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job_organization_name

city

state

<h3>Job Description</h3>
About Us
Perform Properties is a best-in-class, diversified real estate operating platform with expertise in high-quality, grocery anchored shopping centers and premier office assets. Perform is positioned to create more engaging experiences for customers, deliver long-term value for tenants, and drive stronger performance across its portfolio.
Perform has expertise in transactions, development, leasing, and management, and benefits from a multi-sector focus, data driven strategy, and national reach. The company focuses on properties with People-Appeal—dynamic spaces where people and businesses actively choose to work, shop, and gather, enhancing the communities around them.
Formed through the combination of ShopCore, ROIC, and EQ Office, Perform Properties leverages the shared experience, scale, and operational strengths of three leading organizations.
 
Role Summary
We’re looking for a Quantitative Researcher to join our Data &amp; Research team. This role is essential to help us uncover insights through statistical modeling, predictive analytics, and data-driven storytelling. You’ll work closely with a collaborative team that values intellectual curiosity, clear communication, and creative problem-solving.
This role exists to support the Data &amp; Research team’s mission: to build statistical models that uncover meaningful insights and drive smarter decisions. If you’re passionate about data, eager to learn, and enjoy turning complex information into clear, actionable stories, we’d love to hear from you.
This role reports to the Head of Data &amp; Research and is based in the office, 5 days a week.
 
Essential Job Functions
You’ll be responsible for organizing and cleansing datasets to ensure they are ready for use in econometric models, machine learning applications, and data visualizations. Another key task will be using visualization tools like PowerBI and Sigma to create the compelling, high-impact dashboards that will bring our research to life.
As a member of the Data &amp; Research team, you will help create a quarterly slide deck assessing macro trends, industry hot topics, and portfolio analytics with a focus on the Retail and Office sectors. You’ll also maintain our SharePoint site and automate data updates for our standard quarterly PowerPoint presentations, ensuring our materials are always fresh and accurate.
In addition to hands-on data work, you’ll help manage relationships with external data vendors, study emerging data and share your findings with your team.
 
Qualifications and Technical Competencies
• 3-5 years of experience in data research and quantitative analysis
• Experience building forecast models for predictive analytics
• Intermediate-to-advanced coding and coding library searches (ex. Python)
• Data visualization (PowerBI, Sigma)
• Expert proficiency in Microsoft applications (Excel, PowerPoint, PowerBI, SharePoint, Teams)
 
Benefits &amp; Compensation
Benefits: The Company provides a variety of benefits to employees, including health insurance coverage, retirement savings plan, paid holidays and paid time off (PTO).
Base Salary Range: $150,000-$200,000. This represents the presently-anticipated low and high end of the Company’s base salary range for this position. Actual base salary range may vary based on various factors, including but not limited to location and experience.
The additional total direct compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility.
 
Closing
EEO Statement
Our company is proud to be an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our employment decisions are based on individual qualifications, job requirements and business needs without regard to race, color, marital status, sex, sexual orientation, gender identity and/or expression, age, religion, disability, citizenship status, national origin, pregnancy, veteran status and or any other legally protected characteristics. We are committed to providing reasonable accommodations, if you need an accommodation to complete the application process, please email <a href="mailto:recruiting@performproperties.com" target="_blank">recruiting@performproperties.com</a>
#LI-Onsite

