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<h3>Job Description</h3>
About the Role
Savills is seeking a Research &amp; Strategy Analyst to join its Life Sciences Practice Group. This hybrid role blends market research, strategic insight, and business development support to empower brokers, consultants, and clients with high-impact intelligence.
 
The ideal candidate is analytically sharp, intellectually curious, and eager to contribute across both life sciences-specific initiatives and broader commercial real estate research functions. This is a unique opportunity to work at the nexus of science, data, and strategy in one of the industry’s fastest-growing sectors.
 
Key Responsibilities
Research Operations &amp; Market Data Management
<ul>
<li>Maintain and update proprietary databases tracking inventory, leasing activity, sales comparables, ownership structures, development pipelines, and tenant movements in key markets.</li>
<li>Contribute to the production of quarterly market statistics and collaborate with national and regional teams on sector-specific reports.</li>
<li>Ensure accuracy and consistency of data across platforms to support client-ready deliverables and leadership decision-making.</li>
</ul>
Client-Focused Research &amp; Broker Support
<ul>
<li>Respond to requests for market intelligence to support broker teams and strategic pursuits.</li>
<li>Partner with brokers and across functions to develop data-driven materials for client meetings, pitch decks, and presentations.</li>
<li>Leverage research outputs to support marketing campaigns, graphics, and thought leadership placement tailored to client needs.</li>
<li>Build scalable templates and tools that enhance service delivery across geographies.</li>
</ul>
Life Sciences Industry Intelligence
<ul>
<li>Monitor companies in the biotech, medtech, and pharmaceutical sectors—from early-stage startups to public firms—tracking funding milestones, clinical pipelines, partnerships, and expansions.</li>
<li>Identify real estate decision inflection points (e.g., IPOs, new clinical phases, M&amp;A activity) and align those with broker outreach and opportunity pipelines.</li>
<li>Maintain and regularly update a curated list of strategic targets to support CRM integration and proactive client engagement.</li>
<li>Translate complex industry developments into relevant real estate implications for internal and external audiences.</li>
</ul>
CRM Strategy, Pipeline Tracking &amp; Business Enablement
<ul>
<li>Leverage Savills Salesforce environment to track target companies, contacts, and opportunities aligned with life sciences growth triggers.</li>
<li>Maintain detailed and dynamic CRM records to reflect company stage, activity history, strategic touchpoints, and geographic expansion status.</li>
<li>Collaborate with brokers and marketing to execute targeted outreach campaigns based on funding events, clinical milestones, and relocation trends.</li>
<li>Develop dashboards and reports that visualize pipeline health, deal progress, and prospect engagement across key geographies.</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor's degree required; advanced degree (MBA, MS, PhD) or relevant certifications preferred.</li>
<li>2–6 years of experience in life sciences, research, management consulting, or corporate strategy.</li>
<li>Deep familiarity with biotech, pharma, and/or medtech industries including R&amp;D pipelines, funding dynamics, and commercialization paths.</li>
<li>Exceptional analytical skills with the ability to distill complex data into strategic insights.</li>
<li>Strong written and verbal communication skills; experience writing reports or market commentary is a plus.</li>
<li>CRM platform experience (Salesforce) is preferred.</li>
<li>Highly organized, detail-oriented, and motivated to work in a fast-paced, entrepreneurial environment.</li>
</ul>
 
Why Join Savills Life Sciences?
Savills is a global leader in real estate advisory, with a top-tier Life Sciences team that supports clients ranging from emerging startups to global pharmaceutical companies. Our platform empowers innovation—combining data, insight, and strategy to help clients make real estate decisions that accelerate science.
 
As part of our team, you’ll help shape how we track the future of life sciences and grow our presence in the most exciting markets in North America and beyond.
 
Savills values a diverse work environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, veteran status, or any other protected characteristic. Savills participates in the E-Verify program.

