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<h3>Job Description</h3>
Shift:
Monday through Friday, 8:00AM - 5:00PM
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
Associate Scientist I
Pace Analytical Life Sciences, LLC is a premier Contract Research and Development Organization located just north of Cambridge, MA providing pharmaceutical development services for small molecules, biologics, oligonucleotide therapeutics, and other biopharmaceutical drug candidates.
Compensation: $28.00 per hour
Summary
We seek a motivated Associate Scientist with laboratory experience to conduct analytical testing and development experiments that support our client’s effort to develop oligonucleotide and mRNA therapeutics. Our clients include biotechnology and pharmaceutical companies from new startups to those with global operations. This individual will conduct analytical and bioanalytical testing of samples using written procedures and support the development of new methods. Competitive applicants will be able to demonstrate a knowledge of analytical methods for pharmaceuticals, creative problem solving, an ability to collaborate in a cross-functional team, and clearly communicate scientific results. This is an entry level, full-time bench scientist position in Woburn, MA suitable for a recent graduate or someone of limited pharmaceutical experience.
General Responsibilities:
<ul>
<li>Perform testing with good documentation practices using written methods and procedures</li>
<li>Execute development experiments, analyze data, write analytical test methods.</li>
<li>Present results and planned experiments clearly and concisely both verbally and in written reports.</li>
<li>Strive to meet agreed-upon timelines and regularly communicate progress to other stakeholders.</li>
<li>Follow standard operating procedures and other guidance documents as directed by management.</li>
<li>Maintain scientific instruments and troubleshoot problems as needed.</li>
<li>Maintain a clean and organized laboratory including shared benches, sample storage, etc.</li>
<li>Continuously improve technical skills and acquire knowledge specific to the pharmaceutical industry.</li>
</ul>
An Ideal Candidate will possess skills in one or more of the following areas:
<ul>
<li>Experience using analytical instruments such as chromatography (HPLC/UPLC), electrophoresis (PAGE, CE), spectrometry (LC-MS), and spectroscopy (UV/Vis).</li>
<li>Experience using or developing methods to determine the identity, purity, and assay of drug substance and product samples.</li>
<li>Knowledge of the physical and chemical properties of biological polymers (e.g., RNA, DNA, proteins)</li>
<li>Understand the scientific principles of new analytical techniques as well as the hardware and software needed to operate scientific instruments.</li>
</ul>

Required Education and/or Experience:
<ul>
<li>Education in chemistry, biochemistry, or closely related discipline and a B.S. with 0 – 2 year’s of industry experience performing routine testing or developing analytical methods for nucleic acid-based therapeutics.</li>
<li>Strong understanding of physical sciences at the undergraduate level.</li>
<li>Excellent written and oral communication skills.</li>
<li>Flexibility and outstanding time management skills.</li>
<li>Background maintaining and troubleshooting scientific instruments and equipment.</li>
</ul>
PHYSICAL/MENTAL REQUIREMENTS:
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.
WORKING ENVIRONMENT:
Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gasses, noxious odors and related items in a lab setting.
OFCCP Statement - Pace Analytical is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
Benefits When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Associate Scientist 1

<h3>Job Description</h3>
Job Description
As a PLM Lab Analyst, you will play a pivotal role in our laboratory operations. You will be responsible for the analysis and interpretation of bulk material samples for asbestos, applying your expertise to ensure the precision and quality of our results. We are open to hiring either an experienced professional or someone eager to learn, as we provide comprehensive training. As we continue to expand our operations, we are looking for a skilled and experienced Lab Analyst II to join our team.
 
 
Compensation:
$25 - $35 hourly
Responsibilities:
<ul>
<li>PLM Analysis: Perform Polarized Light Microscopy (PLM) analysis of bulk material samples for asbestos, including sample preparation and examination under a HEPA-filtered hood for complete worker safety.</li>
<li>Quality Control: Maintain strict quality control procedures to guarantee the accuracy and reliability of analytical results.</li>
<li>Instrumentation: Operate and maintain laboratory equipment and instruments related to asbestos analysis.</li>
<li>Documentation: Maintain detailed and organized records of all laboratory activities and results.</li>
<li>Safety: Adhere to laboratory safety protocols and procedures at all times to ensure a safe working environment.</li>
<li>Collaboration: Work closely with the laboratory team to meet project deadlines and maintain effective communication.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in a scientific field (e.g., Chemistry, Geology, Environmental Science) is preferred but not required.</li>
<li>Experience in laboratory analysis is a plus, but not mandatory; we are willing to train the right candidate.</li>
<li>Strong attention to detail and organizational skills.</li>
<li>Excellent problem-solving and analytical abilities.</li>
<li>Ability to work effectively in a team and independently.</li>
<li>Knowledge of laboratory safety protocols and practices.</li>
<li>Strong communication skills, both written and verbal.</li>
</ul>
About Company 
Grey Scope Labs is a leading environmental analysis laboratory specializing in asbestos identification. We are committed to delivering accurate and reliable results to clients, ranging from environmental agencies to industrial organizations.

