director of analytical development

B. Braun

<div><div>Job Description
<div></div><div><div>You&rsquo;re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That&rsquo;s why we would like to keep developing our company with you. Keeping your future in mind, we&rsquo;re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.
</div></div><div><div><div><div>Director, Central Analytical Services
</div></div></div></div><div><div><div><div>Company: B. BRAUN MEDICAL (US) INC
</div></div></div></div><div><div><div><div>Job Posting Location: Daytona Beach, Florida, United States, Irvine, California, United States
</div></div></div></div><div><div><div><div>Functional Area: Quality
</div></div></div></div><div><div><div><div>Working Model: Hybrid
</div></div></div></div><div><div><div><div>Days of Work: Friday, Thursday, Wednesday, Tuesday, Monday
</div></div></div></div><div><div><div><div>Shift: 5X8
</div></div></div></div><div><div><div><div>Relocation Available: Yes
</div></div></div></div><div><div><div><div>Requisition ID: 11101
</div></div></div></div><div><div><div><div>B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap&reg; and CAPS&reg;. 
Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise&reg; philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit www.bbraunusa.com
</div></div></div></div><div><div><div><div>Position Summary: 
The Director of Central Analytical Services is a senior leader responsible for establishing, governing, and optimizing analytical strategy, technical capabilities, and laboratory performance across a network of sterile pharmaceutical manufacturing sites. This role provides scientific leadership, ensures method robustness and compliance, drives harmonization across sites, and supports product lifecycle needs&mdash;including development, validation, transfer, troubleshooting, and regulatory submissions of analytical methods and specification.
 
The Director will lead a Franchise level analytical organization delivering centralized support for chemistry, microbiology, sterility assurance testing, and instrumentation strategy to ensure the highest standards of product quality, regulatory compliance, and operational efficiency across sites. 
Responsibilities: Essential Duties 
<ul><li>Develop and execute a Franchise-wide analytical strategy supporting sterile injectable products and global quality objectives.
</li><li>Establish harmonized policies, standards, and procedures for analytical methods, laboratory investigations, and testing practices across sites.
</li><li>Serve as the analytical subject matter expert (SME) for sterile manufacturing during audits, inspections, and regulatory interactions.
</li><li>Lead method development, validation, transfer, and ongoing monitoring for sterile products, ensuring consistent performance across all sites.
</li><li>Create and oversee a method lifecycle management (MLCM) program including periodic review, trending, and optimization.
</li><li>Drive analytical innovation (e.g., rapid microbiology, automation, PAT, advanced characterization).
</li><li>Provide high-level SME support for complex laboratory investigations, out-of-specification (OOS) results, deviations, and sterility/bioburden failures.
</li><li>Oversee root-cause analysis, CAPA development, and long-term remediation for analytical and sterility assurance issues.
</li><li>Act as escalation and decision authority for cross-site analytical challenges.
</li><li>Align practices in sterility testing, environmental monitoring, endotoxin testing, particulate testing, and chemical analysis.
</li><li>Interface closely with Quality Assurance, Sterility Assurance, Manufacturing, Technical Operations, Regulatory Affairs, and R&amp;D.
</li><li>Ensure that all analytical operations meet applicable regulations (FDA, EMA, ICH, USP, ISO) and good manufacturing practices (cGMP).
</li><li>Support preparation and review of regulatory filings and responses (NDA/BLA/ANDA, supplements, variations).
</li><li>Maintain audit readiness and support internal/external inspections.
</li><li>Build and mentor a high-performing analytical science team across sites.
</li><li>Provide training and capability-building programs for site QC teams to ensure consistent execution.
</li></ul><div></div><div>The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time.
</div><div>General: It shall be the duty of every employee while at work to take reasonable care for safety and health of himself/herself and others 
</div>Expertise: Knowledge &amp; Skills
<ul><li>Strong knowledge of USP, EP, JP, ICH guidelines.
</li><li>Expertise in chromatographic methods, spectroscopy, particulate testing, endotoxin, sterility and microbiological methods.
</li><li>Familiarity with Quality Risk Management (QRM), Lean/Six Sigma, and digital/automation solutions.
</li><li>High proficiency with data integrity expectations (ALCOA+, 21 CFR Part 11).
</li><li>Strategic thinker with the ability to influence across functions and sites.
</li><li>Exceptional communication skills and executive presence.
</li><li>Strong decision-making, prioritization, and problem-solving abilities.
</li><li>Provides strategic leadership and direction across multiple departments, sites, or major Quality functions through supervisors and Subject Matter Experts.
</li><li>Fully accountable for cost, capability, performance, and talent outcomes of the organization.
</li><li>Exercises independent judgment in resolving highly complex, systemic, and enterprise level problems with significant regulatory, financial, and reputational impact
</li><li>Regularly consults and advises senior leadership and Group / Board level stakeholders on Quality strategy, risk, compliance posture, and organizational capability.
</li>Acts as organizational spokesperson on Quality matters related to policy, strategy, and enterprise capability. 
<li>
</li></ul>Expertise: Qualifications -Education/Experience/Training/Etc 
Required:
<ul><li>Bachelor&rsquo;s degree in chemistry, Microbiology, or related discipline required. Master&rsquo;s degree or advanced degree preferred
</li><li>10&ndash;15+ years of experience in pharmaceutical analytical sciences, with strong exposure to sterile injectable manufacturing.
</li><li>Proven leadership of multi-site or global analytical or QA/QC functions.
</li><li>Deep expertise in method development, validation, and troubleshooting for sterile products.
</li><li>Demonstrated success in regulatory inspections and technical interactions with agencies.
</li><li>Track record of driving standardization and performance improvement across multiple labs or sites
</li><li>Regular and predictable attendance
</li>Frequent business travel required, Valid driver's license and passport, Secrecy and invention agreement and non- compete agreement 
<li>
</li></ul>While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds. 
Salary Range- $180,000- $260,000 
</div></div></div></div><div><div><div><div>The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate. 
B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com . 
Through its &ldquo;Sharing Expertise&reg;&rdquo; initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. 
We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here .</div></div></div></div></div></div><div></div>