Research & Strategy Analyst, Life Sciences

<h3>Job Description</h3>
Open to: General Public
Work Week: NE (35-hour) Work Week
Salary: (P19) $58,817.70 - $85,742.00
Opening Date: 8/25/2025
Closing Date: 9/15/2025
Existing Vacancies: 1
 
Program/Location
Department of Environmental Protection
Contaminated Site Remediation &amp; Redevelopment
Environmental Evaluation &amp; Remediation Review
Ground Water Pollution Abatement
401 East State Street
Trenton, NJ 08625
 
Scope of Eligibility
Open to applicants who meet the requirements below.
 
Description
Under the close supervision of a Geologist 3 or other supervisory official in a State department or agency, conducts field and office work pertaining to sub-surface investigations, soil compaction, mineral resources, and other related geological work; compiles and analyzes geological data; does other related duties as required.
 
Specific to the Position
The responsibilities will include providing geologic and hydrogeologic support for Contaminated Site Remediation and Redevelopment (CSRR) for the more technically complex sites. It also includes the issuance of the Discharge to Ground Water Permits and the issuance of the Classified Exception Areas. A more advanced understanding of geology and hydrogeology are critical skills necessary to fulfill the job duties. Depending on the level of expertise, the person may also be responsible for completing geologic and hydrogeologic reviews for the lead programs. In this situation, the staff person is responsible for reviewing ground water issues related to Unregulated Heating Oil Tank (UHOT) cases and working with the Bureau of Field Operations, in addition to publicly funded and direct oversight cases. Represents the Bureau of Ground Water Pollution Abatement in dealing with the Ground Water and Surface Water Quality Standards.
 
Preferred Skill Set
This position is responsible for the review of workplans, reports, correspondence, proposals and studies which pertain to geology and hydrogeology, site remediation, well injection and other areas to ensure scientific accuracy and compliance with CSRR regulations, policies and procedures for Licensed Site Remediation Professional &amp; Publicly Funded and Case Management cases. It requires the individual to advise and make recommendations on technical and policy matters.
 
Requirements
Applicants must meet one of the following or a combination of both experience and education. Thirty (30) semester-hour credits are equal to one (1) year of relevant experience.
 
Five (5) years of professional experience in geology, geophysics, and/or hydrogeology.
OR
 
Possession of a bachelor's degree from an accredited college or university in geology, or a bachelor's degree including or supplemented by thirty (30) semester-hour credits in geological subjects; and one (1) year of the above-mentioned professional experience.
 
OR
 
Possession of a master's degree in geology from an accredited college or university.
 
NOTE: All U.S. degrees and transcripts must be from an accredited college or university. All foreign degrees and transcripts must be evaluated for accreditation by a recognized evaluation service by the closing date of this posting. Failure to provide documentation may result in ineligibility.
 
License
Appointees will be required to possess a driver's license valid in New Jersey only if the operation of a vehicle, rather than employee mobility, is necessary to perform the essential duties of the position.
 
Benefits
As a New Jersey State Department, NJDEP offers a comprehensive benefits package that includes:
<ul>
<li>Paid Benefit Leave</li>
<li>Holiday Pay</li>
<li>Alternative Workweek Program*</li>
<li>Telework*</li>
<li>Pension</li>
<li>Deferred Compensation</li>
<li>Health Benefits (medical, prescription drug, dental &amp; vision care) and Life Insurance</li>
<li>Flexible and Health Spending Accounts (FSA/HSA)</li>
<li>Commuter Tax Savings Program</li>
<li>Public Service Loan Forgiveness (PSLF)</li>
<li>Tuition Reimbursement*</li>
</ul>
*Pursuant to the State/Department's policy, procedures, and/or guidelines.
 
Veteran's Preference
To qualify for New Jersey Veteran's Preference/status, you must establish Veteran's Preference through the Department of Military and Veteran's Affairs. Please submit proof of your Veteran's Preference along with your resume as indicated. For more information, please visit <a href="https://www.nj.gov/military/veterans/services/civil-service-preference/" target="_blank">https://www.nj.gov/military/veterans/services/civil-service-preference/</a>
 
Residency
All persons newly hired on or after September 1, 2011, have one year from the date of employment to establish, and then maintain principal residence in the State of New Jersey subject to the provisions of N.J.S.A. 52:14-7 (L.2011, Chapter 70), also known as the “New Jersey First Act”.
 
