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<h3>Job Description</h3>
Job DescriptionSalary: Unpaid Internship 
The Department of Innovative Research at ARCH Collaborative is seeking a dedicated and inquisitive intern to join a special qualitative research project titled: Psychobiographical Analysis of Life Stories of Commercially Sexually Exploited Children (CSEC) Survivors. 
 Project Overview: Psychobiography is a qualitative research method that applies psychological theories to better understand an individual's life journey and personal development. This unique project explores how survivors of CSEC construct meaning in their lives and move toward healing, growth, and agency. 
Key Responsibilities:
<ul>
<li>Conduct literature reviews and contribute to theoretical framing of the study.</li>
<li>Assist in conducting narrative interviews with clients (under supervision).</li>
<li>Support the transcription, psychobiographical analysis, and writing of case narratives.</li>
<li>Collaborate with a multidisciplinary team of clinicians and case managers.</li>
</ul>
Eligibility Criteria:
<ul>
<li>Must be enrolled in or a recent graduate of a program in Psychology, Social Work, Counseling, Social Sciences, or a related field. Masters students in these fields are welcome to apply.</li>
<li>Strong writing, analytical, and interpersonal skills.</li>
<li>Must be willing to participate in an intensive orientation and training on psycho-biographical research methods.</li>
<li>Demonstrated interest in trauma-informed research or working with vulnerable populations.</li>
<li>Previous experience with qualitative research is not required. </li>
</ul>
Internship Details:
<ul>
<li>This is a part-time internship</li>
<li>Duration: Minimum of 3 months, with flexible scheduling.</li>
</ul>
This is a rare opportunity to contribute to meaningful, ethically responsible research that centers the voices and experiences of survivors. If youre passionate about applying psychological insight to real-world stories and systems change, we encourage you to apply. One SAFE Place and Childrens Legacy Center are separate legal entities. Arch Collaborative is a fictitious business name (DBA) of Childrens Legacy Center. Under the DBA Arch Collaborative, and a signed management services agreement, Childrens Legacy Center assists One SAFE Place with operations and enhances OSPs impact. By creating Arch Collaborative, and working alongside other organizations with similar heartbeats, we have created a network of organizations that respond effectively to trauma, violence, and exploitation in our community while maintaining the legal status of each organization.

Psychobiographical Research Intern

<h3>Job Description</h3>
Job DescriptionSalary: 
Site Description
Childrens Research Triangle (CRT) is a mental health non-profit that seeks to provide therapy to children and families in underserved communities. CRT has also been in the forefront of many issues related to maternal substance abuse in pregnancy, the outcomes of children prenatally exposed to alcohol and drugs, the child welfare implications of substance abuse in families, as well as the treatment of youth who have been exposed to trauma. The staff at CRT has written articles that have been published in Pediatrics, The American Journal of Occupational Therapy, Journal of Developmental and Behavioral Pediatrics, Research in Developmental Disabilities, and numerous other leading medical and psychological journals.
 
Intern description
The CRT research team is offering part-time unpaid research internships to qualified undergraduates in the Chicago area.Most of the work is remote; however,interns are expected to come into the office at least once a week in order to help with tasks on site.The Summer cohort typically starts mid-Mayand goes throughmid-August, although scheduling can be flexible.Interns will be involved in multiple ongoing projects, such as:
<ul>
<li>ongoing evaluation of the Trauma Treatment Program</li>
<li>evaluation of a grant program providing training in Youth Mental Health First Aid</li>
<li>the development of a database about children 0 to 18 who have participated in psychological evaluations at CRT</li>
<li>evaluation of the Youth MIND program, which provides trauma-informed screening, assessment, and therapy to youth and families in the Chicago area</li>
<li>evaluation of a gun violence prevention program being implemented in schools around the city</li>
</ul>
 
Interns will be actively involved in most aspects of the research process including searching for relevant literature, putting together research materials, interviewing families, inputting and cleaning data in Excel and IBM SPSS, and helping with data management and analysis. This internship does not provide any clinical experience, i.e., direct contact with children, but is geared for students who would like to learn more about the research/program evaluation work at a non-profit organization. Students will receive the necessary training to do these tasks on these projects and will receive supervision from research team members led by a licensed clinical psychologist. Interns are expected to work at least 6 hours per week, but more hours can be accommodated. Internships can be set up for one, two, or more semesters.
 
