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<h3>Job Description</h3>
Job Description
We are seeking a motivated, detail-oriented Underground Geologist to support ore control and daily production activities at an active mining operation. This role is key in ensuring accurate material classification and efficient movement of ore and waste. The Underground Geologist will work closely with operations, survey, and engineering teams to perform in-mine mapping, sampling, material tracking, and data management.
10–12 month project (may extend based on operational needs)
Key Responsibilities
Ore Control &amp; Material Management
<ul>
<li>
Execute daily ore control tasks, including face sampling, muck pile sampling, and material delineation.
</li>
<li>
Classify ore vs. waste based on sampling and mapping data to guide production decisions.
</li>
<li>
Monitor tonnage movements and ensure proper routing of material to stockpiles or mill feed.
</li>
</ul>
Underground Geological Mapping &amp; Sampling
<ul>
<li>
Conduct geological face mapping and update underground maps daily.
</li>
<li>
Collect channel/face samples and ensure proper handling, labeling, and chain of custody.
</li>
<li>
Maintain sampling quality standards and ensure accurate spatial data capture.
</li>
</ul>
Data Entry, Reporting &amp; Interpretation
<ul>
<li>
Enter sample and geological data into digital databases and ore control software.
</li>
<li>
Compile daily, weekly, and monthly production reports.
</li>
<li>
Provide interpretations and observations that support short-term production decisions.
</li>
</ul>
Cross-Department Liaison
<ul>
<li>
Coordinate with mine operations, survey, engineering, and mill departments to support safe and efficient ore movement.
</li>
<li>
Communicate material routing plans and updates to shift supervisors and production teams.
</li>
<li>
Participate in shift handoff meetings and provide clear updates on ore control status.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor's degree in Geology, Earth Sciences, or related field.
</li>
<li>
Previous experience in underground geology, ore control, or production geology preferred.
</li>
<li>
Strong mapping, sampling, and geological data interpretation skills.
</li>
<li>
Proficiency in digital data entry and geological/ore control software.
</li>
<li>
Excellent communication and interpersonal skills; able to work effectively cross-functionally.
</li>
<li>
Ability to work independently underground in a physically demanding environment.
</li>
<li>
Strong attention to detail and commitment to data accuracy.
</li>
<li>
Authorized to work in the US without work visa sponsorship.
</li>
</ul>

Geologist

<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 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.
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.
Job Description 
The person in this role is responsible for maintaining instrumentation; tuning and calibrating instruments daily; analyzing quality control and client samples; reviewing and assembling this data in an efficient manner, with a high degree of quality, to meet client requirements.
Essential Duties and Responsibilities:&nbsp;
<ul>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Maintains instrumentation</li>
<li>Tunes and calibrates equipment&nbsp;</li>
<li>Analyzes samples&nbsp;</li>
<li>Reviews and assembles all supporting data&nbsp;</li>
<li>Reads, understands, and carries out SOPs</li>
<li>Understands and uses appropriate computer programs and databases and other software in a Windows-based environment</li>
<li>Demonstrates and maintains awareness of technical innovations and progress in environmental field (including periodic literature examination for relative scientific information)</li>
<li>Makes calibration standards or other quality control samples</li>
<li>Trains new personnel as required</li>
<li>Writes SOPs as needed</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>Bachelor's Degree in Chemistry or related field, or equivalent relevant experience in the field&nbsp;</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Ideal Candidates will have:&nbsp;
<ul>
<li>BS in Chemistry&nbsp;</li>
<li>Analytical Chemistry coursework&nbsp;</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Previous experience in a lab setting&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
 Additional Information 
Pay range: $18-20/hour + 10% shift differential&nbsp;
Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary 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.
*The benefits package offered will vary based on the employee’s full-time or part-time regular status.
We support your development! 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! 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! 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/&amp;nbsp" target="_blank">https://careers.eurofins.com/&amp;nbsp</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 Eurofins Scientific 2/2 March 2023 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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 2022, Eurofins generated total revenues of EUR 6.7 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.

