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<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>
Responsible for generating and processing single-cell, spatial, and functional genomics data, as well as supporting standard immunoprofiling activities such as cell culture and flow cytometry.
</li>
<li>
Follow existing lab standard operating procedures to: Participate in sample collection of murine and human tissues, including the preparation of tubes, interfacing with in vivo scientists to retrieve samples, isolation of primary immune cells, and standard mammalian cell culture
</li>
<li>
Participate in sample preparation of murine and human tissues, including tissue fixation, dissociation, sectioning, and antibody staining
</li>
<li>
Generate spatial and single-cell data via a number of commercial workflows, including 10x Genomics and Parse Technologies
</li>
<li>
Interpret quality control metrics for spatial, single-cell and cytometry experiments
</li>
<li>
Typical bench work, including sitting, pipetting, lifting &lt;10lb items
</li>
<li>
Reports to a scientific director of the Systems Immunology Lab
</li>
<li>
Collaborates with and supports several multi-disciplinary experimental teams on a per-project basis
</li>
</ul>
REQUIREMENTS
<ul>
<li>
Masters + 3 years of experience in Biology, Immunology, or a related field; OR
</li>
<li>
PhD +0 yrs experience in Biology, Immunology, or a related field
</li>
<li>
3+ years of hands-on experience with standard immunoprofiling technologies, including:
<ul>
<li>
Flow Cytometry
</li>
<li>
Single-cell library preparation (ideally 10x Genomics or Parse Technology)
</li>
<li>
Preparation and loading of Illumina sequencing libraries
</li>
<li>
Bonus: generation of spatial transcriptomics data (any technology)
</li>
</ul>
</li>
<li>
3+ years of experience with primary immune cells, including:
<ul>
<li>
Primary immune cell isolation
</li>
<li>
Maintenace of immune cell lines
</li>
<li>
Cell culture and in vitro stimulation of primary immune cells
</li>
<li>
Bonus: experience with CRISPR mediated functional genomics, including electroporation of primary immune cells
</li>
</ul>
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist Cellular Genomics

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Manufacturing Sciences and Technology (MSAT) Upstream Group is looking for a highly motivated and versatile candidate to join our multidisciplinary team of scientists and engineers in Andover, MA.
</li>
<li>
MSAT supports portfolio of late-stage development of commercial biopharmaceuticals and vaccines, and is responsible for process troubleshooting, process improvements and second- generation process development.
</li>
<li>
We are looking for someone who is eager to contribute independent thinking and technical excellence to the upstream fermentation team.
</li>
<li>
The Scientist will be a part of a diverse and motivated team of scientists, engineers, and technical professionals that are focused on fermentation processes to produce biotherapeutics.
</li>
<li>
The role is well-integrated into the rest of the MSAT Microbial Team.
</li>
<li>
This role will collaborate with other MSAT scientists to setup bioreactors and execute well-designed experiments, including but not limited to basic analytics, data acquisition and documentation of work.
</li>
<li>
The candidate would also be responsible for user-level maintenance of the relevant equipment and associated documentation.
</li>
<li>
Plan and execute upstream process experiments at benchtop scales
</li>
<li>
Participates and significantly contributes to discussions in lab and project team meetings on design of experiments (bioreactor and shake flask) and interpretation of experimental data.
</li>
<li>
Acts as a technical resource within the upstream group. Provides formal/informal mentoring to junior colleagues within work group/project team.
</li>
<li>
Works under limited supervision with periodic review of achievement of results and experimental approaches employed.
</li>
<li>
Manages own time to meet agreed targets. Develops plans for short-term work activities on own projects.
</li>
<li>
Ensures effective, high-quality, timely and appropriate documentation in electronic laboratory notebooks and internal technical reports; presents data/ strategy to scientists and management in appropriate internal and external venues (technical meetings, project team meetings, conferences) as appropriate.
</li>
<li>
Contributes to safe, efficient, effective and harmonious lab environment, ensures appropriate cleanliness and status/ operability of shared or assigned lab space or equipment; strong lab citizen and collaborative team player; approaches the job with energy and commitment; frequently demonstrates initiative.
</li>
<li>
Participate in multi-disciplinary teams to resolve complex issues
</li>
<li>
Assist in manufacturing investigations and process troubleshooting
</li>
<li>
Assist on process improvement projects
</li>
</ul>
Qualifications
<ul>
<li>
Ph. D. with 0-4 years of experience in biotechnology ;OR
</li>
<li>
Master's degree in a relevant discipline with at 3-5 years of applicable bioprocess experience ;OR
</li>
<li>
Bachelor's degree with at least 7 years of experience
</li>
<li>
Proficient in aseptic technique (required)
</li>
<li>
Proficient in benchtop bioreactor operation and associated analytical tools (required)
</li>
<li>
Experience with bench scale cell culture and/or bacterial fermentation (required)
</li>
<li>
An in-depth knowledge of bioreactor operations fed-batch, perfusion, and continuous modes of cell culture
</li>
<li>
Strong trouble-shooting skills and extreme attention to detail required
</li>
<li>
Ability to troubleshoot technical issues, plan and carry out experiments independently, and work with complex instrumentation and software.
</li>
<li>
Excellent oral and written communication skills.
</li>
<li>
Strong analytical and computer skills.
</li>
<li>
Involves typical bioprocessing lab activities
</li>
<li>
Ability to routinely lift 50 lbs.
</li>
<li>
Standing for prolonged periods of time, walking, bending, and using tools.
</li>
<li>
Ability to perform mathematical calculations and ability to perform complex data analysis.
</li>
</ul>
Preferred:
<ul>
<li>
Prior experience developing and maintaining scale down models of commercial biopharmaceutical processes
</li>
<li>
Prior experience in developing commercially relevant cell culture processes to produce pharmacologically active proteins
</li>
<li>
Experience with control and data acquisition systems
</li>
<li>
Demonstrated experience developing or introducing new technology into commercial processes
</li>
<li>
Knowledge of all aspects of cell culture/fermentation, including batch, fed-batch, perfusion and harvest/clarification operations
</li>
<li>
Familiarity with DoE and other statistical tools
</li>
<li>
Experience with processing and interpreting large data sets
</li>
<li>
Familiarity with regulatory filings, cGMP requirements and operational constraints
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Senior Scientist, Upstream Process Development (MSAT)

