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Principal Scientist- Laurelton, NY. Develop &amp; validate analytical methods for a wide range of pharmaceutical products. Lead the development of robust analytical methods for Assay, Dissolution, Related Substances, &amp; Nitrosamine Impurities techniques, including High-Performance Liquid Chromatography, Gas Chromatography, &amp; Liquid Chromatography-Mass Spectrometry. Manage the validation of analytical methods. Conduct multimedia dissolution studies for bioequivalent generic product development. Perform compatibility studies to identify suitable excipients for formulation development. Reqs: Master's in Pharmaceutical Sci, Chem, Biochem, or related +2yrs exp as Principal Scientist, Chemist, or related. Salary: $115,000/year. Resume: Epic Pharma, 227-15 N. Conduit Avenue, Laurelton, NY, 11413

Principal Scientist

<h3>Job Description</h3>
Job Description
Job Description
The Chemist III independently conducts research, analysis, and experimentation to develop ink, paint, and other chemical product formulations. This is a hands-on position with significant time spent at the lab bench, along with associated administrative duties related to product development. The role involves collaboration with personnel in quality control, manufacturing, product management, and sales to support existing product lines.
Responsibilities
<ul>
<li>Develop and invent new products in line with company goals and objectives.</li>
<li>Collaborate closely with sales and product management to develop products meeting end user cost, performance, and color requirements.</li>
<li>Manage development projects by establishing and adhering to timelines, communicating progress, and maintaining detailed records.</li>
<li>Acquire thorough experience and knowledge of any new product uses and applications.</li>
<li>Troubleshoot chemical-related production problems in conjunction with plant supervisory personnel.</li>
<li>Scale up new products to production size in conjunction with the manufacturing team.</li>
<li>Research and respond to customer technical questions as needed.</li>
<li>Develop formulas, processes, and methods for the solution of technical problems.</li>
<li>Analyze organic and inorganic compounds to determine chemical and physical properties.</li>
<li>Conduct research on manufactured products to develop and improve products.</li>
<li>Prepare standards and specifications for processes, facilities, products, and tests.</li>
<li>Maintain up-to-date lab notebooks detailing specific project work.</li>
<li>Prepare reports, write technical papers, and deliver technical presentations as appropriate.</li>
<li>Conduct technical training for internal and external customers.</li>
<li>Perform other duties as needed.</li>
</ul>
Essential Skills
<ul>
<li>4-7 years of experience in R&amp;D product development for inks, paints, and coatings.</li>
<li>Bachelor's or Master's degree in Chemistry or a related field.</li>
<li>Experience in an industrial manufacturing setting following GMP standards.</li>
</ul>
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 Permanent position based out of Wood Dale, IL.
Pay and Benefits
The pay range for this position is $91000.00 - $102000.00/yr.
standard benefits package
Workplace Type
This is a hybrid position in Wood Dale,IL.
Application Deadline
This position is anticipated to close on Nov 22, 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.

