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<h3>Job Description</h3>
Job DescriptionDescription:
This role offers the chance to become a key contributor to our private equity research team, focusing on the thorough evaluation of private equity managers across buyout, growth, and venture strategies. You'll be responsible for managing the due diligence process from start to finish, conducting detailed analysis of general partners to help inform investment decisions.
 
In this position, you'll spend your time analyzing manager track records, conducting introductory manager meetings, on-site visits, and preparing comprehensive research reports that support our investment committee process. You'll also help manage our research pipeline, keeping track of current and upcoming fundraising opportunities while maintaining relationships with existing managers in our portfolio.
 
The role involves coordinating with various stakeholders - from the general partners you're evaluating to internal teams and clients who rely on your research. You'll have the opportunity to develop expertise across different private equity strategies while contributing to the growth and improvement of our research capabilities.
 
This is a great opportunity for someone looking to leverage and deepen their knowledge of private markets while working in a collaborative environment. You'll have direct exposure to high-quality investment managers and gain valuable experience in institutional-level due diligence processes and private equity implementation across a client base of endowments, foundations, and family offices. The position is based in either Portsmouth, NH, or Boston, offering flexibility in location.
 
Key Responsibilities
<ul>
<li>Develop and sustain a comprehensive pipeline of private equity manager ideas (spanning buyout, growth, and venture) that are either currently in the market or expected to enter within the next 12 months through industry relationships and market intelligence</li>
<li>Create and maintain market maps for private equity segments while tracking industry trends and identifying emerging opportunities across private markets</li>
<li>Lead comprehensive due diligence processes on private equity managers, including analysis of manager organizations, investment strategies, track records, and portfolio performance</li>
<li>Conduct manager evaluation activities, including leading manager meetings, site visits, and reference calls to validate investment thesis and identify potential red flags</li>
<li>Prepare clear and comprehensive investment reports with recommendations based on qualitative and quantitative analysis, incorporating insights from manager interactions and due diligence findings</li>
<li>Monitor existing managers on an ongoing basis through attending annual meetings, general updates, and maintaining regular communication to track performance and strategic developments</li>
<li>Communicate market intelligence and investment ideas to internal teams and clients, presenting investment opportunities and market trends in a clear and actionable format</li>
<li>Support client private equity implementation processes, including portfolio construction analysis, manager selection processes, and fund recommendations tailored to client objectives</li>
<li>Manage information flow between managers, clients, and internal teams to ensure seamless communication and decision-making processes</li>
<li>Serve as subject matter expert on private markets for both internal colleagues and external clients, providing insights on market conditions, strategy performance, and investment opportunities</li>
</ul>
What You'll Bring
 
Required Qualifications
<ul>
<li>Bachelor's degree required; MBA, CFA, or CAIA designation (or progress toward these credentials) preferred</li>
<li>10+ years of experience conducting due diligence on private equity managers, preferably from an investment consultant, investment office, or fund of funds</li>
<li>Fund manager evaluation as the candidate's primary responsibility at prior firm(s)</li>
<li>Specialized experience in segments of the private capital markets (i.e., venture capital, growth equity, buyouts)</li>
</ul>
Professional Skills &amp; Experience
<ul>
<li>Demonstrated qualitative and quantitative analytical skills with the ability to synthesize complex investment issues</li>
<li>Strong written and verbal communication skills and able to present in front of senior professionals in the industry</li>
<li>Demonstrated relationship-building skills and established network in private capital, including general partners, placement agents and limited partners</li>
<li>Experience using Quickbase, Tableau, Pitchbook, Refinitiv, or other private capital data and analytics providers</li>
<li>Strong Excel and PowerPoint skills</li>
</ul>
What We Offer
At Prime Buchholz, a proud B-Corp organization, we believe in aligning our success with a positive impact on the world. We also believe that great work deserves meaningful rewards. In addition to a competitive annual salary and bonus plus comprehensive medical, dental, and vision coverage, you'll enjoy a range of perks designed to support your well-being, including:
<ul>
<li>Flexibility &amp; Balance: Enjoy the flexibility of working from home up to two days a week, with a weekly anchor day in the office to foster team collaboration and connection.</li>
<li>Savings: Plan for your future with our 401(k) match and profit-sharing program, designed to help you build long-term financial security.</li>
<li>Community: We support your commitment to giving back with matching charitable contributions and paid volunteer time for causes that matter to you.</li>
<li>Time: Take time to recharge with our flexible time-off policy and 11 paid holidays. Plus, we offer additional time off to support you through life’s major milestones, including family growth.</li>
</ul>
Prime Buchholz is committed to building and preserving a culture where individuals from different personal and professional backgrounds can thrive, contribute and grow. The collective sum of our individual differences, knowledge, life experiences, and unique talents is the foundation for our accomplishments and impact.
 
