing the signal for sourcing, manufacturing, packaging, and distribution for development products and non-Merck marketed products. ----Analyzes and anticipates project risks as they relate to clinical supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. ----Responsible for authoring the Clinical Supplies section of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. ----Participate in Interactive Voice Response (IVR) System development and User Acceptance Testing (UAT) for assigned studies. - - CSPM Program Manager Specific: - ----Oversees all bulk drug supply management and ensures proper allocation of drug product as needed across assigned program(s) ----Responsible and accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s) ----Responsible for identifying significant supply risks associated with clinical bulk requirements. ----Responsible for the clinical supply budget for respective program(s) and for supporting all protocol and program cost estimates requested by Product Development Teams ----Chairs the Clinical Supply Program Team (CSPT) and works closely with Clinical Team Leads, Project Management (PM), CMC, Regulatory and other functional area representatives to negotiate timelines and strategy for clinical supplies across all assigned program(s) ----Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities. ----Ensures GCS Planning Leadership is aware of program pipeline forecast to ensure proper resourcing of all levels of planning support - Minimum education required: - ----Bachelor's degree in a scientific, business, or related discipline required, MS/MBA preferred. - Required Experience and Skills: - ----At least 8 years of experience in project management ----At least 3 years of experience in planning, scheduling, coordination and processing of clinical supply activities, or the equivalent ----Understanding of MRP systems and demand planning principles ----Strong organizational, time management and problem solving skills ----Results oriented with the proven ability to execute on collaborative projects and develop subject matter expertise Exceptional written and verbal communication and relationship skills along with high personal integrity, credibility, and energy. ----Ability to prioritize tasks and initiatives appropriately to mitigate supply risks. ----Advanced proficiency in Microsoft Excel, PowerPoint, and Word. ----Experience with change management and leading process improvement initiatives. - Preferred Experience and Skills: - ----Demonstrates ability to negotiate, resolve conflicts and engage in decision making as well as partner and influence across functional areas and organizations. ----Strong knowledge of the principles of project management and clinical customer relationship management. ----Knowledge of drug development, production, distribution, shipping, destruction, and reconciliation processes and procedures. ----Knowledge of order management, supply chain operations and document control. ----Experience leading teams and developing direct reports ----Familiarity with data analytics/visualization software. ----Familiarity with SAP as an ERP/MRP system. ----Familiarity with GMP requirements, quality procedures, and SOP execution.
Requirement:
This posting is for the Hiring Our Heroes, Corporate Fellowship 2026 - Cohort 3. Candidates must be transitioning service member fellows who will complete the program within the last 180 days of transition from military service. The fellowship will be 12 weeks long.
- US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-For more information about personal rights under the U.S. Equal Opportunity
Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement•
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts
This is an unpaid, 12-week training fellowship hosted by our company, aligned with DoD SkillBridge guidelines. This is not an offer of employment. Participants are ineligible to receive employment benefits. This opportunity is exclusively for active participants in the Hiring Our Heroes (HOH) Corporate Fellowship Program.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Vacancy posted 24 days ago
Similar jobs that could be interesting for youBased on the Clinical Supplies Project Manager (Hiring Our Heroes Corporate Fellow) in Rahway, NJ vacancy
- ...single day!About the RoleThe Corporate Operations Associate provides... ..., data analysis, and special projects. The successful candidate will... ...initiatives assigned by management.Assist with training and documentation... ...in Business, Operations, Supply Chain, or related field...SuggestedWork at office
Turtle
Clark, NJ5 days ago - ...Accountable for achieving the final clinical deliverable (usually clean... ...customer. Interprets data on project issues and makes good... ...experienced team members or line manager. Works to ensure that all clinical... ...the study and according to corporate standard policies....SuggestedContract workLocal area
$53.5k - $68k
