field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Location: Oceanside, CA 92056 Duration: 5 months+ (Possible Extension) Pay Rate: $42.00 - $48.50/Hour. on W2 Hours: Monday – Friday, 8 am – 5 pm Essential Duties and Job Functions:
<ul>
<li>Under general supervision, develops and validates bioassays to support biological drug development.</li>
<li>Plans and executes assigned experiments that support Process Development activities and project goals.</li>
<li>Proactively seeks out senior personnel to discuss potential solutions to problems.</li>
<li>Participates in group meetings to share test results.</li>
<li>Demonstrates ability to recognize anomalous and inconsistent results and interpret experimental outcomes.</li>
<li>Develops skills in data analysis and ability to evaluate quality of data.</li>
<li>Operates scientific equipment (Plate reader and Softmax software for ELISA, cell culture techniques), selects appropriate methods and techniques to perform experiments, and prepare related reports</li>
<li>Plans and organizes details of experiments with guidance.</li>
<li>Demonstrates good verbal communication skills and interpersonal skills to provide insight into the processes used to achieve results of assigned tasks.</li>
<li>Be able to work in a fast-paced and highly collaborative working environment.</li>
<li>Must have basic understanding of ELISA and cell based assays.</li>
<li>Responsible for data analysis using SoftMax Pro software and graphic display of data using Excel and Power Point presentation formats.</li>
</ul>
 Academic Level: BSc or MSc Knowledge, Experience and Skills:
<ul>
<li>2+ years of experience with BS degree in a relevant scientific discipline.</li>
<li>1+ years of experience with MS degree in a relevant scientific discipline.</li>
</ul>
 #sczr2

Research Associate

<h3>Job Description</h3>
Job Description
Stability. Innovation. Industry Leader - We are Silgan.
We are proud to be an essential part of the world’s food supply chain and are looking for team members who will take this job as seriously as we do! Now hiring for a Coatings Scientist in our Downers Grove, IL office. – Apply now!
**What we offer you:
**
<ul>
<li>
Opportunity to work with leading coating manufacturers to develop and specify products.
</li>
<li>
Opportunity to see your work in use at your local grocery store.
</li>
<li>
A great manufacturing and team culture.
</li>
<li>
Competitive salary based on experience. Salary range $105k - $115k.
</li>
<li>
Achievements are recognized, acknowledged, and celebrated.
</li>
<li>
A comprehensive benefits package, including medical, dental, vision, company-paid life insurance, 401k plan with company match, paid time off, wellness programs, educational assistance, training, and more!
</li>
</ul>
**What you’ll do:
**
<ul>
<li>
Formulate, source and specify coating and materials for plastic and metal food closures.
</li>
<li>
Work with vendors to develop and specify new coatings.
</li>
<li>
Organize and run materials projects from conception to production.
</li>
<li>
Provide technical support for project teams.
</li>
<li>
Design experiments and run both pilot trials and manufacturing trials at plant locations.
</li>
<li>
Analyze chemical data including FTIR, GC, DSC, TMA and rheology in order to develop relationships between material properties and coating performance.
</li>
<li>
Assist in customer and manufacturing problem analysis.
</li>
<li>
Write comprehensive reports.
</li>
<li>
Provide support for regulatory compliance.
</li>
</ul>
**You’ll love it here if you:
**
<ul>
<li>
Like to develop and specify materials for steel, plastic and aluminum closures.
</li>
<li>
Have a solid knowledge of coating chemistries and application.
</li>
<li>
Like to manage material projects from conception to production.
</li>
<li>
Like to run pilot lab and manufacturing trials and provide customer/manufacturing technical support.
</li>
</ul>
**What you’ll need to have:
**
<ul>
<li>
Bachelor’s degree in chemistry, polymers, materials science, engineering or related field.
</li>
<li>
Minimum 8 years of related experience
</li>
<li>
Computer literate – specifically with Microsoft Word, Excel and PowerPoint
</li>
<li>
Ability to travel domestically up to 30%.
</li>
<li>
Knowledge of metal coating formulations, their application and processing.
</li>
<li>
Experience with food contact materials.
</li>
<li>
Project management experience
</li>
<li>
Preferred Qualifications:
<ul>
<li>
Knowledge of rheological and thermal analysis
</li>
<li>
Experience in regulatory compliance of food packaging materials
</li>
<li>
Knowledge of polymers
</li>
<li>
Experience with gasket and liner materials for food packaging
</li>
<li>
Master’s degree in related field
</li>
<li>
Knowledge of Design of Experiments - DOE
</li>
</ul>
</li>
</ul>
**Who we are:
**
<ul>
<li>
Global Fortune 500 packaging company with 109 manufacturing facilities in North and South America, Europe, and Asia
</li>
<li>
A supplier of sustainable metal and plastic packaging solutions for consumer goods products for food, beverage, health care, garden, home, personal care, and beauty products
</li>
<li>
A stable, reliable, and environmentally conscious company
</li>
</ul>
LIMITATIONS AND DISCLAIMER
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required for the position.
All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees.
This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws.
Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Continued employment remains on an "at-will" basis.
Silgan is an Equal Opportunity Employer. We consider applicants for all positions without regard to race, color, religion, sex, national origin, age, marital status, or the presence of a disability, which would not prevent the performance of essential job duties with, or without reasonable accommodation of any other protective status.
Silgan is a drug-free workplace.
You should be proficient in:
<ul>
<li>Bachelor's Degree</li>
<li>Project Management</li>
<li>Food Safety and Quality Assurance (FSQA)</li>
<li>Basic Computer Skills</li>
<li>Microsoft Excel</li>
</ul>