Director, Central Analytical Services

Moderna

<div>The Role:
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.
In this role, you will serve as a critical bridge between Analytical Development and Quality Control, ensuring that cell-based bioassays are robust, transferable, and fully operational across development, clinical, and commercial testing environments.
 
As a Principal Research Associate, you will bring deep technical expertise in potency assays to translate development-stage methods into QC-ready assays, proactively addressing challenges related to transfer, readiness, and lifecycle performance.
 
Working as an individual contributor in a 100% onsite environment in Norwood, you will collaborate cross-functionally while leveraging advanced digital tools and Generative AI to enhance assay transfer, troubleshooting, and continuous improvement.
Here&rsquo;s What You&rsquo;ll Do:
<ul><li>Serve as a liaison between Analytical Development and Quality Control, ensuring alignment on cell-based bioassay expectations, readiness, and performance
</li><li>Represent bioassay method development in cross-functional forums with Analytical Sciences &amp; Technology (AS&amp;T) and QC
</li><li>Ensure bioassays are designed to meet appropriate technical, operational, and regulatory requirements prior to qualification or validation
</li><li>Serve as bioassay subject matter expert for investigations and troubleshooting of assay performance issues across development and QC environments, identifying root causes, testing hypotheses, and implementing solutions
</li><li>Lead assay optimization and continuous improvement efforts based on operational feedback, robustness requirements, and lifecycle needs
</li><li>Collaborate with Quality and AS&amp;T teams to support deviation investigations, CAPAs, and change controls related to analytical methods
</li><li>Analyze and interpret complex datasets to inform bioassay performance, variability, and comparability
</li><li>Author and review technical documentation including protocols, reports, and method lifecycle documents
</li><li>Contribute to cross-functional strategy discussions related to bioassay and analytical control strategies
</li></ul>The key Moderna Mindsets you&rsquo;ll need to succeed in the role:
&ldquo;We behave like owners. The solutions we&rsquo;re building go beyond any job description.&rdquo;
&ldquo;We remove viscosity to encourage collective action.&rdquo;
Here&rsquo;s What You&rsquo;ll Need (Basic Qualifications)
<ul><li>BS degree with 5 years, or MS degree with 2 years of relevant industry experience in Biochemistry, Cell Biology, Immunology, Biological Engineering or related field
</li><li>Strong hands-on experience with cell-based bioassays and/or other relevant bioanalytical methods
</li><li>Experience with flow cytometry, ELISA, HPLC, mass spectrometry, and/or reporter-based assays
</li><li>Demonstrated experience with analytical method transfer to QC or external laboratories
</li><li>Proven ability to troubleshoot complex assay issues and lead investigations in a GMP or late-stage development environment
</li><li>Understanding of CQA frameworks, assay lifecycle management, and regulatory expectations
</li><li>Experience working cross-functionally with Quality, QC, and/or manufacturing organizations
</li><li>Strong analytical thinking and ability to interpret data to drive decisions and improvements
</li><li>Excellent communication skills with the ability to translate technical concepts across functions
</li><li>Ability to manage multiple priorities in a fast-paced, highly collaborative environment
</li><li>Self-motivated, proactive, and comfortable operating with a high degree of ownership
</li><li>This position is site-based, requiring you to be at Moderna&rsquo;s site full-time. This position is not eligible for remote work.
</li><li>At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.
</li></ul>Pay &amp; Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That&rsquo;s why our US benefits and global well-being resources are designed to support you&mdash;at work, at home, and everywhere in between.
<ul><li>Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
</li><li>A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
</li><li>Family planning benefits, including fertility, adoption, and surrogacy support
</li><li>Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
</li><li>Savings and investment opportunities to help you plan for the future
</li><li>Location-specific perks and extras
</li></ul>The salary range for this role is $89,900.00 - $143,800.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual&rsquo;s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.&amp;#xa;&amp;#xa;The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We&rsquo;re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com .
Export Control Notice&amp;#xa;This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant&rsquo;s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.&amp;#xa;#LI-TR2
<ul><li></li></ul></div>

