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<h3>Job Description</h3>
Job Description
Description
Independently perform advanced laboratory testing of raw materials using Gas Chromatography (GC), following approved test methods and in full compliance with QC procedures, company SOPs, and cGMP standards. Operate a range of GC instruments, including those equipped with headspace and direct injection capabilities. Develop GC methods autonomously as needed. Execute method validation, process validation, and cleaning validation testing, along with all associated documentation. Carry out method verification, validation, optimization, and transfer activities as required. Support lab management in conducting investigations and handling deviations; assist in preparing for and responding to audits and regulatory inspections. Perform internal laboratory audits as necessary. Maintain accurate, organized, and cGMP-compliant documentation for all testing activities, including lab notebooks, chromatograms, report forms, Certificates of Analysis (C of A), specification sheets, and glassware labeling. Provide training, guidance, and mentorship to Level 1 and Level 2 chemists. Promote and adhere to all laboratory health, safety, and housekeeping protocols; take a leadership role in lab clean-up efforts and related initiatives. Ensure proper handling and documentation of controlled substances in strict accordance with federal and company regulations. Complete assigned projects with precision and timeliness, minimizing errors, repeats, and analyst-related deviations; follow management directives to meet deadlines and priorities. Actively participate in laboratory and company meetings and training sessions.
 
Skills
Chemistry, gc, method validation, pharmaceutical, gas chromatography, method development, Hplc, Mass spectrometry, Titration, Wet chemistry
 
Top Skills Details
Chemistry,gc,method validation,pharmaceutical,gas chromatography,method development
 
Additional Skills &amp; Qualifications
Bachelor’s degree in Chemistry or a closely related scientific discipline required. A minimum of 4–5 years of laboratory experience is preferred, ideally within a pharmaceutical setting focused on solid dosage forms. Strong verbal and written communication skills, including proficiency in technical writing for reports and the ability to interpret technical documents, instructions, diagrams, and schedules. Excellent interpersonal skills for effective collaboration with colleagues and supervisors. Proven expertise in analytical testing within a cGMP-compliant laboratory environment. Exceptional time management and attention to detail to ensure accurate project completion with minimal errors. Fluent in English with strong command of both verbal and written communication. Ability to consistently deliver high-quality work in a pharmaceutical environment regulated by agencies such as the FDA and DEA. Demonstrated proficiency in operating advanced laboratory instrumentation and associated software. Capable of working under pressure, following detailed instructions, and managing priorities in a deadline-driven setting. Comfortable working with chemicals, reagents, and solvents, involving physical activity in the laboratory.
 
Experience Level
Expert Level
Job Type &amp; Location
This is a Contract to Hire position based out of Laurelton, NY.
Pay and Benefits
The pay range for this position is $80000.00 - $85000.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Laurelton,NY.
Application Deadline
This position is anticipated to close on Nov 6, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

GC Chemist

<h3>Job Description</h3>
Job Description
 Conducts chemical and physical laboratory tests of solid materials, liquids, and gases and analyzes test data.&nbsp; Primary Responsibilities: Operate performance testing equipment and analytical instrumentation as well as insuring proper maintenance, calibration, and repairs when needed. Perform detailed ASTM, SAE, and FTM testing of key characteristics for raw materials, intermediates, production batches, and R&amp;D/Technical Service samples Aviation-specific performance testing, Viscometric testing, tribology testing, foam/emulsion testing, grease testing Characterization of ultra-clean requirements using Spectroscopic light scattering particle counters Quantitative gravimetric Millipore filtration analysis Wet chemical titration methods including Karl Fisher, total acid/base number Specific Gravity, Pour/Flash/Fire Point, Electrical properties Analytical analysis using ICP, HPLC, GC, and FTIR Perform routine control charting on critical tests and troubleshoot/communicate deviations or trends Operate Production laboratory to test inline packaged material and authorize line approvals to package manufactured product as well as provide support to Production for maintaining product quality and integrity Maintain accurate, well-organized, and defensible documentation of all results interface with software such as SAP Participate in both internal quality audits and external customer audits of the laboratory performance Perform PTHAs, JSAs, and support plant/department Safety and 5S initiatives
Company DescriptionDella Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations. 
<h3>Company Description</h3>
Della Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations.

