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<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
The professional scientific staffing services role is a position within the supplier’s organization under which lab work is conducted at a Client facility.&nbsp; Work is assigned by a supervisor from the supplier company, but is executed within Client labs using Client instrumentation and supplies.&nbsp; Technical feedback and final review of data are the responsibilities of Client personnel, but all performance feedback and day-to-day supervision will be provided by the supplier supervisor.
Specific duties for the role include (1) the support of development and qualification of methods overseen by a Client scientist, and (2) the execution of a limited number of techniques for the analysis of routine samples. Techniques within scope are chromatography (LC and GC), USP dissolution (apparatus I and II), particle size distribution and compendial methods. Responsibilities also include basic lab organization and maintenance, as well as excellent documentation skills.
<ul>
<li>Execute testing of assigned analysis type (specific test methods) for routine sample submissions</li>
<li>Support development and qualification of new methodsE</li>
<li>Identify and help to resolve equipment and basic test method issues</li>
<li>Develop expertise to serve as a backup executor of a limited number of other analysis types (other test methods)</li>
<li>Provide feedback to Client scientists on the performance of existing assays / test methods</li>
</ul>
Qualifications 
<ul>
<li>B.S in a science related firled and 3-4 years of industry experience or a M.S. in a sicnece related field with 1 year of experience&nbsp;</li>
<li>Prior knowledge and experience with operating, troubleshooting, and optimizing LC, HPLC/UPLC, GC, dissolution by USP apparatus I and II, and particle size distribution instrumentation.</li>
<li>Dissolution Testing experience is also required for this role</li>
<li>Other techniques of interest would be MS, NMR and IR spectroscopy.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday, 8 am-5 pm.&nbsp; Candidates living within a commutable distance of Cambridge, MA, are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ site, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Scientist - Chromatography

<h3>Job Description</h3>
In Vivo Resources (IVR) Associate, Pharmacology 
 
Our client, a biopharmaceutical company, has an opportunity for a temporary in vivo technician supporting in vivo studies within their rodent-based, drug discovery research program. Responsibilities include animal husbandry, in vivo study support (compound administration, blood collection, necropsy/tissue collection), and facility maintenance. Candidates must be able to work both independently and within a team environment. Hours of operation are flexible.
 
Responsibilities
<ul>
<li>Working closely with the IVR team and pharmacologists, provide research support for in vivo studies including:</li>
<li>Compound administration (PO, SC, IP, IV),</li>
<li>Clinical observations and data collection (body weights, body condition scoring)</li>
<li>Euthanasia procedures</li>
<li>Tissue collection (blood collection, necropsy, tissue collection/preparation,</li>
<li>Sample processing (centrifuge and running both hematology/chemistry analyzers)</li>
<li>Perform daily health checking and husbandry including identifying and responding to clinical conditions.</li>
<li>Perform facility maintenance including receiving/stocking supplies, sanitization/sterilization of equipment and environment, waste management, and monitoring environmental parameters.</li>
<li>Confirmation and adherence of program compliance with IACUC and EHS regulations/standards. Maintain personal compliance with Agios institutional expectations (training, timecards, etc.).</li>
<li>Perform receipt and housing of animal shipments.</li>
<li>Other operational/technical opportunities as required/presented</li>
</ul>
Qualifications
Education/Knowledge
<ul>
<li>English comprehension (reading, writing, verbal)</li>
<li>High School degree with 1-3 years laboratory animal experience</li>
<li>Recognition and response to normal/abnormal animal conditions &amp; behaviors (preferred)</li>
<li>Experience with genetically engineered rodent models (preferred)</li>
<li>Working knowledge of institutional, local and federal animal welfare regulations (preferred)</li>
<li>Microsoft Office, Outlook and data base knowledge.</li>
</ul>
Abilities
<ul>
<li>Experience with/exposure to rodent care (husbandry, technical support, clinical identification)</li>
<li>Familiarity with research facility operations (stock &amp; waste management, organization, sanitation) (preferred)</li>
<li>Lift, push, pull up to 50lb, stand for extended periods of time and perform repetitive motions</li>
</ul>

