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<h3>Job Description</h3>
Job Description
Location: Waltham, MA
**This role will require full-time on-site presence at our client site in Waltham, MA.**
**This role is NOT eligible for relocation assistance**

The Zifo Lab Computing Analyst provides both consulting, analytical and technical laboratory services, including multivendor instrument, information technology as well as in-lab validation/compliance services when applicable. The individual will provide the consulting skills required to analyze customer needs and gaps to propose solutions for the desired state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support team. 
Requirements
Required Skills:
<ul>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests</li>
<li>Ability to troubleshoot complex instrument and technology issues</li>
<li>Strong oral and written communication skills</li>
<li>Ability to identify, track and complete tasks for multiple projects </li>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code</li>
</ul>

Responsibilities:
As a Lab Computing Analyst, beneficiary would perform following key responsibilities:
<ul>
<li>Requirements Management and onsite Validation/Compliance support </li>
<li>IT Consulting</li>
<li>Customer Liaison</li>
<li>Onsite Lab IT Support </li>
</ul>
 Requirements Management
<ul>
<li>Understand problem statement/challenges</li>
<li>Define scope </li>
<li>Gather requirements.</li>
<li>Assist with Validation/Compliance activities (IOPQ) as required.</li>
<li>Analyze current state business processes and requirements.</li>
<li>Assist in building plans for process improvement</li>
</ul>
IT Consulting
<ul>
<li>Analyze gaps/opportunities for improvement based on industry Best Practice</li>
<li>Evaluate Industry trends to identify areas for optimization</li>
<li>Evaluate vendor solutions and facilitate demos of prototypes as Proofs of Concept</li>
<li>Recommend process improvements that fit business needs</li>
</ul>
Customer Liaison:
<ul>
<li>Meeting with internal/external service groups/leads</li>
</ul>
<ul>
<li>Liaise between System/Lab owners and third parties to coordinate best times for services</li>
<li>Provide weekly planning schedules for review at status meeting with customer leads</li>
<li>Monthly Operational review meetings/ Quarterly metrics reporting with department heads</li>
</ul>
On Site Lab IT Support:
<ul>
<li>Perform break/fix support for all Instrument connected systems</li>
<li>Implement Windows based security policies as required</li>
<li>Ensure adherence to client’s corporate policies through periodic reporting &amp; compliance programs</li>
<li>Acts as the technical support contact for field service engineers and external vendors</li>
<li>Provide technical subject matter expertise for new system validation and change management</li>
<li>Create and maintain a physical inventory of lab equipment, PC’s, software, and any other information pertinent to the environment if applicable</li>
<li>Perform system preventative maintenances based on client’s schedule, if applicable</li>
</ul>

Requirements
<ul>
<li>Bachelor’s/Master’s degree or equivalent in Pharmaceutical, Bio-technology, Bio-medical, Chemical </li>
<li>At least 2 years of directly relevant experience, including:</li>
<li>At least 1 year in software development and testing.</li>
<li>At least 1 year of experience in business requirement analysis and gathering.</li>
<li>Demonstrated domain area knowledge.</li>
<li>Candidate must possess excellent analytical and interpersonal skills along with a proven track record in system design, implementation, have demonstrated ability to guide the activities of colleagues, and have demonstrated ability to gain client’s confidence and trust.</li>
<li>Candidate must demonstrate in-depth understanding in one or more of the following areas of Bio/Pharma industry:</li>
<li>Drug Discovery &amp; Development Processes</li>
<li>Clinical study planning &amp; Data management</li>
<li>Lab Workflows</li>
<li>Chemical &amp; Biologics material Management</li>
<li>Sample Management</li>
<li>Robotic Systems Integration &amp; Qualification</li>
<li>Operations KPI and Metrics tracking</li>
<li>Optional requirement: Candidate needs to be familiar with the US and International Regulations and Standards governing the development of technical solutions such as GLP, GMP, 21 CFR Part 11, Part 210, Part 211, Part 820</li>
<li>Technical Skills:</li>
<li>Operating System familiarity with at least 1 of the following: Unix, Windows, MVS</li>
<li>Software Methodology familiarity with: Object Oriented Programming, Structured Programming</li>
<li>Software Development Process familiarity with: Waterfall, Agile</li>
<li>Change Control Management and Risk Management </li>
<li>Office Tools proficiency required in : MS Word, Excel, PowerPoint</li>
<li>Office productivity tool proficiency in at least 1 of the following: Visio, MS Project, SharePoint </li>
</ul>
Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

