Quality Control Analyst jobs at Resilience

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Job Summary The Quality Technician II, Aseptic Control (Day Shift) is responsible for autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. This a Day Shift position working 6am - 6:30pm. 2 days on, 2 days off, 3 days on, 3 days off and the rotation starts over again. Job Responsibilities: * Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts, from technical documentation * Maintain accurate and complete records (i.e., laboratory notebooks, quality records, and sample receipts) * Complete required training * Perform visual inspections * Use the Environmental Monitoring System to collect and analyze samples * Guide others on SOPs, control documents, and/or other work instructions. Coordinate activities of support groups * Ensure that others carry out laboratory duties in a manner consistent with cGMP * Perform regular audits of SOPs and/or work instructions * Perform routine sampling activities and associated data entry * Wearing gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities * Read and interpret diagrams, drawings, and other schematics * Recommend and initiate activities to ensure area and equipment is maintained in a state of compliance * Provide 24/7 "on-call" support to others * Provide feedback on service and issues on a timely basis Minimum Qualifications: * Prior experience in a pharmaceutical production environment * Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language * Thorough attention to detail is required * Must be capable of keeping accurate records and performing mathematical calculations Preferred Qualifications: * High school graduate, vocational school graduate, or equivalent * Working knowledge of MODA, Microsoft applications, SAP, KRONOS * Experience working in a LEAN manufacturing environment * Knowledge of cGMPs and FDA policies/procedures The items described here are representative of those that must be met successfully to perform the essential functions of this job. Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $30.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

As part of our Compliance & Product Services Liability team, you will help shape the technical development of new and revised insurance programs that respond to today's evolving business environment. You'll work across key commercial lines of business, including general liability, umbrella liability, and commercial crime, while keeping customer satisfaction, product quality, and compliance at the forefront. About the Day to Day Responsibilities of the Role * Draft policy language and develop manual rules that guide insurers in issuing and rating policies, and also develop related information, including filings and announcements to customers. * Review laws, regulations and case law for impact on ISO products and insurer procedures. * Develop policy language and rules for major program updates that provide valuable insurance enhancements to products used by the entire insurance industry. * Review state laws and requirements and make revisions to ensure program updates are compliant and relevant in each state. * Leverage insurance expertise and researching skills to provide timely, thoughtful responses to insurer inquires over a wide range of insurance topics. * Develop and present items to panels of insurers on emerging trends and potential revisions. * Collaborate with all stakeholders including Product Development, Law Department, Government Relations, Actuarial, etc., inviting perspectives, contributions, and partnerships within the team, the unit, the company, and with our customers and business partners. * Work in conjunction with the Product Development team to research and review new products, consider impact on other products, and collaborate with others in bringing products to market. About You and How You Can Excel in this Role * Bachelor's degree or equivalent insurance experience. * At least two years P&C insurance experience with product development, claims, underwriting and/or submitting filings with insurance regulators. Experience involving analyzing and development of forms, rules, and/or rating preferred. * Excellent verbal and written communication skills and attention to detail. * Strong organization, research and analytic skills. * Ability to both work independently and collaborate in a team environment. * Knowledge of ISO commercial general liability insurance line procedures is a plus. * CPCU exam study or completion is a plus. #LI-SM1 #LI-Hybrid

Summary/Objective The Quality Control Associate is responsible for the day-to-day functionality of inspecting picked orders for accuracy. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Department Duties - Review picked orders for accuracy and that all stated requirements for the order are met. - Receive, identify, mark and place materials sent to the warehouse according to established procedures. - Prepare various merchandise for delivery; prepare packages for shipping according to established procedures. - Communicate with various personnel, departments, product managers and others to provide and receive information, resolve questions and issues, and coordinate activities. - Maintain work time records per company policy. - Operate a computer to process reports and forms and maintain an inventory of warehouse materials as required. - Assist team to help ensure the facility is maintained in a safe, clean and orderly condition. Competencies - Good organization skills and basic warehouse understanding of picking, shipping, receiving, issuing materials, proper and orderly storage, optimum space utilization and/or stock inventory procedures. - Ability to clearly read/listen and understand work instructions. - Ability to work well in time-sensitive situations. - Basic knowledge of Microsoft Excel - Team-oriented operating style with effective interpersonal skills that allow successful interactions with individuals of a variety of work styles, personalities, and career levels. Requirements Work Environment Warehouse Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. - Ability to move and handle merchandise weighing 1 ounce - 50 pounds - Ability to stand, bend and stoop for an extended period of time Education and Experience Preferred: - At least one (1) year of prior job-related experience in a Quality Control environment - High School diploma or equivalent education Position Type/Expected Hours of Work - Monday through Friday, 40 hours per week with possible overtime Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the associate for this job. Duties, responsibilities and activities may change at any time with or without notice. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the company. EEO Statement Wild Republic is an Equal Opportunity Employer. Applicants for employment, recruitment, hiring, training, transfer, promotion, pay, benefits, lay-off, demotion or termination of employment will be made without consideration of race, color, religion, sex, sexual orientation or preference, gender identity, national origin, age, disability, military status, ancestry, veteran status, or any other protected classification under applicable federal, state or local law.