IVR Associate

<h3>Job Description</h3>
Job Description
.The Enterprise Applications Manager helps us care for our guests and our teams by leading the strategic direction, management, and support of our enterprise IT infrastructure and business-critical applications. This role is responsible for ensuring high availability, scalability, and security of IT systems while driving modernization and digital transformation initiatives. The ideal candidate will have strong leadership skills, technical expertise, and a proactive approach to optimizing IT operations. Support and maintenance of IT services and applications are key functions of this role.
Responsibilities
Infrastructure Management: Oversee the design, implementation, maintenance, and support of IT infrastructure, including cloud and hybrid environments. Enterprise Applications: Lead the administration, optimization, and support of core business applications (ERP, CRM, HRIS, collaboration tools, etc.). SSO &amp; Identity Management: Implement and manage Single Sign-On (SSO) solutions and identity management systems to enhance security and user experience. Strategic IT Planning: Develop and execute technology strategies aligned with business objectives, ensuring future scalability and innovation. Security &amp; Compliance: Ensure IT systems adhere to cybersecurity best practices, compliance requirements, and data governance policies. Vendor &amp; Stakeholder Management: Collaborate with key business units and external vendors to drive performance, manage contracts, and negotiate service agreements. Team Leadership: Lead and mentor a team of IT professionals, fostering a culture of innovation, efficiency, and continuous improvement. Incident &amp; Change Management: Establish and enforce ITIL-based processes to enhance system reliability, minimize downtime, and ensure seamless change implementation. Budget &amp; Cost Management: Oversee IT budgets, optimize costs, and drive cost-effective technology investments.
Requirements
BachelorÃ¢â‚¬â„¢s degree in Information Technology, Computer Science, or a related field 7+ years of experience in IT infrastructure and enterprise applications management, with at least 3 years in a manager level or above role. Experience in cloud computing, networking, and cybersecurity frameworks.Ã‚Â&nbsp; Hands-on experience managing enterprise applications such as ERP, CRM, and ITSM platforms. Strong knowledge of ITIL, DevOps, and Agile methodologies. Experience with identity and access management (IAM) solutions, including SSO and multi-factor authentication (MFA). Excellent leadership, project management, and problem-solving skills. Strong communication and stakeholder management abilities. Track record of adaptability in a fast-paced, complex environment.#zip

Enterprise IT Applications Sr. Manager

<h3>Job Description</h3>
Job DescriptionDescription:
Are you looking to take the next step in your IT Career? Let's chat and see if we are a good match!
 
Opportunity:
Virtual Service Operations is searching for highly motivated and career-driven individuals to join our growing team as Desktop Support in Woburn, Massachusetts. In this role you would be a part of our growing relationship with one of our great clients and have responsibilities in Desktop Support such as:
<ul>
<li>Provide Workstation Software Break Fix support</li>
<li>IMAC – PC Install, Moves, Adds and Changes</li>
<li>Image Loads</li>
<li>Asset Recovery</li>
<li>Asset tagging</li>
<li>Printer Support</li>
<li>Client Center (Tech Bar) Support</li>
<li>IT Service Management Updates</li>
<li>Other Client Support duties needed to maintain Workstation operations and customer satisfaction may be assigned</li>
</ul>
Qualifications:
<ul>
<li>Previous working experience in Desktop Support is desired, however, training will be provided for all entry-level new hires</li>
<li>Knowledge of PC Imaging</li>
<li>Experience with change management and incident management</li>
<li>Experience with using tools such as: ServiceNow, Bomgar, LapLink and Secure Disk Wipe</li>
</ul>
Preferred Qualifications:
<ul>
<li>Certified Dell Technician</li>
<li>Expertise in Inventory Control</li>
</ul>
Requirements:
<ul>
<li>Must be within driving distance of Woburn, Massachusetts, and be willing to work onsite.</li>
<li>Please note that pursuant to a government contract, this specific position requires U.S. citizenship status.</li>
<li>Must be able to lift up to 40 lbs</li>
<li>Must be able to stand or walk for extended periods of time</li>
<li>Must be able to walk up and down stairs or ramps</li>
<li>Must be able to kneel and work under desks or in confined spaces</li>
</ul>
What is Important to Us:
<ul>
<li>You are an excellent communicator in writing and speaking.</li>
<li>You have the ability to work independently but also value teamwork.</li>
<li>Your problem-solving skills are excellent.</li>
<li>You are looking for a job where performance appraisals occur regularly, and you look forward to advancing your career.</li>
<li>You seek a community of virtue-centered co-workers and clients.</li>
</ul>
What we offer you: As part of the VSO company, you will be part of a virtue-centered team who value their work and teammates. We provide ongoing learning and development opportunities to foster continuous growth.
 