Qualified Applicants will be undergraduate students who have:
<ul>
<li>Completed at least one introductory course in psychology, behavioral science, child development, or social work with a grade of B or above, or enrolled in a pre-medical course of study,</li>
<li>Demonstrated merit in their undergraduate studies up until the present time,</li>
<li>Expressed an interest in pursuing future careers or further education in empirical research or medicine, and</li>
<li>Displayed the ability to work well with other people in a team-oriented atmosphere.</li>
</ul>
 
Compensation
Interns may be offered authorship on submitted papers to which they have contributed substantially.
 
To Apply
The Research Team interviews candidates throughout the year, but it is typically divided into three cohorts: Spring, Summer, and Fall. Interested candidates should fill out the job links for their intended cohort. If there are any questions, please email Lorenz Cabe, the Research Internship Manager, <a href="mailto:atlcabe@cr-triangle.org" target="_blank">atlcabe@cr-triangle.org</a>.
 
Application Deadline
Applications for the summer cohort must be submitted by March 1st.
 
Interviewing Timeline
Interviews for our cohorts typically start two months before the cohort begins, based on the availability of space for new interns. Interviews for the Summer cohort will take place from March 1st-April 30th of the year in which you are applying.

Research Internship(Summer 2026)

<h3>Job Description</h3>
Job DescriptionSalary: 
Join Luxaviation USA as a Senior Charter Broker
 
Luxaviation Group delivers excellence in a comprehensive range of business aviation services tailored to our clients and partners. We are committed to the highest safety standards and strive to create a fulfilling work environment by fostering genuine, open, and engaging relationships with passionate professionals.
 
To strengthen our presence in the U.S. market, Luxaviation USA is actively seeking an experienced Senior Charter Broker, ideally based in or with a strong network in New York, Los Angeles, Miami, or Houston.
 
About the Role
As a Senior Charter Broker, you will be responsible for developing and managing a portfolio of high-net-worth and corporate clients. You will play a key role in the end-to-end coordination of on-demand charter flights from quote to execution ensuring a flawless client experience.
 
Key Responsibilities
<ul>
<li>Proactively develop and manage a high-value client portfolio (UHNWI, corporate accounts, family offices, etc.)</li>
<li>Identify and convert new business opportunities through strategic networking and industry intelligence</li>
<li>Build and deliver bespoke commercial offers and charter quotes in a competitive environment</li>
<li>Negotiate, close, and manage contracts tailored to client needs with the highest service standards</li>
<li>Oversee the complete charter process: from flight planning, aircraft sourcing, and coordination to post-flight follow-up</li>
<li>Collaborate with flight operations, crew, and handling agents to ensure operational excellence</li>
<li>Provide high-touch client service including VIP meet &amp; greet when relevant</li>
<li>Be available for on-call duties (evenings/weekends on a rotating basis)</li>
<li>Ensure proper invoicing, payment follow-up, and budgetary compliance for each operation</li>
</ul>
 
Profile and Qualifications
<ul>
<li>Minimum 5 years of experience in private jet charter brokerage or a similar high-end sales role</li>
<li>Proven track record of closing deals and managing demanding clients</li>
<li>Strong understanding of charter operations and aircraft performance</li>
<li>Exceptional interpersonal, communication, and negotiation skills</li>
<li>Strategic, autonomous, and results-driven mindset</li>
<li>Fluent English required; Spanish or any additional language is an advantage</li>
<li>Ability to work under pressure, with discretion and a client-first attitude</li>
<li>Strong organizational and reporting skills</li>
<li>Valid drivers license and ability to pass background checks</li>
</ul>
 
