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job_organization_name

city

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<h3>Job Description</h3>
Job Description
R&amp;D Scientist I
INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!
Job Description
We are seeking a dedicated Lab Technician to conduct chemical and physical analyses in support of the development of manufacturable multisource pharmaceutical products. The role involves providing analytical support for the release of registration materials in support of regulatory submissions, assisting in analytical method validation, and transfer activities.
Responsibilities
<ul>
<li>Prepare samples, perform standard weighing, dilutions, wet chemistry, titrations, and operate HPLC and NGI equipment.</li>
<li>Conduct admitted dose analyses.</li>
<li>Support product development, registration lot release, and pre and post regulatory submission activities.</li>
<li>Perform analytical tasks within assigned timelines and in compliance with cGXP's and company practices.</li>
<li>Follow work instructions, SOPs, and company practices while documenting analytical activities accurately and in a timely manner.</li>
<li>Identify execution challenges of analytical methods and support troubleshooting activities.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in sample preparation, chemistry, biochemistry, wet chemistry, titration, and dilutions.</li>
<li>Experience in physical and chemical testing of organic materials.</li>
<li>Ability to work in a team environment and handle multiple tasks in a fast-paced setting.</li>
<li>Good written and verbal communication skills.</li>
<li>Capability to work under supervision using scientific judgment and professional competency.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS in Chemistry or related field; entry-level graduates with lab experience from school are welcome.</li>
<li>Lab experience outside of academia is strongly preferred.</li>
<li>Experience with data acquisition software is desirable.</li>
</ul>
Work Environment
The team consists of Scientist I's, II's, and III's working collaboratively to accomplish tasks. The position is based in a state-of-the-art lab within a very clean GMP environment. The dress code is business casual, and the work schedule is Monday to Friday, 8 a.m. to 4:30 p.m. This role offers ample opportunity for growth within a large pharmaceutical manufacturing company that promotes from within.
Job Type &amp; Location
This is a Contract to Hire position based out of Columbus, OH.
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 Columbus,OH.
Application Deadline
This position is anticipated to close on Jan 24, 2026.
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.

Pharmaceutical R&D Scientist I

<h3>Job Description</h3>
Job Description
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cutting-edge online programs designed to educate future leaders in policy research, human rights, and related disciplines. Our mission is to deliver world-class skill enhancing programs to candidates globally, equipping them with the knowledge and skills to influence policy and drive positive change in their communities.
Applications are invited for Senior Research Fellowship (for candidates enrolled / passed Masters / Doctoral in any discipline).
Program Overview
<ul>
<li>Learn and follow our methodology to draft research paper in one of the researchable areas. (No prior experience in research paper writing is required, Candidates will receive comprehensive mentorship and guidance throughout the process / tenure.) Program Certification fee of Eur498 is applicable. As a Certified Senior Research Fellow is a significant achievement a valuable addition to your CV that can impress future employers, universities, or scholarship committees. It helps set you apart with a unique edge.</li>
</ul>
What You'll Do:
<ul>
<li>Learn and Lead Groundbreaking Research: Know how to Tackle important policy issues and devise groundbreaking solutions.</li>
<li>Collaborate with Experts</li>
<li>Strategic Analysis: Utilize data to create influential policy recommendations.</li>
<li>Publish &amp; Impact: Contribute your findings to esteemed academic and policy publications.</li>
</ul>
Candidate will be choosing one of the researchable research areas for their research.
Research papers produced by candidates will be published with a Digital Object Identifier (DOI), ensuring the work is uniquely identifiable and accessible through our open-source publication portal.
Eligibility Criteria / Who Can Apply:
<ul>
<li>Open to candidates who are currently enrolled in or have completed a Masters or Doctoral program. Candidates enrolled or passed Bachelor degree but not enrolled in Masters are not eligible to apply.</li>
<li>Applicants from all academic disciplines are welcome, including but not limited to Law, Human Rights, International Relations, Management, Political Science, Social Sciences, Engineering, Medicine, Business, and related fields.</li>
<li>Working / non working professionals in any sector are encouraged to apply. This includes lecturers, professors, advocates, medical professionals, journalists, engineers, historians, managers, environmental scientists, government officials, social activists, and those involved in politics or any relevant field.</li>
<li>Candidates must demonstrate the ability to work independently in a virtual environment and effectively meet deadlines.</li>
</ul>
How to Apply
Interested candidates should submit their updated CV.
Shortlisted candidates will be contacted with complete details.
Note: Applicants are advised to submit only one application. Multiple applications for different positions or locations may result in the cancellation of all submitted applications.