Principal Research Associate, Analytical Development

Catalent Pharma Solutions

<div>Project Manager
Position Summary:<ul><li>
Work Schedule: M-F 1st shift
</li><li>100% on-site</li></ul>
Catalent&rsquo;s Kansas City facility is home to our Oral &amp; Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring a Project Manager. Overall responsibility for the leadership and management of projects as assigned. Depending upon experience and knowledge manage projects that maybe simple and residing in one business line or site, or complex and reside within multiple business lines or may cross multiple Catalent sites. May take on Global PM, Multi site or Lead PM for clients
The Role:<ul><li>
Leads and builds multi-disciplinary project teams comprising of representatives from relevant 
functions and in some cases, cross-functional, multi-site activities for complex projects</li><li>
Manages the execution of the customer&rsquo;s requirements in accordance with an agreed-upon program of activities to achieve established goals and deliverables</li><li>
Compiles and maintains up-to-date project plans, identifies and captures new scope via proposals or change orders</li><li>
Ensures that key milestones in agreement with internal/external customers are achieved and good 
communication is maintained</li><li>
Tracks progress of all activities against plan and notifies the relevant personnel of changes, potential delays and/or issues</li><li>
Engrained in kick-off and methodical approach to managing the project throughout the duration of 
the project scope</li><li>
Understands escalation pathway and when necessary, has the ability to mitigate</li><li>
Demonstrates ability to facilitate risk assessment</li></ul>
The Candidate:<ul><li>
Bachelor's degree in a scientific discipline or equivalent combination of 
education and experience (Associate&rsquo;s degree and 2+ years of experience OR high school diploma 
and 4+ years of experience.</li><li>
Approximately 2 years of experience in project management, the pharmaceutical 
industry or appropriate business-related area preferred</li></ul>
Why you should join Catalent:<ul><li>
Defined career path and annual performance review and feedback process</li><li>
Diverse, inclusive culture</li><li>
Positive working environment focusing on continually improving processes to remain innovative</li><li>
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives</li><li>
152 hours of PTO + 8 paid holidays</li><li>
Several Employee Resource Groups focusing on D&amp;I</li><li>
Dynamic, fast-paced work environment</li><li>
Community engagement and green initiatives</li><li>
Generous 401K match</li><li>
Medical, dental and vision benefits effective day one of employment</li><li>
Tuition Reimbursement - Let us help you finish your degree or start a new degree!</li><li>
WellHub- program to promote overall physical wellness</li><li>
Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. 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. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Project Manager, Biologics Analytical Services

<div>The Role:
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.
In this role, you will operate at the interface of product biology and analytical methodology, translating complex biological mechanisms into robust, high-performing cell-based bioassays.
 
As a Senior Research Associate, you will independently generate and interpret high-quality data that informs product understanding, assay performance, and lifecycle progression from early development through commercialization.
 
