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field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve.
 
Chemical Handler Shift: 1st shift: 7-3:30pm (Mon-Fri) Notes:
Summary: Accurately and efficiently assembles/tests a variety of moderate to semi-complex products to achieve customer quality and on-time delivery schedules. Performs job under direct supervision or with guidance from more experienced team members. Primary Responsibilities/Essential Functions:
<ul>
<li>Cleans, etches, degreases and passivates components through acid and other chemicals baths.</li>
<li>Performs heat treat process and hardness analysis per internal standards, industry standards and customer requirements; maintains operational logs.</li>
<li>Performs dry film lubricant and epoxy operations.</li>
<li>May be required to assist with wire-on and pressure testing.</li>
<li>Performs moderately complex assembly/test functions utilizing mechanical skills, hand and power tools, mechanical/electronic tools, test equipment, and inspection measurement equipment in a manufacturing environment.</li>
<li>Sets up moderately complex test equipment on a variety of products to measure and record valve or system conformance to test specifications.</li>
<li>Performs evaluation and rework of conformity of components according to blueprints and work instructions.</li>
</ul>
Secondary Responsibilities/Non-Essential Functions:
<ul>
<li>May inspect assemblies that conform to product specifications. Assembles and tests to customer and/or industry standards</li>
<li>Maintains a satisfactory high level of performance while following appropriate procedures and observing all pertinent safety rules and requirements</li>
<li>Maintains appropriate knowledge and ability levels to efficiently perform all assigned work and utilizes this knowledge base to become proficient in new/unfamiliar assignments.</li>
<li>Assists in managing waste and scraps to minimize department expenses; develops cost reduction ideas to allow for continuous improvement in processes and procedures.</li>
<li>May monitor and verify quality in accordance with statistical process or other control procedures.</li>
<li>Observes all company policies and procedures, including safety rules, and maintains a clean and orderly work area.</li>
<li>Actively participates in lean/continuous initiatives by identifying and providing suggestions on areas for improvement. Applies lean concepts and tools in work areas</li>
<li>Knowledge of P.P.E (personal protective equipment) and properly uses this equipment.</li>
<li>Note: This job description is not intended to be all-inclusive. Employees may perform other related duties as required to meet the ongoing needs of the organization.</li>
</ul>
Qualifications (relevant experience, education and training):
<ul>
<li>Requires high school diploma or equivalent and 1-3 or more years’ related experience working in a manufacturing process environment.</li>
<li>Fully qualified in majority of operations and products and demonstrated ability to meet or exceed production and quality standards. Must be able to acquire Certified Operator stamp once eligible.</li>
<li>You must wear personal protective equipment, including respirator, steel toe boots, arc flash protective equipment, or other equipment as required by SPD safety guidelines. Must pass pulmonary function test if required.</li>
<li>Thorough knowledge of policies, procedures and systems in functional area.</li>
<li>Proficient in reading, understanding and following follow blueprints, engineering orders, specifications, and verbal instructions. Able to perform basic mathematical calculations.</li>
<li>Effectively applies lean/continuous improvement initiatives. Maintains and can interpret operational and quality metrics and actively contributes improvement suggestions.</li>
<li>Demonstrates effective verbal, written, and interpersonal communication skills, as well as the ability to work in a team environment. Able to participate and provide input to engineering or other leaders on operational status or performance.</li>
<li>Interprets reports and uses job specific software applications (e.g. production control/tracking systems). Able to use employee self-service systems to access on-line information and use specialized automated systems (i.e., PA+, TORS, e-mail).</li>
<li>Effectively demonstrates team member competencies and participates in goal setting, performance feedback, and self-development activities</li>
</ul>