Associate Chemist - Environment Testing - 2nd Shift, Tues-Sat

<h3>Job Description</h3>
Job Description
Chief Therapeutic Medical Physicist (CTMP) - Baltimore, MD (#R10217)
Location: Baltimore, MD Employment Type: Part-Time 20hr/wk Hourly Rate: $97.98
About Greenlife Healthcare Staffing: 
Greenlife Healthcare Staffing is a leading nationwide recruitment agency dedicated to connecting healthcare professionals with top-tier opportunities. We partner with hospitals, clinics, nursing homes, multi-specialty groups, and private practices to match talented individuals with roles that align with their skills and career goals.
Position Overview:
Greenlife Healthcare Staffing Inc., a minority and women-owned business with over ten years of experience in healthcare staffing, is seeking a Board-Certified Chief Therapeutic Medical Physicist to provide on-site radiation oncology support at the VA Maryland Health Care System. The Chief Therapeutic Medical Physicist will oversee all physics and dosimetry operations, ensure compliance with ACR/ASTRO/AAPM standards, and support a culture of safety and quality for Veterans receiving radiation therapy.
Why Join Us?
<ul>
<li>Competitive Compensation: Earn a strong hourly rate of $97.98.</li>
<li>Work Schedule: Part-Time 20hr/wk, on-site position.</li>
<li>Professional Growth: Gain valuable experience in a collaborative, innovative, and supportive environment at a leading VA healthcare system.</li>
<li>Impactful Work: Contribute to a mission-driven organization dedicated to improving patient outcomes for our nation's Veterans.</li>
</ul>
Qualifications:
<ul>
<li>Education: Ph.D. in Medical Physics or a related discipline.</li>
<li>Licensure: Board Certification in Medical Physics or Therapeutic Medical Physics (ABR) is required.</li>
<li>Experience:</li>
<ul>
<li>Minimum of 5 years of post-board certification experience.</li>
<li>At least 3 years of continuous work in the last five years in the field.</li>
<li>Proven experience leading QA programs and performing acceptance testing and commissioning of linear accelerators.</li>
</ul>
<li>Technical Skills: Experience with Varian Edge Linear Accelerators, Eclipse TPS, ARIA R&amp;V, Siemens SOMATOM go.Open Pro CT Simulator and Sun Nuclear/SunCHECK platform.</li>
<li>Soft Skills: Excellent organizational, communication, and leadership skills.</li>
</ul>
Key Responsibilities:
<ul>
<li>Oversee and supervise all radiation oncology physics and dosimetry operations.</li>
<li>Provide quarterly Quality Assurance reports to the VA Radiation Safety and Quality Assurance Committees.</li>
<li>Ensure adherence to national radiation safety standards and manage all QA data and documentation.</li>
<li>Conduct shielding surveys and maintain radiation safety compliance per NHPP requirements.</li>
<li>Participate in peer review conferences and multidisciplinary quality initiatives.</li>
<li>Supervise the development and maintenance of the Quality Management Program (QMP).</li>
</ul>
How to Apply: 
If you are ready to take the next step in your career and make a difference in the healthcare industry, we want to hear from you! Submit your Resume/CV to <a href="mailto:hr@glhstaffing.com" target="_blank">hr@glhstaffing.com</a> or call our office at (800) 608-4025 to learn more about this opportunity and others we offer.
Greenlife Healthcare Staffing - Empowering Healthcare Professionals, Enriching Lives.

Chief Therapeutic Medical Physicist (CTMP)

<h3>Job Description</h3>
Job DescriptionDescription:
Want to work for a company that supports and invests in its employees? Cosmos Corporation has a healthy workplace culture guided by a clear vision, mission, promise, and values! Our culture is intentionally fostered daily by how employees live out our values. The result is a place where employees genuinely enjoy coming to work every day!
 
Cosmos Corporation is a recognized leader in natural health, wellness, and care products. Cosmos creates and distributes people and pet-approved liquid products with the most responsible, effective, high-quality ingredients people trust. Our brands bring innovative products with unique benefits that help people and pets look and feel their very best. We do all of this at our headquarters located in O’Fallon, Missouri.
 
We are looking for a new ideal team player as a process chemist to join the Formulation Team! The Process Chemist is responsible for developing, optimizing, and implementing robust manufacturing processes and formulas to support product development and production. The role involves creating and maintaining master mixing records, conducting pilot and bench batches, troubleshooting with Quality Control, and collaborating with Engineering, Maintenance, and other teams to ensure process efficiency and compliance. This position provides technical support across departments, ensures adherence to GMP and safety practices, and contributes to continuous process improvements to enhance product quality and manufacturing performance.
 