<h3>Job Description</h3>
Central Processing Supervisor, Core Laboratory - Evening Shift
Location: Boston Teaching Hospital
 
<ul>
<li>Evening Shift: 3p – 11:30p ($3/hr evening diff in addition to base salary).</li>
<li>Must be ASCP certified (or equivalent).</li>
</ul>
 
Responsibilities:
<ul>
<li>Responsible for coordinating the daily operation of the front office of the core laboratory.</li>
<li>Oversees all Pre and Post analytic activity on the evening shift, in close conjunction with the day shift MT Operations Coordinator, reference lab staff, and other individuals who oversee areas that have an overlapping operating relationship with Central Processing.</li>
<li>Ensures that all activities, processes and policies are carried out in strict compliance with governmental regulations, licensing agency standards, and hospital policies and procedures.</li>
<li>Responsible for day-to-day general management including staffing, schedules, payroll, performance management, training, education, development of policy and protocol, compliance, and safety.</li>
<li>FTE's: 25+/-.</li>
<li>Reports to the Technical Director of Pre/Post Analytics in the Core Laboratory.</li>
</ul>
 
Qualifications:
<ul>
<li>MT (ASCP) or equivalent.</li>
<li>Bachelor’s Degree in Medical Technology or physical sciences.</li>
<li>4+ years of hospital laboratory experience, including knowledge of &amp;/or experience with pre/post analytics &amp;/or central processing.</li>
<li>1+ years of leadership experience.</li>
<li>Preferred: experience overseeing non-exempt hourly staff.</li>
</ul>

Central Processing Supervisor, Core Laboratory

<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 
<ul>
<li>Clean room Environmental Monitoring sampling</li>
<li>Water sampling&nbsp;&nbsp;</li>
<li>Clean steam sampling</li>
<li>Compressed gas sampling</li>
<li>Bioburden testing&nbsp;&nbsp;</li>
<li>General lab duties (cleaning, stocking, cold room 5S, etc.)</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Knowledge of cGMP&nbsp;</li>
<li>Experience working in a laboratory setting&nbsp;</li>
<li>Experience with Environmental Monitoring and Water Sampling&nbsp;</li>
<li>Knowledge of LIMS&nbsp;</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>High school Diploma with 2-5 years of experience OR</li>
<li>Associates Degree with 1-3 years of experience OR</li>
<li>Bachelor's Degree with 0-1 years of experience&nbsp;</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship&nbsp;</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute On-Site Visit&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday - Friday. The hours are 8 am-5 pm.&nbsp;Candidates living within a commutable distance of Andover, MA, and the surrounding areas are encouraged to apply.&nbsp;
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>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