Chemical Handler

<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;Twitter,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube&nbsp;and&nbsp;LinkedIn.&nbsp;
Job Description 
Key Responsibilities
&nbsp;
<ul>
<li>Design &amp; conduct critical experiments that further project goals.</li>
<li>Implement &amp; may innovate new experimental protocols/techniques.</li>
<li>Understand goals &amp; maintain a high proficiency in his/her projects &amp; overall program.</li>
<li>Interpret results &amp; draw conclusions from own multistage experiments, note significant deviations, then suggest, design, &amp; pursue relevant experiments.</li>
<li>Understand relevant scientific literature &amp; apply theoretical framework to solving problems within scientific discipline in a timely manner.</li>
<li>Perform routine &amp; complex tasks competently &amp; independently &amp; generate reliable &amp; consistent results.</li>
<li>Impact projects mostly through lab &amp;/or pilot plant-based activities.</li>
</ul>
Qualifications 
Education &amp; Experience
Must have a Bachelor’s in biology, biotechnology, or biomedical engineering or equivalent &amp; 3 years&nbsp;of academic &amp;/or industry experience executing&nbsp;pharmaceutical drug development &amp; pharmacology of drugs.
Of experience required, must have 3 years in each of the following:
<ol>
<li>preparing &amp; delivering written &amp; oral presentations to peers, management &amp; business stakeholders in a matrixed organization;</li>
<li>working&nbsp;with internal &amp; external cross functional teams; &amp;</li>
<li>executing &amp; interpreting experiments that involve molecular biology, including DNA/RNA/protein biochemistry &amp; cell biology, including cell culture technique &amp; cellular imaging.</li>
</ol>
&nbsp;
Alternatively, would accept a Master’s in biology, biotechnology, or biomedical engineering or equivalent &amp;&nbsp;1 year&nbsp;of academic &amp;/or industry experience executing pharmaceutical drug development &amp; pharmacology of drugs. Of experience required, must have 1 year of each of (i), (ii), &amp; (iii).
Work experience may be gained concurrently.&nbsp;Employer will accept combination of education, training &amp; work experience.
 Additional Information 
Salary Range: $106,870.00 - $107,500.00 per year.
Apply online at <a href="https://careers.abbvie.com/en" target="_blank">https://careers.abbvie.com/en</a> or send resume to <a href="mailto:Job.opportunity.abbvie@abbvie.com" target="_blank">Job.opportunity.abbvie@abbvie.com</a>. Refer to Req ID:&nbsp;REF49201N
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.&nbsp; This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
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>

Associate Scientist II, Precision Medicine Immunology

<h3>Job Description</h3>
Job DescriptionJob Title: Senior Associate Scientist Location: Cambridge, MA 02142 Duration:12 Months+ Pay Range: $45 - $50/hr. on w2 Job Summary: The Senior Associate Scientist, Specifications will be responsible for specification support of siRNA drug substances and drug products. This is an onsite position. Summary of Key Responsibilities: 
<ul>
<li>Initiate and manage specification change controls in a GMP setting.</li>
<li>Expected contributions to general operations including review of data and authorship/review of technical documentation. Provide technical support as needed.</li>
<li>Author and review SOPs and protocols in accordance with company and regulatory guidelines.</li>
<li>Contribute to data review, analytical and stability sections of regulatory submissions. Assist with responses to agency requests on these sections.</li>
<li>Contribute to specification assessment of existing and new products.</li>
<li>Provie support in maintaining platform program specification documents. </li>
</ul>
 Knowledge/Experience/Skill:
<ul>
<li>BS or MS in Chemistry, Biochemistry or related disciplines. </li>
<li>Minimum of 2 years of previous experience in a cGMP analytical laboratory environment.</li>
<li>Preferred previous experience with stability studies designed and conducted in accordance with ICH guidelines.</li>
<li>Must be a team player and open to change.</li>
<li>Must have excellent communication and speaking skills. Can prepare presentations and present.</li>
<li>Preferred – experience with HPLC and physico-chemical test methods of oligonucleotides. Alternatively - experience with HPLC and physico-chemical test methods of oligosaccharides or proteins.</li>
</ul>
 Accountabilities:
<ul>
<li>Meet Client goals supporting studies and defining specifications for new molecules in development.</li>
<li>On-time and compliant completion of review and verification of stability data to support clinical supply.</li>
<li>Implementation of stability and release specifications for product registration. </li>
<li>Adhere to Client core values.</li>
</ul>
 Competencies:
<ul>
<li>Ability to write clear technical documents and provide meaningful presentations. </li>
<li>Ability to work independently and in compliance with company policies and regulatory guidelines. </li>
<li>Excellent team skills, organization, and strong interpersonal communication skills (written and verbal)</li>
</ul>
 #sczr2