Working as an individual contributor in a 100% onsite environment in Norwood, you will collaborate cross-functionally while leveraging advanced digital tools and gaining exposure to Generative AI to enhance analytical insights, assay development, and decision-making.
Here&rsquo;s What You&rsquo;ll Do:
<ul><li>Independently execute and optimize cell-based bioassays to assess functional activity of mRNA-based therapeutics and vaccines
</li><li>Design and perform experiments to elucidate the relationship between product biology, mechanism of action, and assay readouts
</li><li>Contribute to assay development strategies by evaluating assay formats, controls, and critical parameters
</li><li>Analyze and interpret complex datasets to support assay performance, comparability, and deep product understanding
</li><li>Troubleshoot assay variability and performance issues, identifying root causes and implementing robust improvements
</li><li>Support assay qualification activities in alignment with regulatory expectations
</li><li>Author and review technical documentation, including protocols, reports, and method lifecycle documentation
</li><li>Collaborate cross-functionally with Analytical Development, Quality, Process Development, and Research teams to support method transfer, characterization studies, and lifecycle management
</li><li>Evaluate and implement new technologies or innovative approaches to enhance assay robustness, sensitivity, and throughput
</li></ul>The key Moderna Mindsets you&rsquo;ll need to succeed in the role:
&ldquo;We obsess over learning. We don&rsquo;t have to be the smartest we have to learn the fastest.&rdquo;
&ldquo;We pursue options in parallel to make the best choice later.&rdquo;
Here&rsquo;s What You&rsquo;ll Need (Basic Qualifications)
<ul><li>BS degree with 2 years of relevant industry experience, or MS degree with 0 years of experience in Biochemistry, Molecular Biology, Cell Biology, Immunology, Biological Engineering, or a related field
</li><li>Strong hands-on experience with mammalian cell culture and cell-based bioassays
</li><li>Proficiency with techniques such as ELISA, flow cytometry, or luminescence/fluorescence-based reporter assays
</li><li>Familiarity with nucleic acids (e.g. RNA, DNA) and delivery systems (e.g. LNP, lipoplex, AAV)
</li><li>Ability to independently design experiments, analyze data, and draw scientifically sound conclusions
</li><li>Demonstrated troubleshooting and problem-solving skills in assay development contexts
</li><li>Strong organizational and communication skills, with experience documenting and presenting data
</li><li>Collaborative, proactive, and detail-oriented mindset
</li><li>This position is site-based, requiring you to be at Moderna&rsquo;s site full-time. This position is not eligible for remote work.
</li><li>At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.
</li></ul>Pay &amp; Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That&rsquo;s why our US benefits and global well-being resources are designed to support you&mdash;at work, at home, and everywhere in between.
<ul><li>Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
</li><li>A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
</li><li>Family planning benefits, including fertility, adoption, and surrogacy support
</li><li>Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
</li><li>Savings and investment opportunities to help you plan for the future
</li><li>Location-specific perks and extras
</li></ul>The salary range for this role is $74,000.00 - $118,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual&rsquo;s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.&amp;#xa;&amp;#xa;The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We&rsquo;re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com .
Export Control Notice&amp;#xa;This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant&rsquo;s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.&amp;#xa;#LI-TR2
<ul><li></li></ul></div>