We are proud to be an equal opportunity employer. We do not discriminate on the basis of race, color, religion, national origin, sex (including pregnancy), sexual orientation, gender identity or expression, age, physical or mental disability, veteran status, marital status, genetic information, or any other characteristic protected by state, federal or local law. We strive to create a supportive community where we are all comfortable and confident to be authentic, open and curious.
Requirements:

Director, Research (Private Equity)

<h3>Job Description</h3>
Job DescriptionDescription:
Work Where it Matters
 
LDRM, a joint venture comprised of Lockwood Hills Federal, an Akima company, and DTSV, is not just another technical support contractor. As an Alaska Native Corporation (ANC), our mission and purpose extend beyond our exciting federal projects as we support our shareholder communities in Alaska.
 
At LDRM, the work you do every day makes a difference in the lives of our 15,000 Iñupiat shareholders, a group of Alaska natives from one of the most remote and harshest environments in the United States.
 
For our shareholders, LDRM provides support and employment opportunities and contributes to the survival of a culture that has thrived above the Arctic Circle for more than 10,000 years.
For our government customers, LDRM provides technical, operational, and administrative support services to federal agencies, including Department of State and the U.S. Patent and Trademark Office.
As an LDRM employee, you will be surrounded by a challenging, yet supportive work environment that is committed to innovation and diversity, two of our most important values. You will also have access to our comprehensive benefits and competitive pay in addition to growth opportunities and excellent retirement options.
 
Here’s why we want you to consider LDRM:
<ul>
<li>Tuition reimbursement program.</li>
<li>Platinum-level New Hampshire Veteran Friendly Business</li>
<li>Daytime hours, and no weekends</li>
<li>401(k), health, dental and vision plans, and other insurances you can use</li>
<li>An Employee Assistance Plan that’s ready when you need it</li>
<li>Paid training and paid time off</li>
</ul>
This is an external pipeline posting. The successful candidates will get an active offer, be taken through the federal security clearance process, and will then wait for a vacant position to start work. 
 
 
Job Summary:
 
As our Operations Research Analyst, you are responsible for making assessments after reviewing and evaluating information presented to you. You handle data set research and evaluation to draw conclusions, ensure compliance, and identify trends. You’ll team with multiple stakeholders to achieve optimal results. One of your primary responsibilities includes record keeping and report generation. As the person in this critical investigative position, you will gather domestic and international assignment information. Once you’re here, our benefits package helps take care of you and your family in many ways, including an excellent Employee Assistance Program. Career development is as important to us as it is to you, which is why we love to promote from within.
 