Chemistry Technician

<h3>Job Description</h3>
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Pall Corporation, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.&nbsp;
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper—everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation.
Learn about the Danaher Business System which makes everything possible.
The Sr. Scientist is responsible for the development, validation and execution of broad array of methods supporting analysis of filtration media and integrated filtration, purification or separation devices/systems.
This position reports to the Sr. Manager, Metrology, Analysis and Applications and is part of the Global R&amp;D organization located in Port Washington, NY and will be an on-site role.
In this role, you will have the opportunity to:
<ul>
<li>Develop and refine SOPs for analyzing components or products in filtration, purification, and separation devices.</li>
<li>Document experiments and findings in lab notebooks and technical reports.</li>
<li>Identify and implement improvements in analysis and characterization methods.</li>
<li>Act as SME, providing analytical expertise to cross-functional teams and project stakeholders.</li>
<li>Coordinate lab operations, including scheduling, test parameter reviews, and preventive maintenance with equipment vendors.</li>
</ul>
The essential requirements of the job include:
<ul>
<li>Bachelor’s, or Master’s degree in chemistry with a focus on analytical chemistry</li>
<li>5+ years of experience in an industry lab environment</li>
<li>Hands-on experience developing methods for analytical tools (e.g. ICP-MS, LC-MS, GC-MS, IC, AA, TOC, etc.)</li>
</ul>
Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
The annual salary range OR the hourly range for this role is $100,000 - $110,000.&nbsp; This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
#LI-LM3
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

Senior Scientist - Analytical Chemist

<h3>Job Description</h3>
Job Description
Restoration Ecologist
 
 
ORGANIZATIONAL OVERVIEW
The Natural Areas Conservancy (NAC) is the only nonprofit organization in New York City focused on the care of our 20,000 acres of forests, wetlands, and grasslands. For over a decade, we’ve worked closely with the New York City Department of Parks &amp; Recreation to champion urban natural areas in dozens of parks across the five boroughs through critical research, advocacy, trails work, workforce development initiatives, and community programming. Through these efforts we’re ensuring that everyone has access to high-quality natural areas and understands their benefits because we believe that by working together–with New Yorkers, our partners, and NYC Parks–we can create healthy and thriving natural spaces and more resilient and connected communities. We also convene the Forests in Cities network, a 26-city coalition of experts dedicated to preserving, improving, and expanding urban forests nationally.
 
POSITION OVERVIEW
Reporting to the Senior Manager of Conservation Science, the Restoration Ecologist will be responsible for overseeing NAC forest restoration projects in collaboration with the NYC Parks Department, forest restoration contractors, and other non-profit conservancies. 
 
The Natural Areas Conservancy is tasked with ensuring the effectiveness of forest restoration activities across multiple sites within NYC parks. The Restoration Ecologist will be responsible for coordinating projects across these sites to ensure consistent framing, measurable success metrics, and overall efficiency in all aspects of forest restoration, from initial site design to implementation and subsequent monitoring. Under the guidance of the Senior Manager, Conservation Science, this position will function as the primary project manager for forest restoration initiatives, establishing a comprehensive project management cycle that ensures scientifically sound and ecologically appropriate site preparation, design, planting palettes, implementation, and monitoring. The Restoration Ecologist will be responsible for communicating directly with contractors, tracking and verifying day to day activities and creating reports. The Restoration Ecologist will collaborate closely with the NYC forest practitioner community to disseminate best practices and contribute to the community of practice. This role will occasionally involve supervising college interns.
 
PRIMARY RESPONSIBILITIES 
<ol>
<li>
Manage forest restoration contracts. Under the guidance of NAC senior staff, the Restoration Ecologist will supervise, track, and manage the day-to-day activities of forest restoration contractors. This includes meeting the contractor on-site to scope work, supervising site work, communicating clearly and effectively with contractors and project stakeholders, and tracking progress by daily and weekly logs. The job also includes tracking daily activities against the overall project tasks and timelines. 
</li>
<li>
Coordinate with partners conducting implementation. Coordinate forest restoration activities with partner organizations (e.g., NYC Parks, Prospect Park Alliance, New York Restoration Project, Forest Park Trust) and NAC staff. Liaise with project partners, conduct site visits and track overall project progress and assist with monitoring, reporting, and evaluation activities at each site. 
</li>
<li>
Project management and tracking. Using internal project management tools, track project activities across multiple sites against a timeline and keep up to date. Incorporate contractor work logs, partner-led conservation activities, and volunteer stewardship activities under the same project scope. Using established data systems for forest restoration in NYC (Natural Areas Management Activities database), complete entries for contractors and partners as needed. Keep permits and correspondence on file and organized. Keep the overall project on track and all partners and staff in the loop. 
</li>
<li>
Coordinate and participate in forest restoration activities. Procure plant material, direct and assist with plant deliveries, conduct pre-post monitoring, and participate in volunteer stewardship activities and tree planting. 
</li>
<li>
Communicate outcomes and contribute to science-driven tools and products that advance the care of natural areas, including management recommendations and best practices. Building on the NYC Forest Management Framework and working with colleagues and partners, synthesize project outcomes into case studies, reports, tools, and management plans for practitioner and policy audiences, specifically those focused on Forest Restoration in NYC. Under the direction of the Senior Manager, Conservation Science, supports strengthening the local community of practice through events, communication, and participation in meetings. Communicate outputs to stakeholders and partners with a focus on the practitioner community. 
</li>
</ol>
 