The Insights product is a new offering for Guidepoint's Institutional investment and corporate clients, that offers teleconferences, surveys, and in-person events. The teleconferences live in a transcript library portal, which covers a wide of industries/topics that enables our clients to make informed decisions. All content features experts from Guidepoint's proprietary global network and is conceptualized and hosted by former investment professionals (i.e. private equity/hedge fund), sell-side equity research analysts, and industry professionals. This position can be remote within the United States. WHAT YOU'LL DO: Monitor a coverage universe of public companies within a sector by tracking earnings releases, investor presentations, SEC filings, sell-side research and industry news Create and moderate teleconferences on timely topics featuring an expert from Guidepoint's network with the goal of producing actionable insights for clients Review teleconference transcripts to ensure quality of content WHAT YOU HAVE: Bachelor's degree or Master's degree Minimum 10 years buy-side analyst experience Must follow bottoms-up, fundamental approach to investment research focusing on individual companies Must be current on multiple subsectors within Industrials (aerospace & defense, multi-industrial, building products, transportation & logistics etc..) in terms of news flow and what issues matter to the buyside at any given time Ability to work in a fast-paced entrepreneurial environment Outgoing personality with the ability to speak with people at all professional levels Intellectual curiosity and desire to learn Effective time management and organizational skills Demonstrated ability to work both individually and as part of a team; must be willing to train and mentor junior professionals Must be based in the US and available on East Coast hours if remote WHAT WE OFFER: This is a 3-month full-time consultant role with an expected annual salary of $175,000 - $225,000. This rate may vary depending on job-related knowledge, skills, and experience, as well as geographic location. You will also be eligible for the following benefits: Friday happy hour, “Summer Fridays”, and free snacks Casual work environment, team building, and other social events ABOUT GUIDEPOINT: Guidepoint is a leading research enablement platform designed to advance understanding and empower our clients' decision-making process. Powered by innovative technology, real-time data, and hard-to-source expertise, we help our clients to turn answers into action. Backed by a network of nearly 1.75 million experts and Guidepoint's 1,600 employees worldwide, we inform leading organizations' research by delivering on-demand intelligence and research on request. With Guidepoint, companies and investors can better navigate the abundance of information available today, making it both more useful and more powerful. At Guidepoint, our success relies on the diversity of our employees, advisors, and client base, which allows us to create connections that offer a wealth of perspectives. We are committed to upholding policies that contribute to an equitable and welcoming environment for our community, regardless of background, identity, or experience. #LI-KH1 #LI-Hybrid Base salary may vary depending on job-related knowledge, skills, and experience, as well as geographic location. Additionally, this position is eligible for an annual discretionary bonus based on performance. Compensation$750-$750 USD

CREATIVITY IS OUR SUPERPOWER. It's our heritage and it's also our future. Because we don't just make toys. We create innovative products and experiences that inspire, entertain and develop children through play. Mattel is at its best when every member of our team feels respected, included, and heard-when everyone can show up as themselves and do their best work every day. We value and share an infinite range of ideas and voices that evolve and broaden our perspectives with a reach that extends into all our brands, partners, and suppliers. The Team: This position supports the American Girl/Mattel quality and compliance standards throughout the operations processes at San Bernardino Distributiipn Center to ensure that the business and the customer's expectations are met. Job Description The Opportunity: The Quality Assurance Associate is responsible for ensuring that our products meet or exceed our customers' high levels of expectations. This is accomplished through incoming inspections, process auditing of assembly/rework projects / business to business fulfillment accuracy and review of consumer returns for quality related issues. What Your Impact Will Be: Quality Assurance Processors will inspect targeted incoming shipments, audit internal production/processes to ensure that quality and compliance standards are being maintained. Will be cross trained to assist in other departments as needed. Perform inspections (regular, “hot”, 100%) within established procedures and guidelines. Determine acceptability of product based on knowledge of company's quality and compliance standards. Document all inspection results in proper computer files (Oracle, WMS, spreadsheets). Maintain QC sample inventory and distribute QC samples to the DC's. Communicate, document and schedule non-compliance meetings appropriately and within a set timeline. Perform minor rework and/or repackaging of rejected products. Follow up with supervisor and other departments on 100% inspection progress. Audit products from Production Lines, Publication Shipments, Pick Towers, Ship Alones, Returns/Rework to ensure that process integrity is met. Documentation and data entry into the computer must be timely and accurate. Approve a statistical sampling of Pub. Shipments for accuracy in quantity & compliance to the various shipping manuals, routing guides and company quality and compliance regulations. Communicate all quality findings to the various Floor Supervisors and summarize in a written report. Qualifications What We're Looking For: Required Qualifications Intermediate and above Microsoft Office skills Developed math and reading skills. Ability to work independently with little guidance Able to adapt to varying tasks and multiple demands Able to collaborate with employees and vendors Must be flexible and work overtime to meet the needs of the business. Preferred Qualifications Bilingual in English and Spanish, not required, but beneficial. WMS and EQ system experience Essential Duties: Lift 30 lbs. on a frequent basis and up to 50 lbs. on occasion. Stand and/or walk on concrete floors 8-10 hours a day. Perform tasks which include continuously pulling, pushing, grasping, bending, and reaching. Wear required PPE equipment for the role hired. (Such as: Gloves, Safety Glasses, Steel Toe shoes, etc.). Rotate to all positions rotate to all operational positions as requested to support the business. Able to stand / walk for extended periods of time. Potential to step into Seasonal Leadership Role (Trainer, SST, Supervisor) Ability and willingness to flex between all roles within the warehouse as needed Developed math and reading skills. Bilingual in English and Spanish, not required, but beneficial. Must be flexible and work overtime to meet the needs of the business. The pay range is indicative of projected hiring range, however base pay will be determined based on a candidate's work location, skills and experience. Mattel offers competitive total pay programs, comprehensive benefits, and resources to help empower a culture where every employee can reach their full potential. Additional Information What It's Like to Work Here: We are a purpose driven company aiming to empower the next generation to explore the wonder of childhood and reach their full potential. We live up to our purpose employing the following behaviors: We collaborate: Being a part of Mattel means being part of one team with shared values and common goals. Every person counts and working closely together always brings better results. Partnership is our process and our collective capabilities is our superpower. We innovate: At Mattel we always aim to find new and better ways to create innovative products and experiences. No matter where you work in the organization, you can always make a difference and have real impact. We welcome new ideas and value new initiatives that challenge conventional thinking. We execute: We are a performance driven company. We strive for excellence and are focused on pursuing best in class outcomes. We believe in accountability and ownership and know that our people are at their best when they are empowered to create and deliver results. Who We Are: Mattel is a leading global toy company and owner of one of the strongest catalogs of children's and family entertainment franchises in the world. We create innovative products and experiences that inspire, entertain and develop children through play. We engage consumers through our portfolio of iconic brands, including Barbie, Hot Wheels, Fisher-Price, American Girl, Thomas & Friends, UNO and MEGA, as well as other popular intellectual properties that we own or license in partnership with global entertainment companies. Our offerings include film and television content, gaming, music and live events. We operate in 35 locations and our products are available in more than 150 countries in collaboration with the world's leading retail and ecommerce companies. Since its founding in 1945, Mattel is proud to be a trusted partner in empowering children to explore the wonder of childhood and reach their full potential. Visit us at ************************ and ******************************* . Mattel is an Affirmative Action/Equal Opportunity Employer where we want you to bring your authentic self to work every day. We welcome all job seekers including minorities, females, veterans, individuals with disabilities, and those of all sexual orientations and gender identities. All your information will be kept confidential according to EEO guidelines. Pursuant to the Los Angeles Fair Chance Ordinance and the California Fair Chance Act, qualified applicants with arrest or conviction records will be considered for employment. Videos to watch: The Culture at Mattel Mattel Investor Highlights

