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<h3>Job Description</h3>
Job Description
Production Technician – Biotechnology
We’re seeking a detail-oriented and safety-conscious Production Technician to join our biotechnology team. In this role, you’ll be responsible for executing defined production procedures in a GMP-regulated environment, supporting manufacturing operations, and maintaining a clean, organized, and safe workspace.
Responsibilities:
<ul>
<li>Perform production tasks according to established schedules and procedures.</li>
<li>Ensure compliance with company policies and cGMP regulations.</li>
<li>Maintain a safe work environment and actively participate in site safety initiatives.</li>
<li>Execute lab start-up and shutdown procedures.</li>
<li>Keep work areas clean and well-stocked with necessary supplies.</li>
<li>Operate and monitor equipment including spectrophotometers, pH meters, and automated systems.</li>
<li>Perform routine tasks such as buffer preparation, pH testing, UV measurements, and fraction collection.</li>
<li>Support synthesis and purification processes, including equipment cleaning, solution prep, and column packing.</li>
</ul>
Qualifications:
<ul>
<li>Biotechnology certificate or college degree preferred.</li>
<li>2–5 years of experience in a GMP-regulated environment.</li>
<li>Hands-on experience with pH testing, aseptic technique, buffer preparation, and chromatography.</li>
<li>Strong attention to detail and ability to follow SOPs and safety protocols.</li>
</ul>
Top Skills:
<ul>
<li>pH testing</li>
<li>Aseptic technique</li>
<li>Buffer preparation</li>
</ul>
Pay and Benefits
The pay range for this position is $30.00 - $31.25/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Milford,MA.
Application Deadline
This position is anticipated to close on Sep 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Manufacturing Chemist

<h3>Job Description</h3>
Job Description
Adecco Staffing is assisting a facility in Devens MA in sourcing for an Clean RoomOperator on 1st shift! Ideal candidates have a direct background in a clean-room environment operating machines!

Shift Hours: 5:00AM -4:00PM, Monday-Thursday Pay Rate: $19/hr Job Responsibilities:
• Assisting with 5S and Safety tasks associated with good manufacturing practices • Manufacturing of Extruded tubing • Manufacture of Liquid Silicone Rubber Moulded (LSR) parts • Collecting and recording relevant process data • Assisting engineering with validation and experimental activities • Identifying opportunities for improvement throughout the manufacturing process and working with team members to recommend and implement solutions • Following Clean room policies- gowning up and wearing a mask that covers nose and mouth. • Maintain the tools used to create products. • Keep a clean and well-maintained workspace. • Comply with company regulations and operating procedures • Maintain a helpful and collaborative culture through communication and a strong work ethic • Carry out any other activities to support the business as required Essential Skills and Experience: • Strong Attention to Detail • Troubleshooting &amp; Repairs • Strong Mechanical Background • Direct Background in a Clean Room Environment
 INTERESTED? If so, please apply directly to this posting!
 Pay Details: $19.00 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://uat.adecco.com/en-us/candidate-privacy" target="_blank">https://uat.adecco.com/en-us/candidate-privacy</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>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Clean Room Operators

