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<h3>Job Description</h3>
Title: Quality Specialist
Location: Oxford, MS
Base Salary: $25-$35 per hour
 
Company Overview:
Our client is a rapidly growing, vertically integrated manufacturer serving the regenerative and sustainable farming sectors. Headquartered in the Southeast, the company operates five facilities across the U.S. and Canada.
 
Position Overview:
We are seeking a Chemical Quality Specialist initiatives focused on manufacturing efficiency, productivity, and quality. This role will drive process optimization, equipment validation, data analysis, and innovation while supporting new product development, process enhancements, and system upgrades. Will oversee all aspects of chemical process engineering within a full-scale, 24/7 high-volume manufacturing operation, including coordination with a prototype lab.
 
Key Responsibilities
<ul>
<li>Assist in the tech transfer and scale-up of new processes from development into manufacturing.</li>
<li>Participate in equipment and process troubleshooting and provide on-floor technical support.</li>
<li>Collect, analyze, and interpret process data to identify trends, improve efficiency, and enhance product quality.</li>
<li>Support compliance and documentation, including SOPs, process flow diagrams, technical reports, deviations, and change controls.</li>
<li>Collaborate with R&amp;D, Manufacturing, Quality, Engineering, and Supply Chain to support trials and new product development.</li>
<li>Contribute to capital and expansion projects, including ROI evaluations and capital expenditure requests.</li>
<li>Support equipment validation (IQ/OQ/PQ) and process monitoring in coordination with QA and safety teams.</li>
<li>Identify opportunities for process automation, cost reduction, and energy savings.</li>
<li>Maintain accurate records and adhere to GMP and safety requirements.</li>
<li>Perform other engineering duties as assigned.</li>
</ul>
 
Required Qualifications
<ul>
<li>BS degree in Chemical, Mechanical, Industrial, Biochemical, or Process Engineering (or related field).</li>
<li>1+ years of experience in a GMP manufacturing, pharmaceutical, biotechnology, or chemical process environment.</li>
<li>Understanding of basic chemical/biochemical processes and lab/plant operations.</li>
<li>Strong organizational, problem-solving, and troubleshooting skills.</li>
<li>Familiarity with process control systems and equipment operation.</li>
<li>Proficiency in Microsoft Office (Excel, Word, PowerPoint).</li>
<li>Effective verbal and written communication skills.</li>
</ul>
 
Preferred Qualifications
<ul>
<li>Knowledge of regulatory standards in food, pharmaceutical, or chemical manufacturing.</li>
<li>Experience with CAD software for process and equipment design.</li>
<li>Exposure to multi-site or global engineering initiatives.</li>
<li>Basic knowledge of statistical methods and data analysis.</li>
<li>Familiarity with project management tools and practices.</li>
</ul>
 
Skills &amp; Competencies
<ul>
<li>Strong foundation in unit operations (e.g., heating, evaporation, centrifugation, drying, fluid transport).</li>
<li>Knowledge of equipment selection and evaluation for food, nutraceutical, pharmaceutical, or chemical industries.</li>
<li>Hands-on understanding of plant operations; able to adapt to extended hours if required.</li>
<li>Detail-oriented with strong documentation and technical presentation abilities.</li>
<li>Effective communicator across technical and non-technical teams.</li>
<li>Independent yet collaborative, with a strong sense of accountability.</li>
<li>Innovative thinker focused on efficiency, safety, and cost savings.</li>
<li>Capable of managing multiple projects simultaneously.</li>
</ul>
 
Benefits:
<ul>
<li>401k contribution match</li>
<li>PTO</li>
<li>Medical, Dental, and Vision coverage</li>
<li>Short term and long term disability insurance</li>
</ul>

Chemical Technician

<h3>Job Description</h3>
Job Summary
The Research Associate III will conduct research, development, and manufacturing laboratory experiments to support projects within the PHCS division. This role involves designing and executing complex experiments, analyzing results, and contributing to project strategies in alignment with GMP, GLP, and Design Control standards. The ideal candidate will bring strong scientific expertise, problem-solving ability, and a collaborative mindset to a fast-paced R&amp;D environment.
Key Responsibilities
<ul>
<li>Design, plan, and execute a wide range of experimental protocols.</li>
<li>Conduct bench experiments, record detailed observations, and analyze data.</li>
<li>Prepare technical reports, summaries, and quantitative analyses.</li>
<li>Identify and implement process and workflow improvements in the lab.</li>
<li>Collaborate across cross-functional technical teams for investigations or development activities.</li>
<li>Serve as a subject matter expert and train junior team members.</li>
<li>Troubleshoot experimental or process issues and implement corrective actions.</li>
<li>Ensure compliance with GMP, GLP, and Design Control policies.</li>
<li>Maintain complete and accurate laboratory documentation.</li>
</ul>
Qualifications
<ul>
<li>Education: Bachelor’s degree in a scientific discipline (Biology, Biochemistry, Chemistry, Biotechnology, or related field).</li>
<li>Experience: Minimum 4 years of relevant hands-on laboratory or research experience in biotech, pharmaceutical, or diagnostics environments.</li>
<li>Skills:</li>
<li>Proficiency in a range of experimental and analytical techniques.</li>
<li>Strong data analysis, documentation, and presentation abilities.</li>
<li>Proficient with Microsoft Office and scientific software tools.</li>
<li>Familiarity with scientific literature research.</li>
<li>Soft Skills: Excellent analytical, communication, and teamwork capabilities.</li>
</ul>

