Cytiva

5,001-10,000 employeeshttp://www.cytiva.com/

Description

We’re the Life Sciences newcomer you already know. Cytiva is bringing our long-standing expertise to the forefront of science, to fuel research, discovery, and development with technologies, instruments, and software. We drive customer-centered innovation in 11 facilities across Asia, Europe and America from idea to commercial development stages.

Locations

The company has not entered any location yet.

Qualification Services Project Manager (Remote Role)

Biotech and Pharma

5 days ago | Rochester, New York, United States | Cytiva

Qualification Services Project Manager (Remote Role)

5 days ago | Rochester, New York, United States | Cytiva

Cytiva

Opening date:November 25

Closing date: December 23 2021

Industry:Biotech and Pharma,

Type:Full Time

Job description

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

What you’ll do!

As a result of our growing customer needs to ensure maximum lifecycle utilization of their equipment, we are looking for a Global Services Qualification Services Project Manager.

  • Lead Commissioning and Qualification projects for large scale pharmaceutical production projects.
  • Communicate current state to customers and senior management to secure deliverables.
  • Manage all customer project milestones deliverables; handle urgent tasks, regional communication to display actions made and in progress.
  • Collaborate and connect with cross-functional project leaders and key partners to secure qualification product deliverables.
  • Manage quality objectives, regulatory requirements, schedules, program risks and making decisions based on business objectives.
  • Ensure compliance/closure of regulatory and quality requirements before approving program milestones.
  • Maintain budget and timelines.
  • Identify and assess changes in scope.
  • Act as point of contact to respond/resolve internal & external issues requiring management intervention
  • Support customer meetings as needed
  • Visit customer sites as needed to kick off projects and ensure proper execution of protocols at the site.
  • Work cross functionally with other function in qualification services.
  • Use DBS as appropriate
  • Travel as needed – 10-15%

Who You Are

  • Bachelor's degree in Science, Engineering or related area or relevant work experience.
  • 8-10 years of relevant project management experience.
  • Experience from biopharma industry as well as understanding of cGMP compliance and 21 CFR Part 11 is an advantage
  • Experience with Risk-Based Approach to Commissioning and Qualification.
  • Proven knowledge and experience working with the project management life cycle.
  • Demonstrated capability of cross-functional and cross-site interactions and ability to drive project plans to completion.
  • Experience interacting with regulatory and third-party representative is helpful
  • Effectively manage numerous projects/priorities and approaches to meet objectives; excel in a fast-paced environment
  • Excellent communication skills including the ability to effectively communicate across organizational levels and functions.

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

Danaher Corporation and all Danaher Companies require all US and Puerto Rico employees to be vaccinated against COVID–19 as a condition of employment, subject to reasonable accommodation as required by law.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at .......@danaher.com to request accommodation.

If you’ve ever wondered what’s within you, there’s no better time to find out.

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Staff Technical Project Manager

PMP

Biotech and Pharma

23 days ago | Rochester, New York, United States | Cytiva

Staff Technical Project Manager

23 days ago | Rochester, New York, United States | Cytiva

Cytiva

Opening date:November 07

Closing date: December 07 2021

Industry:Biotech and Pharma,

Type:Full Time

Job description

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

Responsible for wing-to-wing execution of technical MES projects to deliver high quality outcomes to internal and external customers. Partners with functional product owner to define features backlog and requirements, works with technical team to ensure outcomes delivery on time, within scope and budget and of desired quality. Makes sure project management practices are followed and improved as needed.

What You'll Do

  • Collaborate with business partners and technology leadership in defining features backlog and specifying requirements
  • Drive technology discussion and strategy in line with business needs and company reference architecture
  • Define execution plan and approach based on project scope, expected timeline and available budget/resources
  • Facilitate convergence of functional and technical knowledge and build project teams
  • Work with globally located technical team often comprising of members of separate organizations to coordinate daily execution as per outlined plan
  • Cooperate with and handle external vendors as required. Manage procurement and onboarding process
  • Ensure pre-defined project management processes and practices are followed. Drive simplification and improvement as necessary
  • Support execution team with resolution of roadblocks and interdependencies. Partner with technical and functional teams external to the project to ensure their tasks are completed as required
  • Manage project risks, scope changes and other non-standard events throughout the life of the project
  • Manage partner communication and progress reporting
  • Ensure quality of results is verified and matching stakeholder expectations
  • Track project outcomes realization and customer satisfaction levels through established metrics against service level. Ensure lessons learned are collected

Who You Are

  • Bachelor's Degree in Information Systems, Information Technology (IT), Computer Science, or Engineering
  • A minimum of 8 years of professional experience

Desired Characteristics:

  • Experience in managing MES projects, managing functional and technical design phases through to factory acceptance testing and implementation
  • Experience with Siemens, Rockwell solutions
  • Experience with Tacton integration, Boomi Middleware interfaces
  • Experience managing projects with the supply chain and manufacturing functions
  • Experience leading Oracle ERP projects
  • PMP, ScrumMaster or related Project Management certifications
  • Proficiency with Aha!, JIRA, Microsoft Project Plan, Teams
  • Standout colleague – collaborates well with others to solve problems and actively incorporates input from various sources
  • Experience working with others on a global basis
  • Demonstrated customer focus – evaluates decisions through the eyes of the customer, builds strong customer relationships, creates processes with customer viewpoint and partners with customers to help shape their future initiatives
  • Strong analytical and strong problem-solving skills - communicates in a clear and succinct manner and effectively evaluates information / data to make decisions, anticipates obstacles and develops plans to resolve, creates practical strategies and operational plans
  • Change oriented – actively generates process improvements, champions and motivates change initiatives, confronts difficult circumstances in creative ways, balances multiple and competing priorities and performs accordingly
  • Ability to work in fast paced, global environment

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

Danaher Corporation and all Danaher Companies require all US and Puerto Rico employees to be vaccinated against COVID–19 as a condition of employment, subject to reasonable accommodation as required by law.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at ......@danaher.com to request accommodation.

If you’ve ever wondered what’s within you, there’s no better time to find out.

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