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<h3>Job Description</h3>
Position Description If you love engaging in high-profile projects supporting the U.S Navy and our U.S Naval Ships, Serco has a great opportunity for you! Serco is hiring a Senior Marine Electrician to be part of a dynamic team supporting our US. Navy located in the beautiful surroundings of Norfolk, Virginia. In this role, your primary work location will be Norfolk with the possibility of work in Chesapeake, Newport News, and/or Portsmouth VA. Serco supports our US Naval Ships with successful and safe work by providing cabling, equipment, and C5ISR system installations for our Military. You will join an amazing team to fabricate, and assemble various electromechanical and electronic assemblies by applying appropriate safety techniques This position requires the ability to obtain and maintain an active DoD Secret clearance post-employment You play a critical role in ensuring that successful and safe work is performed on-board U.S. Naval Ships and our Military installations, which is vital to our Mission to protect and serve our Military. In this role you will: 
<ul>\n
<li>Receive initial instructions, equipment requirements, and advice from supervisor or engineer as needed; performs recurring work independently; work is reviewed for technical adequacy or conformity with instructions including troubleshooting and correcting malfunctions.</li>
\n
<li>Conduct various tests or experiments which may require minor modifications in test setups or procedures as well as subjective judgments in measurement; selects, sets up, and operates standard test equipment and records test data. </li>
\n
<li>Perform assignments that are not completely standardized or prescribed such as: Constructs components, subunits, or simple models or adapts standard equipment. </li>
\n
<li>Gather and maintains specified records of engineering data such as tests, drawings, etc.; performs computations by substituting numbers in specified formulas; plots data and draws simple curves and graphs.</li>
\n
<li>Perform simple or routine tasks or tests such as tensile or hardness tests; operates and adjusts simple test equipment; records test data. </li>
\n
<li>Rely on your experience and judgment to plan and accomplish goals and you will typically report to a supervisor in a safe work environment.</li>
\n</ul>
\n Meet Your Recruiter! Qualifications To be successful in this role you will have: 
<ul>\n
<li>A High School Diploma or equivalent.</li>
\n
<li>The ability to obtain and maintain and active DoD Secret Clearance post-employment</li>
\n
<li>The ability to obtain and gain access to shipyards (NAVSTA &amp; DBIDS), undergo a background investigation and pass a drug screening</li>
\n
<li>The ability to obtain an OSHA 10 certification</li>
\n
<li>The ability to get respirator qualified and wear PPE throughout the work shift.</li>
\n
<li>A minimum of 8 years experience in electrical work in a related field.</li>
\n
<li>A minimum of 8 years of Shipboard experience.</li>
\n
<li>A Multipin Connector certification.</li>
\n
<li>Fiber Optic certifications. </li>
\n
<li>Experience managing a crew of various trades. (6-10 people)</li>
\n
<li>A combination of experience in the following areas:
<ul>\n
<li>Competency attaching fiber optic, RJ-45, DB type connectors</li>
\n
<li>Read drawings (Tradesman level)</li>
\n
<li>QCI instruct of lower techs</li>
\n
<li>Implement safety program/SRAR Qual/CP</li>
\n
<li>Prelim QA testing, MCTs, space closeouts</li>
\n
<li>Multipin competent</li>
\n
<li>Elec testing reqs, i.e. ground checks, RSPT testing</li>
\n
