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<h3>Job Description</h3>
Title: Business Analyst – Pharma Research IT
Location: Lexington, MA 02421 (Hybrid, flexible depending on work needs)
Duration: 1 year
 
TOP 3 SKILLS:
<ul>
<li>Strong background in business analysis within a pharmaceutical Research environment</li>
<li>Deep understanding of scientific workflows and data management needs</li>
<li>Good knowledge on Research systems such as Electronic Lab Notebooks (ELN), Scientific Data Management Systems (SDMS), and research databases</li>
</ul>

Business Research Analyst

<h3>Job Description</h3>
Job Description
Job Title: Biostatistician
Job Location: Waltham, MA, USA
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: 
Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. As part of our clinical research portfolio, our CorEvitas evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on – now and in the future. Location/Division Specific Information Remote, USA The Biostatistical team uses its’ specialized statistical expertise for performing analyses such as investigating prescribing patterns, comparing effectiveness between treatments, and investigating differences in safety outcomes. #CorEvitas Discover Impactful Work: The Biostatistician will work under the guidance of a Biostatistical Team Lead to complete statistical analysis plans (SAPs) involving complicated longitudinal registry data. The Biostatistician will help to compile appropriate analytic summaries and context for reports and publications. 
<ul>
<li> Query work: We design, analyze and report on research projects, aka queries, with our clients to produce publications for the public domain (e.g. abstracts, posters, podium presentations, manuscripts, etc.) </li>
</ul>
Each query is a team effort with a: 
<ul>
<li> biostatistician lead who designs and leads the potentially complicated analysis</li>
<li>epidemiologist/clinical research manager that coordinates the whole endeavor</li>
<li> clinical epidemiologist who helps with design and frames the overall message</li>
<li> biostatistician analyst who performs the analysis (biostatistician I/II/III)</li>
<li> Pharmacovigilance (PV) work: Through close collaboration with the PV team, we design, analyze and report on long-term post approval safety studies with our pharma clients to provide real-world evidence of safety</li>
<li> Registry work: We work cross-functionally with the Engineering, Clinical Data Management and Project Management teams on all the registry data taking into account client requests from our query and PV work </li>
</ul>
A day in the Life: 
<ul>
<li> Compiles, analyzes and reports statistical data for various projects</li>
<li> Carries out complex statistical analyses with supervision according to a statistical analysis plan</li>
<li> Assists Biostatistical Team Lead in the development of new statistical methodology for measurement and analysis of data</li>
<li> Applies advanced statistical methods, which may include simulation models and other statistical programming as needed</li>
<li> Assesses relevant literature as well as existing data, evaluates the quality of data used in reports and assists with preparation and distribution of periodic reports</li>
<li> Prepares written reports and summarizes data for investigators with minimal supervision.</li>
<li> Makes original contributions to research projects, takes initiative in professional activities and beginning to be more independent in their statistical decision making</li>
<li> Closely collaborates and participates in knowledge sharing with other statistical analysts</li>
<li> Utilizes various database management systems as required </li>
</ul>
Keys to Success: Education Master's degree in Biostatistics, Statistics, Bioinformatics, Mathematics or related field required Experience 
<ul>
<li> Required 3-5 years of applied statistical experience</li>
<li> Preference is given to applications with &gt;2 years of experience with complicated longitudinal datasets and applied advanced statistical methods</li>
<li> Experience with data science techniques including machine learning and associated software a plus </li>
</ul>
Knowledge, Skills, Abilities 
<ul>
<li> Knowledge of statistical software packages such as R, Stata and SAS is required, with preference given to those with in-depth R experience</li>
<li> Must be highly organized and detail-oriented, with excellent time management skills and ability to multi-task</li>
<li> Must possess strong communication and writing skills and be able to work independently and as part of a team </li>
</ul>
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! <a href="http://jobs.thermofisher.com" target="_blank">http://jobs.thermofisher.com</a> Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process. 
<ul>
<li>This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. </li>
</ul>
 