More About VSO: VSO is a hybrid cloud and managed services consulting firm. Much of VSO’s success can be attributed to our deep partnerships with IT services industry leaders such as AWS, IBM, Microsoft and others. VSO leverages numerous other partner relationships so as to provide our customers with optimal support. Additionally, we take pride in taking care of our employees. We offer a wide variety of benefits for eligible employees related to health, retirement, professional development, and more! For more information, please visit our website at <a href="https://vso-inc.com/careers" target="_blank">https://vso-inc.com/careers</a>

Desktop Support in Woburn, Massachusetts

<h3>Job Description</h3>
Job DescriptionCompany Description 
To create revolutionary, story-driven RPGs which go straight to the hearts of gamers — this is our mission. Want to dive deeper into our company’s culture? Explore our social media and check out our&nbsp;YouTube channel&nbsp;where we share behind-the-scenes insights and stories direct from our team members!
Job Description 
CD PROJEKT RED is looking for an Engineering Director to join our office in Boston and drive the gameplay systems of Cyberpunk 2.
In this position, together with the rest of the team, you will help push the envelope for the next, immersive game in the Cyberpunk universe, creating an emotional, open-world experience that will stay with gamers. As an Engineering Director, you'll combine your leadership skills with your deep technical expertise to shape the future of our gameplay systems, driving innovation and delivering unforgettable gaming experiences.
Daily Responsibilities
<ul>
<li>Establish and oversee the architecture and technical strategy for gameplay features and systems.</li>
<li>Lead and mentor a team of talented engineering managers and engineers, fostering a collaborative and innovative environment.</li>
<li>Develop strategic plans for the gameplay teams, including resource allocation, project timelines, and technology roadmaps.</li>
<li>Collaborate closely with art, animation, design, and other engineering teams to align gameplay features &amp; systems with the creative vision for the project.</li>
<li>Drive standards for clean, high-quality, and efficient C++ code, ensuring best practices in optimization, readability, and maintainability.</li>
<li>Ensure thorough documentation, both in-code and for broader knowledge-sharing, enabling smooth onboarding and collaboration within the team and across departments.</li>
<li>Direct efforts to proactively identify and resolve issues, ensuring that character systems contribute to an overall polished and performant product.</li>
<li>Stay up-to-date with the latest industry trends, emerging technologies, and best practices in gameplay technology and bring innovative ideas to the team.</li>
</ul>
Qualifications 
<ul>
<li>Min. 10 years professional experience and at least 5 years of experience within the games industry.</li>
<li>Experience in creating an AAA title for game consoles, debugging, and profiling these games in a console environment.</li>
<li>Proven track record in managing a team.</li>
<li>Good knowledge of Unreal Engine 5 environment - especially features and systems related to the gameplay area.</li>
<li>Practical knowledge of gameplay features &amp; systems implementation.</li>
<li>Experience with Abilities Systems.</li>
<li>Experience with NPCs and crowds.</li>
<li>Experience with removing gameplay systems from the Main Thread.</li>
<li>Knowledge of modern game gameplay systems architecture.</li>
<li>Deep knowledge of C++.</li>
<li>Math &amp; algorithmic skills.</li>
<li>Good &amp; practical knowledge of code parallelization.</li>
<li>Experience working in an Agile development environment is a plus.</li>
<li>Focused on delivering the best results.&nbsp;</li>
<li>Good spirit and team player approach with a mindset geared towards adaptability, collaboration, and continuous improvement.</li>
<li>Excellent communication and interpersonal skills, with the ability to effectively communicate complex technical concepts to both technical and non-technical stakeholders in a multilingual environment.</li>
</ul>
 Additional Information 
This job requires working in Boston, US.
Working mode: in-office, in a hybrid, or full-time capacity.
Health &amp; Well-being
<ul>
<li>Company paid medical healthcare (dental vision &amp; mental).</li>
<li>Paid Leave — 20 days of holiday for every team member per year (26 days after two years).</li>
<li>No dress-code — we like to keep it casual.</li>
<li>401K with employer matching.</li>
<li>Gym Membership Reimbursement.</li>
</ul>
Perks &amp; Professional Growth
<ul>
<li>Flexible working hours.</li>
<li>Trainings, lectures and courses — internal workshops, knowledge-sharing initiatives, online tutorials, and e-learning classes are all available. There’s always something to learn!</li>
<li>Merch — gifts for newborn rebels and regular chances to nab some cool swag!</li>
<li>A welcome pack filled with goodies — to help you feel right at home once you join the team.</li>
</ul>
Life in the Office
<ul>
<li>Dog-friendly office — dog owner? Bring your pooch with you and look after them while working! There’s always a furry friend or two to meet at the studio.</li>
<li>Truly international working environment — a chance to meet and work with a diverse selection of people from all around the world. &nbsp;</li>
</ul>
If you have observed any irregularities in our recruitment process please click&nbsp;here&nbsp;to report them.