REQUIRED SKILLS AND QUALIFICATIONS
<ul>
<li>
Undergraduate degree in forestry, natural resource management, ecology, or similar 
</li>
<li>
Knowledge of forest ecology and management, forest conservation, silviculture, and/ or urban forestry.
</li>
<li>
3-7 years of work experience in natural resource management, forestry, forest research, or technical assistance—urban experience is a plus.
</li>
<li>
Experience in project management tracking systems, geo-spatial tools, and using maps to direct and orient field-based work. 
</li>
<li>
Demonstrated ability to communicate effectively, and develop effective relationships with internal staff, partners, and peers to achieve project goals or objectives. 
</li>
<li>
Knowledge of NYC forested natural areas, tree species ID, understory ID, forest restoration principles. 
</li>
<li>
Proven ability to solve problems, listen to partner needs, and adapt project goals to achieve impact. 
</li>
<li>
Ability to spend time outside in inclement weather, carry 25lbs, hike on steep slopes and through brush. 
</li>
<li>
Valid driver’s license and no driving restrictions.
</li>
<li>
Satisfactory proof of identity and legal authorization to work in the United States, and your completion of an Employment Eligibility Verification Form I-9
</li>
</ul>
 
PREFERRED SKILLS
<ul>
<li>
Experience in managing forest restoration contracts in NYC, complex project management, and knowledge of the NYC Forest Management Framework. 
</li>
<li>
Experience with engaging with community groups, students, or other constituencies through environmental stewardship.
</li>
<li>
Experience in field-based monitoring for forest restoration projects. 
</li>
</ul>
 
JOB LOCATION
NAC currently offers a hybrid remote work schedule as projects allow, with staff reporting to the Manhattan office a minimum of two days a week with offices likely moving to Queens in 2026. This role should be willing to work from a primary office location in Manhattan, and field work reporting locations in all five boroughs of New York City up to 5 days a week. Some occasional domestic travel is expected for this position. 
 
COMPENSATION/BENEFITS
<ul>
<li>
Salary Range: $72,000 - $95,000 depending on experience
</li>
<li>
Competitive benefits package including generous Paid Time Off, eligibility for medical/dental/vision insurance, 401K, and professional development funds.
</li>
</ul>
 
APPLICATION
Include a cover letter, resume, and writing sample as one PDF. Applications will be reviewed on a rolling basis until the position is filled. Please address any questions to <a href="mailto:jobs@naturalareasnyc.org" target="_blank">jobs@naturalareasnyc.org</a>.
 
WORK AUTHORIZATION
Candidates must currently possess and maintain legal authorization to work in the United States. The Natural Areas Conservancy (NAC) utilizes the E-Verify system and does not offer, transfer, or sponsor employment-based non-immigrant or immigrant work visas (e.g., H-1B, permanent residency).
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin. 
Updated: October 31, 2025