Senior 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 
Purpose:
The Cell Culture Development organization within Operations leads the process development and tech transfer of cell culture processes for clinical manufacturing and commercialization of therapeutic proteins in the AbbVie pipeline. In addition, we provide subject matter expertise and experimental support for the manufacture of commercial biologics.
A successful candidate would be one of the senior leaders in the Cell Culture Development group and would be responsible for guiding a team of scientists and engineers in the definition and resolution of complex challenges presented by AbbVie’s robust, diverse biologics pipeline. The candidate would be expected to work together with cell culture scientists at AbbVie Bioresearch Center and other AbbVie sites to define and implement strategies for pre-clinical, early and late stage cell culture development and to identify and prioritize scientific and technological opportunities for investment that will result in robust, high-yielding processes.
Responsibilities:
<ul>
<li>Leads a group of 5+ scientists and engineers with BS/MS and PhDs focused on bioprocess modeling, PAT and advanced bioreactor monitoring and control.</li>
<li>Leads cell culture process development for monoclonal antibodies, bi-specifics, ADCs, fusion proteins and other molecular formats for early and late-stage clinical assets.</li>
<li>Leads PPQ enabling cell culture process characterization activities.</li>
<li>Leads/participates in cross-functional CMC teams and reviews relevant sections of regulatory submissions (e.g. IND, BLA, MAA, etc.).</li>
<li>Advances technical expertise within the cell culture development field. Tracks emerging trends and technologies within the field through internal and external sources, assesses their relevance to AbbVie and facilitates their internal adoption by effectively communicating their value to the business. Pro-actively advises and shares knowledge with the team, peers and senior management.</li>
<li>Mentor and enhance staff performance to create a climate of excellence to achieve business and scientific objectives.</li>
<li>Develops, communicates and implements a vision for development of strategic capabilities.</li>
<li>Identifies and drives technical innovations that will contribute to future business developments and improvements.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree in&nbsp;Biology, Biochemistry, Chemical Engineering or related field&nbsp;with 16 years of related work; Master’s Degree Science or PharmD with 14 years of related work; PhD in Science or related field with 8 years of related work experience. Exceptional candidates with less experience will be considered.</li>
<li>Outstanding record of accomplishment in the Biotech and/or Biopharmaceutical field.</li>
<li>Proven ability to innovate with a history of new or improved product releases.</li>
<li>Has demonstrated the ability to lead scientists and engineers through urgent situations by developing actionable goals and robust implementation plans.</li>
<li>Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators.</li>
<li>Must have a results oriented work ethic and a positive, can-do attitude.</li>
<li>Excellent written and oral communication skills are expected.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Demonstrated proficiency in bench scale bioreactor, shake flask, and other culture systems for the optimization of cell culture processes.</li>
<li>Experience with or ability to lead a team with focus on development and application of hybrid, machine learning, mechanistic and other advanced modelling techniques.</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 thetime&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.&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>
</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.&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 II

<h3>Job Description</h3>
Job DescriptionJob Title: Senior Associate Scientist Location: Cambridge, MA Duration: 12 Months Job Description: The Senior Associate Scientist, Specifications will be responsible for specification support of siRNA drug substances and drug products. This is an onsite position. Summary of Key Responsibilities: • Initiate and manage specification change controls in a GMP setting. • Expected contributions to general operations including review of data and authorship/review of technical documentation. Provide technical support as needed. • Author and review SOPs and protocols in accordance with company and regulatory guidelines. • Contribute to data review, analytical and stability sections of regulatory submissions. Assist with responses to agency requests on these sections. • Contribute to specification assessment of existing and new products. • Provie support in maintaining platform program specification documents Accountabilities • Meet Alnylam goals supporting studies and defining specifications for new molecules in development. • On-time and compliant completion of review and verification of stability data to support clinical supply. • Implementation of stability and release specifications for product registration. • Adhere to Alnylam core values. Hiring Requirements Knowledge/Experience/Skill: • BS or MS in Chemistry, Biochemistry or related disciplines. • Minimum of 2 years of previous experience in a cGMP analytical laboratory environment. • Preferred previous experience with stability studies designed and conducted in accordance with ICH guidelines. • Must be a team player and open to change. • Must have excellent communication and speaking skills. Can prepare presentations and present. • Preferred – experience with HPLC and physico-chemical test methods of oligonucleotides. Alternatively - experience with HPLC and physico-chemical test methods of oligosaccharides or proteins. Scope The Senior Associate Scientist Specifications will be responsible for specification support of developmental and clinical siRNA drug substances and drug products. Physical/Environmental Factors (Complete if appropriate for role) • Must be able to adhere to all laboratory safety requirements • Must be able to travel between Alnylam sites Competencies • Ability to write clear technical documents and provide meaningful presentations. • Ability to work independently and in compliance with company policies and regulatory guidelines. • Excellent team skills, organization, and strong interpersonal communication skills (written and verbal) #ZRCompany DescriptionFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website <a href="http://www.talentburst.com" target="_blank">www.talentburst.com</a> or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX &amp; downtown San Francisco, CA 
<h3>Company Description</h3>
Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website <a href="http://www.talentburst.com" target="_blank">www.talentburst.com</a> or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX &amp; downtown San Francisco, CA

Clinical/Development - Senior Associate Scientist

<h3>Job Description</h3>
Job Description
Grow with Welch's! 
Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary!
At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you.

