Science Salary in Cary, NC

Project Manager - Staff Augmentation for Compli LLCCompli LLC provides project management services for the construction of critical environments which are common in the pharmaceutical, biotech, mission critical and other regulated industries. This position will focus on our client•s mission critical business which consists of the design/construction of server farms and data centers. The ideal candidate will be relationship focused, both with internal and external clients. Strong problem solving and negotiation skills will be key areas needed for success.Responsibilities: Willingness and ability to lead a design-build or CM@Risk team and run a project or project(s) for a given client from bidding/ buyout phase through completion and closeout phases and serve as the main point of contact for the client. Teach, coach, and mentor staff on best practices and procedures, client interactions, soft skills, etc. Interact with clients and design teams as needed to resolve issues and expedite the project. Assist with estimating department during preconstruction and during bidding phases. Review project estimates with operations team (field and office) to ensure completeness and accuracy. Perform quality control reviews of design documents and field reviews. Develop and manage project schedules. Establish project budgets and forecast budgets to project completion including financial oversight and management of the project•s budget. Manage project bidding and buyout • both negotiated and hard bid projects. Prepare/create subcontract scopes of work and initiating subcontracts. Enforce EHS requirements of the clients and Compli LLC. Provide subcontractor and vendor management from contracting to contract closeout. Requirements: Degree in Construction Science and/or Management and 5+ years of construction project management experience or 10+ years of project management and construction field management experience. Demonstrate a detailed understanding of project accounting. Demonstrate a strong fundamental knowledge of the construction project cycle. Partnership approach to working with superintendents, PM•s, architects, and engineers. MS Office Suite knowledge and excellent computer skills. Excellent listening, communication, and problem-solving skills. Demonstrate ability to be a team player. Must be self-motivated and have excellent time management skills. Preferred: Specific experience in mission critical facilities • data centers and telecommunications preferred.

Equal Employment Opportunity/M/F/disability/protected veteran statusAzzur GroupAzzur Lab is actively searching for a Senior Director of Lab services to serve as the site lead for our laboratory facility in Raleigh, NC. The ideal candidate will be a cross-functional leader capable of overseeing our Advanced Therapies and Microbiology teams. Core responsibilities of this role include overall site leadership, collaborating with sales and business development to win new business, attracting and retaining people, managing finances and operations, and contributing to the strategic direction of the site. Responsibilities:Responsible for the laboratory's delivery of high-quality science by providing subject matter expertise, overseeing technical execution, quality assurance, and providing hands-on support.Collaborating with Sales and Business Development to win and maintain positive relationships with new and existing clients.Supporting the attraction, hiring, development, and retention of skilled resources for the delivery of servicesManaging and maintaining revenue and profitability, as defined on an annual basis (i.e., the profit and loss (P&L))Contributing to planning the strategic direction for the lab, focusing on future business growthCollaborate with other regional offices or functional areas on shared clients and needs (such as multi-site companies/clients, GMP Library, and audits)Translate new and existing client needs into actionable value-added projects/results.Prepare capability presentations, proposals, and agreements for new and existing clients.Monitor and report the status of projects and key performance indicators as needed.Develop annual forecasts and track and report on progress quarterly.Develop business revenue and profitability projections and monitor/correct performance. Required Work Experience10+ years in regulated environment within the biotechnology, pharmaceutical, or cell and gene therapy (CGT) industries5 years of experience with gene and cell therapy test methodologies (PCR, Flow Cytometry, ELISA, Mycoplasma and cell-based assays)5+ years of experience in Plasmid Monitoring, vector integration, residuals, mycoplasma, in vitro assays for adventitious viruses, qPCR, PERT.5+ years working in laboratory testing within a life science organization.3+ years of experience in business management, planning, and financial oversight3+ years of experience in personnel management, including hiring, supervision, and evaluation.Demonstrated experience in performing established microbiological methods such as USP 797, 61, 62, sterility, endotoxin, TOC, and environmental monitoring.Experience with multi-color flow detection assays and cell-based potency assays for lot-release and characterization purposes. Preferred Work ExperienceProven and established healthcare life sciences (HLS) network in a designated regionExperience with sterile culture technique, cell preservation studies, and subsequent analytical assessment platforms for both drug substances and drug products.Experience with client-facing tech transfer process and internal