Restoration Ecologist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Leap Consulting Group supports clinical diagnostics and clinical research organizations through a full range of services supporting the end-to-end digital and technology needs of the lab, from the digital front door to the pre-analytical lab bench process (LIMS, instrumentation, automation, etc.), and all of the complex processes for report writing, revenue cycle, and patient engagement before and after testing.
Leap provides turnkey services starting with strategic planning through full implementation and everything in between for CLIA, CAP, NYS CLEP, and FDA-compliant laboratories. Leap’s lab practice is led and staffed by veteran laboratory leaders from high-volume, high-complexity laboratories across the United States. In addition to lab-centric capabilities, Leap offers full capabilities across digital, cloud, and the rest of the IT ecosystems.
Job Description 
We’re looking for experienced laboratory professionals — former bench technologists, R&amp;D scientists, or lab operations specialists — who are excited to apply their laboratory expertise to be client-facing and working directly on client lab projects building the latest and greatest in clinical laboratory workflows and laboratory software system implementations.
This is a hands-on, problem-solving role — you’ll work alongside scientists, engineers, and clinicians to make lab systems work better, not sell software or convince people why they need to do better - everyone is working together to make it better.
This role is not a generic IT business analyst position — it’s designed for individuals with deep understanding of how labs actually function, from sample accessioning to reporting. If you have great IT analyst skills we need those too, but we are currently not hiring for those. Please do not apply here if you are not deeply experienced in clinical laboratory and/or LIMS.
This is a role reporting into our Healthcare Practice Lead focused on supporting several laboratory initiatives including digital-front-doors, preanalytical systems, LIMS, lab automation, bioinformatics, revenue cycle, and other related needs. The role requires Laboratory Operations and/or Laboratory IT awareness, a background in digital transformation or information systems, and ideally exposure to clinical laboratory revenue cycle. The person in this role would be a smart, inquisitive, experienced clinical laboratory or health system technology business analyst or functional technical analyst.&nbsp;
From Buy vs. Build Analysis, to System Sourcing projects, to big picture planning, and down to the real roll-up-your-sleeves implementation requirements gathering, technical design, and partnering with your software engineering peers to deliver solutions. In this position, you will work closely with Leap client’s business, clinical, and technology leaders to understand their needs, design and develop innovative solutions, and tackle complex challenges. The people in this role will help clients articulate their requirements, prioritize their needs, develop detailed specifications, and at times will lead implementations in Agile methodologies often supporting a mixed team of both Leap provided and client employee engineering resources. The ideal candidate will be well spoken, extremely organized, and able to succinctly capture every detail. You should also be able to ask questions to clients to ensure there are no gaps in the analysis conducted and be an effective communicator when there have been changes in the requirements.
As is the nature of digital transformation consulting, the right people for this role find themselves adaptable and flexible in an environment where change is the only constant. The ideal candidate finds clarity in ambiguity and shifts priorities quickly as new client considerations, challenges, and opportunities arise.&nbsp;
You should excel in managing projects, driving product development, and analyzing business needs, all while thriving in a fast-paced and collaborative environment.
This role is a hybrid position based in our Bergen County NJ offices. Hybrid expectations include 4 days a week in office, 1 day remote, exclusive of client-related-travel which would be as required.
Key Responsibilities:
<ul>
<li>
Portfolio and Program Management:
<ul>
<li>
Partner with clients to define a product or program vision, strategy, and roadmap in alignment with business goals and stakeholder needs
</li>
</ul>
</li>
<li>
Business Analysis:
<ul>
<li>
Able to understand complex lab workflows and communicating future state changes to developers
</li>
<li>
Perform gap analysis to identify discrepancies between current processes and desired outcomes
</li>
<li>
Translate bench-side workflows into system requirements
</li>
<li>
Document process maps that mirror the flow of specimens through the lab
