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Substation Civil/Structural Engineer On-site role near Spring Valley, NY Salary Range: $89,000 – $106,000 About the Role We’re looking for a Substation Civil/Structural Engineer to play a key role in the design and development of critical electrical infrastructure projects. This role offers the opportunity to lead detailed engineering phases, mentor junior staff, and contribute technical expertise to projects that strengthen and modernize the power grid. What You’ll Do Lead civil/structural design efforts for substations, including planning, scheduling, and coordination with other disciplines. Apply advanced judgment and analysis to new designs and modifications of existing systems. Provide technical reviews and mentorship for junior engineers. Ensure compliance with quality standards, safety requirements, and project work plans. Recommend improvements to design processes, materials, and construction methods. Monitor progress against project schedules and budgets, ensuring timely delivery. What We’re Looking For Bachelor’s degree in Civil, Structural, or Electrical Engineering. Professional Engineer (PE) license required. Minimum 4 years of engineering experience within civil/structural or substation projects. Strong understanding of engineering principles with hands-on application in real-world projects. Proficiency in Revit, AutoCAD, MicroStation, mFAD, LPile, SACS, or related software. Familiarity with QA/QC standards and industry best practices. Effective communicator with leadership skills and the ability to collaborate across teams. Proficiency in Microsoft Office; involvement in professional engineering organizations is a plus. Why Join This is a chance to be part of projects that directly impact the future of power delivery—covering everything from traditional fossil fuels to renewable energy and modern intelligent protection systems. You’ll be joining a collaborative, forward-thinking environment where your expertise helps shape safe, efficient, and resilient infrastructure. #M1 Ref: #275-Eng Kansas City

Job Description Position Summary: : Freshline Produce LLC., a premium fresh fruit and vegetable processor based in Mahwah, NJ, is seeking a talented Quality Assurance Technician, for its 1st shift, to join its fast growing organization. This is perfect opportunity for a candidate looking to begin their QA career in the food industry. Responsibilities: • Incoming Raw Materials/ Inspection/ Inform QA Manager and Operations Manager if there are quality issues. Fill out Receiving Log, • Identify, label, date, and make a daily inventory list of all WIP products in the coolers, • Production Line Quality Checks including product quality, case quality, Tsunami checks, Metal detector check and room temperature checks, • Practice and enforce GMP regulations - (Hand washing, no jewelry, no gum), • Recognize and examine all inventory at all times, • Good communication, training and interpersonal skills, • Very detail oriented, • Strong problem solving skills, • Bi-lingual (English and Spanish) is preferred, • Experience in the food industry is a plus, • Effective organizational skill; Able to manage priorities and complexities, • Intermediate computer skills, • Proficiency with Microsoft Word, Excel and Outlook, • Strong multi-tasking skills

