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<h3>Job Description</h3>
Job Description
This is a remote position.
The Biostatistician will play a critical role in designing, analyzing, and interpreting clinical trial data to support drug development and regulatory submissions. This position collaborates with clinical, data management, and regulatory teams to ensure statistical rigor in trial design, data analysis, and reporting. The ideal candidate brings strong analytical skills, regulatory knowledge, and proficiency with statistical programming tools. Key Responsibilities: Collaborate with clinical and regulatory teams to design statistically sound clinical trials (e.g., sample size calculation, randomization methods). Develop and review statistical analysis plans (SAPs) in compliance with regulatory guidelines. Perform statistical analyses using SAS, R, or other statistical software on clinical trial datasets. Interpret results and present findings in clinical study reports, regulatory submissions, and scientific publications. Provide statistical support during protocol development, including endpoints and methodology. Ensure statistical deliverables meet internal quality standards and regulatory requirements (e.g., FDA, EMA, ICH). Review case report forms (CRFs) and data validation rules for accuracy and consistency with statistical needs. Collaborate with Data Management and Clinical Operations to ensure data integrity and resolve data discrepancies. Stay up to date on industry best practices, methodologies, and relevant regulatory guidance. Minimum Qualifications: Master’s or Ph.D. in Biostatistics, Statistics, Mathematics, or a related quantitative field. Minimum of 3 years (for MS) or 1 year (for PhD) of relevant experience in the pharmaceutical, biotechnology, or CRO industry. Proficient in statistical programming languages such as SAS and/or R. In-depth knowledge of ICH-GCP, CDISC standards (SDTM, ADaM), and regulatory guidance documents. Strong understanding of clinical trial design, methodology, and regulatory requirements. Excellent communication skills with the ability to interpret and present statistical findings clearly. Strong attention to detail and a commitment to data quality and accuracy. In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. Be part of our network of Subject Matter Experts. E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.

Biostatistician

<h3>Job Description</h3>
Job Descriptionjob summary: 
Our client is seeking a scientist to join their Systems Immunology Lab in the Inflammation &amp; Immunology Research Unit. The successful candidate will be responsible for generating massive single-cell perturbational data using functional genomics and single cell transcriptomics technologies in collaboration with a small team.
 location: Cambridge, Massachusetts job type: Contract salary: $44.00 - 45.95 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Generate custom lentiviral libraries and maintain extensive cell cultures.</li>
<li>Generate edited pools of cells via lentiviral transduction and arrayed electroporation.</li>
<li>Develop, modify, and customize such procedures as needed to succeed in specific cell lines and types, and at large scale.</li>
<li>Generate single-cell data via several commercial workflows, including from 10x Genomics.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelors or Masters + 3 years of experience in Biology, Immunology, or a related field</li>
<li>3+ years of hands-on experience with standard cell culture techniques including primary immune cells handling and isolation, maintenance of cell lines and in vitro stimulation of primary immune cells, experience with standard molecular biology techniques including lentivirus infection, qPCR, western blot, and flow cytometry.</li>
</ul>
Preferred:
<ul>
<li>Bonus: direct experience in pooled cell screening of immune cells using CRISPRi, CRISPRa, and other methods of in vitro gene editing.</li>
</ul>
#LI-CV1
 skills: Molecular Biology, Immunology, Biology, In Vitro, Flow Cytometry, Cell Cultures, Western Blot, CRISPR 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Scientist II - Inflammation & Immunology

<h3>Job Description</h3>
Job Title: Radiation Physicist Location: Danville, Pennsylvania Job Category: PhD, Diagnostic Services Schedule: Days Work Type: Full time Department: Radiation Oncology Division Date Posted: 02/26/2025 Job ID: R-73852 Job SummaryThe Department of Radiation Oncology at Geisinger Health System is seeking applications for medical physicists to join our team in central Pennsylvania. The successful candidate will be involved in all aspects of clinical physics services. Responsibilities include supervising and supporting dosimetry, calibration, treatment planning, and safety equipment operations. The role involves maintaining equipment and regulatory records, as well as billing for services rendered. Additionally, the physicist will contribute to departmental research activities and clinical protocols, and provide education for residency programs within Radiation Oncology. Job Duties
Background:
<ul>
<li>Geisinger participates in one or more of over 100 clinical research trials, which include new treatment protocols for various cancers, as well as select trials involving new cancer drugs. We also offer screening and prevention trials for individuals at risk for certain types of cancer. Our more than 30-year alliance with the National Cancer Institute (NCI) and its community research programs enables us to offer advanced care and treatment options close to home. The health system has received the NCI-NCORP designation and is dedicated to active participation in cancer clinical trials.</li>
<li>Geisinger fosters an exciting intellectual environment that includes the Geisinger Commonwealth School of Medicine, more than 50 graduate medical education programs, and fellowship programs in hematology/oncology and palliative medicine. The medical school is recognized for its innovative educational approach, featuring a curriculum that emphasizes active learning, longitudinal clinical experiences, and community engagement.&nbsp;</li>
<li>Our patients contribute to the MyCode Community Health Initiative with &gt;275,000 patient genomes sequenced for research and real-time clinical applications. Providers interested in clinical, or informatics research collaborate within Geisinger and across organizations to benefit our patients and the scientific community</li>
</ul>