</li>
<li>
Collaborate with engineers to digitize and automate R&amp;D and QC processes
</li>
<li>
Be able to handle changes in workflow and how to address them when those blockers occur
</li>
<li>
Facilitate meetings to gather requirements, develop solution plans, and drive alignment with business stakeholders
</li>
<li>
Participate in detailed design sessions with the technical teams to define the implementation approach based on requirements gathered
</li>
</ul>
</li>
<li>
Project Management:
<ul>
<li>
Handle project ambiguity, complexity, and interdependencies with an organized and structured approach
</li>
<li>
Assess and prioritize new information and requirements, integrating them seamlessly into project deliverables
</li>
<li>
Identify and manage project risks and issues
</li>
<li>
Maintain project documentation, ensuring all project deliverables are documented, updated, and communicated effectively
</li>
</ul>
</li>
<li>
Facilitation &amp; Communication:
<ul>
<li>
Maintain situational awareness and resolve conflicts efficiently to keep projects on track
</li>
<li>
Ensure clear and effective communication across all levels of the organization
</li>
</ul>
</li>
<li>
Adaptability &amp; Creative Problem Solving:
<ul>
<li>
Demonstrate a proactive approach to identifying and addressing challenges
</li>
<li>
Embrace and manage chaos with a continuous learning mindset, adapting to evolving requirements and challenges
</li>
</ul>
</li>
<li>
Detail Orientation &amp; Strategic Vision:
<ul>
<li>
Dive into the details to ensure precision and accuracy while maintaining a strategic, high-level perspective
</li>
<li>
Communicate complex technical concepts in a way that is accessible to non-technical stakeholders, effectively bridging the gap between technical and business perspectives
</li>
<li>
Stay strategic without losing the detail - it is an art more than a science
</li>
</ul>
</li>
<li>
Execution &amp; Results:
<ul>
<li>
Demonstrate dependability and reliability with a focus on clear thinking and meticulous attention to detail
</li>
<li>
Produce detailed stories to drive development and be reliable for QA testing
</li>
</ul>
</li>
</ul>
If you are an energetic and multifaceted professional who can embrace uncertainty, think on their feet, and effectively manage shifting priorities to drive projects forward, with the ability to navigate both technical details and strategic business goals, we encourage you to apply and help us drive impactful solutions for our clients!
Keywords:&nbsp;LIMS, LIS, ELN, middleware, automation, genomics, pathology, molecular diagnostics, assay development, quality control, sample tracking, data integrity, CLIA, CAP, HL7, FHIR, lab workflow optimization
Qualifications 
Minimum Qualifications:
<ul>
<li>
Education: BA/BS Required
</li>
<li>
Experience: Minimum of 3-5 years working at the bench and/or as a Business Analyst or Functional Technical Analyst, preferably in a clinical laboratory&nbsp;
</li>
<li>
Be comfortable communicating in-person, by phone, over video, as well as collaboration chat tools such as Slack and Teams
</li>
<li>
Be a self-starting independent team player who is both professional and kind to colleagues and customers
</li>
<li>
Be tech savvy and ideally consider yourself 'fairly technical'
</li>
<li>
Proven experience in project management, product management, and business analysis
</li>
<li>
Strong facilitation, communication, and conflict resolution skills
</li>
<li>
Ability to manage multiple projects simultaneously and prioritize tasks effectively
</li>
<li>
Ability to manage complexity and ambiguity in a structured and organized manner
</li>
<li>
Demonstrated ability to drive results and deliver innovative solutions
</li>
<li>
Proficiency in discussing technical details and translating them into business value
</li>
<li>
Experience in performing gap analysis and creating business process flows
</li>
</ul>
Preferred Qualifications:
Knowledge, experience, or proficiency in most or all of the following:&nbsp; &nbsp; &nbsp;
<ul>
<li>
Acting as a liaison between technical operations and solutions providers
</li>
<li>
Documenting, analyzing, and recommending solutions to complex problems
</li>
<li>
Information Technology and Software Development business cycles
</li>
<li>
Healthcare Digital Physician and/or Patient Portals
</li>
<li>
Revenue Cycle Management
</li>
<li>
Laboratory Operations
</li>
<li>
Bioinformatics
</li>
</ul>
 Additional Information 
<ul>
<li>Be comfortable communicating in-person, by phone, over video, as well as collaboration chat tools such as Slack</li>
<li>Be a self-starting independent team player who is both professional and kind to colleagues and customers</li>
<li>Be tech savvy and ideally consider yourself 'fairly technical'</li>
</ul>
All your information will be kept confidential according to EEO guidelines.

