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<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Pharmaceutical Technician Job Description
We are seeking a dedicated Clean Room Pharmaceutical Technician for our 2nd Shift (1pm - 11:30pm), working Sunday through Wednesday with a schedule of four 10-hour shifts. This position plays a crucial role in operating production equipment, including non-sterile filling machines, packaging, and labeling machines. The role involves supplying materials to assigned positions, cleaning equipment and production areas, and inspecting parts and items according to standard operating procedures. Additionally, this position requires basic troubleshooting and training assistance.
Responsibilities
<ul>
<li>Operate assigned equipment per established methods and procedures, including setup, operation, and cleaning.</li>
<li>Ensure configurations are correct, check for leaks or abnormalities, and communicate any issues immediately.</li>
<li>Complete operational documentation as per SOP and manage returned and rejected items.</li>
<li>Review and verify area production documentation for accuracy and real-time recording.</li>
<li>Maintain open communication with management regarding production updates, deviations, and corrective measures.</li>
<li>Exchange work status information with the department, management, and co-workers.</li>
<li>Maintain a clean work environment using appropriate cleaning solutions and methods.</li>
<li>Clean and sanitize designated equipment and tools per established methods and schedules.</li>
<li>Handle and procure raw materials and components as per prescribed methods and procedures.</li>
<li>Maintain Aseptic Process Area sterile gowning qualifications.</li>
<li>Respond immediately to equipment alarms or malfunctions and communicate conditions to experts.</li>
<li>Assist co-workers in the production of finished products according to SOPs and manufacturing instructions.</li>
<li>Receive and ship plant uniforms and scrub uniforms for cleaning.</li>
<li>Stock garments and supplies for clean rooms and sterile core, prepare garments for shipping and sterilization.</li>
<li>Assist with special projects as required or requested.</li>
<li>Promote a safe and harmonious work environment.</li>
<li>Maintain compliance with SOPs, GMPs, and all company policies.</li>
</ul>
Essential Skills
<ul>
<li>Associate or Bachelor's Degree from a regionally accredited institution.</li>
<li>One or more years of previous work experience in a hospital or manufacturing environment or clean room filling preferred.</li>
<li>Experience in a production environment, ideally in a clean room setting.</li>
<li>Basic mechanical skills related to equipment operation.</li>
<li>Knowledge and skill in operating specialized equipment such as filling, wash, and sanitizing equipment.</li>
<li>Knowledge of clean room procedures, preferred but not required.</li>
<li>Knowledge of and compliance with GMP regulations, preferred but not required.</li>
<li>Proficiency in general computer functions like Microsoft Office programs and spreadsheets.</li>
<li>Ability to handle multiple projects or tasks simultaneously.</li>
<li>Advanced problem safety sensitivity to recognize potential safety issues.</li>
<li>Strong time management techniques.</li>
<li>Attention to detail and focus on quality, accuracy, sterility, and aseptic technique.</li>
<li>Effective communication skills with coworkers and management.</li>
<li>Proficiency in math with understanding of measurements and conversions.</li>
<li>Ability to recognize deviations from procedures and communicate immediately.</li>
<li>Critical thinking ability.</li>
<li>Ability to maintain confidentiality of information and processes.</li>
<li>Ability to follow hygiene standards and wear protective attire as required.</li>
<li>Ability to solve practical problems and handle variables where limited standardization exists.</li>
<li>Flexibility in work hours.</li>
<li>Ability to provide motivational support.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in clean room procedures and compliance with GMP regulations is preferred but not mandatory.</li>
</ul>
Work Environment
This role is situated in a clean room, lab, and production environment. Employees must adhere to strict hygiene standards and safety procedures, wearing protective attire as necessary. The position operates during the 2nd shift hours, providing a structured yet flexible work schedule.
Job Type &amp; Location
This is a Contract to Hire position based out of Syracuse, New York.
Pay and Benefits
The pay range for this position is $24.00 - $26.60/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 Syracuse,NY.
Application Deadline
This position is anticipated to close on Nov 12, 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.

