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<h3>Job Description</h3>
Position Title
Senior Scientist / Postdoctoral Researcher / Lecturer / Professor
— Focus on Materials Science —
&amp;#x1F539; Urgent Hiring – Materials-Related Fields
We are urgently recruiting PhD holders in the following areas:
<ul>
<li>Materials Science &amp; Engineering</li>
<li>Polymer Science</li>
<li>Functional Materials</li>
<li>Energy Materials</li>
<li>Catalysis &amp; Reaction Engineering</li>
<li>Green Chemistry &amp; Sustainable Materials</li>
<li>Biomedical or Electronic Materials</li>
</ul>
Both full-time (in China) and part-time remote collaboration are welcome.
About the Program
Partnering with top universities, institutes, and listed companies in Jiangsu Province, we aim to build world-class international research teams. The program focuses on industry-academia collaboration, research excellence, and innovation transformation.
Key Responsibilities
<ul>
<li>Conduct high-level independent or collaborative research</li>
<li>Publish in reputable academic journals</li>
<li>Apply for national/international grants</li>
<li>Mentor graduate students (if applicable)</li>
<li>Engage in international and industrial collaborations</li>
</ul>
Compensation &amp; Support
<ul>
<li>&amp;#x1F4B0; Annual Salary: $40,000 – $250,000+ (negotiable)</li>
<li>&amp;#x1F680; Startup Funding: Up to $400,000</li>
<li>&amp;#x1F3E0; Housing/Relocation Support: Up to $400,000</li>
<li>&amp;#x1F6E0;️ Full support for visa, residence, healthcare, children's education, and relocation</li>
</ul>
Career Tracks
<ul>
<li>Academic: Lecturer → Professor</li>
<li>Research: Assistant → Senior Scientist → Group Leader</li>
<li>Support for national talent programs and international collaborations</li>
</ul>
Candidate Requirements
<ul>
<li>PhD in Materials Science, Chemical Engineering, or related fields</li>
<li>Degree from a top global university (QS Top 200 preferred)</li>
<li>Strong publication and research record</li>
<li>Willingness to collaborate with Chinese institutions</li>
<li>Open to candidates of all nationalities</li>
</ul>
How to Apply
Please send your CV to:
 &amp;#x1F4E7; <a href="mailto:yz2994317@gmail.com" target="_blank">yz2994317@gmail.com</a>
 &amp;#x1F4E7; <a href="mailto:Yijing.Zhong@suruntalent.com" target="_blank">Yijing.Zhong@suruntalent.com</a>
Email subject: "Application + Research Direction + Your Name"

Senior Principal Scientist

<h3>Job Description</h3>
Job Description
Description
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
 
Skills
Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry
 
Top Skills Details
Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control
 
Additional Skills &amp; Qualifications
Frist Shift- General Shift: 8:30AM – 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They’re hiring across levels (QC Chemist II &amp; III). QC Chemist II should be between 2-3 years’ experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I’d prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. • Bachelor's degree (BS or BA), physical sciences required • Master's degree preferred • Minimum of 3-5+ years' experience. • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets.
 
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 28, 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.

Quality Control Chemist II, III

<h3>Job Description</h3>
DESCRIPTION: We are seeking a highly motivated Research Associate to support the analytical testing of cell therapy products to support development activities. The role requires hands-on laboratory work, including mammalian cell culture, flow cytometry, and PCR-based testing as well as data analysis. The Research Associate will work as part of a team under the guidance of Senior Project/Team Leads.
 
PRIMARY RESPONSIBILITIES:
- Performing aseptic cell culture, flow cytometry, and molecular assays
- Testing development samples on a routine basis to support process/formulation activities
- Documenting work and analyzing experimental results
- Reporting results out to project lead accurately and on time
- Support general lab maintenance including restocking and ordering supplies and equipment maintenance.
 
MINIMUM REQUIREMENTS:
- 1 year of hands-on experience with adherent mammalian cell culture
- 1 year of hands-on experience with flow cytometry
- Be able to follow established techniques/SOPs in aseptic cell culture, cell and molecular biology to generate and analyze data in an accurate and reproducible manner.
- Capable of maintaining accurate records in electronic laboratory notebooks or paper forms/SOPs, appropriate databases, and inventories in a timely manner.
 
