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<h3>Job Description</h3>
Job Description
The research coordinator is responsible for coordinating research patient visits according to the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience/knowledge and the needs of the organization, which are subject to change from time to time.
Compensation:
$19 hourly
Responsibilities:
<ul>
<li>Coordinate and schedule subject visits within study/subject-specific windows per protocol guidelines</li>
<li>Prepare visit-specific documentation and charts for the Clinical Research Coordinator</li>
<li>Observe Coordinator in patient care and management</li>
<li>Assist the Coordinator in monitoring subject flow and assist in subject care and management</li>
<li>Observe, assist, collect and record all necessary data for follow-up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 3; NO Gene Therapy)</li>
<li>Transcribe subject study information from source documents to the Electronic Case Report Forms</li>
<li>Administer all mandatory questionnaires to study subjects</li>
<li>Set up, prepare subjects, and conduct electrocardiograms (ECG) on subjects as required per the study protocol</li>
<li>Promptly request all necessary medical records for Serious Adverse Event Reporting</li>
<li>Process and ship laboratory biological samples for analysis</li>
<li>Perform intraocular pressure checks after injections</li>
<li>Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)</li>
<li>Inform subjects and obtain written re-consents in regard to ICF’s</li>
<li>Perform other duties as assigned</li>
<li>Obtain any applicable additional/required sponsor training and/or certification</li>
</ul>
Qualifications:
<ul>
<li>Possess high energy, and have a positive, professional attitude</li>
<li>Strong communication skills with a team-player approach</li>
<li>Critical time management skills</li>
<li>Certifications/Trainings</li>
<li>ICH GCP Training/Certificate</li>
<li>IATA Certification</li>
<li>Adhere to ongoing training and education</li>
<li>Demonstrate effectiveness by showing courtesy, diligence, integrity, and teamwork</li>
<li>Other functions may be assigned, and management retains the right to add or change the duties at any time</li>
</ul>
About Company 
<ul>
<li>Benefits: Paid Time Off + Holidays, Medical Insurance, Vision, Dental, 401(k), Life Insurance</li>
<li>Travel within 120 miles is required (company-provided transportation, day trips only), which can mean early mornings and long days</li>
<li>Schedule varies depending on the assigned role and/or assigned physician</li>
<li>Physical Demands and Abilities: Ability to stand and walk for long periods, ability to lift more than 30 lbs</li>
</ul>

Research Assistant

<h3>Job Description</h3>
Job DescriptionChemical Operator
Job Description
We are seeking an experienced Chemical Operator who can work independently and efficiently. The successful candidate will communicate ideas effectively, request actions, and formulate plans or policies under supervision. This role involves developing, monitoring, interpreting, and understanding policies and procedures to ensure alignment with organizational strategies and objectives. The Chemical Operator will organize, prioritize, and oversee activities to meet business objectives and apply safe systems of work. The role also involves creating and reviewing reports, motivating employees, managing risks in production processes, and ensuring compliance with regulations.
Responsibilities
<ul>
<li>Develop, monitor, interpret, and understand policies and procedures.</li>
<li>Plan, organize, prioritize, and oversee activities to efficiently meet business objectives.</li>
<li>Manage and apply safe systems of work.</li>
<li>Create and review relevant reports.</li>
<li>Motivate employees to learn, grow, and develop.</li>
<li>Identify, assess, prioritize, and manage risks in production processes.</li>
<li>Achieve compliance with applicable rules and regulations.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemical mixing, compounding, and GMP.</li>
<li>Basic equipment operation.</li>
<li>Ability to carry out routine tasks and follow strict, detailed instructions.</li>
<li>Knowledge of chemistry.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Ability to carry out operational tasks following established processes.</li>
<li>Experience in installing and maintaining equipment.</li>
<li>Support the quality function by adhering to strict quality standards.</li>
<li>Follow mandatory work instructions, including the use of personal protective equipment.</li>
</ul>
Work Environment
The work environment operates on a quarterly swing shift, alternating between day and night shifts every three months. The company is based in Germany and is committed to employee retention, offering opportunities for cross-training and internal promotions.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Birmingham,AL.
Application Deadline
This position is anticipated to close on Sep 22, 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.