<h3>Job Description</h3>
Job Description
Part Time Shift: Every other Saturday and Sunday 7:00am-3:30pm Hourly Pay Range: $25.00-$30.00 (Based on experience)
POSITION SUMMARY 
Performs lab testing and associated activities within the Microbiology section, including Serology, Virology and Parasitology.
Essential Position Duties 
<ul>
<li>Reviews the daily specimen management report.</li>
<li>Troubleshoots and maintains the LIS and instruments interface and software.</li>
<li>Performs Clostidium difficile assays.</li>
<li>Resolves client problems as needed.</li>
<li>Performs and records all quality assurances systems required to maintain precision and accuracy, including proficiency testing.</li>
<li>Performs other tasks and procedures in Microbiology as required which are commensurate with education, training and experience.</li>
<li>Assists in maintaining adequate inventory of supplies.</li>
<li>Record lot numbers and ensures compliance with State requirements for documentation of lot numbers with quality control and specimen records.</li>
<li>Performs all clerical functions associated with the department.</li>
<li>Reads bacterial and viral cultures. Performs biochemical identification procedures as necessary and record MIC results. </li>
<li>Follows all safety protocols as outlines in safety manual.</li>
<li>Identifies and pursues self improvement needs.</li>
<li>Seeks coaching/mentoring when appropriate.</li>
<li>Performs other duties as assigned</li>
</ul>
Compliance Responsibilities 
<ul>
<li>Participates in required orientation, Compliance and HIPAA training programs.</li>
<li>Cooperates with monitoring and audit functions and investigations.</li>
<li>Participates, as requested, in process improvement responsibilities.</li>
</ul>
POSITION QUALIFICATIONS 
Core Competencies/Skill Sets 
<ul>
<li>Excellent verbal and written communication skills.</li>
<li>Detail oriented and organizational skills.</li>
<li>Exercises accuracy and precision in completion of prescribed tasks and treatments.</li>
</ul>
Professional Experience/Educational Requirements 
<ul>
<li>Bachelor’s degree or MT (ASCP or equivalent preferred); Associates degree with MLT</li>
<li>Minimum of one (1) year experience in the area of Microbiology.</li>
<li>Some computer experience required.</li>
</ul>
Certification/Licensure
<ul>
<li>Must qualify as a clinical laboratory technologist under CLIA regulations.</li>
</ul>
Benefits:
TridentCare offers a competitive wage and robust benefit package to full time employees. Part time employees are eligible for many of the same below, pro-rated. Benefits include:
<ul>
<li>Two weeks of vacation time</li>
<li>Health Insurance after 30 days!</li>
<li>Sick time</li>
<li>8 paid holidays</li>
<li>Same day pay available</li>
<li>Medical insurance allowance, giving you the freedom to customize your plan to fit your needs</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Disability insurance</li>
<li>Company paid life insurance</li>
<li>401(k)</li>
</ul>
#MBX

Microbiologist/ MLT, Microbiologist

<h3>Job Description</h3>
Job DescriptionProduct Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a roduct Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing novel coatings platforms from lab-to-scale to address customer needs. A bachelor’s degree or higher in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science,or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop novel coating platforms, test metrics, and design experiments by working in a lab-based environment with minimal day-to-day guidance.</li>
<li>Develop hypotheses and conduct experiments to improve understanding and performance of actnano’s coating technology by coordinating with various team members.</li>
<li>Communicate technical advances internally with other members of the company and interact with external vendors, independent testing laboratories, and customers to explain and troubleshoot application of the technology.</li>
<li>Support scaling of coating from lab or pilot scale to a manufacturing environment.</li>
<li>Collaborate with sales or technical service to address customer requests.</li>
<li>Expand actnano’s coating portfolio by innovating on current coating technology and developing new coating platforms.</li>
<li>Some international and domestic travel required. </li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $75,000 – $90,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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I3Y9Z3UrYH