You Key Responsibilities Will Be:
<ul>
<li>Develop, optimize, and scale up robust manufacturing processes for all formulations.</li>
<li>Create and maintain master mixing records and documentation for new and existing products.</li>
<li>Conduct bench and pilot batches to support formulation and initiation to the mixing team.</li>
<li>Collaborate with Quality, Engineering, and Operations to troubleshoot issues and improve efficiencies.</li>
<li>Provide technical support across teams and drive continuous improvements in process, quality, and safety.</li>
</ul>
Requirements:
<ul>
<li>5 years of related experience</li>
<li>Superior math mathematical skills</li>
<li>Excel at problem solving.</li>
<li>Excels at computer skills.</li>
<li>Experience with formulation in finished goods</li>
<li>Bachelor’s degree in chemistry, chemical engineering, or related science</li>
</ul>
 
Your Competencies &amp; Skills You Hold Are as Follows:
<ul>
<li>Collaboration &amp; Communication </li>
<li>Team player</li>
<li>Analytical &amp; Critical Thinking Skills </li>
<li>Technical Proficiency</li>
<li>Data Driven Mindset</li>
<li>Process &amp; Scale-Up Expertise.</li>
<li>Attention to Detail </li>
<li>Innovation &amp; Continuous Improvement </li>
<li>Ingredient &amp; Formulation Knowledge </li>
<li>Adaptability &amp; Learning Agility </li>
<li>Safety &amp; Compliance Mindset </li>
</ul>
 
A Day In the Life At Cosmos:
No two days look the same. You might start in the lab running a bench batch to evaluate a new formula, then move to the plant floor to oversee a pilot batch and ensure scale-up parameters align with production equipment. Midday could be spent troubleshooting a manufacturing issue with Quality Control or working with Engineering on process improvements. You will update and refine master mixing records, review data for accuracy, and provide technical guidance to cross-functional teams. Along the way, you will balance hands-on experimentation with problem-solving—leveraging data, technology, and collaboration to keep product quality, efficiency, and innovation at the forefront.
 
Every Wednesday, you will head to the lunchroom at 11:40 a.m. for the weekly Cosmos Minute, where the entire company meets at 11:45 a.m. to learn about other team members and special company announcements at Cosmos.
 
 
What's In It For You?
At Cosmos Corporation we truly care about investing in our employees, these are the benefits and perks at Cosmos! 
<ul>
<li>Medical Health Insurance</li>
<li>Dental Insurance</li>
<li>Vision Insurance</li>
<li>Life Insurance</li>
<li>Short- &amp; Long-Term Disability Insurance</li>
<li>Flexible Spending Accounts</li>
<li>Critical Illness</li>
<li>Accident Coverage </li>
<li>401(k) Contribution</li>
<li>Robust Employee Assistance Program</li>
<li>Vacation Time Off</li>
<li>8 Paid Holidays (and sometimes more!)</li>
<li>Paid Sick Leave</li>
<li>5 Paid Mission Days</li>
<li>Parental Leave </li>
<li>Maternal Leave</li>
<li>Growth &amp; Development Opportunities</li>
<li>Lunch &amp; Learns</li>
<li>Employee Referral Bonus Program</li>
<li>Cosmos Cash Recognition Program</li>
<li>Better Book Club</li>
<li>Excellent Culture</li>
<li>So much more!!</li>
</ul>
 
Equal Opportunity Employer
Cosmos Corporation is an equal-opportunity employer. We prohibit discrimination and harassment of any kind. Cosmos Corporation makes hiring decisions based solely on qualifications, merit, and business needs at the time.

Process Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
Enhance your career at raSmith as a Wetland Ecologist in our Municipal Services division and discover why we’re ranked #2 as a Top Workplace.
 
raSmith is a growing multi-disciplinary consulting civil and structural engineering and land surveying firm with over 45 years of experience. We work with clients on projects nationwide from our six office locations in Wisconsin, Illinois, and California.
 
Are you ready to contribute your talents to a variety of projects that positively impact communities across the country? Consider this opportunity:
 
Wetland Ecologist – Primary Responsibilities:
<ul>
<li>Wetland and waterway delineation, as well as reporting and permitting.</li>
<li>Navigability and Ordinary High Water Mark (OHWM) Determinations.</li>
<li>Rare species habitat assessments and presence/absence surveys.</li>
<li>Proficiency in using GPS equipment (Trimble) to collect field data.</li>
<li>Experience with computer-aided mapping software (e.g., ArcMap, Field Maps, etc.) is a plus.</li>
<li>Experience with Microsoft Office (Work, PowerPoint, and Excel).</li>
<li>Create cost estimates and project scopes.</li>
</ul>
Wetland Ecologist - Benefits:
raSmith has a strong history of maintaining a people-oriented culture that provides a great work-life balance and a highly competitive compensation and benefit package. We support and encourage professional development opportunities and provide career growth charts for our supervisors and employees.
 
