Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Finance team as a Finance Intern. In this role, you will gain hands-on experience supporting the FP&A team, with additional exposure to Sales Operations and Accounting.

As part of your internship, you will contribute to a core project focused on building pro forma P&L scenarios using research on industry peers, market trends, growth opportunities, and potential expense savings.

How you will make an impact: 

• Support the FP&A team with financial analysis and reporting
• Build and analyze pro forma P&L scenarios based on market and competitive research
• Interpret data to identify trends, drivers, and anomalies
• Assist in evaluating growth opportunities and cost-saving initiatives
• Collaborate cross-functionally with Sales Operations and Accounting teams
• Present findings clearly through written and verbal communication
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• Currently pursuing an undergraduate degree in Finance, Business, or a related discipline
• Foundational understanding of GAAP accounting (preferred)
• Strong analytical and problem-solving skills
• Ability to work both independently and collaboratively
• Proficiency in Microsoft Excel
• Exposure to ERP systems (e.g., SAP, Oracle, NetSuite) and/or BI tools (e.g., Tableau, Power BI) is a plus

The anticipated salary range for this position is $25.00 per hour. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. 

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team at TriLink BioTechnologies as a Manufacturing Intern. In this role, you will gain hands-on experience supporting mRNA-based workflows while developing a strong foundation in nucleic acid production.

As part of your core project, you will contribute to the design and validation of untranslated region (UTR) sequences for mRNA. The Manufacturing Intern will partner with scientists in the Operations Technical Support team to design, optimize, and implement standard protocols for PCR methods. The intern will utilize the following skills:

• Primer design
• PCR amplification of DNA
• In-vitro transcription of mRNA
• Silica purification of mRNA
• Fragment Analysis of mRNA and DNA, along with data interpretation
• Analysis of advanced mRNA analytics
• SOP and batch record use and drafting
• Process transfer to manufacturing
• Building production cost models

 The skills and experience that you will bring:

• Currently pursuing an undergraduate degree in Biology, Chemistry, Bioengineering, or a related life science discipline
• Foundational understanding of molecular biology concepts (e.g., DNA, RNA, gene expression) preferred
• Strong analytical and problem-solving skills
• Ability to work both independently and collaboratively in a team environment

Program details:

• 9-week Summer Internship Program
• Program dates: June 1, 2026

The anticipated salary range for this position is $25.00 per hour. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. 

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Operations team as an Operations Intern. In this role, you will gain hands-on experience across multiple operational workflows, including Manufacturing, Quality Control, and Order Fulfillment, with additional exposure to MSAT, Facilities, and Engineering.

This internship is designed to provide a comprehensive understanding of operational processes, automation systems, and continuous improvement methodologies within a manufacturing environment.

How you will make an impact: 

• Rotate through key operational areas including Manufacturing, Quality Control, and Order Fulfillment
• Learn end-to-end workflows, including inputs, processes, outputs, and system purpose
• Develop an understanding of quality standards, specifications, and process nuances
• Gain hands-on exposure to automated manufacturing equipment, including operation, safety, maintenance, and troubleshooting
• Participate in Continuous Improvement (CI) projects using A3 methodology:
  • Problem definition
  • Root cause analysis
  • Solution implementation
  • Validation and lessons learned
• Initiate and execute CI projects aimed at improving quality and/or productivity
• Present progress and findings to stakeholders at key project milestones
• Collaborate with cross-functional teams and learn from subject matter experts
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• Currently pursuing an undergraduate degree in Engineering, Operations, Supply Chain, or a related field
• Strong analytical and problem-solving skills
• Interest in manufacturing operations and process improvement
• Ability to work both independently and collaboratively
• Strong communication skills, with the ability to present findings clearly
• Willingness to learn and work in a hands-on, operational environment

Program details:

• 9-week Summer Internship Program
• Program dates: June 1, 2026

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our manufacturing team as a Temporary Manufacturing Associate I, Oligo. As a Temporary Manufacturing Associate I, Oligo, you will support daily production operations by performing basic production tasks, preparing equipment and materials, executing routine workflows, and maintaining proper documentation. Works under close supervision within ISO-classified manufacturing spaces to produce research and clinical-grade components. Learns and applies operational procedures while developing foundational skills in oligo production technologies.

