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<h3>Job Description</h3>
Job Description
Location: Cambridge, MA
*This role will require regular presence at our client sites in Cambridge, MA*
**This role is not eligible for relocation assistance**
The Zifo Lab Automation Analyst provides technical laboratory automation services, including multivendor instrument, information technology and validation/compliance services when applicable. The individual will work as part of Zifo’s Lab Automation team to implement customer needs and address gaps to propose solutions for the desired automated state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support teams.  
Requirements
<ul>
<li>Provides technical support of customer laboratory environments </li>
<li>Ensure that common automation equipment is properly maintained and in good working order. This includes stand-alone liquid handlers (Hamilton, Echo, Tecan, etc), plate readers (SpectraMax, Envision, Neo2, etc) plate washers/dispensers, as well as several fully integrated robotic systems. </li>
<li>Install, operate, maintain, QC, troubleshoot problems, create methods/scripts, and train users on instruments is required. </li>
<li>Configured in-lab settings for automation software (eg: Cellario, Green Button Go) as required to train robotic equipment. </li>
<li>Perform unit test scripts for in-Lab automation equipment to validate the remote programmed software. </li>
<li>Able to build and operate debugging scripts and perform simple parallel development in the production environment. </li>
<li>Modify existing systems, instruments, methods and software to meet evolving needs. </li>
<li>Work collaboratively with discovery, engineering and expression groups at the local sites to optimize research efficiencies through implementation of automation process improvements and novel technologies </li>
<li>Ensures adherence to client’s corporate policies through periodic reporting and compliance programs </li>
<li>Document procedures, policies, troubleshooting and best practices </li>
<li>Perform system preventative maintenances based on client’s schedule, if applicable </li>
</ul>
Required Skills: 
<ul>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code </li>
<li>Experience in the operation, maintenance, troubleshooting and scripting for liquid handlers, dispensers, plate washers, plate readers, Octet, etc. required. </li>
<li>Programming experience using Python, Java, C# or VB.NET </li>
<li>Experience with scheduling, operation, training and troubleshooting of fully integrated robotic systems </li>
<li>Expertise with Hi-Res BioSolutions’ Cellario or Biosero’s Green Button Go scheduling software is a plus. </li>
<li>Experience with Titian Mosaic is a plus </li>
<li>Exemplary interpersonal skills including the ability to work with other automation engineers and non-automation scientists. </li>
<li>Excellent organizational skills, as exemplified by an aptitude for clear record-keeping and data analysis, and the ability to prioritize work across multiple projects. </li>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests </li>
<li>Ability to troubleshoot complex instrument and technology issues </li>
<li>Strong oral and written communication skills </li>
<li>Ability to identify, track and complete tasks for multiple projects </li>
</ul>
About you: 
<ul>
<li>Independent, self-motivated &amp; results driven individual </li>
<li>Willingness &amp; ability to acquire quickly new technical skills &amp; business principles </li>
<li>Ability for Critical Thinking and Logical Reasoning  </li>
<li>Good understanding of pharmaceutical research and drug Discovery &amp; development processes and biologics workflows (preferred, not required) </li>
</ul>
Required Education/Experience:
<ul>
<li>Bachelor of Science in computer science, life science or equivalent industry experience </li>
<li>2+ years of relevant technical experience including (but not limited to); biotech/pharmaceutical company or an automation provider. </li>
<li>Experience with scientific instrumentation (preferred) </li>
</ul>
Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Lab Automation Analyst

<h3>Job Description</h3>
Job Description
Join a fast-paced, hands-on cannabis team where quality and collaboration drive everything we do. As a Post Processing Technician 3, you'll take the lead in our Processing department, overseeing daily operations while actively contributing to every step of the process-from harvest to cure. Working closely with the Processing Supervisor, you'll help coordinate team tasks, uphold quality standards, and keep our workflow running smoothly across trimming, bucking, inspections, sorting, and inventory control.
This role is ideal for someone who thrives in a structured environment but brings flexibility, focus, and a sharp eye for detail. You'll be training new team members, guiding daily priorities, and ensuring everything is done to spec, all while staying hands-on in a production setting. You'll also play a role in writing and improving standard operating procedures, supporting scheduling efforts, and helping manage team performance with input from leadership and HR.
We're looking for someone with excellent communication skills and the ability to maintain clarity and respect in a team setting. You should be comfortable with physically demanding work, including standing for long periods, lifting up to 50 pounds occasionally, and using fine motor skills for manual tasks. Previous experience is preferred but not required-we're happy to train the right person with the right attitude.
If you're ready to grow your career in a supportive, start-up environment where no two days are the same, we'd love to hear from you.