GxP Lab Computing Analyst

<h3>Job Description</h3>
Job Description
Microbiology Manager
Essential Skills
<ul>
<li>Bachelor’s degree in Microbiology, Food Science, or related field (Master’s preferred).</li>
<li>Minimum 5–7 years of experience in food microbiology testing, with at least 2 years in a management role.</li>
<li>Strong knowledge of dairy and pet food microbiology, pathogens, and spoilage organisms.</li>
<li>Familiarity with ISO accreditation and regulatory requirements (FDA, USDA, AOAC methods).</li>
<li>Excellent leadership, communication, and organizational skills.</li>
<li>Ability to manage multiple priorities in a fast-paced laboratory environment.</li>
</ul>
Salary Min:
$85,000.00Salary Max:$100,000.00
Additional Skills &amp; Qualifications
<ul>
<li>Strong knowledge of ISO17025 and PCR.</li>
<li>Experience in people management.</li>
<li>Skills in food microbiology, PCR, plating, and VIDAS.</li>
</ul>
Job Description
The Microbiology Department Manager will lead and oversee all microbiological testing operations within our accredited third-party food testing laboratory. This role is responsible for ensuring the accuracy, compliance, and efficiency of testing services for dairy and pet food products. The manager will provide technical leadership, supervise laboratory staff, maintain quality standards, and ensure regulatory compliance with industry and client requirements.
Responsibilities
<ul>
<li>Manage daily operations of the microbiology department, including scheduling, workflow, and resource allocation.</li>
<li>Supervise, train, and mentor laboratory technicians and analysts.</li>
<li>Foster a culture of safety, quality, and continuous improvement.</li>
<li>Ensure proper execution of microbiological testing methods such as pathogen detection, indicator organisms, and spoilage organisms.</li>
<li>Review and approve test results, reports, and data integrity.</li>
<li>Troubleshoot technical issues and implement corrective actions.</li>
<li>Maintain compliance with ISO/IEC, FDA, USDA, and other relevant regulatory standards.</li>
<li>Oversee internal audits, proficiency testing, and corrective/preventive actions.</li>
<li>Ensure adherence to Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).</li>
<li>Serve as a technical resource for clients, providing guidance on microbiological testing and interpretation of results.</li>
<li>Collaborate with customer service and business development teams to support client needs.</li>
<li>Manage special projects, method validations, and new service offerings.</li>
<li>Monitor departmental KPIs, turnaround times, and productivity metrics.</li>
<li>Implement process improvements to enhance efficiency and accuracy.</li>
<li>Manage departmental budget, equipment procurement, and maintenance.</li>
</ul>
Work Environment
The laboratory hosts a team of 53 professionals specializing in chemistry and microbiology. The manager will oversee two supervisors who each manage teams of 7-8 individuals. Our facility stands as the showroom for state-of-the-art equipment and instrumentation, making it the largest third-party food testing company in the U.S
Job Type &amp; Location
This is a Permanent position based out of Springfield, MO.
Pay and Benefits
The pay range for this position is $85000.00 - $100000.00/yr.
Medical Insurance  Health Savings Account (HSA)  Dental Insurance  Vision Insurance  Contribution Rates  Additional Benefits  Life and Disability  Worksite Accident Critical Illness Hospital Indemnity  Legal and ID Theft  Flexible Spending Account (FSA)  Employee Assistance Program (EAP)  Commuter and Student Loan Assistance  401(k)
Workplace Type
This is a fully onsite position in Springfield,MO.
Application Deadline
This position is anticipated to close on Jan 15, 2026.
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.