Engineering Director - Gameplay

<h3>Job Description</h3>
Job DescriptionCompany Description 
Come join our team and become part of what the Boston Globe has recognized as one of the Top 100 Women-Led Businesses in Massachusetts 2018 -&nbsp;2024!&nbsp;
Saving lives through organ and tissue donation is the mission uniting our employees and drives the work we do.&nbsp;
New England Donor Services (NEDS) coordinates organ and tissue donation in Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, the eastern counties of Vermont and Bermuda.&nbsp;Responsible for one of the largest of the 55 Organ Procurement Organizations (OPOs) that make up the nation’s donation system, NEDS works with over 200 hospitals and serves nearly 15 million people in our region, screening nearly 55,000 potential donor referrals annually. With approximately $140M in operating revenues, NEDS employs 360 clinical and non-clinical staff members throughout New England and across the country.
Our vision is to be a leader in the development and implementation of strategies to increase the life-saving and life-enhancing gifts of organ and tissue donation through effective relationships with our clinical partners, donor families and the communities we serve.
Job Description 
The Quality Systems Specialist (QSS) will be responsible for ensuring compliance with all internal Standard Operating Procedures and all pertinent regulatory and accreditation requirements. Duties include the following: perform QA review of organ and tissue donor records and associated data entry; collects, documents and distributes all relevant information to complete donor records and assure regulatory compliance; and ensures tissue processors and transplant centers are provided with all donor information required to help ensure the safety of the recipients of donated organs and tissues. Each level assumed the competencies of the essential job functions of the previous level.
This is a hybrid role that requires 1-2 days in office per week after a successful orientation period. There is a weekend coverage rotation once every 7/8 weeks.&nbsp;
<ul>
<li>Collaborates with QSS team members to develop a staffing schedule that ensures QSS coverage 7 days a week (including holiday on call coverage).</li>
<li>Completes tissue donor record review (preliminary and final) to ensure compliance to policies and procedures of NEDS and other governing bodies. This includes reviewing for all required data entry, test reporting and information sharing.</li>
<li>Completes organ donor record review (preliminary and final) to ensure compliance to policies and procedures of NEDS and other governing bodies. This includes reviewing for all required data entry, test reporting and information sharing.</li>
<li>Completes additional information requests by processors in a timely manner.</li>
<li>Maintains all Electronic Medical Records (EMR) access.</li>
<li>Communicates effectively within NEDS and with all outside agencies including tissue processors and transplant centers.</li>
<li>Acts as a resource to all employees who document in donor records and perform other critical functions.</li>
<li>Maintains confidentiality of all donor and recipient information as described by current laws and regulations.</li>
<li>Attends regularly scheduled department meetings.</li>
<li>Implements the Quality Assessment and Performance Improvement plan.</li>
<li>Ensures the accuracy, security, confidentiality and availability of records in compliance with policies and procedures of NEDS and other governing bodies.</li>
<li>May include other responsibilities as assigned by Director, Quality Assurance.</li>
</ul>
Knowledge, Skills and Abilities:
<ul>
<li>Organ/Tissue Experience: strong working knowledge of organ and tissue donation processes and procedures. Knowledge of regulations and standards applicable to organ and tissue donation.</li>
<li>Detail Oriented: meticulous attention to detail</li>
<li>Computer &amp; Application Literacy: proficiency in Microsoft Word, Excel, PowerPoint, Outlook, SharePoint and the ability to learn NEDS’ internal systems including, but not limited to, the clinical database.</li>
<li>Workload Management and Organization: ability to prioritize workload, adapt to changing priorities and deadlines. Manages a complex workload and competing priorities with strong attention to detail, organization and time management.</li>
<li>Interpersonal and Communication Skills: ability to critically think, problem solve and work individually and as a team to manage the daily workload. Demonstrates a high degree of service and support to both external and internal customers. Ability to foster a collaborative team environment.</li>
<li>Emotional Intelligence: demonstrates the ability to understand, use and manage emotions in positive ways to relieve stress, communicate effectively, overcome challenges and diffuse conflict.</li>
</ul>
Qualifications 
<ul>
<li>Undergraduate degree preferred, or a minimum of one years’ experience in organ/tissue banking, medical records or Quality Assurance.</li>
<li>Working knowledge of medical terminology preferred.</li>
</ul>
What You’ll Be a Part Of:
You will be part of a team that supports the NEDS mission, to Save and Heal Lives, through the gift of Organ and Tissue Donation.&nbsp;&nbsp;As an NEDS employee, our benefits include:
<ul>
<li>Generous&nbsp;paid time-off program</li>
<li>Health, Dental, Vision, and Mental Health insurance coverage</li>
<li>2x Annual Salary Life Insurance</li>
<li>Fertility Benefits</li>
<li>LGBTQIA+ Focused Healthcare Programs</li>
<li>Flex Spending Account Options</li>
<li>403(b) Retirement Plan with Organizational Contributions</li>
<li>Tuition Reimbursement</li>
<li>Employee Assistance Program (EAP)</li>
<li>Pet Insurance</li>
<li>Working Advantage discounts Program.</li>
<li>Personal career and skill development opportunities</li>
</ul>
You can also participate in&nbsp;Corporate sponsored events&nbsp; like the annual Blue &amp; Green Walk, Community Volunteering opportunities, Organization-wide team-building outings, and more!
 Additional Information 
HIRING ALERT:&nbsp;NEDS is actively taking precautions to protect our community, staff and partners during this time of medical emergency due to COVID-19.&nbsp;In order to be employed at NEDS, you must be vaccinated and boosted for COVID-19.
When you join New England Donor Services you can expect competitive salaries and a great benefit package. Benefits include a generous paid time off program, BCBS Health and Dental Insurance, Healthcare Reimbursement Account, 2x Annual Salary Life Insurance, Pet Insurance, Flexible Spending Account (FSA),&nbsp;Short-Term and Long-Term Disability Coverage, 403(b) Retirement Contribution, Tuition Reimbursement, Employee Assistance Program and Discounts through Working Advantage.
New England Donor Services is an equal opportunity employer and welcomes candidates from all backgrounds to apply to meet the needs of the communities we serve.
Hear from some of our employees at <a href="http://www.neds.org/careers" target="_blank">www.neds.org/careers</a>