and external analyst training. Required KnowledgeBusiness management experience across multiple business linesExperience in business development, profit and loss (P&L) management, and budgetingStrong understanding of FDA and cGMP regulations and documentation practicesKnowledge of GMP, GxP, ICH, and 21 CFR part 11 regulations relevant to a QC lab operation.Knowledge of the develop and qualification of various stability-indicating, cell-based, potency assays for both lot-release and product characterization of cell and gene therapy drug productsWell-versed in different analytical instruments such as flow cytometers, multi-mode plate readers, stemVision, MSD, ProteinSimple units, and use of 3rd party data analysis software Required EducationBS degree in Biology, Microbiology, Molecular Biology, or equivalent technical degree and/or industry experienceFulltime Employment with Azzur Can Offer YouFlexible PTOTraining and Development Opportunities401(k) matchBonus EligibilityMedical BenefitsPaid HolidaysCompany provided laptop About the Azzur LabFounded in 2012, Azzur Labs is a contract laboratory that serves the pharmaceutical, medical device and biotechnology industries. We believe that the world of research is always on the brink of amazing discoveries and advances that will allow us to live healthier and happier lives. Our goal is to help these companies move from the drug discovery phase to delivery by supporting their microbiological and analytical testing and ensuring regulatory compliance.From Discovery to DeliveryTM, Azzur Group provides the life science community full life-cycle solutions for all their GxP needs. From Azzur Cleanrooms on DemandTM facilities, to our labs, training centers and consulting offices across the nation, Azzur Group helps organizations start, scale, and sustain their growing enterprises. With nearly four decades of service to the life science community, we have become a trusted partner to the world’s leading pharmaceutical, biotechnology, medical device, and healthcare companies, as well as their supply chain. Azzur Group provides clients with the consulting, facility solutions, engineering, validation, IT, technical, training, and laboratory services and solutions they need to remain innovative and competitive. #LI-PK Azzur Lab is actively searching for a Senior Director of Lab services to serve as the site lead for our laboratory facility in Raleigh, NC. The ideal candidate will be a cross-functional leader capable of overseeing our Advanced Therapies and Microbiology teams.PI239121967

Equal Employment Opportunity/M/F/disability/protected veteran statusAzzur GroupAzzur Lab is seeking a meticulous and detail-oriented QC Microbiologist to join our team. The ideal candidate will have a strong background in microbiology and proficiency in various quality control (QC) techniques, including testing sterility, bioburden, environmental monitoring (EM), qualification validation, investigation CAPA, and adherence to SOPs. The candidate will play a crucial role in ensuring the quality and safety of our products through rigorous testing, analysis, and reporting.Responsibilities:Perform routine microbiological testing, including sterility testing, bioburden determination, and EM monitoring.Execute qualification and validation studies for equipment, processes, and methods according to regulatory requirements.Investigate and implement corrective and preventive actions (CAPA) to address deviations and ensure continuous improvement in QC processes.Maintain and update QC documentation, including SOPs, method reports, and validation protocols.Collaborate with cross-functional teams to troubleshoot issues, identify root causes of deviations, and implement effective solutions.Participate in internal and external audits, providing necessary support and documentation as required.Maintain a clean and organized laboratory environment, ensuring safety guidelines and regulations compliance.Stay informed about industry trends, regulatory changes, and best practices in microbiological QC testing.Train new employees on QC procedures, techniques, and safety protocols.Contribute to developing and optimizing QC methods and processes to enhance efficiency and accuracy.Qualifications:Bachelor’s degree in biology or related field.6-8 years of experience in a QC microbiology role in pharmaceutical, biotechnology, or related industries.Proficiency in aseptic techniques, microbial identification, and microbial enumeration methods.Demonstrated experience in performing USP and ISO microbiological methods such as USP 797, 61, 62, 71, 85, and ISO 14698Strong understanding of regulatory requirements (e.g., FDA, EMA) and industry standards related to microbiological QC testing.Experience with validation and qualification processes, including writing protocols and reports.Excellent analytical and problem-solving skills, with a keen attention to detail.Ability to work independently and collaboratively in a fast-paced, dynamic environment.Effective communication skills, with the ability to convey technical information clearly and concisely.Prior experience with electronic documentation systems and QC software is preferred.Required Education:Bachelor of Science or Bachelor of Arts in the field of the life sciences.Required Work Experience: 6 years’ experience in Microbiology Lab. 1-2 years of QC activities, including CAPAEnvironmental monitoring experienceRequired Knowledge:Universal Blood and Body Fluid PrecautionsCommon laboratory equipment, methods, and protocolsFulltime Employment with Azzur can offer you: Flexible PTOTraining