Job Description Electrical Commissioning Engineer - Montvale, NJ Our client is a Engineering Design and Commissioning Company that has a national footprint and specializes in MEP critical facilities design. They provide design, commissioning, consulting and management expertise in the Critical Facilities Space. They have a mindset to provide reliability, energy efficiency, sustainable design and LEED expertise when providing these consulting services for Enterprise, Colocation and Hyperscale Companies. This career-growth minded opportunity offers exciting projects with leading-edge technology and innovation as well as competitive salaries and benefits. Execute onsite commissioning plans, provide and gather specifications, and execute assignments in a multidisciplinary engineering Commissioning role for large facility projects. The commissioning experts adhere to a thorough quality management - QM /QA / QC process and procedures that validate and document our client's systems. Commissioning methodology covers a wide range of procedures to verify the integrity and performance of their customer's mission critical support infrastructure. Responsibilities: • Participate in daily commissioning activity meetings which services include:, • Equipment pre-start-up and start-up procedures; Development of standard operating procedures (SOP's) and Methods of Procedures (MOPs); Comprehensive Commissioning documentation, • Prepare commissioning test procedures and reports; Develop and maintain commissioning logs, equipment checklist, and other tools to track commissioning projects; Write comprehensive reports which include the following sections: recommendations for optimizing building operations, functional checklists, list of deficiencies, equipment operation and maintenance manuals, • Review design criteria, specifications, drawings, equipment submittals, and other documentation pertinent to commissioning, • Integrated system testing; Load Bank Testing; Compilation of all testing procedure results, • Develop and administer functional tests for various systems, such as: electrical distribution systems, UPS, standby generators, etc., • System Assembly; Commission plan preparation ; Follow company QC process and procedures, • Help lead and manage any external resources; Schedule and direct periodic commissioning meetings; Attend construction and coordination meetings if required for the project ; Interface with clients, contractors, equipment vendors and owners agents as needed; Execute project assignments; Interface with project contractors, vendors, and testing technicians; Interact with all facets of the company: engineering, design, etc., • 4-10+ years experience with Electrical Power Systems, • Bachelor's / Associates Degree as an Electrical Engineer a plus, • Experience commissioning enterprise data centers, colos, and hyperscale companies, • Willingness to travel, • A/E experience working in complex facilities or mission critical projects a big plus, • Previous Data Center / Mission Critical experience a must, • Excellent communication skills, both written and verbal (this role requires heavy amount of writing, documentation, and client interaction), • Electrical equipment testing experience in a Critical Facilities / facility environment, • Previous experience conducting Level 1-5 Commissioning, • Possess basic knowledge of systems design for various projects, • Previous Military experience a plus - Navy Nukes, Seabees, Maritime, etc., • Possess basic knowledge of systems design for various projects After applying, if you have further questions, you may call 973-895-5200 and ask for Iggy. You can also submit via our career portal and take a look at other Critical Facility openings we are working on at, If this job is not for you, feel free to forward this along. WE PAY FOR REFERRALS!! Company offers competitive salaries and benefits package including medical insurance, a 401(k) plan EOE/AA Employer M/F/D/V Pkaza LLC is a third-party employment firm. All fees assessed by Pkaza LLC will be paid by our employer that we represent and not by the candidate

Job Description Location: In person/ Hybrid – Montebello, NY Overview: We are looking for a seasoned Senior .NET Developer with full stack expertise to join our development team. The ideal candidate will have strong experience building scalable .NET applications, robust frontend skills (especially with Angular), and a solid track record delivering enterprise software solutions. Prior experience in healthcare projects is preferred but not required. Key Responsibilities: • Design, develop, and maintain full stack web applications using .NET (C#), Angular, and SQL Server., • Implement responsive and intuitive user interfaces using HTML, CSS, and JavaScript., • Develop and consume RESTful APIs and microservices, handling JSON and XML data formats., • Collaborate with product owners, designers, and QA engineers to deliver high-quality software., • Participate in code reviews, architecture discussions, and continuous improvement of development practices., • Troubleshoot, debug, and resolve software issues across the stack., • Follow SDLC best practices and maintain high standards for code quality and maintainability., • 6+ years of professional experience in .NET (C#) development., • 4+ years of frontend development experience using HTML, CSS, JavaScript, and Angular., • Proven experience in full stack software development projects using .NET technologies., • Strong understanding of software architecture, design patterns, and clean coding principles., • Proficiency in building and consuming RESTful APIs and microservices., • Solid grasp of the software development lifecycle (SDLC) and agile methodologies., • Familiarity with development tools such as Visual Studio, VS Code, and SQL Management Studio., • Experience using version control systems like Git., • Excellent analytical, debugging, and problem-solving skills., • Effective verbal and written communication skills, with the ability to work collaboratively in a team environment.