Quantitative Researcher

<h3>Job Description</h3>
Job DescriptionAdvanced Chemical Mixer, $17/hr – Pontiac, MIAre you experienced in chemical mixing and looking for a role where you can fast-track into more advanced liquid mixing operations? Are you ready to grow within a company that specializes in surface chemistry solutions with over 40 years in the industry? If you're eager to take on more responsibility and be part of a growing team, this opportunity is for you!Qualifications:
<ul>
<li>At least 1–2 years of experience mixing chemicals in a manufacturing or industrial setting </li>
<li>Must be able to stand, walk, and crouch throughout the shift </li>
<li>Ability to lift up to 50 lbs </li>
<li>Comfortable with PPE and safety procedures around chemicals </li>
</ul>
Skills:
<ul>
<li>Strong attention to detail and understanding of batch formulations </li>
<li>Ability to follow written and verbal instructions and record accurate data </li>
<li>Basic math and measurement skills required </li>
<li>Familiarity with industrial mixers and the ability to troubleshoot minor equipment issues </li>
<li>Team player with a positive attitude and willingness to learn new processes </li>
</ul>
As an Advanced Chemical Mixer, you'll be responsible for mixing chemical powders and liquids used in surface treatments for metal forming and industrial applications. You’ll begin with dry mix processes and will be fast-tracked to handle liquid mixing responsibilities. Attention to detail, safety, and process accuracy are crucial in this role. This is a great opportunity for someone who is ready to grow into a lead mixing position. Let’s go to work! Apply online today. Workbox Staffing Benefits:
<ul>
<li>Weekly Pay </li>
<li>Hire-in Opportunities </li>
<li>Benefits including Health, Life, and Dental </li>
<li>Veteran Friendly and Equal Opportunity Employer </li>
</ul>

1st shift - Advanced Chemical Mixer

<h3>Job Description</h3>
Job Description
Everytown for Gun Safety, the nation’s largest gun violence prevention advocacy group, is seeking a Research Intern for the Fall 2025 semester. Everytown’s Research Department studies how gun violence occurs in America and identifies the best policies and interventions to prevent and address it. In this role, the Intern will support and contribute to Everytown’s research of various types of gun violence, who it impacts, and how it impacts different communities in diverse ways. Interns are expected to work 15 hours (combination of in-person and remote) per week.
Primary Responsibilities:
<ul>
<li>
Conduct and write literature reviews, and critically analyze new research to support both day-to-day and longer-term research on gun violence prevention in the US;
</li>
<li>
Contribute to drafts of analytically rigorous and credible research materials, including memos, factsheets, and blog posts for a wide range of audiences;
</li>
<li>
Collect, clean, and conduct basic data analysis of gun violence-related datasets;
</li>
<li>
Collaborate on the development and execution of online content;
</li>
<li>
Assist the team in routine research administrative tasks, as and when required;
</li>
<li>
Support data accuracy for EveryShot by reviewing entries, flagging errors, and helping ensure incidents are categorized and displayed correctly;
</li>
<li>
Interact regularly with Everytown staff across all departments to ensure effective coordination and delivery of research program activities.
</li>
</ul>
Note: This position can be hybrid, with some days in the New York City office, or fully remote.
The minimum pay rate for this position is $17.00 per hour.
Dates: Anticipated start date September 22, 2025 through January, 2026
The candidate must meet the following requirements:
<ul>
<li>
Be currently enrolled in an undergraduate program;
</li>
<li>
Demonstrated ability to write well &amp; produce written materials for non-technical audiences;
</li>
<li>
Have exceptional attention to detail;
</li>
<li>
Some previous experience conducting basic data analysis on social science datasets is preferred;
</li>
<li>
Willingness to take initiative on projects;
</li>
<li>
Ability to quickly learn and adapt to a fast-paced environment;
</li>
<li>
Excellent collaboration and communication skills. 
</li>
</ul>
 
Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
About Everytown for Gun Safety Support Fund
Everytown for Gun Safety Support Fund (the “Everytown Support Fund”) is the education, research, and litigation arm of Everytown for Gun Safety, the largest gun violence prevention organization in the country with nearly ten million supporters. The Everytown Support Fund seeks to improve our understanding of the causes of gun violence and help to reduce it by conducting groundbreaking original research, developing evidence-based policies, communicating this knowledge to the American public, and advancing gun safety and gun violence prevention in communities and the courts. Learn more at <a href="http://www.everytownsupportfund.org" target="_blank">www.everytownsupportfund.org</a>.
Everytown for Gun Safety provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws.
Candidates who identify as members of historically underrepresented groups are highly encouraged to apply. 
You can learn about the framework that guides our work by viewing Everytown's Organizations Values