*Microbiology Manager*

<h3>Job Description</h3>
Job DescriptionGeotechnical Engineer
Job Description
We are seeking a Geotechnical Engineer with experience in geotechnical investigations and construction inspections. The ideal candidate will have a B.S in Civil or Geotechnical Engineering and at least three years of relevant experience. This role involves both field and office work, with significant opportunities for career growth and development.
Responsibilities
<ul>
<li>Design earth structures, deep foundations, support of excavation, and underpinning systems.</li>
<li>Assist project managers with field work coordination and project management support.</li>
<li>Scope and oversee geotechnical investigations and construction projects.</li>
<li>Periodically perform inspections of geotechnical construction as needed.</li>
<li>Coordinate investigations and assist in geotechnical report writing.</li>
<li>Prepare standard logs and field forms, including drilling and test pit logs, field investigation dailies, and chain of custody logs.</li>
</ul>
Essential Skills
<ul>
<li>3+ years of experience in geotechnical investigations and construction inspections.</li>
<li>BS in Civil or Geotechnical Engineering.</li>
<li>Experience with investigation and field work coordination.</li>
<li>Field experience in earthwork, driven and drilled pile construction, footings subgrade and backfill inspection, and retaining wall design/construction.</li>
<li>Valid driver's license and reliable transportation.</li>
<li>Comfortable with field work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in geotechnical analysis and design.</li>
<li>Ability to prepare geotechnical reports and documentation.</li>
<li>Strong communication and project management skills.</li>
</ul>
Work Environment
<ul>
<li>The role involves 50-75% fieldwork, with the day starting at 7 AM. Fieldwork may require being outside in various weather conditions. </li>
<li>When not in the field, the engineer will work in the office. </li>
<li>Typically, fieldwork is scheduled for a few days to a week at a time, followed by office work to balance workload and reduce burnout. </li>
<li>The team consists of 17 members, with opportunities for upward growth. Benefits include work-from-home options (2 days a week), 2 weeks of PTO (with additional PTO for more experienced employees), free lunch every Wednesday and free breakfast every Thursday, and a $500 home office stipend.</li>
</ul>
Job Type &amp; Location
This is a Permanent position based out of Philadelphia, PA.
Pay and Benefits
The pay range for this position is $70000.00 - $92000.00/yr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a hybrid position in Philadelphia,PA.
Application Deadline
This position is anticipated to close on Jan 16, 2026.
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.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Chemical Operator (Night Shift: 7 PM – 7 AM)

Capital Resin Corporation (CRC) is passionate about innovation and pushing the boundaries of customer service. Our focus is helping companies create new and innovative organic chemistries, improving upon current chemistries, and delivering greater consistency and process stability. 

We manufacture and sell engineered chemistries as well as design and build chemical processes for a variety of Fortune 500 companies. 

Who we are.
Capital Resin Corp. is a 24/7 production environment dedicated to quality &amp; customer responsiveness. We’ve had significant growth in the past few years and are continuing to build upon that growth. Our company is seeking individuals who are adaptive, creative, responsive, logical, and able to make quick decisions to join our team. Chemical operators, supervisors, chemists, engineers, and salespersons are just to name a few positions that we seek.

We have an immediate opening for “Chemical Operator” positions.
Summary:
The Chemical Operator position will assist in meeting the schedule by completing assignments. The position will participate in daily ‘huddles’ to discuss continuous improvement opportunities and filling out visual production boards.

The Chemical Operator position will typically work 12-hour shifts. The schedule for “Night Shift” is 7:00 PM to 7:00 AM. Over a 2-week period, associates are typically scheduled to work three (3) 12-hours days one week, followed by four (4) 12-hour days the following week, or vice versa. Candidates must be willing to work additional days as required. Initial training may be on Day Shift (7:00 AM to 7:00 PM) until sufficiently trained to work night shift. 