Product Development Engineer / Scientist

<h3>Job Description</h3>
Job Description
Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future!
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness. We offer a competitive benefits package that includes health, dental, vision, wellness programs, employee discounts, retirement plans, tuition reimbursement, ongoing development, advancement opportunities and more. 
Founded in 1846, today HP Hood is one of the largest and most trusted food and beverage manufacturers in the United States. Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more.
Job Summary: HP Hood, LLC is looking for a food science intern to join our R&amp;D team in Wilmington, MA. Our Summer Intern program offers students a paid opportunity to work in an R&amp;D environment that will provide real-life experiences and to apply your education. Responsible for the completion of assigned project work related to product development initiatives to develop and introduce new products, improve product quality, productivity, and or capacity in operations. You will be part of various day to day R&amp;D projects and be a valued member of our team. We look forward to providing an enriching and exciting opportunity for a student to learn more about the Food &amp; Beverage Industry.
NOTE:This paid internship is for 2026, temporary full-time for up to 3 months during normal business hours M-F. Intern will be working in our Wilmington, MA R&amp;D Facility.
Essential Duties and Responsibilities:
<ul>
<li>Conducts assigned projects while increasing the incumbent's level of understanding of projects, processes, and methods.</li>
<li>Provides technical or scientific direction through research on assigned project.</li>
<li>Exhibits innovation in discovery, advancement, and evaluation of new technologies in the area food process/research development.</li>
<li>Provide innovative and timely cost effective improvements, concepts, developments, or scientific insight and understanding with respect to new or existing products or processes.</li>
<li>Maintains a professional record of the work completed.</li>
<li>Schedules equipment and orders ingredients to ensure adequate raw materials, resources, and timing for lab and/or pilot plant testing.</li>
<li>Assists in the executions of food production in the lab, pilot plant, and/or manufacturing plant.</li>
</ul>
Education and Experience:
<ul>
<li>Food Sciences, Chemistry, Biochemistry, Biology, Microbiology, and other Biological Sciences, and Science Ph.D. candidates.</li>
</ul>
Skills and Competencies:
<ul>
<li>Able to apply math, statistics, science, and other technical knowledge to solve real world problems and develop robust solutions.</li>
<li>Seeks out knowledge and is able to quickly grasp technical concepts and grow personal expertise.</li>
<li>Manages time effectively by understanding assignment requirements, prioritizing objectives, and scheduling tasks accordingly.</li>
<li>Listens and communicates well in a team environment.</li>
<li>Provides and receives honest and open feedback in a constructive manner.</li>
<li>Is analytical; uses sound judgment in decision making by basing decisions on factual information.</li>
<li>Show personal initiative and drives for results to ensure deliverables meet cost and schedule requirements.</li>
<li>Exhibits high level of integrity and directness/candor.</li>
<li>Displays excellent written/oral communication skills.</li>
<li>Meets deadlines regularly and works well in fast paced environment.</li>
<li>Drives for results to ensure Engineering deliverables meet cost and schedule requirements.</li>
<li>Demonstrates a positive and mature attitude.</li>
<li>Works hands on in the lab independently and with their team members.</li>
</ul>
HP Hood is an Equal Opportunity Employer Female/Minority/Veteran/Disabled" VERVRAA Federal Contractor"
Exact compensation may vary based on skills, experience and location.
The pay range for this position is$27—$27 USD
HP Hood is an Equal Opportunity Employer 
Female/Minority/Veteran/Disabled
"VERVRAA Federal Contractor"
Privacy Policy
CCPA
For Applicants in Massachusetts - It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Employment is subject to verification of an applicant's identity and eligibility for employment in the United States as required by immigration laws. We are unable to assist with sponsorship at this time.

Research & Development 2026 Summer Internship (Engineering Team)