Clean Room Pharmaceutical Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
 Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
 With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners.
 Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more.
Job Description 
Eurofins Built Environment Testing is looking for an experienced TEM Asbestos Analyst in our Seattle, WA location.&nbsp; Relocation assistance may be available for the right candidate.
The Analyst performs analysis of bulk and air for asbestos mineral fibers using TEM -Transmission Electron Microscopy. &nbsp;&nbsp;Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation.
Responsibilities:
<ul>
<li>Prepare and analyze environmental samples for asbestos using TEM microscopy.</li>
<li>Adherence to EPA, NVLAP, ELAP, OSHA, and NIOSH standards for asbestos identification</li>
<li>Accurately enters and reports analytical data using the LIMS</li>
<li>Performs independent data reviews for other analysts’ work</li>
<li>Performs analysis of reference materials, proficiency samples and other quality control samples as needed</li>
<li>Maintains client service and provides technical support as needed</li>
<li>Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests</li>
<li>Performs confirmation of lab results as needed by client services personnel</li>
<li>Performs and completes all analytical testing QA related tasks as needed</li>
<li>Assists in pursuing, receiving and maintaining necessary laboratory accreditations</li>
<li>Maintains and updates all necessary Training and QA documents onsite as necessary</li>
<li>Co-ordinates and manages projects according to their rush status and due time for timely delivery</li>
<li>Assists co-workers on analytical questions, as necessary</li>
<li>Participates in Lean initiatives and projects when called upon</li>
<li>Follows company policies and procedures and ensures that coworkers are doing the same</li>
</ul>
Secondary Duties:
<ul>
<li>Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed</li>
<li>Manages and disposes analyzed samples as needed</li>
<li>Trains new asbestos testing Analysts as needed</li>
<li>Recommends and coordinates sample transfer as necessary</li>
<li>Establishes and maintains laboratory reference samples</li>
<li>Performs root cause analysis and determines and implements corrective actions for errors and issues as necessary</li>
<li>Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed</li>
<li>Routinely communicates available capacity to Regional Manager</li>
<li>Supports other departments within the lab (mycology, asbestos, bacteriology, and other) when appropriate and as needed</li>
<li>Other responsibilities as deemed necessary by the Supervisor/Manager</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>1+ years of experience performing asbestos microscopy&nbsp;</li>
<li>Must have an undergraduate degree in Geology, Biology or related science, or TEM Asbestos training course&nbsp;</li>
<li>Experience utilizing a Transmission Electron Microscope preferred</li>
<li>Must be willing to relocate to Seattle, WA</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li>
</ul>
 Additional Information 
Compensation range: $23 - $27 per hour depending on qualifications and experience.
<ul>
<li>Position is Full-time Monday - Friday , 8AM - 5PM shift with overtime or weekend work as needed.&nbsp;</li>
<li>Candidates currently living within a commutable distance of Seattle, WA&nbsp;or are willing to relocate are encouraged to apply.&nbsp;&nbsp;</li>
</ul>
Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
We support your development!&nbsp;Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity!&nbsp;Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us!&nbsp;We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR 6.95 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