Responsibilities:
<ul>
<li>Monitors batch while in process and make any adjustments as required. Properly communicates to supervisor when it appears that a goal or deadline will not be met.</li>
</ul>
<ul>
<li>Measure and mix chemicals according to specified formulas.</li>
<li>Monitor and adjust process variables such as temperature, pressure, and flow rates.</li>
<li>Follows all provisions of operating instructions. Responsible for the completion and accuracy of all batch ticket data entry. Responsible for meeting standard batch ticket cycle times while maintaining safety and quality.</li>
</ul>
<ul>
<li>Perform quality control checks on finished products. Monitors quality of output and takes appropriate action, including shutdown of process, to prevent or limit production. Follows all quality policies and production procedures to ensure quality product is produced.</li>
<li>Operates and monitors chemical processing equipment - Follow standard operating procedures to ensure safe and efficient production.</li>
<li>Stages raw materials and puts away finished product. Responsible for raw material and finished goods location integrity. Package and label finished products for shipment.</li>
</ul>
<ul>
<li>Maintain a clean and organized work area. Follow all safety protocols and wear appropriate personal protective equipment (PPE). Report any equipment malfunctions or safety hazards to the supervisor.</li>
<li>Other duties as assigned.</li>
</ul>

Requirements:
<ul>
<li>High School Diploma or GED</li>
<li>Technical manufacturing experience in a chemical facility a bonus.</li>
<li>Standing for extended periods of time, ability to lift, push and pull up to 55 pounds frequently, exposure to outside conditions and ability to work any shift.</li>
<li>Previous experience in chemical manufacturing or related field preferred.</li>
<li>Familiarity with machining, packaging, warehouse, or materials handling is a plus.</li>
<li>Ability to read and interpret technical documents and instructions.</li>
<li>Strong attention to detail and ability to follow precise instructions.</li>
<li>Good communication skills and ability to work well in a team environment.</li>
<li>Basic computer skills for data entry and equipment monitoring.</li>
</ul>
If you are a motivated individual with a strong attention to detail and a passion for chemical manufacturing, we encourage you to apply for the position of Chemical Operator. 

We offer competitive pay, benefits, and opportunities for career growth within our organization.
 

EOE M/F/D/V

Chemical Operator - Night Shift

<h3>Job Description</h3>
Job Description
Description
These openings are for B1- APR (Automatic Pour Room): This is the petri dish area, they make the media that is dispensed into the petri dishes. **This position may involve seeing sheeps blood in bags and/or cleaning petri dishes off. (Building 1) Shifts are as follows: 1st - Shift (Monday- Friday 6:00am-2:30pm) $17/hr 2nd - Shift (Monday- Friday 2:00pm-10:30pm) $19.55/hr 3rd - Shift (Sunday-Thursday 10:00pm-6:30am) $19.55/hr These roles require lifting/twisting/pushing up to 30 lbs repetitively, filing out paperwork throughout their shift and performing basic math with a calculator, working on their feet the entire shift. -packing, quality assurance, production, documentation of packaging procedures, and other warehouse duties. -Disqualifiers: Previously worked at Thermo Fisher and had a bad finish, or bad work history/attendance record Submittal Process: Send over a short sub package, shift they're interested in, Beeline info (last 4 of social, DOB, email, and dubbed resume), also include what time they can tour on Thursday (1pm-3pm) **They have to fully clear BG and DT before starting so make sure your candidates are okay with waiting for everything to clear. Could take 1-2 weeks** We have a waiver for Education.
Skills
production, packaging, picking, packing
Top Skills Details
production, packaging, picking, packing
Additional Skills &amp; Qualifications
Must have high school diploma/GED equivalent
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of LENEXA, KS.
Pay and Benefits
The pay range for this position is $17.00 - $20.70/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 LENEXA,KS.
Application Deadline
This position is anticipated to close on Jan 17, 2026.

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.

Cleanroom Technician - Building 1

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
This position will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations.
Responsibilities
<ul>
<li>Prepare and follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and logbooks</li>
<li>Able to identify, design, and implement process improvements</li>
<li>Comply with GMP protocols</li>
<li>Operate large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)</li>
<li>Assist other chemists within the Manufacturing group during synthesis and purification of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Mobile phase preparation</li>
<li>Column Packing</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Perform oligonucleotide/intermediate analysis via LCMS</li>
<li>Assist in scale up/process development from small/mid-scale chemistry</li>
<li>Communicate with cross-functional groups such as Process Development, Analytical Development, Quality Control, Quality Assurance, etc.</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
<li>Track and update raw material usage in D365 ERP software</li>
<li>Act as production campaign lead</li>
<li>Assist with new personnel training</li>
<li>Address and resolve production challenges proactively, utilizing analytical and critical thinking skills</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in a scientific field</li>
<li>5-10 years experience in a similar position</li>
<li>Good verbal and written communication skills</li>
<li>Ability to work in a team environment</li>
<li>Ability to pay attention to detail</li>
</ul>
Preferred:
<ul>
<li>Experience working in a GMP setting and controlled documentation</li>
</ul>
Wisconsin pay range $85,000—$95,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Associate Manufacturing Scientist III