Research Intern - Fall 2025

<h3>Job Description</h3>
Job Description
Ergon's Paragon Technical Services is seeking an experienced Analytical Chemist to lead laboratory-based research and development efforts focused on bituminous materials used in the asphalt paving industry, in our Hattiesburg, MS, location. This role requires expertise in High-Performance Liquid Chromatography (HPLC) and Gel Permeation Chromatography/Size Exclusion Chromatography (GPC/SEC) to analyze the properties of asphalts, polymers, and process oils. The ideal candidate will thrive in a dynamic, research-driven environment and contribute to innovative product development.
Education and Experience Requirements:
<ul>
<li>Bachelor's degree in chemistry required (Graduate degree preferred).</li>
<li>Minimum 3 years of experience in analytical chemistry (5+ years preferred).</li>
<li>Proven expertise in HPLC and/or GPC/SEC instruments; experience with Agilent equipment is a plus.</li>
<li>Strong ability to work independently in a deadline-driven research setting.</li>
<li>Effective time management and organizational skills.</li>
<li>Commitment to data accuracy, integrity, and laboratory excellence</li>
</ul>
Duties and Responsibilities:
<ul>
<li>Conduct and oversee HPLC and GPC/SEC testing for bituminous materials.</li>
<li>Develop a deep understanding of the SAR-AD instrument and its applications.</li>
<li>Ensure laboratory data integrity, verifying accuracy and reevaluating questionable results.</li>
<li>Maintain meticulous lab records and documentation that align with industry standards.</li>
<li>Stay current with relevant testing requirements and methodologies (ASTM, AASHTO, etc.).</li>
<li>Perform routine calibration and maintenance of laboratory equipment.</li>
<li>Organize lab space effectively, ensuring cleanliness and proper inventory management.</li>
<li>Collaborate with the Technical Director and Research Team, providing updates on ongoing projects.</li>
<li>Comply with Environmental, Health &amp; Safety (EHS) regulations and company policies.</li>
<li>Support broader research initiatives through analysis, reporting, and teamwork.</li>
<li>Optional: Contribute to peer-reviewed publications based on research findings.</li>
</ul>
Why Ergon Inc.? 
At Ergon, we are a relationship-driven, family-owned company that values each employee's growth and contributions. Headquartered in Flowood, Mississippi, we take pride in maintaining a close-knit, small-company atmosphere while offering exceptional career opportunities. Our comprehensive benefits package includes:
<ul>
<li>Competitive pay</li>
<li>401(k) matching &amp; profit sharing</li>
<li>Health, Dental, Vision, and Life Insurance</li>
<li>Short- and Long-Term Disability Plans</li>
<li>Additional voluntary benefits</li>
<li>Paid holidays, vacation, and sick leave</li>
<li>Tuition assistance</li>
</ul>
At Ergon Inc., we live by our core values: 
<ul>
<li>Empowered Service: Together, we're committed to delivering unparalleled service. We do what's right, provide solutions, and foster stronger relationships with our teams and customers. Employee safety is our top priority and the first consideration in all aspects of our service. That's empowered service.</li>
<li>Selfless Leadership: We lead with compassion and put those around us before ourselves. We don't say we're experts; we demonstrate it through technical expertise, category innovation, and care for what we do. We call this selfless leadership.</li>
<li>Purposeful Growth: We believe employee and company growth go hand in hand. We build our legacy together to ensure future success through purposeful growth. The company has continually reinvested tremendously back into the business, not just growing for the sake of growing but growing carefully and strategically.</li>
<li>Respectful Relationships: Together, we foster a culture of respect, acceptance, and diversity of ideas and people. Our differences make us stronger. We're united by our shared values, constantly forging respectful relationships.</li>
</ul>
Come and join the Ergon team!
Must be able to pass a pre-employment drug screen and background check. A clean MVR is required.
We are an EEO/AAP employer.
Job Role: Analytical Chemist
Location: Hattiesburg, MS
 Job Posted by ApplicantPro

Analytical Chemist

<h3>Job Description</h3>
Job Title: Microbiology Technician/Associate Scientist 
Location: Pleasanton, CA (Onsite)
Duration: 6-month initial contract on W2
Pay Rate: $20- $26 per hour on W2
 