Specific benefits include:
<ul>
<li>Generous paid time off and 8 paid holidays</li>
<li>Flexible work schedules</li>
<li>Paid parental leave</li>
<li>Medical/prescription drug, dental, and vision insurance</li>
<li>Health Savings Account (HSA) and Flexible Spending Account (FSA) options</li>
<li>Wellness programs for health insurance savings</li>
<li>Identity Shield and LegalShield programs</li>
<li>Life assistance programs</li>
<li>Corporate wear reimbursement</li>
<li>Employee referral bonus</li>
<li>401K plan with immediate employee participation and generous company match</li>
<li>Tuition and professional licensure/certification reimbursement program</li>
<li>Paid memberships to professional organizations</li>
<li>Paid seminars and conferences</li>
<li>A variety of mentoring and training programs</li>
<li>Company picnics and seasonal events</li>
<li>Social and team-building opportunities</li>
<li>Fun sports leagues such as softball, basketball, bowling, cycling, disc golf, and others</li>
</ul>
Requirements:
Wetland Ecologist – Skills and Requirements:
<ul>
<li>Bachelor of Science degree in Environmental Science or related degree from a U.S. accredited college or university (MS or PhD a plus).</li>
<li>5+ years of related work experience.</li>
<li>Excellent oral, written and analytical skills.</li>
<li>Self-motivated, positive, organized and must be able to work independently.</li>
<li>Be able to travel as projects require and be willing to work in various field situations.</li>
<li>Applicable U.S. based work experience.</li>
</ul>
We are proud to be an EOE/Affirmative Action/Veterans/Disabled employer. Visit raSmith.com to explore some of our projects, check out testimonials from staff and clients, and learn more about what makes us stand out in our industry.

Wetland Ecologist

<h3>Job Description</h3>
Job Description
 
EQUAL OPPORTUNITY EMPLOYER
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.
 
CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with &gt; 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.
Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, &amp; Carbohydrates; Injectables; Highly Potent &amp; Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.
SUMMARY
Performs research and development activities for the purpose of transferring and designing/improving a process or technology. Provides process engineering support for manufacturing processes in assigned group or plant through developing and implementing continuous improvements. And through troubleshooting methods and equipment used in the production of bulk pharmaceutical intermediates and active pharmaceutical ingredients.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.
<ul>
<li>Provides day-to-day support to assigned processes, at times requiring attention outside of the normal work hours</li>
<li>Evaluates new process fits into manufacturing with supervisory oversight, including consideration of safety, cost, equipment, chemistry, and unit operation technological needs</li>
<li>With supervisory input, performs process development via process modeling or testing at lab scale, concentrating on key scale up parameters to scale up from kilo-scale to full production scale</li>
<li>Participates in technology transfer from one manufacturing site to another; develops plans for successful tech transfers, and implements processes into pilot or commercial facilities, with supervisory oversight. Assembles technology transfer packages</li>
<li>Implements process improvements and optimization that reduce costs; improve yields, cycle times or product quality; resolve or prevent environmental, health and safety impacts; reduce down time; improve process consistency; and improve process robustness</li>
<li>Performs process troubleshooting to resolve operating or product problems; identifies and implements solutions to improve process robustness</li>
<li>Supports manufacturing through compiling technical requirements for batch record generation; providing technical input on equipment setup requirements; providing process training for operators; providing technical support in production for processes in development; writing process validation protocols; providing technical input on deviations and investigations; and writing campaign summary reports. Ensures that documentation is consistent with the process filing</li>
<li>Contributes to meeting Process Safety Management compliance by participating in Process Hazard Analysis reviews; and by providing mass and energy balances and other engineering data for the assigned process</li>
<li>Strives to improve professional skills by participating in on-the-job training, attending guest lectures, being an active member of a professional organization, and attending formal training courses and conferences</li>
</ul>
LEADERSHIP &amp; BUDGET RESPONSIBILITIES
As part of a cross functional team, this position is responsible and accountable for addressing process engineering requirements for assigned projects.
SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES
Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
A BS in Chemical Engineering and 1 year experience in Process Engineering in a Pharmaceutical or Fine Chemicals Manufacturing environment.
LANGUAGE SKILLS
Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors.
MATHEMATICAL SKILLS
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
REASONING ABILITY
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
CERTIFICATES, LICENSES, REGISTRATIONS
None.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently required to stand, sit, and talk or hear. The employee is occasionally required to walk; work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, low levels of toxic or caustic chemicals, outside weather conditions, and vibration. The noise level in the work environment is usually moderate.
CORE COMPETENCIES
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
<ul>
<li>Expands knowledge of plant-scale unit operations, scale-up, and plant design considerations; builds on technical knowledge in chemical engineering and process improvement methodology </li>
<li>Emerging knowledge of regulatory issues in pharmaceutical manufacturing including cGMPs, PSM, OSHA, and EPA requirements</li>
<li>Develops computer skills, in the areas of: Microsoft Office Products – Word, Excel, PowerPoint; Batch +, statistical analysis programs, and chemical engineering simulation software</li>
<li>Explores training opportunities in technical areas that will strengthen skills for current assignments; acquires training to use common tools that support job (for example, Batch Plus) </li>
<li>Regularly applies basic science and engineering principles to assigned projects</li>
<li>Participates in and understands the importance of regulatory compliance systems such as PHAs and incident reporting; completes assignments, i.e., action items, in a timely manner</li>
<li>Conducts basic technical and economic evaluations</li>
<li>Demonstrates problem analysis and troubleshooting skills, data compilation, and simple analysis; draws conclusions from data</li>
<li>Demonstrates a trend toward working independently – and decreasing reliance on mentors and supervisors to guide work and daily activities</li>
<li>Executes assigned, well-defined tasks and seeks assistance when appropriate; and begins to offer some input on assigned projects</li>
<li>Follows established methods and procedures; generally, implements existing standards and technical solutions; or implements new ideas that were generated by others</li>
<li>Displays initiative to drive ideas or issues that he/she supports, and follow through to completion</li>
<li>Understands and applies the Corden values </li>
<li>Familiar with manufacturing department’s activities and Corden’s business goals and strategy</li>
<li>Learns basics of project economics and product line cost structure and is familiar with the product standards manual</li>
<li>Demonstrates clear, concise writing skills, targeting detailed reports on specific subjects, often requiring review by more senior personnel </li>
<li>Presentation skills are developed through frequent ‘short and to the point’ presentations; generally targeting technical staff, process team, and project groups</li>
<li>Demonstrates willingness to work in teams and to contribute in technical, plant support and staff meetings</li>
<li>Demonstrates emerging leadership skills, and influence over others in small groups and small projects; knows and uses key facility contacts required to make progress on projects</li>
</ul>
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
<ul>
<li>401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service </li>
<li>Accident Plan</li>
<li>Critical Illness Insurance</li>
<li>Dental Insurance</li>
<li>Disability Insurance</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Account</li>
<li>Health Insurance PPO/HSA</li>
<li>Hospital Indemnity Plan</li>
<li>ID Theft Protection</li>
<li>Life Insurance</li>
<li>Paid Maternity/Paternity Leave</li>
<li>Tuition Reimbursement</li>
<li>Wellness Program</li>
<li>Vacation – Three Weeks 1st Year</li>
<li>Vision Insurance</li>
</ul>
This post will expire on December 8, 2025

Chemical Process Engineer

<h3>Job Description</h3>
Job Description
Company Overview:
At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world’s largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs.
Summary:
Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&amp;E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively.
What will you do?
<ul>
<li>Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems.</li>
<li>Work independently with minimal guidance from the laboratory manager.</li>
<li>Act as a mentor to junior development chemists.</li>
<li>Maintain a clear and orderly record all observations and data.</li>
<li>Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting.</li>
<li>Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts.</li>
<li>Provide legal and archival documentation for patent applications.</li>
<li>Comply with safety regulations and lab procedures.</li>
<li>Provide technical service and knowledge to customers and sales associates based upon the chemist’s current level of expertise. Visit customers when required.</li>
<li>Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems.</li>
<li>Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.</li>
<li>Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.</li>
</ul>
Education, Experience, Skills &amp; Competencies:
<ul>
<li>This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Master’s Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience.</li>
<li>Knowledge of colloid chemistry, surfactants, and tribology is required.</li>
<li>Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired.</li>
<li>Understanding of applied statistics and experimental design is not required, but highly desired.</li>
<li>Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically.</li>
<li>Must have good prioritization and communication skills (oral and writing).</li>
<li>Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community.</li>
</ul>
What's in it for you:
<ul>
<li>Competitive pay programs with excellent career growth trajectory</li>
<li>Opportunities to see your efforts contribute toward the success of the business</li>
<li>Work for a global leader in the industrial process fluids industry</li>
</ul>
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran’s status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities.Applicants with a disability who need assistance applying for a position may email <a href="mailto:OneHR@quakerhoughton.com" target="_blank">OneHR@quakerhoughton.com</a>.