Quality Systems Specialist

<h3>Job Description</h3>
Job Description
Location: West Roxbury, MA
Country: United States
Salary: $75K-$85K
Only US Citizens or Green Card Holders
Description:
We are seeking a highly organized and detail-oriented Assistant Project Manager to support the successful execution of construction projects. This role involves assisting in project oversight, subcontractor/vendor management, scheduling, and project documentation. The ideal candidate will have a strong understanding of construction processes, contract management, and scheduling coordination.
KEY RESPONSIBILITIES
<ul>
<li>Assist in managing all aspects of assigned projects, ensuring smooth execution and adherence to project plans.</li>
<li>Oversee subcontractor and vendor coordination, including scope negotiations and pricing agreements.</li>
<li>Ensure comprehensive coverage for all aspects of the project's scope of work.</li>
<li>Work with scheduling consultants to update the Project Master Schedule and coordinate trade work to meet deadlines.</li>
<li>Develop and manage the Project Submittal Schedule, reviewing submittals and maintaining communication with architects, owners, and awarding authorities.</li>
<li>Support the preparation and processing of Requests for Information (RFIs), proposal requests, and change orders.</li>
<li>Assist in the review and approval process for purchase orders, contracts, and applications for payment.</li>
<li>Oversee and review project documentation, material requests, and reports using Procore project management software.</li>
</ul>
QUALIFICATIONS
<ul>
<li>Bachelor’s degree in Project Management, Construction Management, or a related field.</li>
<li>Minimum of two years of relevant experience in project management or construction administration.</li>
<li>Strong organizational skills with the ability to manage multiple priorities.</li>
<li>Proficiency in Procore or similar project management software is a plus.</li>
<li>Excellent communication skills to coordinate effectively with subcontractors, architects, and project stakeholders.</li>
</ul>
BENEFITS
<ul>
<li>401(k) retirement plan with employer matching</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off (PTO)</li>
<li>Professional development assistance</li>
<li>Vision insurance</li>
</ul>
This position is ideal for a motivated and detail-oriented professional looking to advance their career in project management within the construction industry. If you have the required experience and skills, we encourage you to apply.