TEM Asbestos Analyst located in Seattle, WA - Eurofins Built Environment Testing

<h3>Job Description</h3>
Job DescriptionWho is BlueRock? BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investigational cell therapies, bemdaneprocel (BRT-DA01) for the treatment of Parkinson’s disease and OpCT-001 for the treatment of primary photoreceptor diseases are clinical stage programs. BlueRock was founded in 2016 as a joint venture of Versant Ventures and Leaps by Bayer. Our culture is defined by the courage to persist regardless of the challenge, the urgency to transform medicine and deliver hope, integrity guided by mission, and community-mindedness with the understanding that we are all part of something bigger than ourselves. What Are We Doing? Our&nbsp;foundational science&nbsp;harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit. We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options. We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. BlueRock Therapeutics is seeking an enthusiastic and driven individual to fill an exciting Research Associate (RA) level position at the RAI or RAII levels in New York City, NY.&nbsp; The successful candidate will support the development of cell therapy products and platforms at BlueRock by executing molecular and cell-based assays and will join the Myeloid Biology teamwithin the Neurology program based on their qualifications.&nbsp; Candidates in this role will be responsible for collaborating with various functional groups including research teams, discovery analytics, in vivo sciences, and gene editing to advance projects, including the coordination of sample testing, data analysis, and reporting. The ideal candidate will be a highly motivated, self-starting individual who enjoys hands-on scientific execution, collaboration, and is seeking valuable career experience.Responsibilities:
<ul>
<li>Be responsible for data generation, collection, interpretation, and communication of results under supervision.</li>
<li>Mammalian cell culture; maintenance of cell lines and primary cells under stringent sterility conditions.</li>
<li>Execute plate reader assays (for example, ELISA, Luminescence, biochemical assays).</li>
<li>Perform DNA/RNA-based, flow cytometric, immunofluorescence and other analytical assays as required.</li>
<li>Perform cell-based assays to evaluate cell function, behavior, phenotype</li>
<li>Analyze and document experimental data in electronic laboratory notebooks in a timely and accurate manner in accordance with the company quality management system.</li>
<li>Present scientific data to colleagues in group meetings, prepare and present internal and external presentations (presentations, posters, publications) as required.</li>
<li>Collaborate with other team members as needed to advance our programs.</li>
<li>Perform additional duties to support the safe and efficient operation of the laboratory, and other duties as assigned.</li>
<li>This position requires the employee to be on-site due to hands-on laboratory work.</li>
<li>This position requires occasional compensated overtime on the weekend.</li>
</ul>
Minimum Requirements:
<ul>
<li>Degree in Biological Sciences (Cell Biology, Stem Cell Biology or Molecular Biology etc.) or related discipline is required. B.S. with 0-5 years or M.S. with 0-2 years of experience.</li>
<li>Experience with&nbsp;microglia/macrophage&nbsp;cells is highly desired but not required</li>
<li>Prior hands-on experience with cell-based assays, characterization methods and cell culture (for example, human stem cells and primary cells) is required </li>
<li>Minimum of 1+ year experience in executing cell culture procedures under strict aseptic conditions</li>
<li>Ideal candidate has experience with standard molecular testing procedures, equipment and software including, but not limited to, DNA/RNA analysis (extraction, quantitation), qPCR, etc.</li>
<li>Great team player, ability to effectively communicate and collaborate with the larger team</li>
<li>A proven ability to be highly productive and successful in a high-paced work environment with excellent attention to details and meticulous bench work.</li>
<li>Excellent record-keeping skills required</li>
</ul>
$74,000 - $88,000 annually with bonus.#LI-AL1 BlueRock Therapeutics Company Culture HighlightsWinner of Boston Business Journal's Best Places to Work (Mid-size Company) 2023Winner of Comparably's Award for Best Company for Diversity 2022Winner of Comparably's Award for Best Company for Women 2022Winner of Comparably's Award for Best CEO 2022BlueRock Therapeutics is ranked in the top 5% of companies for Overall Culture on Comparably.Engineering Department is ranked in the top 5% of companies for Overall Culture on Comparably. Check us out on Comparably:&nbsp;<a href="https://www.comparably.com/companies/bluerock-therapeuticsFollow" target="_blank">https://www.comparably.com/companies/bluerock-therapeuticsFollow</a> us on Linkedin: <a href="https://www.linkedin.com/company/bluerocktx/" target="_blank">https://www.linkedin.com/company/bluerocktx/</a> Equal Opportunity Workplace:At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace.&nbsp; Please let us know if you require disability-related accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs.
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.

Research Associate II, Research (Myeloid Biology)

<h3>Job Description</h3>
Job Description
LNK International, Inc. is one of the nation's largest manufacturers of solid and liquid dose, over-the-counter (OTC) pharmaceuticals. For over 40 years, we have built a reputation for delivering the highest quality products, outstanding service and product innovation.
What sets LNK apart? We believe it is our employees. From our lab scientists who assists in various experiments and research, working under the direction of lead scientists and researchers to develop new analytical methods and techniques, as well as reviewing and interpreting results to provide insights and recommendations for further research.
Our full time employees enjoy competitive benefits including:
<ul>
<li>401(k) with generous employer match</li>
<li>Health Insurance</li>
<li>Dental Insurance</li>
<li>Paid holidays</li>
<li>Paid vacation</li>
</ul>
As a microbiologist you will work with and collaborate with a talented and dedicated group of experts.
Job Description:
<ul>
<li>Perform Media Preparation with growth promotion.</li>
<li>Maintain stock cultures weekly in the lab for positive controls.</li>
<li>Perform Water testing using the Water filtration method</li>
<li>Perform general micro lab duties and housekeeping including glassware cleaning and preparation.</li>
<li>Perform calibration and monthly maintenance of different equipment.</li>
<li>Perform Environmental Monitoring of all zones of the micro lab.</li>
<li>Sterilize biohazardous material by running autoclave cycles.</li>
<li>Perform Microbial limits on solid and liquid finished products at LNK International, Inc</li>
<li>Perform Antimicrobial Effectiveness testing on Liquid Products.</li>
<li>Prepare final reports.</li>
<li>Conduct and write Investigation reports for Out of Specification results.</li>
<li>Writing/ reviewing procedures.</li>
<li>Perform Microbial identification as per procedures.</li>
<li>Checking USP for any change in specification and/ or procedure.</li>
<li>Monitoring the microbiology laboratory testing and reviewing of other microbiologist(s) work.</li>
<li>Perform microbial testing on active and excipients of raw materials using USP/In-House method.</li>
</ul>
Requirements
<ul>
<li>Bachelor's degree.</li>
<li>Preference will be given to candidates with experience in the pharmaceutical field.</li>
<li>Excellent communications and presentation skills - written and verbal; fluent in English.</li>
</ul>
The salary listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as permitted by law. 
LNK provides equal employment opportunities to all applicants and prohibits discrimination of any type on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and pregnancy-related conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information or any other characteristic protected by applicable federal, state or local laws.
 Job Posted by ApplicantPro