Job Description Position Summary The Entry-Level Associate, Quality Assurance supports the Quality Management System (QMS) and documentation processes at the Chestnut Ridge site. This role is designed for individuals beginning their career in pharmaceutical quality assurance and provides hands-on experience in maintaining compliance and supporting documentation workflows in a regulated environment. Roles and Responsibilities • Assist in organizing and maintaining QMS documentation including SOPs, CAPAs, deviations, and complaints., • Support the preparation and tracking of quality metrics and trending reports., • Help coordinate internal audits and document audit responses., • Participate in documenting product quality complaints and adverse event records., • Aid in digitizing logbooks and checklists using electronic systems., • Collaborate with cross-functional teams to ensure timely and accurate documentation updates., • Provide administrative support for change control processes and quality-related meetings., • Assist in preparing documentation for regulatory inspections and external audits., • Maintain document control systems and ensure timely review and archival of QA records., • Support training documentation and tracking for QA-related procedures., • Help with data entry and analysis for quality reports using basic statistical tools., • Monitor document lifecycle and ensure version control compliance., • Required Education: Bachelor’s degree in Pharmaceutical Sciences or a related field., • Preferred Education: Master’s degree is a plus., • Experience: 1–3 years in a pharmaceutical or regulated industry (internships or co-op experience acceptable)., • On-site role at Chestnut Ridge, NY., • Standard work hours: 8 AM to 5 PM., • No travel required.

Job Description Strides Pharma Inc. is seeking an experienced and detail-oriented Analytical Quality Assurance Supervisor to lead our AQA operations in Chestnut Ridge, NY. The AQA Supervisor will be responsible for overseeing the review and approval of analytical data, ensuring compliance with cGMP regulations, and supporting product release and regulatory submissions. This role will collaborate cross-functionally with the Quality Control, Regulatory Affairs, and Manufacturing departments to maintain high standards of product quality and integrity. Responsibilities • Manage all Analytical and Quality Control (QC) activities to ensure compliance with cGMP, FDA, EMA, and ICH guidelines., • Lead a team of data reviewers, ensuring accurate, complete, and timely review of raw data, analytical results, and laboratory documentation., • Supervise the Stability Program and Coordinator, including protocol approval, sample pull scheduling, data review, and reporting., • Ensure analytical data integrity through implementation and oversight of robust review processes and audit trails., • Collaborate with QC, QA, and R &D departments to support method validations, transfers, and investigations., • Review and approve analytical documentation such as CoAs, method validation/verification protocols and reports, and stability summaries., • Lead or support investigations into out-of-specification (OOS), out-of-trend (OOT), deviations, and laboratory incidents., • Support regulatory inspections and internal/external audits, providing documentation and subject matter expertise., • Drive continuous improvement initiatives in QA/QC processes and systems to ensure operational excellence and regulatory readiness., • Mentor, coach, and develop the AQA team to build a high-performing quality organization, • Coordinate workload sharing with other groups in QC and develop action plans to improve the working environment and for maximization of laboratory efficiency., • Prepare monthly report of the issues, work done, any employee related issues and conduct bi-weekly audits of the analyst’s notebooks., • Review/Approve SOP’s, procedures and monographs for the QC Group as needed., • Review and comment on the articles affecting QC in the USP Supplements and Pharmacopeial Forums., • Conduct periodic audits of the analyst notebooks and instrument logbooks to ensure compliance of cGMP’s., • Evaluate potential candidates for QA; performance evaluation of direct reports., • Coordinate data review for analytical tests, including but not limited to HPLC, UV-Vis, IR, and Raw Material, Finished Product, Stability testing. Qualifications • Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related field (Master’s or Ph.D. preferred), • Minimum of 10 years of experience in pharmaceutical analytical quality assurance or quality control, • Proven leadership or supervisory experience in a GMP-regulated environment, • Experience with analytical instrumentation (HPLC, GC, UV, IR, etc.) and associated data review, • Demonstrated management and leadership experience with strong interpersonal and influencing skills., • Strong understanding of FDA regulations, cGMP, ICH guidelines, USP/EP compendia, • Knowledge of pharmaceutical manufacturing processes and laboratory practices, • Familiarity with regulatory submission requirements (ANDA, NDA, etc.), • Proficiency with laboratory software and documentation systems (e.g., Empower, LIMS, TrackWise), • Organizational Support - Follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values; benefits organization through outside activities; supports affirmative action and respects diversity., • Leadership - Exhibits confidence in self and others; inspires and motivates others to perform well; effectively influences actions and opinions of others; accepts feedback from others; gives appropriate recognition to others., • Supervising People - Includes staff in planning, decision-making, facilitating and process improvement; takes responsibility for subordinates' activities; is available to staff; provides regular performance feedback; develops subordinates' skills and encourages growth; solicits and applies customer feedback (internal and external); fosters quality focus in others; improves processes, products and services.; continually works to improve supervisory skills., • Quality - Demonstrates accuracy and thoroughness; looks for ways to improve and promote quality; applies feedback to improve performance; monitors own work to ensure quality., • Demonstrated flexibility in carrying out varied assignments in a high quality work environment., • Excellent written and oral communications skills with a strong emphasis on organizational capabilities., • Excellent analytical thinking and problem-solving skills, • Strong attention to detail with a commitment to quality and compliance, • Effective leadership, team management, and interpersonal communication, • Ability to prioritize and manage multiple tasks in a fast-paced environment, • Proficient in technical writing and reviewing complex data and reports Physical Requirements • Ability to sit or stand for extended periods, • Occasionally lift up to 25 pounds, • Use of personal protective equipment (PPE) as required in laboratory or production areas, • Ability to work in office, laboratory, and manufacturing settings as needed, • The work environment is representative of a group laboratory environment.