Coatings Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Toxins group within the Product Development, Science &amp; Technology (PDS&amp;T) - Biologics organization supports manufacturing, process validation, regulatory submission, and continuous improvement for late-stage and commercial manufacturing of biological toxin products at AbbVie. We have an exciting opportunity for a senior scientist I position based in Irvine, CA. This role involves leveraging scientific and bioengineering principles to develop bioassays for analytical testing at drug substance and drug product release and stability time points. The candidate must possess in-depth knowledge and hands-on experience in a range of techniques, including but not limited to molecular cloning, mammalian cell culture, PCR, Western blot, cell sorting, bioassay, microscopy, transfection, HPLC, and mass spectrometry. Moreover, excellent communication skills and the ability to thrive in a multi-disciplinary and cross-functional team environment are essential for success in this role.
Key responsibilities include:
<ul>
<li>Lead scientific initiatives by generating innovative technical ideas and strategic approaches to advance research objectives and overcome experimental challenges.</li>
<li>Demonstrate a strong understanding of project goals, aligning research activities with broader objectives and adapting experimental plans as needed based on new data, project developments, or shifting priorities.</li>
<li>Independently design, execute, and interpret complex experiments with rigorous methodology to ensure reproducibility and accurate data interpretation. Develop, optimize, and implement novel experimental protocols by leveraging emerging technologies to drive scientific progress and solve technical issues.</li>
<li>Maintain advanced, up-to-date expertise in relevant scientific and technical disciplines, applying this knowledge to experimental design, troubleshooting, method development, and integration of best practices from current literature.</li>
<li>Establish and manage clear experimental timelines, closely tracking progress and ensuring timely completion of project deliverables through strong organizational and time-management skills.</li>
<li>Deliver high-quality scientific communication by drafting and editing SOPs, technical reports, publications, presentations, and patent applications according to industry and regulatory standards. Effectively organize, analyze, and present scientific ideas and experimental data to cross-functional teams and stakeholders through impactful written and oral communications.</li>
</ul>
Qualifications 
<ul>
<li>Advanced degree in a relevant field: Ph.D. (with 6+ months biopharmaceutical industry experience preferred), Master’s degree (6+ years industry experience) and Bachler’s degree (8+ years industry experience) in Cell and Molecular Biology, Biochemistry, Biochemical or Biomedical Engineering, Biotechnology, , or closely related disciplines.</li>
<li>Robust research background in neuroscience, with direct expertise in neural cancer cell and primary cell culture, 3D cell models, and complex co-culture systems preferred. Demonstrated hands-on experience in developing and optimizing these models for scientific study or drug discovery applications.</li>
<li>Proficient in RNA microinjection for protein expression and functional evaluations, with a solid understanding of related molecular techniques. Also experienced in the generation of stable cell lines and the design and execution of novel cell-based assays.</li>
<li>Highly skilled in high-resolution imaging and live-cell imaging techniques, including advanced confocal microscopy, fluorescence-based assays, and related methodologies for monitoring cellular processes in real time.</li>
<li>Extensive laboratory experience with molecular cloning, mammalian cell culture, PCR, Western blotting, cell sorting, bioassays, advanced microscopy, transfection procedures, HPLC, and mass spectrometry.</li>
<li>Knowledgeable in genome editing approaches—including CRISPR/Cas9—with a thorough understanding of design, execution, and validation of gene editing experiments.</li>
<li>Previous GxP experience and attention to detail in documentation preferred.</li>
<li>Demonstrated proficiency in computer skills essential for scientific research, including word processing, spreadsheets, presentation software, and advanced data analysis. Capable of analyzing, interpreting, and presenting complex data sets using specialized scientific software (e.g., Python, R, JMP). Experience with laboratory automation platforms (such as Hamilton) is highly desirable.</li>
<li>Proven scientific leadership, demonstrated by being the main author on published research papers and holding patents. Skilled at designing experiments, solving problems creatively, developing thorough experimental plans, and independently troubleshooting and validating results.</li>
<li>Demonstrated ability to stay current with scientific advances, critically assess relevant literature, and quickly integrate emerging concepts and techniques into research projects.</li>
<li>Detail-oriented work style, with a proven record of delivering high-quality and reproducible data within tight timelines.</li>
<li>Strong interpersonal and collaborative skills, enabling effective teamwork within multidisciplinary, cross-functional teams. Able to communicate complex scientific information clearly through both spoken presentations and technical documentation.</li>
<li>Self-motivated and adaptable, with a passion for scientific discovery and a commitment to continuous learning and process improvement.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;ofthis posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location,and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of anybonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's soleand&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist I, Cell/Molecular Biology