The Role: The Microbiology Technician – Cleaning R&amp;D position is in alignment with the Cleaning Business strategy to lead with #1 brands in the cleaning, sanitization, and disinfection categories. This role supports critical internal R&amp;D formulation development required to establish robust products and method development for various initiatives across all of Clorox’s businesses. The focus of this role will be on parterning closely with a Senior Microbiologist to develop and validate our internal capabilities for testing our Professional products against tuberculosis. This role is responsible for the prep, execution, and data analysis of laboratory testing in conjunction with the guidance of Scientists and oversight of the Group Manager. The Microbiology Technician is also responsible for implementing tools, resources and practices which serve to increase our microbiological acumen on tuberculosis testing while working safely alongside other team members.
 
The Microbiology Technician – Cleaning R&amp;D applies technical microbiological knowledge (with a primary focus on surface sanitization and disinfection) to new and existing test methods, while supporting projects and programs across the businesses by working collaboratively with Scientists and other Technicians on the Microbiology Team. The day-to-day activities of this role includes various tasks, but not limited to; media prep, routine testing execution, new test method development &amp; validation, data analysis and related lab maintenance.
 
Requirements:
o Execute a variety of simple to complex microbiological laboratory experiments in collaboration with other technicians and scientists to support the Clorox business.
o Collaborate with scientists to collect, evaluate, and present data to inform teams to enable project decisions.
o Manage the microbiology laboratory for this specific project, including laboratory upkeep, maintenance, and ordering equipment and supplies.
o Contributes to the operating principles and best practices of this new capability by working safely and with the highest integrity.
o Contributes to knowledge management practices with standardization and consistency.
o Ability to effectively network internally and externally.
o Excellent communication skills with ability to present critical information.
o Ability to collaborate cross-functionally with individuals in a wide variety of disciplines and backgrounds and build effective relationships.
Preferred candidates have:
o Background in biology, biotechnology, or microbiology
o Ideal candidate should have experience with aseptic techniques and dilution procedures.