Chemical Operator

<h3>Job Description</h3>
Job Description
!!!! HIRING IMMEDIATELY - Clean Room Assembler: All Shifts Open - $20/hr !!!!
APPLY NOW 
Shift:
<ul>
<li>1st 6am to 2pm - $17.00</li>
<li>2nd 2pm to 10pm - $19.55</li>
<li>3rd 10pm to 6am - $20.40</li>
<li>Weekend Shift PM or AM - $20.40</li>
</ul>
Responsibilities
• Assemble small parts with precision using tweezers.
• Operate machinery by placing parts in a jig and aligning them on a computer.
• Conduct quality checks using microscopes and magnifying glasses.
• Work in a clean room environment when needed.
• Operate a laser etching machine occasionally.
Essential Skills
• 1+ year of experience in roles requiring attention to detail and quality control using microscopes, micrometers, or calipers.
Additional Skills &amp; Qualifications
• Experience working in a medical-related position is a plus.
• 1+ year of ERP experience is beneficial.
Why Work Here?
Enjoy a generous benefits package that includes 3 weeks of PTO, 11 paid holidays, and a 401k plan with a 6% match. Health, dental, and vision insurance are available from the first day of employment. Additionally, there is an opportunity for tuition reimbursement, supporting your continuous learning and development.
Work Environment
The work environment allows for casual attire, such as jeans and a polo or nice t-shirt. Safety goggles are provided due to the use of lasers, while steel toe boots are not required. If working in the clean room, employees will need to suit up each day.
Job Type &amp; Location
This is a Contract to Hire position based out of Kettering, Ohio.
Pay and Benefits
The pay range for this position is $19.55 - $20.40/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 Kettering,OH.
Application Deadline
This position is anticipated to close on Sep 22, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

!!! URGENTLY HIRING - Clean Room Assembler - $20/hr - APPLY NOW !!!!

<h3>Job Description</h3>
Job Title:&nbsp;Southeast USA Area Research Manager
Location:&nbsp;Southeast USA / Thonotosassa, FL (Near Tampa, FL)
 
Lead a High-Impact Research Station in the Southeast
We're growing and we’re seeking a senior-level research scientist and proven team leader to manage one of our premier research stations in the Southeast. This is a strategic and hands-on leadership role, responsible for both scientific direction and operational oversight of a cross-functional team—including researchers, technicians, and farm staff.
 
You’ll lead multidisciplinary field, greenhouse, and lab trials focused on crop protection, sustainable agriculture, and product development. You’ll also drive client success by ensuring high-quality trial design, data integrity, and proactive communication.
 
If you're passionate about applied research and team leadership—and ready to make an impact in a dynamic, growth-oriented company—this role offers the platform and autonomy to lead meaningful innovation.
 
What You’ll Do
<ul>
<li>Oversee day-to-day operations of a regional research station, including scientific research staff and farm/technical support teams</li>
<li>Design and manage field, greenhouse, and laboratory trials for evaluating crop protection products, particularly foliar, soil, and seed-applied treatments</li>
<li>Develop and maintain strong working relationships with clients and cooperators</li>
<li>Lead proposal development and transform opportunities into ready-to-sign research contracts</li>
<li>Coordinate staffing, trial scheduling, data collection, and reporting workflows</li>
<li>Ensure excellence in data management, trial execution, and final client deliverables</li>
<li>Lead virtual and in-person meetings with cross-functional teams</li>
<li>Maintain research infrastructure, equipment, and facility compliance</li>
<li>Investigate emerging research methods and market trends to identify new service opportunities</li>
<li>Support professional development and licensing compliance for team members</li>
<li>Represent the station’s capabilities and results in both internal and external settings</li>
</ul>
 