QC Microbiologist Scientist

<h3>Job Description</h3>
Job Title: Biotechnologist Associate 
Location: Portsmouth, NH, 03801 
Duration: 12 Months
Job Type: Contract 
Work Type: Onsite 
Shift: 12 Hour Shift - Night Shift from 07:00 PM to 07:00 AM - Rotating Shift
Job Description:
<ul>
<li>The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. </li>
<li>They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. </li>
<li>Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. </li>
<li>Attain qualification for all assigned tasks and maintain individual training plan. </li>
<li>Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. </li>
<li>Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. </li>
<li>Must be willing to gown and work in a "clean room" environment. </li>
<li>Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects. </li>
<li>Perform other duties as assigned. </li>
<li>High School Diploma or equivalent experience minimum with an AS/BS preferred </li>
<li>Preferred area of study: Science related field, degrees in Genetics are relevant. </li>
<li>Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred. </li>
<li>Prior experience with Aseptic Techniques and gowning procedures is preferred. </li>
<li>Working experience in manufacturing; cGMP setting preferred. The ideal candidate will have experience within the Cell and Gene Therapy field. </li>
<li>Able to follow documentation procedures for day-to-day tasks in a regulated industry </li>
<li>Proven logic and decision-making abilities, critical thinking skills. </li>
<li>Strong written and verbal communication skills.</li>
</ul>

Research Assistant

<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 
We are looking for a highly motivated scientist to join our Rheumatology team at our Cambridge, MA office. The ideal candidate should be driven, experienced, collaborative, adaptable, and productive. They will support in vitro research efforts for our existing early-stage through late-stage discovery portfolio programs. Responsibilities include conducting, analyzing, and reporting on in vitro assays to explore key biological questions related to rheumatic diseases, such as RA, Systemic Sclerosis and Psoriatic Arthritis. The candidate should apply fundamental scientific principles to research and be skilled in laboratory techniques such as pipetting, cell culture, molecular biology and ELISA. In addition, a candidate with experience in fibroblast cultures and functional assays (proliferation, migration and invasion) is preferred.
Responsibilities
<ul>
<li>Scientific Research: Design and execute precise in vitro experiments to advance understanding of rheumatic disease biology.</li>
<li>Lab Techniques: Skillfully use methods like pipetting, cell culture, molecular biology, ELISA, fibroblasts functional assays (proliferation, migration, invasion) and flow cytometry to collect quality data.</li>
<li>Cell culture: Maintenance and expansion of primary cells. Experience in fibroblasts and macrophage differentiation protocols would be preferred.</li>
<li>Data Analysis: Analyze and interpret results accurately, creating reports and presentations to share with teams.</li>
<li>Protocol Development: Follow and adapt experimental protocols while implementing new methods as needed.</li>
<li>Lab Management: Maintain equipment and manage supplies to ensure efficient lab operations.</li>
<li>Literature Review: Review literature for insights that aid experimental design and contribute ideas.</li>
<li>Collaboration: Work with cross-disciplinary teams, offering scientific expertise to drive project progress.</li>
<li>Documentation: Accurately maintain and update lab notebook and lab inventories of cell stocks, reagents etc.</li>
</ul>
Qualifications 
<ul>
<li>Education/ Years of Experience: Bachelor’s or master’s degree in biology or a closely related discipline with typically 0-2+ years’ (MS) or 3-5+ (BS) years’ experience.</li>
<li>Professional Experience: Demonstrated proficiency in cell culture techniques with a strong grasp of molecular biology, including practical expertise in fibroblasts culture. Fibroblasts related functional assays and ELISA are strongly preferred.</li>
<li>Communication Abilities: Excellent verbal and written communication skills, with the capability to explain complex scientific ideas clearly and encourage collaborative dialogue.</li>
<li>Interpersonal Capabilities: Proven ability to thrive in a team-oriented setting, displaying strong interpersonal and teamwork skills.</li>
<li>Organizational Skills: Outstanding time management and organizational abilities, adept at handling multiple priorities and tasks effectively.</li>
<li>Learning Aptitude: A proactive and adaptable learner with the ability to independently generate and assess data, while quickly acquiring and applying new skills.</li>
</ul>
Position will be hired based on level of experience - Associate Scientist II or Scientist I&nbsp;
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive 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 determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