Assistant Project Manager

<h3>Job Description</h3>
Job Description
 Why should you join the Analogic team?
At Analogic, we work together to create life-changing technology. We value your unique skills and abilities and invite you to join our team in saving lives by supplying health care workers with high-tech medical products and transportation security professionals with leading-edge aviation security screening equipment. We offer great benefits, a 9/80 work schedule and career advancement. To learn more about our culture, mission and vision please visit <a href="http://www.analogic.com" target="_blank">www.analogic.com</a>
Essential Duties and Responsibilities: 
<ul>
<li>Creates and successfully executes unbiased run plans for the collection of bag images on both checkpoint and checked baggage systems. This will include working with explosives, explosive simulants, prohibited items, and creating Stream of Commerce (SOC) images.</li>
<li>Supports data collection and test activities at customer sites including reporting of progress/results, coordination with the Manager, Data Collection and Analysis and algorithm staff to ensure collected data meets the objectives and quality standards.</li>
<li>Uses software tools to label and “truth” images and their contents to support developments of the algorithm team. In addition, the candidate will be asked to review work by other labelers in the organization for accuracy.</li>
<li>Uses OS and software tools for tasks such as copying, converting, and archiving data to varied file formats using tools in Linux or emulator software.</li>
<li>Reports software bugs and other anomalies in tracking systems such as JIRA.</li>
<li>Researches, Maintains, utilizes, and expands an inventory of test items and prohibited items as needed for internal and external customer efforts. Works with the team to specify required test and evaluation articles to support data collection and system validation efforts</li>
</ul>
Education, Work Experience, Skills and Competencies Requirements:
<ul>
<li>BS/BA in Physics, Data Science, Chemistry or similar accredited education and/or experience</li>
<li>Currently hold or eligible to obtain a US Government Secret Clearance (must be a US citizen).</li>
<li>Experience with MSOffice tools such as Teams, Excel, Word and Project. Experience using Linux and Linux database software strongly preferred.</li>
<li>Experience in the aviation security industry preferred.</li>
<li>4-8 years of experience working in an engineering team environment. Ability to effectively lead small teams in execution of time-sensitive tasks in a regulated environment. </li>
<li>Up to 20% travel may be required to regulator sites, airports and other potential sites for data collections and other activities.</li>
</ul>
What We Offer:We appreciate that our employees work diligently to contribute to our success as an organization. We also recognize the importance of work-life balance and therefore developed a competitive total rewards package including programs that offer employees flexibility to balance their work and life including:
<ul>
<li>9/80 work schedule – enjoy every other Friday off!</li>
<li>Flexible Vacation – employees can take time off as is reasonably needed</li>
<li>Comprehensive benefits including medical, dental, vision, life insurance and disability plans.</li>
<li>HRA (for PPO plan participants) /HSA (Health Savings Account for high deductible plan participants) contribution</li>
<li>401K with company match and immediate vesting</li>
<li>Continuous Education Assistance</li>
<li>Supportive culture that values innovation, collaboration, and excellence</li>
</ul>
To learn more about our culture please visit: <a href="https://www.analogic.com/careers/" target="_blank">https://www.analogic.com/careers/</a>
Follow us on LinkedIn: <a href="https://www.linkedin.com/company/analogic/" target="_blank">https://www.linkedin.com/company/analogic/</a>