How you will make an impact: 

• Reviews daily production tasks and follows established procedures for material preparation, equipment set-up, and execution of routine processes.
• Assists in preparing production areas for cGMP project initiation or changeover.
• Documents production activities by accurately completing forms, logs, and batch-related records in compliance with GDP.
• Operates and cleans equipment following established instructions and escalates equipment issues or deviations.
• Supports execution of batch records and follows SOPs; may assist in SOP revisions under guidance.
• Participates in training and completes required cGMP and company training within defined timelines.
• Maintains a clean and safe work environment by following SOPs and housekeeping expectations.
• Communicates progress, issues, and observations to supervisors or senior associates.
• Collaborates with Manufacturing Associate II staff and other support groups to ensure workflow alignment.
• Performs basic oligo synthesis, purification, processing steps, and associated documentation with supervision.
• Performs other functions and duties as required

 The skills and experience that you will bring: 

• Bachelor's Degree in life science field or related field preferably in Chemistry/Biochemistry/Biology/Molecular Biology or equivalent experience
• 1+ years of experience in a Biochemistry manufacturing laboratory preferred
• Exposure in a cGMP/ ISO 7/ ISO 8 clean room environment desired
• Experience with executing SOPs
• Proficiency in Microsoft Office Suite desired
• Display strong organizational skills, detail-oriented, and demonstrated problem-solving abilities
• Excellent written and verbal communication skills
• Self-motivated and able to organize and prioritize multiple tasks

The anticipated salary range for this position is $20.00 - $25.00. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. 

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our CDMO team as a Senior Process Development & Manufacturing Specialist. The Senior Process Development & Manufacturing Specialist is responsible for leading the transfer, execution, and optimization of processes supporting GMP-grade oligonucleotide and mRNA production within a CDMO environment. This role combines advanced technical expertise in IVT synthesis, downstream purification, and wet chemistry operations with ownership of process performance, scalability, and manufacturing readiness. The position is a subject matter expert, driving process improvements, supporting client programs, and ensuring successful technology transfer from development into GMP manufacturing. With a high degree of autonomy, this role partners cross-functionally with Manufacturing, Quality, and Commercial teams to deliver high-quality and scalable solutions for external clients.

How you will make an impact: 

• Lead execution and optimization of manufacturing processes for GMP-grade oligonucleotides and mRNA, ensuring product quality, consistency, and process efficiency.
• Lead tech transfer activities, translating development processes into robust, scalable GMP manufacturing workflows.
• Drive process improvement and scale-up initiatives by analyzing process data, identifying bottlenecks, and implementing sustainable solutions.
• Support equipment performance and process reliability by troubleshooting issues, identifying root causes, and collaborating on corrective and preventive actions.
• Author, review, and implement GMP documentation, including batch records, SOPs, and technical reports in accordance with Good Documentation Practices.
• Serve as a technical subject matter expert, providing guidance, training, and mentorship to manufacturing staff and supporting cross-functional problem-solving.
• Collaborate with internal stakeholders and client-facing teams to support technical discussions, custom process requirements, and successful program execution.
• Conduct characterization and process development studies to support continuous improvement and product scalability.
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, or related scientific discipline with 5–8+ years of relevant experience, or advanced degree with industry experience.
• Strong hands-on experience in GMP manufacturing environments, including oligonucleotide or mRNA production, purification (HPLC), and scale-up.
• Demonstrated expertise in process development, tech transfer, and process optimization within regulated environments (ICH Q7, ISO cleanrooms).
• Proven ability to analyze process data, troubleshoot technical issues, and implement process improvements.
• Experience authoring and reviewing GMP documentation, including SOPs, batch records, and technical reports.
• Strong communication and leadership skills, with experience mentoring staff and supporting cross-functional and client-facing interactions.

The anticipated salary range for this position is $90,000 - $100,00.  In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package.  The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role.  

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Customer Service team as a Temporary Customer Service Representative I. As a Temporary Customer Service Representative I, you will be the first point of contact for our customers, playing a key role in delivering exceptional service and fostering brand loyalty. Your primary responsibilities will include responding to customer inquiries, processing orders, and ensuring accurate documentation in accordance with established procedures. You will collaborate with internal teams to meet customer needs while embodying TriLink’s mission and values. This is an entry-level role designed to build a strong foundation for growth within the Customer Service team. 