 
In this role you will:
<ul>
<li>Conduct research on cases prior to these being sent for adjudication by gathering information from a variety of sources, including but not limited to: petitions, applications, and supporting documents, the internet, telephone calls, government, commercial and open-source databases</li>
<li>Evaluate data sets and interpret the relevance of data gathered including numerical statistics, legal documents, and open-source material with regard to cases</li>
<li>Perform analyses on research conducted and information received from various locations to identify possible fraudulent activity related to cases</li>
<li>Ensure the integrity of recordkeeping systems and the veracity of data collected prior to entering the data into the record keeping systems</li>
<li>Write reports in a clear and concise manner that summarize the information gathered and identified during research</li>
<li>Coordinate and network with agency personnel, other government agencies, and coworkers to facilitate information sharing on cases that involve fraud or potential criminal activity</li>
<li>Handle appropriately any Law Enforcement Sensitive (LES) information</li>
<li>Perform analyses on petitions being returned to identify trends that may be useful in future research that is being conducted prior to the cases being sent overseas. Identify errors and areas for improvement in memos associated with these petitions</li>
<li>Maintain a working knowledge of a variety of resources related to eligibility requirements</li>
<li>Make phone calls to collect information on a personalized basis, and create reports based on the information provided</li>
<li>Evaluate the case at hand, analyze the specific and adapted questions that need to be asked, and communicate in an unscripted manner</li>
</ul>
You may be required to perform other duties as assigned to advance the unit’s mission of supporting case pre-adjudication.
 
Requirements:
Your Minimum Qualifications to be a Research Analyst:
<ul>
<li>Bachelor’s Degree and experience with research and/or reporting</li>
<li>Ability to effectively communicate orally and in writing</li>
<li>Report preparation and document analysis to establish authenticity and for evaluation against government standards</li>
<li>Ability to establish and maintain effective communications with peers and with government officials</li>
<li>Ability to use databases to obtain and validate information</li>
<li>Ability to comprehend government regulations</li>
<li>Ability to conduct telephonic interviews to obtain and/or validate petition</li>
<li>Ability to analyze and evaluate data and interview responses to prepare concise reports and records of findings</li>
<li>Ability to accept feedback</li>
<li>Ability to think flexibly (open-mindedness with no absolutes), and think outside of the box</li>
<li>Proficient use of Microsoft Office suite of products</li>
</ul>
You must be a U.S. citizen. Additionally, you must successfully complete a credit and criminal background check and be able to obtain a Secret-level federal security clearance. AGAIN, this is a pipeline position which, after you receive a federal clearance, may require a wait to begin work.
 
Physical Demands:
 
While performing the duties of this job, you may occasionally be required to stand; walk; sit; lift up to 20 lbs.; bend; reach; carry; stoop; kneel; use hands and fingers to handle, or feel objects, tools or controls; use fingers and hands to type or write; speak; or hear. Specific vision abilities may be required to perform the job which may include close vision, distance vision, color vision, peripheral vision, depth perception, or the ability to adjust focus.
 
At LDRM, honesty and integrity govern our activities. We fulfill our commitments, and we treat everyone with dignity and respect. As an Alaskan Native company, our mission is to improve the quality of life for our shareholders and our people by maximizing economic growth, protecting and enhancing our environment, and by promoting healthy communities with decisions, actions, and behaviors consistent with our core principles.

Research Analyst - DAYS - PIPELINE

<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>
The successful candidate will join the Genomic Medicine Drug Product Development group. This individual will be an integral part of a dynamic and growing group of scientists and engineers developing adeno-associated virus (AAV) based gene therapy products within the larger organization. This team member will execute studies for the development of AAV formulations, fill-finish processes, and clinical device compatibility to ensure clinical and commercial readiness.
 
You will be responsible for:
<ul>
<li>Execution of formulation studies and non-GMP stability studies for AAV-based drug candidates</li>
<li>Clinical administrative device compatibility and In-use studies for clinical dosing enablement</li>
<li>Supporting the development of GMP fill finish processes</li>
<li>Developing presentations for internal presentations</li>
<li>Technical report authoring and data verification.</li>
</ul>
 
You will need to have:
<ul>
<li>BS in Pharmaceutics, Biochemistry, Chemical Engineering, or relevant field with 2+ years, a MS with 1+ years of relevant experience</li>
<li>Hands on experience with biologic drug development</li>
<li>Understanding of protein chemistry, formulation, and degradation</li>
<li>Ability to work effectively in a cross-functional settings</li>
<li>Excellent interpersonal and communication skills</li>
</ul>
 