Post Processing Technician 3

<h3>Job Description</h3>
Job DescriptionAbout UsDeep Genomics is at the forefront of integrating artificial intelligence and complex biology to transform drug discovery. Our proprietary machine learning platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, genetics, chemistry and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how medicines are created. About the RoleThe Principal Research Associate/ Research Scientist will join our in vivo Pharmacology team within the Platform Biology group and will be a key player in driving our cutting-edge AI RNA therapeutics discovery platform. In this role, you will be responsible for helping lead in vivo therapeutic efficacy testing efforts of novel RNA therapeutics in various animal models. You will also support target validation, therapeutic lead optimization and drug profiling through the implementation and execution of novel molecular assays to advance our internal therapeutics portfolio. The ideal candidate will have a strong molecular biology background with expertise in processing tissue samples as well as experience with rodent models. Relevant knowledge of RNA modalities such as ADAR, ASO, mRNA and/or siRNAs is also highly beneficial. The successful candidate should demonstrate initiative and be able to thrive in a dynamic work environment with cross-functional teams working together to achieve company goals. Title is commensurate with prior experience.&nbsp; This position is onsite at our Cambridge, MA site.Key Responsibilities
<ul>
<li>Perform standard molecular biology techniques in a consistent and reproducible manner (e.g. PCR, qPCR, ddPCR, ELISA, Western blot, Jess/Leo capillary-based Western blot, etc.).</li>
<li>Support the development of novel molecular, cellular and functional assays on animal samples for our internal therapeutic pipeline.</li>
<li>Plan and execute in vivo rodent studies to enable drug discoveryCollaborate with a cross-functional team in a dynamic, matrixed environment to achieve shared company deadlines.</li>
<li>Clearly document experiments, standard operating procedures (SOPs) and data in an electronic lab notebook (ELN).</li>
<li>Communicate and present experimental design and findings with colleagues and project teams</li>
</ul>
Basic Qualifications
<ul>
<li>Degree in Pharmacology, Biology, Molecular Biology, Genetics, Biochemistry or a related field with a BS and 6-8+ years of relevant experience, a MS and 4-6+ years of relevant experience, or a PhD and 0-2+ years of relevant pharmaceutical or biotechnology experience.</li>
<li>Strong understanding of molecular biology and tissue sample processing for RNA and protein readouts as well as a familiarity with Next-Generation Sequencing techniques (NGS).</li>
<li>Experience with rodents, running animal studies, and in vivo study design is highly desirable.</li>
<li>Experienced in design,&nbsp; execution and analysis of molecular assays.</li>
<li>Excellent communication, organizational skills and a willingness to learn.</li>
<li>Ability to work independently and manage priorities in a fast-paced technical environment</li>
</ul>
Preferred Qualifications
<ul>
<li>Hands-on experience using liquid handlers is preferred (ex. Beckman Echo, Agilent Bravo and Hamilton STAR/STAR V.).</li>
<li>Past experience with RNA editing and/or RNA oligonucleotides.</li>
<li>Knowledge of histology and immunohistochemical assays and quantification is a bonus.</li>
<li>Demonstrated experience working in cross-functional teams.</li>
<li>Experience working in an advanced data and computing environment.</li>
</ul>
What we offer
<ul>
<li>A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery.&nbsp;</li>
<li>Highly competitive compensation, including meaningful stock ownership.</li>
<li>Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program.&nbsp;</li>
<li>Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days.</li>
<li>Maternity and parental leave top-up coverage, as well as new parent paid time off.&nbsp;</li>
<li>Focus on learning and growth for all employees - learning and development budget &amp; lunch and learns.</li>
<li>Facilities located in the heart of Toronto - the epicenter of machine learning and AI research and development, and in Kendall Square, Cambridge, Mass. - a global center of biotechnology and life sciences.</li>
</ul>
Deep Genomics welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process. Deep Genomics thanks all applicants, however only those selected for an interview will be contacted.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Principal Research Associate/Research Scientist, in vivo Pharmacology