How you will make an impact: 

• Serve as the primary contact for customers, addressing inquiries via phone, email, or other communication channels with professionalism and efficiency. 
• Process customer orders, quotes, and requests accurately and in a timely manner using ERP and CRM systems. 
• Ensure all customer interactions are documented thoroughly and align with established Standard Operating Procedures (SOPs). 
• Collaborate with internal departments, including Sales and Shipping, to meet customer scheduling and delivery expectations. 
• Resolve customer complaints by gathering relevant information and escalating complex issues to the Customer Service Supervisor as needed. 
• Assist in maintaining and updating customer accounts, ensuring compliance with regulatory standards and internal protocols. 
• Provide basic product information, answer routine questions, and offer support on order tracking and shipping inquiries. 
• Support team training initiatives by contributing feedback and participating in process improvement discussions. 
• Uphold Maravai’s mission and values, demonstrating a commitment to creating positive customer experiences. 
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• High school diploma or equivalent required; a bachelor's degree in business or a related field is preferred. 
• 0-2 years of experience in a customer service role, ideally in a manufacturing or life sciences environment. 
• Familiarity with ERP and CRM systems (e.g., Oracle/NetSuite, Salesforce) is a plus. 
• Strong organizational skills with excellent attention to detail. 
• Effective communication skills, both written and verbal. 
• Ability to work collaboratively in a team environment while managing individual tasks independently. 
• Customer-focused mindset with a proactive approach to problem-solving. 
• Basic proficiency in Microsoft Office Suite (Word, Excel, Outlook). 

The anticipated salary range for this position is $20.00 - $25.00. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. 

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team as a Manufacturing Associate II (Dry Lab). As a Manufacturing Associate II, you will support the production of phosphoramidites and related products used in DNA/RNA synthesis. This role is primarily focused on packaging, order processing, and shipping activities to ensure timely and accurate delivery of products.

Glen Research operates in a dynamic, small-company environment where flexibility and adaptability are essential. Teamwork and individual contributions play a key role in the company’s success. Responsibilities may evolve over time to support business needs and growth.

How you will make an impact: 

• Column Preparation: Inspect and assemble columns to ensure readiness for use.
• Product Preparation: Weigh and aliquot products; seal, label, and inspect finished goods; store inventory appropriately.
• Clean Up: Maintain cleanliness of product distribution areas and ensure general lab and storage housekeeping.
• Order Processing: Verify item availability; coordinate with Dry Lab and Customer Service on production needs and backorders; pull items and enclosures; process orders in the ERP system.
• Operations Support: Manage designated Dry Lab processes and contribute to additional projects as needed.
• Other Duties: Perform additional responsibilities as assigned.

 The skills and experience that you will bring: 

• BS in Chemistry, Biology, or related science.
• 3 years previous work experience in similar role.
• Knowledge and experience in safely handling organic solvents and other laboratory chemicals.
• Strong attention to detail.
• Experience with NetSuite or other ERP system preferred. 
• Ability to work in a fast-paced environment.
• Excellent computer skills, organization skills, time management.
• Self Motivated

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Senior QA Operations Specialist. In this role, you will lead the maintenance and continuous improvement of the Quality Management System, review and approve product and new product development documentation, and track and report on key quality metrics. You will also ensure compliance with company policies and procedures, as well as applicable domestic and international standards and regulations, including but not limited to ISO 13485.

How you will make an impact: 

• Responsible for reviewing and approving Quality Events (e.g. deviations, non-conformances, OOS, CAPAs, and complaints) to ensure appropriate investigations are thorough and completed in a timely manner.
• Reviews and approves change control of materials, equipment, processes, and procedures including appropriate documentation.
• Maintains the control of documents and records.
• Provides oversight for training program and conduct quality related training. Train or supervise junior team member, as required.
• Conducts quality investigations to assess root cause, corrections, corrective actions, preventive actions, and monitor effectiveness. 
• Leads cross-functional teams in risk identification, mitigation activities, and quality improvement projects.
• Reviews and approves product documentation for disposition of finished goods.
• Compiles, maintains, reports, and presents quality metrics during site Quality Management Reviews to ensure visibility of QMS health, including creating trending graphs for weekly, monthly, and quarterly reports.
• Leads the audit program, including conducting internal audits and hosting external or third-party quality audits (e.g. customers, ISO, etc.).
• Ensures compliance with all in-house or external specifications to standards such as ISO or customer requirements.
• Supports supplier quality by maintaining the approved supplier list, administering supplier surveys, quality agreements, approved supplier list, and performing critical supplier audits as needed.
• Identifies quality issues/ discrepancies and effectively resolves these within the organization.
• Perform other functions and duties as required.