<h3>Job Description</h3>
Job Description
Leukemia Research Scientist: Tampa, FL
Children's Cancer Research Group Laboratory is looking for a research scientist to direct, plan, supervise and execute laboratory research projects regarding the etiology of acute leukemias. A Ph.D., an appropriate background and experience is required. Must be able to personally perform the laboratory tests.&nbsp; Competitive salary and benefits provided. Resumes ONLY (do not personally deliver a resume. It will not be considered) Please send resume with the required qualifications only to:
<a href="mailto:ctebbi@childrenscancerresearchgroup.org" target="_blank">ctebbi@childrenscancerresearchgroup.org</a>&nbsp;

Leukemia Research Scientist

<h3>Job Description</h3>
Job Description
Fresno, CA
Full-Time | 7:00 AM – 3:30 PM, Monday–Friday
Pay: Starting at $30.77/hr, to be hired in at a higher rate
This is a safety‐sensitive position
About the Role
A growing organization in the food and chemical sector is seeking a skilled Chemist to support food safety inspection, product testing, and quality control operations. This role is ideal for someone who enjoys hands‐on laboratory work, problem‐solving, and ensuring products meet strict safety and quality standards.
Key Responsibilities
• Conduct chemical testing on finished products and raw materials.
• Perform food safety inspections and document findings.
• Provide technical and chemical expertise to internal teams, suppliers, and customers.
• Monitor and verify the repackaging of chemical products for resale.
• Maintain quality control for bulk and packaged chemical products.
• Prepare chemical solutions, reagents, and standards as needed.
• Ensure compliance with company procedures and regulatory requirements.
Qualifications
• Bachelor’s degree in Chemistry (required).
• 2–5 years of relevant laboratory or chemical testing experience.
• Strong understanding of chemical analysis, quality control, and safety practices.
• Ability to work independently and communicate technical information clearly.
• High attention to detail and commitment to maintaining a safe work environment.
Company DescriptionSkySource Solutions believes in attaining success. We know success is important to our clients, applicants, candidates, and our internal staff and want to be an integral part of that process. The SkySource Difference: We are not just another staffing firm! We truly care about our candidates long-term success and how we get there together. So the BIG Question is... How do we get there? Our team of Recruiters come with 5 plus years of industry experience and are not looking to just find you a job. We truly care about your short-term and long-term career goals and understand what's important in making that next career move. We want to understand what you are looking for from a cultural, compensation and benefits perspective. Apply today and experience the SkySource difference! 
<h3>Company Description</h3>
SkySource Solutions believes in attaining success. We know success is important to our clients, applicants, candidates, and our internal staff and want to be an integral part of that process.\r\nThe SkySource Difference: We are not just another staffing firm! We truly care about our candidates long-term success and how we get there together. So the BIG Question is... How do we get there?\r\nOur team of Recruiters come with 5 plus years of industry experience and are not looking to just find you a job. We truly care about your short-term and long-term career goals and understand what's important in making that next career move. We want to understand what you are looking for from a cultural, compensation and benefits perspective. \r\n\r\nApply today and experience the SkySource difference!