Job Description About the Role: We are seeking an experienced Technical Business Analyst (BA) to join our team, with a focus on Healthcare Workforce Management (WFM) solutions. In this role, you will serve as the bridge between business stakeholders, healthcare operations teams, and our product/engineering teams, translating complex business needs into clear, actionable technical requirements. Your work will directly impact how healthcare organizations manage labor costs, optimize scheduling, and ensure compliance. Key Responsibilities: • Gather, document, and analyze business and functional requirements related to workforce management in healthcare settings (e.g., scheduling, time & attendance, credentialing, labor compliance)., • Conduct discovery sessions and process mapping with healthcare stakeholders (e.g., Nursing Directors, HR, Operations)., • Translate business needs into detailed user stories, process flows, and acceptance criteria., • Collaborate closely with product managers, designers, and engineers to design scalable, user-friendly WFM solutions., • Assist in the evaluation and selection of third-party WFM integrations or build options., • Partner with QA teams to ensure test plans align with business expectations., • Identify gaps between current system capabilities and healthcare workforce regulatory requirements (e.g., PBJ reporting, overtime rules, union contracts)., • Analyze and validate data to support WFM optimizations and compliance reporting., • 4+ years experience as a Business Analyst, with at least 2+ years in healthcare or healthcare technology., • Strong understanding of Healthcare Workforce Management (e.g., staff scheduling, labor law compliance, PBJ, credential tracking)., • Experience working with SaaS-based HCM or WFM platforms (e.g., Kronos, Smartlinx, Empeon, Workday, etc.)., • Familiarity with healthcare staffing models (e.g., Skilled Nursing Facilities, Homecare, Acute Care)., • Excellent skills in process mapping (e.g., BPMN), requirements gathering, and documentation., • Strong technical acumen — comfortable discussing APIs, data models, and integration concepts with technical teams., • Proficient in Agile methodology (JIRA, Confluence) and writing user stories., • Exceptional communication and stakeholder management skills.