(SRFP)-Research Fellow-Senior (Code:EU7255)

<h3>Job Description</h3>
Job Description
About Certified Group
 At Certified Group, we deliver expert solutions and rigorous testing our customers can trust—on time, every time—so the world can have confidence in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification and audit services, Certified Group brings together trusted brands including Food Safety Net Services (FSNS), FSNS Certification &amp; Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc.
We support a wide range of industries, including food &amp; beverage, dietary supplements &amp; NHPs, cosmetics, OTC and personal care products, tobacco, nicotine, cannabis, and hemp.
We are united by a shared culture and core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team—including believing in you.
The Opportunity
 We are seeking a Lab Services Supervisor to play a critical leadership role within our laboratory operations. This position is ideal for a hands-on leader who is passionate about training, quality, and developing high-performing teams.
In this role, you will oversee and deliver laboratory training, mentor staff, and partner closely with management to ensure operational excellence, regulatory compliance, and a positive, professional work environment. 
Key Responsibilities
<ul>
<li>Lead, deliver, and oversee training for new and current laboratory personnel. </li>
<li>Mentor and coach team members, providing ongoing performance feedback and development support. </li>
<li>Evaluate training effectiveness and manage corrective action plans when needed. </li>
<li>Maintain a collaborative, respectful, and safety-focused workplace culture.</li>
<li>Ensure compliance with the FSNS Quality Manual, SOPs, QC standards, and ISO 17025 guidelines. </li>
<li>Conduct internal audits related to training and test performance. </li>
<li>Maintain trainer qualifications and required certifications.</li>
<li>Process samples and perform testing as needed across multiple laboratory areas. </li>
<li>Maintain the ability to perform all functions reporting to the supervisor. </li>
<li>Oversee test results and reporting, including communication of out-of-specification results. </li>
<li>Address client needs in collaboration with the Management Team.</li>
<li>Work closely with Operations and Technical Managers to support lab priorities and schedules. Identify opportunities to improve operational efficiency through effective training. </li>
<li>Stay current with industry trends, scientific literature, and professional development opportunities.</li>
<li>Promote and uphold safety standards for yourself and others. Ensure proper use of PPE and adherence to laboratory safety protocols.</li>
</ul>
Education &amp; Experience
<ul>
<li>Bachelor’s degree in Life Sciences or a related field required. </li>
<li>Master’s degree in Life Sciences or a related field preferred. </li>
<li>Minimum of two years of analytical laboratory experience and at least one year of experience managing or supervising personnel, or an equivalent combination of education and experience. </li>
<li>Familiarity with GMP, OSHA, FDA, BAM, APHA, and Compendium methods is required. </li>
<li>Working knowledge of LIMS and Microsoft Office is required.</li>
</ul>
Skills &amp; Competencies
<ul>
<li>Strong written, verbal, and interpersonal communication skills. </li>
<li>Excellent organizational and time-management abilities. </li>
<li>Critical thinking and independent problem-solving skills. </li>
<li>Ability to interpret written, verbal, and visual instructions. </li>
<li>Comfortable working in a fast-paced, deadline-driven environment.</li>
<li>Ability to lead and supervisor a team.</li>
</ul>
 Sunday -Thursday Sunday shift starting at 10am Monday-Thursday shift starting at 2pm

