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job_organization_name

city

state

<h3>Job Description</h3>
Job Description🧼 2nd Shift Cleanroom Technician
Location : Placentia, California
*Espanol esta bien*
Hours: Monday–Friday, 2:00 PM–10:30 PM (overtime available)
Are you reliable, detail-oriented, and looking for steady, hands-on work? Join a leading manufacturer of medical products used in hospitals and healthcare facilities! No specific experience is required — just a good work ethic and some general work experience in any field. We’ll train you.
💪 What You’ll Do:
<ul>
<li>Assemble and package medical products in a cleanroom environment</li>
<li>Inspect products for quality and follow safety procedures</li>
<li>Keep accurate production records</li>
<li>Maintain a clean and organized workspace</li>
<li>Work closely with your team to meet production goals</li>
</ul>
&amp;#x1F31F; What We’re Looking For:
<ul>
<li>Any prior work experience (production, warehouse, retail, etc.)</li>
<li>Ability to lift up to 25 lbs and stay focused on quality</li>
<li>Team player with good communication skills</li>
<li>Comfortable following detailed instructions and cleanliness standards</li>
</ul>
💵 Why You’ll Love It:
<ul>
<li>Contract-to-hire – opportunity for permanent employment after 4 months</li>
<li>Full benefits (medical, dental, vision) once hired</li>
<li>Clean, friendly, small-team environment (only 4 people per room)</li>
<li>Growth and leadership opportunities for motivated employees</li>
</ul>
Join a team that helps make medical care safer and better every day!
👉 Apply today — no special experience needed, just a willingness to learn!
Job Type &amp; Location
This is a Contract to Hire position based out of Placentia, CA.
Pay and Benefits
The pay range for this position is $17.50 - $17.50/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 Placentia,CA.
Application Deadline
This position is anticipated to close on Nov 21, 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.

2nd Shift Cleanroom Tech (Entrylevel)

<h3>Job Description</h3>
Job DescriptionQC Analytical Chemist- Torrance, California&nbsp; Rate: $32.00 to $35.00 Analyzes Raw Materials, In-Process Samples and Finished Goods Includes the following: Other duties may be assigned.
<ul>
<li>Analyzes compounds to determine chemical and physical properties.</li>
<li>Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples.</li>
<li>Monitor and trend QC data results </li>
<li>Follows established procedures and documents all findings and results timely, concisely, clearly and accurately.</li>
<li>Prepares standards and specifications for processes, facilities, products, and tests.</li>
<li>Measures products for compliance to standards and specifications and reports same.</li>
<li>Provide updates/escalations at daily and weekly site-specific and cross-site meetings. </li>
<li>Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations</li>
<li>Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration assays, FTIR) in cosmetic and OTC manufacturing environment to support QC testing, data reviews, &amp; COA generation to support testing and release.</li>
<li>Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211). Knowledge of regulatory requirements for data integrity and practices. </li>
<li>Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits</li>
<li>Assessment of GMP systems currently in place to ensure compliance.</li>
<li>Proficiency in MS Word, Excel, Power Point and other applications</li>
<li>Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment</li>
<li>Works with development of formulas, processes, and methods for solution of technical problems.</li>
<li>Provides input to the development of procedures.</li>
<li>Strives toward continuous self-improvement in personal productivity.</li>
<li>Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities</li>
<li>A minimum of 3 years’ experience and BS or BA. </li>
</ul>
Preferred:
<ul>
<li>Demonstrated leadership and management skills, including establishing direction and goals, and building good work ethics for the team</li>
<li>Supervising/managing experience.</li>
<li>Experience with microbiological testing methods.</li>
</ul>
What we’re offering: ●Competitive compensation package. ●Health, dental, and vision benefits. ●401K program. ●The spirit of a startup with the security of an established, profitable industry leader. ●The opportunity to make waves in a $250B industry. At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer. &nbsp;
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QC Analytical Chemist- Torrance, California