Development Chemist III

<h3>Job Description</h3>
Job DescriptionSalary: $160,000 - $180,000 
About Acrivon Therapeutics
 Acrivon is a clinical stage biopharmaceutical company discovering and developing precision medicines utilizing its proprietary Generative Phosphoproteomics AP3 platform. The platform allows the company to interpret and quantify compound specific, drug-regulated pathway activity levels inside the intact cell in an unbiased manner, yielding terabytes of proprietary data and delivering rapid, actionable insights. The Generative Phosphoproteomics AP3 platform is comprised of a growing suite of powerful, internally-developed tools, including the AP3 Data Portal, converting multimodal data into structured data for generative AI analyses, the AP3 KaiSR Kinase Substrate Relationship Predictor, and the AP3 Interactome. These distinctive capabilities enable the company to go beyond the limitations of traditional drug discovery, as well as current AI-based target-centric drug discovery, and rapidly design highly differentiated compounds with desirable pathway effects through intracellular protein network analyses and advance these agents into the clinic for streamlined development.
 
Acrivon is currently advancing its lead program, ACR-368 (also known as prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2b trial for endometrial cancer. The company has received Fast Track designation from the Food and Drug Administration, or FDA, for the investigation of ACR-368 as a monotherapy based on OncoSignature-predicted sensitivity in patients with endometrial cancer. The FDA has granted a Breakthrough Device designation for the ACR-368 OncoSignature assay for the identification of patients with endometrial cancer who may benefit from ACR-368 treatment. In addition, the company has initiated a third arm to the Phase 2b study without the need for a pre-treatment biopsy to evaluate ACR-368 with ultra-low-dose gemcitabine (ULDG) sensitization in all-comer, biomarker-unselected 2nd line patients with endometrial cancer who have all received prior treatment with chemotherapy and anti-PD-1.
 
Acrivon is also leveraging its proprietary Generative Phosphoproteomics AP3 platform for developing its co-crystallography-driven, internally discovered pipeline programs. These include ACR-2316, the companys second clinical stage asset, a novel, potent, selective WEE1/PKMYT1 inhibitor designed for superior single-agent activity through strong activation of not only CDK1 and CDK2, but also of PLK1 to drive pro-apoptotic cell death, as observed in preclinical studies against benchmark inhibitors. The Phase 1 trial of ACR-2316 is advancing with enrollment in the first three dose-escalation cohorts completed. Drug target engagement was observed at DL1 and 2 using the companys clinical mass spectrometry-based AP3 profiling, with evidence of approximate dose proportionality based on plasma pharmacokinetic analyses, and initial clinical activity and confirmed partial response. In addition, the company is advancing a preclinical program directed against an undisclosed cell cycle regulatory target.
Position Overview:
This position will apply technical expertise to support biomarker assaysprimarily digital imaging, analysis and associated workflows, data analysis, scripting and LIMSwithin our CLIA/CAP framework, and work closely with our biomarker platform team to advance our precision medicines in oncology.
Location:
This position will report to the CLIA Laboratory Director and be based at least 60% in our Watertown, MA facility, with no more than 40% in a home office.
Duties and Responsibilities:
<ul>
<li>Execute validated slide scanning and quantitative image analysis protocols for highcomplexity tests, including IHC and multiplex immunofluorescence assays.</li>
<li>Develop and execute validation plans for equipment and assay procedures including software and electronic workflow.</li>
<li>Collaborate with cross-functional teams to develop image analysis algorithms, scripts and workflows to support clinical and research assay development.</li>
<li>Lead all LIMS efforts including configurations, validations, document support and training.</li>
<li>Provide technical guidance on laboratory automation, data tracking and workflow optimization.</li>
<li>Assist with biostatistics for validation protocols and result analysis.</li>
<li>Collaborate with Quality, Regulatory, and IT teams to maintain a compliant, efficient laboratory.</li>
<li>Participate in proficiency testing and regulatory compliance.</li>
<li>Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.</li>
<li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.</li>
<li>Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, or Laboratory Director.</li>
<li>Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.</li>
<li>Work on special projects as assigned by management.</li>
</ul>
Required Skills/Abilities:
<ul>
<li>Minimum of masters degree in computer science, medical technology, histology, biology, or related field.</li>
<li>Minimum of 5 years of experience in clinical or research pathology laboratory.</li>
<li>Expertise in digital pathology platforms including multispectral imaging systems.</li>
<li>Familiarity with histology and IHC (including both bright field and fluorescence techniques).</li>
<li>Proficiency in Python, RStudio, HTML and laboratory information systems.</li>
<li>Familiarity with machine learning/AI applications</li>
<li>Detailoriented, precise, and adept at working in regulated environments.</li>
<li>Excellent communication, problem-solving, and leadership skills.</li>
<li>Ability to participate constructively on cross-functional and diverse teams.</li>
<li>Visual acuity for microscopic examination and computer use.</li>
</ul>
Acrivon Therapeutics is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation, or genetics. In addition to federal law requirements, Acrivon Therapeutics complies with applicable state and local laws governing nondiscrimination in employment.