What You Bring
<ul>
<li>Master’s or Ph.D. in Agronomy, Entomology, Plant Pathology, Crop Protection, Biology, or related agricultural sciences</li>
<li>Minimum of 5 years of experience in research management and agricultural product development</li>
<li>Proven ability to manage scientific teams and agricultural staff in a research station setting</li>
<li>Strong background in crop pest management, pesticide efficacy, and disease trials across field, greenhouse, and lab environments</li>
<li>Expertise in research proposal development, scientific reporting, and client-facing presentations</li>
<li>Understanding of soil pest biology and sustainable agricultural practices</li>
<li>Excellent leadership, organizational, and interpersonal communication skills</li>
<li>Proficiency in Microsoft Office and research data management tool</li>
</ul>
 
Why This Role?
<ul>
<li>Join a respected organization with deep roots in applied agricultural research</li>
<li>Lead a well-established research facility with a capable team and strong client base</li>
<li>Shape high-impact research that supports innovation in sustainable agriculture</li>
<li>Competitive compensation and benefits package</li>
<li>Opportunities for long-term growth and national visibility</li>
</ul>
 
Additional Requirements
<ul>
<li>Ability to lift up to 50 pounds regularly</li>
<li>Willingness and ability to travel 15–20% of the time</li>
</ul>
 
Benefits:
<ul>
<li>401(k)</li>
<li>Cell phone reimbursement</li>
<li>Dental insurance</li>
<li>Employee assistance program</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Professional development assistance</li>
<li>Referral program</li>
</ul>

Southeast USA Area Research Manager at Florida Ag Research

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
The Quantitative, Translational &amp; ADME Sciences (QTAS) department is seeking a highly motivated fulltime contract Scientist to join the In Vitro ADME Sciences group (IVAS).
</li>
<li>
Work in collaboration with other team members to characterize the CYP Induction properties of candidate drug molecules and may work on other in vitro ADME assays.
</li>
<li>
Works very closely with other disciplines (medicinal chemistry, pharmaceutical sciences, pharmacology, toxicology etc.) to conduct preclinical studies, support clinical evaluation and contribute to IND and NDA filings.
</li>
<li>
In this role, you will be a scientist with hands-on experience in conducting in-vitro ADME assays including CYP450 induction assays to characterize candidate drug molecules for potential to induce CYP450 enzymes.
</li>
<li>
Provide support to project teams to enhance mechanistic understanding of complex drug-drug interactions.
</li>
<li>
Routinely conduct (hands-on) evaluation of CYP450 induction
</li>
<li>
Conduct qPCR assay
</li>
<li>
Interpretation of in vitro CYP induction data derived from assays in human hepatocytes or reporter gene systems
</li>
<li>
Perform human and rodent hepatocytes cell culture, seeding and maintenance
</li>
<li>
Perform cell viability assessments and use microplate reader to measure endpoints
</li>
<li>
Contribute to the design of invitro ADME assays and data interpretation
</li>
<li>
Analyze data and maintain detailed, accurate and comprehensible study documentations
</li>
<li>
Use BioELN and GraphPad Prism for data analysis
</li>
</ul>
Qualifications:
<ul>
<li>
BS (1-3 years relevant experience) or MS in Biochemistry, Chemistry or Biology
</li>
</ul>
California Fair Chance Act:
Synectics Inc. will consider qualified applicants with a criminal history pursuant to the California Fair Chance Act. You do not need to disclose your criminal history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if Synectics Inc. is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. Find out more about the Fair Chance Act by visiting calcivilrights.ca.gov/fair-chance-act/.
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist

<h3>Job Description</h3>
Job Description
Process Expert (Chemical Operator)
Overview:
Celanese&nbsp;is a Fortune 500 global chemical and specialty materials company that engineers and manufactures products essential to everyday living. With global headquarters in Dallas, Texas, Celanese employs approximately 13,300 dedicated people working at more than 50 owned and operated manufacturing facilities across 27 countries. We are committed to employee growth and creating shareholder value, and strive to make a difference in the communities where we operate. Our company focuses on the safety of its employees, provides competitive compensation (including benefits starting Day 1), and emphasizes giving back to the community.&nbsp;
Responsibilities:
Purposeand Summary of position:
<ul>
<li>Process expert (chemical operator) in production unit will be responsible, with training, for operating and troubleshooting equipment, assisting maintenance, and maintaining environment</li>
<li>Operators will be required to learn all jobs in the unit including floor operations, control room, material movement, and filtration</li>
<li>Understand and follow all Site and Unit Safety procedures and protocols</li>
<li>Perform all functions necessary including operation of all equipment</li>
<li>Perform preliminary troubleshooting on equipment and process malfunctions and be prepared and able to make first attempt repairs where appropriate</li>
<li>Support maintenance in the unit through LOTO of equipment and issuing Safe Work Permits when required</li>
<li>Strictly follow all batch recipe sheets and SOCs</li>
<li>Maintain accurate records of all observations and results</li>
<li>Accurately and thoroughly reporting these data via written (Logbook &amp; PGRs), to the shift relieving process experts, and to process leaders</li>
</ul>
Qualifications:
<ul>
<li>High School Diploma or GED or 10 years of manufacturing experience with some high school education</li>
<li>Some technical college a plus&nbsp;</li>
<li>2 years of mechanical aptitude experience.</li>
<li>Chemical Manufacturing/Operations experience&nbsp;</li>
<li>Solid equipment and mechanical skills</li>
<li>Strong initiative and ability to troubleshoot "on the fly"</li>
<li>Good work ethic as indicated by work record</li>
<li>Ability to work on a team</li>
<li>Strong computer skills</li>
<li>Ability to work independently as well as a member of the team</li>
<li>Strong oral and written communication skills, excellent observation skills</li>
<li>Solid safety regulation understanding/practice</li>
<li>Ability to learn and acquire information in both a computer-based and hands on environment</li>
</ul>
Desirable Knowledge/Skills/Abilities:
<ul>
<li>Knowledge, experience and demonstrated good performance in chemical processes</li>
<li>DCS or control room operator experience</li>
<li>Aptitude to learn and acquire various different operational and maintenance skills</li>
</ul>
 Celanese is an Equal Opportunity Employer. Celanese does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
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orzQfwpJSU