Highly Valued:
<ul>
<li>Experience developing stabilizing, clinically acceptable formulations, and fill finish processes for biologics.</li>
<li>Experience with biopharmaceutical assays (CE, SEC, SVP analysis, DLS, etc.).</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Job Description🧪 Quality Control Lab Analyst – Contract to Hire
📍&nbsp;Location: Hadley, MA
🕒&nbsp;Schedule: Monday–Friday, 8:30 AM–4:30 PM or 9:00 AM–5:00 PM
🔬&nbsp;Join a growing team in a cutting-edge lab environment
&amp;#x1F31F;&nbsp;Help Us Ensure Quality from Molecule to Market
Are you a hands-on chemist with a passion for precision and product safety? Join our expanding team as a&nbsp;Quality Control Lab Analyst&nbsp;and play a critical role in testing and validating the ingredients that power health and wellness products. You’ll work in a dynamic lab setting, using advanced instrumentation and wet chemistry techniques to ensure every batch meets the highest standards.
This is a fantastic opportunity for someone who thrives in a collaborative, science-driven environment and wants to grow with a company that values innovation and integrity.
💼&nbsp;What You’ll Do
<ul>
<li>Prepare and test samples using GC and wet chemistry methods (pH, titrations, LOD).</li>
<li>Run calibration curves and system suitability tests to ensure accuracy.</li>
<li>Perform first-line instrument care and basic troubleshooting (GC, HPLC).</li>
<li>Support method validation efforts (accuracy, precision, LOD, LOQ).</li>
<li>Maintain lab inventory, cleanliness, and documentation standards.</li>
<li>Draft and review SOPs and participate in notebook peer reviews.</li>
</ul>
✅&nbsp;What You Bring
<ul>
<li>Bachelor’s degree in Chemistry (Master’s preferred).</li>
<li>3–5 years of QC lab experience in food, supplements, or natural products.</li>
<li>Independent operation of&nbsp;GC and HPLC&nbsp;instruments.</li>
<li>Experience with lipid-rich or natural product matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with&nbsp;USP/AOAC methods&nbsp;and&nbsp;cGMP documentation.</li>
<li>Proficiency in chromatography software (OpenLab, ChemStation).</li>
<li>Strong lab safety mindset and attention to detail.</li>
</ul>
&nbsp;Why You’ll Love This Role
<ul>
<li>Work in a growing organization with room to influence lab operations.</li>
<li>Be part of a team that values scientific rigor and continuous improvement.</li>
<li>Enjoy a stable weekday schedule with flexibility in start time.</li>
<li>Opportunity to transition into a permanent role with long-term growth potential.</li>
</ul>
Ready to make your mark in quality control?
Apply today and help us deliver safe, effective products backed by science.
Pay and Benefits
The pay range for this position is $30.00 - $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 Hadley,MA.
Application Deadline
This position is anticipated to close on Sep 12, 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.