<h3>Job Description</h3>
Job Description
Apply Today! Great Company to work for! 
Job Duties:
<ul>
<li>Responsible for maintaining a sterile environment by garbing, cleaning, and acting according to the CGMP guidelines for clean room procedures.</li>
<li>Measure, cut, position, and align tubing and small components for assembly.</li>
<li>Operate cable guns, tubing spreader, bag sealers, tubing cutter and manual cutting devices.</li>
<li>Read instructions and drawing assemblies to identify product specifications.</li>
</ul>
Qualifications:
<ul>
<li>High School diploma or equivalent desired, with a minimum of six months related experience; or equivalent combination of education and experience.</li>
<li>Possess industry-specific training on how to assemble intricate parts or products in a controlled room or facility.</li>
<li>Prepares and assembles necessary parts/products based on Work Order</li>
</ul>
Monday-Friday
Company DescriptionDiscover a workplace that empowers you to thrive, innovate, and build the career you’ve been dreaming of. 
<h3>Company Description</h3>
Discover a workplace that empowers you to thrive, innovate, and build the career you’ve been dreaming of.

Cleanroom Assemblers - 1st shift & 2nd shift

<h3>Job Description</h3>
Job Description
Geotechnical Consultants Inc. (GCI) is a 46-year-old civil engineering company specializing in geotechnical engineering, environmental consulting, field and construction services, special inspections, building envelope services, and steel testing.
We are seeking a full-time Geotechnical Field Representative in the Youngstown, OH area. This position will be responsible for assisting engineers on construction site locations to perform routine testing for project documentation. GCI is looking for individuals who enjoy working outside, ability to work independently, excellent client communication skills, “can do” attitude, willingness to learn new concepts, and ability to achieve needed testing certifications.
General Roles and Responsibilities:
· Provide technical support to the Project Manager through on-site inspections and testing of soils, concrete, asphalt, and other construction materials.
· Perform computations and communicate results through field reports.
· Consistent communication with Project Mangers, client representatives, general contractors, and others to obtain project-appropriate objectives.
· Responsible for maintaining strict quality control and safety standards including cleaning and maintenance of equipment.
· Authority to reject and resolve conflict within scope of authority.
· Willingness to grow and achieve certifications as needed.
Desired Certifications (or ability to achieve):
· Concrete – ACI Field Testing Technician Grade 1-2, NICET Level 1-3, ICC Reinforced Concrete Special Inspector.
· Soils – NICET Level 1-3, ICC Soils Special Inspector.
· Asphalt – NICET Level 1-3, ODOT Level 1-2.
· Masonry – ICC Structural Masonry Special Inspector.
· Structural Steel – ICC Bolt &amp; Weld Special Inspector, AWS Certification.
· ICC Fireproofing Special Inspector
Qualifications:
<ul>
<li>3-5 years' experience in a construction related job, or education related experience, preferred.</li>
<li>Ability to pass drug test and general background check.</li>
<li>Effective speaking and written communication skills.</li>
<li>Valid driver’s license and insurance</li>