Laboratory Information and Workflow Manager, CLIA Immunohistochemistry (IHC) Laboratory

<h3>Job Description</h3>
Job Description
POSITION SUMMARY
Summarize the primary purpose &amp; key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (It may be helpful to complete this section after you have finished the other sections of the document.
• NMR Scientist – Contract | San Diego, CA (Onsite)
• Are you passionate about NMR and ready to make an impact? Join Client’s dynamic team in San Diego, where we run thousands of automated experiments and deliver rapid small molecule structure elucidations every month.
• Troubleshoot and resolve technical issues with NMR spectrometers
• Solve complex regio- and stereoisomer structures by NMR
• Lead and coordinate NMR lab relocation activities
• Drive automation and workflow improvements
• Advanced degree in Chemistry or related field, with demonstrated NMR structure elucidation experience
• Proficiency in Bruker NMR platforms
• Experience with NMR hardware and troubleshooting
• Excellent interpersonal and communication skills
• Commitment to safety and collaboration
• Be part of a collaborative team making a real difference in drug discovery
• Work onsite in a state-of-the-art lab environment
Hard Skills:
• Experience with NMR hardware and troubleshooting
• Solve complex regio- and stereoisomer structures by NMR
• Lead and coordinate NMR lab relocation activities
Why Patients Need You
Purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Cleint’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.

What You Will Achieve
As a Senior Scientist in the Oncology Analytical and Synthesis Technologies Open Access group, you will be at the center of a pivotal operation within Medicinal Chemistry. You will be part of a group in Client that comprises experts in the major scientific disciplines involved in the discovery and preclinical development of small molecule drugs. Specifically, you will be involved in the structural analysis of a broad range of achiral/chiral small molecule compounds primarily through NMR spectroscopy as well as responsible for implementing novel technologies/workflows to expedite such processes.
You will play a vital role as a key contributor in large, multi-disciplinary matrix teams from project inception through to delivery of clinical drug candidates. You will provide key contributions to the implementation of analytical chemistry strategies through development and execution of innovative techniques that help to revolutionize expedite our approach to the discovery and development of small molecule and synthetically derived drugs.
Your significant experience of applying knowledge of principles, concepts, and practices of the analytical chemistry discipline and specifically NMR will make you a critical member of the team. Your skill and knowledge will help in making decisions that require choosing among limited options. You are proactive in contributing to all team discussions and creating an environment of collaboration.
It is your innovative scientific temperament that will help in making Client ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
• Contribute to achievement of immediate work group goals and collaborate with other team members.
• Build effective partnerships with other research lines, in particular synthetic medicinal chemistry, technology, pharmaceutical sciences and process chemistry groups.
• Develop efficient approaches to the structural elucidation of primarily small molecule compounds through developing an expertise in NMR-based methodologies.
• Drive the utilization of the most contemporary and effective analytical/purification instrumentation combined with automated technologies.
• Communicate work clearly and concisely to internal stakeholders through written and verbal communications.
Qualifications
Must-Have
• Bachelor's Degree
• 2+ years of experience
• Experience in compound structural analysis by NMR-based and Mass Spectrometry methods.
• Working knowledge of NMR-instrumentation and hardware.
• Familiarity with standard laboratory techniques and working knowledge of HPLC and purification techniques.
• Interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment
• Effective communication skills

Nice-to-Have
• Broad knowledge of various analytical software packages (e.g. Agilent, ACD Labs, Bruker, etc).
• Proficiency with basic NMR instrument upkeep and troubleshooting issues.
• Experience with logistics around lab set-up after a site move.
• Familiarity with development/execution of workflows for the parallel purification and analysis of compound libraries.
Company DescriptionWe believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list. 
<h3>Company Description</h3>
We believe in service that helps you solve a problem, move forward with a project, manage a difficult situation, or simply check something off your list.