Clinical Lab Business Analyst - Hybrid On-site

<h3>Job Description</h3>
Job DescriptionQuality Control Microbiology Analyst II, IIIAllendale, NJ QC Microbiology Analyst II The Quality Control Microbiology Analyst II serves as a support role to clinical and commercial production. Microbiology Analyst II will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. This position will report into the Manager of QC Microbiology.
<ul>
<li>Environmental monitoring in controlled environments; Non-viable particulate monitoring, Active viable air monitoring Personnel monitoring, Surface sampling, Passive air monitoring</li>
<li>Equipment monitoring; Ensure equipment is in proper working conditions, Ensure all equipment is properly maintained/calibrated, Program equipment with proper workflows, Assist with routine laboratory testing, Plate reads and incubations</li>
<li>Shipping of test samples and equipment to contract laboratories for testing</li>
<li>Produce documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)</li>
<li>Writing/conducting investigations pertaining to environmental monitoring and testing</li>
<li>Develop and train QC Microbiology Analyst I personnel on relevant business processes</li>
</ul>
REQUIREMENTS
<ul>
<li>BA/BS in a science or relevant field required or equivalent experience; Minimum 2-4 years of experience with environmental monitoring or within the biopharmaceutical industry.</li>
<li>GxP/GDP, Safety Trained</li>
<li>Proficient with computer software such as; Microsoft Office, MODA/LIMS</li>
<li>Familiarity with ISO and EU standards</li>
<li>Strong written and oral communication skills.</li>
<li>Technical training ability.</li>
<li>Must have the ability to work in a team-oriented environment and with clients</li>
<li>Must be able to work during the weekend, holidays, and as required by the company.</li>
<li>Must be able to handle the standard/moderate noise of the manufacturing facility.</li>
<li>The QC Microbiology Analyst II must be able to maintain aseptic behavior within a cleanroom environment for an extended period.</li>
<li>Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities.</li>
</ul>
While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. QC Microbiology Analyst III The Quality Control Microbiology Analyst III serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst III will coordinate data for batch release, participate in project/client meetings, and author/revise environmental monitoring procedures. Additionally, the QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring.
<ul>
<li>Documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).</li>
<li>Coordinates data for batch release.</li>
<li>Participation in project/client meetings and communications, providing scientific and technical expertise.</li>
<li>Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols.</li>
<li>Review of investigations and documentation of non-confirming events and environmental excursions.</li>
<li>Apply expertise of compliance requirements to maintain an inspection-ready state.</li>
<li>Participate and act as subject matter expert during audits/inspections.</li>
<li>Develop and train QC Microbiology Analyst II on relevant business processes.</li>
<li>Processing of purchase orders for outsourced testing and lab supplies.</li>
<li>Coordinates work orders.</li>
</ul>
REQUIREMENTS
<ul>
<li>BA/BS in a science or relevant field required or equivalent experience; Minimum 5-7 years of experience with environmental monitoring or within the biopharmaceutical industry</li>
<li>GxP/GDP Trained</li>
<li>Proficient with computer software such as; Microsoft Office, MODA/LIMS, Microsoft Visio (preferred), Netsuite (preferred), Maximo Asset Management System (preferred)</li>
<li>Proficient knowledge of ISO and EU standards</li>
<li>Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review.</li>
<li>Strong written and oral communication skills</li>
<li>Strong technical writing skills</li>
<li>Technical training experience</li>
<li>Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities</li>
<li>Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen.</li>
<li>Must have the ability to work in a team-oriented environment and with clients</li>
<li>Must be able to work during the weekend, holidays and as required by the company</li>
<li>Must be able to handle the standard/moderate noise of the manufacturing facility</li>
</ul>
All PositionsWorking Environment
<ul>
<li>While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.</li>
<li>Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen.</li>
<li>Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy.</li>
<li>Must have the ability to work in a team-oriented environment and with clients</li>
<li>Must be able to work during the weekend, holidays, and as required by the company</li>
<li>Must be able to handle the standard/moderate noise of the manufacturing facility</li>
</ul>
Please note these job descriptions are not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

QC Microbiology Analyst II, III

<h3>Job Description</h3>
Job Description
<ul>
<li>
The R&amp;D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. This position combines hands-on laboratory research with product development responsibilities, including experimental design, material characterization, prototype development, and compliance with design control requirements. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing. This role bridges early discovery and applied development, requiring both strong scientific skills and practical problem-solving. Key Responsibilities
</li>
<li>Plan, execute, and analyze laboratory experiments involving biomaterials, regenerative matrices, and medical device components.</li>
<li>Contribute innovative ideas for new products, testing methods, or process improvements to enhance R&amp;D capabilities.</li>
<li>Develop, build, and refine prototypes to meet defined specifications and clinical needs.</li>
<li>Generate accurate technical documentation, reports, and protocols in compliance with FDA, ISO, and Design Control requirements.</li>
<li>Characterize materials and prototypes using analytical, biochemical, and mechanical testing methods.</li>
<li>Perform risk assessments, troubleshoot technical issues, and propose solutions to improve product performance or process robustness.</li>
<li>Support technology transfer from R&amp;D to manufacturing, including process documentation, validation support, and training of personnel.</li>
<li>Collaborate with cross-functional teams (Manufacturing, Quality, Regulatory, Marketing, and Clinical) to align product development with business and clinical requirements.</li>
<li>Engage with external consultants, and customers to gather feedback and translate needs into product features.</li>
<li>Mentor and provide technical guidance to junior staff on laboratory practices, data analysis, and project tasks.</li>
<li>Present findings and project updates to management, peers, and cross-functional stakeholders.</li>
<li>Maintain laboratory operations, including equipment calibration, safety compliance, and method updates.</li>
<li>Qualifications</li>
<li>MS with 1–2 years or BS with 3–5 years in Biomedical Science, Materials Science, Chemistry, or related field.</li>
<li>Experience in medical device research and development, biomaterials, or regenerative technologies preferred.</li>
<li>Knowledge of laboratory techniques for material characterization, tissue-derived biomaterials, or device testing.</li>
<li>Familiarity with Design Controls, GLP/GMP, and ISO standards.</li>
<li>Proficiency with experimental design, data/statistical analysis, and technical problem-solving.</li>
<li>Experience with CAD, prototyping tools, or modeling software is a plus.</li>
<li>Strong organizational skills with the ability to manage multiple studies and projects simultaneously.</li>
<li>Excellent communications and presentation skills for cross-functional collaboration.</li>
<li>Demonstrated ability to work independently, manage multiple priorities, and deliver high-quality results.</li>
</ul>