Laboratory Services Supervisor

<h3>Job Description</h3>
Job Description
Duties:
<ul>
<li>Perform environmental monitoring of cleanrooms</li>
<li>Collect water samples to ensure all sample collected per schedule and tested on time</li>
<li>Perform and review microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden and Plate Reading</li>
<li>Perform and review visual inspection of final product</li>
<li>Data entry and trend data as needed and prepare slides for management</li>
<li>Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures</li>
</ul>
 
Qualifications:
<ul>
<li>&nbsp;AA Degree and 1+ years’ experience in Microbiology lab/Environmental Monitoring OR</li>
<li>HS Degree and 2+ years’ experience in Microbiology lab/Environmental Monitoring </li>
<li>Experience in the application of microbiological techniques such as environmental air monitoring, water testing, surface monitoring</li>
<li>Experience in aseptic techniques and clean room operations</li>
<li>Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs.</li>
<li>Ability to pass vision exam for visual inspection</li>
<li>Knowledge of GMP, SOPs and quality control processes for commercial manufacturing</li>
</ul>
 
Why Choose R&amp;D Partners?
As an employee, you have access to a comprehensive benefits package including:
<ul>
<li>Medical insurance – PPO, HMO &amp; HSA</li>
<li>Dental &amp; Vision insurance</li>
<li>401k plan</li>
<li>Employee Assistance Program</li>
<li>Long-term disability</li>
<li>Weekly payroll</li>
<li>Expense reimbursement</li>
<li>Online timecard approval</li>
</ul>
&nbsp;
Pay Scale:
$48,000 (Dependent on Experience)
&nbsp;
R&amp;D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research &amp; engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
&nbsp;
R&amp;D Partners is an equal-opportunity employer.
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Quality Control Microbiology Tech

<h3>Job Description</h3>
Job Description
 
LABORATORY SUPERVISOR 
Corporate Job Title
Laboratory Supervisor
Reporting Relationships
Laboratory Manager
Position Summary
Assists Management in the responsibility for all day-to-day laboratory operations. Represents the policies, ethics, and culture of the company in a leadership role. Assists and understudies Lab Manager through closely monitoring lab-related customer service, troubleshooting, and problem solving. Supervises and coordinates activities of personnel engaged in performing chemical and physical tests required for quality control of processes and products
Minimum Requirements
• Bachelor’s degree from four-year college or university or Associates degree or equivalent from two-year college or technical school; or a minimum of three years related experience and/or training; or equivalent combination of education and experience. 
• Ability to define problems, collect data, establish facts, and draw valid conclusions. 
• Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Responsibilities
<ul>
<li>Ensures all lab staff has adequate resources to perform all aspects of work required.</li>
<li>Ensures all lab staff are adequately trained to safely perform all required job functions and that competency records are maintained.</li>
<li>Ensures compliance with all corporate policy procedures in the laboratory.</li>
<li>Assists Lab Manager regarding sales, profits, costs and expenses to meet/ exceed budgeted financial expectations for the laboratory.</li>
<li>Provides employee motivation and champions the Quality system, including SQC, Calibrations, Quality Assurance, Training, and Round Robins.</li>
<li>Communicates with lab staff and management to promote empowerment and accountability.</li>
<li>Obtains and maintains an in-depth knowledge of local market requirements.</li>
<li>Understands customer requirements and organizes lab procedures, schedules and staffing to provide for meeting/exceeding same.</li>
<li>Fosters customer confidence in CCC laboratory work.</li>
<li>Supports the ISO certificate(s) and manages corrective/preventive actions.</li>
<li>Reviews local laboratory operations for all aspects of the continuous improvement process.</li>
<li>Recommends measures to improve testing procedures, use of equipment, and needs for new equipment. Conducts research to develop custom procedures as needed, working in conjunction with senior lab management.</li>
<li>Maintains open communication with the Lab Manager.</li>
<li>Represents CCC by appearance and conduct. Behaves ethically at all times; Ensures compliance in all areas</li>
<li>Ensures laboratory practices meet or exceed company policy and industry standards.</li>
<li>Establishes or adjusts work schedules to meet testing requirements and control costs.</li>
<li>Assists with maintaining time, training, calibration, QC and testing records.</li>
<li>Other duties as may be assigned by Lab Management, and/or senior management.</li>
<li>Other job duties as defined.</li>
</ul>
Fitness for Duty – Physical Demands
The physical demands described here represent those that must be met by an employee to successfully perform the essential functions of the Lab Supervisor role within a testing and inspection environment. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
<ul>
<li>Mobility: Must be able to move about laboratory, testing, and field environments for extended periods, including standing and walking for up to 6–8 hours per day.</li>
<li>Lifting &amp; Carrying: Ability to lift, move, and carry laboratory equipment, samples, and materials weighing up to 25–50 pounds occasionally.</li>
<li>Manual Dexterity: Frequent use of hands and fingers required to operate laboratory instruments, computers, and precision tools.</li>
<li>Posture &amp; Movement: Regular bending, stooping, reaching, and kneeling may be required when handling samples, setting up test equipment, or accessing storage areas.</li>
<li>Visual Acuity: Must have close, distance, and color vision adequate to read and interpret instruments, test results, safety labels, and technical documentation.</li>
<li>Hearing &amp; Communication: Must be able to hear equipment alarms, verbal instructions, and environmental sounds in laboratory and industrial settings. Clear verbal communication is essential for supervising staff and ensuring safety compliance.</li>
<li>Environmental Tolerance:</li>
<li>Exposure to laboratory and industrial conditions including noise, dust, chemicals, and temperature variations.</li>
<li>Must be able to wear appropriate personal protective equipment (PPE) such as safety glasses, gloves, lab coats, and occasionally respirators or hearing protection.</li>
</ul>
This document contains Confidential and Proprietary information which is the property of Camin Cargo Control. None of the information contained herein may be disclosed, reproduced, distributed or used without prior written consent from Camin. All rights reserved.
 