What We Offer
<ul>
<li>A competitive compensation package including base salary + attractive commissions based on performance</li>
<li>A key role within a globally recognized aviation group</li>
<li>Access to Luxaviations worldwide fleet and resources to support your success</li>
<li>A dynamic and supportive team with international reach</li>
</ul>

Senior Charter Broker - USA

<h3>Job Description</h3>
Job DescriptionOverview:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world, headquartered in Leverkusen, and areas of business include pharmaceuticals; consumer healthcare products, agricultural chemicals, seeds and biotechnology products.&nbsp;&nbsp;&nbsp; Job Title: Chemical Process EngineerLocation: Kansas City, MO, 64120&nbsp;Duration: 6 Months&nbsp;&nbsp;Job Type: -Temporary Assignment&nbsp;Work Type: &nbsp;Onsite&nbsp; &nbsp;&nbsp;Job Description:&nbsp;&nbsp;&nbsp;Responsibilities and Duties&nbsp;
<ul>
<li>Collaborate with site technical and operational team members to advance technical resolution to outstanding PHA, MOC, optimization, and other action items for 1-4 chemical processes operating within Site 4 AI.&nbsp;</li>
<li>Complete technical definition, validation and reporting for environmental data required for permitting and annual reporting requirements.&nbsp;</li>
<li>Review and improve plant documentation, aimed at improving the readability, detail and clarity of startup, shutdown and normal operations procedures and P&amp;IDs.&nbsp;</li>
<li>Complete technical definition, documentation and execution of pressure safety design packages.&nbsp;</li>
<li>Collaborate with plant engineering resources to scope, document and define implementation plans for process and reliability improvement projects.&nbsp;</li>
<li>Support improvements to plant training programs.&nbsp;</li>
</ul>
Skills and Qualifications&nbsp;
<ul>
<li>Bachelor’s degree in Chemistry, Chemical Engineering or other engineering discipline&nbsp;</li>
<li>BS 5+ years experience in process measurement and applications in a manufacturing or industrial or engineering environment.&nbsp;</li>
<li>Knowledge of chemical processes to effectively analyze, make recommendations and provide resolution to complex problems. </li>
<li>Knowledge of OSHA PSM/EPA RMP requirements and associated risk management techniques.&nbsp;</li>
<li>Ability to lead small groups of people as well as to work independently.&nbsp;</li>
<li>Demonstrated verbal and written communication skills in both technical and non-technical areas.&nbsp;</li>
<li>Intermediate computer skills.&nbsp;</li>
</ul>
TekWissen® Group is an equal opportunity employer supporting workforce diversity.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen® is an equal opportunity employer supporting workplace diversity.&nbsp;

Chemical Process Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
Cogent Scientific, an insourced contract research organization in Indianapolis, is looking for the right people to accomplish our Mission: partnering in the global effort to improve lives through innovative science with an experienced workforce.
 
We typically hire scientists with the following backgrounds:
 
* BS/MS - Chemistry, Biochemistry, Organic Chemistry, Molecular Biology and related fields.
* Industrial experience in pharma/biotech arenas.
* Laboratory skills sets such as: organic synthesis, purification and formulation; analytical chemistry utilizing LC, LC/MS, wet chemistry techniques; molecular biology using PCR, cell culture, Western blot.
* Team players who embody our Core Values:
<ul>
<li>Client Focused: We only succeed when our clients succeed.</li>
<li>Outstanding: We deliver meticulous results through outstanding performance.</li>
<li>Good: We act ethically and morally.</li>
<li>Employee-Centric: We honor and support our employees.</li>
<li>imble: We are prepared to adapt in an ever-changing industry.</li>
<li>Team-Oriented: We collaborate with each other and with our clients.</li>
</ul>
If you do not see a job posted on our employment page that fills your skills and experience, feel free to upload your information and resume here. We are continually growing and look forward to working with you soon!