PREFERRED EXPERIENCE:
- Cellular therapy laboratory experience
- Experience in mRNA/DNA extraction and qRT-PCR/ddPCR
- Experience with ELISA
- Experience with pluripotent stem cells
- Experience with Good Documentation Practices

Research Associate - Cell Therapy Analytical Testing

<h3>Job Description</h3>
Job Title: Research Associate - Cell Therapy Analytical Testing
Location: Westborough, Ma
Zip Code: 01581
Duration: 3 Months
Pay Rate: $50/hr.
Keyword's: #ResearchAssociatejobs; #CellTherapyAnalyticalTestingjobs; #Westboroughjobs;
Start Date: Immediate
 
JOB DESCRIPTION: 
We are seeking a highly motivated Research Associate to support the analytical testing of cell therapy products to support development activities. The role requires hands-on laboratory work, including mammalian cell culture, flow cytometry, and PCR-based testing as well as data analysis. The Research Associate will work as part of a team under the guidance of Senior Project/Team Leads.
 
PRIMARY RESPONSIBILITIES:
- Performing aseptic cell culture, flow cytometry, and molecular assays
- Testing development samples on a routine basis to support process/formulation activities
- Documenting work and analyzing experimental results
- Reporting results out to project lead accurately and on time
- Support general lab maintenance including restocking and ordering supplies and equipment maintenance.
 
MINIMUM REQUIREMENTS:
- 1 year of hands-on experience with adherent mammalian cell culture
- 1 year of hands-on experience with flow cytometry
- Be able to follow established techniques/SOPs in aseptic cell culture, cell and molecular biology to generate and analyze data in an accurate and reproducible manner.
- Capable of maintaining accurate records in electronic laboratory notebooks or paper forms/SOPs, appropriate databases, and inventories in a timely manner.
 
PREFERRED EXPERIENCE:
- Cellular therapy laboratory experience
- Experience in mRNA/DNA extraction and qRT-PCR/ddPCR
- Experience with ELISA
- Experience with pluripotent stem cells
- Experience with Good Documentation Practices
 
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

Associate Researcher

<h3>Job Description</h3>
Job Description
Mitsubishi Electric Research Laboratories (MERL) invites qualified candidates to apply for the position of Research Scientist in the Multiphysical Systems Group. Current areas of interest include physics-based modeling and numerical simulation of thermofluid and mechatronic systems, control system design and development, nonlinear state estimation, and applications of machine learning. Successful candidates will be expected to perform original, relevant research in the areas of nonlinear state estimation and system inversion for complex multiphysical systems.
The Multiphysical Systems Group at MERL conducts fundamental, academically-oriented research in model-based design and analysis of complex multiphysical systems, emphasizing thermofluid, electrical power, and mechatronic applications. Using state-of-the-art languages, we construct system-level dynamic models and use them to design new estimation and control algorithms, analyze dynamic behaviors, optimize product performance, and prototype new products and services that are enabled by these tools and methods. Current research interests include data-driven optimization and estimation for large-scale, nonlinear system models, development of next-generation tools for scientific computing, and design and analysis of robust nonlinear control and model predictive control. Specific areas of interest include state and parameter estimation for physics-based models comprised of hybrid (discrete and continuous state) nonlinear differential algebraic equations, particle filtering and ensemble estimation methods, variational methods for data assimilation and model inversion, and other cutting-edge estimation technologies. The successful candidate will bring an independent research agenda and a track record commensurate with experience and be capable of working within interdisciplinary R&amp;D teams.
Responsibilities for this position include:
<ul>
<li>Conducting innovative and relevant research on modelling, estimation and control for multiphysical systems</li>
<li>Developing and advancing a research agenda impacting the scientific community and company technology</li>
<li>Publishing results in leading technical journals and conferences, and drafting patent applications </li>
<li>Partnering with business units, corporate R&amp;D, and academic groups in the execution of R&amp;D projects</li>
<li>Transferring results and technology to Mitsubishi Electric corporate research laboratories</li>
</ul>
Qualifications for this position are:
<ul>
<li>A Ph.D. or equivalent from an internationally recognized institution in mechanical engineering, chemical engineering, electrical engineering, applied mathematics, or other related fields, with a focus on estimation, control theory, and/or data assimilation</li>
<li>Extensive experience with physics-based modeling, simulation, and dynamic analysis of multiphysical systems</li>
<li>Expertise in thermofluid systems is preferred, but background in mechatronic or other systems will also be considered</li>
<li>Strong programming skills, in at least some of Julia, Modelica, C/C++, Python, and Matlab</li>
<li>A strong publication record in leading conferences and journals, consistent with experience</li>
<li>A record for independently proposing and executing research programs with academic impact</li>
<li>Strong teamwork, communication (oral and written), teaching, and listening skills</li>
</ul>
The pay range for this position at the commencement of employment is expected to be between $135,000 and $170,000 per year. Actual base pay will depend on a variety of individualized factors, including job-related knowledge, skills, and experience.
In addition to base salary, the total compensation package will include an annual performance-based bonus and a comprehensive benefits program encompassing medical, dental, and vision coverage; a generous 401(k) match; commuting and home office stipends and various paid time off programs (including vacation, sick time, personal and parental leave). Specific details regarding participation in these programs will be provided upon an offer of employment.
Employment is considered “at-will,” and the Company reserves the right to modify base salary or any other compensation program at any time, including for reasons related to individual performance, departmental or Company performance, and market conditions.
PRINCIPALS ONLY. No phone calls please.
Mitsubishi Electric Research Laboratories, Inc. is an Equal Opportunity Employer.
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL's employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions.