Grow with Welch's! 
Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary! 
At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you.
Position Summary: 
Welch's is modernizing its R&amp;D digital ecosystem through the implementation of a new ERP and an upgraded Product Lifecycle Management (PLM) system. As a Senior Scientist Product Systems on the R&amp;D team, you will play a pivotal role in designing, building, and validating PLM functionality, ensuring that product data, formulation workflows, and specification structures are accurate, scalable, and aligned with business needs.
During the implementation phase, you will serve as a technical lead representing R&amp;D in enterprise design discussions, system configuration, and cross-functional testing. Once the new PLM system is successfully deployed and stable, your role will expand to include creation and stewardship of product, ingredient, formula, and analytical specifications within the PLM system.
This role is ideal for a highly technical, detail-oriented scientist who excels in digital tools, structured data, formulation workflows, and cross-functional problem-solving.
Where You'll Work: 
This role will be based out of our Waltham, MA headquarters where you will be immersed in a dynamic workplace where innovation thrives and collaboration is key. 
Our company in-office schedule is designed to maximize collaboration &amp; relationship building balanced with flexibility and well-being with 3 days in office and Thursdays/Friday being remote, flex days.
What You'll Do:
<ul>
<li>Serve as a core R&amp;D technical lead in the implementation of Welch's new PLM and ERP systems.</li>
<li>Translate R&amp;D formulation workflows, product data needs, and technical requirements into system logic and configuration.</li>
<li>Lead R&amp;D's execution of system testing, including writing test scripts, validating data structures, and troubleshooting issues.</li>
<li>Partner with IT, Supply Chain, Quality, and external vendors to design and refine digital workflows that reflect R&amp;D processes accurately and efficiently.</li>
<li>Support customization and build activities to ensure PLM functionality meets R&amp;D's operational needs.</li>
<li>Identify and drive improvements in data governance, workflow efficiency, and system usability across the R&amp;D organization.</li>
<li>Develop training materials, processes, and user guidance to support system adoption within R&amp;D.</li>
<li>After ERP/PLM stabilization, become a primary author and steward of product, formula, ingredient, and analytical method specifications in the new PLM system.</li>
<li>Create and maintain high-quality, audit-ready specifications with strong attention to metadata, version control, and technical accuracy.</li>
<li>Collaborate with Product Development, Quality, Supply Chain, and Operations to gather accurate inputs and finalize specifications.</li>
<li>Continuously optimize templates, workflows, and data structures within PLM to improve long-term system performance and data integrity.</li>
</ul>
 Who You Are: 
<ul>
<li>A technically strong scientist with experience in formulation, analytical methods, product development, or structured product data.</li>
<li>A systems thinker who enjoys understanding how digital workflows, product data, and technical processes fit together.</li>
<li>Exceptionally organized and detail-oriented, with a natural ability to create accurate technical documentation and manage structured data.</li>
<li>Skilled at breaking down complex R&amp;D processes and translating them into clear system requirements and digital workflows.</li>
<li>A collaborative partner who communicates clearly and effectively across IT, Quality, Supply Chain, Operations, and R&amp;D.</li>
<li>Comfortable working in an environment undergoing major digital transformation—able to bring structure, clarity, and problem-solving when processes are evolving.</li>
<li>A proactive troubleshooter who can identify root causes, propose solutions, and improve how systems and data function.</li>
<li>Someone who enjoys supporting others, creating training materials, and helping teams adopt new tools and workflows.</li>
<li>Motivated to take on future responsibility for specification authoring once the new PLM system is stable</li>
</ul>
What You'll Need: 
<ul>
<li>Bachelor's degree in Food Science, Chemistry, Engineering, Information Systems, or related fields.</li>
<li>5+ years of experience in PLM, ERP, product data systems, digital transformation, or R&amp;D systems roles within food, beverage, consumer goods, or related manufacturing sectors.</li>
<li>Hands-on experience leading system implementations or upgrades.</li>
<li>Strong technical documentation skills and comfort working in structured, data-driven environments.</li>
<li>Ability to work cross-functionally (IT, FSQ, Supply Chain, Operations), influence without authority, and drive alignment across technical teams.</li>
<li>Strong critical thinking and troubleshooting skills, with the ability to diagnose workflow or system issues quickly.</li>
<li>Experience training others, developing user documentation, or supporting digital tools is beneficial.</li>
<li>Proficient in Microsoft Office</li>
</ul>
What You'll Enjoy: 
<ul>
<li>Organization with a bold, clear purpose &amp; vision for the future</li>
<li>Inclusive Culture: Be a part of an inclusive workplace where you not only belong but also have the opportunity to be the best version of yourself</li>
<li>Passionate Community: You are encouraged to have a voice, share your opinions, and have individual impact on the success of the business</li>
<li>Hybrid work model: Flexible &amp; collaborative work environment to maximize well-being &amp; success</li>
<li>Paid Time Off and Holidays: Available immediately for you to enjoy time away from the office to rest and recharge</li>
<li>Paid Volunteer Time Off: Enjoy time away from the office to rest and recharge</li>
<li>Development &amp; Advancement: Access to LinkedIn Learning as well as both formal and informal opportunities to develop and grow your career</li>
<li>Compensation Package Consisting of Competitive Base Salary and Annual Incentive Plan (Bonus)</li>
<li>401K plan with Generous Company Match</li>
<li>Flexible Benefits from your first day: Choose the benefits that meet your needs and preferences:</li>
<li>Health, Dental &amp; Vision Insurance</li>
<li>Health Savings Accounts </li>
<li>Life and accident insurance </li>
<li>Employee Assistance Programs </li>
<li>Tuition reimbursement program</li>
<li>Additional benefits available through Perks at Work</li>
<li>Paid parental (and adoption) leave – Available after 12 months of employment</li>
</ul>
The anticipated hiring base salary range for this position is $110,000 to $120,000 annually for US-based employees. This range reflects the minimum and maximum for the position across all US locations, is based on a full-time work schedule, and is Welch's good faith estimate as of the date of this posting. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. In addition to base salary, this role is eligible for participation in a bonus plan.
#LI-Hybrid