Chemist

<h3>Job Description</h3>
Job Description
CHEMICAL OPERATOR
Our company is currently seeking a skilled and experienced PETN Chemical Operator for our explosive manufacturing facility. The ideal candidate will have some mechanical and chemical experience, excellent communication skills, and a high degree of mechanical and chemical aptitude. The successful applicant will be responsible for operating production line equipment, handling and packaging finished goods, loading raw materials, monitoring the production process, operating loading machinery, maintaining work area and equipment, carrying out basic quality and testing checks, data logging, and reporting any issues with equipment directly to supervision. The applicant must be willing and able to cross-train into all positions within the PETN process. The applicant must understand and follow Standard Operating Procedures (Work Instructions) and production directives without deviation. Must be able to lift up to 50 lbs., sit, stand, climb stairs and qualify for all required PPE.
ABOUT AUSTIN POWDER
Austin Powder manufactures a full line of industrial explosives and provides blasting services to customers in the quarrying, mining, construction, and oil and gas industries -- all for the purpose of providing aggregate, energy, and mineral products to consumers.
Our values of commitment to safety, attention to detail, and the power of family are the very bedrock upon which our company's culture is built. We truly value our team which is why we offer competitive opportunities for career growth and advancement.
WORK EXPERIENCE / REQUIREMENTS
<ul>
<li>Must have basic understanding of computers</li>
<li>Must be able to handle working in chemical manufacturing environment</li>
<li>Must be self-starter capable of working in team or sole contributor</li>
<li>Good organization and record keeping skills</li>
<li>Excellent communication skills</li>
<li>Must be able to lift 50 lbs</li>
<li>Ability to work overtime when applicable</li>
<li>Swing Shift 12 hour shift schedule</li>
</ul>
EDUCATION REQUIREMENTS
<ul>
<li>Minimum of a high school education or equivalent mandatory</li>
</ul>
PREFERRED EXPERIENCE
<ul>
<li>1 year of experience in Chemical Operations</li>
<li>Previous working experience with Process Safety Management</li>
<li>Explosive or chemical manufacturing</li>
<li>Mechanically inclined</li>
<li>Previous working experience with Microsoft Word, Excel</li>
</ul>
ARE YOU READY TO JOIN OUR TEAM?
If you feel that you would be right for this night shift position, please fill out our initial 3-minute, mobile-friendly application so that we can review your information. We look forward to meeting you!
This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, national origin, and for inquiring about, discussing or disclosing compensation. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
 

 Job Posted by ApplicantPro

Chemical Operator

<h3>Job Description</h3>
Job Description???? Now Hiring: Chemical Operator | Join Our Team and Power the Process!
???? Location: Rock Hill, SC. ???? Schedule: Full-Time | 8-, 10-, or 12-hour shifts (Overtime &amp; Weekend Opportunities!) ???? Pay Type: Hourly | Non-Exempt
Are you ready to get hands-on in a fast-paced, safety-first manufacturing environment? We're looking for a Chemical Operator to join our operations team and play a key role in producing high-quality chemical products that make a difference. If you’re dependable, detail-oriented, and thrive in a production setting, this is your chance to grow your career in industrial manufacturing!
???? What You’ll Do:
✅ Operate and monitor a variety of process equipment including reactors, pumps, centrifuges, filters, and more ✅ Load/unload raw materials and finished goods safely and efficiently ✅ Monitor gauges and instruments, record data, and adjust valves and controls to ensure safe operations ✅ Troubleshoot and report mechanical/process issues as they arise ✅ Perform basic equipment maintenance and keep your work area clean and orderly ✅ Wear PPE and follow all HSEQ (Health, Safety, Environment &amp; Quality) protocols ✅ Communicate clearly with team members and participate in shift handovers
???? What You Bring:
✔️ High School Diploma or GED required ✔️ At least 1 year of experience in a manufacturing or chemical plant environment ✔️ Forklift experience (or willing to be trained) ✔️ Strong attention to detail and commitment to safety ✔️ Ability to work flexible hours, including overtime and weekends as needed
???? Bonus if you have: • WorkKeys Certification (SC) • 2+ years of relevant industry experience
???? Why You’ll Love Working Here:
???? Career growth potential ???? Team-oriented environment ???? On-the-job training ????️ Opportunity to work with cutting-edge equipment ???? Make a real impact in production
Ready to operate with purpose? ???? Apply today and bring your skills to a team that values your work and keeps safety at the core of everything we do.
Click below to schedule a conversation today: ???? Book a time here
or email me at: <a href="mailto:cwhitehead@qworksgroup.com" target="_blank">cwhitehead@qworksgroup.com</a>
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