Plm Analyst

<h3>Job Description</h3>
Job DescriptionJob title: Diagnostic Radiological Medical Physicist Schedule: Weekdays; mission-essential coverage possible What you’ll do Provide diagnostic imaging physics support, QA, and regulatory compliance across modalities to ensure safe, high-quality imaging services. Key responsibilities: • Perform acceptance/annual testing for CT, MRI, X-ray, fluoroscopy, mammography • Radiation safety consults; protocol optimization; technologist education • Documentation to meet DHA, Joint Commission, and NCR standards Qualifications: • CAMPEP-accredited graduate degree and imaging residency; ABR (Diagnostic Radiological Physics) or equivalent; BLS • 3–5+ years post-residency preferred • U.S. citizenship; mission-essential status possible Compensation: Estimated $95.00-$103.00 per hour&nbsp;&nbsp;&nbsp;&nbsp;#ICSP&nbsp;
Federal Staffing Resources (FSR)&nbsp;is an Equal Opportunity Employer and a proud partner in the Federal Government’s commitment to diversity and inclusion. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, protected veteran status, disability, or any other characteristic protected by law.

Diagnostic Radiological Medical Physicist

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

GC Chemist

<h3>Job Description</h3>
Job Description
Ironwood Cancer &amp; Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, social service support, nutritionist, integrative services, and genetic counseling.
Mission Statement: To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.
Overview: We are looking for a qualified and experienced Physicist to work in our fast-paced out-patient oncology clinic. The Medical Physicist conducts all aspects of radiation therapy physics, including clinical medical physics support, equipment calibration and commissioning, maintenance of appropriate quality assurance programs for equipment and treatment delivery, compliance with radiation safety, licensing issues and other pertinent regulatory requirements. 
Schedule: Full-time, Monday through Friday day shift position. 
Essential Duties and Responsibilities: 
<ul>
<li>Responsible for all physics of radiotherapy treatments.</li>
<li>Responsible for Calibration and QA of all treatment devices.</li>
<li>Responsible for Calibration and QA of treatment simulators.</li>
<li>Responsible for Calibration and QA of treatment planning systems.</li>
<li>Responsible for Calibration and QA of the physics test equipment.</li>
<li>Review of treatment plan calculations.</li>
<li>Review of weekly chart checks.</li>
<li>Commissioning of new radiologic systems.</li>
<li>Establish new commission &amp; QA criteria for new radiologic programs.</li>
<li>Establish new treatment protocols for safe and effective treatment delivery.</li>
<li>Consult with and assist radiation therapists, dosimetrists and radiation oncologists.</li>
<li>Provide training for new clinical systems and programs.</li>
<li>Provide radiation safety training.</li>
<li>Provide treatment planning for special procedures like HDR and SBRT.</li>
</ul>
Knowledge and Skills:
<ul>
<li>Ability to communicate frequently with front office staff, radiation therapists, dosimetrists, other physicists and radiation oncologists. Must be able accurately exchange detailed information in each situation.</li>
<li>Must remain calm and solve problems in highly stressful situations with limited time.</li>
<li>Constantly working around occupational levels of radiation exposure and hazardous materials.</li>
<li>Constantly operates computer and office equipment.</li>
<li>Must be able to maintain stationary position for up 6 hours per day.</li>
<li>Must be able to read medical charts on a computer screen for up to 6 hours per day.</li>
<li>Ability to use office equipment, computer, and typing is essential.</li>
</ul>
 Education and Experience:
<ul>
<li>Master’s Degree or PhD in Medical Physics or closely related field.</li>
<li>2 years clinical experience.</li>
</ul>
We offer a competitive salary and a comprehensive benefit package including health/dental/vision and life insurance, 401K, and a caring work environment. We are an E.O.E.
Please visit our website at <a href="http://www.ironwoodcrc.com" target="_blank">www.ironwoodcrc.com</a>. "Outsmarting Cancer One Patient at a Time"