Qc Lab Analyst

<h3>Job Description</h3>
Job Description
Position: Supervisor, Senior Scientist – In Vivo Pharmacokinetics
Salary Range: $120,000 - $135,000 / yr
Location: Boston, MA
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit <a href="http://www.pharmaron.com" target="_blank">www.pharmaron.com</a>.
Job Overview:
We are seeking a Supervisor, Senior Scientist with deep expertise in In Vivo Pharmacokinetics (PK) studies to lead and contribute to our DMPK team. This role combines hands-on scientific work with leadership responsibilities, including supervising technical staff, overseeing rodent PK study design and execution, and ensuring compliance with AAALAC and IACUC guidelines.
Key Responsibilities
<ul>
<li>Establish, train and provide scientific direction, oversight, and guidance to the technical staff that support in vivo studies.</li>
<li>Design, supervise, and conduct rodent PK studies, ensuring compliance with AAALAC and IACUC guidelines.</li>
<li>Draft, review, and interpret study protocols, data, and reports with scientific rigor and accuracy.</li>
<li>Ensure efficient scheduling of studies and staff to optimize capacity and deliver high-quality results on time.</li>
<li>Partner with project management, business development, and bioanalysis teams to ensure seamless client interactions and study execution.</li>
<li>Act as a technical representative in sales discussions with new and prospective clients.</li>
<li>Implement harmonized processes, best practices, and state-of-the-art methodologies for PK studies.</li>
<li>Recommend and implement strategies to improve productivity, increase efficiency, and maintain scientific excellence.</li>
</ul>
What We're Looking For:
<ul>
<li>PhD, MS, or BS in Pharmacokinetics, Chemistry, Biochemistry, or related discipline.</li>
<li>5+ years of laboratory experience in a CRO environment.</li>
<li>3+ years of management experience, including staff development and budget oversight.</li>
<li>Strong expertise in rodent PK studies, including dosing, sampling, and tissue collection/processing.</li>
<li>Proficiency with noncompartmental analysis (Phoenix WinNonlin) is required.</li>
<li>Proven ability to manage multiple projects while maintaining attention to detail and high-quality standards.</li>
<li>Excellent written and verbal communication skills, with a client-focused mindset.</li>
</ul>
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
<ul>
<li>Insurance including Medical, Dental &amp; Vision with significant employer contributions</li>
<li>Employer-funded Health Reimbursement Account</li>
<li>Healthcare &amp; Dependent Care Flexible Spending Accounts</li>
<li>100% Employer-paid Employee Life and AD&amp;D Insurance, Short- and Long-Term Disability Insurance</li>
<li>401k plan with generous employer match</li>
<li>Access to an Employee Assistance Program</li>
</ul>
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-MC1

Supervisor, Senior Scientist - In Vivo Pharmacokinetics

<h3>Job Description</h3>
Job DescriptionHiring for a Quality Control Lab Analyst in Hadley!
Job Description
We are seeking a dedicated Quality Control Lab Analyst to join our growing team. This role involves conducting GC testing of raw materials, in-process samples, and finished goods. The successful candidate will play a key role in ensuring the quality and safety of our products.
Responsibilities
<ul>
<li>Prepare samples across various matrices and run calibration curves and system suitability tests.</li>
<li>Perform wet chemistry tests, including pH, titrations, and loss on drying (LOD).</li>
<li>Provide first-line instrument care, such as column maintenance and addressing leaks and pump seals, following IQ/OQ/PQ guidelines.</li>
<li>Conduct basic troubleshooting and maintenance of laboratory instruments.</li>
<li>Support method validation work, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Flexibly support lab needs, including inventory management, lab cleanup, and notebook peer review.</li>
<li>Draft and review Standard Operating Procedures (SOPs).</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry is necessary; a Master's degree in Chemistry or Analytical Chemistry is preferred.</li>
<li>3-5 years of experience in a QC lab within the food or supplement industry.</li>
<li>Demonstrated independent operation of HPLC and GC.</li>
<li>Experience with natural product or lipid-rich matrices, including small molecule testing like vitamins, fats, emulsifiers, and actives.</li>
<li>Working knowledge of USP/AOAC methods and cGMP documentation.</li>
<li>Proficiency in chromatography software such as OpenLab and ChemStation.</li>
<li>Strong lab safety mindset and approach to work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience as a bench lab analyst or chemist.</li>
<li>Proficiency in titration and wet chemistry.</li>
<li>Experience with ICP-MS.</li>
</ul>
Work Environment
The position is based in a laboratory/manufacturing setting. The work schedule is Monday through Friday, with working hours from 8:30 am to 4:30 pm or 9 am to 5 pm. As a smaller organization looking to expand, this role offers significant opportunities for growth and influence in the day-to-day operations of the lab.
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, Massachusetts.
Pay and Benefits
The pay range for this position is $30.00 - $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 Hadley,MA.
Application Deadline
This position is anticipated to close on Sep 19, 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.