<li>Ability to travel up to 4 hours a day and walk/stand up to 8 hours a day.</li>
<li>Desire to work outside in all weather conditions.</li>
<li>Ability to safely lift varying weights from 10-50 pounds, and safely traverse construction sites and project sites</li>
</ul>
&nbsp;
Company DescriptionGCI is an Equal Opportunity Employer committed to compliance with all applicable federal, state, and local equal employment opportunity laws. Since opening our doors in 1979, we’ve upheld the principles of quality work, honest fees, exceptional service, and delivering solid value to our clients. We welcome motivated, self-sufficient individuals who thrive in a team environment and are seeking long-term career growth. GCI offers competitive pay, benefits, paid training, and profit sharing to all full-time employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information, marital status, protected veteran status, political affiliation, military service, parental status, or any other status protected by law. GCI also provides reasonable accommodation for qualified individuals with disabilities, pregnancy-related conditions, and sincerely held religious beliefs, observances, and practices, unless doing so would impose an undue hardship. 
<h3>Company Description</h3>
GCI is an Equal Opportunity Employer committed to compliance with all applicable federal, state, and local equal employment opportunity laws. Since opening our doors in 1979, we’ve upheld the principles of quality work, honest fees, exceptional service, and delivering solid value to our clients.\r\nWe welcome motivated, self-sufficient individuals who thrive in a team environment and are seeking long-term career growth. GCI offers competitive pay, benefits, paid training, and profit sharing to all full-time employees.\r\nAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information, marital status, protected veteran status, political affiliation, military service, parental status, or any other status protected by law. GCI also provides reasonable accommodation for qualified individuals with disabilities, pregnancy-related conditions, and sincerely held religious beliefs, observances, and practices, unless doing so would impose an undue hardship.

Geotechnical Field Representative, Youngstown Ohio Area

<h3>Job Description</h3>
Job Description
We are currently seeking a Soils Technician to join our team! Immediate opening available. Minimum of 1 year of experience as soils technician required. Experience in testing and observing placement of compacted fill (sand cone, nuclear gauge), grading, preparation of field reports, plotting density test results. Salary commensurate with experience.
Benefits:
<ul>
<li>Medical, dental, vision, life, and long-term disability insurance</li>
<li>401(k) with company 3% contribution and profit sharing</li>
<li>Paid time off</li>
</ul>
Responsibilities:
<ul>
<li>Observing the placement of compacted soils and rock fill</li>
<li>Testing of compacted fill using sand cone and/or nuclear density gauge</li>
<li>Ability to work on projects throughout southern California with focus in San Diego County</li>
<li>Ability to compile test results, read plans, and write field reports</li>
</ul>
​Qualifications:
<ul>
<li>Ability to lift and carry heavy samples and equipment over rough terrain</li>
<li>Driver's license and clean driving record</li>
</ul>