Physicist - Medical

<h3>Job Description</h3>
Job Description
Job Title: 2nd Shift Cleanroom Technician
Job Description
A leading supplier of surgical one-time-use items, instruments, and kits for hospitals and healthcare product manufacturers is seeking a Cleanroom Technician Assembler to work on their production line. The position is on the 2nd shift from 2:00 PM to 10:30 PM, Monday to Friday, with opportunities for overtime on weekdays or Saturdays.
Responsibilities
<ul>
<li>Count, cut, measure, fold, or otherwise modify raw materials as per directions found in the Device Master Record, and complete necessary inspections and documentation of quantities, control numbers, and other requirements per QS &amp; GMP policy.</li>
<li>Perform on-line inspections of each device as it is produced and report problems to the Production Supervisor for disposition.</li>
<li>Seal products in final packaging configurations, ensuring procedures and machine settings for the sealer are followed properly.</li>
<li>Prepare packaged work in progress for sterilization and complete necessary documentation and control numbers per QS &amp; GMP.</li>
<li>Maintain proper inventory control procedures including product staging, segregation, and rotation.</li>
<li>Perform and document scheduled facility cleaning per QS.</li>
<li>Understand and conform to proper Clean Room etiquette.</li>
<li>Perform other duties as deemed necessary by the Production Supervisor.</li>
<li>Communicate and work well with production, purchasing, quality, and management in accomplishing assigned goals and objectives.</li>
<li>Meet objectives of the quality management system and recommend improvements as needed.</li>
</ul>
Essential Skills
<ul>
<li>General production skills in a cleanroom setting</li>
<li>Experience in medical device or medical assembly</li>
<li>Ability to operate basic production equipment</li>
<li>Strong attention to detail and motivation to work</li>
<li>Good communication skills, both verbal and written</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Preferred one year of experience in cleanroom, medical assembly, or warehouse</li>
<li>Must be able to lift up to 25 lbs</li>
<li>Proven team leader capabilities</li>
<li>Basic English proficiency to read work orders and communicate with auditors/supervisors</li>
<li>Comfortable in a Spanish-only environment for tenured employees</li>
</ul>
Why Work Here?
This is a contract-to-hire position with potential for permanent employment after four months. Employees benefit from medical, dental, and vision coverage. The company fosters a collaborative environment where teamwork is encouraged to achieve company goals. Leadership opportunities are available for those who demonstrate initiative and enthusiasm.
Work Environment
The work environment is a clean room with a total of four employees in a new department. Employees must wear clean room gear, including scrubs, a white coat, gloves, hair net, and follow grooming restrictions such as no makeup, jewelry, eyelashes, or nails. Employees can drink water or take bathroom breaks but must inform the lead due to gowning procedures. Breaks are scheduled after four hours of the shift.
Job Type &amp; Location
This is a Contract to Hire position based out of Placentia, CA.
Pay and Benefits
The pay range for this position is $17.50 - $17.50/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 Placentia,CA.
Application Deadline
This position is anticipated to close on Nov 14, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

2nd Shift Cleanroom Tech

<h3>Job Description</h3>
Job Description
Job Title: GCMS Chemist
Job Description
The GCMS Chemist primary responsibility is to provide support to laboratory staff as needed in all areas of laboratory operations. They will report to the general manager and/or operations manager for their daily assignment. The needs of the laboratory will change on a daily basis, as will the role.
Responsibilities
<ul>
<li>Independently prepare and analyze samples after appropriate training, using analytical SOPs and instrumentation specific to the department and analytical methodologies.</li>
<li>Perform routine operation, maintenance, and calibration of laboratory instruments and equipment.</li>
<li>Assist with validation and MDL studies.</li>
<li>Assist with investigation and preparation of responses to client inquiries and corrective action requests (CARs).</li>
<li>Input and maintain technical information as needed to support laboratory functions and operations.</li>
<li>Maintain laboratory notebooks where applicable.</li>
<li>Adhere to internal standards, policies, and procedures.</li>
<li>Perform other duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Proficient in extraction, titration, and pH testing.</li>
<li>Comfortable handling various acids, bases, and reagents with appropriate personal protective equipment (PPE).</li>
<li>Experience in organic extraction, metals, and/or as a GC or GCMS technician.</li>
<li>Knowledge of general chemistry including wet chemistry, titrations, dilutions, and viscosity.</li>
<li>Experience with laboratory equipment and sample analysis.</li>
<li>Must have experience with Microsoft Office Suite (Excel, Word, Outlook, Access, PowerPoint, etc.).</li>
<li>Effective communicator who can work under minimal guidance and multi-task with shifting priorities each day.</li>
<li>Experience with EPA methods 8260 and 624, targeting VOCs in environmental matrices</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in sciences through education, work-related experience, or a combination.</li>
<li>Knowledge and concern for environmental issues is a plus.</li>
<li>Demonstrates the utmost level of integrity and shows respect towards others and company principles.</li>
<li>Excellent time management skills, including the ability to balance multiple projects concurrently and arrange necessary resources.</li>
</ul>
Work Environment
The work takes place in a chemistry lab specializing in extractions. The position requires a willingness to work a flexible schedule, as longer hours, evenings, and/or weekend work will frequently be necessary as job duties demand. Business hours are Monday through Friday, 8:00 AM to 5:00 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Dayton, New Jersey.
Job Type &amp; Location
This is a Contract to Hire position based out of Dayton, NJ.
Pay and Benefits
The pay range for this position is $20.00 - $24.00/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 Dayton,NJ.
Application Deadline
This position is anticipated to close on Nov 11, 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.