Associate Scientist II or Scientist I, Rheumatology

<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.
Process Chemist Scientist Notes-
<ul>
<li>BS with 2-3 years XP -OR- PhD with academic XP, -AND-
<ul>
<li>Small molecule XP</li>
<li>HPLC, GC, NMR, UCMS, crystallization</li>
<li>Large scale up (100+ grams)</li>
</ul>
</li>
</ul>
<ul>
<li>Looking for Process Chemist • Open to degree -PhD, MS, BS • Experience is a scale up lab • Someone from CRO would work well. • Reaction optimization experience ideal. • Large scale up experience -100s grams/kilos scale up would be ideal • Small molecule work • Medicinal Chemist is typically not ideal • Mix of inorganic or organic is fine • HPLC, GC, NMR, UCMS, crystallization • Chemdraw and Microsoft Word/Excel is a must</li>
<li>MUST HAVE experience in organic synthesis &amp; lab experience</li>
<li>Knowledge in setting up reactions</li>
<li>Organic chemistry knowledge</li>
</ul>
 Process Chemist Scientist Job Description Seeking a talented individual to join our process chemistry group in Boston, MA. This role will support drug substance development programs at company performing synthetic organic chemistry in the laboratory at a high level to design and execute syntheses of challenging compounds, troubleshoot a diverse range of chemistry issues and devise corrective solutions, and analyze complex data sets that leads to clear conclusion or recommendations to guide the synthetic decision. In addition, the individual is expected to work both independently and in a matrix team environment.
Key Responsibilities · Designs, executes, and interprets synthetic organic experiments with a high degree of reliability, independence, and attention to detail · Proficient in application and utility of a variety of analytical tools (NMR, HPLC, LCMS, Biotage) to monitor and analyze experiments · Generate effective hypotheses to pursue synthesis goals and set new experimental direction · Multitask to execute multiple experiments in an efficient manner · Makes conceptual contributions to development activities and scientific strategies · Develops novel and creative solutions to overcome synthetic and manufacturing obstacles · Employs new principles and technologies to promote progress in the synthesis · Maintains accurate records of experiments and results in a laboratory notebook and authors reports as assigned · Draft, review and submit required documentation pertaining to the development and preparation of drug substances under cGMP environment · Be familiar with SOPs and GMPs and ensure compliance with all applicable regulations and SOPs · Possess excellent written and verbal communication skills · Perform other duties as assigned
Minimum Education and Experience Requirements: · PhD with 0 – 3 years relevant synthetic chemistry experience or · MS with over 2 – 6 years relevant synthetic chemistry experience or · BS with over 2 – 10 years relevant synthetic chemistry experience
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