AMC Networks is home to many of the greatest stories and characters in TV and film and the premier destination for passionate and engaged fan communities around the world. We create and curate celebrated series and films across distinct brands and make them available to audiences everywhere. Our portfolio includes targeted streaming services AMC+, Acorn TV, Shudder, Sundance Now, ALLBLK and HIDIVE; cable networks AMC, BBC AMERICA, Independent Film Company, Sundance TV and We TV; and film distribution labels Independent Film Company and RLJE Films. The company also operates AMC Studios, our in-house studio, production, and distribution operation behind acclaimed and fan-favorite originals including The Walking Dead Universe and the Anne Rice Immortal Universe, and AMC Networks International, our international programming business. We are currently seeking a Quality Control Technician to join our Media Operations & Engineering team based in our Bethpage, NY office. JOB RESPONSIBILITIES * Responsible for the quality control evaluation of AMCN Broadcasting & Technologies client Network's program materials - both digitally delivered files and physical tapes. * Utilize and understand industry and departmental quality control procedures, guidelines, and department document database for proper and complete media evaluation. * Provide full and accurate metadata entries and reports of quality control assignments, giving great attention to detail and accuracy. * Maintain effective and productive communication channels with various AMCN B&T departments and colleagues, as they relate to scheduled work assignments and troubleshooting. * Understand and properly use all technical equipment related to work completion. * Report and document equipment issues and anomalies. Qualifications (Required & Preferred) * Bachelor's degree in relevant field major (i.e. Communications, TV Production, etc.) preferred. * At minimum, two years of relevant work experience in a broadcast television environment. * Excellent research, evaluation, and troubleshooting skills. * Outstanding communication skills, both verbal and written. * Comprehensive knowledge of time code, reference, frame rates, resolution, aspect ratios, audio formats (PCM) and types (surround/stereo), digital file formats. * Advanced knowledge of NTSC, PAL and HD video/audio broadcast standards and specifications. * General understanding of digital file codecs/wrappers and transcoding workflows. * Willingness to maintain flexible work schedule including nights, weekends, and holidays at management's discretion. * Strong analytic skills & critical thinking * Ability to absorb and retain information quickly * Excellent interpersonal skills. * High level of attention to detail. * Ability to interact and collaborate with all levels of management, co-workers and other departments. * Ability to quickly adapt to new technologies and workflows in a rapidly evolving environment. * Ideal candidate will be well versed in file based workflows. * Experience with the Evertz Mediator platform a plus. * Exposure to delivering digital files and elements to Electronic Sell Through platforms a plus. * Experience delivering media to VOD services a plus. The base compensation for this position is $52,000 to $55,000 commensurate with experience. AMC Networks additionally offers a comprehensive benefits package including Medical, Dental, Vision, Prescription Drug Coverage, 401k Plan, Wellness Program, Life Insurance, Tuition Reimbursement, Paid Time Off, Paid Parental Leave and Adoption Services, among other benefit plan options, subject to eligibility requirements. AMC Networks values the benefits achieved through in-office collaboration, but we provide our employees with the flexibility to work from home one day per week. The Company is committed to policy of nondiscrimination in its employment and personnel practices. Applicants are considered for all employment without regard to race, color, religious creed, religion, alienage, citizenship, gender, gender identity, national origin, ancestry, genetic predisposition or carrier status, age, marital status, familial status, military or veteran status, status as a victim of domestic violence, stalking or sexual assault, sexual orientation, disability or any other characteristic protected by federal, state or local law.