 
 4 days on 4 days off (Rotational). 12-hour shifts

Laboratory Supervisor

<h3>Job Description</h3>
Job Description
Our Story
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow.
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program (ESOP) and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage — with medical premiums either paid by Superior or highly subsidized — so you and your family can access great benefits with minimal cost.
You’ll also join a supportive team, where paid training and experienced coworkers help you learn, grow, and succeed from day one.
At SUPERIOR, you get more than a job — you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to success.
What We’re Looking For
We are currently seeking a Chemical Handler to work at our Arnold, MO location.
This role is responsible for:
<ul>
<li>Daily production</li>
<li>Unloading raw materials</li>
<li>Completing paperwork</li>
<li>Maintaining a safe operation</li>
</ul>
Schedule:
<ul>
<li>Full-time, 1st shift</li>
<li>Monday–Friday, 7:30 a.m. – 5:00 p.m.</li>
<li>Additional hours may be required</li>
</ul>
What You’ll Do
You will:
<ul>
<li>Transfer products into and out of pails, drums, and totes using transfer pumps and hoses</li>
<li>Read paperwork with chemical amounts and blending instructions</li>
<li>Pull product samples and submit them to the Lab for quality control</li>
<li>Label containers and secure closures</li>
<li>Inspect, label, store, and prepare products for shipment</li>
<li>Stage, load, and unload pails, drums, and totes</li>
<li>Operate a forklift</li>
<li>Wear required PPE for safety</li>
<li>Keep your work area safe, clean, and orderly</li>
<li>Lift and/or move 55 lbs</li>
<li>Cross-train in areas such as shipping/receiving, bulk handling, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventive maintenance, and yard truck spotting</li>
</ul>
Candidates Should Possess
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Effective verbal and written communication skills to work with co-workers, chemists, administrative staff, delivery personnel, and management</li>
</ul>
What We Offer
At Superior, we take care of our people. Our comprehensive benefits package includes:
<ul>
<li>Medical Insurance – 100% company-paid HDHP or a low-cost PPO option</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>401(k) Retirement Plan</li>
<li>Flexible Spending Accounts (FSA)</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Dental, Vision &amp; Life Insurance</li>
<li>Short-Term &amp; Long-Term Disability (STD &amp; LTD)</li>
<li>Paid Training from day one</li>
</ul>
Join a company that invests in you — personally, professionally, and financially.
EOE including disability/veteran/drug free