 The skills and experience that you will bring: 

• Minimum, Bachelor's Degree in scientific discipline (Chemistry, Biology, Bioengineering, etc.).
• Quality professional with a minimum of 5 years relevant experience in a life science industry.
• Requires knowledge of ISO 13485 standards (or ISO 9001).
• Proficient at the use of root cause analysis tools, such as 5-Why's, FMEA's, DMAIC, Cause and Effect Diagrams, Process Mapping, etc.
• Strong and effective verbal and written communication skills.
• Strong interpersonal, teamwork and customer interfacing skills.
• Strong problem-solving skills and analytical skills applied to investigations.
• Self-motivated and able to organize and prioritize multiple tasks.
• Ability to identify quality issues/discrepancies and effectively resolve discrepancies within the organization.
• Proficient in Microsoft Office
• Experience with NetSuite ERP and Qualio is a plus

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team as a Manufacturing Associate II. As a Manufacturing Associate II (Wet Lab), you will be responsible for formulating and testing products for DNA synthesis. This position requires a chemistry background, preferably a BS degree in Chemistry or relevant experience.  This position requires experience with wet-bench chemistry, HPLC, spectrophotometers as well as general chemistry techniques.

How you will make an impact: 

• Manage raw materials and supplies for the lab
• Manage reanalysis of products and raw materials in a timely manner
• Lead department when Lab Manager is not present and coordinate with outside departments 
• Prepare catalog products using manufacturing instructions, procedures and protocols
• Associated tasks include packaging, labeling, and storing of product; maintaining inventory of catalog products and raw materials
• Conduct preventative maintenance
• Prepare equipment and glassware; general inventory and organization of supplies
• Assist with general shipping and receiving of hazmat products and materials
• Maintain proper storage, handling, and disposal of organic solvents, hazardous chemicals, and waste is essential
• Provide proper documentation and accountability of tasks performed 
• Maintain an organized work environment
• Conduct general laboratory duties and other work as assigned
• Assist with customer order fulfilment including preparing shipping documentation will be a priority. Receiving and processing incoming materials from vendors and suppliers is a key function
• Provide General warehouse duties
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• BS in Chemistry or related science
• 2 years of previous laboratory experience
• Excellent written and verbal communication skills
• Knowledge and experience in safely handling organic solvents and laboratory chemicals.  
• Ability to follow direction and work in a fast-paced work environment
• Experience with databases, ERP, and document control systems

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Quality & Regulatory team as a Part-Time Document Control Associate I. As a Part-Time Document Control Associate I, you will be responsible for maintaining the document and record control systems and ensuring they meet Quality Management System (QMS) requirements. This position is responsible for coordinating the issuance, revision, review and approval of SOPs and other documents. 

How you will make an impact: 

• Issue document change order numbers, route and track new and revised documents for approval, file controlled documents and other documentation provided to QA, and ensure that all documentation follows the change control procedures  
• Review documents for completeness, adherence to company guidelines on formatting, and authorization for approvals  
• Monitor status of in-process document changes to ensure timely completion  
• Organize filing systems for electronic and paper based GMP/research documents  
• Support the establishment and improvement of quality systems  
• Facilitate continuous improvements efforts of quality systems  
• Assist in quality audits, including document preparation and record retrieval.  
• Update and maintain quality metrics as needed  
• Support after hours and weekends as needed  
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• BS Degree in scientific area preferred. 
• Minimum of 1-2 years hands-on experience with document control management, preferably in a life science industry  
• Experience with ISO 9001, ISO 13485,  21CFR820, 21CFR 211, or other regulated industry a plus. 
• Experience with MasterControl or other document management system a plus but not required. 
• Demonstrated ability to work independently and as part of a team  
• Good writing skills, high degree of organization and excellent attention to detail. 
• Good computer skills with working knowledge of MS office suite and Adobe Acrobat. 
• Must be able to support after hours and weekend as needed. 
• Self motivated and able to organize and prioritize multiple tasks.  