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Biostatistician

<h3>Job Description</h3>
Job Description
We are seeking a Scientist to join our Analytical Method Development team. In this critical role, you will serve as aSubject Matter Expert (SME) in analytical method transfer and validation, supporting the development and quality control of lipid nanoparticles (LNPs). You will also play a key role in continuous improvement initiatives and provide technical leadership in investigations and root cause analyses.
Please note:This role will evenutally need to relocate to North Dakota. Relocation assistance is available.
Key Responsibilities:
<ul>
<li>Act as SME for analytical method transfer and validation.</li>
<li>Support method and process validation activities.</li>
<li>Contribute to QC testing and development for lipid nanoparticles (LNPs).</li>
<li>Lead or support investigations into deviations, OOS results, and CAPAs.</li>
<li>Drive continuous improvement in analytical methodologies and lab practices.</li>
<li>Mentor and support the development of junior scientists.</li>
</ul>
Required Skills &amp; Expertise:
<ul>
<li>Strong background inanalytical chemistry,method development, andquality control.</li>
<li>Hands-on experience withHPLC,capillary electrophoresis,PCR, andprotein assays.</li>
<li>Proficiency inELISA,protein chemistry, and regulatory compliance (e.g., FDA guidelines).</li>
<li>Demonstrated ability to troubleshoot and optimize analytical methods.</li>
</ul>
Qualifications:
<ul>
<li>PhDin a relevant scientific discipline with5+ yearsof experience, or</li>
<li>Master’s degreewith7+ years, or</li>
<li>Bachelor’s degreewith10+ yearsof relevant experience.</li>
<li>Proven experience mentoring junior team members is highly desirable.</li>
</ul>
Work Environment:
<ul>
<li>100% onsiterole, Monday–Friday, 9:00 AM – 5:00 PM.</li>
<li>Individual contributor role with mentoring responsibilities.</li>
<li>Reports to theSr. Manager of Method Validation.</li>
<li>Collaborative team environment with nine scientists.</li>
</ul>
Pay and Benefits
The pay range for this position is $100000.00 - $110000.00/yr.
They will receive health, dental, vision, 401k. They will get holidays and vacation time as well and a yearly bonus of 10%.
Workplace Type
This is a fully onsite position in Waltham,MA.
Application Deadline
This position is anticipated to close on Jul 31, 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.

Senior Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Operator Job Description
Join our team as a Clean Room Operator where you will play a vital role in maintaining a clean room environment. You will be responsible for packing equipment and collaborating with a team to ensure efficient operations.
Responsibilities
<ul>
<li>Operate within a clean room environment, adhering to all safety and cleanliness protocols.</li>
<li>Pack equipment efficiently and accurately.</li>
<li>Collaborate with team members to ensure smooth workflow and operations.</li>
</ul>
Essential Skills
<ul>
<li>Experience in general production, warehouse operations, including pick, pack, load, and unload tasks.</li>
<li>Ability to work effectively in a clean room setting.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Ability to read and write in English.</li>
<li>Physical capability to lift up to 20lbs.</li>
</ul>
Why Work Here?
Employees enjoy long tenure and the opportunity for career progression. This is a contract-to-hire position, offering long-term prospects and the potential for advancement to lead or manage a department.
Work Environment
Work in a clean room environment with a focus on precision and teamwork. The role involves handling equipment in a structured setting, ensuring adherence to safety standards.
Job Type &amp; Location
This is a Contract to Hire position based out of Attleboro Falls, Massachusetts.
Pay and Benefits
The pay range for this position is $18.00 - $18.50/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 Attleboro Falls,MA.
Application Deadline
This position is anticipated to close on Jul 31, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Operator

<h3>Job Description</h3>
Job Description
Description
This position is ideal for someone who thrives in a collaborative environment and is eager to learn, grow, and make meaningful contributions. Prepare biological samples—including cells, tissues, and plasma—for LC-MS analysis Perform protein lysis, immunoprecipitation, enzymatic digestion, filtration, and concentration Design and execute experiments in close collaboration with cross-functional scientists Develop, optimize, and validate analytical methods for protein characterization Analyze and interpret data, documenting results in electronic lab notebooks Present findings and actively contribute to team discussions and troubleshooting Uphold rigorous standards for lab safety, data integrity, and scientific excellence
Skills
lc-ms, cell culture, tissue culture, mass spectrometry, Gmp, data entry, Laboratory
Top Skills Details
lc-ms,cell culture,tissue culture,mass spectrometry
Additional Skills &amp; Qualifications
BS in Chemistry, Biochemistry, or related field + 3–5 years of experience OR MS + 1–3 years of experience Note: This role is not open to fresh graduates or PhD holders Master 2-3 yrs working exp BS 3-5 yrs Strong experience with LC-MS sample preparation workflows Familiarity with proteomics and immunoanalytical techniques Exposure to Parallel Reaction Monitoring (PRM) is a plus Comfortable operating lab equipment and following complex protocols Excellent data organization and communication skills Hands-on role in protein mass spectrometry, supporting innovative research in pharmacokinetics and metabolism. Emphasize LC-MS sample prep as the core skill—candidates with strong experience here are highly valued. PRM and proteomics are preferred but trainable—encourage candidates with LC-MS and immunoassay backgrounds to apply. Designed for BS/MS-level scientists—a great opportunity for those who want to stay hands-on in the lab and deepen their expertise. Not a postdoc or academic transition role—ideal for industry-minded professionals.
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $30.00 - $35.00/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 Andover,MA.
Application Deadline
This position is anticipated to close on Aug 8, 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.