<h3>Job Description</h3>
Job Description
Job Description
We are seeking a Chemical / Process Engineer to join our team. The ideal candidate will develop, maintain, and optimize our chemical finishing processes while ensuring safety, quality, and compliance with industry standards. This role is hands-on and requires close collaboration with production, quality, and environmental health &amp; safety teams.
Responsibilities
<ul>
<li>
Develop, implement, and improve electroplating, anodizing, conversion coating, and passivation processes.
</li>
<li>
Monitor and control chemical bath conditions, ensuring consistent performance and compliance with specifications.
</li>
<li>
Troubleshoot and resolve process issues related to adhesion, corrosion resistance, and finish quality.
</li>
<li>
Support audits and maintain compliance with NADCAP, ISO, AS9100D, and customer specifications.
</li>
<li>
Drive process improvements using Lean, Six Sigma, and data-driven problem solving.
</li>
<li>
Ensure compliance with environmental, health, and safety regulations for chemical handling and waste treatment.
</li>
<li>
Document standard operating procedures, work instructions, and process records.
</li>
<li>
Collaborate with cross-functional teams to meet production, quality, and cost goals.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s degree in Chemical Engineering, Materials Science, Chemistry, or a related field.
</li>
<li>
3+ years of experience in chemical or surface finishing processes (electroplating, anodizing, coatings, etc.).
</li>
<li>
Strong understanding of process control, bath chemistry, and troubleshooting.
</li>
<li>
Familiarity with NADCAP, ISO, and AS9100 requirements preferred.
</li>
<li>
Knowledge of safety practices for handling hazardous chemicals.
</li>
<li>
Excellent problem-solving, analytical, and communication skills.
</li>
<li>
Ability to work hands-on in a production environment.
</li>
</ul>
Preferred Certifications (Not Required)
<ul>
<li>
Lean Six Sigma (Green Belt or higher).
</li>
<li>
Certified Quality Engineer (CQE).
</li>
<li>
OSHA / HAZWOPER or other EHS-related training.
</li>
<li>
Professional Engineer (PE) license is a plus.
</li>
</ul>
Benefits
<ul>
<li>
Competitive salary with performance-based incentives.
</li>
<li>
Health, dental, and vision insurance.
</li>
<li>
Retirement plan with company match.
</li>
<li>
Paid time off and holidays.
</li>
<li>
Opportunities for career growth and professional development.
</li>
</ul>
Company DescriptionCentral Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver. 
<h3>Company Description</h3>
Central Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver.

Chemical Process Engineer

<h3>Job Description</h3>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $70,000 - 90,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

QC Chemist II

<h3>Job Description</h3>
Job Description
Chemical Packager
KEY ACCOUNTABILITIES

<ul>
<li>Safely handle chemicals by following detailed instructions for filtering, packaging and cleaning.</li>
<li>Proper execution of packaging instructions for batch travelers.</li>
<li>Follow detailed instructions for filtering and or packaging chemicals.</li>
<li>Clean mix vessel and other equipment, using detergents, brushes, or scrapers.</li>
<li>Able to operate within and follow established Company quality and safety standards.</li>
<li>Move product inventory to and from appropriate areas.</li>
<li>Work under close supervision.</li>
<li>Other duties as assigned to support the efficiency of the packaging operation.</li>
<li>Works on quality initiatives such as 5’s and safety projects</li>
<li>Updates the packaging MPC and keeps packaging logs up to</li>
</ul>

JOB QUALIFICATIONS

<ul>
<li>High School education or GED</li>
<li>Ability to read and write English</li>
<li>Good communication skills</li>
<li>Computer skills a plus</li>
</ul>
WORK ENVIRONMENT

<ul>
<li>Ability to tolerate moderate noise levels.</li>
<li>Ability to tolerate OSHA safe levels of solvents, airborne particles and toxic or caustic chemicals with a minimum of discomfort, as is sometimes experiences in a laboratory and/or manufacturing environment.</li>
</ul>
PHYSICAL REQUIREMENTS
<ul>
<li>May require lifting 50 pounds on a regular basis</li>
<li>Ability to wear personal protective equipment</li>
<li>Ability to stand for long periods of time</li>
</ul>
Company DescriptionBlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers. 
<h3>Company Description</h3>
BlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers.