NMR Scientist

<h3>Job Description</h3>
Job DescriptionMicrobiologist (Associate) — ISO/IEC 17025 Cannabis Testing Lab
Location: Tucson, AZ (on-site) Schedule: Full-time, Mon–Fri Reports to:&nbsp;Lab Director Level: Associate / Microbiologist I–II (slightly above entry level; strong entry-level candidates welcome)
About the Role
Join Full Spectrum Lab, an ISO/IEC 17025–accredited lab serving Arizona’s cannabis and hemp industry. You’ll perform microbiological safety testing across diverse matrices (flower, concentrates, edibles, beverages, topicals, and environmental swabs) and help us deliver accurate, defensible results on time.
Responsibilities
<ul>
<li>
Run microbiology methods aligned to AOAC/USP/FDA-BAM and Arizona State Department of Health rules:
<ul>
<li>
Pathogens: Salmonella spp., STEC
</li>
<li>
Fungal targets: Aspergillus spp. (A. flavus, A. fumigatus, A. niger, A. terreus)
</li>
<li>
Environmental monitoring &amp; indicators: TYMC/TAC, coliforms/Enterobacteriaceae, BTGN
</li>
</ul>
</li>
<li>
Execute and troubleshoot qPCR (e.g., AriaMX or similar), enrichments, plating/Petrifilm; interpret Cq values and growth results with defined acceptance criteria.
</li>
<li>
Prepare media/reagents; maintain cultures and positive/negative/IPC controls; follow aseptic technique in a BSL-2 environment.
</li>
<li>
Document work in LIMS with full traceability; contribute to report review and release.
</li>
<li>
Support method verification/validation (selectivity, recovery, LoD/LoQ, ruggedness) and uncertainty inputs.
</li>
<li>
Maintain/calibrate pipettes, incubators, biosafety cabinets, thermometers, autoclaves, and qPCR instruments (basic IQ/OQ/PQ tasks).
</li>
<li>
Participate in OOS/CAPA investigations, proficiency testing, internal audits, and continual improvement under ISO/IEC 17025.
</li>
<li>Help train technicians and cross-train with Chemistry as needed</li>
</ul>
Addition responsibilities may include sample intake, accessioning, and generalized sample prepMinimum Qualifications
<ul>
<li>
B.S. in Microbiology, Molecular Biology, or related field (M.S. a plus).
</li>
<li>
0–3+ years hands-on microbiology in an accredited/regulated lab (ISO 17025/CLIA/FDA/USDA/pharma) or equivalent internships/co-ops.
</li>
<li>
Competency with qPCR and culture-based workflows; strong aseptic technique and contamination control.
</li>
<li>
Familiarity with ISO/IEC 17025 concepts (verification/validation, traceability, equipment control, records, impartiality).
</li>
<li>
Comfortable with LIMS and good documentation practices (ALCOA+).
</li>
<li>
Able to lift 30+ lb and stand for extended periods in a fast, high-throughput setting.
</li>
</ul>
Nice to Have
<ul>
<li>
Cannabis/hemp matrix experience (Arizona ADHS awareness).
</li>
<li>
Environmental monitoring program experience.
</li>
<li>
SOP authorship and basic statistics (control charts, trend reviews).
</li>
<li>
Prior use of Confident LIMS or AriaMX.
</li>
</ul>
What Success Looks Like
30 days: Trained on SOPs/LIMS; independently running core qPCR and culture workflows. 90 days: Cross-trained on all matrices; zero late results; contributing small CAPA/5S wins. 180 days: Acting SME for a method area; supporting PT and validations with reduced reruns/contamination.
Compensation &amp; Benefits
<ul>
<li>
Salary: $60,000 per year
</li>
<li>
Benefits: Medical, dental, and vision; paid time off; company holidays
</li>
</ul>
Work Environment &amp; Safety
<ul>
<li>
BSL-2 procedures, PPE compliance, chemical and biohazard waste handling per SOPs and state regulations.
</li>
</ul>
Equal Opportunity
We’re an equal opportunity employer and committed to a safe, inclusive workplace.
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