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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>
This role involves integrating and staging both tabular and spatial GIS datasets into a database environment, developing tools or scripts to automate data processing, and building a program or workflow to execute the defined data model and generate outputs. 
 
JOB DESCRIPTION: 
 
<ol>
<li>Design, develop, and maintain a relational database (e.g., PostgreSQL/PostGIS or equivalent) to store, organize, and manage GIS and tabular data</li>
<li>Develop a data model and associated processing workflows to evaluate parcel-level compliance.</li>
<li>Collaborate with the Systems team to access, clean, and stage GIS reference data for integration into the project database.</li>
<li>Develop scripts, tools, or applications (in Python, SQL, or similar languages) to automate data ingestion, transformation, and analysis.</li>
<li>Ensure data accuracy, integrity, and performance through quality control checks and optimization of spatial queries.</li>
<li>Produce reproducible data outputs and reports to support policy analysis.</li>
<li>Document database schema, data model logic, and workflow processes to support long term maintenance and transparency.</li>
</ol>

Geographic Information System Developer

<h3>Job Description</h3>
Research Operations Coordinator
The Research Operations Coordinator plays a key role in supporting the Community Insights Team by managing market research logistics and project coordination. This position is well-suited for those looking to get hands-on experience in market research, project management, and operational excellence.
As an integral junior team member, the coordinator will gain exposure to a wide range of real-world research projects across diverse industries, with opportunities to broaden their skills and take on greater responsibilities over time.
 
Main responsibilities: 
<ul>
<li>Responding to and troubleshooting basic respondent inquiries and triage incoming issues</li>
<li>Recruiting/scheduling for online qualitative interviews/focus groups</li>
<li>Programming and leading quality assurance checks (QA) for research instruments and deliverables</li>
<li>Managing respondents and data quality in our research platform</li>
<li>Supporting account teams in driving logistics and management tied to kicking off new Finch communities when relevant</li>
</ul>
Required Experience &amp; Skills
<ul>
<li>0-1 years of experience is required, but ideal candidate will come with some history of applied business skills (via internship and/or entry level role)</li>
<li>Candidates will ideally have experience and interest in Business/Management, Operations, Communications, Project Management, or Market Research.</li>
<li>Proficiency in Outlook and MS Excel- including data manipulation, formulas, lookups, and formatting.</li>
</ul>
Required Candidate Attributes
<ul>
<li>Organized &amp; attentive to detail, with an eye for catching errors &amp; mistakes</li>
<li>Strong time management, with the ability to prioritize needs across multiple priorities at once</li>
<li>Exceptional communication skills, with the ability to write clearly and concisely</li>
<li>Process-oriented – motivated to create, refine, and follow repeatable systems to support research operations at scale</li>
<li>Willingness to learn/manage new tools or platforms</li>
<li>Customer service-oriented, leading with empathy and professionalism when engaging with internal team members and research respondents</li>
</ul>
 
Nice-to-Have Additional Skills or Experience 
<ul>
<li>Experience in market research</li>
<li>Recruitment: knowledge of sample management and panel quality</li>
<li>Survey programming</li>
<li>Quality assurance</li>
<li>Experience in project management and/or vendor management</li>
<li>Prior experience supporting online communities or panels</li>
</ul>
 
Company Description
Finch Brands is a real-world brand consultancy. We exist to help brands win when it matters most. We do this by blending insight, intuition, and creativity to shape brand strategy and drive people to action.
Founded in 1998 by pioneering minds instrumental in the ascent of David’s Bridal and IKEA, the Finch Brands team has extensive experience building, running and growing successful brands. Along with years of agency service, this includes important tenures at Campbell Soup, Kimberly-Clark, Urban Outfitters, Target, and more.