Chemical Packager- Hiring ASAP (Up to $23/hr)!!!

<h3>Job Description</h3>
Job Description
Description
The client is seeking a motivated full time contract Biostatistician. This is a hybrid position (requires minimum of 1 day/ week in the office in Watertown, MA). In this role, you will be supporting all statistical activities across multiple studies at the biotech including study monitoring, reporting, simulation studies and generating real word evidence. The position reports to the Head of Biometrics.
Responsibilities
• Perform simulations, modeling, and validation of datasets, tables, listings, and figures to ensure accuracy and compliance.
• Independently perform statistical analyses as per the analysis plan. Collaborate with study teams to ensure the delivery of high-quality outputs according to the timelines. Identify and anticipate issues arising in the study design, conduct and propose scientifically sound approaches. 
• Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.
• Work collaboratively with multifunctional study teams.
Additional Skills &amp; Qualifications
• Minimum Ph.D. in Statistics or related field
• Strong proficiency in R and Python 
• Extensive experience in simulation, various data visualization, and analytics
• Previous internship or work experience at a biotech or CRO is a plus 
• Excellent communication skills, strong organizational skills, and ability to work independently in a fast-paced setting.
Job Type &amp; Location
This is a Contract position based out of Watertown, MA.
Pay and Benefits
The pay range for this position is $45.00 - $55.00/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 hybrid position in Watertown,MA.
Application Deadline
This position is anticipated to close on Nov 14, 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.

Biostatistician

<h3>Job Description</h3>
Job Description
Position: Scientist – Immunology Discovery
Location: Cambridge, MA
Type: Contract | Onsite
A leading biotech company in Cambridge, MA is seeking a passionate and detail-oriented Scientist to join its Immunology Discovery team. This role is ideal for someone with hands-on experience in cell-based assays, organoid culture, and immunological techniques who thrives in a fast-paced, collaborative research environment.
Key Responsibilities
<ul>
<li>Culture and maintain human colon organoids for experimental use.</li>
<li>Perform cell-based assays using mammalian cell lines and primary cells to assess proliferation, cytokine release, and gene expression.</li>
<li>Utilize advanced molecular and cellular biology techniques including flow cytometry, ELISA, MSD, HTRF, and qPCR.</li>
<li>Process animal and human tissue ex vivo and isolate immune cells as needed.</li>
<li>Independently design, execute, and interpret experiments to support project goals.</li>
<li>Collaborate across teams to support organoid needs and share data insights.</li>
<li>Innovate and implement new protocols and techniques.</li>
<li>Analyze and report data clearly and consistently in both individual and group settings.</li>
</ul>
Required Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Biological Sciences or related field with 2+ years of industry experience.</li>
<li>Strong experience in in vitro cell culture, including sterile techniques and handling of challenging cell types.</li>
<li>Experience with human colon organoids and primary epithelial cells.</li>
<li>Hands-on experience with immune cells (e.g., monocytes, macrophages, dendritic cells).</li>
<li>Proficiency in immunoassays such as flow cytometry, ELISA, MSD, and HTRF.</li>
<li>Skilled in gene expression analysis via qPCR.</li>
<li>Excellent organizational, communication, and problem-solving skills.</li>
<li>Ability to work independently and collaboratively in a dynamic environment.</li>
<li>Flexibility to work weekends and holidays as needed.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience with ex vivo animal tissue processing.</li>
<li>Familiarity with GMP documentation and cleanroom gowning.</li>
<li>Knowledge of regulatory standards (USP, EP, JP, ICH guidelines).</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Job Type &amp; Location
This is a Contract position based out of Cambridge, MA.
Pay and Benefits
The pay range for this position is $35.00 - $38.00/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 Cambridge,MA.
Application Deadline
This position is anticipated to close on Nov 21, 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.