Authorization to Work
Selected candidates must be authorized to work in the United States per the Department of Homeland Security, United States Citizenship, and Immigration Services regulations. NOTE: The State of New Jersey does not provide sponsorship for citizenship to the United States.
 
Equal Opportunity Employment
The State of New Jersey seeks to increase the richness and diversity of its workforce, and in doing so, become the employer of choice for all people seeking to work in State Government. To evaluate the effectiveness of our efforts to attract and employ a diverse workforce, applicants are asked to voluntarily answer a few brief questions on the NJ Affirmative Action Information Form. All information is considered confidential and will be filed separately with the agency's affirmative action officer. This information will not be part of your application for employment and will not be considered in any hiring decision.
 
DEP Notices of Vacancy have a 4:00 p.m. deadline on the closing date. When filing for these opportunities, please be sure to have your letter of interest and credentials sent electronically before 4 p.m. on the closing date.
 
The New Jersey Department of Environmental Protection is an Equal Opportunity Employer and is committed to inclusive hiring and a diverse workforce. We strongly encourage people from all backgrounds to apply. Accommodations under ADA will be provided upon request.

Geologist 1

<h3>Job Description</h3>
Position: Imagery Analyst (FMV)
Location: Suitland, MD
Clearance: TS/SCI
Salary Range: 80-90K
 
Job Description:
Mission Essential is seeking Maritime Imagery Analysts to support a new mission at
the NMIC with ONI in support of the GEOINT PED Watch for watch positions. Shift work
will be required and rotating shift work will be necessary.
 
Duties include but are not limited to:
• Provide imagery analysis and exploitation support for maritime/operational related issues. The Maritime Imagery Analyst shall provide GEOINT based exploitation reports using multiple formats consistent with GEOINT PED watch SOP. This support shall primarily be the exploitation of tactical airborne sensors within NSG and/or equivalent NSG standard exploitation systems.
• Participate in testing and analysis of new algorithm outputs and capabilities, to include data labeling in support of maritime GEOINT objects.
• Develop and maintain desktop procedures, techniques and methodologies related to ONI, Navy and maritime missions.
• Assist with training of rotating or new personnel that may augment the overall GEOINT PED Watch. This training may include hands-on instruction, analyst-to-analyst exchanges, or working aids.
 
REQUIREMENTS
 
Qualifications:
• 2 years of practical work experience exploiting NTM and/or airborne intelligence, surveillance and reconnaissance imagery – Full Motion Video (FMV)
• 1 year experience writing technical products, reports, and briefs.
• Formal military imagery analysis training or equivalent civilian remote sensing certification
• Familiarity with NTM GEOINT tasking and collection requirements mechanisms and tools.
• Experience using three or more of the following imagery and GIS systems and tools (or equivalent): Socet GXP, RemoteView Pro, iSPY, Advanced Motion Platform (AMP), Orchestration Services (formally Cedalion), National Consolidated Library (NCL), or Imagery Exploitation Capability (IEC)
 
Desired Qualifications:
• NSG GPC-F certification – not required upon consideration for the position but certification and training materials will be provided
• Knowledge of the following areas (not required): UAS, tactical GEOINT collection, exploitation, analysis and production workflow processes, CGS, DCGS, GI&amp;S, DOT

Geospatial Analyst

<h3>Job Description</h3>
We are seeking a highly motivated chemists to join our dynamic team at Rockville, Maryland. In this role, you will be responsible for designing, synthesizing, and optimizing novel linkers and payloads for our ADC projects. Your expertise in organic synthesis, bioconjugation, and analytical techniques will be critical for advancing our drug discovery pipeline.
Responsibilities:
1. Design and synthesize novel linker-payload molecules for ADC development
2. Optimize synthetic routes for efficient and scalable production of linker-payloads
3. Characterize and analyze synthesized molecules using analytical techniques such as HPLC, LC-MS and NMR
4. Collaborate with cross-functional teams to support ADC projects from discovery to preclinical and clinical development stages
5. Stay current with the latest developments in ADC chemistry and contribute to the advancement of ADC technology
Qualifications:
1. PhD degree in Organic Chemistry with more than 3 years experience in in designing, synthesizing, and characterizing ADC linkers and payloads, preferably within a pharmaceutical or biotechnology setting.
2. Innovative team-player with high energy for fast-paced environment
3. Proficiency in modern synthetic methods and techniques
4. Strong analytical and problem-solving skills