Welch's is an Equal Employment Opportunity Employer. We are committed to the prevention of employment discrimination based on race, religion, color, sex, gender identity, national origin, age, marital status, disability and/or military or veteran status, sexual orientation or any other action covered by federal or applicable state/local laws.
Welch's offers more than just a job - it's an opportunity to grow, innovate, and make a global impact with a passionate community.

Senior Scientist Product Systems

<h3>Job Description</h3>
Job DescriptionPsiThera&nbsp;is&nbsp;seeking&nbsp;a talented and creative medicinal chemist with a strong&nbsp;track record&nbsp;of advancing small molecule projects from&nbsp;initial&nbsp;hits through to development candidate&nbsp;selection&nbsp;to join our dynamic, multidisciplinary team.&nbsp;Our science&nbsp;and&nbsp;our&nbsp;team&nbsp;are focused on&nbsp;combining medicinal chemistry with our&nbsp;cutting-edge&nbsp;computational platform to rapidly&nbsp;identify&nbsp;and&nbsp;optimize&nbsp;molecules into&nbsp;innovative medicines for patients.&nbsp; We are looking for a self-motivated individual who thrives in a fast-paced, highly collaborative environment that integrates&nbsp;computational and&nbsp;experimental data&nbsp;to drive our programs to the clinic. The ideal candidate will&nbsp;have direct&nbsp;experience&nbsp;integrating&nbsp;a&nbsp;deep knowledge of&nbsp;synthetic and&nbsp;medicinal chemistry&nbsp;with&nbsp;in&nbsp;silico&nbsp;drug discovery methods&nbsp;to perform&nbsp;multiparameter&nbsp;optimization, including ADME/PK&nbsp;considerations, and rapidly advance programs from hit&nbsp;identification&nbsp;to lead&nbsp;selection&nbsp;to development candidate&nbsp;nomination.&nbsp;A&nbsp;successful candidate will have&nbsp;strong synthetic&nbsp;chemistry skills,&nbsp;expertise&nbsp;in creative and practical small molecule design,&nbsp;experience guiding teams of CRO chemists&nbsp;and excellent communication skills to present strategies and results to the broader team.&nbsp;This individual will report to the Director of&nbsp;Medicinal Chemistry&nbsp;and collaborate closely across functions including&nbsp;computational chemistry, biophysics, structural biology, and&nbsp;biology&nbsp;teams to provide actionable insights and strategic guidance.&nbsp;Key Responsibilities
<ul>
<li>Advance small molecule programs&nbsp;from hit&nbsp;selection&nbsp;to&nbsp;development candidate&nbsp;selection&nbsp;</li>
<li>In collaboration with CADD, biophysics,&nbsp;structural&nbsp;biology&nbsp;and biology&nbsp;design&nbsp;small molecules&nbsp;to achieve program goals and meet timelines&nbsp;</li>
<li>Plan, prioritize and implement synthetic and medicinal chemistry&nbsp;&nbsp;</li>
<li>Manage teams of external synthetic chemists to ensure&nbsp;timely&nbsp;delivery of complex target molecules for biological testing&nbsp;</li>
<li>Review analytical data to&nbsp;ensure&nbsp;identity and&nbsp;quality of samples&nbsp;</li>
<li>Stay current&nbsp;with&nbsp;chemistry, medicinal&nbsp;chemistry&nbsp;and&nbsp;project-relevant&nbsp;literature&nbsp;as well as&nbsp;with&nbsp;new&nbsp;patent&nbsp;application filings.&nbsp;</li>
</ul>
Requirements
<ul>
<li>Minimum&nbsp;qualifications:&nbsp;3-5&nbsp;years&nbsp;experience&nbsp;driving small molecule&nbsp;discovery&nbsp;programs&nbsp;from&nbsp;hit to lead&nbsp;through lead optimization&nbsp;as&nbsp;demonstrated&nbsp;by peer reviewed publications and/or&nbsp;inventorship status on patent applications&nbsp;</li>
<li>Preferred qualifications: 5-10&nbsp;years&nbsp;experience&nbsp;with&nbsp;experience driving small molecule discovery programs from hit to&nbsp;lead through&nbsp;development candidate&nbsp;selection. Experience with project leadership is a plus</li>
<li>BS, MS or PhD in organic chemistry, medicinal&nbsp;chemistry&nbsp;or a closely related field&nbsp;</li>
<li>Proven&nbsp;track record&nbsp;of creative solutions to solve&nbsp;medicinal chemistry&nbsp;challenges&nbsp;</li>