Chemist

<h3>Job Description</h3>
Job Description
OMIC USA Inc. is seeking motivated and skilled Chemist 2s (Analytical Chemists) to join our expanding laboratory teams. This posting covers several open positions across three of our main analytical departments: Inorganic, Gas Chromatography, and Liquid Chromatography. Applicants will be reviewed for all Chemist 2 roles, and final placement will be based on each candidate’s technical background, experience, and best departmental fit. Whether your strengths are in trace element analysis, pesticide residue testing, or general instrumental quantitation, we invite you to apply and become part of a rewarding, collaborative analytical laboratory environment.
OMIC USA, Inc. is an International Analytical Testing Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients.
MISSION OF THE ROLE:
 Chemist 2 performs an essential role in the Residue Chemistry and Inorganic Laboratories by providing analytical services and results accurately, efficiently, and in a timely manner to clients through (1) analyzing samples by GC, LC, or ICP instrumentation using conventional, MS, MSMS, and other analytical detection techniques, (2) proposing improvements, (3) stabilizing analytical processes, and (4) contributing to innovation to achieve the Company’s mission and objectives.
RESPONSIBILITIES: Other duties may be assigned.
<ol>
<li>Performs sample analysis as per documented methods and Standard Operating Procedures (SOPs).</li>
</ol>
This includes but is not limited to:
<ol>
<ol>
<li>Operating analytical instrumentation, chromatographic and other, such as a GC, LC, or ICP that is equipped with conventional, MS, and MSMS detection.</li>
<li>Utilizing multiple vendor acquisition and quantitative analysis software packages to evaluate, interpret, and report test results, including QA/QC data. Vendors could include, Agilent, SCIEX, Waters, CETAC, LECO, and others.</li>
<li>Entering data into the LIMS for the tests performed and is responsible for the results.</li>
<li>Independently performing analysis for simple and complex test methods for routine and non-routine samples and matrix types. Issues with complex analyses are discussed with and potential solutions proposed to the Group Leader.</li>
<li>Depending on skill level and training, test responsibility may include more complex or challenging analyses, advanced data interpretation, and independent decision making with little supervision or consultation needed.</li>
<li>Scheduling activities to provide accurate and timely service to support business requirements. </li>
<li>Ensuring that samples are extracted and analyzed in accordance with registered and in-house validated methods.</li>
<li>Ensuring that reference materials and working standards are maintained and documented according to relevant regulated documents and SOPs.</li>
<li>Compiling and maintaining Internal Quality Control (IQC) data for analytes and tests assigned and performing periodic assessments of positive fortification extraction efficiency/recovery trends. Consults with Group Leader to determine cases where QC or analytical data do not meet acceptable criteria based on established procedures and suggests course(s) of action.</li>
<li>Remaining informed of hazards associated with chemicals, equipment, and their use in a laboratory setting. Works in a safe manner, using appropriate safeguards and personal protective equipment, to prevent injury to self and co-workers. Reports all accidents or unsafe working conditions to the safety committee or management.</li>
</ol>
<li>Performs responsibilities and duties of Chemist 1 (Extraction Chemist); this may include extractions, as needed, assigned, and directed by the Group Leader.</li>
<li>Troubleshoots issues with analytical procedures and coordinates with Chemist 3 (Senior Chemist) or Group Leader on resolutions.</li>
<li>Troubleshoots and performs routine and preventative maintenance, verification, and calibration of chromatographic and other analytical instrumentation possessing conventional, MS, and MSMS detectors in accordance with documented procedures. Escalates to Chemist 3 or Group Leader if issues cannot be resolved.</li>
<li>Develops and updates controlled documents and SOPs, ensuring that current versions are up to date and are available to other Chemists.</li>
<li>As directed by Group Leader, may perform secondary review on data packages submitted by other Chemists for quality, accuracy, consistency, and completeness ensuring proper procedures are followed for ISO17025 compliance.</li>
<li>Participates in special analytical projects, as directed by Group Leader.</li>
<li>Develops improved and/or new methodology using published sources and finalizes supporting data which is verified by Chemist 3 or Group Leader.</li>
<li>Assists Chemist 3 and Group Leader with new equipment recommendations, implementation, instrument verification, and method optimization.</li>
<li>Assists Chemist 3 in R&amp;D projects.</li>
<li>Contributes to the continuous improvement of laboratory operations by proposing and implementing changes for improving extraction and analysis method quality and performance, reducing cost, and increasing efficiency.</li>
<li>Obtains and retains an up-to-date knowledge of analytical techniques, equipment, and technologies. Participates in internal and external training as assigned. Participates in external professional and technical meetings for obtaining latest market insights, new technologies, and building networks as assigned and directed by Group Leader or Management.</li>
<li>Trains and mentors Chemists within department and is a resource to other Chemists as needed or directed.</li>
<li>Supports and provides assignments for Chemist 1 as directed by Group Leader.</li>
</ol>
SUPERVISORY RESPONSIBILITIES:
This role has no direct supervisory responsibilities.
SKILLS AND EXPERIENCE:

EDUCATION
Bachelor's degree (B.S. or B.A.) in Chemistry or related science from a four-year college or university or equivalent combination of education and experience.
CERTIFICATES, LICENSES, REGISTRATIONS
None
SKILLS &amp; EXPERIENCE
<ul>
<li>At least 1 year of successful experience working independently with and proven competency in daily operation, maintenance, and troubleshooting of Gas or Liquid Chromatographic or Inductively Coupled Plasma Spectrometric instrumentation utilizing conventional, MS, and MSMS detectors (GC, GCMS, GCMSMS, HPLC, LCMSMS, ICPMS, etc.).</li>
<li>Experience routinely analyzing and producing data packages for small and larger data sets.</li>
<li>Thorough understanding and demonstrable working knowledge of analytical instrumentation and data analysis software packages such as: Agilent MassHunter, Agilent OpenLAB CDS, SCIEX Analyst, SCIEX MultiQuant, SCIEX OS, Waters Acquity or equivalent.</li>
<li>Successful experience collaborating with different or dissimilar business departments.</li>
<li>Familiar with the commercial fast-paced laboratory business environment.</li>
<li>Experience with and participation in improvement and learning initiatives.</li>
<li>Ability to handle multiple priorities and deadlines.</li>
<li>Able to gather and communicate technical information clearly, both orally and through writing, with respect to analytical and problem-solving skills.</li>
<li>High Emotional Intelligence.</li>
<li>Good cultural awareness and ability to communicate with people of diverse backgrounds.</li>
<li>Experienced user of MS Office and Adobe Acrobat.</li>
</ul>
PERFORMANCE FACTORS 
<ul>
<li>Quality of Work</li>
<li>Communication</li>
<li>Adaptability</li>
<li>Teamwork</li>
<li>Time Management</li>
<li>Knowledge and Skills</li>
<li>Initiative</li>
<li>Dependability</li>
</ul>
LANGUAGE SKILLS 
Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write Standard Operating Procedures, analytical methods, reports, business correspondences, and additional laboratory documentation.
MATHEMATICAL SKILLS 
Ability to apply advanced mathematical concepts such as exponents, logarithms, and quadratic equations. Ability to apply mathematical operations to tasks such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
REASONING ABILITY 
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.

SKILLS &amp; EXPERIENCE
<ul>
<li>3 or more years of experience with GCMS, GCMSMS, LCMS, LCMSMS, and/or ICPMS instrumentation; routinely creating and running analytical sequences, performing primary data analysis and review, as well as compiling and submitting finalized data package deliverables in a commercial high-throughput laboratory environment.</li>
<li>3 or more years of experience in analytical method development with an emphasis on optimization of MS and MSMS instrumentation and data acquisition parameters.</li>
<li>3 or more years of experience working with one or more of the following software platforms: Agilent MassHunter, Agilent OpenLAB CDS, SCIEX Analyst, SCIEX MultiQuant, SCIEX OS, and Waters Acquity.</li>
<li>3 or more years of experience routinely analyzing, which includes screening, quantitation, and reporting, of large-scale pesticide panels (&gt; 100 compounds per sample) or moderate metal and minerals panels.</li>
<li>Proficient hands-on experience and expertise in employing the QuEChERS extraction technique, along with processing and analyzing the resulting data.</li>
<li>Proficient hands-on experience employing microwave acid digestions for metals and minerals testing.</li>
<li>At least 1 year of experience with sample processing and extraction method development, particularly for pesticides, process contaminants, and/or metals and minerals in food matrices.</li>
<li>Experience with high resolution accurate mass spectrometry (HRMS), Time of Flight (TOF), and/or other cutting-edge analytical technologies.</li>
<li>Knowledge of other relevant laboratory technologies.</li>
<li>Successful experience in mentoring and training others, specifically in extraction, analytical, and instrument methodology.</li>
<li>Experience interacting with representatives of relevant external agencies and organizations.</li>
<li>Experience working in international businesses.</li>
</ul>
OTHERS:
TRAINING REQUIREMENTS
OJT in understanding company operating systems, including the maintenance and operation of laboratory extraction and analytical equipment, and passing the Initial Demonstration of Capability (IDOC) for existing SOPs or other laboratory procedures.
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
WORK ENVIRONMENT 
Works in a laboratory using laboratory extraction and analytical equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Chemist 2