<li>Layout &amp; cutting of electrical enclosures, electrical hook-ups &amp; multiple meter knowledge</li>
\n
<li>Reading drawings (Apprentice level)</li>
\n
<li>Band/pack MCTs/RISE</li>
\n
<li>Layout &amp; mount small equipment as needed</li>
\n
<li>Basic knowledge of tools, QA documents, meter</li>
\n
<li>Safety: Actively participates in safety surveillances &amp; walk-thrus</li>
\n</ul>
\n</li>
\n
<li>Familiarization with NAVSEA, standard concepts, practices, and procedures within the field of electrical repair, fabrication, and installation</li>
\n
<li>The ability to work in high heat spaces, climb shipyard dry dock stairs/ladders, work in kneeling position for layout of cable runs under false decking, lift up to 50 pounds with 80% of work requiring carrying, pushing, and/or pulling up to 40 pounds for majority of shift while being in a standing, crouching, or walking position.</li>
\n
<li>Attention to safety, which is critical</li>
\n
<li>The ability and willing to travel up to 10% to various work sites</li>
\n
<li>The ability to work on-site in Chesapeake, VA and travel to Newport News, VA.</li>
\n</ul>
\n Additional desired experience and skills: 
<ul>\n
<li>An active DoD Secret clearance</li>
\n
<li>An OSHA Certification</li>
\n</ul>
\n If you are interested in supporting and working with passionate Serco team- then submit your application now for immediate consideration. It only takes a few minutes and could change your career! Military Veterans and Spouses encouraged to apply! Company Overview Serco Inc. (Serco) is the Americas division of Serco Group, plc. In North America, Serco's 9,000+ employees strive to make an impact every day across 100+ sites in the areas of Defense, Citizen Services, and Transportation. We help our clients deliver vital services more efficiently while increasing the satisfaction of their end customers. Serco serves every branch of the U.S. military, numerous U.S. Federal civilian agencies, the Intelligence Community, the Canadian government, state, provincial and local governments, and commercial clients. While your place may look a little different depending on your role, we know you will find yours here. Wherever you work and whatever you do, we invite you to discover your place in our world. Serco is a place you can count on and where you can make an impact because every contribution matters. To review Serco benefits please visit: <a href="https://www.serco.com/na/careers/benefits-of-choosing-serco" target="_blank">https://www.serco.com/na/careers/benefits-of-choosing-serco</a>. If you require an accommodation with the application process please email: [email&nbsp;protected] or call the HR Service Desk at 800-628-6458, option 1. Please note, due to EEOC/OFCCP compliance, Serco is unable to accept resumes by email. Candidates may be asked to present proof of identify during the selection process. If requested, this will require presentation of a government-issued I.D. (with photo) with name and address that match the information entered on the application. Serco will not take possession of or retain/store the information provided as proof of identity. For more information on how Serco uses your information, please see our Applicant Privacy Policy and Notice. Serco does not accept unsolicited resumes through or from search firms or staffing agencies without being a contracted approved vendor. All unsolicited resumes will be considered the property of Serco and will not be obligated to pay a placement or contract fee. If you are interested in becoming an approved vendor at Serco, please email [email&nbsp;protected]. Serco is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Senior Marine Electrician (Norfolk, VA)