...(SRP) which provides supervision, case management, and social service connections to thousands... ...Supervised Release Program, such as; Clinical, Case Management, Community Engagement and... ...and truthful information throughout the hiring process. Any misrepresentation,...SuggestedHourly payFull timeTemporary workWork at officeLocal areaImmediate startWork visaFlexible hoursWeekend workAfternoon shiftWeekday work- ...opportunity to grow alongside a highly collaborative team? We're partnering with an exciting clinical research organization that is continuing to expand its project management team. This is an opportunity for an experienced Clinical Project Manager to join a warm,...Suggested
$35 - $42 per hour
...Clinical Research Coordinator - Somerset, NJ Work Set-Up: On-site Scheduled... ...with maintaining regulatory binders, managing study supplies, and updating study portals. Strong... ...IQVIA is committed to integrity in our hiring process and maintains a zero tolerance...SuggestedHourly payFull timePart timeImmediate startWorldwideIQVIA
Linden, NJ2 days ago$65k - $80k
...trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter expertise... ...a proactive, self-starting individual who can effectively manage patient-facing responsibilities while ensuring strict adherence...Full timeTemporary workWork at officeLocal areaMonday to FridayVitalief
Rahway, NJmore than 2 months ago$65k - $80k
Vitalief, located in Rahway, NJ, is seeking a Clinical Research Coordinator to support cardiovascular clinical trials at community hospital... .... The role includes coordinating trial activities, managing patient interactions, and ensuring regulatory compliance. Benefits...- ...22395681Reference Number: 24-00464Title: Supply Chain ManagerLocation: Iselin, NJ, 08830Posted... ...: HAN Staffing Job Title: Materials Manager Location: Chicago, IL - Onsite Job Description... ...manufacturing level, cross functional project teams, and our network of vendors. You...Contract workWork at office
- ...recruiting for a Senior Procurement Manager. This position will be located... ...: Ensure compliance with corporate policies, ethical standards,... ...Skills: Bachelor’s degree in supply chain management, Business Administration... ...policies and date of hire, Employees are eligible for the...Full timeTemporary workWork experience placementLocal areaImmediate startFlexible hours
$173.2k - $272.6k
...difference.Value Chain Management (VCM) is the... ...Manufacturing Division product supply chain strategy in alignment... ..., cost of goods projections, and post-approval product... ...of CMC and clinical strategy to bring a product... ...candidates can engage in a hiring process that exhibits...Full timeFor contractorsLocal areaFlexible hours$129k - $203.1k
...DescriptionJob DescriptionSupply Chain Management (SCM) coordinates all aspects of supply through planning, sourcing,... ...pharmaceutical or biotech industry.Prior project management experience in a cross-... ...that candidates can engage in a hiring process that exhibits their true...Full timeFor contractorsLocal areaFlexible hours- ...coordinating payroll scheduling, ensuring accurate documentation and compliance. As part of the team, you will facilitate training for new hires, handle routine inquiries, and help maintain club policies. Regular attendance and teamwork are essential in this fast-paced retail...
$90.2k - $128.5k
MANAGER, CUSTOMER SUPPLY CHAINDivision: Consumer Products DivisionLocation: Clark, NJHello, we’re L’Or... ...executions are progressing to plan.Project Leadership: Lead or participate in specific... ...processes and to advocating for hiring and promoting each candidate in an ethical...Work experience placementSummer workWork from homeWorldwideFlexible hours2 days per week$60k
Strategic Corporate Recruiter | High-Volume Talent Partner | Human-First, AI-Enhanced Hiring Expert Come lead the Procurement team at the Newark... ...role of the Procurement Manager is to assist in successfully managing SSP America's Supply Chain Programs. The Procurement...Full timeLocal area$95k - $105k
...purpose is to keep customers' supply chains flowing and enable the... ...Posting Title: Operations Manager Time Type: Full Time The... ...management responsibilities include hiring and training, planning and... ...expected to comply with all corporate and site-specific policies....Full timeContract workTemporary workTraineeshipWork at officeLocal areaFlexible hoursNight shiftAfternoon shiftDSV Air & Sea
Port Reading, NJ4 days ago- ...Operations Manager Location: Port Reading, USA The Operations... ...responsibilities include hiring and training, planning and assigning... ...expected to comply with all corporate and site-specific policies.... ...needed changes in levels of supplies, equipment, or staffing needs...Contract workTraineeshipWork at officeLocal areaFlexible hoursNight shiftAfternoon shift
DSV
Port Reading, NJ4 days ago $103.45k - $197.73k
.... The Opportunity As a dedicated Manager, Claims Operations, you will lead... ...for career progression Supports projects by serving as a subject matter expert. Hires, develops, and coaches claims employees... ...pay incentives based on overall corporate and individual performance and at...Work at officeRemote workRelocation packageFlexible hoursUSAA