Microbiology Technician/Associate Scientist

<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 
The Local Delivery Translational Sciences (LDTS) organization at AbbVie, leads the strategy, generation, analyses, interpretations, and reporting of non-clinical data and communications/agreements with global regulatory agencies in the areas of Translational Pharmacology, Non-clinical Pharmacokinetics, Exposure-Response, Immunogenicity, and Biopharmaceutics. &nbsp;The organization supports all phases of non-clinical development, supporting all new molecular entities across multiple therapeutic areas.
The organization is responsible for defining the relationship between drug exposure (e.g., concentrations in blood/ local tissue) and efficacy and safety measures in non-clinical models to select the optimal dose, dosing intervals, and biomarkers for FIH studies.
The organization provides critical support for conducting technical due diligence of new business opportunities (both in-licensing and out-licensing) by assessing probability of success for achieving the Target Product Profile (TPP). It also contributes to responses to defend our intellectual properties and extension of patent protection, provides critical support for life-cycle management of marketed products, responds to questions from post-marketing safety, legal, pharmaceutical manufacturing and regulatory for marketed products world-wide, and publication of scientific information in patents and manuscripts.
The LDTS group at AbbVie, is seeking a Principal Research Scientist – Modeling and Simulation.&nbsp; As a member of multidisciplinary teams, this individual will contribute both Pharmacokinetic and Modeling and Simulation (M&amp;S) expertise to lead efforts to build in silico drug models that describe the relationship(s) between exposure (drug, antibody, biomarker) and response (pharmacodynamic, toxicodynamic) for both desired and undesired effects.&nbsp; These models will support formulation development as well as early-stage clinical development activities utilizing various sources of data from both nonclinical models and humans.&nbsp; This individual should be comfortable with exploratory analyses and non-conventional modeling beyond systemic drug development including ophthalmology, neurotoxin, and aesthetics/dermatology.&nbsp; This scientist should be proactive, inquisitive, a self-starter who is eager to learn and thrives in a fast pace and independent environment, with a desire to interact as a modeling and simulation expert with matrix project teams.
Specific responsibilities include:
<ul>
<li>Apply PK and PK/PD modeling/simulation to guide the design and execution of in vivo preclinical animal experiments and/or early-stage clinical trials.</li>
<li>Identify opportunities to apply and develop modeling and simulation strategies across the R&amp;D portfolio, with a focus on ophthalmology, neurotoxin, and aesthetics/dermatology.</li>
<li>Integrate M&amp;S knowledge to contribute to optimizing translational sciences strategies.</li>
<li>Analysis of PK/PD data, both clinical and nonclinical, through the use of sophisticated mathematical and statistical modeling and simulation tools to support dose selection, study design and proof-of-concept.</li>
<li>Identify and monitor vendors and consultants or engage internal resources as appropriate to meet project deliverables.</li>
<li>In collaboration with other stakeholders, conduct and integrate data analyses and summarize modeling outcomes to support IND, CTA, IMPD, NDA, and BLA filing and regulatory correspondences.&nbsp;</li>
<li>Exploratory analyses and non-conventional modeling beyond systemic drug development with a focus on locally-administered/acting products.</li>
<li>Maintain awareness of current technologies in PK/PD and PBPK modeling.</li>
<li>Develop close and effective partnerships with other nonclinical and clinical pharmacology/PKPD and biomarker scientists, safety scientists, research scientists, clinicians and project teams.</li>
<li>Design and provide scientific oversight of preclinical PK/TK studies</li>
<li>At project level, establish and maintain effective collaborations with key stakeholders to facilitate data integration for biomarker selection, candidate nomination/selection, and human dose prediction</li>
</ul>
Qualifications 
<ul>
<li>BS with typically&nbsp;14+ years of experience OR MS with typically 12+ years of experience OR&nbsp;PhD with typically 6+ years of experience in Pharmaceutical Sciences, Quantitative Pharmacology, Biomedical/Chemical Engineering, Pharmacometrics or related field,</li>
<li>&nbsp;2+ years of experience in PK/PD modeling &amp; simulation, quantitative pharmacology, and/or applied population PK in the pharmaceutical industry.&nbsp;&nbsp;</li>
<li>Academic and/or industry experience in either physiologically-based pharmacokinetic (PBPK) modeling or population PK/PKPD modeling.</li>
<li>Strong knowledge of biology (mechanism of action)/pharmacology, toxicology, clinical immunology, protein sciences, statistics, and pharmaceutical development</li>
<li>Ability to learn new areas of biological sciences and build on solid foundation of quantitative skills to develop models.</li>
<li>Data manipulation and programming skills and ideally with the use of programs such as SAS, R, S+ or similar programs.</li>
<li>Experience using Phoenix WNL,GastroPlus, and SimCyp</li>
<li>Scientific publications in area of specialization.</li>
</ul>
<ul>
<li>Effective written and verbal communication skills.</li>
<li>Strong ability to collaborate with others.</li>
<li>Ability to keep up-to-date with and propose the implementation of scientific and technological developments in the area of modeling.</li>
<li>The successful candidate is required to have ability to work within a diverse workforce.</li>
</ul>
Preferred Experience
<ul>
<li>Experience with biologics including gene therapy</li>
<li>Experience with general programming and data analysis tools/languages such as R, Matlab, Berkeley Madonna, ADAPT, etc.</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. ​
</li>
<li>
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.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
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;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Principal Research Scientist - Modeling and Simulation

<h3>Job Description</h3>
• We are looking for an energetic and experienced mass spectrometry scientist to join our Research ADC Characterization team in the Protein Solutions and Bioanalytical department. This individual will help us grow our mass spectrometry capabilities, lead the development of new or improved techniques for the characterization of proteins and antibody drug conjugates in various matrices, as well as maintain our shared mass spectrometers. They will also participate in collaborative, cross-functional teams to enable cancer therapeutic development and aid in exploring scientific questions surrounding antibody-based therapeutic activity and behavior.
 