Job Duties and Responsibilities:
<ul>
<li>Clinical support of linear accelerator treatments, including patient simulation, image fusion, treatment planning, secondary dose calculation, plan quality assurance and reviews of treatment plan safety and quality.</li>
<li>Special emphasis on stereotactic radiosurgery (SRS), stereotactic body radiotherapy (SBRT), HDR, and TBI treatment planning, secondary dose verification and plan quality assurance.</li>
<li>Clinical support of brachytherapy procedures, including patient simulation, treatment planning, secondary dose verification, treatment delivery and reviews of treatment delivery safety and quality; high dose rate equipment purchase, maintenance and quality assurance; and permanent seed implants, including ordering, assays, implant support and planning and documentation.</li>
<li>Preparation and updates of physics and dosimetry policies and procedures as required.</li>
<li>Maintenance of daily, monthly and annual quality assurance testing for software and equipment, both diagnostic and therapeutic, throughout the department.</li>
<li>Involvement in the departmental residency program, including the development of, and instruction, in a new radiobiology curriculum for both physicist and radiation oncologist residents.</li>
<li>Coordination of physics aspects of the department’s research program, including support for existing departmental and national research protocols, as well as developing original physics-oriented research projects.</li>
<li>Travel, including interdepartmental travel as needed; training for new equipment, software or modalities; and participation in national meetings and conferences.</li>
<li>Other physics duties as needed, including but not limited to commissioning of both software and new equipment for treatment or diagnostic use, radiation shielding calculations, and in vivo measurements for verification of patient dose.</li>
<li>Radixact and/or CyberKnife experience is desired.</li>
<li>Perform other related duties as assigned.</li>
</ul>

Colleagues, Facility and Equipment:
The department staff comprises six experienced medical physicists who are actively involved in various clinical, teaching, and research activities. Additionally, the department includes ten radiation oncologists, nine dosimetrists, one medical physics resident, and a dedicated IT specialist. The department is equipped with seven Varian linear accelerators, which include one Trilogy, five TrueBeam machines, and one Halcyon. It also has one CyberKnife, one Radixact Tomotherapy machine, and two HDR brachytherapy afterloaders (Elekta Flexitron), along with five CT simulators from GE Medical Systems. Furthermore, the department has three-year and ten-year long-term plans for the system upgrade and an additional cancer center is currently under construction and is expected to open in Summer 2025. Perhaps just as important, we encourage an atmosphere of collaboration, cooperation and collegiality.
 Position Details
Work is typically performed in a clinical environment. Accountable for satisfying all job specific obligations and complying with all organization policies and procedures. The specific statements in this profile are not intended to be all-inclusive. They represent typical elements considered necessary to successfully perform the job. Additional competencies and skills outlined in any department-specific orientation will be considered essential to the performance of the job related to that position.
 EducationMaster's Degree- (Required) Certification(s) and License(s)Specialty Certification - Default Issuing Body Our Purpose &amp; ValuesOUR PURPOSE &amp; VALUES: Everything we do is about caring for our patients, our members, our students, our Geisinger family and our communities. KINDNESS: We strive to treat everyone as we would hope to be treated ourselves. EXCELLENCE: We treasure colleagues who humbly strive for excellence. LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow. INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation. SAFETY: We provide a safe environment for our patients and members and the Geisinger family We offer healthcare benefits for full time and part time positions from day one, including vision, dental and domestic partners. Perhaps just as important, from senior management on down, we encourage an atmosphere of collaboration, cooperation and collegiality. We know that a diverse workforce with unique experiences and backgrounds makes our team stronger. Our patients, members and community come from a wide variety of backgrounds, and it takes a diverse workforce to make better health easier for all. We are proud to be an affirmative action, equal opportunity employer and all qualified applicants will receive consideration for employment regardless to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