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist
Job Description
The Quality Control Chemist will support method development for GC, HPLC, and UPLC and engage in analytical chemistry work. The role involves identifying and performing proper characterization methods and writing, preparing, and presenting technical data, reports, and standard operating procedures (SOPs) for internal use.
Responsibilities
<ul>
<li>Support method development for GC, HPLC, and UPLC.</li>
<li>Perform analytical chemistry work.</li>
<li>Identify and implement appropriate characterization methods.</li>
<li>Write, prepare, and present technical data, technical reports, and SOPs for internal use.</li>
<li>Execute and oversee chemistry methods to support the chemistry team.</li>
<li>Drive research and development within the department.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in Chemistry, HPLC, UPLC, and method development.</li>
<li>Experience with analytical chemistry, gas chromatography, capillary electrophoresis, conductivity, FTIR, GCMS, UVVIS, and wet chemistry.</li>
<li>Quality control expertise.</li>
<li>Hands-on experience with empower systems.</li>
<li>Experience with CE methods, such as CE-SDS and cIEF, for analyzing biological materials.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's or Master's degree in Chemistry, Biochemistry, or related field.</li>
<li>3-5 years of experience in method development with various chemistry instrumentation.</li>
<li>Detail-oriented, collaborative, and hardworking.</li>
</ul>
Work Environment
The position requires 100% onsite work in the Quality Control chemistry group. The work environment is business casual, with a first shift schedule from Monday to Friday. The team values individuals who are detail-oriented, collaborative, and dedicated to their work.
Job Type &amp; Location
This is a Contract position based out of Bedford, Massachusetts.
Pay and Benefits
The pay range for this position is $35.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bedford,MA.
Application Deadline
This position is anticipated to close on Sep 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
🧪 Lab Technician – Chemical Analysis &amp; Quality Support
📍&nbsp;Location: Hadley, MA
🕒&nbsp;Schedule: Monday–Friday | 10-Hour Shifts + Overtime Available
🔁&nbsp;Contract-to-Hire Opportunity
We are seeking a dedicated Lab Technician to perform chemical analysis of plating baths and process solutions using titration, spectrophotometry, and other methods. The ideal candidate will play a vital role in ensuring the quality and compliance of our processes with industry standards.
Responsibilities
<ul>
<li>Conduct chemical analysis of plating baths and process solutions using titration, spectrophotometry, and other methods.</li>
<li>Prepare and maintain standard solutions, reagents, and laboratory equipment.</li>
<li>Monitor bath chemistry to ensure compliance with internal specifications and industry standards.</li>
<li>Assist in maintaining records of analysis, solution concentrations, and corrective actions.</li>
<li>Support environmental testing and wastewater treatment monitoring.</li>
<li>Collaborate with production teams to troubleshoot quality issues or solution variances.</li>
<li>Maintain a clean, safe, and organized laboratory workspace.</li>
<li>Adhere to all safety and environmental protocols.</li>
</ul>
Essential Skills
<ul>
<li>Quality control</li>
<li>Laboratory experience</li>
<li>Titration expertise</li>
<li>Experience with metal finishing</li>
<li>Chemistry knowledge</li>
<li>GMP (Good Manufacturing Practice)</li>
<li>Quality control and assurance</li>
</ul>
Must Haves:
<ul>
<li>Hands-on experience in a lab setting (no degree required).</li>
<li>Strong skills in titration and wet chemistry.</li>
<li>Familiarity with metal finishing processes (preferred).</li>
<li>Understanding of GMP and quality control practices.</li>
<li>Motivated, reliable, and safety-conscious mindset.</li>
</ul>
Pay and Benefits
The pay range for this position is $25.00 - $27.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Springfield,MA.
Application Deadline
This position is anticipated to close on Sep 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Plating Lab Technician

<h3>Job Description</h3>
Job Description
Description
Support development and research of new methods and analytical techniques to be used to release new and existing products 
Validation and verification of analytical methods
perform investigations of out of specification, out of trends, equipment failure, etc. 
Present trending data to support development and validation following GMP guidelines
Perform analytical testing for organic and inorganic chemicals by using FTIR, HPLC, NMR LCMS, GCMS, ICP- MS, GC and wet chemistry
Create test procedures and provide analytical support for certain research products
Top Skills Details
NMR,GCMS,Hplc,FTIR,wet chemistry,analytical chemistry,LCMS
Additional Skills &amp; Qualifications
MS in chemistry or biochemistry with 3-5 years experience or a BS with 5-7 years experience
Experience working with FTIR, HPLC, LCMS, GCMS, ICPMS, NMR
Vast knowledge of following GMP guidelines and procedures
Willingness to train and develop team members
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $75000.00 - $85000.00/yr.
Company provides holiday, vacation, and 401k benefits. They will be able to gain bonuses past on company and personal performance.
Workplace Type
This is a fully onsite position in Tewksbury,MA.
Application Deadline
This position is anticipated to close on Sep 25, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Chemist