and Development Opportunities401(k) matchBonus EligibilityMedical BenefitsPaid HolidaysCompany provided laptopWho we are: Azzur Group is dedicated to providing clients with efficient, innovative quality and compliance solutions from Discovery to Delivery. With more than 500 industry partners, including 80% of the top pharma/biotech manufacturers in the U.S., Azzur Group provides carefully calibrated and efficiently executed project management, process engineering, and compliance services. As one of the fastest-growing private companies in America, Azzur Group provides clients with consulting, facility solutions, engineering, validation, IT, technical, training, COD, laboratory services, and solutions they need to remain innovative and competitive. #LI-PK Azzur Lab is seeking a meticulous and detail-oriented QC Microbiologist to join our team. The ideal candidate will have a strong background in microbiology and proficiency in various quality control (QC) techniques, including testing sterility, bioburden, environmental monitoring (EM), qualification validation, investigation CAPA, and adherence to SOPs. The candidate will play a crucial role in ensuring the quality and safety of our products through rigorous testing, analysis, and reporting.PI239121991

Reliability ConsultantCompli LLC is a full-service regulatory compliance consulting services company specializing in pharma and biotech as well as food and beverage, chemical, and discrete manufacturing industries. We are seeking an experienced Reliability Consultant to join our growing Asset Management and Reliability (AMR) Services team. The successful candidate will assist our clients across the United States in providing innovative solutions. This position will be responsible for delivering technical Maintenance, Engineering and Reliability expertise across multiple projects in a professional and timely manner.Responsibilities: Support and work alongside Senior Consultants through all phases of delivery including discovery, information and data gathering and analysis, best practices gap identification, findings, recommendations, and project improvement plan development. Provide the technical assistance needed to support on-site maintenance activities. Adhere to delivering technically sound and fundamentally consistent work with established company intellectual property, processes, forms, and templates. Develop and maintain trusted relationships with client and industry partners at all levels of the organization. Leverage professional network to generate new opportunities through quality delivery and technical excellence. Establish credibility through thought leadership (technical papers, industry publications, digital media, etc.) and participation in industry associations, conferences, etc. Support efforts to increase the firm's market share for consulting services in the chosen area(s) of focus by identifying additional projects and clients. Periodically develop and deliver training courses to our clients in the fields of your areas of expertise. All other duties as assigned. Required Qualifications: Possess an in-depth understanding of industry best practices in a minimum of five of the following disciplines: M&R Best Practices Gap Assessment and Improvement Plan Development Computerized Maintenance Management Systems (CMMS) review Asset Criticality Ranking (ACR) education and facilitation Work Management/Process Workflow review and development Preventive Maintenance (PM) program review and optimization Job Plan and Work Instruction writing Predictive Maintenance (PdM)/Condition Monitoring program implementation Failure Modes and Effects Analysis (FMEA) development Reliability Centered Maintenance (RCM) education and facilitation Materials Management (MRO) program review and optimization Maintenance Training program review and optimization/implementation Maintenance Metrics and Scorecards Total Productive Maintenance (TPM)/Operator Care review and enhancement Shutdown Management program review and improvement Change Management practices Ability to play a key role in the delivery of a M&R solution utilizing our tools, systems and methodologies. Ability to communicate with client leadership and stakeholders ensuring they understand and recognize the value being created by the M&R project. Possess a minimum of five years related-work experience. Demonstrate strong communication skills • written, verbal and presentation skills. Utilize good analytical and critical thinking skills. Must be thorough and detail oriented. Is a good team-player with strong facilitation skills. Possesses excellent organizational and time management skills. Has a good work ethic and treats documents with confidentiality. Proficiency in all MS Office software and spreadsheet applications. Ability to learn quickly and work under pressure in a fast-paced environment. All candidates must be legally eligible to work in the United States. Must be willing to travel up to 90% of their worktime regionally in the Midwest. Preferred Qualifications: Bachelor's degree in engineering, computer science, business, or related field from an accredited curriculum. Industry certifications such as those listed next would be considered a plus: CMRP, CMRT, CRL, LM1, LM2, LME, PMP, or RCM . M&R Consulting experience preferred. Minimum of three years of Pharmaceutical/ Bio-Tech or Food and Beverage, Chemical or discrete Manufacturing industry experience. Proficient in the use of planning/scheduling software such as Maximo, Upkeep, etc. Past and current participation in industry associations or technical groups.