Research Associate

<h3>Job Description</h3>
Job Description
Description
Assembles assigned product parts on assembly line in accordance with production guidelines as well as performs spot checks of products to ensure adherence to approved quality standards.
- Notifies management of product discrepancies or equipment malfunctions.
- Adheres to established company policies and procedures paying special attention to safety regulations.
- Wears personal protective equipment in accordance with training guidelines.
- Performs other related duties as assigned.
Working in a cleanroom environment utilizing a microscope daily to assemble medical devices. 
Skills
Assembly, Cleanroom, Microscope, Hand tool, Production, Medical assembly, Catheter, Medical device, Inspection, Mechanical assembly, Work instruction, Hand dexterity
Top Skills Details
Assembly, Cleanroom, Microscope, Hand tool, Production, Medical assembly, Catheter, Medical device, Inspection
Additional Skills &amp; Qualifications
Written Communication Skills
Physical Dexterity
Reading Skills
Time Management
Mechanical Skills
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $22.00 - $24.00/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 NASHUA,NH.
Application Deadline
This position is anticipated to close on Aug 1, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
???? We’re Growing at Eckert &amp; Ziegler Radiopharma, Inc. – Join Us in Wilmington, MA!
Eckert &amp; Ziegler Radiopharma, Inc. is entering an exciting phase of growth as we build and scale operations to support the future of radiopharmaceuticals. Based in Wilmington, MA, we're hiring across several key functions and looking for mission-driven individuals who thrive in a fast-paced, collaborative environment.
If you're passionate about making a real impact in healthcare — or know someone who might be — we’d love to connect. We’re building something special here at Eckert &amp; Ziegler Radiopharma, Inc., and there’s plenty of opportunity for talented, motivated professionals to grow with us.
Position Summary
We are seeking a Senior QC Microbiologist to lead microbiological testing, environmental monitoring, and contamination control programs in our GMP manufacturing facility. This hands-on role is critical to ensuring product quality and compliance with regulatory requirements for sterile radiopharmaceutical products.
Key Responsibilities
<ul>
<li>Perform microbiological testing including bioburden, endotoxin, sterility, and microbial identification.</li>
<li>Lead and support environmental monitoring (EM) of classified cleanroom spaces.</li>
<li>Assist in the development and execution of site-wide strategies for environmental control, contamination prevention, and sterility assurance.</li>
<li>Review and trend EM data and investigate excursions or out-of-specifications (OOS).</li>
<li>Author and revise SOPs, protocols, and technical reports related to microbiology.</li>
<li>Train and mentor staff on aseptic technique, gowning, and cleanroom behavior.</li>
<li>Support aseptic process simulations (media fills) and cleanroom qualifications.</li>
<li>Participate in internal audits, regulatory inspections, and quality investigations.</li>
<li>Stay current with FDA, EMA, USP, and ICH microbiology guidance and best practices.</li>
<li>Contribute to continuous improvement and regulatory readiness initiatives.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s or Master’s degree in Microbiology, Biology, or related life science field.</li>
<li>6–8+ years of microbiology experience in a cGMP pharmaceutical, biologics, or sterile manufacturing environment.</li>
<li>Strong understanding of aseptic technique, contamination control, and microbiological testing methods.</li>
<li>Familiarity with cleanroom classifications and environmental monitoring programs.</li>
<li>Excellent documentation and communication skills.</li>
<li>Experience supporting audits and regulatory inspections is a plus.</li>
</ul>
Work Schedule &amp; Conditions
• Standard day shift; flexibility for occasional off-hours support. • Must be able to stand for extended periods, lift up to 25 lbs, and gown for cleanroom access.
Why Join Us?
<ul>
<li>Work in a purpose-driven environment focused on innovation and patient impact.</li>
<li>Contribute to high-value, small-batch clinical production.</li>
<li>Be part of a supportive, collaborative team with opportunities for growth.</li>
</ul>