Radiation Physicist

<h3>Job Description</h3>
Job DescriptionBilingual Middle School Math Specialist 
Bilingual Middle School Math Specialist 
Are you passionate about teaching and learning? Are you motivated to make a positive impact in the lives of urban, working-class youth? If yes, this position with SmartStart Education is right for you! 
The Job: 
SmartStart Education seeks a small group Bilingual Math Specialist tutor to work with small groups of middle school students on Mondays through Thursdays. Each small group consists of 1-4 students. Each group consists of students who have been identified as students who are struggling with fundamental Math skills. Students are from all grade levels, including 6th through 8th. 
The tutor will work with each group several times throughout the week at a middle school in Bronx, NY. Groups will take place within the classroom (push-in services) or outside of the classroom (pull-out services). Tutors should be flexible and comfortable with both settings. Each tutor will be given the responsibility of taking daily attendance and monitoring student progress using a personal device (mobile phone). 
Job Details: 
The tutoring position begins January 26, 2026 and ends on April 20 2026. The schedule will be 8am through 2:20pm. Applicants are encouraged to schedule interviews as soon as possible to allow ample time to complete onboarding steps. Failure to do so may result in a position being unavailable. 
Salary Range: $193.70 to $213.07 per day.
Qualifications: 
If you believe that this position aligns with your qualifications and showcases your exceptional skills, we kindly request your confirmation regarding your ability to meet the following minimum requirements: 
<ul>
<li>Possession of a bachelor's degree from an accredited institution in any field is mandatory. ***Please note that applications with anticipated graduation dates will not be considered.</li>
<li>Bilingual Spanish Proficiency is REQUIRED. </li>
<li>Demonstrated experience of at least one year in teaching or tutoring, either within a school environment or another educational setting.</li>
<li>Comprehensive understanding of the unique challenges faced by urban students, schools, and communities, encompassing racial disparity, socio-economic disparity, and cultural disparity.</li>
<li>Mastery of middle school math concepts and skills, substantiating proficiency in the subject matter.</li>
<li>Display of genuine passion and unwavering commitment towards fostering the success of students.</li>
<li>Exemplary punctuality, ensuring timely attendance and adherence to established schedules.</li>
<li>Proficiency in communication skills, enabling effective and articulate interaction with students, colleagues, and interested parties.</li>
<li>Ability to comfortably commute to the designated location.</li>
</ul>
If you are confident in meeting these minimal qualifications, we encourage you to proceed with your application.
<ul>
<li></li>
</ul>
 
Compensation details: 193.7-213.07
 
PI4e7ff9196bc2-25405-39415271

Bilingual Middle School Math Specialist

<h3>Job Description</h3>
Job DescriptionOur Story
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow.
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program (ESOP) and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage — with medical premiums either paid by Superior or highly subsidized — so you and your family can access great benefits with minimal cost.
You’ll also join a supportive team, where paid training and experienced coworkers help you learn, grow, and succeed from day one. 
At SUPERIOR, you get more than a job — you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to success.
What We’re Looking For
We are currently seeking a Chemical Handler to work at our Louisville, KY location.
This role is responsible for:
<ul>
<li>Daily production</li>
<li>Unloading raw materials</li>
<li>Completing paperwork</li>
<li>Maintaining a safe operation</li>
</ul>
Schedule:
<ul>
<li>Full-time, 1st shift</li>
<li>Monday–Friday, 8:00 a.m. – 4:30 p.m.</li>
<li>Additional hours may be required</li>
</ul>
What You’ll Do
You will:
<ul>
<li>Transfer products into and out of pails, drums, and totes using transfer pumps and hoses</li>
<li>Read paperwork with chemical amounts and blending instructions</li>
<li>Pull product samples and submit them to the Lab for quality control</li>
<li>Label containers and secure closures</li>
<li>Inspect, label, store, and prepare products for shipment</li>
<li>Stage, load, and unload pails, drums, and totes</li>
<li>Operate a forklift</li>
<li>Wear required PPE for safety</li>
<li>Keep your work area safe, clean, and orderly</li>
<li>Lift and/or move 55 lbs</li>
<li>Cross-train in areas such as shipping/receiving, bulk handling, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventive maintenance, and yard truck spotting</li>
</ul>
Candidates Should Possess
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Effective verbal and written communication skills to work with co-workers, chemists, administrative staff, delivery personnel, and management</li>
</ul>
What We Offer
At Superior, we take care of our people. Our comprehensive benefits package includes:
<ul>
<li>Medical Insurance – 100% company-paid HDHP or a low-cost PPO option</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>401(k) Retirement Plan</li>
<li>Flexible Spending Accounts (FSA)</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Dental, Vision &amp; Life Insurance</li>
<li>Short-Term &amp; Long-Term Disability (STD &amp; LTD)</li>
<li>Paid Training from day one</li>
</ul>
Join a company that invests in you — personally, professionally, and financially.
EOE including disability/veteran/drug free