Scientists - General Consideration

<h3>Job Description</h3>
Job DescriptionSalary: $85K-$115K, depending upon experience 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge whileworking among experts in their fields and with cutting-edge instrumentation. 
 
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values:
 
Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. imble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients.
 
We currently have a role available for an Expert Small Molecule Purification Chemist.
Job duties include, but are not limited to:
<ul>
<li>Identifying, characterizing and purifying small molecule pharmaceutical compounds using analytical and chromatographic techniques (UPLC, RP-HPLC, SFC, LC-MS, etc.).
<ul>
<li>Accustomed to purifying samples weighing between milligram - over 100 g samples; completing 50+ samples/wk.</li>
<li>This DOES NOT include protein, oligonucleotide and other large molecules.</li>
</ul>
</li>
<li>Rapidly developing unique and effective methods on LC and SFC.
<ul>
<li>Extensive experience with SFC and chiral/achiral purification is required.</li>
</ul>
</li>
<li>Specifying alternative LC-MS columns/methods for specific projects.</li>
<li>Using tools such as KNIME and MNOVA to facilitate and automating the processing and storage of large amounts of data in shared databases.</li>
<li>Conducting preventative maintenance and troubleshooting on instrumentation as needed.</li>
<li>Providing critical feedback to improve workflow and chemistry performance andimplementation of best practices.</li>
</ul>
Job requirements include, but are not limited to:
<ul>
<li>MS in Chemistry, Analytical Chemistry or related field with 5+ years of pharma laboratory experience outside of academia/academic research.
<ul>
<li>BS in Chemistry or related field with 8+ years of experience will also be considered.</li>
</ul>
</li>
<li>Extensive theoretical knowledge of UPLC, LC, LC-MS required, as well as hands-on experience with Waters and Agilent systems.</li>
<li>SME (developer/administrator) with MNOVA and other laboratory software.</li>
<li>Excellent communication skills verbal and written.</li>
<li>Demonstration of excellent team player and collaboration skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions.</li>
<li>The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinaryenvironment with flexibility and an adaptable approach to goal delivery.</li>
</ul>

Expert Small Molecule Purification Chemist

<h3>Job Description</h3>
Job DescriptionSalary: $50K - $55K 
Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. GMGI is looking for a Research Associate to join our team studying the biology of exceptionally long-lived marine animals. Our goal is to translate evolutionary insights from these exceptional animals into interventions that promote human healthspan and combat age-related diseases, using zebrafish as a development platform. This position will conduct zebrafish genetics work and husbandry, testing these evolutionary targets to extend healthy functionality. This project will use modern genetic editing techniques and apply new assays to modulate and test the molecular mechanisms of aging.
The ideal candidate will have experience with aquatic husbandry, standard molecular biology techniques, excellent communication skills, attention to detail, and the ability to work with a multi-disciplinary team of collaborators. This is an extraordinary opportunity for a dynamic and motivated individual to learn a powerful genetic model and to advance aging research in an entrepreneurial and exciting work environment.
 
Responsibilities:
<ul>
<li>Standard molecular biology and genetics experimental research.</li>
<li>Contribute to the maintenance of the aquatic facility, including feeding, water quality, and health monitoring.</li>
<li>Contribute to the generation and maintenance of transgenic zebrafish lines, including microinjection, mutant screening, and genotyping.</li>
<li>Apply assays to quantify biological aging in zebrafish, including taking tissue samples, performing histology, and compound neuro-muscular functionality.</li>
<li>Maintain a comprehensive electronic lab notebook.</li>
<li>Contribute to grant proposals and publications, and present results at lab meetings and other venues.</li>
<li>Participate in institutional fund-raising activities and community outreach activities.</li>
</ul>
 