GCMS Chemist

<h3>Job Description</h3>
Job Description
Salary, Benefits and Hiring level: $95,488 – $128,689 starting, DOE; (promotion potential to GS-13 step 10, equivalent to $147,615 in 2025) . In addition, the Pacific Council offers generously competitive insurance and retirement benefits.
Organizational Culture
At the Pacific Council, we value respect, integrity, curiosity, and collaboration. Our team is mission-driven and supportive, combining analytical rigor with a genuine commitment to sustainable fisheries and fishing communities. We work together in a transparent, collegial environment that celebrates teamwork, innovation, and diverse perspectives. 
Summary
The Pacific Fishery Management Council (Pacific Council) is one of eight regional councils established under the Magnuson–Stevens Fishery Conservation and Management Act. The Council manages fisheries in federal waters off Washington, Oregon, and California through transparent, science-based decision-making that sustains fish populations and the communities that depend on them. 
Our work covers groundfish, salmon, highly migratory species, and coastal pelagic species, and increasingly addresses issues such as climate change, offshore wind energy, and aquaculture. Council staff support this mission by conducting analyses, coordinating advisory bodies, and ensuring open, inclusive public processes in collaboration with stakeholders as well as state, tribal, and federal partners. 
Position Overview 
The Pacific Council is seeking a Fisheries Scientist (Staff Officer) with a Ph.D. or equivalent experience in fisheries science, marine biology, oceanography, ecology, or a related discipline. 
This position plays a central role in the development of scientific processes, the review of scientific analyses, and providing recommendations and insights for informing Council decisions. The successful candidate will apply strong analytical and problem-solving skills to complex fishery management issues, work collaboratively with diverse experts and stakeholders, and communicate scientific information clearly to policymakers and the public. 
Key Responsibilities 
<ul>
<li>Lead or contribute to scientific analyses, reports, and discussion papers supporting Fishery Management Plans, plan amendments, and regulatory actions.</li>
<li>Conduct or review biological, oceanographic, and ecological analyses relevant to fisheries management decisions.</li>
<li>Integrate information from stock assessments, ecosystem models, and monitoring programs into management advice.</li>
<li>Foster evidence-based decision making via the development and application of peer review processes.</li>
<li>Coordinate with state, tribal, and federal scientists to ensure analytical rigor and consistency across disciplines.</li>
<li>Facilitate and coordinate the meetings and agendas of Council advisory bodies and scientific review panels.</li>
<li>Present complex scientific information clearly and objectively to decision-makers, advisory bodies, and the public.</li>
<li>Maintain neutrality and professionalism in a dynamic, sometimes contentious policy environment.</li>
</ul>
Qualifications 
 Desired Minimums 
<ul>
<li>Ph.D. (or equivalent experience) in fisheries science, marine biology, oceanography, ecology, or a closely related field.</li>
<li>Demonstrated ability to design, conduct, or synthesize scientific analyses related to living marine resources.</li>
<li>Excellent writing and verbal communication skills, including the ability to convey complex concepts to non-technical audiences.</li>
<li>Strong organizational, analytical, and problem-solving skills.</li>
<li>Ability to work collaboratively with individuals from diverse scientific and technical backgrounds.</li>
<li>High professional and ethical standards, with a commitment to objectivity and public service.</li>
</ul>
 Additional Preferred 
<ul>
<li>Familiarity with West Coast fisheries and the Council’s management process.</li>
<li>Experience contributing to peer review, stock assessments, or ecosystem-based management.</li>
<li>Experience leading or supporting multidisciplinary or interagency projects.</li>
<li>Knowledge of federal fisheries policy frameworks and the Magnuson–Stevens Act.</li>
</ul>
Physical Demands
Staff Officers operate at the intersection of science, policy, and public engagement. The position requires occasional travel throughout the West Coast (typically 4–8 days per trip) and occasional international travel. A primarily remote work arrangement is not available. 
Work Environment
The work is primarily in an office environment. Frequent use of a keyboard and other computer hardware is required, often for lengthy periods of time. Use of other typical office equipment may also be required. Extended periods of continuous work beyond eight hours per day is often required. Lifting of light to moderately heavy boxes and equipment and unloading and loading boxes and equipment into and from vehicles, may be required. 
Hiring Requirements
Employment will be contingent upon successful completion of a background check.
 