We're Hiring!Commercial Data Analyst NAAt Envu, we partner with our customers to design world-class, forward-thinking innovations that protect and enhance the health of environments around the world. We offer dedicated services in: Professional Pest Management, Forestry, Ornamentals, Golf, Industrial Vegetation Management, Lawn & Landscape, Mosquito Management, and Range & Pasture.Envu brings together diverse points of view to look beyond chemistry and dare to explore new paths forward. Guided by our inclusive culture, we embrace change and flexibility, tackling our customers' toughest challenges proactively, passionately and with an entrepreneurial spirit.We pursue our ambitions collaboratively because we know that a unified and empowered team is an unstoppable force, allowing us to achieve our vision of healthy environments for everyone, everywhere. Join Us.FUNCTION: Commercial Americas(CA)LOCATION: Cary North CarolinaTYPE: PermanentGET TO KNOW YOUR AREA: This position will contribute to the strategy and lead execution of commercial excellence efforts for NA, improving sales analytics via power bi to support the go-to market, fact-based approach we are seeking. This role also will be a critical driver of the sales analytics around goals, progress to objectives, and analytics for customer feedback. This position will provide support across all businesses, with key focus around channel segmentation/strategy, account planning, sales analytics around pricing and program effectiveness, sales training, and customer-facing execution, in collaboration with the business heads for development of sales reporting tools, and timely updates on key sales metrics, as well as the sales incentive plans.Identify in collaboration with the businesses regional execution and identification of cross-business upskilling andintegration of best practices, including standardization and KPIs. Lead strong field adoption of virtual/digital tools, and efforts to strengthen digital mindset.This position is core to ES's ability to deliver business commitments, including sales, EBITDA, pricing and program excellence, and OPEX mgmt.YOUR MISSION WILL BE TO: Contribute to ES NA commercial excellence initiatives, together with Commercial excellence lead and business leaders to build sales excellence capacity/capabilities, develop and execute channel/customer segmentation strategies, KAM planning, and go-to market approach, working in strong collaboration with business and customer engagement team, to achieve business objectives.Lead development and execution of Power BI reports to support the main objectives of the sales organization, including clarity of established goals and KPIs to track progress.Lead development of valuable and timely sales tools to help sales organization steer the business, track progress, to success, as well as provide an early warning system to business challenges.Develop tools and processes to ensure pricing excellence and improve program effectivenessSupport efforts to Strengthen Account Planning through tools to help Customer/Account Needs Assessment, Interaction Management, and Account Sales and Resource PlanningDrive sales performance by determining, tracking, and measuring field force KPIsTrack progress of go-to market pricing strategies, and help develop potential improvements to go-to market (agency/title transfer) models using Power BI.Provide the business with tools to facilitate a strengthened institutional knowledge of key customers, products, pricing, and competitive activities in all segments, and to track the same.Engage and align commercial organization, in collaboration with business leads, in digital strategies and new business models.Global impact and contribution as member of the global Customer Excellence Team.ARE YOU READY FOR THE ROLE?Main requirements: POWER BI Dashboards and Reporting Experience- min 2 yearsBBS/BA degree in business, analytics, or related field.Strong analytical, financial, and strategic skillsIncumbent requires 6 years of applicable exp.Key traits are customer focus, entrepreneurial mindset, results orientation, collaborative skills, time management, and negotiation skills.Demonstrated problem solving skills necessary to deal with volatile, rapidly changing market conditions.Strong Digital mindset and openness to experimentation.Strong interpersonal and collaborative skillsExcellent oral and written communicationsEnvironmental Science U.S. LLC is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.By applying for this position, you agree that your personal data are going to be processed and recorded by Envu for recruitment purposes only. For candidates who are not selected for this position, personal data will be kept for a period of two years and then permanently deleted.We will soon be in touch to let you know the next steps to be taken!