<h3>Job Description</h3>
Job Description
QC Scientist – Weekend Shift 
📍 Location: St. Louis, MO, USA
🧪 Department: Quality Control – Analytical Team
🕒 Schedule: Friday to Monday | 4x10 Hour Shifts | Flexible Start Times (7 AM–5 PM or 8 AM–6 PM)
Why Join Us?
Be part of a growing, innovative team at the forefront of pharmaceutical quality control. As a QC Scientist, you’ll play a vital role in ensuring the safety and efficacy of life-changing biologic products. This is a unique opportunity to join a newly formed weekend team, receive comprehensive training, and contribute to meaningful work in a collaborative, fast-paced environment.
What You’ll Do
As a QC Scientist, you’ll work hands-on in a state-of-the-art laboratory, performing advanced analytical testing to support GMP manufacturing. Your responsibilities will include:
<ul>
<li>Conducting analytical tests using HPLC, UPLC, CGE, iCE, Cell-Based Assays, and Compendial Testing (pH, UV, Osmolality, Appearance).</li>
<li>Supporting commercial product testing, stability studies, and client-driven projects.</li>
<li>Reviewing laboratory data packets and authoring investigations.</li>
<li>Collaborating with cross-functional teams including Quality Assurance and Data Review.</li>
<li>Ensuring compliance with GMP standards, SOPs, and safety protocols.</li>
<li>Participating in lab operations such as safety inspections and inventory management.</li>
</ul>
What You Bring
<ul>
<li>Education: Bachelor’s degree in Chemical Pharmaceutical, Biology, Chemistry, Biotechnology, or a related field.</li>
<li>Experience: 1–5 years in a GMP-regulated environment, preferably in pharmaceuticals.</li>
<li>Hands-on experience with analytical instruments and techniques: HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, Cell-Based Bioassays.</li>
<li>Familiarity with EMPOWER, MS Office, and laboratory software.</li>
<li>Strong organizational skills, attention to detail, and a collaborative mindset.</li>
</ul>
Training &amp; Team Environment
You’ll be part of a tight-knit team of 6 Scientists and 1 Supervisor, supported by a larger QC Analytical group of 80+ professionals. Expect 3–6 months of structured training, with hands-on testing and mentorship before transitioning to weekend operations
Job Type &amp; Location
This is a Contract to Hire position based out of Jennings, MO.
Pay and Benefits
The pay range for this position is $28.00 - $38.00/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 Jennings,MO.
Application Deadline
This position is anticipated to close on Nov 20, 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 Chemist

<h3>Job Description</h3>
Job DescriptionIrvine Clinical Research, a research site specializing in late phase clinical trials in Mild Cognitive Impairment, Alzheimer’s Disease, and Depression, is seeking applicants for a Research Assistant. They will provide administrative support to our team of physicians, psychologists, and research coordinators. This position is designed for an ambitious individual who is willing to start at an entry-level role and work their way up quickly.Job Duties
<ul>
<li>Warmly greet and assist study participants at the front and back office, especially older adults</li>
<li>Coordinate and troubleshoot scheduling for participant visits</li>
<li>Learn complex research protocols quickly and assist with data entry and quality</li>
<li>Assist doctors, clinicians, and research coordinators with study participant visits as needed</li>
<li>Provide clerical and administrative support</li>
</ul>
Job Requirements
<ul>
<li>Excellent communication and social skills in spoken and written English</li>
<li>Attention to detail and the ability to handle multiple tasks with precision</li>
<li>Willingness to commit to at least 2 years of growth and development</li>
</ul>
This is a full-time employment position based in-person at our clinic in the Alzheimer’s Orange County building in Irvine. The starting salary for this position is approximately $23/hr (approximately $47,480 per year). Depending on job performance, there is a possibility for growth. The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Research Assistant