POSITION RESPONSIBILITIES:
• Determine and develop novel and appropriate LC-MS methods for the characterization of intact ADCs, antibodies, and other proteins
• Develop and optimize both broadly applicable and fit-for-purpose methodologies for the capture, characterization, and quantification of proteins and conjugates from biological samples
• Perform peptide mapping to deeply characterize proteins and bioconjugates
• Provide care, maintenance, and troubleshooting of shared LC-MS instrumentation, including training new users and developing and maintaining best practices
• Provide technical and scientific advice and support to scientists of all levels, advise on LC and mass spectrometry related questions, and provide sample processing and data analysis for non-MS users
• Practice continuous improvement to refine methods and optimize processes, staying in touch with relevant literature and state of the art technologies
• Maintain strong communication and collaborative relationships with mass spectrometry groups outside of Research
• Create and organize technical information to deliver effective presentations in multiple forums
 
 
EDUCATION AND EXPERIENCE:
• A Ph.D. or equivalent experience in bioanalytical chemistry, analytical chemistry, pharmaceutical sciences, or a related discipline with recognized and established expertise in mass spectrometry
• 4+ years of research experience in the biotech/pharmaceutical industry or closely related academic areas
• Demonstrated experience in the operation and maintenance of mass spectrometers, their software, and applicable data analysis software
• Established capability in biological characterization and data analysis, specifically utilizing mass spectrometry techniques
• Attention to detail and a strong analytical mindset capable of proposing sound experimental strategies and developing new LC-MS protocols
• Uses critical thinking to solve complex problems, address challenges, overcome obstacles, and anticipate areas for growth
• Established safe laboratory skills and accurate record keeping
• Ability to work independently on routine experiments
 
TECHNICAL SKILLS REQUIREMENTS:
Preferred qualifications include:
• Hands-on experience working with a Waters Xevo G2S QTof, Thermofisher Q Exactive, and/or SCIEX X500B QTOF
• Familiarity with affinity purification of proteins, peptides and/or metabolites.
• Experience analyzing all types of recombinant proteins
• Experience identifying and characterizing post-translational modifications or enzymatic modifications of proteins
• Experience with protein conformational analysis, such as Hydrogen deuterium exchange mass spectrometry
• Familiarity with Protein Metrics software and reporting, including high throughput data processing
• Experience or familiarity with mass spectrometry automation
• Knowledge of SEC-MALS biological analysis methods

Senior Scientist

<h3>Job Description</h3>
Key Responsibilities:
<ul>
<li>Perform testing of resin products using specialized instruments to meet customer requirements</li>
<li>Record and report test results accurately; maintain proper documentation</li>
<li>Complete production work orders per established procedures</li>
<li>Ensure compliance with corporate quality policies and safety standards</li>
<li>Maintain a clean, safe, and organized laboratory environment</li>
<li>Actively participate in safety and continuous improvement initiatives</li>
</ul>
 
Qualifications:
<ul>
<li>High school diploma or equivalent required</li>
<li>No previous work experience required</li>
<li>Preferred: Experience in manufacturing, operations, or laboratory environments</li>
</ul>
 
Skills and Abilities:
<ul>
<li>Understanding of Good Laboratory and Manufacturing Practices</li>
<li>Strong mathematical, organizational, and problem-solving skills</li>
<li>Ability to follow written procedures and verbal instructions</li>
<li>Comfortable using basic hand tools (e.g., wrenches, torque drivers, tweezers)</li>
</ul>