Research Operations Coordinator

<h3>Job Description</h3>
This position is based in Cambridge, Massachusetts or San Francisco, Califonia. Remote work from certain states may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines. Candidates interested in remote work are encouraged to apply.
Purpose and Scope:
The Modality Intelligence Lead is a scientific subject matter expert within the Oncology Research Intelligence group, specializing in the strategic analysis of emerging therapeutic modalities such as next gen ADCs, engineered biologics, or small molecules. Reporting to the Head of CI&amp;RPM, this role provides deep, cross-oncology research portfolio insights on modality trends, competitor activities, platform technologies, and translational relevance to inform Oncology Research strategy. In addition to ongoing landscape monitoring and intelligence synthesis, the Modality Intelligence Lead proactively identifies high-potential external opportunities and leads the development of evaluation proposals for internal consideration. By collaborating closely with External Innovation Partners, Oncology Research Leadership, relevant PF (ie. PF-IO and PF-TPD) and Business Development, the role ensures timely, well-informed assessments that support strategic research alignment and external innovation prioritization.
Essential Job Responsibilities:
Modality Landscape Monitoring &amp; Strategic Foresight:
<ul>
<li>Continuously monitor scientific, clinical, and technological advances across prioritized therapeutic modalities.</li>
<li>Identify emerging trends, breakthroughs, and risks with implications for Astellas' oncology research strategy and modality capabilities.</li>
<li>Develop structured landscape assessments and foresight reports highlighting implications for internal pipeline differentiation and innovation gaps.</li>
</ul>
External Opportunity Assessment &amp; Strategic Framing:
<ul>
<li>Collaborate with External Innovation Partners and Business Development to assess novel platforms, technologies, and innovation opportunities aligned with prioritized therapeutic modalities and the overarching Oncology Research Strategy.</li>
<li>Support nonclinical-stage opportunity assessments by providing strategic modality insights, and lead the development of internal opportunity briefs and evaluation proposals for potential collaborations, partnerships, or in-licensing opportunities.</li>
</ul>
Collaboration &amp; Influence:
<ul>
<li>Act as a trusted advisor to CI&amp;RPM and other sub-function units in Oncology Research, and other scientific stakeholders on modality trends and strategic implications.</li>
<li>Partner with Innovation Intelligence analysts and Research Strategy Leads to ensure data-driven modality insights inform broader Oncology Research Strategy development.</li>
<li>Contribute to the enhancement of intelligence infrastructure (e.g., databases, dashboards, horizon scanning tools) with a modality focus.</li>
</ul>
Qualifications:
Required
<ul>
<li>Advanced degree (PhD, MD, MBA, or equivalent) in life sciences, pharmacology, medicinal chemistry, bioengineering or related field.</li>
<li>Minimum 8 years of experience in pharmaceutical R&amp;D, external innovation, academic collaboration, or scientific partnering.</li>
<li>Deep technical understanding of one or more modality platforms (e.g., engineered biologics, engineered small molecules, next generation ADCs).</li>
<li>Strong analytical skills with the ability to synthesize complex datasets and scientific trends into actionable strategy.</li>
<li>Proven experience influencing research or portfolio decisions through strategic insights.</li>
<li>Familiarity with the external innovation ecosystem including biotech start-ups, platform companies, and academic research.</li>
<li>Experience working closely with Research Leadership and Business Development on strategic evaluations.</li>
<li>High digital literacy and familiarity with CI or analytics tools/platforms.</li>
<li>Effective communication skills, with ability to convey scientific and strategic ideas to both technical and executive audiences.</li>
</ul>
Salary Range
$175K – $240K (NOTE: Final salary could be more or less, based on experience)
Benefits:
<ul>
<li>Medical, Dental and Vision Insurance</li>
<li>Generous Paid Time Off options, including Vacation, Sick time, plus national holidays including Heritage Days, and Summer and Winter Breaks</li>
<li>401(k) match and annual company contribution</li>
<li>Company paid life insurance</li>
<li>Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions</li>
<li>Long Term Incentive Plan for eligible positions</li>
<li>Referral bonus program</li>
</ul>
Category CI &amp; Research Program Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Modality Intelligence Lead, Oncology Research Intelligence

<h3>Job Description</h3>
Manufacturing Lab Associate (Night Shift)
Location: Novato, CA.
6-12 Month Assignment
Pay Rate: $28/hr. / $30.80 / $32.20 (Depends on shift)
Open Shifts: SET Schedule/ Room for OT
 
Night Shift: Wednesday-Saturday 6:00 PM – 7:00 AM (3x12/4x12 schedule alternating weekly on Saturday) OR Sun-Tue / Every other Wednesday 6 PM - 7 AM) 
 
 
On behalf of our client a pharmaceutical company specialized in developing therapeutics for patients dealing with life threatening rare-genetic diseases. We are seeking for a Manufacturing Associate with hands-on experience in large-scale bioprocess operations, buffer/media preparation, and cGMP-compliant environments. Skilled in cell culture, purification, and formulation processes with a strong foundation in scientific principles and operational excellence.
 
Key Responsibilities
<ul>
<li>Operate large-scale equipment supporting Cell Culture and Purification operations.</li>
<li>Prepare buffer and media solutions for production batches.</li>
<li>Learn and execute biopharmaceutical manufacturing techniques including tangential flow filtration, chromatography, and formulation.</li>
<li>Follow SOPs and document processes in accordance with GDP and regulatory guidelines.</li>
<li>Identify, troubleshoot, and escalate process issues while contributing to resolution strategies.</li>
<li>Support integration of new technologies and practices into established processes.</li>
<li>Suggest and assist with procedural improvements and updates.</li>
</ul>
 
Education and Qualifications
<ul>
<li>Bachelor's degree in a science-related field or engineering</li>
<li>OR. Associate's degree in a science-related field or Biotech Certificate with 2+ years' experience in biotech manufacturing or other regulated industries</li>
<li>Physically demanding role with frequent bending, lifting (up to 25 lbs.) reaching, stair and ladder use</li>
<li>Will require night shift work and flexibility with off-hours as needed</li>
</ul>
 
Please submit a copy of your resume in a Word or PDF format to be considered.