<li>Firsthand experience in&nbsp;structure-based and computer-aided drug discovery&nbsp;</li>
<li>Experience with working collaboratively&nbsp;across&nbsp;drug discovery disciplines, including biology,&nbsp;structural biology,&nbsp;computational&nbsp;chemistry&nbsp;and&nbsp;biophysics&nbsp;</li>
<li>Experience leading&nbsp;and&nbsp;managing&nbsp;teams of external chemists&nbsp;&nbsp;</li>
<li>Excellent communication and collaboration skills, with the ability to work well in a multidisciplinary environment&nbsp;</li>
<li>Excellent organizational skills and attention to detail, with a strong passion for learning new concepts and technologies&nbsp;</li>
</ul>
Additional Qualifications
<ul>
<li>Experience as a project team lead&nbsp;</li>
<li>Direct experience with DEL&nbsp;screen follow-up&nbsp;and fragment-based&nbsp;drug discovery&nbsp;</li>
<li>Experience&nbsp;with&nbsp;progressing programs&nbsp;through lead&nbsp;optimization&nbsp;for immunology targets&nbsp;</li>
<li>Familiarity&nbsp;with molecular modeling tools&nbsp;</li>
<li>Proficiency&nbsp;with data analysis tools (Spotfire, KNIME)&nbsp;</li>
</ul>
PsiThera offers a competitive base salary plus discretionary annual bonus and company ownership through stock options. We also support employees with subsidized medical/dental/vision insurance, 20 days vacation, and a 401k match. Salary for this opportunity will be commensurate with experience.About&nbsp;PsiThera&nbsp;PsiThera&nbsp;is creating better therapeutics through an integrated molecular design paradigm that&nbsp;leverages&nbsp;best-in-class physics-based and AI technologies honed through decades of research and innovation.  Our focus is first-in-class inflammation and immunology (I&amp;I)&nbsp;small&nbsp;molecule therapeutics. We have assembled a diverse team with extensive experience across disciplines ranging from physics and computer science to chemistry, biology, biochemistry, and structural biology.  This continuum of complementary skills drives our scientific vision to deliver meaningful therapeutics to patients in need.  We are patient-inspired, perseverant, synergistic, supportive, intrepid, and inclusive. If&nbsp;you’re&nbsp;passionate about advancing medicine in a fast-paced, innovative environment, and eager to contribute to a team that blends advanced computation with drug discovery,&nbsp;PsiThera&nbsp;might be the perfect fit for you.&nbsp;At&nbsp;PsiThera, we are a lean, high-performing team dedicated to pushing boundaries and achieving growth—both personally and scientifically.  We seek individuals who are smart, collaborative, and thrive in a dynamic, early-stage biotech environment.&nbsp; Read More About Us&nbsp;·       Our Story:             <a href="https://psithera.com/company/&amp;nbsp" target="_blank">https://psithera.com/company/&amp;nbsp</a>;·      &nbsp;Platform: <a href="https://psithera.com/quaisar-platform/&amp;nbsp" target="_blank">https://psithera.com/quaisar-platform/&amp;nbsp</a>;·       Team:                  &nbsp;&nbsp;&nbsp;<a href="https://psithera.com/company/team-and-leadership/&nbsp;&nbsp;Psivant" target="_blank">https://psithera.com/company/team-and-leadership/&nbsp;&nbsp;Psivant</a> Therapeutics,&nbsp;Inc. (d/b/a&nbsp;PsiThera)&nbsp;is proud to be an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. We&nbsp;comply with&nbsp;all applicable laws and regulations, ensuring that all qualified applicants receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, genetic information, or any other legally protected status.&nbsp;&nbsp;Please note that we do not accept unsolicited resumes and kindly request that recruiters do not contact our team&nbsp;regarding&nbsp;this job posting. If a resume is&nbsp;submitted&nbsp;without a prior agreement, we will not be&nbsp;obligated&nbsp;to pay any referral or placement fees. Thank you for&nbsp;your understanding!&nbsp;
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior/Principal Scientist, Medicinal Chemistry