Microbiologist

<h3>Job Description</h3>
Job Description
COMPANY OVERVIEW:
CERTERRA (formerly RMA Companies) is a growing national provider of testing, inspection, and certification services that support innovation in new product development, quality assurance, for project delivery, and engineered solutions for asset management. We are passionate about contributing to the sustainable development of the communities we serve.
We are a national firm with a global reach serving national and international clients from 30+ offices located in 10 states and are ranked on ENR’s Top 500 list alongside the nation’s top firms.
With a 60-year history, CERTERRA has a passion for high-end services, constant innovation, and investment in the development of world-class laboratory facilities, and interactive management technologies. Each member of our staff is committed to service, innovation, and the success of our clients.
 
Job Summary: We are seeking a Lab Supervisor to oversee our laboratory operations and ensure the highest quality of testing services. The supervisor will be responsible for supervising staff, assisting the Lab Director in developing and implementing lab policies and procedures, and maintaining compliance with regulatory standards. Qualifications
<ul>
<li>Associate’s degree in Engineering (preferred).</li>
<li>Minimum of 3+ years of experience with laboratory testing of construction materials, with at least 1+ years in a supervisory or managerial role</li>
<li>Strong knowledge of laboratory operations, quality control, and regulatory requirements</li>
<li>Excellent leadership, communication, and problem-solving skills.</li>
<li>Must have excellent interpersonal, verbal, and written communication skills.</li>
</ul>
Responsibilities
<ul>
<li>Oversee daily operations of the laboratory, including scheduling, staffing, equipment calibration and verification, and workflow management</li>
<li>Assist Lab Director in developing and implementing lab policies, procedures, and quality assurance programs</li>
<li>Ensure compliance with regulatory standards, accrediting agencies, and best practices</li>
<li>Lead and mentor laboratory staff, providing training and guidance as needed</li>
<li>Collaborate with other departments to ensure seamless integration of lab services</li>
<li>Handle any issues or concerns related to lab services promptly and effectively.</li>
</ul>
Technical Requirements:
<ul>
<li>American Concrete Institute (ACI) Certifications:</li>
<li>Aggregate Testing Technician - Level 1 or 2</li>
<li>Aggregate/Soils Base Testing Technician</li>
<li>Concrete Strength Testing Technician</li>
<li>Concrete Field-Testing Technician - Grade 1</li>
<li>Concrete Laboratory Testing Technician - Level 1 or 2</li>
<li>National Institute for Certification in Engineering Technologies (NICET): Construction Materials Testing: Asphalt, Concrete, Soils (Levels I, II, or III)</li>
<li>NJSAT Certifications: HMA Plant Technologist Level 1</li>
</ul>
Other Miscellaneous Qualities:
<ul>
<li>Familiarity with Lab Information Management Systems (LIMS)</li>
</ul>