Laboratory Associate

<h3>Job Description</h3>
Job Responsibilities &amp; Requirements:
<ul>
<li>Execute Geotechnical project assignments including engineering analysis, report preparation, field exploration and laboratory services.</li>
<li>Provide project-level development of reports and proposals.</li>
<li>Field and laboratory sampling and testing.</li>
<li>Oversight and testing on geotechnical projects during design and construction and respond to customers’ inquiries concerning testing progress and reporting.</li>
<li>Implement and oversee department policies, goals, objectives, and procedures.</li>
<li>Follow-up laboratory tests of various construction materials including soil, aggregate, concrete, asphalt, etc.</li>
<li>Analyze test data and conduct corrective action to prevent non-conforming products.</li>
<li>Ensure tests are carried out in accordance with relevant standard test methods and according to agreed customers’ requirements.</li>
<li>Conduct analysis as required after receiving tests results from technicians and ensure compliance with standards.</li>
<li>Ensure all site equipment and instruments are fit for use by provision of necessary resources for the implementation of calibration and maintenance programs.</li>
<li>Any duties or responsibilities assigned by the management.</li>
</ul>

Education and Related Requirements:
<ul>
<li>B.S. degree (M.S. degree or Ph.D. is preferred) in Civil or Environmental Engineering, Geology or a related field.</li>
<li>Successfully passed the E.I.T. or G.I.T. exam preferred.</li>
<li>Strong oral and written communication skills.</li>
<li>Demonstrates performance of independent analysis as well as strong problem-solving and organizational skills.</li>
<li>Strong personal safety awareness.</li>
</ul>

Geotechnical Staff Engineer

<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!

QC Chemist III (3rd Shift)

<h3>Job Description</h3>
Job Responsibilities:
<ul>
<li>Lead safety efforts for team and ensure team follows safety rules and guidelines. Responsible for creating and modeling a safe work environment; demonstrating safety practices. Promote pre-task planning for all projects.</li>
<li>Mentor, develop and train staff both technically and for leadership roles.</li>
<li>Manage progress of all geotechnical projects to ensure quality and timely deliverables within budget and immediately coordinate with clients for scope changes.</li>
<li>Manage the execution of geotechnical project assignments including supervising or performing complex engineering analyses, report review and report preparation. Critical review of field and laboratory test data as well as geotechnical recommendations.</li>
<li>Oversee and prepare technical proposals, manage client expectations and overall client satisfaction.</li>
<li>Access and manage risk at the project execution level including quality assurance of technical aspects and support the Regional Operations Leader (ROL) on proposal level and non-technical aspects of the department.</li>
<li>Support the ROL on risk assessment for both conventional and alternate delivery contracts. </li>
<li>Oversight and responsibility for geotechnical design aspects including but not limited to:</li>
</ul>
<ol>
<li>Shallow and deep foundations.</li>
<li>Tunnels (lined and unlined) and earth and rockfill dams. </li>
<li>Pavement evaluations, engineering analyses and design, pavement management experience a plus. </li>
<li>Shoring and bracing systems for deep excavations.</li>
<li>Earth retaining structures.</li>
<li>Pipe/culvert foundations and machine foundations in water/wastewater, power, and chemical plants.</li>
<li>Ground improvement and ground modification systems.</li>
<li>Groundwater dewatering and analysis, pump, and slug tests.</li>
<li>Pile driving including knowledge in Pile Driving Analysis (PDA) and Case Pile Wave Equation Analysis Program (CAPWAP).</li>
<li>Instrumentation systems and evaluation of data therefrom.</li>
<li>Geo-forensic evaluations.</li>
</ol>
<ul>
<li>Contribute to increasing MC²’s geotechnical engineering consulting footprint in the market.</li>
<li>Bring advanced and insightful solutions to clients in Geotechnical Engineering.</li>
<li>Promote continuous quality monitoring and improvement on projects. Monitor quality standards and practices.</li>
<li>Responsible for conceptualizing the initial design and/or investigative approach for a major phase of a large project or have overall responsibility for the engineering work on a project of moderate scope.</li>
<li>Plan, schedule, conduct, and/or coordinate all engineering work involving conventional and complex engineering practices.</li>
<li>Conduct field inspections or investigations, when required.</li>
<li>Follow and support all site safety policies and procedures.</li>
<li>Participate in social industry events with clients and other stakeholders.</li>
</ul>

Education and Related Requirements:
<ul>
<li>M.S. degree or Ph.D. in Civil Engineering with a concentration in Geotechnical Engineering</li>
<li>10+ years of relevant hands-on experience in heavy civil projects</li>
<li>Knowledge of commercially available geotechnical software such as APILE, LPILE, SLOPE/W or SLIDE, GRLWEAP, MSEW, PLAXIS etc. required for slope stability, settlement, deep foundations, finite element modeling, etc.</li>
<li>Conversant in both AASHTO (LRFD) as well as LFD/ASD procedures applicable for analyses.</li>
<li>Familiarity with FL/GA geology and local field and design practices is preferred </li>
<li>Familiarity with GDOT and FHWA procedures for foundations, walls, and pavement analyses. </li>
<li>Excellent analytical, written, and verbal communication skills</li>
</ul>

Preferred Licenses, Registrations or Certifications:
<ul>
<li>Professional Engineer (PE)</li>
<li>Membership in applicable technical associations</li>
</ul>

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