<h3>Job Description</h3>
Job Description
Job Description
The Chemist III independently conducts research, analysis, and experimentation to develop ink, paint, and other chemical product formulations. This is a hands-on position with significant time spent at the lab bench, along with associated administrative duties related to product development. The role involves collaboration with personnel in quality control, manufacturing, product management, and sales to support existing product lines.
Responsibilities
<ul>
<li>Develop and invent new products in line with company goals and objectives.</li>
<li>Collaborate closely with sales and product management to develop products meeting end user cost, performance, and color requirements.</li>
<li>Manage development projects by establishing and adhering to timelines, communicating progress, and maintaining detailed records.</li>
<li>Acquire thorough experience and knowledge of any new product uses and applications.</li>
<li>Troubleshoot chemical-related production problems in conjunction with plant supervisory personnel.</li>
<li>Scale up new products to production size in conjunction with the manufacturing team.</li>
<li>Research and respond to customer technical questions as needed.</li>
<li>Develop formulas, processes, and methods for the solution of technical problems.</li>
<li>Analyze organic and inorganic compounds to determine chemical and physical properties.</li>
<li>Conduct research on manufactured products to develop and improve products.</li>
<li>Prepare standards and specifications for processes, facilities, products, and tests.</li>
<li>Maintain up-to-date lab notebooks detailing specific project work.</li>
<li>Prepare reports, write technical papers, and deliver technical presentations as appropriate.</li>
<li>Conduct technical training for internal and external customers.</li>
<li>Perform other duties as needed.</li>
</ul>
Essential Skills
<ul>
<li>4-7 years of experience in R&amp;D product development for inks, paints, and coatings.</li>
<li>Bachelor's or Master's degree in Chemistry or a related field.</li>
<li>Experience in an industrial manufacturing setting following GMP standards.</li>
</ul>
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 Permanent position based out of Elk Grove Village, IL.
Pay and Benefits
The pay range for this position is $91000.00 - $102000.00/yr.
standard benefits package
Workplace Type
This is a hybrid position in Elk Grove Village,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.

<h3>Job Description</h3>
Job Description
Job Description
The Chemist III independently conducts research, analysis, and experimentation to develop ink, paint, and other chemical product formulations. This is a hands-on position with significant time spent at the lab bench, along with associated administrative duties related to product development. The role involves collaboration with personnel in quality control, manufacturing, product management, and sales to support existing product lines.
Responsibilities
<ul>
<li>Develop and invent new products in line with company goals and objectives.</li>
<li>Collaborate closely with sales and product management to develop products meeting end user cost, performance, and color requirements.</li>
<li>Manage development projects by establishing and adhering to timelines, communicating progress, and maintaining detailed records.</li>
<li>Acquire thorough experience and knowledge of any new product uses and applications.</li>
<li>Troubleshoot chemical-related production problems in conjunction with plant supervisory personnel.</li>
<li>Scale up new products to production size in conjunction with the manufacturing team.</li>
<li>Research and respond to customer technical questions as needed.</li>
<li>Develop formulas, processes, and methods for the solution of technical problems.</li>
<li>Analyze organic and inorganic compounds to determine chemical and physical properties.</li>
<li>Conduct research on manufactured products to develop and improve products.</li>
<li>Prepare standards and specifications for processes, facilities, products, and tests.</li>
<li>Maintain up-to-date lab notebooks detailing specific project work.</li>
<li>Prepare reports, write technical papers, and deliver technical presentations as appropriate.</li>
<li>Conduct technical training for internal and external customers.</li>
<li>Perform other duties as needed.</li>
</ul>
Essential Skills
<ul>
<li>4-7 years of experience in R&amp;D product development for inks, paints, and coatings.</li>
<li>Bachelor's or Master's degree in Chemistry or a related field.</li>
<li>Experience in an industrial manufacturing setting following GMP standards.</li>
</ul>
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 Permanent position based out of Wood Dale, IL.
Pay and Benefits
The pay range for this position is $91000.00 - $102000.00/yr.
standard benefits package
Workplace Type
This is a hybrid position in Wood Dale,IL.
Application Deadline
This position is anticipated to close on Nov 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job DescriptionJob TitleChemist / Senior ChemistJoin Our TeamWe are seeking a Chemist to join our Eljen Technology team in Sweetwater, Texas. The Chemist will support chemical manufacturing, product development and quality control in compliance with health and safety requirements. To be successful in this role, you will need a science background with excellent written and verbal communication skills and diligence. If you are an enthusiastic initiative-taker, we encourage you to apply for this exciting opportunity. We offer a competitive salary and benefits package, opportunities for professional growth, and a supportive, collaborative work environment.Job TypeFull-Time, In-PersonSalaryDepends on Qualifications/ExperienceBenefits
<ul>
<li>401(k)</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
Job Requirements 
<ul>
<li>Bachelor of Science with related laboratory work experience required.</li>
<li>Master degree preferred.</li>
<li>Excellent chemistry background including product development</li>
<li>Excellent organizational skills and attention to detail.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Proficient with Microsoft Office Suite.</li>
<li>Proficient with or possesses the ability to quickly learn software and applications used for chemical tests and analysis.</li>
<li>Prolonged periods of sitting at a desk and working on a computer.</li>
<li>Must be able to lift 15 pounds at times.</li>
<li>Exposure to various chemicals and compounds.</li>
<li>Must identify, select and use proper PPE at all times</li>
</ul>
Job Responsibilities &nbsp;
<ul>
<li>Performs laboratory tasks safely with due attention to safety data sheets and in compliance with environmental Health &amp; Safety standards.</li>
<li>Follows standard operation processes sufficiently and satisfactorily</li>
<li>Identifies and recommends improvements to processes, products and quality.</li>
<li>Writes and presents laboratory reports.</li>
<li>Maintains comprehensive documentation on assigned projects and reviews same with peers and/or manager.</li>
<li>Collaborates with lab and interdepartmental teams.</li>
<li>Operates, maintains, and tests laboratory equipment; identifies problems when equipment fails and conducts or recommends repairs.</li>
<li>Drafts standard operating procedures and safety materials.</li>
<li>Performs other duties as assigned.</li>
</ul>
LMI is an Equal Opportunity Employer. We embrace diversity and are committed to creating an inclusive environment for our employees. OFCCP Equal Employment Opportunity Posters
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<h3>Job Description</h3>
Job Description
The Chemist II performs an essential role in the Gas Chromatography (GC) department by providing analytical services and results accurately, efficiently, and promptly to clients through: Analyzing samples using GC, conventional, MS, MSMS, and other detection techniques, proposing improvements, stabilizing analytical processes, and contributing to innovation to achieve the company's mission and objectives
 