Shift: graveyard/night shift (11pm start) Compensation: $21-31/hr To support our Digital Cinema department, we are seeking a swing-shift QC Technician who can fulfill the responsibility of linear QC for Digital Cinema Package (DCP) in a theatrical and/or production suite environment, while ensuring that all security protocols are followed when dealing with sensitive material. The ideal candidate will have a good understanding of DCP including image, audio, accessibility and immersive elements. They should have knowledge and experience with Digital Cinema playback servers, audio, captioning, motion devices and other equipment required to carry out the QC workflows. In addition, QC experience with other formats and media including IMP, video, discs are pluses. They should be highly motivated, possess a flexible attitude, keen eye for details and a highly effective communicator especially with clients. They should also able to work as part of a team that deals with changing priorities and workloads. Responsibilities: · Perform theatrical QC services · Perform QC on other materials such as sources from clients (for example DCDM, DSM, video, audio on workstations such as DVS Clipster, Resolve, Colorfront's Transkoder etc) · Perform the above QC internally or/and with clients · Manage client engagements in the theaters where appropriate · Ingest materials via physical media or electronic transmission to playback servers or devices such as Dolby IMS2000, GDC, Doremi etc · Create detailed QC reports · Follow internal as well as client specific security protocols · Must be willing to work weekends, holidays and past their normal scheduled shift if needed · Create stereography maps for foreign language versioning · Other related tasks as assigned to fulfill responsibilities Requirements · Experience in QC workflows within a theatrical environment preferred · Excellent knowledge and understanding of media including audio, video, subtitles and other immersive elements such as 3D, ATMOS, DTSX, D-Box preferred · Requires accurate and methodical approach to QC. A very detailed attention and focused attitude to audio, video and film impairments and artifacts, while making subjective decision to the severity of an issue and delivering appropriate feedbacks · Experience in working directly with clients and an excellent communicator · Passionate about quality, customer experience and customer service excellence · Ability to work on own initiative and also be a good team player · A positive attitude when experiencing obstacles and enthusiastic towards getting work done · Ability and willingness to learn new methods, procedures, or techniques and take on new tasks Experience: • Minimum one (1) to two (2) years of experience in quality assurance within a theatrical environment is preferred.

Job Description Shift: graveyard/night shift (11pm start) Compensation: $21-31/hr To support our Digital Cinema department, we are seeking a swing-shift QC Technician who can fulfill the responsibility of linear QC for Digital Cinema Package (DCP) in a theatrical and/or production suite environment, while ensuring that all security protocols are followed when dealing with sensitive material. The ideal candidate will have a good understanding of DCP including image, audio, accessibility and immersive elements. They should have knowledge and experience with Digital Cinema playback servers, audio, captioning, motion devices and other equipment required to carry out the QC workflows. In addition, QC experience with other formats and media including IMP, video, discs are pluses. They should be highly motivated, possess a flexible attitude, keen eye for details and a highly effective communicator especially with clients. They should also able to work as part of a team that deals with changing priorities and workloads. Responsibilities: · Perform theatrical QC services · Perform QC on other materials such as sources from clients (for example DCDM, DSM, video, audio on workstations such as DVS Clipster, Resolve, Colorfront's Transkoder etc) · Perform the above QC internally or/and with clients · Manage client engagements in the theaters where appropriate · Ingest materials via physical media or electronic transmission to playback servers or devices such as Dolby IMS2000, GDC, Doremi etc · Create detailed QC reports · Follow internal as well as client specific security protocols · Must be willing to work weekends, holidays and past their normal scheduled shift if needed · Create stereography maps for foreign language versioning · Other related tasks as assigned to fulfill responsibilities Requirements · Experience in QC workflows within a theatrical environment preferred · Excellent knowledge and understanding of media including audio, video, subtitles and other immersive elements such as 3D, ATMOS, DTSX, D-Box preferred · Requires accurate and methodical approach to QC. A very detailed attention and focused attitude to audio, video and film impairments and artifacts, while making subjective decision to the severity of an issue and delivering appropriate feedbacks · Experience in working directly with clients and an excellent communicator · Passionate about quality, customer experience and customer service excellence · Ability to work on own initiative and also be a good team player · A positive attitude when experiencing obstacles and enthusiastic towards getting work done · Ability and willingness to learn new methods, procedures, or techniques and take on new tasks Experience: • Minimum one (1) to two (2) years of experience in quality assurance within a theatrical environment is preferred.

Shift: graveyard/night shift (11pm start) Compensation: $21-31/hr To support our Digital Cinema department, we are seeking a swing-shift QC Technician who can fulfill the responsibility of linear QC for Digital Cinema Package (DCP) in a theatrical and/or production suite environment, while ensuring that all security protocols are followed when dealing with sensitive material. The ideal candidate will have a good understanding of DCP including image, audio, accessibility and immersive elements. They should have knowledge and experience with Digital Cinema playback servers, audio, captioning, motion devices and other equipment required to carry out the QC workflows. In addition, QC experience with other formats and media including IMP, video, discs are pluses. They should be highly motivated, possess a flexible attitude, keen eye for details and a highly effective communicator especially with clients. They should also able to work as part of a team that deals with changing priorities and workloads. Responsibilities: * Perform theatrical QC services * Perform QC on other materials such as sources from clients (for example DCDM, DSM, video, audio on workstations such as DVS Clipster, Resolve, Colorfront's Transkoder etc) * Perform the above QC internally or/and with clients * Manage client engagements in the theaters where appropriate * Ingest materials via physical media or electronic transmission to playback servers or devices such as Dolby IMS2000, GDC, Doremi etc * Create detailed QC reports * Follow internal as well as client specific security protocols * Must be willing to work weekends, holidays and past their normal scheduled shift if needed * Create stereography maps for foreign language versioning * Other related tasks as assigned to fulfill responsibilities