<h3>Job Description</h3>
Job Description
Job Title: Chemical Operator
Job Description
As a Chemical Operator, you will be responsible for performing kettle and holding tank washouts compliant with departmental and formula requirements. You will record raw material details, including lot and batch numbers, and ensure all paperwork and container labels are accurately completed. Additionally, you will submit samples for quality control testing and approval, ensuring formula batches meet the specified requirements.
Responsibilities
<ul>
<li>Follow Production Order Instructions and processes to ensure formula batches meet required specifications.</li>
<li>Safely use tools such as pumps, hoses, transfer lines, and valves to transfer raw materials and formulas.</li>
<li>Lift up to 50 pounds regularly and wear all applicable PPE while adhering to the Production Floor Employee Dress Code.</li>
<li>Execute housekeeping tasks in Compounding work areas to maintain a safe and clean environment.</li>
<li>Replace and maintain hoses, gaskets, and connectors for safe material transfer.</li>
<li>Assist in troubleshooting transfer pumps.</li>
<li>Operate a forklift and/or pallet jack as needed.</li>
</ul>
Essential Skills
<ul>
<li>Attention to detail</li>
<li>Adherence to all safety procedures</li>
<li>Knowledge of manufacturing and production processes</li>
<li>Chemical mixing and compounding</li>
<li>Batch making</li>
<li>Forklift operation</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Chemical experience preferred</li>
<li>Basic math, reading, and writing skills</li>
</ul>
Why Work Here?
Enjoy comprehensive health, dental, and vision benefits, a 401K with matching contributions, and a Health Savings Account contribution. Experience a supportive family culture with room for growth, as many supervisors began as production workers. Additionally, you will receive paid time off and vacation time to maintain a healthy work-life balance.
Work Environment
The work environment is a clean and well-lit chemical setting, where safety is a priority and attention to detail is essential. Employees adhere to a dress code and utilize PPE to ensure safety and compliance.
Job Type &amp; Location
This is a Contract to Hire position based out of Cartersville, Georgia.
Job Type &amp; Location
This is a Contract to Hire position based out of Cartersville, GA.
Pay and Benefits
The pay range for this position is $24.00 - $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 Cartersville,GA.
Application Deadline
This position is anticipated to close on Nov 21, 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.

Chemical Operator

<h3>Job Description</h3>
Job Description
 This is a position within Keller Executive Search and not with one of its clients. This senior position will lead AI &amp; Innovation for Keller Executive Search in Albuquerque, NM, United States, shaping strategy, building scalable processes, and partnering across the firm to deliver measurable impact. Key Responsibilities: - Define the AI &amp; Innovation vision, roadmap, and annual operating plan aligned to business goals. - Build and lead a high‑performing AI &amp; Innovation team; set clear objectives and coach managers. - Own AI &amp; Innovation KPIs and reporting; drive continuous improvement and operational excellence. - Establish scalable policies, processes, and tooling for AI &amp; Innovation across regions. - Partner with executive leadership and cross‑functional stakeholders to deliver outcomes. - Manage budgets, vendors, and risk within the AI &amp; Innovation portfolio. 
Requirements
 - 7+ years of progressive experience in AI &amp; Innovation with 4+ years leading managers. - Proven track record building programs at regional or global scale. - Strong analytical skills; ability to translate data into decisions. - Excellent communication and stakeholder‑management skills. - Bachelor’s degree required; advanced degree or relevant certification preferred. - Experience in professional services or recruitment industry is an advantage.
Benefits
 - Salary range: $215,000–$270,000 USD - Opportunities for professional growth. - Company culture: Flat management structure with direct access to decision-makers. Open communication environment. 
Equal Employment Opportunity Statement: Keller Executive Search provides equal employment opportunities to all qualified applicants and employees. Employment decisions are based on merit, qualifications, and business needs, without regard to protected characteristics under applicable law. Commitment to Diversity: An inclusive and equitable workplace is actively fostered. Hiring, development, and advancement practices are designed to broaden representation and ensure fair access to opportunity. Data Protection and Privacy: Personal data is processed solely for recruitment and employment purposes, in accordance with applicable data‑protection laws (including GDPR where relevant). Information may be retained for compliance and legitimate interests, subject to data minimization and security controls. Pay Equity: Compensation practices are reviewed to support pay equity for substantially similar work, accounting for bona fide factors such as experience, education, and performance. Health and Safety: Workplace health and safety obligations are observed in line with applicable national and local requirements. Employees are expected to follow all safety policies and promptly report hazards. Compliance with Law: All recruitment, selection, and employment practices are conducted in compliance with applicable laws and regulations in the jurisdiction of employment.
Note: This job posting may be for a position with Keller Executive Search or one of our clients. The specific employer will be identified during the application and interview process. Employment laws and requirements may vary depending on the employer and location.