Research Associate

<h3>Job Description</h3>
Position Title: Gas Measurement Specialist (Hybrid)
Location: Detroit, MI, USA
Duration: 06- months Contract on W2 (Possible extension)
 
Position Description:
<ul>
<li>Validates gas measurement data for reasonableness and timeliness using the Gas Measurement system.</li>
<li>Independently ensures defensible gas measurement data by leveraging industry standards for large volume customers, pipeline transportation interconnects, and production metering locations.</li>
<li>May occasionally mentor other team members on best practices.</li>
<li>Participates in the review and support of the company’s LAUF (lost and unaccounted for) efforts.</li>
</ul>
 
Key Accountabilities:
<ul>
<li>Evaluates and identifies possible measurement anomalies and errors using trend charts.</li>
<li>Collaborates with field operations to quickly remediate equipment issues or to optimize field measurement conditions.</li>
<li>Implements approved enhancements to gas measurement systems to ensure compliance with changing company and industry standards.</li>
<li>Prepares volumetric reports for internal and external gas customers.</li>
<li>Evaluates the usage of customers with volume corrector instruments (VCI) to ensure accurate measurement</li>
<li>Develops billing correction strategies in SAP billing system applications and implements with input from others.</li>
<li>Seeks customer input on individual services provided to upstream and downstream business partners.</li>
<li>Performs daily/monthly system balancing analyses to identify lost gas.</li>
<li>May occasionally lead special cross-functional measurement projects to develop new or enhance existing processes.</li>
<li>Implements moderate to complex decisions with occasional oversight from supervision.</li>
</ul>
 
Minimum Education &amp; Experience Requirements:
<ul>
<li>Bachelor's degree in Business, Accounting/Finance, Mathematics, Economics, Engineering or a related discipline</li>
<li>3 years of experience in gas measurement, or working in data analytics</li>
</ul>
 
Preferred:
<ul>
<li>Experience in the accounting practices of utilities</li>
<li>Broad knowledge of gas transmission, distribution, and gathering systems</li>
</ul>
 
Other Qualifications:
<ul>
<li>Proficient in Excel, Database systems</li>
<li>Proficient verbal, written, and presentation skills; communicates clearly, with credibility and confidence</li>
<li>Strong written and verbal communication skills with proven abilities to defend and justify recommendations</li>
<li>Flexibility and the ability to work with shifting priorities as well as embrace new and evolving responsibilities</li>
<li>Ability to defend data adjustment decisions using company and national gas measurement standards</li>
<li>Ability to analyze large datasets consisting of complex operational data and develop recommendations Competencies</li>
</ul>
 
Additional Information:
<ul>
<li>Incumbents may engage in all or some combination of the activities and accountabilities and utilize a variety of the competencies cited in this description depending upon the organization and role to which they are assigned.</li>
<li>This description is intended to describe the general nature and level of work performed by incumbents in this job.</li>
<li>It is not intended as an all-inclusive list of accountabilities or responsibilities, nor is it intended to limit the rights of supervisors or management representatives to</li>
<li>assign, direct and control the work of employees under their supervision.</li>
</ul>

Gas Measurement Analyst

<h3>Job Description</h3>
Position: Chemist/Analytical chemist
Location: Hershey, PA 
Duration: 3 Months with a possible extension 
Job Type: Temporary Assignment 
Work Type: Onsite
Pay Rate: $30.00-$30.00/hr
 
Overview: 
 
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is an American multinational company and one of the largest chocolate manufacturers in the worldIt also manufactures baked products, beverages and many more that are produced globally
 
Job Details: 
 
<ul>
<li>The successful candidate will provide laboratory support to facilitate the commissioning of workflows that will be used for projects important to key long-term company initiatives.</li>
<li>These laboratory activities will include method development and optimization, routine testing, and process/equipment troubleshooting as necessary.</li>
<li>The candidate will need to be familiar with analytical techniques of mixed complexity and be able perform tasks under varying degrees of supervision.</li>
</ul>
 