Chemical Handler

<h3>Job Description</h3>
Job Description
Summary of Position: 
Under direct supervision, this role leads the formula design, validation and implementation of new products, line extensions, product improvements and cost savings initiatives. This role will also serve as technical assistance to the manufacturing sites and supervisor. 

Essentials for the Role: 
<ul>
<li>Under direct supervision, define the formulation, nutritional and process parameters needed to develop a new product which meets customer expectations and project objective(s) </li>
<li>Work collaboratively in the execution of development from bench to production scale for new products, product improvements and cost savings projects</li>
<li>Create new prototypes for product development initiatives and identify, evaluate and approve potential ingredients and manufacturing suppliers</li>
<li>Identify opportunities for competitive market advantage through product benchmarking</li>
<li>Contribute significantly, directly and continually to attain results through the generation and application of advanced, specialized knowledge</li>
<li>Understand product requirements, plantequipmentand processes to enable the creation of detailed product specifications</li>
<li>Understand the commercialization process and contribute to the organization, implementation and management of work streams</li>
<li>Generate and support pipeline work to drive cost optimization through formulation and processing efficiencies</li>
<li>Manage calibration of laboratory equipment </li>
<li>Work collaboratively with manager and teammate at other locations to execute individual and team goals </li>
<li>Exhibit strong communication skills within technical and non-technical community</li>
</ul>
Important Details: The duties and responsibilities described are not a comprehensive list of all tasks. Additional tasks and duties may be assigned from time to time as necessitated by business needs. 
You’ll fit right in if you have: 
<ul>
<li>Bachelor’s Degree Required: Food Science, Engineering, Chemistry or related field</li>
<li>1- 3years of technical experience in industry; internships or coops considered </li>
<li>Ability to communicate effectively and openly while working with a cross-functional team</li>
<li>Must be a self-starter, independent, organized, energeticand resourceful</li>
<li>Excellentwrittenandverbalcommunicationsskills</li>
<li>Aptitude fororganizationand project management</li>
<li>Invests time and effort in professional development and supporting customer-centric culture.</li>
</ul>


Work Environment: 
This job operates in a professional manufacturing and R&amp;D lab environment. Must be able to conduct themselves accordingly. Lab hygiene and Good Manufacturing Practices (GMPs) must be followed. 

Physical Demands: 
Role is a hybrid of computer-based work and lab/product development-based work. May require lifting boxes of up to 40 lbs. The physical demands described here are representative of those that must be met by the employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. 

Expected Work Hours: 
This is a full-time position. The employee must be available during “core” business hours between 8:00-5:00 pm, Monday through Friday. 

Travel: 
20 – 30% Headquarters in TN and 3 Manufacturing Facilities in PA 

Equal Employment Opportunity: 
MBC Companies is committed to providing equal opportunity for all employees and applicants without regard to race, color, religion, national origin, sex, age, marital status, sexual orientation, disability, political affiliation, personal appearance, family responsibilities, matriculation, or any other characteristic protected under federal, state, or local law. Each person is evaluated on the basis of personal skill and merit. MBC Companies’ policy regarding equal employment opportunity applies to all aspects of employment including recruitment, hiring, job assignments and promotions, working conditions, scheduling, educational and recreational programs.