Elizabeth, NJ5 days ago- ...ahead and will know what people want before they do—and you’ll never miss a beat. Become a pro in inventory management, financial management, and procurement. SUPPLY AND LOGISTICS JOBS IN THE NAVY LOGISTICS SPECIALIST How do you launch F/A-18 Hornets off an...Full timePart timeWorldwideOverseas
U.S. Navy
Elizabeth, NJ7 hours ago - ...they do—and you’ll never miss a beat. Become a pro in inventory management, financial management, and procurement. LOGISTICS SPECIALIST... ...F/A−18 Hornets off an aircraft carrier without a stocked supply of new tires on board? You don’t. That's why the Navy relies on...Full timePart timeWorldwideOverseas
U.S. Navy
Elizabeth, NJ1 day ago $23.18 - $34.77 per hour
...competency to perform the role through ongoing education and training. Follows best practice guidelines as outlined by the NJSN management team. Shift and rotating days, nights, weekend and holiday assignments. Occasional overtime may be required. Responsible for timely...Hourly payTemporary workBank staffH1bLocal areaFlexible hoursShift workNight shiftRotating shiftDay shift$190.5k - $254k
...Today, we add value to our customers' entire supply chain by transporting, storing, packaging... ...leadership by delivering advanced Order Management, Freight Management and Supply Chain... ...EmploymentDSV Air & Sea Inc. employees are hired for an undefined period of time as “at will...Temporary workWork experience placementWork at officeLocal areaMonday to FridayFlexible hours- ...goods worldwide. Summary The Carrier Procurement Manager is responsible for developing and executing... .... Additional duties, responsibilities, and projects as assigned. Education & Experience Bachelor’s degree in Supply Chain, Logistics, Business, or a related field...Contract workWork at officeLocal areaRemote workWorldwide
- Vitalief is seeking a Clinical Research Coordinator in New Brunswick, NJ, to manage Oncology-related trials. Responsibilities include patient screening, consent, and managing patient care, while collaborating with healthcare teams. A Bachelor's degree and 1-2 years of clinical...
- Vitalief in New Brunswick, NJ is seeking a dedicated Senior Clinical Research Coordinator to support clinical trials, particularly in Oncology. The role involves patient interaction, data management, and ensuring regulatory compliance. Candidates must have a Bachelor’s...Full time
$70k - $80k
...intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise... ...consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and...Full timeTemporary workWork at officeRemote workVitalief
New Brunswick, NJ29 days ago$103.56k - $125.5k
...who do it. Position Summary The Clinical Trial Manager (CTM) is accountable for end-to-end study... ...effective coordination, and successful project execution. Key Responsibilities... ...Occasional local travel requirement We hire for skills and capabilities, not just credentials...Hourly payFull timeSummer workLive inLocal areaRemote workFlexible hoursBristol-Myers Squibb Company
New Brunswick, NJ3 days ago$110k - $140k
...ABOUT VITALIEF Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing... ...seeking an experienced Pre & Post-Award Clinical Research Grants Project Manager to support a major statewide clinical research initiative for...Full timeTemporary workWork at officeRemote workVitalief
New Brunswick, NJ15 days ago$70k - $95k
...Procurement/SCM Location Job Description Sanmina Corporation (Nasdaq: SANM) is a leading integrated... ...system accuracy and plan stability. Manages ECOs developing implementation strategies and executing changes across the supply chain and production floor. Releases required...Permanent employmentContract workWork experience placementFlexible hoursSanmina
Newark, NJ3 days ago$70k - $95k
...Procurement/SCM Location Job Description Sanmina Corporation (Nasdaq: SANM) is a leading integrated... ...system accuracy and plan stability. Manages ECOs developing implementation strategies and executing changes across the supply chain and production floor. Releases required...Permanent employmentContract workWork experience placementFlexible hoursSanmina
Newark, NJ1 day ago$65k - $78k
...Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional... ...and research leadership to support the successful execution, management, and ongoing operations of the vascular medical device...Full timeTemporary workWork at officeRemote work2 days per week3 days per weekVitalief
Newark, NJmore than 2 months ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Supplies Project Manager (Hiring Our Heroes Corporate Fellow). Be the first to apply!
Related searches
- projects Rahway, NJ
- project controls Rahway, NJ
- senior implementation project manager Rahway, NJ
- software implementation project manager Rahway, NJ
- implementation project manager remote Rahway, NJ
- retail project merchandiser part time Rahway, NJ
- special projects Rahway, NJ
- project finance Rahway, NJ
- capital projects Rahway, NJ
- recruiting specialist Rahway, NJ