Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do

• Responsible for quality release of finished good products to packaging for shipment.
• Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
• Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
• Issue Certificate of Quality for final product release when all release requirements have been verified and met.
• Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
• Collaborate timely with Cross functional teams to aid effective investigations & problems solving
• Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
• Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
• Continually identify, recommend and implement process improvements with a lean and quality focus.
• Comply with EHS regulations & policies.
• Responding to routine quality related queries from other departments.
• Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.

Who you are

• Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
• Demonstrated collaboration, negotiation & conflict resolution skills.
• Effective communication skills (written and oral).
• Ability to multi-task & handle tasks with competing priorities effectively.
• Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
• Experience with generating, tracking and interpreting quality metrics.
• Demonstrate support to a positive quality culture
• 1-year experience in a medical device or pharmaceutical industry.
• 1-year experience with CA/PA systems, including complaint handling.
• Thorough familiarity with cGMPs of sterile product manufacture.
• Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

The Senior Manager, Brand Strategy is responsible for building and quarterbacking a brand strategy and go-to market plan for the Capterra brand. This leader will play a key role in breaking down operational silos and driving alignment across marketing and the business.

What You Will do:

Collaborate with marketing leadership and brand GMs to develop and implement a brand marketing strategy
Demonstrate leadership through command of the strategy, knowledge about cross-functional initiatives relevant to the brand, and employee engagement initiatives
Maintain the brand narrative, messaging, and positioning for the brand.
Develop and manage media, content and PR campaigns by partnering with internal teams to create campaign and measurement plans, and assets; and communicate direction and updates to ensure end to end success for marketing programs
Develop the brand KPI forecast based on inputs from cross-functional marketing leaders, sales, and GMs
Consistently report on core KPIs, and overall performance for area of ownership
Manage brand marketing budget to ensure ROI and efficiency
Assist CMO, and brand GMs in preparing presentations and reports relevant to brand marketing plan for executive leadership and Key Initiative meetings

What You Will Need:

Bachelor’s Degree (preferred: business, communications, marketing, public relations, economics, mathematics/statistics) or applicable marketing experience.
Approximately 7-10 years of applicable experience
Has managed cross team or functions, demonstrated ability to influence without authority
Demonstrated ability to deliver through others in a matrixed or dotted line structure
Prior experience and proven ability to manage multiple business functions and multiple direct reports
Experience in leading media, content and PR initiatives end-to-end – planning, executing and delivering results
Leadership Experience -- managing across teams.
Strategic Thinker

What We Offer:

Limitless growth and learning opportunities
A collaborative and positive culture — Your team will be as smart and driven as you
Outstanding compensation — Plus competitive benefits and generous time off
A chance to make an impact — Your work will contribute directly to our strategy

In this important role you will help drive storytelling efforts to bring the SF Fed brand to life and forge a strong connection between SF Fed employees and the Bank's vision and strategic priorities. You will develop engaging content and help shape high-level Bank-wide messaging that inspires and galvanizes employees and that is strategically used for distribution to other Bank partners. This position will balance creative, analytical, and critical thinking to understand employee and other partner needs, and will help develop a dynamic content strategy that strengthens our brand positioning.

Essential Responsibilities:

• Drive content and brand strategy for executives, employees, and other key partners to support Bank vision and strategic priorities through storytelling and key messaging.
• Collaborate with representatives from key internal and external communication teams to take a holistic and synchronized approach to content strategy and development.
• Coach executive leaders on Bank-wide messaging, working closely with them to role model that messaging and develop bylined content and spoken communications to meet objectives.
• Shape high-level Bank-wide messaging to guide communication teams across the Bank.
• Craft compelling and memorable content-from articles and blog posts to video assets and talk tracks-to be distributed across the Bank's internal channels and leveraged for our external channels to inspire and engage partners.
• Build positive relationships and drive alignment across communications teams, and meet the needs of internal and external partners.
• Ensure all internal content is on brand, and reflects the Bank's vision, strategic priorities, and values.

Additional duties:

• Create and drive goals and performance metrics for content campaigns; monitor regularly to understand effectiveness of strategy and creative, making recommendations for continuous improvement.
• Ensure cross-communication dependencies and resources are identified and coordinated to ensure effective communications.
• Collaborate closely with the creative team to develop engaging multi-media communication assets.
• Lead the communications life cycle through the development of complex communication plans.

Requirements:

• Bachelor's degree in English, Communications, or other related field or equivalent work experience. Master's in Business or Project Management, preferred.
• Typically requires eight or more years of brand management, communications, or marketing work experience and three or more years in diverse roles, with increasing responsibilities across major projects and programs.
• Significant experience leading a portfolio of sophisticated communications and key partners is required.
• Proven experience in developing formal communication plans and strategies is required.
• Proven experience in influencing key decision makers at all levels in an organization including executive.
• Excellent interpersonal skills, emotional intelligence, collaboration and consensus building skills.
• Experience crafting and implementing performance metrics to measure success of content/campaigns is preferred.
• Published author preferred.

At the Federal Reserve Bank of San Francisco, we offer a wonderful benefits package including: Medical, Dental, Vision, Pretax Flexible Spending Account, Backup Child Care Program, Pretax Day Care Flexible Spending Account, Vacation Days, Sick Days, Paid Holiday's, Pet Insurance, Matching 401(k), and an unheard of Retirement / Pension.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

At the Federal Reserve Bank of San Francisco, we believe in the diversity of our people, ideas, and experiences and are committed to building an inclusive culture that is representative of the communities we serve. The Federal Reserve Bank of San Francisco is an Equal Opportunity Employer.