Hourly Rate: $24.00 - $29.00 (Based on Experience) Benefits Offered: 401K, Life, Dental, Medical, Vision Shift: 1st Shift: Monday - Friday 7:00 am to 4:00 pm We are seeking a driven and detail-oriented Quality Control Technician who is committed to building a long-term career in Quality. This role is well-suited for individuals with foundational experience in manufacturing or inspection who take pride in precision, integrity, and continuous improvement. The Quality Control Technician reports directly to the Quality Manager and plays a vital role in maintaining the integrity of our products, processes, and documentation. You will perform inspections, maintain quality records, support root cause analysis, and collaborate with production teams to uphold ISO 9001 and customer requirements. Key Responsibilities: Conduct thorough inspections of products and assemblies to verify compliance with specifications and quality standards. Monitor the effectiveness of quality control processes and support improvements within assigned areas. Document inspection findings accurately and maintain complete, organized quality records. Assist in investigations of non-conformances, contributing to root cause analysis and corrective actions. Collaborate with production teams to identify issues early and resolve quality concerns efficiently. Follow established ISO 9001 procedures and support the ongoing development of the Quality Management System. Participate in internal audits and support readiness for customers or third-party audits. Uphold a high level of professionalism and represent the Quality department with integrity in all interactions. Qualifications: 1-3 years of experience in manufacturing, inspection, or quality-related work. High School Diploma or equivalent required; technical training or an associate degree is preferred. Strong attention to detail with a natural ability to notice small inconsistencies or defects. High personal integrity - consistently doing the right thing, even when it is inconvenient solid communication skills, both written and verbal, with the ability to collaborate across departments proficiency in Microsoft Office Suite; familiarity with quality management software is a plus Strong organizational skills and the ability to maintain accurate, reliable documentation A proactive problem-solver who can follow detailed processes, manage multiple tasks, and work with minimal supervision.

Job Description Hourly Rate: $24.00 - $29.00 (Based on Experience) Benefits Offered: 401K, Life, Dental, Medical, Vision Shift: 1st Shift: Monday - Friday 7:00 am to 4:00 pm We are seeking a driven and detail-oriented Quality Control Technician who is committed to building a long-term career in Quality. This role is well-suited for individuals with foundational experience in manufacturing or inspection who take pride in precision, integrity, and continuous improvement. The Quality Control Technician reports directly to the Quality Manager and plays a vital role in maintaining the integrity of our products, processes, and documentation. You will perform inspections, maintain quality records, support root cause analysis, and collaborate with production teams to uphold ISO 9001 and customer requirements. Key Responsibilities: • Conduct thorough inspections of products and assemblies to verify compliance with specifications and quality standards. • Monitor the effectiveness of quality control processes and support improvements within assigned areas. • Document inspection findings accurately and maintain complete, organized quality records. • Assist in investigations of non-conformances, contributing to root cause analysis and corrective actions. • Collaborate with production teams to identify issues early and resolve quality concerns efficiently. • Follow established ISO 9001 procedures and support the ongoing development of the Quality Management System. • Participate in internal audits and support readiness for customers or third-party audits. • Uphold a high level of professionalism and represent the Quality department with integrity in all interactions. Qualifications: • 1-3 years of experience in manufacturing, inspection, or quality-related work. • High School Diploma or equivalent required; technical training or an associate degree is preferred. • Strong attention to detail with a natural ability to notice small inconsistencies or defects. • High personal integrity - consistently doing the right thing, even when it is inconvenient • solid communication skills, both written and verbal, with the ability to collaborate across departments • proficiency in Microsoft Office Suite; familiarity with quality management software is a plus • Strong organizational skills and the ability to maintain accurate, reliable documentation • A proactive problem-solver who can follow detailed processes, manage multiple tasks, and work with minimal supervision.