Main Duties:
 
Project Assistance -
 
<ul>
<li>Assist current scientists with project work, working under varying degrees of supervision as necessary, including supporting GC, GC/MS, and HPLC workstreams.</li>
<li>Provide technical input to current projects and assist in scoping new projects.</li>
</ul>
 
Routine Testing -
 
<ul>
<li>Perform simple to complex sample analysis as instructed from extraction through data analysis &amp; reporting.</li>
<li>Prepare equipment, reagents, standards and controls. Perform data interpretation and analysis.</li>
<li>Maintain and troubleshoot equipment. Assist in the interpretation of results when requested.</li>
</ul>
 
Method Development -
 
<ul>
<li>Assist in development, optimization, and/or qualification of new or existing methods as instructed.</li>
</ul>
 
Typical Day:
 
Top Three Technical Skills:
 
<ul>
<li>Wet analytical chemistry</li>
<li>Chromatography, including HPLC &amp; GC, with prior GC/MS exposure.</li>
<li>Familiar with common laboratory software, including Agilent Masshunter, Waters Empower, Labware LIMS, and/or similar.</li>
</ul>
 
Must Haves (i.e., years of experience?)
 
<ul>
<li>Previous hands-on experience with Chromatography instruments.</li>
<li>Experience in maintaining + troubleshooting general lab equipment</li>
</ul>
 
Software Skills and Purpose (if applicable): 
 
<ul>
<li>Familiar with Labware LIMS</li>
<li>Proficient in MS suite of programs</li>
<li>Attention to detail</li>
<li>Ability to work supervised &amp; unsupervised</li>
<li>Ability to adapt schedule &amp; reprioritize work as projects change &amp; evolve.</li>
</ul>
 
TekWissen® Group is an equal opportunity employer supporting workforce diversity

Chemist/Analytical chemist

<h3>Job Description</h3>
Astrix is proud to partner with a globally recognized contract research, development, and manufacturing organization (CDMO) serving the pharmaceutical and biotech industries. We are seeking a motivated and detail-oriented Quality Control (QC) Chemist to join the team.
If you're passionate about laboratory science, quality assurance, and contributing to life-saving innovations, this is your chance to work in a high-impact environment with room to grow.
 
Pay: 35-44/hr.
Schedule: 6pm-6am, Monday-Friday
 
Key Responsibilities:
<ul>
<li>Perform analytical testing on raw materials, in-process and final products, and stability samples using balances, pipettes, pH meters, UV/Vis spectrophotometers, TOC analyzers, and more.</li>
<li>Conduct chromatography (HPLC, GC) testing following comprehensive training and qualification.</li>
<li>Execute wet chemistry assays and routine water sample collections.</li>
<li>Maintain and calibrate QC analytical instruments and general lab equipment.</li>
<li>Support QC laboratory housekeeping and audit readiness efforts.</li>
<li>Assist in reviewing QC data and summarizing findings for management.</li>
<li>Participate in deviation investigations, CAPAs, and out-of-specification (OOS) documentation under guidance from QC Management.</li>
<li>Serve as backup for sample receipt, shipment, result distribution, and external lab coordination.</li>
</ul>
 
Qualifications:
Required:
<ul>
<li>Bachelor’s degree in Chemistry or a related scientific field.</li>
<li>3 years of experience in a pharmaceutical QC Chemist or analytical laboratory role.</li>
</ul>
Preferred:
<ul>
<li>Experience working in a cGMP, GLP, or FDA-regulated environment.</li>
</ul>
Key Competencies &amp; Skills:
<ul>
<li>Strong understanding of analytical chemistry principles and lab techniques.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to manage time effectively and work independently in a fast-paced environment.</li>
<li>Proficiency with Microsoft Office and laboratory data systems.</li>
<li>Working knowledge of FDA regulations (21 CFR 211, 820, 600) and ISO standards (9001, 13485) is a plus.</li>
<li>Familiarity with statistical analysis, report writing, and documentation best practices.</li>
</ul>
Physical Requirements:
<ul>
<li>Must be able to sit, stand, walk, kneel, or crouch for extended periods.</li>
<li>Ability to lift up to 50 lbs as needed.</li>
<li>Requires fine motor skills, visual focus, and manual dexterity for laboratory work.</li>
</ul>
 
Why Join Us?
<ul>
<li>Be part of a company with a national and global impact in pharmaceutical development.</li>
<li>Gain valuable experience in an FDA-regulated environment with career advancement opportunities.</li>
<li>Work alongside a collaborative team that values innovation, quality, and continuous learning.</li>
</ul>
 
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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