Senior AI & Innovation Manager

<h3>Job Description</h3>
Job DescriptionGlobal Strategy Group (GSG) works at the intersection of business, politics, and causes. Our team is made up of a great group of professionals who come from various backgrounds in strategic communications, research, and public affairs. Our culture and values play an integral role in how we operate, and we work hard to bring passion, energy, and drive to everything we do! Global Strategy Group is the go-to public affairs, communications, and research partner for brands, causes, and campaigns. We work with our clients to build their reputation, tackle big challenges, and win.&nbsp;We are seeking a Director to join our Insights research team. This role focuses on consumer insights, corporate, and market research—- helping brands define the optimal positioning, strengthen their reputation, guide public affairs initiatives, and craft compelling messages that resonate with key stakeholders.&nbsp;Qualified candidates must have experience managing quantitative (surveys) and qualitative (focus groups and online discussion boards) research projects from beginning to end. Ideal candidates will thrive in a fast-paced, deadline-oriented environment, and enjoy driving projects forward every step of the wayResponsibilities
<ul>
<li>Manage qualitative and quantitative research projects from beginning to end with full accountability for the success of the project. </li>
<li>Conceptualize and produce client-ready survey questionnaires and qualitative research screeners and guides that require minimal edits from account lead.</li>
<li>Conceptualize and produce analyses of research projects – both written analyses and visual PowerPoint presentations that require minimal edits from account lead. </li>
<li>Provide insights and strategy to clients with a strong strategic voice. </li>
<li>Ability to manage projects and client relationships independently with minimal oversight from account lead. This includes successfully manage day-to-day needs and expectations, including responding to clients in a timely fashion, anticipating client needs, and regularly updating clients. </li>
<li>Moderate qualitative research engagements, including in-depth interviews, focus groups, and online discussion boards.</li>
<li>Oversee and coordinate research projects by actively keeping track of project details, organizing tasks, and keeping team's adherence to timelines without prompting.</li>
<li> Responsible for overseeing project fielding, i.e., review partials, provide edits, discuss weighting targets with data team, actively troubleshoot project fielding issues.</li>
<li>Responsible for training, managing, and overseeing junior staff on the execution of projects. Must exhibit basic supervisory skills of any direct reports to manage their work and professional development, with guidance.</li>
<li> Lead the development of new business proposals, including producing, editing, and delivering presentations with senior staff oversight and guidance.</li>
<li>·Conceptualize and develop research designs and methodological approaches for new business in order to meet client research objectives.</li>
</ul>
Qualifications
<ul>
<li>6-8 years of experience in primary research. Experience in market research methodologies and consumer insights is valuable, though the primary focus for this role will be on corporate reputation and public affairs research.</li>
<li>Experience in executing every stage of a research project – both quantitative and qualitative.&nbsp; </li>
<li> Excellent project management and organizational skills.</li>
<li>A proven ability to successfully juggle multiple projects.</li>
<li>Ability to work efficiently and quickly produce high-quality work products.</li>
<li>Experience with the new business process (i.e., writing proposals and producing pitch decks, developing methodologies and research programs, etc.).</li>
<li>Experience with client-facing responsibilities, including leading client engagements. </li>
<li>Strong Presentation skills</li>
<li>Excellent communication and writing skills.</li>
<li>Experience with moderating in-depth interviews and online discussion boards, moderating focus groups a plus.</li>
<li>Strong analytical skills – going beyond descriptive findings to tell a story with actionable recommendations.</li>
<li>Team player with the ability to collaborate and maintain strong working relationships.</li>
<li>Ability to mentor, train, and manage entry-level employees.</li>
<li>Strong attention to detail and experience with catching mistakes and being detail oriented. </li>
<li>Expertise with Microsoft Office Suite (PowerPoint, Excel Word).</li>
<li>Experience/coursework with statistics and advanced quantitative methods, a plus.</li>
</ul>
The base salary for this position is between $ 110,000- $120,000 commensurate with experience plus eligibility of a discretionary bonus. GSG provides a comprehensive benefits package including excellent coverage for medical, vision, and dental insurance; paid parental leave; generous time off and holidays; 401k with employer match; and additional benefits.&nbsp;&nbsp;If this sounds like an opportunity for you, please send your information our way!&nbsp;When submitting your resume, please include a cover letter which highlights your relevant experience, along with why you want to be part of the team at GSG. We are interested in candidates who align with our mission and want to contribute to our continued growth. &nbsp;Candidates who match the needs for the position will be contacted via email.&nbsp;If you are an individual with a disability and would like to request a reasonable accommodation to complete your online application or participate in the interview process, please reach out to <a href="mailto:hr@globalstrategygroup.com" target="_blank">hr@globalstrategygroup.com</a> or you may call (212) 260-8813 and ask to speak to someone in Human Resources – Talent Acquisition. &nbsp;&nbsp;Global Strategy Group, LLC.Global Strategy Group (GSG) is a full-service research, public affairs, and communications agency tackling some of today’s most complex and important challenges. With more than two and half decades of experience and a team of 150+ talented professionals, we protect and build corporate reputations, influence public affairs decision makers, advocate on important social issues, and win campaigns. We combine unparalleled subject matter expertise with data-driven insights and innovative methodologies to generate urgency among stakeholders and key audiences, delivering tangible success for our clients.&nbsp; &nbsp;Global Strategy Group is an Equal Opportunity Employer. &nbsp;At GSG, we are distinguished by our depth of talent. Our people are team players, straight shooters, and problem solvers. We bring passion, energy, and drive to everything we do. This all comes from our closely held firm values, which have guided us since the day GSG opened its doors. We are committed to ensuring that our workplace provides a diverse, inclusive, and culturally rich atmosphere and are always looking for talented individuals to add to our culture. &nbsp;We do not discriminate against any applicant for employment on any legally recognized basis including, but not limited to: race, religion or creed, color, national origin, sex, age, disability, marital status, sexual orientation, genetic information, citizenship status, veteran status, uniform service member status, or any other protected class under federal, state or local statute.&nbsp;&nbsp;&nbsp;
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Director, Research (Insights)