Axiom Space is collaborating with Astrolab, Inc. to develop a Lunar Terrain Vehicle (LTV) for future Artemis missions, combining Axiom's advanced AxEMU spacesuit with Astrolab's FLEX rover to enable groundbreaking scientific exploration on the Moon's surface. This partnership reflects Axiom Space's broader mission to build era-defining space infrastructure that drives exploration and fuels a vibrant space economy that will empower our civilization to transcend Earth for the benefit of every human, everywhere. Axiom Space fosters a work environment inclusive of all perspectives. We are the pioneers of commercial space, leading the transformation of low-Earth orbit into a global space marketplace. Our mission-driven team is seeking a bold and dynamic Senior Quality Technician who is fueled by high ownership, execution horsepower, growth mindset, and driven to understand our world, science/technology, and life itself, for the benefit of all on Earth and beyond. Employment in this role is contingent on Astrolab/Axiom being selected as a winner of NASA's LTVS contract. POSITION SUMMARY We are looking for a resilient, high-energy, experienced Senior Quality Control Technician with a good eye for detail. You will be responsible for performing standardized quality control checks on our company products to ensure they meet the required legal and company standards for safety and quality. You may also be required to maintain tool control records, calibrated test & inspection equipment, prepare test data, and identify areas for quality control improvement. Additional responsibilities may require you to operate company vehicles to store and transport materials and products. Lastly, you must be able to perform all tasks as directed by supervisor. KEY DUTIES & RESPONSIBILITIES Developing and maintaining company inspection reports Inspecting goods or products according to quality and safety standards across all stages of production Ensuring company tools and equipment are calibrated and working correctly Reporting quality anomalies to the supervisor Collating test data and drafting quality reports Identifying possible areas for improvement in quality control processes and implement new methods accordingly Comply with safety regulations and maintain clean and orderly work areas Urgently communicate quality, safety, or compliance concerns Communicating project progress, status, and potential issues to stakeholders and leadership Implementing and maintaining agile project management methodologies throughout the project lifecycle Perform additional job duties as assigned QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education & Experience High School diploma or GED Minimum of 10+ years of inspection experience Understanding of advanced mathematical concepts including fractions, ratios, and proportions Track record of delivering outcomes in ambiguous, fast-moving environments Uses good judgement to problem-solve proactively, positively impacting hard challenges Proven to deliver high quality results under tight deadlines Grit Passion for space and the mission Entrepreneurial, growth mindset Perseverance Resourceful, adaptable Skills GD&T experience Experience with Coordinate Measuring Machine (CMM) Advance Experience with Quality Inspection Tools Executes priorities with precision and pace High EQ and ability to collaborate within teams and cross-functionally Tech-savvy in using systems and tools to move faster and smarter Excellent written and verbal communication skills Competencies: Embody our core values of leadership, innovation, and teamwork. In addition, to perform the job successfully, an individual should demonstrate the following competencies: Accountability Sense of Urgency Extreme Ownership Execution and Delivery Efficiency Effectiveness WORK ENVIRONMENT: Generally, an office environment, but can involve inside or outside work depending on the task. Requirements Must be able to complete a U.S. government background investigation. Management has the prerogative to select at any level for which the position is advertised. Proof of U.S. Citizenship or US Permanent Residency is a requirement for this position. Must be willing to work evenings and weekends as needed to meet critical project milestones. Physical Requirements Work may involve sitting or standing for extended periods (90% of the time) May require lifting and carrying up to 25 lbs. (5% of the time) Equipment and Machines Standard office equipment (PC, phone, printer, etc.) Axiom Space is proud to be an equal opportunity employer. Axiom Space does not discriminate on the basis of race, regional color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with disability, or other applicable legally protected characteristics.

As our Quality Control Technician you will assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining adjustments for batches that do not conform to requirements, documenting inspections, and insuring calibration of testing equipment. Solving challenges is the very foundation of who we are. After all, in the beginning, our founder, sea captain Robert Fergusson, didn't particularly care about paint. When he founded our company in 1921, he just wanted to keep his ship intact and stumbled upon a valuable solution. Today, that discovery is Rust-Oleum Corporation. The same passion that drove the Captain to spend his next few years creating the world's first rust-preventative paint still drives us today. When we see a problem, we work diligently until we've perfected a solution, which has led to some of the most cutting edge, durable and innovative products in the industry. Our creative and talented team of over 2000 people across every corner of the world, help us remain the global leader in protective paints and coatings for both home and industry. Here's what you can expect every day: Perform testing of production batches, incoming raw materials, finished goods, and components to determine conformance to specifications. Judge as “fit for release” production batches, incoming raw materials, finished goods, and components that are in conformance to all specifications and visually acceptable. Determine and communicate batch adjustments for any batches that do not conform to requirements, utilizing batch history, adjustment guidelines, and consultation with the QC Manager. Perform validation testing during filling to insure integrity of finished goods, including labeling, packaging, and fill weights. Communicate current status of inspections to QC Manager. Communicate issues with work instructions and procedures to QC Manager. Document inspection results. Required Experience: 1-3 years of production/manufacturing/quality control experience preferred but not required High school diploma or equivalent, Associate's or Bachelor's degree a plus Some background in physical sciences and algebra Ability to accurately read and enter computer data through a variety of tests Proficiency in Excel, Word, and other MS Office applications Experience in SAP recommended but not required Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