Associate Food Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
<ul>
<li>Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.</li>
<li>Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.</li>
<li>Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.</li>
<li>Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure compliance with international regulations such as FDA and EMA.</li>
<li>Work collaboratively with R&amp;D and production teams to support product development and release.</li>
<li>Provide technical support and training to junior team members or other departments.</li>
</ul>
Essential Skills
<ul>
<li>3-7 years of routine testing experience using HPLC and dissolution techniques.</li>
<li>Proficiency in working with solid oral dosage forms, raw materials, and finished products.</li>
<li>Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.</li>
<li>Strong understanding of Pharma GMP practices.</li>
<li>Competence in laboratory applications including wet chemistry, titration, and chromatography.</li>
<li>Basic computer skills in MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>Ability to document and record analytical experiments and results as per cGMP guidelines.</li>
<li>Strong problem-solving skills and attention to detail.</li>
<li>Knowledge of regulatory guidelines such as GMP and GLP.</li>
</ul>
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type &amp; Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $35.00/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 East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 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.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Job Description

POSITION SUMMARY The Microbiology Supervisor is responsible for the operation of Microbiology section of the clinical laboratory.&nbsp; The Microbiology Supervisor facilitates the implementation of hospital and laboratory policies and procedures.&nbsp; Responsible for assisting in training new employees, supervising both Clinical Laboratory Scientists and laboratory phlebotomist’s workload organization, and monitoring daily maintenance and quality control. This person will report to the Lab Manager Implements good public relations by representing the laboratory directly to patients, physicians and hospital staff at all times.
ESSENTIAL DUTIES AND RESPONSIBILITIES
<ul>
<li>Responsible for assisting with the selection of methodology and instrumentation to perform laboratory tests appropriate for the patient population served.&nbsp; Responsible for the validation and implementation of new instrumentation.&nbsp; Ensures the standardization of tests methodologies, procedures, instrumentation, and reference ranges.</li>
<li>Verifies test procedures performed and established the laboratory’s test performance characteristics, including, but not limited to the linearity, precision and accuracy of each test and test system.</li>
<li>Ensures participation in and successful completion of a quality control and approved proficiency testing program commensurate with the services offered.&nbsp; Troubleshoots any problems with the proficiency testing program.&nbsp; Establishes parameters for acceptable level of analytic performance.&nbsp; Ensures that quality is maintained throughout entire testing process from order entry through results reporting.</li>
<li>Reviews the work of others to ensure that tests are performed in accordance with prescribed standards.</li>
<li>Assists in maintaining and optimizing work standards to assure a reasonable turnaround time of test results.</li>
<li>Troubleshoots equipment problems.</li>
<li>Maintains inventory control of supplies and reagents in his/her section(s).</li>
<li>Schedules, organizes and delineates duties of personnel.</li>
<li>Assists manager in performance evaluations of the employees in his/her sections.</li>
<li>Responsible for the operation of the Microbiology department.</li>
<li>Works closely with the Laboratory Manager to meet the administrative and financial goals of the department</li>
<li>Responsible for meeting the service and quality goals of the department. Assumes responsibility for daily operations and meets CLIA requirements for microbiology</li>
<li>Provides clinical microbiology consultations to medical and hospital staff</li>
<li>Present micro data reports clearly and concisely to management, including QC performance metrics and trends</li>
<li>Proactively identifies and implements improvements and lean initiatives</li>
<li>Responsible for the technical and scientific oversight of the department including assisting in hiring of personnel, training/competency assessment and input for performance review of the staff in their designated area.</li>
<li>Responsible for making clinical/technical decisions in the resolution of testing/reporting issues, maintenance of the quality and security of department instrumentation, quality control documentation and meeting hospital goals to ensure accurate and timely patient care.</li>
<li>Responsible for maintaining procedure manuals for all testing performed and the documentation required for regulatory and licensing organizations</li>
<li>Oversee and manage team schedule of staff and PTO request.&nbsp;</li>
<li>Work collaboratively with other department leaders to have a more efficient workflow for the Clinical laboratory.&nbsp;</li>
<li>Responsible for ensuring staff compliance with hospital policies and meeting regulatory requirements within their assigned areas (e.g. coordinate meal breaks, corrected reports, attendance, overtime and punctuality)</li>
<li>Setting an example- must always be conscious of how his / her words and actions will be perceived.</li>
<li>Attend minimum of three (3) leadership seminar/workshop annually</li>
<li>Performs additional duties as directed by the by the Laboratory Director or Manager which are necessary for the efficient operation of the laboratory.</li>
</ul>
Job Requirements

POSITION REQUIREMENTS
A.&nbsp; &nbsp;Education
<ul>
<li>Bachelor’s degree – Science</li>
</ul>
B.&nbsp; Qualifications/Experience
<ul>
<li>2-5 years Microbiology Clinical Laboratory Experience</li>
<li>CA Clinical Laboratory Scientist License or Clinical Microbiologist Scientist License</li>
<li>2 years leadership experience in an acute care setting required</li>
</ul>
C.&nbsp; &nbsp;Special Skills/Knowledge
<ul>
<li>Strong interpersonal and organizational skills.&nbsp; Proficient with computer.</li>
</ul>
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#LI-AJ1