<h3>Job Description</h3>
ALOIS Healthcare is seeking a travel Physicist for a travel job in Oakland, California.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 11/10/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
They have three main components of work: clinical service and consultation, research and development, and teaching. A medical physicist might: Plan radiation treatments for cancer patients. Study how radiation effects the body.
ALOIS Healthcare Job ID #17269734. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Physicist Acute
About ALOIS Healthcare
Why ALOIS Healthcare?
ALOIS means “brave warrior” and that’s what you are- Warrior in Scrubs! Just as you advocate for your patients, we will advocate for you. The pay you deserve. The support you need. We’re in your corner for every battle – because you shouldn’t settle for anything less when it comes to your career.
We offer:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Industry-leading pay
<ul>
<li>Generous cost of living and housing stipends</li>
</ul>
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Opportunities for referral, sign-on, and extension bonuses
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Weekly health insurance or health insurance Marketplace weekly bonus
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Continuing education credits
We’re proud to be recognized globally as a certified minority-owned staffing supplier.
At ALOIS Healthcare:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Everyone Matters
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;We are Performance Driven
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;We are Open, Honest and Direct
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;We are Transparent
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;We are Inclusive
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;We Do the Right Thing
We care about you - and your success is our success.

Travel Physicist

<h3>Job Description</h3>
Job Description
Company Summary: 
Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose laundry and dish products, facial wipes, and baby wipes. With manufacturing plants and
warehouses in Chicago and Long Island, NY, the company provides customers with private-label solutions and contract manufacturing services for products found in retail and institutional markets.
Through its commitment to agility, innovation, trust and reliability, and sustainable creation, Radienz Living is passionate about providing its customers with products that support a cleaner way of living
and a more radiant world. The company has undergone a remarkable transformation over the last two years, focusing on two product lines: Unit Dose products, where it is the undisputed leader in Private Label and Contract Manufacturing, and Personal Care Wipes, where it manufactures the wipes for the country's #1 beauty care brand. 
Our commitment to operational excellence is supported by robust quality systems, multiple GMP certifications, and a comprehensive suite of in-house labs—including FDA/EPA-certified microbiology,
quality control, chemistry, and R&amp;D facilities. This infrastructure enables us to deliver innovation, safety, and performance at every stage of the product lifecycle.
 
Background: 
The Lab Technician/Lab Assistant supports the daily operations of the Microbiology Laboratory by preparing samples and materials for testing in accordance with established procedures and quality standards. This includes completing and organizing all required documentation, logging samples into laboratory records and systems, and preparing media, solutions, and other testing materials. The role is also responsible for monitoring and recording equipment temperatures, cleaning and maintaining laboratory instruments according to schedules and SOPs, and ensuring the lab environment remains clean, safe, and compliant with regulatory and company standards.
 
Responsibilities:
• Record temperatures for incubators, refrigerators, and water baths.
• Operate autoclaves and perform control procedures, including biological indicator checks and temperature verification
• Conduct daily calibration of laboratory instruments such as balances and pH meters.
• Collect water, swab, and environmental air samples for microbiological testing.
• Read ampoules in the dry bath and accurately document results.
• Log all samples into the microbiology sample logbook and complete required documentation for each test.
• Prepare bottles, tubes, and plates for Microbial Limits Testing (MLT) and other microbiological analyses.
• Prepare and adjust the pH of media required for laboratory testing.
• Maintain a clean, organized, and safe laboratory environment, including washing and sterilizing glassware and equipment.
• Run autoclave cycles for biohazard waste, media preparation, and sterilization of filters.
• Monitor and maintain laboratory supply inventory; ensure necessary materials are available and restock as needed.
 
Qualifications &amp; Requirements:
• High school diploma or equivalent required; associate or bachelor’s degree in Biology, Microbiology, or a related scientific discipline preferred.
• Prior experience in a microbiology or quality control laboratory within a manufacturing or regulated environment preferred.
• Familiarity with aseptic techniques, autoclave operation, and environmental monitoring procedures.
• Ability to accurately perform and document routine laboratory tests and calibrations.
• Strong attention to detail and adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Basic computer skills and experience with data entry or laboratory information systems.
• Ability to work independently and collaboratively in a fast-paced production environment.
• Strong organizational and communication skills.
• Physical ability to stand for extended periods and handle laboratory materials and equipment safely.
 
Physical Demands:
• While performing the duties of this job, the employee is regularly required to stand, walk, and use hands to handle or operate laboratory instruments, tools, and materials.
• The role may involve frequent bending, reaching, and lifting or moving objects up to 25 pounds.
• Visual acuity and manual dexterity are required to accurately perform laboratory tests, record data, and handle small equipment and glassware.
• The employee must be able to wear required personal protective equipment (PPE), such as lab coats, gloves, safety glasses, and masks, as necessary.
• Extended periods of standing during testing or media preparation may be required.
 