Job Description Job Summary With advanced and specialized packaging knowledge, oversees and manages the daily operation of a packaging line. Performs functions relating to the packaging of drug products consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP). This role supervises the day-to-day activities of the Operators and provides guidance on tasks that are being performed on the line. Often, this position is involved in the Operator interview process but are not decision makers in terms of hiring decisions, promotions, annual evaluations, etc. This role is recognized as a process expert, and is qualified as a certified trainer and provides training to less senior Operators. Proactively identifies and performs root cause analysis, in conjunction with other operators/technicians, makes recommendations, and aids in implementation. Responsible for the safe and efficient execution of job duties, while ensuring product compliance to established standards. Oversees and coordinates packaging lines for single location. May fill in for supervisor as necessary. Responsibilities Packaging Operations • Coordinates each Operator’s responsibilities during each shift., • Monitors the packaging process to ensure schedule is met within standards., • Conducts final audit of Batch Records, including SAP transactions, prior to going to Packaging BR Reconciler; Is qualified and capable of running all packaging equipment across the entire packaging department., • Conducts preliminary review of all daily Batch Production Record (BPR) for the line and logbook documentation to ensure detail and accuracy., • Accurately reviews BPR's steps for completeness and accuracy., • Request components, labels and inserts per the BPR., • Set up packaging machinery; accurately sets equipment programming according to BPR's and SOP's., • Conduct basic set ups, starts, operates, adjusts, troubleshoots and tears down packaging lines., • Conduct sampling: Collects samples from each batch and submits to QA for retained samples., • Conducts verification of line/equipment cleaning and documents per SOP., • Executes procedures used to clean pharmaceutical packaging equipment and facilities., • Captures and reports metrics; troubleshoots downtime in order to increase operational efficiency., • Lead or participate in Continuous Improvement projects., • Performs defect evaluations and initiates production event logs., • Identifies, reports, and suggests resolutions for processing related issues., • Communicates and coordinates change-overs and other equipment downtime issues to Reliability Technicians., • Is qualified as a certified trainer and provides training to less senior operators., • Contribute to safety audits., • Carries out processing/packaging activities safely, as required, on a daily basis., • Follows all safety and compliance procedures and participates in required training., • Adheres to all cGMP compliance/regulatory mandates and quality requirements., • Participate in safety teams, start-up discussions, incident debriefs, etc., • High school diploma or equivalent., • Thorough knowledge of cGMP regulations and processes., • Ability to oversee and manage the daily operation of a packaging line., • Qualified and capable of running all packaging equipment across the entire packaging department., • Ability to monitors processes to ensure schedule is met within standards., • Ability to conduct final audits of Batch Records, including SAP transactions, prior to going to Packaging BR Reconciler., • Certified Trainer of others., • Ability to analyze metrics and troubleshoot downtime in conjunction with other specialists., • Effectively interfaces with Quality and supervisor to inform of deviations or other line issues., • Demonstrates the ability to work in collaboration with others as a part of a team., • Ability to lead or participate in Continuous Improvement projects., • Good communication skills., • Good attention to detail in order to conduct final audits and reviews., • Ability to follow both verbal and written instructions including SOP’s and Batch Record documentation., • Ability to accurately and precisely record data and batch information., • Ability to work in both independent and team environments., • Must be able to stand for long periods of time (8 or 12 hour shifts), lift at least 35 pounds, climb ladders, wear a dust mask or respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE, including safety glasses, ear plugs, and safety shoes., • Dexterity - ability to quickly move your hand, your hand together with your arm, or your two hands to grasp, manipulate, or assemble objects., • Vision - ability to see details at close range (within a few feet of the observer)., • Multi-limb Coordination - ability to coordinate two or more limbs (for example, two arms, two legs, or one leg and one arm) while sitting or standing.

Job Description Summary: Test Data Management Specialist with min 7 years of IT experience in creating, managing, and validating test data for Member, Claims, and Finance domains within the healthcare insurance industry • Experience with any of the test data management (TDM) tools (e.g., Informatica TDM, IBM Optim, Databricks, or custom scripts)., • Proficiency in SQL, data profiling, and working with relational databases., • Strong understanding of healthcare insurance data models, claim lifecycle, enrollment, billing, and financial transactions., • Should have experience working in cloud environment, • Knowledge of HIPAA, PHI handling, and data masking techniques., • Design, generate, and maintain test data sets for Member, Claims, and Finance workflows in healthcare insurance systems., • Analyze business and system requirements to identify and prepare required test data conditions., • Build synthetic data and subset production data while ensuring HIPAA and data privacy compliance., • Collaborate with QA, developers, and business users to understand scenarios and ensure complete test coverage., • Automate test data creation processes using SQL, scripts, or test data tools.

