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<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 an R&amp;D Process Engineering Intern to join our R&amp;D team in Wilmington, MA. The 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.
The Process Engineering Intern will support equipment, system, and product initiatives by learning to identify, develop, lead, and execute solutions for performance across Hood sites, working with cross functional teams to drive down plant losses through process and packaging improvements, ingredient loss optimization, standard process development, changeover optimization, and/or BOM and Standards updates and optimization. Also, you will help R&amp;D Engineers collect critical data during pilot and plant trials, production start-ups, and/or equipment/technology evaluations. Lastly, you will partner with the product development intern to learn about the entire product commercialization process.
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 approximately 3 months during normal business hours M-F. Intern will be working in our Wilmington, MA R&amp;D Facility. The position requires that the intern reside within commuting distance and have reliable transportation to be onsite according to a weekly schedule. Potential to travel to other Hood facilities as opportunities arise.
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>Develops and maintain material balances and unit operation capability information to ensure optimal production rates, parameters, and formulas.</li>
<li>Identifies, develops, leads, and executes equipment and system improvements that deliver financial benefits (e.g. batch time reduction, line efficiency improvements, new equipment/technology).</li>
<li>Designs experiments and collects data on process improvements.</li>
<li>Analyzes, interprets, and presents findings clearly and concisely.</li>
<li>Provides 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>
<li>Other duties as assigned.</li>
</ul>
Education and Experience:
<ul>
<li>Food Engineering, Food Science/Technology, Agricultural Engineering, Biological Systems Engineering/Technology, Chemical Engineering, Process Engineering, or other related degrees. Sophomore through Graduate Level.</li>
<li>Demonstrates knowledge of ingredients, product, and equipment and unit operations.</li>
<li>Demonstrates understanding of quality metrics, analysis methods and procedures.</li>
<li>Demonstrate clear understanding and execution of human and food safety practices and apply this understanding to all projects and initiatives.</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 DescriptionDescription:
Are you a civil engineering student with a strong interest in geotechnical engineering? Are you looking to further your education with intensive, real-world experience and mentorship from professional engineers? Do you like the idea of spending some time outdoors, getting your hands dirty (literally) while you learn about what it takes to be a successful geotechnical engineer? GeoEngineers is seeking motivated engineering students for our geotechnical Spring 2026 internship opportunities.
 
Essential Duties and Responsibilities
<ul>
<li>Monitors field explorations and construction projects under the guidance of engineers and scientists.</li>
<li>Documents field conditions and completes field reports.</li>
<li>May assist with routine laboratory testing and analyses.</li>
<li>Assists engineers with office and project-related deliverables.</li>
<li>Assists with organizing and maintaining lab and field equipment when needed.</li>
<li>Maintains field readiness and keeps up to date on company training requirements. Conducts work safely and supports the safe work practices of team members.</li>
</ul>
Qualifications
<ul>
<li>High school diploma or equivalent.</li>
<li>Current enrollment in a Bachelor’s or Master’s degree program specializing in Civil or Geotechnical Engineering.</li>
<li>Basic working knowledge of Microsoft Office applications preferred.</li>
<li>Strong written and verbal communication skills.</li>
<li>Ability to work in a team environment and complete tasks in a timely manner.</li>
<li>Valid driver’s license and a reliable form of personal transportation.</li>
</ul>
Physical Requirements / Work Environment
<ul>
<li>All candidates are subject to completing a background check, and reference check.</li>
<li>Ability to perform a wide range of physical activities, regular walking, bending, standing and reaching, and occasional lifting of up to 50 lbs.</li>
<li>Ability to perform consistent work on a PC with prolonged sitting and view of a monitor/screen.</li>
</ul>
Our best estimate of the rate for this role, located in Boston MA, is $25 per hour. Compensation offered will be based on a variety of individual factors, including education and experience, as well as internal equity. GeoEngineers’ salary ranges are reviewed and updated each year and employees are eligible for pay increases based on individual performance. As part of our competitive total rewards package, employees in this role may also be eligible for our annual year-end bonus offering, subject to program eligibility requirements.
 
At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits here.
 
Our Commitment to Belonging at GeoEngineers
 
When people feel they can bring their whole selves to work, that they have a voice and are supported and respected, it creates trust and a feeling of belonging— employees then flourish, grow their careers, and do the best work of their lives. A culture of belonging allows our employees to thrive and our company to prosper. This is a journey, and we are committed to doing the work, learning and evolving as we go.
 
GeoEngineers is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances. 
 
GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at <a href="mailto:hr@geoengineers.com" target="_blank">hr@geoengineers.com</a> or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis. 
 
We welcome and encourage individuals from all backgrounds and experiences to apply for openings on our team. We would love for you to join us!
 