Duties and Responsibilities
 
Sample Analysis
<ul>
<li>Operate GC instrumentation with conventional, MS, and MSMS detection</li>
<li>Utilize Agilent MassHunter and OpenLAB CDS to analyze, interpret, and report test results</li>
<li>Enter data into LIMS and take responsibility for results</li>
<li>Independently perform simple and complex analyses for routine and non-routine samples</li>
<li>Schedule activities to provide accurate and timely service</li>
<li>Ensure samples are extracted and analyzed according to validated methods</li>
<li>Maintain and document reference materials and working standards</li>
<li>Compile and maintain Internal Quality Control data</li>
<li>Work safely with awareness of chemical hazards </li>
</ul>
Instrument Maintenance &amp; Troubleshooting
<ul>
<li>Troubleshoot issues with analytical procedures</li>
<li>Perform routine and preventative maintenance, verification, and calibration of GC instruments</li>
<li>Coordinate with Chemist 3 or Group Leader on the resolution of complex issues </li>
</ul>
Documentation &amp; Quality Assurance
<ul>
<li>Develop and update controlled documents and SOPs</li>
<li>Perform secondary review on data packages (as directed)</li>
<li>Ensure ISO17025 compliance </li>
</ul>
Method Development &amp; Improvement
<ul>
<li>Develop improved and/or new methodology using published sources</li>
<li>Contribute to the continuous improvement of laboratory operations</li>
<li>Propose and implement changes to improve quality and efficiency </li>
</ul>
Knowledge &amp; Professional Development
<ul>
<li>Maintain up-to-date knowledge of analytical techniques and technologies</li>
<li>Participate in internal and external training</li>
<li>Attend professional and technical meetings as assigned </li>
</ul>
Team Support &amp; Mentoring
<ul>
<li>Train and mentor chemists within the department</li>
<li>Support and provide assignments for Chemist 1 (as directed)</li>
<li>Assist Chemist 3 in R&amp;D projects</li>
</ul>
Job Requirements
<ul>
<li>Bachelor's degree (B.S. or B.A.) in Chemistry or related science</li>
<li>At least one year of experience with GC instrumentation (conventional, MS, MSMS detectors)</li>
<li>Experience in analyzing and producing data packages</li>
<li>Practical working knowledge of analytical software (Agilent MassHunter, OpenLAB CDS)</li>
<li>Experience collaborating with different business departments</li>
<li>Familiarity with commercial fast-paced laboratory environments</li>
<li>Ability to handle multiple priorities and deadlines</li>
<li>Strong analytical and problem-solving skills</li>
<li>Clear technical communication (oral and written)</li>
<li>High emotional intelligence</li>
<li>Cultural awareness and effective diverse communication</li>
<li>Proficiency in MS Office and Adobe Acrobat</li>
<li>Strong mathematical skills, including statistical analysis</li>
<li>Excellent reasoning ability </li>
</ul>
Preferred
<ul>
<li>3+ years of experience with GC-MS and GC-MSMS instrumentation</li>
<li>3+ years of experience with analytical method development</li>
<li>3+ years of experience with Agilent software platforms</li>
<li>3+ years analyzing large-scale pesticide panels (&gt;100 compounds)</li>
<li>Experience with the QuEChERS extraction technique</li>
<li>Experience with sample processing and extraction method development</li>
<li>Experience with high-resolution mass spectrometry (HRMS/TOF)</li>
<li>Experience mentoring and training others</li>
<li>Experience in international businesses </li>
</ul>
Job Benefits
<ul>
<li>Medical/Vision Insurance</li>
<li>
<ul>
<li>The company covers 100% of EE premiums and 90% of dependents</li>
<li>HSA- the company covers 100% of the premium and contributes to the HSA every month</li>
</ul>
</li>
<li>Dental insurance</li>
<li>LTD</li>
<li>FSA</li>
<li>Supplemental Insurance</li>
<li>LegalShield/IDShield</li>
<li>401(k)</li>
<li>PTO</li>
<li>13 paid holidays</li>
<li>Partnership with Adidas and the Columbia employee stores</li>
<li>Discretionary Annual Bonus</li>
</ul>
Company DescriptionReal People. Real Connections. Real Results. That's the Messina Talent Advantage. For more than 40 years, Messina's Talent practice has continuously evolved to meet the needs of our clients. We not only help our clients fill roles and build their teams, but we also help them better understand their workforce and develop strategic talent initiatives that drive value for their organizations. Messina Talent Advisors, a Messina Group Company, has the network, proven processes, and all the latest technologies to connect the right candidates with the right jobs - faster. 
<h3>Company Description</h3>
Real People. Real Connections. Real Results.\r\n\r\nThat's the Messina Talent Advantage.\r\n\r\nFor more than 40 years, Messina's Talent practice has continuously evolved to meet the needs of our clients. We not only help our clients fill roles and build their teams, but we also help them better understand their workforce and develop strategic talent initiatives that drive value for their organizations.\r\n\r\nMessina Talent Advisors, a Messina Group Company, has the network, proven processes, and all the latest technologies to connect the right candidates with the right jobs - faster.