Process Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
A subsidiary of Veolia group, Veolia North America (VNA) is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. VNA helps commercial, industrial, healthcare, higher education, and municipality customers throughout North America. Headquartered in Boston, Mass., Veolia North America has more than 10,000 employees working at more than 350 locations across the continent. <a href="http://www.veolianorthamerica.com" target="_blank">www.veolianorthamerica.com</a>
Job Description 
Position Purpose:&nbsp;
Operates and maintains water/wastewater treatment, processing, disposal and testing equipment in water/wastewater treatment facility to purify water to meet permit and operational requirements.
Primary Duties/Responsibilities:&nbsp;
<ul>
<li>Tends automatic and semi-automatic machines and related equipment including pumps, engines, generators, valves, gates, mixers, conveyors, blowers, chemical feed and odor control and used to decontaminate wastewater by settling, aeration and sludge processing.</li>
<li>Monitors control panels and adjusts valves and gates manually or by remote control to regulate flow.</li>
<li>Monitors flow meters, gauges, flow ratios, pressures and related controls through instrument panels, computer terminals and programmable logic control units in assigned area.</li>
<li>Monitors and records operating conditions observations and data in area shift log.</li>
<li>Ensures conformance to process specifications.&nbsp; Troubleshoots and diagnoses operational problems and takes corrective action per procedure.&nbsp; Verifies and reports suspected malfunctions and variances to supervisor. Performs routine and preventative maintenance and maintenance related items as assigned.&nbsp;</li>
<li>Performs field tests (chemical, physical and biological) in order to pace chemical dosages for process and odor control units or alter unit processes.</li>
<li>Samples wastewater, sludge and gases (odor control, digester, etc.) according to schedule.</li>
<li>Prepares chemical solutions and services automatic samplers.</li>
<li>Performs lab tests applicable to permit testing and related reports per procedure.</li>
<li>Performs instrument calibration for portable meters including, but not limited to, dissolved oxygen, pH, H2S, percent oxygen, lower explosive limit.</li>
<li>Monitors process chemical supplies and recommend reorder.</li>
<li>Performs manual labor including filling and emptying of machine bins and cleaning equipment, facilities and grounds as required.</li>
<li>Performs minor maintenance including, but not limited to, routine preventive maintenance, lubrication and minor adjustments.</li>
<li>Operates vehicles for plant operational purposes.</li>
<li>Practices good housekeeping in assigned area and properly disposes of waste according to safety and environmental policies.</li>
</ul>
Work Environment:&nbsp;
<ul>
<li>Spends 100% of time in operations environment.&nbsp;</li>
<li>May need to work outside in inclement weather conditions and drive company vehicle to perform duties.</li>
<li>Possible Work Hazards:May be exposed to possible operations hazards including fumes, toxic and caustic chemicals, heavy machinery, high pressure, hot or cold work environment temperatures, slippery surfaces, water hazards and electrical equipment.</li>
</ul>
Qualifications 
Education/Experience/Background:&nbsp;
<ul>
<li>High School education or GED with the ability to read, write and comprehend English (operational, process, safety and quality instructions).</li>
<li>Associate’s degree in a science or technical area strongly preferred.</li>
<li>Experience in a related position with knowledge of the methods, techniques, and practices of wastewater treatment is preferred but not required.</li>
</ul>
Knowledge/Skills/Abilities:&nbsp;
<ul>
<li>Must have the ability to perform basic math equations.</li>
<li>Must demonstrate proficiency in the care and use of all site specific, facility required PPE (Personal Protection Equipment), including respirators, gas detectors, confined space equipment, etc.)</li>
<li>Must consistently demonstrate the ability to operate all machines and equipment meeting or exceeding processing and quality targets under general supervision.</li>
<li>Must demonstrate ability to efficiently operate all equipment in facility which may include pumps, engines, centrifuge, generators, valves, gates, mixers, conveyors, blowers, dryers, chemical feed, odor control, disinfection equipment, sludge processing filters, belt presses and measuring/control devices, testing equipment, and material handling equipment.</li>
<li>Must have the ability to diagnose process problems regardless of complexity, troubleshoot equipment and take corrective action within policy and procedure limitations.</li>
<li>Must demonstrate a working ability to use computer programs for safety training and process control.</li>
<li>Must demonstrate ability to work in a team environment and willingness to assume additional or new responsibilities readily.</li>
<li>Must be able to work overtime if required by site.</li>
</ul>
Required Certification/Licenses/Training:&nbsp;
<ul>
<li>Requires a Massachusetts Wastewater certification .</li>
<li>Must possess a valid driver’s license and a safe driving record.</li>
<li>Employee Orientation, Departmental Operating Procedures, Safety, OSHA and Quality Training.</li>
<li>HAZWOPER (Hazardous Waste Operations and Emergency Response) Level I and II certification if required by site.</li>
<li>Forklift Certification if required at site.&nbsp;</li>
<li>Works toward higher-level Wastewater Treatment certification.</li>
<li>May perform more advanced functions as part of training and development.</li>
</ul>
Physical Requirements:&nbsp;
<ul>
<li>Amount of time spent – Standing 25%, Walking 75% for as many as five miles per shift.</li>
<li>While performing the duties of this job, the employee is regularly required use hands to finger, handle, or feel; reach with hands and arms; and talk or hear.&nbsp;</li>
<li>The employee is occasionally required to stoop, kneel, or crouch and enter confined spaces.&nbsp;</li>
<li>May be required to use ladders or stairs.</li>
<li>The employee must lift and/or move up to 50 pounds (occasionally 60 pounds).&nbsp;</li>
<li>Specific vision abilities required by this job include close vision, distance vision, color vision, and ability to adjust focus. Requires close visual observation to detect process non-conformance and machine malfunction.</li>
</ul>
 Additional Information 
This is a full-time, permanent Union position.
Additional Benefits:
<ul>
<li>Union members are allowed to participate in the Veolia stock program</li>
<li>Union members are eligible for one time bonuses after obtaining a higher wastewater license:</li>
<li>Upon obtaining a MA Grade 6 license, employee receives a one-time bonus of $1000</li>
<li>Upon obtaining a MA Grade 7 license, employee receives a one-time bonus of $1500</li>
<li>Shift differential for off- shift hours</li>
<li>Operator in training makes $27.75 per hour</li>
<li>Grade 4-5 operator makes $30.84 per hour</li>
<li>Grade 6 operator makes $31.81 per hour</li>
<li>Grade 7 operator makes $33.33 per hour</li>
</ul>
Hours: Initial training for 3-6 months hours will be 7am-3pm (M-F), then second or third shift with weekends or overtime as required.
Benefits: Veolia’s comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, savings accounts, tuition reimbursement, paid volunteering and more. In addition, employees are also entitled to participate in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement.
We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