ADC Chemistry Linker-Payload Synthesis, Principal/Senior Scientist

<h3>Job Description</h3>
Job Description Medical Physicist PhD Cert - Troy - Radiation Oncology - FT/First Shift US-OH-Troy Job ID: 2024-50824 Type: Full-Time # of Openings: 1 Category: Physicist KH Troy Overview 
Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it’s by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.
 Responsibilities 
Key Responsibilities:
<ul>
<li>Clinical Support: Provide expert medical physics support for Radiation Oncology procedures, ensuring optimal performance and safety of all equipment. Opportunity to contribute to Gamma Knife and HDR procedures located at main campus.</li>
<li>Equipment Management: Oversee the acquisition, installation, calibration, and acceptance of radiation treatment equipment, maintaining meticulous records and documentation.</li>
<li>Quality Assurance: Ensure compliance with quality measures and standards as set by the State of Ohio, documenting all quality assurance activities.</li>
<li>Professional Development: Maintain up-to-date knowledge and skills within the field, pursuing ongoing professional development and adhering to legal and ethical standards.</li>
<li>Patient Advocacy: Advocate for patient safety and high-quality care, actively participating in performance improvement initiatives and utilizing organizational resources effectively.</li>
<li>Mission Alignment: Uphold the organization’s mission, vision, values, and philosophies in all aspects of work and collaboration with the Radiation Oncology department.</li>
</ul>
 Qualifications 
Qualifications:
<ul>
<li>Education: PhD, DMP, or MS in medical physics or a related field. Board certification in Therapeutic Medical Physics is preferred, but we encourage board-eligible candidates to apply and continue to pursue certification.</li>
<li>Experience: A minimum of two years of recent clinical medical physics experience in Radiation Oncology is preferred.</li>
<li>Certification: Board certification in Therapeutic Medical Physics preferred. Must obtain BLS certification upon hire.</li>
<li>Candidates: MS, DMP, or PhD board-certified or board-eligible candidates are strongly encouraged to apply.</li>
</ul>
#PM21
 
Compensation details: 108.29-151.61
 
PI3fc1de845092-25405-35498376

Medical Physicist PhD Cert - Troy - Radiation Oncology - FT/First Shift

<h3>Job Description</h3>
Job DescriptionManufacturing Chemist
Title: Manufacturing Chemist
Location: Lewisville, TX (75056)
Salary: $75,000 - $90,000
We manufacture leading brands serving the HVAC/R and building-construction tades across North America. We're known for durable, innovative products and dependable support specializing in chemical manufacturing solutions tailored to industrial and commercial applications.&nbsp;
What You Will Be Doing
<ul>
<li>Performing product quality control testing and updating QC protocols.</li>
<li>Developing new formulations and evaluating existing ones to support product innovation and improvement.</li>
<li>Maintaining and updating Safety Data Sheets (SDS).</li>
<li>Ensuring compliance with EPA, DOT, OSHA, and internal safety standards.</li>
<li>Preparing and submitting regulatory reports (e.g., FIFRA, HazMat, Tier II).</li>
<li>Supporting production teams with troubleshooting and process optimization.</li>
<li>Collaborating across lab and manufacturing teams to ensure product consistency and safety.</li>
</ul>
What You Need For This Job
<ul>
<li>Education: Bachelor's degree in Chemistry, Chemical Engineering, or a related field.</li>
<li>Experience: At least 2 years in chemical manufacturing, product development, or quality control.</li>
<li>Regulatory Knowledge: Strong understanding of EPA, DOT, and compliance reporting requirements.</li>
<li>Technical Skills: Ability to develop and refine chemical formulations; strong organizational and technical writing skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>Familiarity with ISO or other quality management systems.</li>
<li>Knowledge of process safety and chemical hazard assessments.</li>
<li>Industry experience in one or more of the following:
<ul>
<li>Liquid blending</li>
<li>Food processing</li>
<li>Paint or coatings manufacturing</li>
<li>Personal care product manufacturing</li>
<li>Aerosol production</li>
<li>Oil/lubricants production</li>
<li>Automotive or janitorial chemical production</li>
</ul>
</li>
</ul>
What's In It For You
Full Benefit's Package (Medical, dental, vision, PTO, 401K &amp; More!!)
If interested, Please send an updated resume with desired salary pay to <a href="mailto:CHRIS.BARBER@CYBERCODERS.COM" target="_blank">CHRIS.BARBER@CYBERCODERS.COM</a>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. This job was first posted by CyberCoders on 09/03/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please contact a member of our Human Resources team to make arrangements.