Soils Technician

<h3>Job Description</h3>
Job Description
At Redo Cabinets, we are looking to add Measure Technicians to our talented team. The Measure Technician is an essential role that is a trusted pro who ensures accuracy and turns designs into flawless kitchen remodeling projects.&nbsp;The primary function of the measure technician position is the technical evaluation of the job site to determine the manner in which the contracted work will be installed.&nbsp;You will be a W-2 employee. We provide a company vehicle, company tools, health insurance, paid time off, 401(k), and steady inside work. Must have experience measuring kitchen cabinets.
Measure Technician
Measure Technician needed to join our professional team; full-time position with great benefits such as health, dental, vision, 401k with company matching, direct deposit, company vehicle, company supplied tools, paid holidays, and paid time off.
About us
Redo Cabinets is a leader in the home improvement industry and is family owned and operated since 1953. We specialize in cabinet refacing. We pride ourselves on excellent customer service and communication to provide the customer with premium quality work.
Essential Functions:
<ul>
<li>Perform accurate measurements of cabinet components to determine the proper ordering of materials</li>
<li>Complete paperwork for ordering of all materials</li>
<li>Examine and record existing conditions in area(s) in which work is to be performed</li>
<li>Produce necessary drawing(s) for the installer to install the job per the contract specifications</li>
<li>Identify job site problems or irregularities to be addressed by the installer and or need to alter contract specifications</li>
<li>Identify job specifications requiring plumbing and/or electrical contractor</li>
<li>Review the contract and checklist with the customer to confirm expected work to be performed, the materials to be installed and any conditions that may affect scheduling and final outcome of the work performed</li>
<li>Collect measure payment from the customer as indicated on the contract if necessary</li>
<li>Adhere to the scheduled measures appointments as closely as possible without deviation</li>
<li>Project manage during the installation coordinating with the installer and customer questions.</li>
<li>Function as an ambassador for the company by presenting a professional appearance, answering customer questions and concerns in a business like manner, and treating the customer with respect at all times</li>
</ul>
Who You Are:
<ul>
<li>Have knowledge of a kitchen’s composition and an understanding of cabinet layout designs and terminology</li>
<li>Excellent attention to detail</li>
<li>Proficient in measuring and recording cabinet and countertop dimensions</li>
<li>Ability to follow directions and to provide feedback to project manager and sales department</li>
<li>Capable of identifying and addressing installation issues</li>
<li>Prior experience in cabinet refacing and cabinet installation a plus</li>
<li>Must have a valid driver's license with a verifiable safe driving record and no physical limitations to perform the tasks required</li>
<li>Experience with plumbing, electrical, and carpentry a plus</li>
<li>Must have a clear criminal background and will be subjected to a zero-tolerance drug policy</li>
</ul>
What We Offer:
<ul>
<li>Competitive compensation based on experience</li>
<li>Excellent benefits package that includes medical, dental, vision, short-term disability, life insurance, 401(k) with company match, paid vacation, and paid holidays</li>
<li>Company-supplied vehicle and tools</li>
<li>Opportunity for growth and advancement</li>
<li>Family-like work environment</li>
<li>Locally owned business that invests in and appreciates its employees</li>
</ul>
Immediate start is available after successful drug and background screening. We are an Equal Opportunity Employer and value diversity. All employment is decided on the basis of qualifications, merit, and business need.
Company DescriptionAt Redo Cabinets, we’re passionate about transforming kitchens and empowering people. Our team thrives on craftsmanship, collaboration, and doing the right thing every day. We’re a tight-knit crew that supports each other, values growth and reliability, and takes pride in turning houses into homes with beautiful cabinetry. If you want to be part of a motivated, adaptable team where your work matters and your voice is heard, Redo Cabinets is the place to build something meaningful—and grow with us. 
<h3>Company Description</h3>
At Redo Cabinets, we’re passionate about transforming kitchens and empowering people. Our team thrives on craftsmanship, collaboration, and doing the right thing every day. We’re a tight-knit crew that supports each other, values growth and reliability, and takes pride in turning houses into homes with beautiful cabinetry. If you want to be part of a motivated, adaptable team where your work matters and your voice is heard, Redo Cabinets is the place to build something meaningful—and grow with us.