Location: Cary, NCSalary: $35.00 USD Hourly - $45.00 USD HourlyDescription: Title- Information Security Analyst - I Location- Temple Terrace, FL; Cary, NC; Ashburn, VA (Remote) Duration- Long-term contractJOB DESCRIPTION: LOCATIONS: Temple Terrace, FL; Cary, NC; Ashburn, VA REMOTE MODEL: 4pm-12am EST shift and/or 12am-8am EST shift The Tier-1 Security Analyst represents the entry point into the Security Operations Center (SOC). The SOC Security Analyst will perform basic security monitoring, handle common issue types, and perform basic incident response activities. The duties of the SOC Security Analyst (Tier 1) include the following: • Provide "eyes on glass" real-time security monitoring in a 24x7 environment by monitoring security infrastructure and security alarm devices for Indicators of Compromise utilizing SIEM and cybersecurity tools; • Performing level 1 assessment of incoming alerts (assessing the priority of the alert, determining the severity of the alert concerning the customer environment, correlating additional details) and coordinating with Senior Analysts for high-priority incidents, if necessary; • Provide basic security event detection and initial triage of security events, opening tickets in designated ticketing systems within SLO and/or SLA guidelines; • Performing administrative routines of SOC like evaluating reports and SIEM dashboards, reviewing ticket escalations ; • Incoming call handling from and initiating trouble tickets, if applicable; • Provide health and availability analysis, opening tickets in designated ticketing systems within SLO and/or SLA guidelines; • Follow documented escalation procedures; • Identify recurring incidents for problem management purposes; • Coordinate with Senior Analysts for high-priority incidents.Required Skills & Expertise: • Associate degree in Computer Science, Information Security, or a similar discipline • Strong documentation and communication skills • Exceptional problem-solving skills • Proactive in engaging with customers, client executives, and client management teams • Basic knowledge of network technologies • Knowledge of Transmission Control Protocol/Internet Protocol (TCP/IP), RCF 1918, and common attacks against TCP/IP protocol • Knowledge of Microsoft Windows and Server Operating Systems • Basic understanding of threat landscape and indicators of compromise • At least 1-3 years Security related experience • Clear and concise written and oral English Desired Skills & Experience: • Bachelor or higher degree in Computer Science, Information Security, or similar discipline • Information Technology security-related certifications like CompTIA A+, Network+, Security+, Linux, Cisco CCNA, Microsoft Certified Azure Fundamentals, AWS Cloud Practitioner or SANS GSEC • Understanding of command line scripting and implementation (i.e. Python, PowerShell, Bash Shell) • Ability to write new content/searches/scripts (e.g., Splunk dashboards, Splunk ES alerts, QRadar, RSA Netwitness, SumoLogic, Sentinel, Chronicle, SOAR, etc.) • Experience with tools such as Active Directory, Cisco IOS, MS Server, AMP, Splunk ES, SNORT, Yara, IronPort, Firepower, SOAR, etc. • Strong understanding of networking (TCP Flags, TCP Handshake, IP addressing, Firewalls, Proxy, IDS, IPS) • Ability to perform NetFlow / packet capture (PCAP) analysis • Experience with basic cyber threat hunting Contact: [email protected] job and many more are available through The Judge Group. Find us on the web at www.judge.com

We're Hiring! Senior Regulatory ManagerAt Envu, we partner with our customers to design world-class, forward-thinking innovations that protect and enhance the health of environments around the world. We offer dedicated services in: Professional Pest Management, Forestry, Ornamentals, Golf, Industrial Vegetation Management, Lawn & Landscape, Mosquito Management, and Range & Pasture. Envu brings together diverse points of view to look beyond chemistry and dare to explore new paths forward. Guided by our inclusive culture, we embrace change and flexibility, tackling our customers' toughest challenges proactively, passionately and with an entrepreneurial spirit. We pursue our ambitions collaboratively because we know that a unified and empowered team is an unstoppable force, allowing us to achieve our vision of healthy environments for everyone, everywhere. Join Us. FUNCTION: Global InnovationLOCATION: Cary, North Carolina - Hybrid and Remote.JOB TYPE: Permanent GET TO KNOW YOUR AREA: • Develop and implement regulatory strategies to obtain and maintain products registration in countries of responsibility• Convey critical knowledge of assigned products/portfolio, current pesticide regulations to company management to alleviate or reduce regulatory impacts or costs for the countries and portfolio assignedYOUR MISSION WILL BE TO: At country level manage the regulatory aspects of registered products and facilitating favorable regulatory outcomes by taking a leadership role in formulating and implementing registration strategies and/or addressing product-specific issues raised by regulatory authorities.Actively engage with Marketing teams to achieve desired business objectives.Provide specific regulatory expertise and lead the preparation of country regulatory dossiers with external consultants.Act as Regulatory Affairs liaison with