Manufacturing Chemist

<h3>Job Description</h3>
Millbrook Support Services is seeking a local contract Physicist for a local contract job in East Orange, New Jersey.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 11/01/2025</li>
<li>Duration: 26 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Local Contract</li>
</ul>
Millbrook Support Services Job ID #25-00269.
About Millbrook Support Services
Millbrook specializes in placing healthcare providers of varying specialties with clients throughout the United States. Want to work for a company that actually invests in your future? Along with offering providers attractive assignments with our world class customer base, Millbrook focuses on value-added training programs to help keep providers up to date in the latest advancements in medicine and technologies. We offer local and travel assignments from 13 weeks to one year. Our qualified staffing specialists are standing by and ready to help match your medical expertise with a thrilling new opportunity!

Local Contract Physicist

<h3>Job Description</h3>
Job Description:
The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines, address excursions and conduct investigations.
 
Essential Job Responsibilities:
⦁ Attire gowning for Grade B/A manufacturing areas and collect EM samples for viable air, non-viable particulates, and surface viable samples.
⦁ Perform QC testing of samples for bioburden, microbial identification, growth promotion, and Endotoxin analysis.
⦁ Receive manufacturing samples for QC analysis, ship samples to the contract labs testing, review data for lot disposition.
⦁ Read and Review routine EM plates, lab testing data, logbooks, and documents for product release and trend reports.
⦁ Understand and follow aseptic behavior, good laboratory and manufacturing practices, and documentation.
⦁ Author/update laboratory procedures, protocols, and help in EM data trend reports.
⦁ Support cleanroom qualification, gowning qualification, aseptic process qualification, and personnel monitoring for manufacturing activities.
⦁ Initiate Incident reports for OOS results and work with the team to find a root cause and corrective actions.
⦁ Perform QC lab support activities like lab set up, housekeeping, instrumentation maintenance, and coordinate instrument calibration.
 
Required:
⦁ B.S. degree in Biology/ or other life science related degree with 0-3 years of relevant industry experience in a quality control role. 
⦁ While working towards a completed B.S. degree, consideration will be given to associate degree in Biology or related life sciences with 2-5 years direct industry experience.
⦁ Excellent knowledge of Aseptic technique and common microbiological testing
⦁ Knowledge of relevant, compliance and guidance documents
⦁ Must be able to gown into cleanrooms in support of testing and manufacturing activities
⦁ Good documentation (ALCOA +) and data organization
⦁ Ability to work weekends is required; while most of the schedule will be during a standard work week, there will be regular weekend work.Interpersonal skills and ability to contribute to the success of a team
 
Preferred:
⦁ Proven history of working in a fast-paced team environment, time management, and meet deadlines.
⦁ Team player with the ability and willingness to support other colleagues in the Quality Control department. 
⦁ This support may include future cross training with analytical assays as needed
⦁ 
⦁ Models our Core Values: Bold, Caring, and Results-Driven - consistently exemplifies the culture we strive to create, operates with transparency, and earns trust.

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