Lab Supervisor

<h3>Job Description</h3>
Job Description
Description: Zifo is working with a large pharma client to build a team of laboratory IT (lab computing, &amp; Lab IT systems) professionals. 
**This role will require a 100% on-site presence in Albany, NY **
**This role is not eligible for relocation assistance**
Requirements
Responsibilities:
· Execute validation test plans once approved by client(s)
· Revise and route Lifecycle documents for review and approval
· Update relevant IT lifecycle documents
· Participate in Sandboxing sessions with multifunctional teams
· Coordinate delivery of PC hardware to various laboratories and manufacturing areas
· Troubleshoot and resolve any IT issues / tickets as needed
Qualifications:
<ul>
<li>Bachelor of Science in computer science, life science</li>
<li>Previous technical experience including (but not limited to); Windows technologies, networking, remote computing and backup systems preferred</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>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code</li>
<li>Experience with virtual machine support (preferred)</li>
<li>Experience with scientific instrumentation (preferred) </li>
</ul>
A successful Zifo-ite is:
<ul>
<li>Independent, Self-Motivated &amp; Results driven</li>
<li>Willing &amp; able to quickly acquire new Technical Skills &amp; Business Principles</li>
<li>A critical thinker who possesses logical reasoning</li>
<li>Curious and always looking for creative solutions to complex problems</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 Computing Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
This position plays a key role in supporting both laboratory operations and team leadership within a technical environment. The role involves overseeing daily lab activities, ensuring compliance and quality standards, and guiding team members to meet performance goals. It requires a balance of hands-on technical work and strategic leadership to drive continuous improvement and operational efficiency.
Laboratory Responsibilities
<ul>
<li>Manage and coordinate the training program for laboratory staff.</li>
<li>Conduct laboratory investigations and prepare reports.</li>
<li>Perform environmental monitoring and collect samples (e.g., compressed gas, water) to support departmental needs.</li>
<li>Coordinate equipment maintenance and calibration schedules.</li>
<li>Review and verify laboratory data through peer review.</li>
<li>Utilize the Laboratory Information Management System (LIMS) for tracking samples, test results, and reporting metrics.</li>
<li>Maintain the microbiological productivity database and generate monthly metrics reports.</li>
<li>Conduct acceptance testing of commercially prepared microbiological culture media, as needed.</li>
<li>Perform microbial identification procedures when required.</li>
</ul>
Leadership Responsibilities
<ul>
<li>Lead direct reports, group leaders, and their teams in technical environments such as laboratories or manufacturing facilities.</li>
<li>Promote and embody the company’s vision and values.</li>
<li>Oversee scheduling, task allocation, and the onboarding process for new hires.</li>
<li>Manage overtime and weekend work schedules as needed.</li>
<li>Develop and implement team-building strategies and initiatives.</li>
<li>Apply Lean principles to drive operational excellence.</li>
<li>Supervise daily operations of the Quality Control (QC) analyst team.</li>
<li>Coach, mentor, and support group leaders while monitoring team productivity.</li>
<li>Assist in the professional development of group leaders.</li>
<li>Coordinate and participate in interviews for new hires.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Chemistry, Life Sciences, Engineering, or a related scientific discipline.</li>
<li>Minimum of 3 years leading dynamic teams in technical or laboratory settings, with a strong emphasis on team development, coaching, and performance management.</li>
<li>At least 3 years of hands-on laboratory experience; prior work in a GMP-regulated environment is strongly preferred.</li>
<li>Demonstrated experience managing day-to-day lab operations, including workflow optimization, equipment oversight, and compliance with safety and quality standards.</li>
<li>Proven ability to serve as a liaison between internal teams and external clients, ensuring effective communication, timely project execution, and high client satisfaction.</li>
<li>Must be authorized to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager</li>
<li>60 Minute Onsite Meeting with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a second shift schedule (Monday through Friday, 2 pm- 10:30 pm), with occasional weekends and overtime required as needed. Candidates located within a commutable distance to Rensselaer, NY,&nbsp;are strongly encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays&nbsp;</li>
<li>Hourly pay ranges from&nbsp;$33&nbsp;to $38, based on education and relevant experience.</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Microbiology Operations Supervisor ( 2nd Shift Mon-Fri)

<h3>Job Description</h3>
Job Description
Geotechnical Engineer
Established consulting engineering firm seeks Geotechnical Engineer:
<ul>
<li>Civil Engineering degree with PE license</li>
<li>8+ years of experience</li>
<li>Foundations, soils, subsurface investigations</li>
<li>Pilings</li>
<li>Report writing and proposals</li>
<li>Project experience with commercial development</li>
<li>Client interaction skills</li>
<li>Project experience in Buffalo area desired</li>
</ul>
#civilmep
#midsenior