Sunset Industries has been manufacturing and assembling high-precision components for more than 60 years across the Aerospace, Nuclear, and Industrial markets. We have a strong reputation for quality and customer service. Pride in our company, the work, the quality, and respect for our customers & staff are reflected in each and every member of our team. Sunset is a professional work environment with motivated, results-oriented contributors. We help each other, we invest in our people, and we provide advancement opportunities so we can grow together. Sunset is a privately held company and we recently moved to a newly renovated 26,000 sqft facility in Mentor, OH - come join us in building the future of manufacturing. The Quality & Inspection Associate is a position within the Quality team. Reporting to the VP of Engineering & Quality, this team member will be key contributor to the quality inspection of our production parts. The successful candidate will be a self-starter who is organized, flexible, analytical, and practical with a willingness to collaborate amongst the team. What you'll do: Support the inspection team by performing operations such as: • Perform first piece inspection after initial set up for production • Perform final inspection after all processing prior to shipment, including the recording of all results • Setup gages to be used for production (dial bore gages) • Continuous improvement of inspection process • Collaborate with the production team to optimize quality when issues arise • Assist with AS 9102 FAIR documentation • Perform inspection of outside service operations • Perform inspection of parts with Keyence Vision System, Coordinate Measuring System (CMM), and hand tools What you'll bring: • Working computer skills, especially Excel and familiarity with software platforms • Passion for continuous improvement • Strong work ethic • Attention to detail • Attitude of helpfulness and support • Self-starter mentality - the ability to work in a timely manner with limited supervision. • Ability to collaborate and contribute as a member of a team. • Flexibility - each day is different from the next and that keeps things interesting. • Integrity and trustworthiness with confidential information. We ensure transparency and honesty are at the core of every interaction. • Ability and opportunities to work overtime as needed • Must be a U.S. Citizen, or hold a valid work visa that does not require sponsorship in order to legally work full-time in the United States. Preferred Skills: • Associate's or Bachelor's Degree preferred • ASQ CQT or CQI preferred • 3 years' experience in Quality Control/Quality Assurance preferred • Ability to read blueprints and understand GD&T tolerances • Ability to use inspection instrumentation (micrometers, calipers, gages, etc.) • Experience with inspection systems preferred, but not required (i.e. Keyence Vision System, Coordinate Measuring Machine (CMMs), etc.) What's in it for you: • Competitive compensation package comprising base hourly rate, performance-based compensation, and profit sharing. • Generous paid time-off. • Fully paid health, dental, and benefits • Pension plan • Collaborative work environment. • We invest in our people and provide growth opportunities for our dedicated and hard-working employees. • A place where your ideas, contributions, and ability to execute are valued. Applicants must be eligible to work in the United States and able to work 7:00am - 3:30pm Monday - Friday. Opportunities may exist for overtime work, but are not required. As an equal opportunity employer, Sunset Industries does not discriminate in hiring or terms and conditions of employment because of an individual's race, color, religion, gender, national origin, age, disability, sexual orientation, or marital status.

GENERAL SUMMARY: Assists with application and monitoring of established quality procedures and methods for production batches and new raw materials. Compiles, tabulates and summarizes QC data for analysis. Prepares and communicates variables and deviations from prescribed standards of quality. Maintains statistical records having to do with quality, nature and causes of defects in D365. Expedites and follows up changes to allow for prescribed quality standards. PRINCIPLE DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Check production batches by comparison to standards Advise batchmaker of any necessary adjustments to apply to product batch Recheck batch after adjustments are made until product is within standard product specifications Use proper analytical tools to compare product to standard specifications and to wet and/or dry samples Record results of comparison in D365 Consult with QC manager on products more than 10% out of product specifications Upon approval of product record data in D365 Check bulk raw materials against standard product specifications upon receipt Consult Quality control manual for specific requirements for product analysis of production batches as well as raw materials Calibrate QC/QA equipment as required Other duties as assigned by supervisor/manager QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience and Education Required High school diploma Proficient math and written communication skills Good computer skills - knowledge of Excel required Up to three years in industry related QC field helpful Prior batchmaking experience helpful Specific Knowledge, Skills, and Abilities Required Successful completion of Munsel Color test, helpful Familiarity with products used in batchmaking processes Familiarity with standard analytical tools Reasoning Ability Employee must work with limited supervision following written and verbal instructions. CERTIFICATES, LICENSES, REGISTRATIONS: N/A PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals to perform the essential functions. Occasional lifting and/or carrying of up to 40 lbs. Is required. Standing for extended periods of time (approximately 90% of 8-hour shift) is required with some sitting, walking, reaching, handling, bending and stooping. WORK ENVIRONMENT: Normal laboratory industry related environment conditions are present in the QC/QA laboratory. Employee on occasion will be required to go into the manufacturing areas, where normal manufacturing environment conditions are present. The company provides any required personal protective equipment. KEY PERFORMANCE INDICATORS (KPI) Turnover of correct production batches QC efficiency as gauged by customer RMA's

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Job Summary The Quality Technician II, Aseptic Control (Day Shift) is responsible for autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. This a Day Shift position working 6am - 6:30pm. 2 days on, 2 days off, 3 days on, 3 days off and the rotation starts over again. Job Responsibilities: * Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts, from technical documentation * Maintain accurate and complete records (i.e., laboratory notebooks, quality records, and sample receipts) * Complete required training * Perform visual inspections * Use the Environmental Monitoring System to collect and analyze samples * Guide others on SOPs, control documents, and/or other work instructions. Coordinate activities of support groups * Ensure that others carry out laboratory duties in a manner consistent with cGMP * Perform regular audits of SOPs and/or work instructions * Perform routine sampling activities and associated data entry * Wearing gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities * Read and interpret diagrams, drawings, and other schematics * Recommend and initiate activities to ensure area and equipment is maintained in a state of compliance * Provide 24/7 "on-call" support to others * Provide feedback on service and issues on a timely basis Minimum Qualifications: * Prior experience in a pharmaceutical production environment * Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language * Thorough attention to detail is required * Must be capable of keeping accurate records and performing mathematical calculations Preferred Qualifications: * High school graduate, vocational school graduate, or equivalent * Working knowledge of MODA, Microsoft applications, SAP, KRONOS * Experience working in a LEAN manufacturing environment * Knowledge of cGMPs and FDA policies/procedures The items described here are representative of those that must be met successfully to perform the essential functions of this job. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $30.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