Sr. Research Associate, Analytical Development

Qiddiya Investment Company

<div>Qiddiya Investment Company is transforming the entertainment landscape in Saudi Arabia, and we are in search of a strategic and commercially driven professional to fill the role of Director - Development Financial Planning within our Sports Business Unit. This position is pivotal in shaping our development strategy through comprehensive business planning, financial strategy, and commercial analysis for proposed world-class sports assets and facilities, with total investment value exceeding several billion dollars.
As the Director of Development Financial Planning - Sports, you will be responsible for establishing the strategic direction and commercial framework for various sports development projects. You will lead a high-performing team that develops comprehensive business plans, investment strategies, and financial models while serving as a key member of the senior leadership team. Your role will be instrumental in driving investment decisions, optimizing capital allocation, and ensuring our projects deliver exceptional returns while aligning with Qiddiya's long-term vision.
Day to day you will be partnering with C-suite executives, development leaders, strategy teams and key stakeholders to shape the future of world-class sports assets and facilities. With that in mind, outstanding commercial acumen, strategic leadership, and the ability to influence at the highest levels are essential, while experience in large-scale sporting events and venues would be beneficial given the role's strategic focus.
Key Responsibilities<ul><li>
Establish and oversee the strategic planning function for the Sports Business Unit, including development of investment strategies, business plans, and financial frameworks for multiple billion-dollar development projects</li><li>
Drive capital optimization and investment strategy, ensuring sophisticated financial modeling and strategic assessment of all investments while maximizing shareholder value</li><li>
Lead the development of innovative commercial models and revenue strategies for sports assets in collaboration with senior leadership teams</li><li>
Direct complex feasibility studies and strategic assessments for major development initiatives, including guidance on capital structure, funding options, and risk management strategies</li><li>
Foster strategic relationships with key stakeholders, financial institutions, and partners to drive business growth and secure optimal financing solutions</li><li>
Spearhead transformation initiatives in financial and commercial strategy to ensure executive decision making is based on best-in-class analysis and thinking</li><li>
Lead strategic due diligence and valuation of potential investments, partnerships, and development opportunities</li><li>
Develop and implement sophisticated financial planning and analysis frameworks to drive strategic decision-making at board level</li><li>
Guide long-term financial forecasting and scenario planning to optimize portfolio performance and returns</li><li>
Direct the creation of board-level business cases and investment proposals, including detailed ROI analysis and risk assessment</li><li>
Establish best practices in business planning and financial strategy across the organization</li><li>
Lead change management initiatives to improve financial planning processes and drive operational excellence</li></ul> 

Requirements 
<ul><li>
Bachelor's degree in finance, economics, real estate, or a related field
</li><li>A minimum of 15-18 years of relevant experience,
</li><li>Early experience at a leading management consultancy and subsequent operational or client-side roles are preferred but not mandatory.</li><li>
Proven track record of leading financial strategy and business planning for large-scale development projects ($1B+)</li><li>
Experience in financial planning and business strategy for major sporting venues or events is highly desirable</li><li>
Demonstrated expertise in capital markets, project finance, and investment strategy</li><li>
Strong background in developing and implementing commercial frameworks and revenue optimization strategies</li><li>
Distinguished expertise in business planning, financial modeling, and strategic analysis for complex development projects</li><li>
Exceptional critical thinking and strategic problem-solving abilities, with demonstrated capability to drive innovation and challenge conventional approaches</li><li>
Outstanding executive presence and communication skills, with proven ability to influence and engage at board and C-suite levels</li><li>
Strong leadership capabilities, with demonstrated success in building and developing high-performing teams</li><li>
Advanced proficiency in financial modeling, strategic planning tools, and enterprise-level planning systems</li></ul></div>

Director- Development Financial Analysis. CDU7

<div>The Role:
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.
In this role, you will support the development, optimization, and execution of cell-based bioassays to enable release and stability testing of mRNA-based therapeutics and vaccines.
 
You will generate high-quality, precise data that underpins clinical and commercial programs, ensuring robustness and reliability across analytical workflows.
 