Qualifications:
<ul>
<li>BS or MS in genetics, molecular or cell biology, or related field, with lab experience.</li>
<li>Experience with standard molecular biology techniques such as DNA/RNA isolation, PCR/qPCR, molecular cloning, and CRISPR gene editing.</li>
<li>Experience with the husbandry of aquatic models.</li>
<li>Experience with zebrafish and histology is desirable.</li>
<li>Ability to work independently to design and execute experiments</li>
<li>Strong data analysis skills using standard bioinformatic and statistic software packages</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Excellent organization skills and the ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and teamwork skills.</li>
<li>Enthusiasm and commitment to GMGIs mission for science and education.</li>
</ul>
This position will report to the Research Scientist.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
Health and Dental Insurance
Medical and Dependent Flex Spending Accounts
Long Term Disability
Life Insurance
Paid Time Off
403(b) Retirement Plan
12 Paid Holidays
Applicants must be authorized to work in the US.
 
About GMGI 
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization and building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

Research Associate I - Marine Biomedical Discovery

<h3>Job Description</h3>
Job Description
Job Title: Quality Control Laboratory Chemist
Employment Type: Full-Time | On-Site Location : Gulfport, MS &nbsp;
About the Role
We are seeking a Quality Control Laboratory Chemist to join our team in supporting the manufacturing of both human and veterinary drug products. This position plays a key role in performing a variety of chemical analyses on raw materials, in-process samples, finished goods, and stability samples in a GMP-regulated environment.
Key Responsibilities
<ul>
<li>Perform chemical testing on raw materials, in-process products, finished products, and stability samples.</li>
<li>Operate, maintain, and calibrate analytical instruments such as HPLC, GC, etc.</li>
<li>Prepare reagents and samples in accordance with SOPs.</li>
<li>Accurately document and report test results in compliance with GMP standards.</li>
<li>Support method development, validation, and transfer activities.</li>
<li>Investigate and troubleshoot testing or equipment issues.</li>
<li>Collaborate with team members and cross-functional departments.</li>
<li>Mentor and support junior chemists, as needed.</li>
</ul>
Required Skills &amp; Experience
<ul>
<li>3–5 years of hands-on experience in a GMP-regulated QC or manufacturing lab.</li>
<li>Strong chromatography background, especially with HPLC, GC, or similar instruments.</li>
<li>Proficiency in analytical tools: UV/VIS, FTIR, AA, IC, ICP-MS, and dissolution testing.</li>
<li>Familiarity with lab software such as Empower and Microsoft Office Suite.</li>
<li>Solid understanding of cGMP, quality systems, and related compliance practices (e.g., change control, deviations, CAPAs).</li>
<li>High attention to detail with excellent communication and time management skills.</li>
<li>Ability to multitask in a fast-paced, regulated environment.</li>
</ul>
Must-Have Requirements
<ul>
<li>3–5 years of direct, hands-on chemistry experience in a GMP-regulated laboratory.</li>
<li>Proven chromatography experience (e.g., HPLC, UV/VIS, FTIR).</li>
<li>Academic/lab research experience alone will not be considered.</li>
<li>Degree not required — practical skills and industry experience are most important.</li>
</ul>
Physical Requirements
<ul>
<li>Must be able to lift 50 lbs or more daily.</li>
<li>Ability to walk, stand, or sit for 8+ hours per day.</li>
</ul>

Quality Control Laboratory Chemist

<h3>Job Description</h3>
Job DescriptionSalary: 
RTI is a leading biomedical contract research organization, providing global clients in both animal health and human health, biopharma, and advanced feed/nutrition industries with premier quality services and product development support. 
 
Job Purpose
The Associate Scientist will perform laboratory assays, maintain laboratory equipment, assist with facility maintenance and completion of testing for submitted samples.
 