Staff - Research Scientist - Multiphysical Systems

<h3>Job Description</h3>
Job DescriptionJob Posting Title
Associate Chemist, Quality Control
Job Description
About TRI-K
 
Since 1974, TRI-K Industries, Inc. has been a leading manufacturer of specialty ingredients, bringing innovative concepts and products to life for the cosmetics industry. TRI-K strives to keep ahead of the curve with a specialization in cosmetic proteins and multi-functional peptides, natural actives, preservatives, and mild surfactants. TRI-K is a member of the Galaxy Group, with sales offices, manufacturing facilities and partners around the world. At TRI-K, we combine an awareness of consumer trends with innovative technologies to maintain our superior offering in the industry. Our in-house development team is constantly pioneering the discovery of new materials, resulting in enhanced consumer benefits. TRI-K Industries is a wonderful place to start your career with opportunities to learn and grow.
 
Role Purpose: Assists QC Manager and performs quality control procedures designed to ensure continuous production and shipment of cosmetic ingredients consistent with established standards. Serves as key member of Proteins Division Quality Unit (PDQU) with authority to test, approve or release FG or RM, following ISO and GMP Protocols.
 
Position Reports to: Quality Control Manager
 
Positions Reporting to this Position: none
 
Position is located in Derry, NH. 
 
Requirements
Role Objectives: 
Essential Duties and Responsibilities include the following. Other duties may be assigned.
<ul>
<li>Secondary responsibility for Quality Control Department (verification, review, approval &amp; release) including Quality testing. Performs Quality functions related to shipping, as needed</li>
<li>Key member of Proteins Division Quality Unit (PDQU)</li>
<li>Accurately analyzes and performs chemical testing of FG, in-process batches, raw materials, according to established standards</li>
<li>Accurately maintains and updates Quality control data base on a daily basis</li>
<li>As part of PDQU, tracks, investigates and reports deviations from established Quality Control Standards</li>
<li>Participates in cross-functional teams to increase efficiency, solve problems and improve quality systems</li>
<li>Secondary responsibility for approval and release of incoming raw materials, maintenance of RM data base and related specifications</li>
<li>Assists with aseptic sampling of products, labeling and proper storage of retains</li>
<li>Become fully trained on PD products, including Specifications, methods and equipment</li>
<li>Member of team who evaluate and respond to quality issues presented by customers</li>
<li>Ability to use and maintain analytical equipment necessary for quality testing</li>
<li>Follow safe laboratory guidelines and plant safety protocols</li>
<li>As part of PDQU, maintains equipment, calibrations, and documentation according to SOP &amp; Work Instructions, following ISO and GMP protocols</li>
<li>Maintains Quality Control objectives, complementary to corporate policies and goals</li>
</ul>
Competencies:
To perform the job successfully, an individual should demonstrate the following competencies:
<ul>
<li>Language Ability- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.</li>
<li>Math Ability- Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry.</li>
<li>Reasoning Ability- Ability to solve problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.</li>
<li>Computer Skills- Knowledge of Word Processing software; Spreadsheet software and Internet software.</li>
<li>Work Environment- While performing the duties of this job, the employee is frequently exposed to work near moving mechanical parts; fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
<li>Physical Demands- While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and taste or smell. The employee is occasionally required to sit; climb or balance and stoop, kneel, crouch, or crawl. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor's degree from four-year college or university, preferably in Chemistry, Biology or a related field. </li>
<li>One to two years related experience and/or training; or equivalent combination of education and experience is a plus.</li>
</ul>
 