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical Production Compounder
Job Description
We are seeking a skilled Chemical Compounding Operator to produce batches of coatings and paints. You will follow Batch Tickets to ensure products meet customer and company specifications.
Responsibilities
<ul>
<li>Produce batches of coatings and paints according to specifications.</li>
<li>Follow Batch Ticket instructions to ensure quality and accuracy.</li>
<li>Engage in chemical mixing, blending, and compounding processes.</li>
<li>Maintain accurate Batch records and adhere to GMP standards.</li>
</ul>
Essential Skills
<ul>
<li>Experience in batching, blending, or manufacturing of liquid-based products.</li>
<li>Ability to follow detailed Batch Ticket instructions.</li>
<li>Positive attendance record.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with chemical operation and manufacturing.</li>
<li>Skills in batch mixing and chemical blending.</li>
</ul>
Work Environment
The position offers a dynamic work environment with opportunities for voluntary overtime, allowing employees to work up to 80 hours a week if desired. Shifts available are 1st Shift from Monday to Friday, 6 a.m. to 2 p.m., and 2nd Shift from Monday to Friday, 2 p.m. to 10 p.m. Training for all shifts will occur from 6:30 a.m. to 2:30 p.m. for one week. Employees can enjoy almost unlimited overtime for those eager to maximize their hours.
Job Type &amp; Location
This is a Contract to Hire position based out of Appleton, WI.
Pay and Benefits
The pay range for this position is $17.75 - $23.75/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 Appleton,WI.
Application Deadline
This position is anticipated to close on Nov 14, 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.