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our engineering team as a Senior Facilities Engineer. As a Senior Facilities Engineer, you will responsible for the technical oversight, reliability, compliance, and continuous improvement of facility infrastructure, laboratory systems, and critical utilities supporting R&D, Manufacturing, and Quality Control operations. This role serves as the subject matter expert for building systems, environmental controls, maintenance strategy, and regulatory compliance within a regulated life sciences environment. The Senior Facilities Engineer ensures facility readiness, safety, and business continuity through proactive maintenance programs, engineering problem solving, vendor management, and cross functional collaboration to support operational performance and regulatory standards.

How you will make an impact: 

• Serve as technical owner for facility infrastructure systems including HVAC, electrical distribution, water systems, compressed air, laboratory gases, environmental controls, and waste systems
• Develop and execute preventive and predictive maintenance programs to improve uptime, asset reliability, and lifecycle management
• Manage facility and equipment asset records, maintenance schedules, and calibration programs within CMMS systems
• Lead troubleshooting and root cause investigations for facility related failures and implement sustainable corrective actions
• Support equipment installation, commissioning, qualification, and validation activities including IQ and OQ where applicable
• Ensure compliance with GMP, ISO 9001 and or ISO 13485, OSHA, and local and federal regulatory requirements
• Oversee hazardous material handling, storage, and disposal in partnership with EHS and approved vendors
• Evaluate and manage external contractors and service providers to ensure cost effectiveness, quality, and timely execution
• Maintain audit ready documentation including SOPs, maintenance logs, calibration records, and validation documentation
• Support capital improvement projects, facility expansions, space planning, and business continuity initiatives
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• Bachelor’s degree in Engineering, Facilities Engineering, Mechanical Engineering, or related technical discipline with 5 years of experience in facilities engineering within a regulated laboratory or manufacturing environment. Equivalent experience considered.
• Working knowledge of GMP regulations and ISO 9001 and or ISO 13485 standards
• Experience supporting HVAC, utilities, laboratory infrastructure, and environmental control systems
• Experience with equipment qualification, validation, and calibration programs
• Proficiency with CMMS systems and Microsoft Office applications
• Strong analytical and problem solving skills with ability to conduct root cause investigations
• Effective communication skills and ability to collaborate cross functionally

The anticipated salary range for this position is $100,000 - $120,000.  In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package.  The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role.  

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our commercial team as a Field Application Scientist (APAC). As a Field Application Scientist (APAC), you will be a client facing technical subject matter expert (SME) that provides custom solutions based on understanding the client’s needs to help grow our TriLink’s mRNA services business. The candidate will work within a cross functional team that includes regional sales/BD representatives, proposals, product management, marketing, R&D, Manufacturing, and Analytical teams. A successful candidate will thrive in a dynamic work environment applying their technical expertise towards creative customer solutions.  

How you will make an impact: 

• Partner with Business Development and Sales teams to improve customer journey by providing technical support and understanding of customer needs during pre-sale activities including but not limited to TriLink’s custom discovery services in mRNA manufacturing, analytical testing, and relevant products. 
• Support customer journey from early discovery on.  
• Represent the company scientifically at conferences, seminars, and webinars alongside R&D. 
• Address inquiries about company technology and manage technical escalations and support cases.    
• Serve as a liaison between customers and internal teams to produce applicable quotes, RFPs, HLEs, Proposals, and SOWs for client-specific technical needs. 
• Highlight the Voice of Customer (VOC) to internal teams to drive business focus and innovation. 
• Stay informed on technological advances, industry trends, and innovations in RNA health. 
• Perform other functions and duties as required 

 The skills and experience that you will bring: 

• Bachelor’s degree in biological field (i.e. molecular biology, biochemistry, or genomics); with at least 4 years of extensive technical experience in nucleic acids lab techniques from biotechnology or pharmaceutical industry. At least 2 years of experience for PhD.  
• Preferred lab experiences in: R&D, Process Development,  QC directly in mRNA. GMP manufacturing is a plus. 
• Strong client-facing skills, task-oriented, and able to communicate scientifically with technical teams. 
• Proven track record working with Business Development, Marketing, and Sales in Life Sciences. 
• Advanced understanding of molecular biology and mRNA/nucleic acid therapeutic applications, including manufacturing and analytical methods. 
• Understanding of clinical development pathways and current regulatory or CMC requirements. 
• Ability to prioritize multiple projects in a fast-paced, deadline-driven environment. 
• Ability to travel up to 30% including semiregular visits to company Headquarters (San Diego, CA) and customer visits as needed 

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Your next role as a Miracle Maker 

Maravai LifeSciences is seeking an experienced, proactive and detail-oriented Financial Reporting and Revenue Manager to join our team. This role is responsible for managing the preparation and filing of all external financial reports in compliance with U.S. GAAP and SEC regulations (including Forms 10-K, 10-Q, and 8-K), and leading the Company’s revenue accounting and recognition process. The Financial Reporting Manager will play a critical role in ensuring the accuracy, timeliness, and integrity of the Company’s financial disclosures as a large accelerated filer. In addition to overseeing SEC reporting, this individual will review customer contracts, write revenue memos, and drive process improvements across revenue accounting and operations.