<h3>Job Description</h3>
Job Description
We are seeking a Scientist to join our client’s Manufacturing Sciences &amp; Technology team in Devens, MA. This role supports the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing.
You will collaborate closely with Manufacturing, Quality Assurance, Quality Control, Supply Chain, and Procurement on cross-functional teams to ensure GMP compliance and continuity of supply.
Key responsibilities include:
<ul>
<li> Qualify alternative raw material suppliers and partner with Procurement to identify new options. </li>
<li> Recommend and lead necessary testing to qualify materials for GMP manufacturing. </li>
<li> Author technical equivalency assessments, specification comparisons, material characterization reports, and change controls. </li>
<li> Support material and consumable manufacturing investigations. </li>
<li> Manage supplier change notifications and evaluate risks to maintain GMP compliance. </li>
<li> Contribute to risk assessments and material specification development. </li>
<li> Partner with cross-functional teams to deliver results in a fast-paced, matrixed environment.</li>
</ul>
Requirements
Bachelor’s or Master’s degree in Material Science Engineering, Chemistry, or related field with 2+ years of industry experience, or a PhD. 
 Strong technical writing skills and ability to author GMP documentation. 
 Experience in cross-matrix team environments and stakeholder collaboration. 
 Proven ability to manage multiple projects in a fast-paced setting. 
 Independent contributor with strong communication and interpersonal skills. 
 Experience with GMP change controls and investigations preferred. 
 Familiarity with analytical techniques (FTIR, SEM-EDS, etc.) and data trending/analysis a plus. 
 Awareness of cGMP regulations and compliance requirements.
Benefits
Competitive hourly rate: $67.20 – $75.20/hr (W-2 only, no C2C)
 Hybrid schedule (50% onsite Tue–Thu; full onsite during the first month) 
 12-month contract with possible extension 
 Health benefits, holiday pay, and 401(k) program 
 Paid time off (UTO) and professional development support 
 Employee referral bonus program 
 Opportunity to contribute to high-impact projects with a leading biopharma company

Scientist - GMP Quality & Technical Writing (Hybrid, Devens MA)

<h3>Job Description</h3>
The Dimensional Inspection Technician helps measure and inspect material and supports calibration activities for the organization working closely with our engineering teams General Responsibilities 
<ul>\n
<li>Interprets mechanical prints.</li>
\n
<li>Collects data and conveys tests results to stakeholders</li>
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<li>Document and record data in accordance with lab procedures.</li>
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<li>Prepares technical reports with recommendations for solutions to technical problems.</li>
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<li>Performs precise calibrations and preventative corrective maintenance on measuring and test equipment and tools.</li>
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<li>Develops calibration operating procedures and documentation for all instruments.</li>
\n
<li>Identify and perform preventative maintenance on equipment.</li>
\n
<li>Perform preventative maintenance on equipment.</li>
\n</ul>
\n Experience / Qualifications 
<ul>\n
<li>Relevant work experience or knowledge of the role</li>
\n
<li>Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands</li>
\n
<li>Strong organization, planning and time management skills to achieve results</li>
\n
<li>Holds self-accountable to achieving goals and standards</li>
\n
<li>Proficient in Microsoft Office programs (Outlook, Word, PowerPoint, and Excel)</li>
\n</ul>
\n Dimensional Inspection activities include: 
<ul>\n
<li>Mechanical print reading and GD&amp;T interpretation</li>
\n
<li>CMM program development</li>
\n
<li>3D Laser scanning</li>
\n
<li>Hand tool measurement</li>
\n
<li>Data collection and reporting</li>
\n</ul>
\n Calibration activities include: 
<ul>
<li>Process various internal calibrations for Sensata in accordance with documented procedures. Calibration parameters include:</li>
</ul>
\n 
<ul>
<li>
<ul>\n
<li>Resistance</li>
\n
<li>Current</li>
\n
<li>Voltage</li>
\n
<li>Pressure</li>
\n
<li>Temperature</li>
\n
<li>Force</li>
\n
<li>Dimensional</li>
\n
<li>Other</li>
\n</ul>
</li>
</ul>
\n 
<ul>\n
<li>Document and record data in accordance with lab procedures</li>
\n
<li>Communicate with equipment owners &amp; requesters to convey test results and to collect/process equipment</li>
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<li>Write and update test procedures</li>
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<li>Identify and perform preventative maintenance on equipment</li>
\n
<li>Identify and execute process and equipment improvement opportunities to drive lab efficiencies</li>
\n</ul>
\n #LI-MY1 #LI-Onsite Hourly Base Pay Range: $28.00 - $38.50 At Sensata, our employees are the key to our success and growth. We recognize that each individual brings their own unique experience, therefore the base salary range information shown above is a general guideline only. Sensata considers several factors when extending an offer, including, but not limited to, a candidate's experience and qualifications, as well as internal equity, market and business considerations. In addition to base salary, Sensata offers competitive medical, dental, vision, life and disability insurance plans, along with education reimbursement, wellness programs, a 401(k) retirement plan with Company matching, and a variety of paid time off, such as vacation or flex-time, sick, bereavement, and parental leave. SmarterTogether 
<ul>\n
<li>Collaborating at Sensata means working with some of the world's most talented people in an enriching environment that is constantly pushing towards the next best thing</li>
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<li>Employees work across functions, countries and cultures gaining new perspectives through mutual respect and open communication</li>
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<li>As OneSensata, we are working together to make things work together</li>
\n</ul>
\n Click here to view Sensata Recruitment Privacy Statement Click here to view our Sensata Recruitment Privacy Statement for China NOTE: If you are a current Sensata employee (or one of our Affiliates), please back out of this application and log into Workday via the Company Intranet to apply directly. Type "FIND JOBS" in the Workday search bar.