We offer a competitive compensation package including:
• Medical
• Dental
• 401 (K)
• Vision
• Paid Time Off
• Life Insurance
• In addition to other programs and plans
 
TRI-K Industries is an equal opportunity employer, and we celebrate and value diversity in our workforce. Hiring decisions are based on qualifications, merit, and business needs.
 Monday-Friday, 1:00 PM to 9:30 PM

Associate Chemist, Quality Control

<h3>Job Description</h3>
Job Description Job Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
About the Role
Are you passionate about chemistry and eager to make an impact in a dynamic laboratory setting? We’re looking for a Bench Chemist who thrives on precision, problem-solving, and innovation. In this role, you’ll work with cutting-edge instrumentation and collaborate with a team dedicated to delivering high-quality results that drive product excellence.
This is an exciting opportunity to join a growing organization where your expertise will directly contribute to advancing science and improving product quality.
What You’ll Do
<ul>
<li>Perform LC and GC testing on raw materials, in-process samples, and finished goods.</li>
<li>Prepare samples, run calibration curves, and ensure system suitability through integration reviews.</li>
<li>Execute wet chemistry techniques such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance and troubleshooting to keep operations running smoothly.</li>
<li>Support method validation efforts focusing on accuracy, precision, and detection limits.</li>
<li>Maintain a clean, organized lab environment and assist with inventory management.</li>
<li>Draft and review SOPs to uphold compliance and quality standards.</li>
</ul>
What We’re Looking For
<ul>
<li>Education: Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Technical Skills: Proficient in HPLC and GC systems, chromatography software (OpenLab, ChemStation), and wet chemistry techniques.</li>
<li>Knowledge: Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Strong commitment to lab safety, accuracy, and continuous improvement.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in organic chemistry, formulation, or R&amp;D.</li>
</ul>
Why Join Us?
<ul>
<li>Work with state-of-the-art equipment in a collaborative, science-driven environment.</li>
<li>Opportunity for career growth through a contract-to-hire pathway.</li>
<li>Be part of a team that values innovation, quality, and professional development.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, MA.
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 Hadley,MA.
Application Deadline
This position is anticipated to close on Nov 28, 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.