Operating as an individual contributor in a 100% onsite environment, you will collaborate cross-functionally while expanding your expertise and leveraging digital and Generative AI-enabled tools to enhance assay performance and data insights.
Here&rsquo;s What You&rsquo;ll Do:
<ul><li>Execute cell-based bioassays to assess potency and functional activity of mRNA-based therapeutics and vaccines
</li><li>Support assay development, optimization, and qualification activities under scientific guidance
</li><li>Perform routine cell culture activities, including maintaining and expanding cell lines with precision
</li><li>Analyze experimental data rigorously, ensuring accuracy, integrity, and clear documentation of results
</li><li>Assist in troubleshooting assay performance issues and investigating deviations to ensure data reliability
</li><li>Follow established protocols, SOPs, and regulatory expectations in a highly controlled environment
</li><li>Contribute to authoring and maintaining technical documentation, including protocols, reports, and data summaries
</li><li>Collaborate cross-functionally with Analytical Development, Quality, Process Development, and Research teams to support project timelines and deliverables
</li></ul>The key Moderna Mindsets you&rsquo;ll need to succeed in the role:
&ldquo;We obsess over learning. We don&rsquo;t have to be the smartest we have to learn the fastest.&rdquo;
&ldquo;We digitize everywhere possible using the power of code to maximize our impact on patients.&rdquo;
Here&rsquo;s What You&rsquo;ll Need (Basic Requirements):
<ul><li>BS degree in Biochemistry, Molecular Biology, Cell Biology, Immunology, Biological Engineering, or related field with 0&ndash;3+ years of relevant experience
</li><li>Hands-on experience with mammalian cell culture and/or bioassays preferred
</li><li>Familiarity with techniques such as ELISA, cell-based assays, or reporter assays is a plus
</li><li>Familiarity with nucleic acids (e.g. RNA, DNA) and delivery systems (e.g. LNP, lipoplex, AAV)
</li><li>Strong attention to detail and ability to follow protocols accurately
</li><li>Basic data analysis and problem-solving skills
</li><li>Strong organizational and communication skills
</li><li>Team-oriented mindset with willingness to learn and grow
</li></ul>Pay &amp; Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That&rsquo;s why our US benefits and global well-being resources are designed to support you&mdash;at work, at home, and everywhere in between.
<ul><li>Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
</li><li>A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
</li><li>Family planning benefits, including fertility, adoption, and surrogacy support
</li><li>Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
</li><li>Savings and investment opportunities to help you plan for the future
</li><li>Location-specific perks and extras
</li></ul>The salary range for this role is $63,200.00 - $100,900.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual&rsquo;s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.&amp;#xa;&amp;#xa;The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We&rsquo;re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com .
Export Control Notice&amp;#xa;This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant&rsquo;s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.&amp;#xa;#LI-TR2
<ul><li></li></ul></div>

Research Associate, Analytical Development

Fusion Group Holding

Business Analyst- Purpose of the JobTo support in identifying and attracting investors and providing them with guidance in order to ensure they a have all the information and resources needed to create and maintain business relationships. Reviewing investor applications, complete all documents, allocating plots and give recommendations to BO director.Main duties and responsibilities<ul><li>Collaborate with the Business Development Director to identify and develop new business opportunities with investors that are aligned with company strategic targets and build on relationships with existing investors.</li></ul><ul><li>Coordinate with PR and Marketing in planning events aimed at attracting potential investors.</li></ul><ul><li>Prepare reports on business development, key activities and achievements and submit to senior management as needed.</li></ul><ul><li>Contribute in creating and maintaining relationships with investors and guide them in understanding the type of services offered by the Zones in terms of opening up a business, including assessment of the business, design, construction, and funding as appropriate.</li></ul><ul><li>Gather, collate and disseminate information such as data on regional market and competition analysis reports, that will help investors analyze their potential investments and assess the feasibility of their potential business in the Zones.</li></ul><ul><li>Collaborate with all relevant departments across comany to ensure investor's inquiries, issues, concerns, interests, etc. are managed and resolved appropriately and in a timely manner.</li></ul><ul><li>Review investors proposals to ensure alignment with company goals and objectives and provide recommendations to the Business Development Director in regards to approving/rejecting investors proposals/applications.</li></ul><ul><li>Support in evaluating potential business opportunities and investments by conducting financial analysis and provide recommendations and prepare any necessary action plans.</li></ul><ul><li>Any other duties requested by Management.</li></ul>QualificationsEducation: <ul><li>Bachelor&rsquo;s degree in business administration, Communications or related field is required.</li></ul>Work Experience:<ul><li>A minimum of 3 years of work experience, preferably in the required discipline.</li></ul>Professional training/ certification:<ul><li>A certification in a relevant discipline from an accredited institution is preferred.</li></ul>Skills:<ul><li>Proficient in Microsoft Office .</li></ul><ul><li>Proficient in English and Arabic .</li></ul><ul><li>Teamwork and collaboration skills</li></ul><ul><li>Communication and interpersonal skills</li></ul><ul><li>Planning and organizing skills</li></ul><ul><li>Analytical and problem solving skills</li></ul><ul><li>Customer service skills</li></ul>Job Type: Contract Contract length: 12 monthsEducation:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Business Analyst: 4 years (Required)</li><li>Business Analysis: 3 years (Required)</li><li>&bull;	Analytical and problem solving skills: 4 years (Required)</li><li>Ability to manage stakeholders and build relationships: 4 years (Required)</li></ul>Language:<ul><li>Arabic (Required)</li><li>English (Required)</li></ul>Work Location: In person

Business Analyst

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