Applications will be accepted until position is filled.

Fisheries Scientist (Staff Officer)

<h3>Job Description</h3>
Job Description
Frontier Medicines is seeking a highly motivated individual to fill the position of Principal Scientist, Computational Chemistry. The successful candidate will play a leading role in developing medicinal chemistry optimization strategies for key drug discovery programs. This individual will review experimental results, develop SAR hypotheses for activity, selectivity, and properties, and make design suggestions to improve the profiles of small molecule drug candidates.
As a covalent drug discovery–focused company, there is the opportunity for method development within this evolving field, in addition to applying the full range of ligand-based and structure-based design approaches and leveraging data from chemoproteomics, AI and quantum mechanics.
This role is key to Frontier Medicines’ success and an opportunity to work in a highly collaborative and energetic environment with short communication lines across functions and departments, and regular interactions with senior leaders. As the senior computational chemist, there is furthermore an opportunity to build out the computational team in the future
Requirements
What will you be doing? 
<ul>
<li>Design, execute, and analyze computational chemistry studies using a wide range of ligand-based, structure-based, and physics-based modeling techniques.</li>
<li>Partner closely with medicinal chemists and biologists to develop and refine structure–activity relationships (SAR), optimize molecular properties, and guide design hypotheses.</li>
<li>Contribute to project strategy and decision-making across all discovery stages, including target assessment, hit identification, lead optimization, and development candidate nomination.</li>
<li>Champion innovative computational tools and workflows, identify and implement emerging technologies that enhance Frontier’s CADD capabilities – specifically with an eye to the applicability to the covalent domain.</li>
<li>Work closely and partner with the AI team to develop and integrate novel AI applications into daily drug design workflows</li>
<li>Communicate scientific results, design rationales, and strategic insights to multidisciplinary teams and senior leadership.</li>
</ul>
What are we looking for? 
<ul>
<li>Ph.D. in Computational/Theoretical Chemistry, Biophysics, or a related discipline with 5+ years of relevant industry experience in drug discovery (biotech or pharma).</li>
<li>Demonstrated expertise in applying computational chemistry to small molecule design and optimization.</li>
<li>Strong experience with leading computational chemistry tools, CCG tools including MOE is highly preferred</li>
<li>Basic knowledge of scripting and programming with Python preferred</li>
<li>Experience with quantum mechanics (QM) is highly preferred</li>
<li>Proven track record of scientific impact, as evidenced by publications, patents, and successful project contributions.</li>
<li>Solid understanding of medicinal chemistry principles, SAR analysis, and ADMET optimization.</li>
<li>Excellent communication, presentation, and cross-functional collaboration skills.</li>
<li>Ability to operate independently and as a scientific leader in a fast-paced, startup environment.</li>
<li>Legally authorized to work in the U.S.</li>
</ul>
Benefits
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
<li>Family Leave (Maternity, Paternity)</li>
<li>Short Term &amp; Long Term Disability</li>
<li>Training &amp; Development</li>
<li>Free Food &amp; Snacks</li>
<li>Wellness Resources</li>
<li>Stock Option Plan</li>
</ul>
At Frontier, we strive to build a diverse and equitable workplace. The salary range for this role is $175,000 - $231,000. Compensation for the role will depend on a number of factors, including candidates' qualifications, skills, competencies and experience. Frontier offers a competitive total rewards package which includes healthcare coverage, 401k and a broad range of other benefits. 
This compensation and benefits information is based on Frontier's knowledge as of the date of publication, and may be modified in the future.