<h3>Job Description</h3>
Job Description
Job Title: Chemist II Location: &nbsp;Monroeville, PA 15146 Duration: 06-month contract on W2 + possible extension or conversion Shift: Mon-Fri 8:00am-5:00pm Schedule: Schedule is flexible after the training period with start times between 6:00am-8:00am, working 8 hours/day.
Pay rate - $25/hr on w2(without Benefits)
JOB DESCRIPTION: Summary: The Chemist II will be a part of the Monroeville Business and Technology Center Photochromics team and involved in the execution of experiments related to product formulation and testing. The goal of this team is to develop new products through fundamental understanding of formulation and application. Specifically, you will work closely with formulators, chemists, and scientists to assist in the growth and development of Transitions products.
Key Responsibilities: • Following standard operating procedures and industry standards for formula mixing, sample preparation, and testing • Precise measurement and mixing of formula ingredients described by a formulation log • Preparing test specimens for a variety of tests • Creating a collaborative and inclusive work environment • Upholding safety standards for the team, including wearing appropriate personal protective equipment and following safety guidelines • Documenting and reporting experimental details • Keen observation of experimental details and external factors • Time management and work efficiency • Independently planning and executing all aspects of an experiment following a discussion of objectives with the supervisor • Interpreting data and making recommendations for future work
Qualifications: • Bachelor’s Degree in a scientific or technical field • 0-1 years of laboratory experience • Experience with coatings formulation is desired • Strong attention to detail and ability to keep track of multiple project tasks
PPE: Any PPE required will be supplied by the client