We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies.
Requirements:

Geotechnical Intern (Spring 2026)

<h3>Job Description</h3>
Job DescriptionCompany Description 
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.&nbsp;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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
We are seeking an Analytical Chemist&nbsp;to support a dynamic client team focused on&nbsp;formulation research and development&nbsp;for cutting-edge drug modalities. This role is ideal for a scientist with&nbsp;strong LC-MS experience&nbsp;and a background in analytical chemistry, who thrives in a fast-paced, collaborative environment.
Key Responsibilities
<ul>
<li>Develop and perform analytical assays focused on&nbsp;lipid nanoparticle and protein characterization&nbsp;using LC-MS, LC-MS/MS, UPLC, SEC-MALS, and related techniques.</li>
<li>Support material characterization, process optimization, and formulation development of&nbsp;lipid-based and protein-based therapeutics.</li>
<li>Write test methods, SOPs, and study reports with a focus on lipid and protein analytics.</li>
<li>Collaborate with cross-functional teams, including genetic medicine, formulation, and analytical development, to ensure the timely delivery of assay data.</li>
<li>Troubleshoot, interpret, and present experimental data in multidisciplinary team meetings.</li>
<li>Maintain detailed records in electronic lab notebooks and sample management systems.</li>
<li>Willingness to take on additional responsibilities as assigned.</li>
</ul>
Qualifications 
Minimum Qualifications
<ul>
<li>B.S. in life sciences with 3–4 years of industry experience or M.S. with 1–2 years of experience.</li>
<li>Hands-on experience with&nbsp;lipid and protein LCMS assay development and optimization.</li>
<li>Experience with&nbsp;QExactive or Orbitrap instrumentation.</li>
<li>Ability to work independently after initial training and troubleshoot experimental results.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience with&nbsp;lipid nanoparticle formulation&nbsp;or&nbsp;protein therapeutic development.</li>
<li>Familiarity with assay qualification following ICH guidance.</li>
<li>Strong communication skills and ability to manage workflows and deliverables.</li>
<li>Authorization to work in the U.S. without restriction or sponsorship.</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 In-Person Meeting over Coffee for a Casual Discussion of the Role with the Team&nbsp;</li>
</ul>
Location:&nbsp;Boston, MA (commutable candidates encouraged to apply)
Schedule:&nbsp;Full-time, Monday–Friday, 8:00 AM–5:00 PM
Compensation:
<ul>
<li>Hourly Rate:&nbsp;$36–$39/hour</li>
<li>Annual Equivalent:&nbsp;$74,880–$81,120 (based on education and experience)</li>
</ul>
Benefits
<ul>
<li>Comprehensive medical, dental, and vision coverage</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Chemist - LCMS

<h3>Job Description</h3>
Job Description
InnoTECH Staffing is looking to hire a fulltime / permanent Senior R&amp;D Polymer Chemist who has at least 3 years of product development experience for a fast-growing and well funded coatings company in the Boston area. 
!!! Must be a US Citizen or Greencard Holder !!!

This position will focus on developing new platform technologies (organic / polymers) for environmental protection and implementing at customers.
** Any additional languages (Mandarin, German and Spanish) are a plus, but not required. 
Some international travel required.

Responsibilities for this role include:
● Developing functional materials, test methods, and implementation solutions for addressing environmental protection of electric vehicles, ADAS systems, and consumer electronics.
● Maintaining project plans, timelines, and deliverables for staying accountable on product launch strategy.
● Communicating technical advances and project strategy internally across a global team comprising technical team members and sales.
● Working autonomously on open-ended projects ranging from new coating development to creation of novel application techniques.
● Expanding Company’s intellectual property portfolio by innovating on current or new coatings and application technology.
● Serving as the subject matter expert on coatings under development and participating in developing strategy for implementing coating solution at customer.
● Collaborating effectively with various functions within sales, technical services, manufacturing, and operations on new product launch.
● Mentoring technicians and co-ops on execution of experiments towards coating development.

Candidate must be legally allowed to work in the US.
*** International and domestic travel is required.

Education:
M.S. or Ph.D. in Mechanical Engineering, Chemical Engineering, Chemistry, Materials Science, or Electrical Engineering or associated technical field. Previous industry or research experience development of coatings preferred.