regulatory authorities and/or 3rd party companies for registration dossiers and defense strategies in the assigned countryRepresent the company on Industry activities of strategic importance with respect to country regulatory trends and regulations.Provide early warning to business and alerting on local regulatory trendsAnticipate future developments/changes and develop appropriate regulatory strategies for the assigned products.ARE YOU READY FOR THE ROLE? Main requirements: Degree preferred in health, physical, natural sciences or agricultureUndergraduate plus 8+ years of experience, MS plus 6+ years of experience or PhD plus 2+ years of experienceHas very broad knowledge of pesticide regulations and requirements;Ability to work in a multi-functional environmentAbility to manage complex situations and good problem-solving skillsStrong communication skills (verbal and written)Detail orientedFluent in English, both written and spoken. Additional languages appreciatedEnvironmental Science U.S. LLC is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. By applying for this position, you agree that your personal data are going to be processed and recorded by Envu for recruitment purposes only. For candidates who are not selected for this position, personal data will be kept for a period of two years and then permanently deleted. We will soon be in touch to let you know the next steps to be taken!

SENIOR MECHANICAL ENGINEERCary, NCDescription:Precis Engineering + Architecture (Precis) (www.precisengineering.com) offers comprehensive design services to our clients in the pharmaceutical, biotechnology, higher education, industrial, commercial, critical utility, and healthcare markets. Together, we design and create important buildings, facilities, and environments that improve and save lives.Precis is recognized for our design expertise and proficiency in providing strategically sensitive and technically complex engineering and architectural services. The Mechanical Department is regularly engaged in a broad spectrum of projects that require creative solutions to challenging building systems and utility issues. This offers an excellent environment for employees to rapidly expand their knowledge and understanding of the key role engineering plays in the success of building renovations and new construction projects.Precis is currently seeking a Senior Mechanical Engineer for our Ambler, PA office. This individual must have a background in Mechanical/HVAC Engineering and a basic understanding of engineering practice within highly regulated industries. We are looking for a resourceful and goal-oriented individual who desires challenging work in a dynamic environment.Responsibilities:Provide mechanical engineering services to design and oversee the design of complete mechanical/HVAC systems supporting facility expansions, renovations, remediation, and new construction projects from concept through detailed design and construction, including equipment, ductwork, piping, building automation, and related building components.Receive supervision and guidance relating to overall objectives, critical issues, new concepts, and policy matters. Receive direction on unusual conditions and developments.Independently apply extensive and diversified knowledge and use advanced techniques in the modification or extension of standard procedures and design criteria to complete assignments, including the development of details, control sequences, and specifications. Assist upper-level management to develop new techniques and improve standards and processes.Supervise all staff necessary to complete project assignments in alignment the defined scopes, schedules, and budgets. Provide thorough review of project documents for conformity with project assignments and quality assurance.Interact with client representatives, equipment vendors, contractors, project managers, and other project team members to coordinate deliverables and breadth of the mechanical design.Periodically visit project sites to survey existing conditions and observe construction activities.Requirements:Bachelor of Science degree in Mechanical or Architectural EngineeringMinimum 8 years industry engineering experienceStrong computer literacy with advanced knowledge and use of Excel, Word, Outlook, and TeamsAdvanced written & verbal communication skillsAdvanced knowledge of applicable codes and industry standards and guidelinesExperience with critical environments and related building systemsProfessional Engineer license

OverviewWe are seeking a full-time DevOps Senior Software Engineer to join the Core Technology Team at our location in Cary, NC or Olathe, KS. This DevOps software engineer will help build and maintain the next generation of Garmin's Continuous Integration / Continuous Delivery (CI/CD) system used to build embedded software for Garmin's award-winning products. Essential FunctionsAutomate routine tasks whenever possibleSupport software engineering applications installations and upgradesCollaborate and add value through participation in peer code reviews, providing comments and suggestionsEvaluate, integrate, administer and support new applicationsSupport monitoring and testing of software engineering applicationsSupport application server capacity planning, backups and other server-based activitiesProvide reliable