Bench Chemist

<h3>Job Description</h3>
Job Description
Job Title: Lab Technician II Location: Braintree, MA, 02184
Pay rate: $20 - $30 an hour
Contract Duration: 6-month contract - temp to perm
Client: Integra LifeSciences Corporation Job ID: IGRAJP00001661
We offer medical, dental, vision, and 401(k) benefits.
My apologies if your profile doesn't suit this job. This is a blast email.
Description:
<ul>
<li>ISO 13485 exp preferred, along with ISO 7 and 8 cleanroom</li>
<li>ISO 5 is even better</li>
</ul>
Must Have:
<ul>
<li>Environmental Monitoring</li>
<li>Water Monitor &amp; Collecting</li>
<li>Microsoft Office experience - Advanced/Proficient</li>
</ul>
Exp with Bioburden testing is great
Responsibilities:
<ul>
<li>Responsible for performing Microbiological testing such as Bioburden, Endotoxin, Growth promotion testing, TOC &amp; Conductivity testing, sending samples for Microbial ID testing and other micro testing.</li>
<li>Perform Environmental monitoring of clean rooms including Viables and Non-viables testing and responsible of water samples collection and testing.</li>
<li>Working knowledge of aseptic techniques and provides database support, generates reports, and analyzes the data as needed.</li>
<li>Inspection and testing of raw materials, in-process, and final product testing.</li>
<li>Assist in trending environmental monitoring data. Report and investigate any monitoring excursions.</li>
<li>Monitors equipment and instrumentation used daily to ensure proper operation and calibration.</li>
<li>Maintains a working inventory of all components, materials and solutions as needed.</li>
<li>Develops and revises SOPs &amp; Forms</li>
<li>Responsible for identifying and alerting supervisor of issues on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions.</li>
<li>Assist in Out of Specification (OOS) Investigations, Non-conformances, and Corrective Action/Preventive Actions (CAPAs).</li>
<li>Assists in the writing and updating of Microbiological test procedures, protocol, logbooks, and checklists.</li>
<li>Assist as needed in test method validation, investigation studies or other product development studies.</li>
<li>Assist in preparing for and participating in FDA audits, customer audits, etc.</li>
<li>All other duties as assigned</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Microbiology, Biology, or a relevant scientific discipline.</li>
<li>A minimum of 2-4 years’ experience in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other cGMP-regulated product environment.</li>
<li>Familiarity with the application of FDA and/or ISO quality standards in a government-regulated industry. Quality Certification (e.g., CQE, CQA, Six Sigma) preferred.</li>
<li>Proficient computer competence, including experience with databases and Microsoft Office software to create reports, spreadsheets, analyze data, and prepare presentations.</li>
<li>Experience with performing Microbiological assays in cGMP cGMP-compliant lab and understanding of aseptic techniques.</li>
<li>Working knowledge of standard laboratory practices and safety.</li>
<li>Ability to follow instructions precisely, recognize deviations, and recommend corrective action.</li>
<li>Experience working in ISO Class 7 &amp; 8 cleanrooms.</li>
</ul>
Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. We serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. We also have national recruiting 
<h3>Company Description</h3>
TechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. \r\n\r\nWe serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. \r\n\r\nWe also have national recruiting

Laboratory Technician (Med Device/Pharma) AO2025

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Independently performs routine and non-routine testing. Performs laboratory testing within a GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data, evaluates results and forms conclusions with minimal outside input. Is able to recognize laboratory technique or instrumental events that could impact the integrity of the test data. Recognizes and resolves simple to moderately complex technical problems. Writes procedures with minimal guidance. Works under the general guidance of a supervisor but can effectively manage their own time to ensure timely completion of assigned duties. Trends data to support assay performance. Effectively writes all types of exception reports.
Responsibilities
<ul>
<li>Performs more complex test methods as written to support product/material release with minimal error.</li>
<li>Understands laboratory techniques and principles performed.</li>
<li>Interprets experimental data for conformance with product/material specifications.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements.</li>
<li>Assists with writing and performs validation assays per approved protocols.</li>
<li>Can effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
<li>Make recommendations for process improvement.</li>
<li>Writes/revises procedures as necessary and provides support for department.</li>
<li>Develops and maintains trend reports, backlog report, and document error reports which support departmental performance.</li>
<li>Authors all types of Investigations and deviations effectively. Assist in troubleshooting assays.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>5-8 years of related work experience</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
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This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
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Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
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Quality Control Scientist-Microbiology (Sunday-Thursday 9am-5:30pm)