<h3>Job Description</h3>
Job Summary
The Onkos Chemist/Process Chemist is responsible for the early and mid stage coating, raw material and general chemistry development of the NanoCeptTM antibacterial coating technology and associated products, through the use of chemistry, chemical engineering and manufacturing principles and internal customer input to achieve the program deliverables (e.g. quality, cost, and delivery).&nbsp;The Chemist leads the hands-on aspects of the NanoCept chemistry process development, raw material development and test piece coating needed to generate performance data to secure regulatory clearance and eventual commercialization of Onkos’ antibacterial coated implant systems.&nbsp;They develop and support process chemistry development, raw material, and analytical processes as they relate to NanoCept coating process and implant testing efforts, conduct process remediation exercises when necessary, root cause and engineering analyses, and work with R&amp;D and Regulatory on design for manufacturability, quality testing, and inspection. &nbsp;&nbsp;They provide focused and expert support of the efforts centered around new material/product research and development, and associated pre-clinical testing critical for regulatory clearances.&nbsp;&nbsp;
Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Works with multidisciplinary project team to develop, implement, and facilitate the following for FDA clearance of safe and effective technology and products:
Ø&nbsp;NanoCept chemical process coating development, part coating and evaluation, and technology transfer with a particular focus on the chemistry and chemical engineering &nbsp;aspects of the coating process and post processing such as packaging and sterilization.
Ø&nbsp;Chemical processing equipment set up and maintenance
Ø&nbsp;Planning and execution of various chemical reactions
Ø&nbsp;Designs of Experiment
Ø&nbsp;Statistical process analysis 
Ø&nbsp;Design Verification testing
Ø&nbsp;Internal / external communications with 3rd party vendors
Ø&nbsp;Creation and management of required materials and process specifications
Ø&nbsp;Leverages and applies fundamental chemistry, chemical engineering and manufacturing rigor to all development of products and processes, such as:
Ø&nbsp;Material and chemical processing techniques
Ø&nbsp;Raw material and coating characterization
Ø&nbsp;Reaction thermodynamics and kinetics
Ø&nbsp;Leads process risk analysis via FMEA
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Generates process quality requirements
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Generates regulatory related documentation and testing protocols
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Assist in preparing comprehensive project timelines with technical objectives, milestones (timing, resource requirements, costs, etc.).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Seek out new technologies for materials and processing through 3rd party relationships.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensures work output is compliant with all current regulatory and quality standards.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Completes all required training in timely fashion.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Other requirements as project needs dictate
 
 
Requirements
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;A minimum of three years of successful chemistry or chemical engineering related technology development in the industrial chemicals, medical device, or pharmaceutical field
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with chemical process development and chemical engineering practices
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum of BS degree in Chemistry or Chemical Engineering, ideally monomer and polymer synthesis through wet chemistry means
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to apply analytical skills, in solving chemistry or chemical engineering problems and developing new technologies 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Demonstrated knowledge of statistically driven Designs of Experiment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Demonstrated computer skills including spreadsheets, word processing, database and other applicable software programs.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent interpersonal skills; self-motivated and flexible to changing schedules.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong attention to detail, good oral and written communication skills&nbsp;
﻿About Onkos Surgical&nbsp;
At Onkos Surgical, we believe individuals with cancer requiring surgery deserve solutions designed specifically for them. These individuals, their caregivers and their support network deserve an organization passionately championing their cause.&nbsp;&nbsp;
We exist to maintain a singular focus on surgical oncology by looking at everything we do through the lens of the cancer surgeon and their patients.&nbsp;&nbsp;
At Onkos Surgical, we will:&nbsp;
<ul>
<li>Find solutions to our patients’ unmet clinical needs and advocate for their cause.&nbsp;</li>
<li>Partner with surgical oncologists through research, education and innovation, to treat their patients more effectively and more efficiently.&nbsp;</li>
<li>Collaborate with regulatory agencies to find pathways to provide timely solutions while upholding the highest standards of quality or compliance.&nbsp;</li>
<li>Fulfill our employees’ desire to make a difference in the lives of the patients they serve while achieving their own professional growth.&nbsp;</li>
<li>Deliver value to our customers and shareholders.&nbsp;</li>
</ul>

<h3>Job Description</h3>
POSITION SUMMARY
 
The Chemist will provide analytical support for QC testing of antibiotic products which include raw materials, in-process samples, stability samples, validation samples, product surveillance, and finished products according to Quality Assurance standard procedures, as assigned. Assist with development and validation of chemical assays. Assist with installing, validating, and trouble-shooting new and existing equipment, including automated systems, as assigned. Accurately generate and document all analytical test results per written procedures and corporate policies and support management in the evaluation and review of all test results and investigations as needed.
 