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development.&nbsp;
We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects.&nbsp;
Job Responsibilities and Requirements:&nbsp;
<ul>
<li>Experience with protein chemistry, protein analytics, and bioprocess technology is required&nbsp;</li>
<li>Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process&nbsp;</li>
<li>Hands on experience and working knowledge on techniques including but not limited to&nbsp; liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet&nbsp;</li>
<li>Hands on experience with SDS-PAGE, ELISA, and&nbsp;experience with protein purification/chromatography at the lab scale is a plus&nbsp;</li>
<li>A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred&nbsp;</li>
<li>Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data&nbsp;</li>
<li>Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices&nbsp;</li>
<li>Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline&nbsp;</li>
<li>BS 2-4&nbsp;years or MS +0-2 years of relevant experience&nbsp;</li>
<li>Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet&nbsp;</li>
</ul>
<ul>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>The position&nbsp;is full-time, on-site, Monday through Friday, 8:00 AM-5:00 PM.&nbsp;</li>
<li>Pay range: $27.00 - $31.00 based on degree level and years of relevant experience&nbsp;</li>
<li>Excellent full-time benefits including:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
</li>
</ul>
Ready to take the next step in your career? Apply today and join a team that’s making a difference in science every day.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioprocess Analytical Chemist (Purification Process Support)

<h3>Job Description</h3>
Job DescriptionAbout Phoenix TailingsPhoenix Tailings is a rapidly growing clean mining and metals production startup dedicated to sustainable and economic critical metals production. Our mission is to be the world's first fully clean mining and metals production company, producing the resources needed for the next generation of our economy.&nbsp; Why Phoenix Tailings&nbsp;At Phoenix, we believe that nothing great is ever accomplished alone or without the passion of people who push and motivate one another. If you are someone who shares our relentless pursuit of a better future, passion for innovation, and are excited about working with some of the top innovators in the world, then this is the place for you.&nbsp; Our Values&nbsp;● You are only crazy if you are wrong, it’s ok to be wrong● Lead with Compassion● Be Resourceful● Listen● Hustle Who We Are Looking For&nbsp;Phoenix Tailings is seeking a highly experienced Head Geologist with deep expertise in tailings and secondary resource geology. You will combine advanced technical skills with strategic insight to identify high-value opportunities, guiding drilling, sampling, and test work to assess the composition, recoverability, and commercial potential of rare earths and other critical minerals. This role is a unique opportunity to redefine the future of critical mineral sourcing by transforming mine waste into the feedstock of tomorrow’s technologies.&nbsp; This pay range reflects the expected compensation for this role and may vary based on experience and qualifications. Salary Range: $120,000/year- $180,000/yearKey Responsibilities:
<ul>
<li>Lead global efforts to identify and prioritize tailings sites rich in critical minerals, including rare earths minerals and other high-value elements.&nbsp;</li>
<li>Conduct geological, mineralogical, and geochemical evaluations to determine resource quality, quantity, and extraction potential.&nbsp;</li>
<li>Design and oversee drilling, sampling, and laboratory analysis programs specific to tailings deposits.&nbsp;</li>
<li>Develop and maintain a database of prospective tailings sites, ranking them by strategic and technical importance.&nbsp;</li>
<li>Collaborate with the VP of Exploration and business development teams to support acquisition and partnership negotiations.&nbsp;</li>
<li>Engage with mine operators, government agencies, and research institutions to access and evaluate tailings data.&nbsp;</li>
<li>Prepare technical reports and presentations to inform internal decision-making and support external stakeholders.&nbsp;</li>
<li>Ensure all exploration activities meet the highest environmental, safety, and ethical standards.&nbsp;</li>
</ul>
Qualifications:
<ul>
<li>Advanced degree in Geology, Geochemistry, or a related field.&nbsp;</li>
<li>Proven track record in mineral exploration, resource estimation, and project evaluation.&nbsp;</li>
<li>Expertise in tailings, secondary resources, or unconventional mineral deposits, with emphasis on rare earths and critical minerals.&nbsp;</li>
<li>Strong knowledge of critical minerals markets, processing pathways, and extraction challenges.&nbsp;</li>
<li>Experience leading field teams and managing multi-disciplinary technical projects.&nbsp;</li>
<li>Proficiency with geological modeling, geochemical analysis, and GIS tools.&nbsp;</li>
<li>Ability to collaborate effectively across commercial, technical, and executive teams.&nbsp;</li>
</ul>
 We offer a competitive compensation package that is based on expertise. We also offer the following benefits:
<ul>
<li>Healthcare, we care about you and your family:&nbsp;100% Medical, dental, and vision coverage&nbsp;</li>
<li>Stock:&nbsp;Ownership in a fast-growing venture-backed company.&nbsp;</li>
<li>Family Focus:&nbsp;Parental leave and flexibility for families.&nbsp;</li>
<li>Time Off:&nbsp;Flexible vacation policy to encourage people to get out and see the world.&nbsp;</li>
<li>Team Fun:&nbsp;Regularly scheduled events, and celebrations.&nbsp;</li>
<li>Learning:&nbsp;Learning and development Opportunities to grow your skills and career.&nbsp;</li>
<li>Great team:&nbsp;Working with fun, hard-working, kind people committed to making a difference!&nbsp;</li>
<li>Flexible culture:&nbsp;We are results-focused. We don’t work at the office every day.&nbsp;</li>
</ul>
At Phoenix Tailings, we have an open culture that values learning, and we are looking to grow the team with enthusiastic individuals who share our vision of sustainable mining.&nbsp;&nbsp;&nbsp;Phoenix Tailings, Inc. is an Equal Opportunity Employer, and we value diversity at all levels. All qualified candidates will receive consideration for employment without regard to race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age, disability or genetic information, or any other applicable protected characteristics, and these characteristics will not be a factor for consideration of any work-related decisions (including but not limited to hiring, firing, compensation, and discipline).&nbsp;
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