Job Description About the Role: We are seeking a motivated and experienced Scrum Master / Project Manager to lead cross-functional teams in delivering high-quality software and driving projects to successful completion. This hybrid role combines Agile facilitation and project management expertise, ensuring alignment between business goals, team execution, and delivery timelines. Our development team works primarily with the following technology stack: C#, .NET, SQL, and Angular. Familiarity with these technologies is a plus, as it will help in understanding the context and flow of development work. Key Responsibilities: • Act as Scrum Master for one or more Agile teams, facilitating all standard ceremonies (Daily Standups, Sprint Planning, Reviews, Retrospectives)., • Serve as Project Manager for broader initiatives, overseeing timelines, risks, and stakeholder communication., • Remove impediments and support team collaboration to ensure high performance and continuous improvement., • Coordinate with Product Owners, Engineers, QA, Designers, and stakeholders to ensure clear requirements and deliverables., • Maintain Jira (or other Agile tools), ensuring transparency of backlog, sprint health, and project progress., • Track and report on key project metrics including velocity, burn-down, and delivery milestones., • Proactively identify risks and dependencies and develop mitigation plans., • 3–6 years of experience as a Scrum Master and/or Project Manager in a software development environment., • Strong understanding of Agile methodologies (Scrum, Kanban) and project management principles., • Proven track record of managing multiple projects and coordinating distributed teams., • Excellent communication, facilitation, and problem-solving skills., • Proficiency with project and collaboration tools such as Jira, Confluence, or similar., • Familiarity with development processes involving C#, .NET, SQL, and Angular is a strong advantage., • Certification such as Certified Scrum Master (CSM), PMI-ACP, or PMP is a plus., • Experience in Healthcare, HCM (Human Capital Management), or SaaS environments is a strong plus.

A recognized company in New Jersey is looking to add a new SAP BODS Consultant to their team. In this role, the SAP BODS Consultant will be responsible for maintaining the smooth operation of the SAP BODS system and developing and supporting data integration solutions. Responsibilities: • Provide round-the-clock Production support and manage user roles and permissions, • Create and manage data sources, • Perform backup and recovery of BODS repositories, • Implement performance tuning techniques, • Deploy code across Development, QA, and Production environments using central repositories, • Develop BODS workflows/dataflows/mapping, • Create models using calculation views and performance tuning, • Load delta records on source and target level CDC on type 1, type 2, and type 3 SCD., • Perform quality testing and beta testing of the applications that are delivered, • Manage Data Warehouse Project Deliverables for SAP BODS ETL SpecificationsQualifications:, • 5+ years of experience in Business Objects Data Services (Admin, workflows, Mapping, dataflows, Data integrator/Data Quality/Platform transformations, etc.), • Bachelor's degree in business (or Management), Computer Science, Engineering, or related discipline, or equivalent work experience, • Experience in Data warehousing., • Experience delivering complex data management engagements, including all phases of the project life cycle from scoping and planning, requirements gathering, design, development, testing, and go-live phases, • Proven experience in SAP HANA Modelling (calculation views), • Strong knowledge of Data Modeling and Star Schemas, • Working knowledge and experience with SQL language, • Proven experience working with a large Data Warehouse, • Proven experience connecting BODS with a REST/SOAP API, • Proven experience in extracting semi-structured data like JSON

Hi Everyone, Greetings !!!! Kindly go through the below mentioned Job Description and let me know your interest. Role: Salesforce Business Analyst Location: NYC, NY (Hybrid) Job Description: ● Analyze and document business needs from stakeholders, then translate them into functional and technical specifications ● Clearly articulate and document the acceptance criteria for the outlined tasks ● Act as a liaison between business stakeholders and the technical team, facilitating communication and ensuring alignment. ● In depth hands on experience using agile project management tools like Jira or similar ● Managing the backlog, write user stories and implement progress reports ● Facilitate solution design sessions with the technical team to plan the implementation of the business requirements to meet the acceptance criteria ● Act as a liaison between the QA / UAT and the technical team, while supporting the testing cycles, ensure solutions are thoroughly tested before moving the tasks through completion stages ● Develop training materials and deliver training sessions to support user adoption of new features ● Familiarity with the Salesforce platform and configuration is a plus