Compounder

<h3>Job Description</h3>
Job Description
Quality Control Associate II (Microbiology | cGMP Lab)
 Location: Norwood, MA 02062 (Onsite – Not Remote) Schedule: Monday–Friday, 9:00 AM–5:00 PM Duration: 6-Month Contract | Target Dates: December 4, 2025 – June 5, 2026 Pay Rate: $50.00 per hour 
About the Role
We’re seeking an experienced and detail-oriented Quality Control Associate II to support cGMP QC microbiology testing and quality systems activities at our state-of-the-art manufacturing site in Norwood, MA.
In this role, you’ll perform routine QC testing for raw materials, drug substances, and finished products, while ensuring compliance with Good Manufacturing Practices (cGMP) and internal quality standards. You’ll work hands-on in a dynamic, fast-paced environment, collaborating with cross-functional teams to uphold quality and operational excellence.Why Join
<ul>
<li>
Opportunity to work in a cutting-edge biotech environment supporting life-changing therapeutics.
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Exposure to advanced QC systems and global quality standards.
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Be part of a passionate, mission-driven team committed to scientific excellence and patient impact.
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</ul>
✅ Ready to take the next step in your quality control career?Apply now to join a world-class organization where your skills will directly contribute to improving global health.FOR MORE IMMEDIATE CONSIDERATION, email a current resume to <a href="mailto:iris.levy@randstadusa.com" target="_blank">iris.levy@randstadusa.com</a>
salary: $49 - $50 per hour shift: First work hours: 9 AM - 5 PM education: Bachelors 
Responsibilities
Key Responsibilities
<ul>
<li>
Perform QC microbiology testing, including bioburden, endotoxin, sterility, TOC, and microbial enumeration.
</li>
<li>
Maintain, calibrate, and troubleshoot laboratory equipment.
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Manage QC laboratory supplies and inventory.
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Author, review, and revise SOPs, protocols, and technical reports.
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Participate in deviations, CAPAs, change controls, and non-conformance investigations.
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<li>
Support audit readiness and continuous improvement initiatives.
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<li>
Ensure strict adherence to cGMP documentation practices and regulatory requirements.
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Maintain a clean, organized, and safe laboratory environment.
</li>
</ul>
Qualifications
Education: Bachelor’s degree in a STEM discipline (Biology, Microbiology, Chemistry, or related field). Experience: 2–3 years of hands-on experience in a cGMP laboratory, preferably in microbiology or biopharma QC.
Preferred Skills &amp; Competencies:
<ul>
<li>
Proficiency in Microsoft Office and electronic systems (LIMS, SAP, eQMS).
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Strong understanding of GMP, aseptic technique, and laboratory instrumentation.
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Knowledge of FDA, EU, and ICH regulatory guidelines.
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Excellent troubleshooting, organization, and communication skills.
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Ability to manage multiple projects in a fast-paced, collaborative environment.
</li>
</ul>
 Skills
<ul>
<li>cGMP (2 years of experience is required)</li>
<li>Microbiology (4 years of experience is required)</li>
<li>Quality Assurance</li>
<li>Quality Control</li>
<li>raw materials</li>
<li>laboratory (4 years of experience is required)</li>
 Qualifications
<li>Years of experience: 4 years</li>
<li>Experience level: Experienced</li>
 Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 
 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. 
</ul>

QC Associate II - Microbiology - cGMP Lab

<h3>Job Description</h3>
Job Description
Job Description
The role involves ensuring adherence to lab safety guidelines, creating and updating Standard Operating Procedures (SOPs), and collaborating with production to test all incoming raw materials.
Responsibilities
<ul>
<li>Adhere strictly to laboratory safety protocols and regulatory compliance standards.</li>
<li>Develop, revise, and maintain Standard Operating Procedures (SOPs) to ensure consistency and quality in laboratory practices.</li>
<li>Collaborate cross-functionally with the production team to conduct comprehensive testing of all incoming raw materials.</li>
<li>Perform routine microbiological analyses, including detection of bacteria, yeast, and mold, as well as identity verification using Fourier-transform infrared spectroscopy (FTIR).</li>
<li>Ensure accurate and thorough documentation of all laboratory procedures, test results, and quality control activities.</li>
<li>Communicate clearly and effectively with team members and other departments to support operational efficiency and continuous improvement.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's Degree in Biology or Microbiology </li>
<li>Experience with Good Manufacturing Practices (GMP).</li>
<li>Proficiency with FTIR testing.</li>
<li>Ability to create and write SOPs.</li>
<li>Experience in microbiology testing, including bacteria, yeast, mold, and identity testing using FTIR.</li>
</ul>
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
Diversity, Equity &amp; Inclusion
At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&amp;I Are Embedded Into Our Culture Through:
<ul>
<li>Hiring diverse talent</li>
<li>Maintaining an inclusive environment through persistent self-reflection</li>
<li>Building a culture of care, engagement, and recognition with clear outcomes</li>
<li>Ensuring growth opportunities for our people</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Mundelein, IL.
Pay and Benefits
The pay range for this position is $20.00 - $26.00/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 Mundelein,IL.
Application Deadline
This position is anticipated to close on Nov 14, 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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