Responsibilities
<ul>
<li>Perform laboratory assays according to Standard Operating Procedures, or other standard methodologies such as FDA BAM, in areas including but not limited to, bacteriology, virology, mycology, and immunology.</li>
<li>Document laboratory work in accordance with RTI Lab's Standard Operating Procedures on appropriate forms and report out results and/or author reports.</li>
<li>Assist with and at times manage laboratory projects, research and order supplies and equipment, and help lab team meet project deadlines.</li>
<li>Ensure diagnostic laboratory processes maintain compliance with ISO 17025 requirements and complete record keeping in compliance with RTI Lab's Standard Operating Procedures.</li>
<li>Train to perform daily tests processes such as media preparation, sample processing, VIs, SNs, and ELISA</li>
<li>Perform Equipment and facility maintenance, equipment calibration/verification, laboratory cleaning, and other general laboratory inventories</li>
<li>Maintain, and perform QC for, RTI Lab's stock cells, viruses, and/or bacteria. Assist in maintaining RTI Lab's stock of monoclonal antibodies (MABs) and pulmonary alveolar macrophages (PAMs)</li>
<li>Document work accurately, appropriately and make timely corrections to errors. Assist with internal review of laboratory data</li>
<li>Maintain competency in diagnostic lab processes and cross train on other laboratory procedures.</li>
<li>Maintain training record, review, and assist with SOP (Standard Operating Procedures) revisions, and/or writing of new SOP's and perform literature reviews.</li>
</ul>
 
Qualification, Training, and Experience Requirements
<ul>
<li>Undergraduate degree in biological sciences or equivalent required and 0-4 years of experience, or</li>
<li>Graduate degree and 0-2 years' relevant experience and demonstration of competency in job role-specific requirements</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: QC Chemist I
Location: Central Islip, NY (Onsite) Job Type: Full-Time | Permanent Shift: 8:30 AM – 5:00 PM (may vary) Industry: Pharmaceutical Experience Required: 2 to 15 years Compensation: *,000 – *,000 Visa Sponsorship: Not available Remote Option: No
Job Overview:
We are looking for a dedicated Quality Control Chemist to join our team and perform analytical testing in a GMP-regulated laboratory environment. The ideal candidate will have experience in pharmaceutical product testing and familiarity with various analytical instruments and techniques.
Responsibilities:
<ul>
<li>
Perform standard and advanced laboratory testing on raw materials, in-process samples, and finished products.
</li>
<li>
Operate lab instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.
</li>
<li>
Ensure compliance with cGMP, data integrity, and good documentation practices.
</li>
<li>
Support deviation investigations, change control activities, and CAPAs.
</li>
<li>
Participate in method validations and support production and quality operations.
</li>
<li>
Maintain accurate and timely documentation in line with regulatory standards.
</li>
<li>
Execute assigned tasks with attention to detail and in alignment with department protocols.
</li>
<li>
Collaborate with team members and other departments to meet project deadlines.
</li>
<li>
Perform other duties as assigned by management.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Bachelor’s degree in Chemistry or a related scientific field.
</li>
<li>
2–15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector.
</li>
<li>
Strong understanding of lab testing and instrumentation.
</li>
<li>
Must be able to read, write, and understand scientific materials in English.
</li>
<li>
Proficiency with MS Office and laboratory software systems.
</li>
<li>
Comfortable working on-site full-time; no remote options.
</li>
</ul>
Preferred Experience:
<ul>
<li>
Hands-on experience with Inhalation dosage forms (MDI) is a strong advantage.
</li>
<li>
Background in testing tablets, capsules, liquids, and solids also acceptable.
</li>
<li>
Prior exposure to GMP, FDA regulatory guidelines, and quality systems.
</li>
<li>
Experience conducting investigations or root cause analyses.
</li>
</ul>
Work Environment &amp; Physical Requirements:
<ul>
<li>
Work in a controlled laboratory or production area wearing PPE (lab coat, gloves, goggles, etc.).
</li>
<li>
Ability to lift up to 10 kg and stand or walk for extended periods during an 8-hour shift.
</li>
<li>
Comfortable using computers and working at a screen for prolonged periods.
</li>
</ul>
Additional Information:
<ul>
<li>
Must be willing to work weekday shifts and occasional weekends depending on business needs.
</li>
<li>
Must be open to working in a pharmaceutical manufacturing environment.
</li>
<li>
No employment sponsorship or visa support available.
</li>
</ul>

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