Work Environment:
• Work is performed primarily in a laboratory and manufacturing environment where exposure to biological agents, chemicals, and disinfectants may occur.
• The role requires adherence to all safety procedures, including the use of PPE and compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• The noise level in the work environment is generally moderate but may vary depending on production activity.
• The laboratory environment is temperature-controlled, but occasional work in production or warehouse areas may be required.
• The employee must maintain a clean, organized, and safe workspace in accordance with company and regulatory standards.
 
Why Join Us?
At Radienz Living, we take pride in making high-quality personal care and household products that people trust every day. As part of our team, you’ll join a company that values safety, teamwork, and continuous improvement. We believe in investing in our people — providing hands-on experience, training, and opportunities to grow your career in manufacturing, quality, and operations.
You’ll work in a clean, professional, and collaborative environment where your contributions make a direct impact on the products we deliver to leading brands and consumers. At Radienz Living, we’re more than a manufacturing company — we’re a community built on respect, reliability, and shared success.
The approximate hourly pay for this position is $18.00-$23.00*. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities as well as geographic location.
 
Radienz Living is an equal employment opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, 
gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to 
inform us confidentially if you may require any special accommodation to participate fully in our recruitment experience. Contact us at 631-952-0100.
 
This position is not eligible for Visa Sponsorship.
 
 1st shift, Monday - Friday; 8am - 4:30pm

Microbiology Lab Tech

<h3>Job Description</h3>
Prime Staffing is seeking a travel Physicist for a travel job in Oakland, California.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 11/10/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours</li>
<li>Employment Type: Travel</li>
</ul>
About the Position
\n
Specialty: Medical Physicist Experience: Minimum 2 years of experience in clinical medical physics (radiation oncology, diagnostic imaging, or nuclear medicine) License: ABR or ABMP certification required Certifications: BLS required; all certifications must be submitted with expiration dates Must-Have: All time-off requests must be submitted with the initial application
\n
Description: We are seeking an experienced Medical Physicist to support radiation therapy or diagnostic imaging services. This role requires at least 2 years of recent clinical experience, preferably in a hospital or cancer center setting. Responsibilities include machine calibration, quality assurance testing, treatment planning support, and compliance with regulatory standards.
\n
Floating within departments may be required. Weekend or holiday duties may apply. Missed shifts must be made up. Compliance and onboarding typically take 4–6 weeks. A voice screening and hiring manager interview are part of the process.
\n
Requirements
\n
Required for Onboarding:
\n
<ul>\n
<li>BLS – AHA (Active)</li>
\n
<li>ABR or ABMP Certification</li>
\n</ul>
Prime Staffing Job ID #34459290. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied / Tech:Physicist,08:00:00-16:00:00
About Prime Staffing
At Prime Staffing, we understand the importance of finding the perfect fit for both our clients and candidates. Prime Staffing utilizes a unique matchmaking approach, providing the most qualified contingent staffing to our clients, and the most competitive contracts to our workforce. Our experienced team takes the time to get to know both our clients and candidates, their needs, and preferences, to ensure that each placement is a success.
We offer a wide range of staffing services including temporary, temp-to-perm, and direct hire placements. Our extensive network of qualified candidates includes nurses, allied healthcare professionals, corporate support professionals and executives.

Travel Radiation Oncology Medical Physicist

<h3>Job Description</h3>
Job Description
Come join our family! Microbac Laboratories is an essential business offering competitive pay and benefits including medical, dental, vision, life insurance, disability, generous paid time off including vacation, holidays and flex-time, a wellness program, referral bonus, tuition reimbursement and more! 
Whether you are just starting your career in science or looking to further it, Microbac will put you on the path of an exciting career with room to grow. Quality, safety, giving back to our communities, diversity and inclusion, customer success and employee wellbeing are part of our core culture. We are looking for motivated individuals to join our family as a Chemist I.
ABOUT MICROBAC
Microbac serves our clients with the utmost expertise and respect for their market requirements, constraints and challenges. We embody a company-wide commitment to exceptional customer experience, which has been refined over nearly 50 years of trusted, analytical and measurement experience.
Through our network of laboratories, offices, and field services, we have the flexibility to meet the unique requirements for each client, project and scope.
As a privately held third-party testing company, Microbac operates with a commitment to safety, quality and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and nutrition and life science markets.