<h3>Job Description</h3>
Job Description
In this vital role you will be developing, qualifying and transferring innovative and fit-for-purpose quantitative assays for the measurement of DNA, proteins and other biological analyzes for manufacturing process development. The Senior Associate in Process Development is instrumental in designing, developing, and optimizing manufacturing processes. They are involved in conducting experiments, analyzing results, and implementing process improvements to enhance efficiency and product quality.
 Responsibilities:
<ul>
<li>Routine testing support for PD DS process related impurity analysis</li>
<li>Preparation of lab buffers and reagents</li>
<li>Lab reagent and materials inventory</li>
<li>Maintenance of critical reagents stocks</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>Provides critical evaluation of analytical data and results to support product development analytical testing activities.</li>
<li>Documentation of assays and laboratory activities in electronic notebook documentation system</li>
<li>Generating, analyzing, and interpreting analytical data</li>
<li>Supporting analytical projects involving method development, qualification, and transfer</li>
<li>Analyzing routine samples by qPCR and ELISA, data interpretation and reporting,</li>
<li>Documentation of results and peer review of electronic notebooks.</li>
<li>Preparation of lab buffers and reagents, maintenance of critical reagents stocks</li>
<li>Sample, reagent and materials inventory tracking and re-stocking</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.</li>
</ul>
Requirements / Qualifications:
<ul>
<li>Associate’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field and 2 years of Scientific experience OR</li>
<li>Bachelor’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field</li>
<li>Experience and expertise with protein assays, especially immunoassays, ELISAs or qPCR.</li>
<li>Experience in GMP lab setting.</li>
<li>Experience and expertise with Microsoft Office software: Word, PowerPoint and Excel.</li>
<li>Enjoys participating in a cohesive, high performing team, establishes effective and adaptable relationships with colleagues, while contributing as an effective independent contributor.</li>
<li>Communication – establishes and maintains effective communication mechanisms to keep colleagues appropriately advised; bridges communication between individuals, team and other organizational units as necessary.</li>
<li>Social skills – communicates optimally, using appropriate tact and sensitivity; makes others feel respected, valued and understood.</li>
<li>ELISA, immunoassays and qPCR technologies</li>
<li>Familiarity with electronic laboratory notebook/record keeping system(s)</li>
<li>Familiarity with working in a GMP/GxP environment</li>
<li>Strong Communication skills</li>
<li>Team player</li>
</ul>
Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search. 
<h3>Company Description</h3>
The Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search.

Associate Scientist

<h3>Job Description</h3>
Job Description
Job Description 
<ul>
<li>
Developing proteomics workflows using advanced high-resolution mass spectrometry techniques. 
</li>
<li>
Key duties include development and optimization of sample preparation methods from cell lines and other matrices for mass spectrometry analysis and data processing with various bioinformatics tools; collaborative work with colleagues; accurately documenting all activities in an electronic lab notebook (ELN). 
</li>
<li>
Applying knowledge of proteomics workflows to develop and implement optimal strategies for the preparation and analysis of cellular samples
</li>
<li>
Working collaboratively with experts in the team to advance innovative proteomics strategies
</li>
<li>
Employing different bioinformatics tools for data analysis and fitting
</li>
<li>
Consistent record keeping using an electronic lab notebook (ELN)
</li>
<li>
Interact daily with the managers and 3-4 colleagues in the cross-functional team for method development, laboratory work prioritization, experiment planning and execution. 
</li>
<li>
Also work on common assignments with colleagues in a larger bioanalytical group at the same location, as needed. 
</li>
<li>
Participate in bi-weekly group meetings and other team meetings and discussions, as relevant to their work.
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
M.Sc with 5+ years experience; OR
</li>
<li>
PhD 0+ years in a relevant scientific field with a documented experience in proteomics and mass-spectrometry desired 
</li>
<li>
Advanced knowledge and documented expertise with mass-spectrometry based proteomics approaches: label- or label-free quantification (TMT or DIA)
</li>
<li>
Experience with high-resolution mass-spectrometry instruments, such as Orbitraps and timsTOF
</li>
<li>
Experience with sample preparation based on enrichment (incl. affinity purification), and universal protein extraction
</li>
<li>
Bioinformatics skills relevant for mass-spec data search, statistical analysis and visualization
</li>
<li>
Experience with membrane protein analysis and/or cell surface proteomics
</li>
<li>
Knowledge of cell culture techniques and experience conducitng cell-based assays
</li>
<li>
Walking, taking the stairs, standing, sitting as appropriate for a laboratory-based position
</li>
<li>
Experience with cell culture and cell manipulation is a plus.
</li>
<li>
Requires expertise in LC-MS based proteomics. 
</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.

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