Chemical Handler

<h3>Job Description</h3>
Job DescriptionPosition:&amp; Microbiologist&amp; Location:&amp; Hershey, PA 17033&amp; Duration:&amp; 7&amp; Months&amp; &amp; &amp; &amp; &amp; &amp; &amp; &amp; &amp; Job Type:&amp; Temporary Assignment&amp; Work Type:&amp; Onsite&amp; &amp; &amp; &amp; &amp; &amp; &amp; Job Description:&amp; &amp; Primary responsibility- Media Preparation&amp; 
<ul>
<li>Prepare the microbiological media for in-house food testing purposes&amp; </li>
<li>Maintain an inventory and well stocked supply of prepared and commercially available microbiological media formats to support testing.&amp; </li>
<li>Coordinate the destruction of samples after&amp; results&amp; entry&amp; </li>
<li>Maintain&amp; autoclave records related to the preparation and destruction of routine analysis&amp; </li>
</ul>
Support food product sample receiving, analyses&amp; 
<ul>
<li>Microbiological analyses of food ingredients,&amp; finished product, and environmental swabs&amp; </li>
<li>Plating for hygiene indicators and molecular testing for food borne pathogens&amp; </li>
<li>Assist&amp; in sample preparation and receiving as needed&amp; </li>
<li>Microbiological data interpretation and review&amp; </li>
</ul>
Qualifications&amp; 
<ul>
<li>Microbiology experience&amp; needed&amp; for this role.&amp; </li>
<li>Food science a&amp; plus, but&amp; not&amp; required.&amp; &amp; </li>
<li>Microbiology is&amp; most&amp; important skill set.&amp; </li>
</ul>
Education:
<ul>
<li>B.S. in Microbiology, Food Science,&amp; Biology&amp; or related field; and 2-3 food microbiology testing experience.&amp; </li>
<li>In lieu of a&amp; Bachelor's&amp; degree,&amp; candidate&amp; must have 5+ years of food microbiology work experience.&amp; </li>
</ul>

Microbiologist

<h3>Job Description</h3>
Job Description
Leukemia Research Scientist: Tampa, FL
Children's Cancer Research Group Laboratory is looking for a research scientist to direct, plan, supervise and execute laboratory research projects regarding the etiology of acute leukemias. A Ph.D., an appropriate background and experience is required. Must be able to personally perform the laboratory tests.&nbsp; Competitive salary and benefits provided. Resumes ONLY (do not personally deliver a resume. It will not be considered) Please send resume with the required qualifications only to:
<a href="mailto:ctebbi@childrenscancerresearchgroup.org" target="_blank">ctebbi@childrenscancerresearchgroup.org</a>&nbsp;

Leukemia Research Scientist

<h3>Job Description</h3>
Job Description
Biocytogen is seeking highly skilled and motivated scientists to join our antibody discovery team. This role is dedicated to optimizing therapeutic antibody binders from our RenBiologics program, which generates an extensive library of therapeutic antibodies targeting thousands of druggable genes. The successful candidate will utilize advanced antibody engineering techniques to improve binding affinity, specificity, stability, and therapeutic functionality. This work supports the development of antibodies across diverse therapeutic areas, including immuno-oncology, inflammatory and autoimmune diseases, neurology, cardiovascular conditions, and metabolic disorders.