JOB SUMMARY
The Chemist I, working in an accredited commercial laboratory, provides a variety of routine scientific tasks under close supervision. Receives specific and detailed instructions as to required tasks and results expected. 
ESSENTIAL FUNCTIONS
<ul>
<li>Following established SOP’s and adhering to state, federal and other accrediting body requirements, prepare and process samples, and collect information about the composition of substances to support the analytical testing needs of clients, for such purposes as quantitative analysis, and product development </li>
<li>Prepare necessary standards, solutions, reagents, media, and samples for sample analyses</li>
<li>Utilize specialized laboratory equipment and instrumentation to process and analyze samples</li>
<li>Perform equipment and instrumentation set up</li>
<li>Accurately record observations and data and basic interpretation of data</li>
<li>Maintain the integrity of procedures and record professional activity for peer review</li>
<li>Monitor and address sample backlog issues</li>
<li>Maintain accurate, up to date logs, notebooks and equipment records</li>
<li>Perform necessary laboratory administrative functions such as filing paperwork, photocopying, reviewing of data, and entering data into computerized LIMS</li>
<li>Comply with and promote Safety, and Quality programs</li>
</ul>
MINIMUM REQUIREMENTS
<ul>
<li>High School Diploma</li>
<li>Basic knowledge of principles, terminology, practices, techniques and instrumentation commonly used in a laboratory setting</li>
<li>Ability to effectively prioritize work and manage time to meet deadlines and rush orders</li>
<li>Computer literacy</li>
<li>Ability to work with delicate laboratory equipment</li>
<li>Ability to communicate effectively in both written and verbal formats</li>
</ul>

WORKING CONDITIONS AND PHYSICAL REQUIREMENTS
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.
Physical Requirements: 
<ul>
<li>While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel objects, tools, or controls; talk or hear; and taste or smell. The employee is occasionally required to stand, walk, and sit.</li>
<li>The employee must regularly lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.</li>
</ul>
Working Conditions: 
<ul>
<li>While performing the duties of this job, the employee frequently works near moving mechanical parts and is frequently exposed to fumes or airborne particles and toxic or caustic chemicals.</li>
<li>The noise level in the work environment is usually moderate.</li>
</ul>