ROLES &amp; RESPONSIBILITIES:
 
<ul>
<li>Maintains the QC laboratories to comply with cGMP and US Antibiotics standards of safety, quality, and cleanliness.</li>
<li>Follows all safety precautions and guidance from training sessions, chemical hygiene plan, MSDSs (Material Safety Data Sheets), and other technical literature and resources.</li>
<li>Performs efficient and reliable analytical tests following validated procedures for raw material, in process, validation, product surveillance, finished product, stability, water, and environmental samples, as assigned.</li>
<li>Documents all results in accordance with cGMPs and written procedures.</li>
<li>Troubleshoots and solves problems with assays and laboratory equipment and reports all observations.</li>
<li>Strictly follows written procedures to minimize analytical variability. Recommends any potential improvements or changes to methods and lab operations (changes implemented via the change control process).</li>
<li>Interprets analytical results correctly, notifying supervision promptly of any situation that indicates analytical issues or product issues.</li>
<li>Participates in analytical method validations or transfers as required.</li>
<li>Performs satisfactorily on all analyst qualification studies, indicating technical proficiency.</li>
<li>Plans, performs, and documents non-routine tests (or special studies) and investigations under the direction of supervisor and/or manager.</li>
<li>Evaluates and utilizes state-of-the-art equipment, including automated systems and computerized systems to perform and document testing and meet the goals of improved performance, including reliability and efficiency.</li>
<li>Maintains and improves proficiency of technical skills through training.</li>
<li>Conducts special studies in accordance with protocols and direction of management. Prepares well-documented reports of results.</li>
<li>Carries out other departmental duties as deemed appropriate by supervisor/manager.</li>
<li>Reviews (i.e., validates) analytical test results for other laboratory personnel, as required.</li>
<li>Assists supervision in conducting analytical failure investigations, as required, following all procedures.</li>
<li>Calibrates and maintains assigned laboratory equipment as needed according to schedules and procedures, documenting all results.</li>
<li>Assists with equipment qualification testing as required by management.</li>
<li>Assists with sampling tasks as required.</li>
<li>Ensures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and those lab operations conform to company standards for safety and performance.</li>
<li>Reports all test results and any concerns with accuracy of analytical data and/or any issues that may impact product quality, efficacy, safety, or purity.</li>
<li>Supports production needs by efficient laboratory turnaround of samples with right-first-time testing.</li>
<li>Evaluates test results versus established test criteria and/or product specifications.</li>
<li>Must be able to follow procedures for investigative analytical results as required.</li>
<li>Advises, in a technical role, less-experienced staff, notifying supervisor or manager of problems/issues or additional training needs.</li>
<li>Initiates ideas for operational changes and continuous improvement in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance.</li>
<li>Must be able to assure the accuracy and integrity of analytical results/documentation generated. Exercises careful attention to testing procedures, and sampling handling and preparation as to avoid known degradation failure modes for materials under test, and to documentation.</li>
</ul>
 
EDUCATION, WORK EXPERIENCE, CERTIFICATIONS:
<ul>
<li>BS/BA degree in Chemistry (or related science) or equivalent related analytical experience.</li>
<li>Minimum of 0-5 years of analytical experience in pharmaceutical industry and/or other scientific experience.</li>
<li>Strong knowledge/experience of cGMPs in areas beyond QC laboratory.</li>
</ul>
 
KNOWLEDGE, SKILLS, AND ABILITIES:
 Skills/Abilities:
<ul>
<li>Demonstrate ability to perform a wide variety of chemical, instrumental, and chromatographic analyses in an efficient, reliable, and safety conscious manner.</li>
<li>Advanced computer skills.</li>
<li>Appropriate interpersonal and leadership skills</li>
<li>Strong verbal communication skills and technical writing skills.</li>
<li>Ability to prioritize and decide appropriate course of actions for routine issues.</li>
<li>Ability to recognize possible compliance, technical, or safety-related issues and notify supervisor or manager promptly.</li>
<li>Ability to suggest appropriate corrective and/or preventive action(s) and assist with implementation.</li>
<li>Ability to work in a multi-disciplinary team environment</li>
<li>Demonstrate visual acuity per SOP requirements</li>
</ul>
Required Knowledge:
<ul>
<li>Understanding of analytical techniques, test methodology, method development, method validation and reporting for data integrity.</li>
<li>Comprehensive skills related to chemical, instrumental, chromatographic analysis, Operational Excellence, statistical applications and tools</li>
<li>Understanding of equipment installation, validation, calibration, and troubleshooting, etc.</li>
<li>Strong knowledge of cGMPs, USP and FDA’s laboratory related requirements.</li>
</ul>

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