<h3>Job Description</h3>
Job Description
What we are looking for:
The Associate Scientist position is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment. In this role, you will be supporting product formulation development and characterization focused on implantable and injectable pharmaceutical devices for controlled drug delivery utilizing Secant Group’s biomaterial platform.
What you will do:
<ul>
<li>Formulate and characterize drug-loaded polymer formulations designed for long-acting implantables, injectables, and oral gastroretention devices to support customer projects and internal investigations</li>
<li>Execute pre-formulation studies, such as drug particle size analysis, SEM, light microscopy, milling, and sieving</li>
<li>Characterize drug-polymer miscibility and physiochemical interactions between polymers and various drugs, using DSC, TGA, rheometry</li>
<li>Analyze formulations using FTIR and Raman spectroscopy to determine drug-polymer mixing efficiency, drug loading, and content uniformity</li>
<li>Setup and run dissolution studies and analyze dissolution media to determine drug release profiles using HPLC to quantify drug concentration</li>
<li>Setup and run degradation studies and analyze sample weight, dimensions, and topography to determine polymer degradation behavior</li>
<li>Perform wet chemistry experiments, like Soxhlet extraction, Karl Fischer titrations, and acid/base titrations</li>
<li>Collaborate with other teammates within R&amp;D to achieve project goals</li>
</ul>
Who you are:
<ul>
<li>BS in chemistry, biochemistry, chemical engineering, biomedical engineering, pharmaceutics, pharmaceutical sciences, or a related discipline with 0-2 years of experience</li>
<li>Knowledge of biomaterials specifically biodegradable polymers or polyurethanes</li>
<li>Exposure to controlled release drug delivery applications</li>
<li>Desire to develop formulation and characterization skills for drug-polymer dosage forms</li>
<li>Ability to learn polymer processing techniques, including dispensing, formulation, mixing, milling, extrusion, dispersions, emulsions, molding, casting, and coatings</li>
<li>Ability to learn test methods and equipment, including mechanical testing (MTS, Instron), DSC, TGA, FTIR, Raman, Dissolution, HPLC, Rheometry, SEM, Light Microscopy, Particle Size Analysis, Titrations, Extractions</li>
</ul>
What we offer:
<ul>
<li>Annual Bonuses</li>
<li>401k with excellent company match</li>
<li>Health Insurance: Medical with Rx plan / Dental / Vision</li>
<li>Company Paid Short-Term and Long-Term Disability</li>
<li>Generous Paid Time off and Holiday Pay</li>
</ul>
Who we are:
The Secant Group is an advanced technology biomaterials company headquartered in Telford, Pennsylvania, with manufacturing facilities in Quakertown and Perkasie, Pennsylvania. Secant provides innovative solutions through next-generation materials, structures, textile designs, and process technologies for the medical device, pharmaceutical, aerospace and energy markets.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY The Metrology Technician will assist Metrology personnel with product, maintenance and equipment calibration issues according to FDA, cGMP and BA Sciences' Standard Operating Procedures. 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Monitors and maintains the water systems.</li>
<li>Installation, maintenance and calibrates stability chambers, incubators, refrigerators and freezers.</li>
<li>On-call Monitoring of stability chambers and controlled rooms.</li>
<li>Calibration of equipment and instrumentation required for tests, including mechanical and chemical tests.</li>
<li>Assists chemists and other company personnel on an as needed basis.</li>
<li>Follows all safety rules and regulations.</li>
<li>Ensures all work performed strictly adheres to cGMP, Company, client and Pharmacopeial methodologies.</li>
<li>Assist in proper management of hazardous waste and compliance with DES hazardous waste rules.</li>
<li>Performs problem solving with minimal rework.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
A high school diploma or GED is required. 0-2 years of related experience. Knowledge of cGMPs and related compliance regulations and guidances is preferred. A Metrology Technician should be willing to attend technical training classes to enhance skills or correct identified deficiencies. Requires the ability to lift and/or move up to 50 lbs.
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>Self-starting motivated person who possesses good interpersonal skills and who is able to effectively interact with all departments with the Company.</li>
<li>Must have good organizational and verbal communication skills.</li>
<li>Basic computer skills required. Experience with cGMP is preferred.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Metrology Technician

<h3>Job Description</h3>
Job Descriptionjob summary: 
As a Senior Formulation/Process Scientist in Central Islip, NY, you will be a key SME on analytical methods, driving the development of new pharmaceutical products. This individual contributor role is responsible for independently developing, assessing, and validating analytical test methods, leading projects related to extractables and leachables (E&amp;L), and providing technical support for product development from pre-formulation through to FDA submissions.
This is a permanent role on-site in Central Islip, NY.
Relocation Candidates welcome to apply.
 location: Central Islip, New York job type: Permanent salary: $90,000 - 105,000 per year work hours: 9 to 5 education: Doctorate responsibilities: 
<ul>
<li>Operate as the subject matter expert (SME) on analytical methods for products that are under development, products that are commercialized and in support of process analytical technologies (PAT) for commercial manufacturing processes.</li>
<li>Operate as the subject matter expert (SME) on analytical methods for various internal and external projects. Independently develop, assess and/or verify and validate analytical test methods for APIs, excipients, packaging components, devices and drug products using industry standard methodologies including QbD principles for analytical methods; US FDA or EU guidance's and requirements; United States Pharmacopoeia (USP) guidelines; International Council for Harmonization (ICH) guidelines. Techniques may include standard tools like HPLC, UPLC, UV, GC, LC-MS, Viscometer, Karl-Fisher, IR, Particle size analyses, XRPD, DVS, Rheometer etc. to more specialized techniques such as LS-MS/MS, NMR, SS-NMR, Synchrotron etc.</li>
<li>Lead and define strategy on all topics extractable and leachables (E&amp;L).</li>
<li>Evaluate material from new vendors for suitability of material based on physico-chemical properties and perform studies in support of vendor qualifications.</li>
</ul>
 qualifications: 
EDUCATION AND EXPERIENCE
<ul>
<li>PhD in Analytical Chemistry, Pharmaceutical Chemistry, Organic Chemistry or Medicinal Chemistry or scientific degree.</li>
<li>Hands-on wet lab experience</li>
<li>1+ years of experience in HPLC</li>
<li>1+ years of experience in Karl Fischer titration</li>
<li>1+ years of experience in inhalation toxicology</li>
</ul>
 #LI-AB1 
 skills: Liquid Chromatography (LC), Karl Fischer (KF) Titration 
 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.