 Depending on skills and experience, this role is paying up to $125K base and also has a bonus and full benefits package

Senior R&D Scientist - polymer chemist - product development - coatings

<h3>Job Description</h3>
Job DescriptionDescription . Plans, conducts and performs a variety of chemical productions and process&nbsp; &nbsp; &nbsp; &nbsp;developments under general supervision. · Utilizes or adapts new methods under guided supervision for updating existing synthesis procedures in order to improve yields, reduce production time and waste.&nbsp; · Keeps abreast of most recent technological developments pertaining to new products and applying to new products R/D under guided supervision&nbsp; · Troubleshoots and resolves standard production problems with full understanding of chemistries and analytical tools for progress of reactions&nbsp; · May supervise activities of lower chemists ensuring guided procedures or scale-ups in effective and safe manner&nbsp; · Attends technical meetings, conferences, seminars and reads current literature to keep up with up to date scientific knowledge.&nbsp; Key Responsibilities · Responsible for maintaining a clear and detailed lab book. · Responsible for maintaining neat, clean and safe work area. · Performs other duties of similar complexity as directed. · Ability to define problems, collect data, establish facts, and draw conclusions · Strong organizational, problem-solving, and analytical skills · Ability to manage priorities and workflow · Ability to work independently and as a member of various teams and committees · Proven ability to handle multiple projects and meet deadlines · Strong interpersonal skills Skills, Knowledge and Expertise · Strong understanding of chemistry · Bachelor’s degree in Chemistry with 10-15 years experience or · Master’s degree in Chemistry with 5-10 year of experience or · PhD in Chemistry with 5-7 years of experience.

Principal Production Chemist

<h3>Job Description</h3>
Job Description
Seeking Senior Summer Camp counselor in Groton Ma. Prefer school teacher.&nbsp; Requires 3 years experience. 8am-4pm M-F. Must be creative, great problem solver, can "think on the go" and work with little direct supervision.&nbsp; Able to lead other counselors.&nbsp; Must be very well organized.&nbsp; Duties include creative planning for the day/week.&nbsp; Excellent compensation with bonuses.

Senior Summer Camp Counselor

<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Analytical/QC Lab Metrologist is responsible for the timely installation, maintenance, repair, calibration, and IQ/OQ of instruments, balances, and other equipment used by the Analytical Development (AD) and Quality Control (QC) groups. This role also ensures Standard Operating Procedures are technically sound and provide full regulatory compliance. This position is critical to supporting high-quality science, operational excellence, and regulatory compliance across both sites.
Core Responsibilities: 
<ul>
<li>Revises and reviews metrology-related protocols and IQ/OQ to ascertain proper functioning of the instrumentation. Ensures that appropriate documentation for the instrument calibration program is in place for compliance with regulatory expectations.</li>
<li>Schedules, executes and supports instrument calibrations and preventative maintenance in such a way so as not disrupt the analysts using the instruments. Responsible in the assignment of instrument custodians, assuring instrument maintenance and usage logbooks have been maintained. Trouble shooting or judging the issue for chromatographic systems mainly LC/GC.</li>
<li>Negotiates and manages contracts with external vendors and contracted services as required. Oversees the work of contracted personnel to install/modify equipment and systems in accordance with the specific needs of the AD and QC groups while meeting all cGMP and USP requirements.</li>
<li>Keep abreast of instrument validation requirements to ensure compliance with respect to USP and cGMP requirements.</li>
<li>Provides assistance in internal and customer audits by providing relevant, up to date documentation related to calibration, qualification and maintenance of appropriate analytical instrumentation used by the analytical groups. </li>
<li>Leads the process to evaluate, purchase and install new instrumentation. Interacts with internal and external vendors to ensure the proper instrumentation is identified to support the needs of the business. Evaluates and recommends appropriate application of new software packages as well as upgrades of software/firmware/hardware.</li>
<li>Directly involved with and supports investigations that are instrument related. Conducts all work in compliance with USP and cGMP standards and all other appropriate Federal, state and local regulations.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s Degree in chemistry or a related science with a minimum of 5 years’ related experience </li>
<li>Familiarity with LC/GC trouble shooting.</li>
<li>Experience in a cGMP environment</li>
<li>Ability to exercise independent judgment in the application of scientific principles pertaining to analyses as related to this business and operation </li>
<li>Proficiency with computers and other software packages relevant to installation, modification, calibration and qualification of instrumentation systems and equipment</li>
<li>Strong communication skills; written and verbal. </li>
<li>Possess strong organizational skills</li>
</ul>
Preferred
<ul>
<li>Experience in lab equipment such as analytical balance, micro balance, KF, OVEN-KF, NMR, ICP-MS, PSD, XRPD, TGA, DSC, etc. </li>
<li>Experience or familiarity with Labware LIMS and the Instrument Manager module</li>
<li>Experience or familiarity with Master Control and Veeva</li>
<li>Recent relevant experience in bulk pharmaceutical/API manufacturing or specialty chemicals</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Analytical/Quality Control Lab Metrologist

<h3>Job Description</h3>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 5+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 5+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
?Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 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.

QC Chemist III

<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 + 4-6 years or MS + 2-4 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>Position is full-time, on-site Monday-Friday 8AM-5PM.&nbsp;</li>
<li>Pay range: $27.00 - $31.00 based on degree level and years of relevant experience with the skills utilized in the role.&nbsp;</li>
<li>Excellent full-time benefits including 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>
<li>#LI-EB1</li>
</ul>
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 Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $70,000 - 90,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
?Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 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.

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