Sr Geotechnical Engineer

<h3>Job Description</h3>
Job Description
About Cleerly
We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. 
Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. 
At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. 
While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter, for some roles like sales or external facing roles travel could be up to 90% of the time.
About the Opportunity
We are seeking a highly skilled Staff Scientist to lead the design, development, validation of
innovative clinical workflow that can directly impact the diagnosis and treatment for heart
disease. In this senior-level role, you are responsible for architecting a cutting-edge product that
integrates our existing technologies while pushing the boundary of innovation in cardiac
vascular imaging. You will also represent the company in strategic research collaborations with
leading academic and clinical institutions, driving innovation at the intersection of AI and
cardiovascular health.
About the Team
You will join our expert Computational Imaging team, where we develop sophisticated algorithms to enhance and improve medical imaging. We are focused on improving the quality and clinical value of medical images, creating powerful, extra software components that correct artifacts, standardize data, and ensure the utmost precision before the final analysis. Our work is essential for elevating the reliability and accuracy of Cleerly's regulated products.

Responsibilities
<ul>
<li>Research and develop state-of-the-art AI and non-AI algorithms for coronary CT/fluoroscopy imaging applications.</li>
<li>Implement an efficient and robust image processing pipeline to solve challenging problems in low latency environments.</li>
<li>Translate product and clinical requirements into algorithmic specifications in collaboration with Product and Clinical teams.</li>
<li>Partner with Regulatory Affairs to support regulatory submissions (e.g., 510(k), De Novo,PCCP), including generating evidence and documentation.</li>
<li>Collaborate with engineering teams to deploy AI and non-AI based solutions in clinical practice.</li>
<li>Communicate findings and strategy to internal stakeholders and leadership through clear technical documentation, presentations, and demos.</li>
<li>Contribute to intellectual property development through patents and scientific publications.</li>
<li>Mentor junior scientists and foster a culture of technical excellence and scientific rigor.</li>
</ul>
Requirements 
<ul>
<li>Ph.D. in Computer Science, Data Science, Biomedical Engineering, Biomedical Imaging, or a related technical field, with 5+ years combined postdoc and/or industry experience; OR an M.S. with 8+ years of relevant experience.</li>
<li>R&amp;D experience in medical image processing, demonstrating subject matter expertise in image quality enhancement, optical flow analysis and 2D&amp;3D rigid/deformable image registration.</li>
<li>Proven track record of publications in top-tier medical imaging or computer vision conferences and journals (e.g., MICCAI, IEEE TMI, CVPR, Medical Image Analysis).</li>
<li>Strong experience in C++ and Python.</li>
<li>Prior experience with ITK, OpenCV, VTK, CMake, Slicer is a plus</li>
<li>Prior experience with cardiac motion modelling or tracking is a plus</li>
<li>Excellent interpersonal, cross-functional, and cross-cultural collaboration skills.</li>
</ul>
Preferred qualifications
<ul>
<li>5+ years of industry experience in AI-based medical device development or clinical deployment.</li>
<li>Experience supporting FDA regulatory submissions for ML-based software, including familiarity with De Novo, 510(k), and PCCP pathways.</li>
<li>Deep domain knowledge in cardiovascular imaging and CT interpretation workflows.</li>
</ul>
TTC*: $265k - $305k
*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.).
Each role at Cleerly has a defined salary range based on market data and company stage. We typically hire at the lower to mid-point of the range, with the top end reserved for internal growth and exceptional performance. Actual pay depends on factors like experience, technical depth, geographic location, and alignment with internal peers.
Working at Cleerly takes HEART. Discover our Core Values:
<ul>
<li>H: Humility- be a servant leader</li>
<li>E: Excellence- deliver world-changing results</li>
<li>A: Accountability- do what you say; expect the same from others</li>
<li>R: Remarkable- inspire &amp; innovate with impact</li>
<li>T: Teamwork- together we win</li>
</ul>
Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.
OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.
By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (<a href="https://cleerlyhealth.com/privacy-policy" target="_blank">https://cleerlyhealth.com/privacy-policy</a>). All official emails will come from @cleerlyhealth.com email accounts. 
#Cleerly

Staff Scientist, Computational Imaging

<h3>Job Description</h3>
Job Description
This is a full-time hybrid role for an Earth Scientist / Geophysicist located in the New York City Metropolitan Area, allowing for some work from home. The Geophysicist will be responsible for conducting geophysical (GPR, EM, etc.) surveys, data acquisition, and data processing. They will also be involved in analyzing geophysical data, preparing reports, and collaborating with cross-functional teams to deliver precise and accurate findings.

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