Measure Tech

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
We are seeking a highly skilled Senior Scientist to join our Global Material and Parenteral Packaging Science team, a core component of Product Development Science &amp; Technology (PDS&amp;T). The successful candidate will help lead the development of Container Closure Systems (CCS) for novel parenteral and biotechnological products (NBEs), supporting the advancement of some of AbbVie’s most strategic pipeline assets, including monoclonal antibodies, antibody-drug conjugates, and therapeutic toxins.
In this role, you will be considered a subject matter expert (SME) in characterizing CCS—including vials, prefilled syringes, and prefilled cartridges—with an emphasis on Container Closure Integrity (CCI). You will lead the design and execution of novel scientific methods to critically evaluate container closure performance and integrity using force analyzers, developing and validating analytical methods, providing technical expertise for CCS qualification in pharmaceutical manufacturing, and evaluating and implementing cutting-edge CCI and characterization technologies.
<ul>
<li>Leverage deep technical expertise and available characterization data (force/torque, dimensional, material properties) to proactively identify, analyze and resolve key project hurdles and critical assumptions related to CCS design and integrity of new parenteral drug products, namely liquid drug preparations of biotechnological drugs in vials, pre-filled syringes and cartridges as well as lyophilizates.</li>
<li>Identify and seize opportunities to investigate and incorporate novel CCS materials, components, or integrity technologies that align with the long-term strategy and enhance product stability and manufacturability.&nbsp; This includes actively contributing to the technical evaluation and implementation of CCIT methods and continuous improvement based on a holistic CCI strategy aligned to current regulatory requirements.</li>
<li>Responsibility for development and validation of robust CCI methods according to GxP requirements, ensuring they are scientifically sound and fit-for-purpose across all phases of drug development.</li>
<li>Technical support of the continuous landscaping programs for innovative CCS, including hands-on implementation and comprehensive characterization based on various CCI techniques.</li>
<li>Initiate and drive strategic technical collaborations with AbbVie partner labs, external contract labs, and manufacturing sites to facilitate method transfer, technology adoption, and successful project delivery.</li>
<li>Coordination of external suppliers for materials, equipment, and contract services needed to perform work.</li>
<li>Authoring comprehensive, scientifically sound reports (e.g. lab reports, development reports or risk assessments) that could serve as critical source documents for authority submissions.&nbsp; Ensure all work is documented according to applicable GxP and internal procedural requirements.</li>
<li>Take responsibility for transferring ownership and maintaining lab equipment. Ensure required maintenance schedule, proper documentation, and training new users.</li>
<li>Mentoring and support for new colleagues and interns/contractors to build group expertise.</li>
<li>Presentation of project data as well as SME topics in internal global teams and effectively communicate technical conclusions and strategic recommendations.</li>
<li>Compliance with all relevant work safety requirements.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Degree from an accredited University in pharmacy/biology/biotechnology/chemistry/process engineering/material sciences/physics or related areas.</li>
<li>Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and typically 4 years of experience.</li>
<li>Possesses thorough technical and scientific understanding of parenteral drug product development and CCI test methods.</li>
<li>Understanding of relevant scientific literature and ability to apply theoretical framework to solving problems within their scientific discipline in a timely manner.</li>
<li>Scientific expertise in statistical data analysis</li>
<li>Knowledge of CAD/3D printing and/or µCT analysis is an advantage.</li>
<li>Ability to work concurrently on multiple projects, work in teams, and manage priority conflicts.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to establish comprehensive scientific and project related documentation.</li>
<li>Ability to communicate CCI strategies and content to broad audiences internally and externally.</li>
<li>Strong motivation and proactive approach to lab responsibilities</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education and typically 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Possess thorough theoretical and practical understanding of own scientific discipline.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, I Global Material and Parenteral Packaging Sciences

<h3>Job Description</h3>
Job DescriptionWe are seeking a detail-oriented Electronics Assembly Technician to join our team. This role involves performing a wide variety of electronic and electro-mechanical assembly operations in a clean room environment.Key Responsibilities:
<ul>
<li>Perform bench-level electronic and electro-mechanical assembly using skilled hand techniques and/or automated production equipment</li>
<li>Interpret technical specifications, drawings, and documentation</li>
<li>Follow established methods and sequences for wiring, component installation, hand soldering, and cable harnessing</li>
<li>Set up and adjust assemblies while holding tight tolerances to blueprint specifications</li>
<li>Maintain clean room standards and procedures</li>
</ul>
Qualifications:
<ul>
<li>Experience working in a clean room environment</li>
<li>High School Diploma or equivalent with a minimum of 4 years of relevant experience OR</li>
<li>Associate’s Degree (or post-secondary education) with 0–2 years of related experience</li>
<li>Strong attention to detail and ability to work from technical documentation</li>
</ul>
This is a great opportunity for someone who enjoys hands-on assembly work in a precision-driven environment. #INDNashua #ZipNashuaCompany DescriptionWe are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing 
<h3>Company Description</h3>
We are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing

Clean Room Assembly NH

<h3>Job Description</h3>
Job Description
We are LOTTE BIOLOGICS! Delivering Therapies That Enable a Healthier World. 
A new company, built on 80 years of tradition. We embody our core values of being Inspired by Science, Embracing Diversity, Fostering Talent, and Connecting Lives. Our mission is to be the most trusted partner in the industry, with high standards of quality and continuous innovation, to reliably deliver benefits for patients worldwide. 
Position Summary
The Senior Scientist is responsible for analytical method development for the testing of biologics, ADC's, and other protein modalities. You will lead the implementation of analytical methods for a variety of instruments and techniques to support pre-clinical to commercial stage client projects. You will perform non-GMP testing, pre-clinical stability studies, reference standard qualification, and comparability studies.
Duties &amp; Responsibilities
<ul>
<li>Lead analytical method development and demonstrate expertise with protein biotherapeutic test methods used to characterize products.</li>
<li>Leverage a strong understanding of the drug substance process to lead testing of upstream and downstream process development samples.</li>
<li>Document results and perform data analysis, interpretation, and trending.</li>
<li>Design, author, and review standard operating procedures, methods, protocols, reports, change controls, and regulatory submission supporting documentation.</li>
<li>Lead technical transfers to quality control and serve as an analytical expert for transfer and validation activities, investigations, method troubleshooting.</li>
<li>Actively mentor less experienced scientists to facilitate their development.</li>
<li>Identify opportunities for technical advancements and implement new analytical technologies.</li>
<li>Lead analytical client interactions, support site inspections, review regulatory filings and prepare CMC inquiry responses as required.</li>
<li>Perform routine laboratory activities including sample management, instrument maintenance and calibration, inventory and ordering of supplies, general housekeeping, and other related activities.</li>
<li>Work in a diverse group environment while focusing on inclusivity and safety to produce high quality, compliant results.</li>
</ul>
Education &amp; Experience
<ul>
<li>B.S. in Biology, Chemistry, or equivalent area of related study with 7-9 years, M.S. with 3-6 years, or Ph.D. with 1-3 years, of industry experience in biologic/protein analytics.</li>
<li>Experience in protein biotherapeutics for a variety of instrumentation (i.e., HPLC/UPLC, qPCR, ELISA, CE-SDS, iCIEF, UV-VIS, MS, GC, and cell-based assays) is required.</li>
<li>Experience with the biopharmaceutical development process, ICH guidelines, compendial requirements, and experimental statistical design/data analysis is required.</li>
<li>Experience authoring, validating, and coordinating timely transfer of test methods with and to Quality Control laboratories is required.</li>
<li>Experience developing bridging studies between new and existing methods, method comparability studies, and product comparability studies required to support CMC changes is preferred.</li>
<li>Experience leading analytical method change controls within a Quality Management System and ensuring all required test data and reports are available to support and justify the change(s) is preferred.</li>
<li>Experience defining analytical control strategy, coordinating the specifications development process, preparing the specification package documents, and driving the process for internal and regulatory approval of the specifications is desired.</li>
</ul>
Knowledge, Skills, Abilities
<ul>
<li>Ability to interpret technical data and results to draw appropriate conclusions, apply risk-based quality principles, and identify logical next steps to ensure good scientific, compliance and regulatory outcomes.</li>
<li>Strong verbal, written, presentation, and interpersonal communication skills with ability to clearly articulate scientific objectives and results to lead discussions, build alignment, and make recommendations.</li>
<li>Ability to prioritize, manage team priorities/resources, and complete project deliverables within given timelines.</li>
<li>Organized, detail oriented, and proficient in writing formal reports, documents, and technical presentations.</li>
<li>Aptitude as a functional mentor/technical point of contact and ability to effectively train others.</li>
</ul>
Physical Demands
<ul>
<li>The role is a combination of laboratory and office-based work.</li>
<li>The laboratory work requires appropriate levels of personal protective equipment (PPE). The role may require contact with biohazardous materials such as live cell cultures and other hazardous chemicals including methotrexate, acids, and caustics. Powdered materials and high temperature liquids and solids may also be handled. Use of a respirator may be required.</li>
<li>Frequent repeated motions such as pipetting, lifting, bending, twisting, squatting, crouching, sitting, kneeling, climbing on stepstools, and reaching may be required. Repetitive use of arms/hands/wrists and grasping may be required.</li>
<li>The role may require unassisted lifting (not to exceed 50 lbs.).</li>
</ul>
Work Environment
<ul>
<li>Position is primarily laboratory and office based with occasional work in a classified GMP manufacturing environment.</li>
<li>Dynamic, fast-paced, interactive, and entrepreneurial environment.</li>
<li>Position is a team and project-based position that may require occasional shift work, weekends, and holidays.</li>
</ul>
Supervisory Responsibilities 
May require supervisory responsibility of up to 3-5 direct reports. Demonstrated leadership experience is preferred.
Travel
&lt;5% of travel required for this position. 
Target Bonus
10%
Work Location:
East Syracuse, NY 
New York Pay Range$85,000—$118,000 USD
We are an Equal Employment Opportunity ("EEO") Employer. 
We believe that women, people of color, veterans and LGBTQ communities must participate in the work we do, so we strongly encourage applications from people with these identities or who are members of underrepresented communities!  If this is the work that you want to do, in a culture of inclusion and excellence with the goal of making our world to be a healthier place, then please apply today!

14,951 Science Jobs