Principal Scientist, Computational Chemistry

<h3>Job Description</h3>
The Cultivation Technician is responsible for plant care in all stages oflife-cycle cannabis growth to include germination, vegetative, flowering and harvest. The Technician journals, monitors and tracks all observations in the company's software tracking system.
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Pay Rate: $17.50/hr + Benefits including PTO, Health, Dental, Vision, Life, Disability, 401K and More!
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Major Areas of Responsibility include:
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<ul>\n
<li>Clone, plant, water, fertilize, and water plants, shrubs, and trees, using hand tools and gardening tools.</li>
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<li>Harvest plants, and transplant or pot and label them.</li>
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<li>Record information about plants and plant growth.</li>
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<li>Feel plants' leaves and note their coloring to detect the presence of insects or disease.</li>
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<li>Fill growing tanks with water.</li>
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<li>Inspect plants and bud ties to assess quality.</li>
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<li>Clean work areas and maintain tools in accordance with sanitation standards.</li>
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<li>Check and water all plants in cultivation facility as outlined in the Daily Room-Checklist.</li>
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<li>Transplanting plants into larger containers as needed.</li>
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<li>Trimming plants in the vegetative stage and creating clones from material.</li>
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<li>Washing pots/trays/lights, etc. retuning them to the appropriate Clean Room.</li>
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<li>Harvesting and Trimming flowering plants.</li>
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<li>Staking weak plants.</li>
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<li>Examining plants for signs of pests or disease.</li>
\n</ul>
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Minimum Qualifications (Skills, Knowledge &amp; Abilities):
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<ul>\n
<li>All applicants must be at least 21 years of age.</li>
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<li>1-3years of experience in a related position with an emphasis in an operations production/manufacturing environment.</li>
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<li>Experience must include hands-on responsibility for the full scope production activities, both operations, and analysis.</li>
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<li>Working knowledge of medical cannabis and cannabis-infused product production from seed to sell. Alternatively, a background in horticulture and a willingness to learn.</li>
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<li>Experience with inventory control methods.</li>
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<li>Strong interpersonal skills including listening, negotiation, and conflict management.</li>
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<li>Excellent written, verbal and non-verbal communication skills.</li>
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<li>Ability to develop strong relationships and experience working with senior level executives.</li>
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<li>Ability to build and maintain positive relationships in order to gain support and achieve results both internally and externally.</li>
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<li>Ability to exercise sound judgment and problem solving.</li>
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<li>Ability to organize and prioritize work.</li>
\n</ul>
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Additional Abilities Required:
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The job requires physical activity, including prolonged standing, repetitive bending, climbing, and lifting or moving up to 25 pounds (or more with a coworker). Good visual acuity, hand-eye coordination, manual dexterity, and ability to perform repetitive motions with accuracy is required. The noise level in the work environment is usually moderate.
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About The Cannabist Company:
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The Cannabist Company, formerly known as Columbia Care, is one of the most experienced cultivators, manufacturers and providers of cannabis products and related services, with licenses in 12 U.S. jurisdictions. The Company operates 77 facilities including 61 dispensaries and 16 cultivation and manufacturing facilities, including those under development. Columbia Care, now The Cannabist Company, is one of the original multi-state providers of cannabis in the U.S. and now delivers industry-leading products and services to both the medical and adult-use markets. In 2021, the Company launched Cannabist, its retail brand, creating a national dispensary network that leverages proprietary technology platforms. The company offers products spanning flower, edibles, oils and tablets, and manufactures popular brands including Seed &amp; Strain, Triple Seven, Hedy, gLeaf, Classix, Press, and Amber. For more information, please visit <a href="http://www.cannabistcompany.com" target="_blank">www.cannabistcompany.com</a>.
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Recognized for its comprehensive benefits, ongoing training opportunities and commitment to diversity and equity inclusion both internally and with external vendors, The Cannabist Company has earned a spot on mg Magazine's America's Top Cannabis Industry Employers list.
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The Cannabist Company provides full-time employees with an excellent benefits and compensation package including but not limited to competitive wages, paid holidays, vacation and sick time, 401K with company match, multiple health plan choices, dental, vision, pet and life insurances, 100% paid short-term disability, optional long-term disability insurance and more!
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#ENGHP
Salary
$17.50 USD per hour

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