Department: Quality Control Reports to: QC Specialist IV

Department: Quality Control Reports to: QC Specialist IV About CTMC CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson's research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed eight INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Responsibilities The Quality Control (QC) Specialist I is responsible for conducting environmental monitoring (EM) and safety testing to support aseptic production and final drug product release. This role ensures compliance with Good Manufacturing Practices (GMP) and regulatory standards, contributing to the overall quality and integrity of the manufactured products. Perform routine environmental monitoring of air, surfaces, and personnel, including sampling using contact plates, viable and non-viable particulate sampling in classified aseptic production areas. Analyze collected samples for microbial contamination, or other relevant parameters. Interpret data and document findings in accordance with company procedures and regulatory requirements. Manage data entry, reporting and review of EM data within an electronic EM system. Perform microbial identification of isolated organisms. Execute media fill simulation in aseptic environments. Ensure timely receipt and submission of samples within the organization. Support the qualification of cleanroom facilities and assist with annual shutdown and restart programs. Perform sterility testing, endotoxin analysis, Gram staining, and basic biochemical testing. Execute growth promotion and pH testing for microbiological media. Conduct stability testing as per protocols for cell therapy and viral supernatant products. Execute daily lab responsibilities and tasks to meet assigned schedule and deadlines. Assist area management to ensure that the lab is always in a state of readiness for a given area of relevant standards and regulations. Perform basic maintenance, calibration, and quality control of laboratory equipment. Maintain inventory and order laboratory supplies as needed. Other duties as required. Qualifications/Skills Bachelor's degree in Biological Sciences, Biotechnology or a related field required. 1+ yr.'s experience in a quality control laboratory including knowledge of environmental monitoring, microbiological testing, and GMP requirements preferred, 0+ yr.'s required or equivalent combination of education and experience. Proven capability to work aseptically in cleanroom environments. Demonstrated ability to collaborate effectively in a multi-disciplinary team. Able to carry out planned laboratory activities with minimal supervision. Shows initiative to take on additional responsibility. Proficient with Microsoft Office (Excel, Outlook, etc.). Able to work flexible work hours to maintain critical testing during manufacturing runs. Capable of working in a fast-paced environment and communicating effectively with a diverse work group. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer Printer Scanner Telephone Lab Equipment Physical Demands- Frequent sitting, standing, walking Carrying packages and moving bins and boxes, lifting up to 10 lbs. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.

Department: Quality Control Reports to: Sr. Manager, Quality Control About CTMC CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson's research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed 8 INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Role Summary As CTMC advances its portfolio of cell therapy products across early- to late-stage clinical development, the Quality Control (QC) team continues to expand its analytical capabilities. We are seeking a QC Specialist IV with strong expertise in analytical method qualification and validation. This role is ideal for an experienced QC professional who can ensure that methods are scientifically sound, phase-appropriate, and compliant with regulatory expectations throughout the product lifecycle. The successful candidate will play a key role in advancing analytical readiness for clinical and commercial manufacturing. Responsibilities Lead and execute analytical method qualification and validation activities for QC assays supporting the release and characterization of cell and gene therapy products. Ensure study design, execution, and reporting are compliant with ICH and FDA expectations. Apply subject matter expertise across key analytical platforms, including: Flow cytometry for phenotyping, purity, and functional marker expression. Molecular assays (qPCR/dd PCR) for vector copy number (VCN) determination. Immunoassays such as IFN-γ ELISA for functional potency assessment. Automated cell counting and viability using systems such as the Cellometer and NC-200. Design, author, and oversee analytical method qualification and validation in compliance with ICH guidelines. Partner closely with Analytical Development to ensure seamless and compliant transfer of analytical methods into QC. Author, review, and approve technical documents including SOPs, validation protocols, qualification reports, and analytical methods. Ensure scientific integrity and regulatory readiness of all deliverables. Provide SME-level guidance and training to QC analysts, fostering technical proficiency and consistency in execution. Support regulatory submissions, audits, and inspections by preparing method validation summaries, presenting data, and defending QC analytical approaches. Lead or contribute to laboratory investigations (OOS, OOT, deviations) with emphasis on method performance, data integrity, and scientifically justified root cause determination. Continuously monitor assay performance, trend analytical data, and implement improvements or requalification as needed. Ensure all QC analytical activities are conducted in full compliance with cGMP, ICH Q2(R2), and applicable global regulatory standards. Engage in external-facing technical discussions with partners, collaborators, and contract laboratories to align on analytical expectations, study designs, and data interpretations. Represent CTMC QC in cross-functional and partner project meetings with professionalism and scientific rigor. Other duties as required. Qualifications/Skills Bachelor's degree in a scientific discipline (advanced degree preferred) with 5+ years of QC or analytical development experience in a GMP-regulated environment or equivalent combination of education and experience. Proven experience in analytical method qualification and validation, including protocol design, execution, and data interpretation. Hands-on expertise with flow cytometry, molecular assays (qPCR/dd PCR), ELISA, and automated cell counting and viability platforms. Demonstrated ability to function as a subject matter expert (SME) for QC analytical methods and provide technical leadership within cross-functional teams. Proficient in authoring and reviewing technical documentation, including SOPs, validation protocols, qualification reports, and investigations. Familiarity with Laboratory Information Management Systems (LIMS) and electronic data workflows to support data integrity and compliance is a. Strong understanding of regulatory guidelines (ICH, FDA, EMA) governing analytical method validation and QC operations. Excellent organizational skills with the ability to manage multiple priorities, projects, and timelines in a dynamic environment. Effective communication and collaboration skills, with the ability to engage confidently across diverse teams and external partners. Able to work flexible work hours to ensure continuity of manufacturing and release activities. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer, printer, fax, and telephone. Physical Demands- Frequent sitting, standing, walking Carrying packages and moving bins and boxes, lifting up to 10 lbs. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.