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Chemist I

<h3>Job Description</h3>
Job DescriptionRetro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. We’re building a mission-driven team of accomplished and kind individuals who embrace our startup culture of rapid iteration, transparency, and versatility. We are seeking a motivated Scientist to support the development of rejuvenation therapies for osteoarthritis (OA). In this role, you will focus on building and executing the in vivo portion of the OA research, in particular, disease model development, drug dosing, and the downstream readouts including histopathology, molecular/cellular characterization, and behavior readouts. You will report to the Tissue Reprogramming lead. About you: You have a good understanding of Musculoskeletal biology and have hands-on experience in related histology. You enjoy hands-on work and value being organized, planning proactively, and paying attention to the details. You’re a highly collaborative team member with a “can-do” attitude and you apply a “Mission &gt; team &gt; individual" mindset to your work. You value direct, clear communication. You’re motivated to work on a forefront of science and produce therapies that improve patients’ health span!In this role you will:
<ul>
<li>Support the development of the osteoarthritis (OA) research pipeline, working collaboratively with in vitro focused team members.</li>
<li>Drive in vivo side of the program, including designing and executing OA studies with either healthy animals or disease models, performing drug administration, histological analysis, and comprehensive characterization (biodistribution, gene expression profiling, PK/PD, and toxicology).&nbsp;</li>
<li>Perform and train technical in vivo team members on surgical induction of osteoarthritis models in mice and rats.</li>
<li>Conduct intra-articular (IA) injections for therapeutic delivery.</li>
<li>Collaborate with cross-functional teams (Vivarium, Computational biology) to integrate preclinical findings.</li>
<li>Maintain accurate records and protocols, analyze and interpret experimental data; provide scientific and development insights and in-depth data interpretation to inform decision-making within the team and for senior leadership.</li>
<li>Work with other departments and CROs as necessary to plan and expedite project objectives.</li>
</ul>
 You will thrive in this role if you:
<ul>
<li>Have a PhD in Cell &amp; Molecular Biology, Biomedical Sciences, Physiology or related field, with at least 2 years of industry or post-doctoral experience.</li>
<li>Have proven experience designing, leading, and conducting in vivo experiments.</li>
<li>Have prior research experiences in musculoskeletal biology and osteoarthritis research.</li>
<li>Hands-on experience in drug dosing, microsurgical model generation for osteoarthritis, histology, immunohistochemistry, and/or immunofluorescence.</li>
<li>Are experienced in analyzing and quantifying histological and imaging data.</li>
<li>Strong collaboration and communication skills; thrives in a highly interdisciplinary, team-first environment</li>
<li>Are passionate about novel translational research and rejuvenation therapies.</li>
<li>Are intellectually curious, timeline sensitive, and detail-oriented; maintaining high standards for research data while actively and accurately communicating your findings.</li>
</ul>
 It’s a bonus if you:
<ul>
<li>Have expertise in structural damage assessment, including histopathology (e.g., OARSI scoring) and advanced imaging modalities.</li>
<li>Are familiar with behavioral and functional assessments relevant to OA (e.g., weight bearing, gait analysis).</li>
<li>Have prior experience in gene therapy development</li>
</ul>
 At Retro, we don’t use titles. New hires join as a “Member of X Team.” Depending on experience, this role could flex from a Scientist to a Senior Scientist level.&nbsp; Total compensation includes competitive base salary, generous equity, and benefits including: - Medical, dental, and vision insurance for you and your family- 401(k) plan with 4% matching- Flexible time off and 10 company holidays per year- Paid parental leave- Annual learning &amp; development stipend- Daily Retro-sponsored lunch and snacks&nbsp;We take pride in cultivating an environment that fosters collaboration, open communication, and authenticity. We believe that great results are best delivered by a highly creative team working in concert. We are an equal opportunity employer; we do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are diverse in background and singular in mission.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

In Vivo Scientist, Musculoskeletal Research

<h3>Job Description</h3>
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: MilliporeSigma in Cleveland, OH is seeking a Quality Control Chemist to join our Quality Control department. In this vital role, you will conduct release testing for raw materials, manufactured goods, purchased materials for repackaging, and packaged good for sale. The department has both an Analytical Chemistry lab and Microbiology lab. You will perform analytical chemistry testing against a multitude of analytical specifications to determine whether the material meets or does not meet requirements. This position involves wet chemistry testing and/or instrumental analysis. Responsibilities: 
<ul>\n
<li>Work closely with Department Supervisor and Team Leads to ensure that departmental tasks are completed on time</li>
\n
<li>Follow all safety requirements and refer to MSDS for PPE and other safety guidance</li>
\n
<li>Practice proper laboratory safety and waste disposal</li>
\n
<li>Maintain Laboratory space and instruments</li>
\n
<li>Perform testing per documented procedure</li>
\n
<li>Recognize out-of-spec (OOS) results and initiate OOS investigation</li>
\n
<li>Perform needed instrument or titrant verification/calibration during scheduled time</li>
\n
<li>Demonstrate Good Documentation Practices (GDP) and Data Integrity Principles</li>
\n</ul>
\n Physical requirements: 
<ul>\n
<li>Wearing of PPE </li>
\n
<li>Lifting up to 25 pounds</li>
\n
<li>Standing for long periods of time </li>
\n</ul>
\n Who You Are: Minimum Qualifications: 
<ul>
<li>Bachelor's degree in Chemistry, Biochemistry or other Life Science field with 2+ years of laboratory experience </li>
</ul>
\n -OR- 
<ul>
<li>Associate degree in Chemistry, Biochemistry or other Life Science field with 3+ years of industry laboratory experience</li>
</ul>
\n Preferred Qualifications: 
<ul>
<li>Experience with the following: FT-IR, Auto-Titrators for Assay and Moisture, Wet Chemistry testing techniques, UV-Vis, pH, and Solution preparations </li>
</ul>
\n
<ul>\n
<li>Ability to perform all functions in a safe and timely manner in accordance with OSHA standards and general rules and regulations governing the workplace</li>
\n
<li>Detail oriented, excellent verbal and written communication skills, well-organized</li>
\n</ul>
\n Pay Range for this position: $24.00 - $44.00/hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Quality Control Chemist 1