Data Collection Engineer

<h3>Job Description</h3>
Job Description
About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger.&nbsp;For more information, visit&nbsp;<a href="http://www.mmsholdings.com&nbsp;or" target="_blank">www.mmsholdings.com&nbsp;or</a> follow MMS on&nbsp;LinkedIn.
Responsibilities:&nbsp;
<ul>
<li>Create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.</li>
<li>Develop phase 1-4 SAPs and make significant contributions to iSAPs. Create SAP TLFs shells for all phases and studies.</li>
<li>Review ADAM and TLFs; work with client and programmers to resolve comments.</li>
<li>Strong programming and logic skills (working knowledge of SAS)</li>
<li>Ability to apply drug development knowledge during production of high quality statistical analyses.</li>
<li>Perform sample size calculations for a variety of scenarios and study designs.</li>
<li>Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor.</li>
<li>Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas.&nbsp;</li>
<li>Understand the various tools that we work with</li>
<li>High level knowledge of drug development as it pertains to biostatistics.</li>
<li>Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.</li>
<li>Review the statistical section of a Sponsor’s protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study. Create the statistical section of the Sponsor’s protocol with minimal support</li>
<li>High proficiency with MS Office applications</li>
<li>Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation.</li>
<li>Provide ICH guideline based input as applicable to statistics.</li>
<li>Prepare and review statistical methods and results sections for the CSR with minimal support in collaboration with in-house medical writers.</li>
</ul>
Requirements:
<ul>
<li>Experience in immunogenicity and serotype vaccine studies preferred &nbsp;</li>
<li>Experience in pediatric studies preferred</li>
<li>College graduate in Biostatistics, Statistics, or Mathematics discipline or related field, masters or PhD preferred, or many years of related experience required.</li>
<li>Minimum of 7 years’ experience in Biostatistics or similar field required.</li>
<li>Expert knowledge of scientific principles and concepts.&nbsp;</li>
<li>Has high level knowledge of drug development as it pertains to biostatistics; has the ability to apply drug development knowledge during production of high quality statistical analyses.</li>
<li>Strong SAS programming, SAS base, SAS macro experience.</li>
<li>Thorough knowledge and understanding of clinical data preferred.</li>
<li>Strong experience with data and production of TLGs.</li>
<li>Excellent scientific writing skills.</li>
<li>Strong resource for biostatistics; willing to guide others in a variety of biostatistical techniques.</li>
<li>Proficiency with MS Office applications.</li>
<li>Hands-on experience with clinical trial and pharmaceutical development preferred.</li>
<li>Good communication skills and willingness to work with others to clearly understand needs and solve problems.</li>
<li>Excellent problem-solving skills.</li>
<li>Good organizational and communication skills.</li>
<li>Familiarity with 21 CFR Part 11, FDA, and GCP requirements.</li>
<li>Basic understanding of CROs and scientific &amp; clinical data/terminology, &amp; the drug development process.</li>
</ul>
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PpEUDGG7w9

Senior Biostatistician - Remote

<h3>Job Description</h3>
Job Description
Help redefine how the DoD makes multi-billion-dollar force-design decisions. In this role, you'll fuse physics-driven simulation, interactive computing, and verified AI code-generation to create next-generation wargaming platforms. We’re seeking an experienced software developer who can own key parts of a larger extensible, cloud-distributed simulation environment, and inspire a small, high-conviction team by leading from the front.
What you’ll do
<ul>
<li>Design &amp; implement a scalable, interactive physics simulation that runs seamlessly in cloud and on-prem clusters.</li>
<li>Own core functionality in modern C++ from multi-threaded performance tuning to continuous integration.</li>
<li>Collaborate with product &amp; AI teams to embed verified, AI-generated algorithms directly into a developer SDK for extending the platform.</li>
<li>Prototype quickly, iterate faster: deliver usable capability to government end-users in weeks, not months.</li>
<li>Set the engineering bar—write clean code, document rigorously, and mentor teammates through code reviews and pair programming.</li>
</ul>
Why Code Metal?
<ul>
<li>Mission with impact: your work shapes the digital battlefield models that influence real-world acquisition.</li>
<li>Velocity: small teams, rapid iteration cycles, and the mandate to ship.</li>
<li>Ownership: no passengers, everyone pushes code that hits production.</li>
</ul>
Requirements
Must-have credentials
<ul>
<li>Bachelor's degree (or equivalent experience) in applied math, scientific computing, physics, or a related field.</li>
<li>Proven expertise in multi-threaded C++ for high-performance applications.</li>
<li>Hands-on experience with large-scale, physics-based simulations.</li>
<li>Active Secret clearance or eligibility to obtain one. </li>
</ul>
Bonus points
<ul>
<li>Master’s (or equivalent experience) in applied math, scientific computing, physics, or similar.</li>
<li>GPU compute chops—OpenCL, CUDA, or both.</li>
<li>Prior work running physics simulations in distributed cloud environments.</li>
<li>TS/SCI clearance.</li>
</ul>
Benefits
<ul>
<li>Health care plan with 100% premium coverage, including medical, dental, and vision.</li>
<li>401k with 5% matching.</li>
<li>Paid Time Off (Uncapped Vacation, plus Sick &amp; Public Holidays).</li>
<li>Flexible hybrid work arrangement.</li>
<li>Relocation assistance for qualifying employees.</li>
</ul>

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