Microbiology Supervisor - Full Time Days

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical EngineerJob Description
We are seeking a skilled Chemical Engineer to perform all chemical process functions related to chemical batching. This role involves conducting root cause analysis (RCA) to troubleshoot batching issues and implementing corrective and preventive actions (CAPAs) for both internal and external challenges. You will be responsible for scaling up and commercializing new formulas, adjusting existing formulas, and validating all manufacturing and quality processes and specifications. Additionally, you will perform in-process batch adjustments, support production scaling to meet product specifications, and analyze production and laboratory data to optimize processes and reduce costs.
Responsibilities
<ul>
<li>Conduct root cause analysis for customer complaints and internal production issues.</li>
<li>Ensure all batch adjustments are executed accurately when raw materials or formulas change.</li>
<li>Scale up and commercialize new formulas and products, ensuring correct implementation.</li>
<li>Analyze production data and quality data to identify optimization and cost reduction opportunities.</li>
<li>Participate in the disposition of non-conforming materials and support deviation management.</li>
<li>Mentor and coach fellow engineers and quality and production personnel in continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>1-5 years of experience in chemical engineering or chemical process engineering.</li>
<li>Ability to diagnose and resolve customer complaints and internal production issues.</li>
<li>Experience with root cause analysis and implementation of CAPA.</li>
<li>Expertise in chemical manufacturing, quality control, and process engineering.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Degree in Chemical Engineering or a related field.</li>
<li>Experience in scale-up and commercialization processes.</li>
<li>Familiarity with chemical equipment and laboratory practices.</li>
<li>Knowledge of new product development and chemical processing.</li>
</ul>
Work Environment
This position operates in a chemical manufacturing environment, working across offices, laboratories, production areas, and production labs. The role follows a first shift schedule from Monday through Friday, with flexible working hours typically ranging from 40 to 45 hours per week, extending to 50 hours during major projects or issues. You will collaborate with various organizational levels, including R&amp;D, Quality, Production, Maintenance, Customers, Sales, and leadership roles.
Job Type &amp; Location
This is a Permanent position based out of Germantown, WI.
Pay and Benefits
The pay range for this position is $90000.00 - $110000.00/yr.
This company offers health insurance, dental insurance, vision insurance, 401k match, bonuses, etc. They also provide paid vacation and paid holiday.
Workplace Type
This is a fully onsite position in Germantown,WI.
Application Deadline
This position is anticipated to close on Jan 23, 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.

Chemical Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist OperatorJob Description
The Chemist Operator will be responsible for producing Active Pharmaceutical Ingredients using chemical reactors. This role requires following specific Batch Records to ensure the production of a consistent product.
Responsibilities
<ul>
<li>Handle various unit operations, such as reactions, filtration, distillation, drying, and milling, on raw materials and various stages of chemical processing according to written manufacturing procedures and SOPs.</li>
<li>Follow and document instructions per batch sheet to produce products in accordance with all cGMP guidelines.</li>
<li>Set up equipment, including vessels, tanks, centrifuges, and dryers, for proper processing. Clean and verify equipment and vessels.</li>
<li>Record observations of operating conditions.</li>
<li>Drive and operate a fork truck.</li>
<li>Make work prioritization or timing decisions with supervisory oversight.</li>
<li>Adjust utilities to maintain reaction parameters.</li>
<li>Maintain process flow through the plant while adhering to all safety, GMP, and environmental regulations and standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in Chemical Operation or Batching, 1-5 years preferred.</li>
<li>Knowledge of GMP guidelines from food, chemical, or pharmaceutical industries.</li>
<li>Understanding of Analytical Chemistry and Chemical Operating.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma with experience, or an Associate's or Bachelor's degree in Sciences, preferably in Chemical Technology or Chemistry.</li>
<li>Experience in GC and Batching processes.</li>
</ul>
Work Environment
The work environment is a clean laboratory and production setting. Initial training will be on the first shift for 3-6 months, after which the role will transition to a permanent shift from 6 p.m. to 6:30 a.m., following a 2-2-3 schedule, including working every other weekend. The company is expanding its innovation hub, offering growth opportunities into leadership positions for those who excel.
Job Type &amp; Location
This is a Contract to Hire position based out of Grafton, WI.
Pay and Benefits
The pay range for this position is $24.00 - $26.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Grafton,WI.
Application Deadline
This position is anticipated to close on Jan 23, 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.

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