Dimensional & Metrology Lab Specialist

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Analytical Chemist – Method Development &amp; Validation
Location:&nbsp;Tewkesbury, MA
Employment Type:&nbsp;Full Time - Permanent 
Experience Level:&nbsp;Intermediate
Overview:
We are seeking a highly skilled&nbsp;Analytical Chemist&nbsp;to join our team in supporting the development, validation, and implementation of analytical methods for pharmaceutical products. This role involves hands-on testing using advanced instrumentation, troubleshooting analytical issues, and ensuring compliance with GMP standards. The ideal candidate will have a strong experience in analytical chemistry and experience with a wide range of techniques and equipment.
Key Responsibilities:
<ul>
<li>Develop and optimize new analytical methods and techniques for product release.</li>
<li>Validate and verify analytical methods in accordance with regulatory and internal standards.</li>
<li>Investigate out-of-specification (OOS) results, out-of-trend (OOT) data, and equipment failures.</li>
<li>Analyze and present trending data to support method development and validation efforts.</li>
<li>Perform analytical testing of organic and inorganic compounds using FTIR, HPLC, NMR, LCMS, GCMS, ICP-MS, GC, and wet chemistry techniques.</li>
<li>Author test procedures and provide analytical support for research and development projects.</li>
<li>Follow GMP guidelines and contribute to continuous improvement initiatives.</li>
<li>Train and mentor junior team members as needed.</li>
</ul>
Required Skills &amp; Expertise:
<ul>
<li>Strong proficiency in analytical techniques including NMR, GCMS, HPLC, FTIR, LCMS, ICP-MS, and wet chemistry.</li>
<li>Deep understanding of GMP regulations and quality systems.</li>
<li>Experience conducting method development, validation, and troubleshooting.</li>
<li>Ability to work independently and collaboratively in a fast-paced environment.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree (MS) in Chemistry or Biochemistry with 3–5 years of relevant experience, or</li>
<li>Bachelor’s degree (BS) in Chemistry or Biochemistry with 5–7 years of experience.</li>
<li>Proven experience working with advanced analytical instrumentation in a pharmaceutical setting.</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
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 12, 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.

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