Operator in Training

<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job Description: We are currently seeking a Chemist II position in Quality Control to join our team. The Chemist II will perform laboratory testing within a fast-paced cGMP environment. Experience with capillary electrophoresis testing is required. Responsibilities:
<ul>
<li>Performs test methods validations for clinical and commercial projects.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Performs a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives.</li>
<li>Authors validation protocols and reports as well as corresponding test methods.</li>
<li>Support laboratory investigations in a timely manner.</li>
<li>Support a variety of testing techniques upon completion of training.</li>
</ul>
Requirements:
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience.</li>
<li>CE-SDS, HPLC or ELISA existing experience and troubleshooting experience.</li>
<li>Empower or Softmax / PLA software experience.</li>
<li>Spectrophotometric concentration determination.</li>
<li>Quality Control testing of phase III and commercial products.</li>
<li>Experience with empower audit trail.</li>
</ul>
Top skills:
<ul>
<li>QC background.</li>
<li>Documentation.</li>
<li>Advance testing/CE-SDS, HPLC or ELISA experience.</li>
<li>Empower or Softmax / PLA software experience is a plus.</li>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience.</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Chemist II

<h3>Job Description</h3>
Job Description
Akkodis is seeking a Senior Scientist, Downstream MSAT for a Contract job with a client in Framingham, MA. The ideal candidate will have experience managing MSAT teams and downstream process development in support of GMP manufacturing, tech transfer, and regulatory filings for late-phase and commercial biologics.
Rate Range: $106/hour to $108/hour; the rate may be negotiable based on experience, education, geographic location, and other factors.
Senior Scientist, Downstream MSAT job responsibilities include:
<ul>
<li>
Lead development and scale-up of robust downstream processes for various biologics (mAbs, bispecifics, fusion proteins, enzymes, etc.)
</li>
<li>
Manage a development team, ensuring successful execution of virus clearance studies, process characterization, and regulatory submissions
</li>
<li>
Oversee technology transfers to internal and external manufacturing sites
</li>
<li>
Conduct DOE studies and support establishment of proven acceptable process ranges
</li>
</ul>
Desired Qualifications:
<ul>
<li>
Ph.D. in Biotechnology or related field with 3–5 years of experience, or M.S. with 5–10 years, or B.S. with 10+ years
</li>
<li>
Strong expertise in chromatography, filtration (TFF/NFF), and downstream GMP biologics production
</li>
<li>
Experience with tech transfer, automated platforms (e.g., GE Healthcare AKTA), and regulatory documentation
</li>
<li>
Proven ability to lead teams, troubleshoot equipment, and support commercial and late-stage development programs
</li>
</ul>
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Shweta.Ojha@akkodisgroup.com
 Pay Details: $106.00 to $108.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.akkodis.com/en/us/candidate-privacy-policy" target="_blank">https://www.akkodis.com/en/us/candidate-privacy-policy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 Company DescriptionGlobal Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level. Diverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set. Commitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish. Continuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career. Inclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard. Our Evolution and Your Role in It Akkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success. Empowering the Future We're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering. Join the Akkodis Community At Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today. 
<h3>Company Description</h3>
Global Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level.\r\n\r\nDiverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set.\r\n\r\nCommitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish.\r\n\r\nContinuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career.\r\n\r\nInclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard.\r\n\r\nOur Evolution and Your Role in It\r\n\r\nAkkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success.\r\n\r\nEmpowering the Future\r\n\r\nWe're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering.\r\n\r\nJoin the Akkodis Community\r\n\r\nAt Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.

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