Senior R&D Scientist, Analytical Chemistry

<h3>Job Description</h3>
Job Description
Create Your Experience of a Lifetime!
Come work and play in the mountains!&nbsp; Whether it’s your first-time seeing snow or you were born on the slopes, joining our team means discovering (or re-discovering!) a passion for the outdoors while building lifelong connections with teammates and guests from around the world.
With 40+ resorts across 3 continents, you can join our team for a season or stay to build a career. From day one, you'll receive some of the highest compensation rates in the industry, free pass(es) along with free ski and snowboard lessons, 40% retail discounts, the chance to grow through Epic Service - our leading training and development experience, and wellness benefits to fuel your success.
Hiring for our seasonal positions occurs on a rolling basis. Applications will be accepted until December 15th or until the positions are filled (whichever is first).
Employee Benefits
•&nbsp;&nbsp; &nbsp;Ski/Mountain Perks! Free passes for employees, employee discounted lift tickets for friends and family AND free ski lessons&nbsp; •&nbsp;&nbsp; &nbsp;MORE employee discounts on lodging, food, gear, and mountain shuttles •&nbsp;&nbsp; &nbsp;401(k) Retirement Plan&nbsp; •&nbsp;&nbsp; &nbsp;Employee Assistance Program •&nbsp;&nbsp; &nbsp;Excellent training and professional development •&nbsp;&nbsp; &nbsp;Referral Program
To Learn More, please review the Benefits Eligibility Summary
Job Summary:
As a Snowmaker, you will brave the elements and help build out the mountain for the skiing guest. Snowmaking is a physically demanding and exciting job. Work with some of the most fascinating equipment on the mountain, and make it snow! Only Swing and Graveyard shifts available
Job Specifications:
<ul>
<li>Starting Wage: $20.00/hr - $22.48/hr</li>
<li>Employment Type: Winter Seasonal 2025/2026</li>
<li>Shift Type: Full Time </li>
<li>Minimum Age: At least 18 years of age</li>
<li>Housing Availability: Yes</li>
</ul>
Job Responsibilities:
<ul>
<li>Operate all snowmaking equipment in a safe and efficient manner</li>
<li>Operate all vehicles, including snowmobiles, in a safe and efficient manner</li>
<li>Perform basic snowmaking equipment maintenance</li>
<li>Work on the production of snow to create the best skiing surface for our guests.</li>
<li>Other duties as assigned</li>
</ul>
Job Requirements:
<ul>
<li>Valid driver's license with no restrictions</li>
<li>Must be able to communicate fluently in English</li>
<li>Able to lift &amp; carry up to 50 lbs.</li>
<li>Basic hand tool knowledge and skill</li>
<li>Able to work extended hours outdoors in an alpine environment</li>
</ul>
The expected pay range is&nbsp;$20.00/hr - $22.48/hr. This is the pay range we reasonably expect to pay for this position. Individual compensation decisions are based on a variety of factors.
In completing this application, and when submitting related documentation, applicants may redact information that identifies their age, date of birth, and/or dates of attendance at or graduation from an educational institution.&nbsp;
We follow all federal, state, and local laws including restrictions on child/minor labor. Minors hired into this position will not be asked or permitted to engage in any activities restricted to adult workers.
Vail Resorts is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or any other status protected by applicable law.
Requisition ID &nbsp;510270 Reference Date:&nbsp;07/19/2025&nbsp; Job Code Function:&nbsp;Snowmaking&nbsp;

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