1.1. Head Geologist

<h3>Job Description</h3>
Job Description
Senior Scientist III (iPSC-Derived Gut Models) Cambridge, MA (Lab Based Position) Pay Rate: $70 -77/hr W2
This 24+ Month Contract Position Has A Tentative Start Date of 2/2/26 Role Overview: We are seeking a hands-on Scientist with strong experimental biology expertise to advance iPSC-derived gut models for evaluating combination therapies for inflammatory diseases (e.g., IBD). Working closely with DAGS, Immunology, and Pharmacology colleagues, the contractor will culture and differentiate human iPSCs into intestinal lineages (e.g., epithelial monolayers and 3D organoids/enteroids), establish microphysiological systems, and design and execute combination therapy studies. The successful candidate will optimize functional assays, perform dose–response and matrixed combination experiments, analyze synergy/antagonism, and deliver clear, actionable data packages to cross-functional teams. Required Qualifications: • MS with 5+ years or PhD with 1–2+ years of relevant experience in molecular/cellular biology, immunology, pharmacology, or related field • Hands-on experience with human cell culture and at least one of: o iPSC maintenance and differentiation into epithelial/endodermal lineages o Intestinal organoids (enteroids) or epithelial monolayers • Proven ability to execute and troubleshoot functional assays; experience running dose–response studies and quantitative assay analysis • Strong documentation, data analysis, and presentation skills; success working in collaborative, cross-functional settings • Following aseptic processes Preferred Qualifications • Direct experience with iPSC-derived intestinal models, including 3D organoids, 2D monolayers, Transwells, and/or gut-on-chip systems • Expertise in barrier function assays (TEER, permeability), imaging-based analyses, and cytokine profiling • Experience with automation, liquid handling, and high-throughput assay development • Background in inflammatory disease biology and prior industry experience in preclinical combination testing or pharmacology Job Description: The Merck Genome Sciences (GS) iPSC disease modeling group within the Department of Data, AI, and Genome Sciences (DAGS) partners with Immunology and cross-functional teams to evaluate therapeutic strategies based on human-relevant models. Our mission is to build and apply robust iPSC-derived systems to understand mechanisms in human disease and to test mono- and combination therapies under controlled, scalable in vitro conditions. We leverage genetic and pharmacological perturbations in iPSC-derived gut models to inform therapeutic combination design and prioritization. The contractor is expected to work both independently and collaboratively in a dynamic early discovery environment. • Develop, optimize, and execute iPSC-derived gut model systems: o Differentiation of iPSCs into 3D intestinal organoids. o Co-cultures with immune cells (e.g., macrophages, dendritic cells, T cells), and 3D organoid model system. o Microphysiological platforms to model barrier and tissue microenvironment • Design and run combination therapy studies: o Plan mono- and pairwise/multi-drug matrices; include biologics, small molecules, and pathway-targeted agents o Execute dose–response and time-course experiments; incorporate inflammatory stimuli (e.g., cytokine cocktails, bacterial products) to model disease-relevant contexts o Analyze combination effects for synergy/additivity/antagonism and generate decision-enabling summaries • Apply quantitative, mechanism-informed readouts: o Barrier integrity and function assays (TEER, permeability, wound healing, mucus layer assays) o Inflammatory and cell-state profiling (cytokine/chemokine panels via ELISA/MSD, qPCR/RT-qPCR, flow cytometry, high-content imaging, immunofluorescence) o Transcriptomic profiling (bulk or single cell preferred) for pathway engagement; collaborate with data scientists for analysis. • Implement perturbations and model qualification: o Genetic and pharmacological perturbations to dissect mechanisms and predict combination responsiveness. o Assess reproducibility, dynamic range, and throughput; adapt assays to plate-based formats (96-/384-well) and support automation readiness. • Collaborate cross-functionally: o Partner with immunology, pharmacology, and data science teams to prioritize combinations, refine hypotheses, and align in vitro models with translational endpoints. o Present experimental plans and results to internal stakeholders, including senior leadership; maintain rigorous documentation and SOPs. • Ensure compliance with safety practices and proper maintenance of cell lines, reagents, and equipment. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.
Company DescriptionOur people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs. We offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. 
<h3>Company Description</h3>
Our people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals.\r\n\r\nJohnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.\r\n\r\nWe offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more.\r\n\r\nJohnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.

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