Job Description With demonstrated packaging knowledge and experience, performs moderate to advanced functions relating to the packaging of drug products consistent with established Current Good Manufacturing Practices (cGMP), customer requirements, and in conjunction with all Standard Operating Procedures (SOP). Is qualified in Filling or Labeling. Assists in troubleshooting process issues. Responsible for the safe and efficient execution of job duties, while ensuring product compliance to established standards. All incumbents are responsible for following applicable Division & Company policies and procedures. Responsibilities: • Competently operates pharmaceutical packaging machinery which may include stamp machines, tape machines, box machines, electronic scales, and other machinery., • Ensures that all equipment is running properly., • Executes processes such as: material handling, capping, outserts/med guides, in-process checks, packing, stacking, cartoning, etc., • Is qualified in Filling and/or Labeling., • May request components, labels and inserts per the BPR/MPR., • May set up packaging machinery; may accurately set equipment programming according to BPR's and SOP's., • Conducts basic sets up, starts, operates, adjusts, troubleshoots and tears down packaging lines., • Executes Batch Production Record (BPR) or Packaging Master Records (MPR) and logbook documentation with detail and accuracy., • Accurately reviews BPR's steps for completeness., • Accuracy conducts sampling: Collects samples from each batch and submits to QA for retained samples., • Demonstrates the ability to execute procedures and complete tasks in a compliant and safe manner, • Executes the procedures used to clean pharmaceutical packaging equipment and facilities., • Conducts Master Cleans or A & B type Cleans and Line Clearances, • Assists in troubleshooting process issues., • Identifies and reports processing related issues to Packaging Supervisor or designee and to Quality personnel, • Executes the required in-process product quality checks and documents accurately., • Demonstrates the ability to work in collaboration with others as a part of a team., • Stays current on SOPs and cGMPs., • May participate in training qualifier classes., • Participate in safety teams, start-up discussions, incident debriefs, etc., • Carries out processing/packaging activities safely, as required, on a daily basis., • Follows all safety and compliance procedures and participates in required training., • Adheres to all cGMP compliance/regulatory mandates and quality requirements., • Ensures compliance with SOPs, Policies and Procedures as required by Par and regulatory agencies, • High school diploma or equivalent., • Qualified in Filling or Labeling., • Competent at all of the following processes:, • Material handling, • Capping, • Outserts/med guides, • In-process check, • Packing, • Stacking, • Cartoning, if applicable, • Competent in setting up and running machinery., • Competent in Master Clean/ Line Clearance or A&B type Cleans., • Competently samples batches., • Ability to follow both verbal and written instructions including SOP’s and Batch Record documentation., • Ability to accurately and precisely record data and batch information., • Ability to work in both independent and team environments., • Ability to assist in troubleshooting process issues., • Ability to participate in Continuous Improvement projects., • Proficient in reading and writing English to understand work instructions and document results. Physical Requirements: • Must be able to stand for long periods of time (8 or 12 hour shifts), lift at least 35 pounds, climb ladders, wear a dust mask or respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE, including safety glasses, ear plugs, and safety shoes., • Dexterity - ability to quickly move your hand, your hand together with your arm, or your two hands to grasp, manipulate, or assemble objects., • Vision - ability to see details at close range (within a few feet of the observer)., • Multi-limb Coordination - ability to coordinate two or more limbs (for example, two arms, two legs, or one leg and one arm) while sitting or standing.

To deliver a great customer experience while safely and efficiently maintaining a neat, clean and organized warehouse.To perform responsibilities that will ensure accurate receiving of all deliveries to protect Company assets.To perform other tasks Dance, Customer Experience, Operations, Retail, QA.

NET applications, robust frontend skills (especially with Angular), and a solid track record delivering enterprise software solutions. Design, develop, and maintain full stack web applications using. Collaborate with product owners, designers, and QA engineers to deliver high-quality software.