Formulation Scientist

<h3>Job Description</h3>
Job DescriptionTitle: Quality Control Microbiologist Location: Durham, North CarolinaHire Type: Long-term Contract, OnsitePay Rate: $24.00/hour (W2, with full employee benefits) Overview:Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive aFull Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental &amp; vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan. Job Summary: The QC Microbiology Analyst is responsible for performing microbiological testing to ensure product quality and compliance with FDA and GMP regulations. This role involves testing product and stability samples, maintaining accurate documentation, supporting investigations, and contributing to continuous improvement initiatives in a fast-paced medical device/diagnostics environment. Job Duties:
<ul>
<li>Perform microbiological testing on finished products, stability samples, and special test requests per SOPs.</li>
<li>Prepare and manipulate microbial cultures and stocks using aseptic technique.</li>
<li>Document and review test results for accuracy and compliance with GDP, GLP, GMP, and HSE requirements.</li>
<li>Support audits by maintaining logbooks, calibration records, and laboratory cleanliness.</li>
<li>Enter and manage data in the Laboratory Information Management System (LIMS).</li>
<li>Assist with laboratory investigations and document invalid test results.</li>
<li>Maintain training compliance with departmental processes and procedures.</li>
<li>Follow PPE and safety protocols in all laboratory activities.</li>
<li>Participate in continuous improvement initiatives and maintain 6S standards in lab areas.</li>
<li>Perform additional duties as assigned.</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor’s Degree in Microbiology, Biology, Biochemistry, or related life science preferred.</li>
<li>In lieu of a Bachelor’s Degree, will consider Associate’s Degree with 2+ years of relevant regulated industry experience (GMP preferred).</li>
<li>Prior microbiology lab and sterile/aseptic technique experience preferred.</li>
<li>Strong organizational, multitasking, and communication skills.</li>
<li>Knowledge of microbiological testing, quality principles, and data entry/analysis software.</li>
<li>Ability to problem solve and troubleshoot independently.</li>
<li>Team-oriented with initiative to drive improvements.</li>
<li>Ability to read and follow SOPs while maintaining safety and HSE compliance.</li>
</ul>
 Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.

Quality Control Microbiologist

<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 
Purpose
We are seeking a highly motivated Peptide Purification Scientist to join our Peptide Synthesis team. The ideal candidate will have hands-on experience in the synthesis, transformation, and purification of peptides. This individual will investigate, identify, develop, and optimize new methods/techniques to generate reliable and reproducible data in a timely manner. The candidate should also be able to demonstrate broad and versatile technical expertise within discipline and be able to collaborate and communicate with other groups across discipline.
Responsibilities:
Laboratory Tasks:
• Perform routine laboratory techniques: pipetting, reagent reconstitution, calculation of concentrations/dilutions, and accurate weighing of raw materials for instrument setup and compound processing.
• Use RP-HPLC/MS for purification, characterization, and analysis of peptides.
• Setup, maintain, and troubleshoot instruments: HPLC, lyophilizers, peptide synthesizers, centrifuges, rotovap, and balances.
• Maintain and optimize peptide purification processes to ensure consistent output, with a strong focus on increasing peptide recovery and overall throughput.
• Follow SOPs for standardized activities; implements data driven improvements/optimization.
• Identify and implement process improvements; conduct optimization experiments when necessary.
• Troubleshoot and correct process or instrument issues.
• Highly autonomous and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.
• Complete hazardous waste training (RCRA/DOT) and manage hazardous waste, including bulking and coordination with handlers.
Data Analysis &amp; Technical Writing:
• Maintain accurate lab notebooks and records of all procedures.
• Analyze and interpret LC/MS data to assess peptide/sample quality.
• Adjust analytical methods for QC and peptide content.
• Contribute to development of new data analysis methods.
• Prepare and review technical reports, SOPs, summaries, and quantitative analyses.
•Stay current with scientific literature relevant to peptide purification and processes. &nbsp;
Inventory &amp; Training:
• Manage inventory of reagents and consumables; order supplies as needed.
• Train new employees in lab techniques and instrument use.
Compliance:
• Comply with all corporate/divisional policies and procedures.
• Adhere to standards regarding code of conduct, safety, handling of hazardous materials, GxP compliance, and animal care (if applicable). &nbsp;
Ideal candidates will demonstrate strong problem-solving skills, meticulous attention to detail, and excellent documentation abilities. Experience with RP-HPLC method development and optimization is a must.
Qualifications 
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
<ul>
<li>Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Possess thorough theoretical and practical understanding in peptide purification and HPLC method development; experience in peptide synthesis is highly desirable.</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;ofthis 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.&nbsp;​
</li>
<li>
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.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
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 anybonus,&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 soleand&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.
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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