<h3>Job Description</h3>
Job Description Production ChemistThis is an exciting opportunity to join a global, industry leading company. The Chemist will formulate products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specificationsResponsibilities:
<ul>
<li>Responsible for bulk formulating products of low to medium complexity including intermediates in accordance with approved written procedures and policies. </li>
<li>Perform data entry and inventory control utilizing the ERP database. </li>
<li>Responsible for completing production documentation and maintaining quality records to GDP/GMP standards.</li>
<li>Coordinate prioritize and plan lab tasks to meet strict deadlines.</li>
<li>Follows controlled Standard Operation Procedures/ documents.</li>
<li>Monitors manufacturing processes and performs adjustments when necessary to meet required yields.</li>
</ul>
Requirements and Desired Experience:
<ul>
<li>Bachelor’s degree in a life science or related field</li>
<li>0-3 years working in a general manufacturing environment formulating products in the areas of biological sciences, life sciences, or an equivalent.</li>
<li>Ability to follow guidelines and handle hazardous materials safely. </li>
<li>Ability to work in a product team and make decision of limited scope, subject to review.</li>
<li>Able to follow detailed procedures and have good documentation skills. Understanding of Good Manufacturing Practices and Good Laboratory Practices. </li>
<li>Must be experienced in using ERP systems- SAP a plus. </li>
<li>Working knowledge of Microsoft Office tools – Excel and Word.</li>
<li>Basic working knowledge of laboratory environments, materials, and equipment.</li>
</ul>
Pay Range (Based on Experience &amp; Qualifications): $31 per hour

Production Chemist

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Technician Job Description
We are seeking a dedicated Chemical Technician to support chemical operations throughout our facility. The successful candidate will assist the team with tasks related to handling chemicals, chemical transfer, and packaging, as well as other duties needed throughout the facility and laboratory.
Responsibilities
<ul>
<li>Support chemical operations within the facility.</li>
<li>Assist with handling chemicals, including chemical transfer and packaging.</li>
<li>Perform various tasks as needed throughout the laboratory and facility.</li>
</ul>
Essential Skills
<ul>
<li>Experience in chemical handling and manufacturing.</li>
<li>Familiarity with Safety Data Sheets (SDS) and Good Manufacturing Practices (GMP).</li>
<li>Strong attention to detail.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>1 year of chemical manufacturing or handling experience preferred.</li>
</ul>
Work Environment
This role is based in a chemical manufacturing environment with working hours from 7 a.m. to 3 p.m., Monday to Friday. There is a possibility for overtime before and after shifts, as well as on Saturdays. Initially, the position will be 5 days per week, but may transition to a 4-day, 10-hour schedule. The facility is involved in the development of new fire suppression products and is currently expanding.
Job Type &amp; Location
This is a Contract to Hire position based out of Green Bay, Wisconsin.
Pay and Benefits
The pay range for this position is $20.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Green Bay,WI.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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