Quality Control Microbiologist

<h3>Job Description</h3>
Job DescriptionJob Title: Sr ScientistJob Description
Join our team as a Sr Scientist, where you will support the Analytical Method Development Team as a Subject Matter Expert. You will be instrumental in test method transfer, analytical test method validation, and driving continuous improvement initiatives. Your expertise will also contribute to test method validation, process validation, and QC testing and development on lipid nanoparticles (LNPs). Additionally, you will support deviations and investigations for Out of Specification (OOS) results, Corrective and Preventive Actions (CAPA), and root cause analysis.
Responsibilities
<ul>
<li>Serve as a Subject Matter Expert for test method transfer and analytical test method validation.</li>
<li>Assist with test method validation and process validation.</li>
<li>Support QC testing and development on lipid nanoparticles (LNPs).</li>
<li>Investigate deviations and support OOS, CAPA, and root cause analysis.</li>
<li>Drive continuous improvements in processes and methodologies.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in method development, analytical chemistry, and quality control.</li>
<li>Experience with HPLC, validation, LNP, and protein assays.</li>
<li>Strong knowledge of analytical method development, protein chemistry, ELISA, capillary electrophoresis, FDA regulations, and PCR.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree with 10+ years of experience, Master's degree with 7+ years of experience, or PhD with 5+ years of experience.</li>
<li>Understanding of HPLC, capillary electrophoresis, and PCR.</li>
<li>Experience mentoring and supporting the development of junior scientists.</li>
</ul>
Work Environment
This role is 100% onsite, operating Monday to Friday from 9:00 am to 5:00 pm. You will be an individual contributor with responsibilities to mentor other scientists, working within a team of nine and reporting directly to the Sr Manager of Method Validation. High degrees of collaboration and communication skills are essential in this dynamic and growth-oriented environment
Pay and Benefits
The pay range for this position is $100000.00 - $110000.00/yr.
They will receive health, dental, vision, 401k. They will get holidays and vacation time as well and a yearly bonus of 10%.
Workplace Type
This is a fully onsite position in Waltham,MA.
Application Deadline
This position is anticipated to close on Jul 31, 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 DescriptionJob Title: Quality Control ChemistJob Description
This position performs routine testing using various chemistry techniques within the pharmaceutical industry. We seek an experienced professional who can make an immediate impact.
Responsibilities
<ul>
<li>Conduct routine testing or other analysis in a specific group or department setting.</li>
<li>Perform advanced or critical testing as required.</li>
<li>Operate specialized equipment or conduct specialized skill testing.</li>
<li>Apply working knowledge of raw materials testing and release.</li>
<li>Utilize instruments such as HPLC, GC, and ICP.</li>
<li>Lead investigation activities.</li>
<li>Ensure compliance with all data integrity and cGMP practices, procedures, and expectations.</li>
<li>Maintain compliance with all good documentation practices.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, GC, ICP, and GC-MS.</li>
<li>Experience in quality control and wet chemistry.</li>
<li>Knowledge of pharmaceutical raw materials and data entry.</li>
<li>Analytical chemistry expertise.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>1-3 years of experience in the industry for Chemist I positions; co-op experience in a cGMP pharmaceutical manufacturing setting is acceptable.</li>
<li>3-5 years of industry experience for Chemist II positions.</li>
</ul>
Work Environment
Work within a small, collaborative team of 15 people in quality, with cross-departmental collaboration. The position operates on the first shift, Monday through Friday, from 8:00 AM to 5:00 PM. The main site for product testing is in Fall River, with a focus on expanding the product line, particularly inhalants.
Relocation Bonus
Up to 6K for relocation bonus offered 
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
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 Fall River,MA.
Application Deadline
This position is anticipated to close on Jul 31, 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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