R&D Scientist

<h3>Job Description</h3>
Title: ArcGIS Developer
Location: NYC NY
On-site/Remote/Hybrid: Hybrid (4 days onsite, 1 day remote)
Duration: 12 Months
Interview Process: 1-2 Rounds
 
Required Skills
<ul>
<li>A minimum of 5-10 years custom GIS Development experience, Asset Management, Transportation experience</li>
<li>Minimum 5 years hands-on experience of experience in supporting ESRI GIS software, Portal of ArcGIS, ArcGIS Server, ArcGIS Desktop, HeXagon, Microsoft products, Microsoft Dynamics, Coding Languages such as: SQL &amp; Python</li>
</ul>
 
Preferred Skills
<ul>
<li>Preferable 2+ years working experience with transportation or logistics industry</li>
<li>Strong analytical and problem-solving skills</li>
</ul>

ArcGIS Developer

<h3>Job Description</h3>
EMM Research is seeking a dynamic and self-motivated Research Associate to join our team in New York City. As a Research Associate, you will play a crucial role in supporting our investment banking operations by providing comprehensive research and analytical support to assist our clients and decision-makers.
 
Responsibilities:
<ul>
<li>Conduct comprehensive market research and analysis, delivering valuable insights into diverse industry sectors, market trends, and investment opportunities.</li>
<li>Gather and synthesize financial data, market reports, and relevant information from various sources to facilitate informed decision-making</li>
<li>Prepare concise and informative research reports, presentations, and investment memoranda for clients and internal stakeholders</li>
<li>Stay updated on industry news, regulatory changes, and economic developments, and provide timely updates to the team</li>
<li>Collaborate with team members to ensure the delivery of high-quality research and analysis</li>
<li>Proactively track project progress and updates in the internal ticketing system, ensuring accurate documentation of events such as calls, meetings, and activity uploads</li>
<li>Utilize timers on all work to accurately capture time spent on tasks and projects, contributing to efficient project management and resource allocation</li>
</ul>
 
Requirements:
<ul>
<li>Bachelor's degree in history, library studies, communications, or a related field</li>
<li>At least one year of corporate experience</li>
<li>Strong analytical and quantitative skills</li>
<li>Excellent communication, both written and verbal</li>
<li>Self-motivated and able to work independently as well as in a team</li>
<li>Demonstrated ability to meet deadlines and manage multiple tasks simultaneously</li>
<li>4x on site, 1 day remote | Central NYC location</li>
</ul>
 
If you are a dedicated and enthusiastic professional looking to advance your career EMM Research offers an exciting opportunity to work with a dynamic team in the heart of New York City.

Research Associate

<h3>Job Description</h3>
Time for Change? Do you want work for one of the most highly respected consulting firms in their field?
 
They are not a recruitment or search agency 
Had enough of 360 recruitment or business development but enjoy research and delivery 
 
Based in New York 
Do you hold an impressive record within University , Collegiate Sport or industry 
 
Do you have 6months - 2years experience within the recruitment and Talent Acquisition environment 
 
Want to be fast tracked for promotion within this lucrative field ? 
 
If the answer is yes then read on 
 
Senior Associate - Client delivery 
 
Sick of corporate politics? No chance of getting promoted unless someone leaves. Whatever you do is not enough ?
 
I was a Senior Director for a well-known firm and no matter how much I tried or how good my numbers were, they would always find fault in my process, it was really demoralising.
 
You might be experiencing the same.
 