This position reports to the Director, Financial Reporting and works closely with Accounting, FP&A, Legal, Investor Relations, and external auditors, providing key technical accounting expertise and supporting the continuous improvement of reporting processes, internal controls, and financial systems. The ideal candidate will have a strong foundation in public company reporting requirements, technical accounting, ASC 606 revenue recognition, and a proven ability to operate effectively in a dynamic, growth-oriented environment.

How you will make an impact: 

• Own the preparation and timely filing of SEC reports, including Forms 10-K, 10-Q and 8-K, ensuring compliance with U.S. GAAP and SEC regulations.
• Lead the drafting and review of financial statements, footnotes, and MD&A disclosures with a strong focus on accuracy, consistency, and technical precision.
• Oversee revenue recognition processes, including contract review, identification of performance obligations, variable consideration analysis, and appropriate revenue treatment under ASC 606.
• Prepare and review technical accounting memos related to revenue recognition and other complex accounting matters.
• Partner with Operations and Sales to streamline revenue-related processes, improve contract flow, and enhance automation and internal controls.
• Perform and review monthly close and reporting activities, including the calculation and analysis of earnings per share (EPS) and review of revenue journal entries.
• Coordinate the preparation of supporting workpapers for quarterly and annual SEC filings by collaborating with cross-functional teams to gather and validate information required for disclosures.
• Liaison with external auditors, as needed, to provide required documentation and respond to inquiries related to quarterly reviews, annual audits, and internal controls testing.
• Develop and manage the quarterly SEC reporting calendar, including key milestones, deliverables, and team assignments to ensure timely execution of all reporting activities.
• Partner closely with the Investor Relations team to support the preparation and review of quarterly earnings materials, ensuring alignment with SEC disclosures and corporate messaging.
• Support the preparation of annual statutory financial statements by coordinating with external consultants and internal teams to compile required schedules and supporting documentation.
• Monitor and assess the impact of new accounting standards and SEC rule changes, develop implementation plans and coordinate with business units to ensure timely adoption and compliance.
• Support SOX compliance efforts, including maintaining and enhancing documentation for policies, procedures, and internal controls related to external financial reporting.
• Drive process improvement initiatives to enhance reporting accuracy, efficiency, and automation within the financial reporting function.
• Maintain and continuously update the related accounting policies to reflect current standards and best practices.
• Coach and mentor team members on SEC reporting requirements, revenue accounting principles, disclosure best practices, and the effective use of reporting tools and systems.
• Prepare ad hoc financial analyses and reports as needed.to support management decision-making and special projects.
•  Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.

 The skills and experience that you will bring: 

• 6+ years of experience in financial reporting, auditing, and/or accounting
• CPA required.
• Experience with ASC 606 revenue recognition.
• Public accounting experience required.
• Ability to appropriately communicate effectively with all levels within the organization.
• Ability to read and interpret Generally Accepted Accounting Principles.
• Able to identify and resolve technical, operational, and organizational problems.
• Ability to prepare written memorandums summarizing accounting research.
• Able to work in a fast-paced, constantly changing environment while managing multiple priorities and meet critical deadlines.
• Proficiency with Microsoft Office Suite required.
• Experience with Workiva required.
• Highly detail oriented and organized in work.
• Ability to work cooperatively and collaboratively with all levels of employees, management, and external agencies, developing strong relationships.

The anticipated salary range for this position is $130,000 - $145,000.  In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package.  The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role.  

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Join our Talent Community!

If you are interested in working with us, but do not see a position open that matches your skillsets, we would still love to hear form you! Please submit your resume and let us know a bit more about you and we will reach out if a position opens up that aligns! 

In the meantime, follow us on LinkedIn to stay up to date on our company and job openings.

www.linkedin.com/company/maravai-lifesciences/

We look forward to connecting with you!