<h3>Job Description</h3>
Job Description
Research Analyst
Location: Fully remote
Reports to: Director of Analysis
Job Type: Full-time
About Greenline Insights
Greenline Insights is a non-partisan, analytically driven research firm empowering smart decision-making in climate, energy, and public policy. We specialize in modeling, analysis, and policy design to help local workforces, businesses, and communities thrive. Our interdisciplinary work spans economics, energy, public health, infrastructure, industry, and innovation — and is rooted in clarity, rigor, and action. We pride ourselves on translating complex research into policy-relevant insights that drive real-world impact, from detailed reports and testimony to stakeholder engagement and modeling tools.
Our Values We value curiosity, intellectual rigor, and mission-driven care. As a research-focused team, we believe clarity — in thinking, methods, and communication — is essential for impactful work.
We look for teammates who bring good energy, analytical grit, and a commitment to problem-solving. We thrive with colleagues who enjoy tackling complexity, asking sharp questions, building structure where none exists, and working collaboratively to generate high-quality, actionable research.
Role Summary
We’re seeking an ambitious, energetic Research Analyst to help drive a wide range of climate, energy, and economic policy research. The ideal candidate is excited by analytical challenges, comfortable working with complex datasets, and eager to translate quantitative findings into clear, actionable policy insights.
As a core member of our research team, you’ll gather, interpret, and analyze data; support modeling efforts across multiple projects; and help shape the evidence base behind high-impact policy decisions. You’ll be joining at a pivotal moment — Greenline Insights is growing quickly, and your work will directly expand our research capacity, sharpen our modeling, and increase our impact.
This role is an opportunity to build deep expertise at the intersection of energy systems, economics, and public policy. As the company scales, there will be meaningful opportunities for increased responsibility, leadership, and ownership of research domains.
Core Responsibilities 
Data &amp; Research
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Identify, collect, clean, and structure key datasets to support energy, economic, and policy modeling.
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Conduct literature reviews and background research to inform modeling assumptions and project design.
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Develop clear, repeatable workflows for data processing and documentation.
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Modeling &amp; Analysis
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Run and support energy policy, economic impact, and emissions modeling tools.
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Analyze and interpret complex data to uncover trends, quantify impacts, and inform policy insights.
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Translate modeling outputs into structured findings that support messaging, recommendations, and decision-making.
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Contribute to the development and refinement of internal models, tools, and analytical systems.
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Writing &amp; Communication
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Draft and contribute to reports, memos, policy briefs, presentations, and technical appendices.
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Summarize technical results in clear, compelling language tailored to policymakers, advocates, and other stakeholders.
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Create charts, figures, and visual summaries to communicate analytical findings.
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What We’re Looking For
Must-Have Qualities
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A graduate degree or 2–4 years of equivalent professional experience in energy, climate, economics, public policy, or a related analytical field.
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Experience working with energy, climate, economic, or environmental datasets — including data cleaning, synthesis, and interpretation.
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Strong analytical skills and comfort with quantitative modeling, scenario analysis, or impact assessment.
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Clear, concise writing and communication skills; ability to explain technical findings to non-technical audiences.
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Curiosity and intellectual grit — you enjoy digging into complex questions, solving problems, and navigating ambiguity.
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A self-starter who is comfortable managing tasks independently while collaborating closely in a small, high-trust team.
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Enthusiasm for learning new methods, adapting to new tools, and growing into project leadership over time.
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Exceptional attention to detail, with the ability to spot data inconsistencies, validate assumptions, and ensure accuracy across datasets, modeling outputs, and written deliverables.
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Commitment to Greenline Insight’s mission and interest in long-term growth with the company.
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Preferred Skills
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Experience with Python or another similar programming language for data analysis or modeling.
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Familiarity with energy/economic modeling platforms, including but not limited to IMPLAN, REMI, system dynamics modeling tools (e.g., Vensim), Energy Policy Simulator, or other economic/energy modeling platforms.
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Experience building data visualizations or communicating quantitative results through charts and figures.
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Background in climate, clean energy, economic modeling, or policy analysis.
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Position Details
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Type: Full-time
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Location: Fully remote. Occasional travel may also be required.
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Salary: $75,000–$85,000, commensurate with experience.
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Benefits: Generous PTO, healthcare/dental benefits, and flexible remote work hours.
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How to Apply
Please fill out the form to submit your resume, cover letter, and contact information. Applications are reviewed weekly on a rolling basis; we encourage early submission.
Equal Opportunity Statement
Greenline Insights is an equal opportunity employer. We value diversity of backgrounds and perspectives and are committed to creating an inclusive environment for all employees and contractors. We encourage applications from individuals of all races, ethnicities, religions, genders, sexual orientations, gender identities, ages, national origins, veteran statuses, and those with disabilities — even if you don’t meet every qualification listed.

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