Not here the company was set up with the ethos of the company cares, based on collaboration and the team will be a success. They do not do corporate politics and people feeling like another cog in the machine. In fact, they have an extremely high retention rate.
 
People join the company at this level and the senior management have worked their way up, so they understand what it takes and how to treat people. The culture starts at the top with the directors having a calm and supportive manner. It is not all about work, a true balance is evident amongst his team
 
Our client a consultancy to the financial services market is looking for their next star performers based in New York.
 
They are looking for candidates who have 6months -2 years exposure to recruitment and talent acquisition market and have the ability and gravitas to network at the C-level
 
You must be able to demonstrate a high achievement with either University, Collegiate sport, or the recruitment and staffing 
 
You will be part of the execution team and have the opportunity to be fast tracked.
 
Successful candidates can expect this to happen within 9-18months
 
You will be trusted from day one and have a real impact on your client’s success
 
As a trusted advisor and a member of the execution team, you will be tasked to deliver market leading industry Senior Advisors. Your work has a direct impact on our clients’ ability to compete on landmark private equity deals across key economic sectors.
 
Responsibilities include :
<ul>
<li>Research: Understanding industry ecosystems</li>
<li>Have the ability to identify and map the key companies and executives relevant to the deal.</li>
<li>Sourcing, interviewing and securing experienced industry expert C-level executives and thought-leaders as advisors to our clients.</li>
<li>Client Management and presentation : Present research findings to their clients and recommend the most relevant advisors for maximum impact on the given deal process.</li>
</ul>
 
Rapid career progression for strong performers - top Associates have been able to earn promotion in as little as 9 months.
The management team is a clear destination for this role
 
Exceptional exposure and opportunity to learn directly from leading industry executives and senior PE professionals.
 
The culture is high performance given the nature of the business you will make a lasting impact on your clients
 
Team culture is paramount in this business as delivery is essential in return you will get a clear roadmap for success and receive a targeted personal development plan.
 
A great place to work is a term used a lot but this company live and breath the culture and have a lot of un along the way
 
This really is a standout opportunity to forge a career in this highly lucrative field
 
Renumeration will start at $75-90k with an excellent OTE
In year 2 this will rise considerably in line with your success and promotions
 
If you are interested in finding out more or would like to discuss your current career options DM me, email <a href="mailto:Sblair@resourcingassociates.com" target="_blank">Sblair@resourcingassociates.com</a>
 
 
If you are an experienced recruitment professional looking for advice and guidance about the recruitment market, please feel free to also submit your details for an open conversation
 
 
Resourcing Associates typically place recruitment professionals in to the following positions:
 
 
<ul>
<li>Financial Services Recruitment</li>
<li>Executive Search</li>
<li>Private Equity Research</li>
<li>I.T. Recruitment</li>
<li>Technology Recruitment</li>
<li>Digital Recruitment</li>
<li>Cyber Recruitment</li>
<li>InfoSec Recruitment</li>
<li>SAP Recruitment</li>
<li>Media Recruitment</li>
<li>Marketing Recruitment</li>
<li>Finance Recruitment</li>
<li>Accountancy Recruitment</li>
<li>Procurement Recruitment</li>
<li>Supply Chain Recruitment</li>
<li>HR Recruitment</li>
<li>Legal Recruitment</li>
<li>Legal Recruitment</li>
<li>Paralegal Recruitment</li>
<li>Investment Banking Recruitment</li>
<li>Public Sector Recruitment</li>
<li>Business support Recruitment</li>
<li>Office Support Recruitment</li>
<li>Pharmaceutical Recruitment</li>
<li>Management Recruitment</li>
<li>C-Level Recruitment</li>
<li>Board Recruitment</li>
<li>Executive Recruitment</li>
<li>Banking Recruitment</li>
<li>Transformation, Recruitment Change Management Recruitment</li>
<li>Insurance Recruitment</li>
</ul>
 
 
Executive Search , Search Associate , Execution and Delivery Associates, Recruitment Consultant , Senior recruitment Consultant , Principal consultant, Managing Consultant Recruitment Team Leader , Recruitment Manager , Recruitment Director , Associate Director , Business Development Director
 
 
Please note we are only able to respond to Candidates who have Exec Search or Recruitment Agency experience. If you have not heard from us within four working days, unfortunately, on this occasion, your application has not been successful.
 
 
Resourcing Associates is a recruitment agency that specialises in placing all levels of recruitment professionals:

638 Science Jobs in New York, NY 10007, USA