Key Responsibilities
Target Selection and Program Design
•Select and evaluate therapeutic targets with a strong understanding of MOA, druggability, and delivery options.
•Design experimental strategies to advance candidates from Biocytogen’s RenBiologics Antibody Binder/Lead Library toward therapeutic development.
Project Management
•Drive projects by assembling resources, managing timelines, and ensuring alignment with program objectives.
Antibody Engineering and Optimization
•Engineer antibodies to improve affinity, specificity, stability, and manufacturability.
•Optimize antibodies through advanced molecular designs, such as Fc engineering or bispecific formats.
 Lead Evaluation and Development
•Evaluate lead antibodies for binding, function, and developability, ensuring readiness for preclinical development.
Collaboration and Reporting
•Work with discovery, manufacturing, and BD licensing teams to advance and out-license antibody assets.
•Maintain clear documentation and present findings to internal and external stakeholders.

Requirements
•PhD in Biochemistry, Molecular Biology, Immunology, or a related field with 2+ years of relevant experience, or MS with 5+ years of experience in antibody engineering and project management.
•Strong expertise in target biology research, including understanding MOA, druggability, and formulation requirements.
•Proven experience in antibody engineering and optimization, including affinity maturation and stability improvement.
•Demonstrated ability to independently drive projects, assemble resources, and meet critical milestones.
•Excellent collaboration and communication skills for working with cross-functional teams and presenting findings effectively.
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>

BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Scientist/Sr. Scientist-Preclinical Antibody Drug Development

<h3>Job Description</h3>
Job Description
WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job training, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today!&nbsp;
Schedule: Compressed 12hr Shift – Nightshift Pay Rate: $25 - $29 Hourly DOE&nbsp; Location: Hillsboro, OR Position Type:&nbsp;Full Time Benefits: This position is eligible for WGNSTAR’s full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. &nbsp; Principal Duties and Responsibilities:
<ul>
<li>May operate metrology tools including electron microscopes, Focused Ion Beam and additional lab equipment to complete analytical requests in the client lab</li>
<li>May perform tests and sampling to include setup and operation of metrology equipment&nbsp;</li>
<li>Will utilize client software and equipment to complete tasks, support processes and product tracking&nbsp;</li>
<li>May provide reports and results of sampling and experiments&nbsp;</li>
<li>May perform PM, troubleshooting and minor maintenance of lab equipment&nbsp;</li>
</ul>
Requirements:
<ul>
<li>Excellent communication, lab protocol and time management skills&nbsp;</li>
<li>Must support 12hr compressed work week schedule&nbsp;</li>
<li>Familiarity with semiconductor manufacturing environment, processes and equipment&nbsp;</li>
<li>Direct experience using metrology &nbsp;and/or electron microscopy equipment&nbsp;</li>
<li>A.S or B.S. degree in STEM or related scientific fields&nbsp;</li>
</ul>
Physical Effort/Activities: May be required to walk up to 5+miles per day, able to be on feet for 8-10 hrs at a time, ability to&nbsp;bend, twist, push/pull, crouch, kneel in confined spaces, work at heights, on a ladder, and lift up to 50 pounds. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities &amp; Career Development Opportunities.&nbsp;
The people who thrive most at WGNSTAR are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, and adapt quickly to changing environments, while leveraging their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success.&nbsp;
This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position.&nbsp;
 This position is not eligible for visa sponsorship. All applicants must be legally authorized to work in the United States without the need for current or future sponsorship (e.g., H-1B, O-1, etc). Additionally, WGNSTAR does not participate in the STEM OPT extension program for this role. Equal opportunities and Social Governance
WGNSTAR is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.
WGNSTAR places an immense emphasis on equal employment, encourages diversity in the workplace, and applies an open-door policy for inclusion of all employees. Our diversity program encourages people from any gender, background, ethnicity, culture, education, and experience to join the company and more importantly build a career through employee development.
Through our Global wellness programs, WGNSTAR ensures our employees and families have access to a full range of wellness services through our Employee Assistance Program (EAP). In the communities that surround our business operations, we support individual and group sponsorships for local sports and those that are vulnerable in society.
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