solutions to a variety of problems using sound problem solving techniquesPerform technical root cause analysis and outlines corrective action for given problemsServe as a mentor to less experienced software engineers (Software Engineer 1/2)Estimate level of effort, evaluate new options of similar technology, offer suggestions to improve processes, and provide comments on some electrical design aspectsApply Garmin's Mission Statement and Quality Policy and enthusiastically exhibit a desire to see Garmin succeedBasic QualificationsQualified candidates will possess a Bachelor of Science Degree in Computer Science, Electrical Engineering, Computer Engineering, Aerospace Engineering, Math or Physics OR a technical field (such as CIS or IT) from a four-year college or university AND a minimum of 5 years relevant experience OR an equivalent combination of education and relevant experience with a 3.0 cumulative GPA or higher. Other requirements include:Must possess a minimum 1 year of work experience automating tools and/or testsExperience with Python or a shell scripting language (ie. Bash, sh, ksh, zsh)Administrative experience with Jenkins automation serverUser level experience with container / orchestrator technology like Docker, Kubernetes, OpenShiftWorking knowledge of GIT or similar source code managerUser level experience with virtualization technologies like VMWare / VirtualBoxExperience with Cloud technology like OpenStack, Amazon AWS, Cloud FoundryAbility to work and collaborate across geographical and organizational barriersDesired QualificationsMotivation for future Leadership opportunities Experience administering Zuul CIExperience with IT Automation tools such as Ansible or TerraformExperience with embedded Software DevelopmentExperience administering in Windows, Linux and Mac OS'sExperience developing in Java, Groovy, C++ or C#Experience working with the entire SDLCExperience with ELK, Kibana, Grafana or other analytic technologyGarmin International is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, veteran's status, age or disability.This position is eligible for Garmin's benefit program. Details can be found here: Garmin Benefits

Regulatory Affairs Specialist The Regulatory Affairs Specialist ensures product safety and legal compliance regarding global chemical regulations in product development across the supply chain. Responsibilities include providing product stewardship support regarding regulatory issues for the company's products and market/applications, monitoring and analyzing regulatory trends and positions in the industry, ensuring the efficient completion of stewardship-related product introduction deliverables, and supporting sustainable development alternatives and concepts for the company's product lines. Responsibilities and Duties: Processing customer inquiries regarding regulatory affairs and product safety. Conflict resolutions. Creation of product safety requests. Review of raw material. Preparation of declarations of conformity Product formulary disclosures Approval process REACh SVHC/banned substances SCIP TSCA Other country chemical registration status ROHS/WEE CONEG US California Prop 65 Conflict Minerals PFOA/PFOS CMR substances Assist with Drug master file filing and updates FDA Food Contact Medical Devices Pharma USP General Chapters < 232> Elemental Impurities-Limits and < 233> Elemental Impurities-Procedures. < 462> Residual solvents Nitosamines EU MDR - SVHC/ BfR-food contact Other food contact research as needed Metal catalysts Tin Platinum Rhodium Residual VOC Pesticides Paper US FSC/EU Timber rules Microplastics Others as legislation is passed Help with registration of compostable/biobased products. Training, email notification, and internet research on new or changed legal requirements. Maintenance of the database with supplier-specific information for the preparation of declarations of conformity. Communication with all Loparex sites. IMDS - Automotive - GADSL. Sampling products for shipping for migration analysis. Perform facility audits regarding regulatory compliance. Other duties as assigned. Qualifications and Skills: Bachelor's Degree in Chemistry or Environmental Science preferred, or equivalent combination of education and experience. 3-5 years of regulatory affairs experience required. Knowledge of silicone/polymer chemistry. Knowledge of engineered films, siliconized papers, and films highly preferred. Ability to work in a cross-functional team. Understanding of the product and market portfolio with respect to how they impact health, safety, and environmental issues. Ability to understand technical information and science as it applies to products, and the ability to translate into a business context. Experience in dealing with internal and external customers. Fluent in English, other languages a plus. Excellent organizational skills. Ability to work accurately and quickly under operational timeframes. Ability to communicate with management and employees efficiently and professionally. Benefits: Medical, Dental, and Vision Insurance Telehealth Health savings account with generous annual employer contribution Fitness reimbursement program Development and career growth opportunities Competitive 401(k) matching program We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other category protected by applicable law.