Biologist II

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
We are seeking an individual who will perform routine single plex and multiplex immunohistochemistry in drug discovery programs. 
</li>
<li>
The successful candidate will work in a group providing research support in target validation, target distribution, animal model development, pharmacology, and exploratory safety studies. 
</li>
<li>
Being detailed oriented is critical to this role. 
</li>
<li>
Specific activities will include immunohistochemistry performed on the Leica Bond Rx platform therefore, familiarity with this technology is important. 
</li>
<li>
Exposure to multiplex using the Lumiphores COMET platform will be available. 
</li>
<li>
Additional tasks include using computer-based laboratory tracking system (Sample Manager), Dream Path, interaction with study pathologists and project teams as well as inclusion in a highly dynamic, motivated team of immunohistochemistry scientists and histotechnologists.
</li>
<li>
Routine work with chemicals
</li>
</ul>
Qualifications:
<ul>
<li>
B.S./B.A. in Biology/Chemistry or related field
</li>
<li>
Microsoft office skills
</li>
<li>
Qualification in IHC (QIHC) preferred but not required
</li>
<li>
Working knowledge of the Leica Bond Rx IHC platform
</li>
<li>
Ability to troubleshoot IHC
</li>
<li>
Ideally 3-5 years of experience within a histology/ pathology laboratory
</li>
<li>
Well organized
</li>
<li>
Attention to detail
</li>
<li>
Adherence to established protocols and laboratory documentation requirements
</li>
<li>
Ability to work and effectively communicate within a team environment
</li>
<li>
Ability to handle multiple projects simultaneously
</li>
<li>
Delivery of high-quality, timely results
</li>
<li>
Excellent oral and written communication skills
</li>
<li>
Enthusiastic
</li>
<li>
Independent, analytical, innovative thinker
</li>
<li>
Proficiency with MS office-Excel, OneNote
</li>
<li>
Immunohistochemistry experience acquired at pharmaceutical, CRO or biotechnology company
</li>
<li>
Team-oriented
</li>
<li>
Comfortable working independently after a thorough period of training and onboarding as well as the ability to prioritize workload to manage several tasks. 
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist

<h3>Job Description</h3>
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These owners, who share the belief that the majority of property loss is preventable, represent many of the world’s largest organizations, including one of every four Fortune 500 companies. They work with FM to better understand the hazards that can impact their business continuity to make cost-effective risk management decisions, combining property loss prevention with insurance protection.
 
The purpose of this position is to develop new scientific knowledge, technologies and engineering solutions to problems in material flammability, fire dynamics and Lithium-ion battery safety research, which can be used for the prevention or control of industrial property loss.&nbsp;&nbsp;&nbsp;
The principal responsibilities are to carry out research projects in the areas of flammability, fire spread, and heat transfer in fires from solid combustible as well as Lithium-ion batteries. Key areas of research include understanding of fire behavior at the medium and large scales via bench-scale experiments and theoretical models on material flammability and flame heat transfer. Projects can also involve advanced flame diagnostic of buoyant turbulent sooty flames and wall fires. The experimental and theoretical studies will be closely integrated with Computational Fluid Dynamic (CFD) model development and validation within the work group.&nbsp;
The position is responsible for all aspects of project management including project proposals, execution, and reporting.
 
The position requires a PhD in Mechanical, Chemical Engineering, Fire Protection Engineering, or related fields with a strong fundamental background in combustion, fluid mechanics, heat transfer, material science and applied mathematics.&nbsp; Extensive experience in experimental methods in thermal fluids, material flammability, heat transfer, combustion/fire, and an understanding of associated numerical methods are required. Research experience with advanced laser diagnostics in flame, experimental measurement in turbulent flame, heat transfer and failure analysis of battery is desirable. Also needed are excellent written and verbal communication skills, as well as demonstrated expertise in developing solutions to challenging technical problems.
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
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