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city

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<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that foster a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
E Ink is seeking an innovative and results-focused Materials Scientist to help engineer materials for better performance, reliability and consistency via modern inverse design techniques. In this role, you will be working with wet / dry lab practices and techniques to determine rapid screening pipelines that enable collection of large datasets related to E Ink-specific material sets. As the glue between collaborators working with materials and AI-focused scientists, you will be expected to connect the worlds to enable accurate, high-throughput models that can be used to accelerate inverse design of materials. As part of our innovative team, you will be instrumental in enabling these pipelines to operate at scale, with the goal of &gt;100x in the throughput over the next year. In this role, you will work in a collaborative development team environment and work closely with other research teams. As a member of this new initiative, you will be expected to take a leadership role in spearheading this new initiative and delivering results. The successful candidate will have strong analytical and communication skills, and a record of driving toward pragmatic solutions to industrial problems.
Responsibilities:
<ul>
<li>Design and maintain reproducible pipelines (software / hardware) that generate experimental data, engineer materials-centric features, and train predictive or generative ML models</li>
<li>Conduct inverse-design campaigns (Bayesian optimization, diffusion models, genetic algorithms, etc.) to recommend new formulations, coordinate lab validation and iterate</li>
<li>Dive deep into fundamental ink dynamics and chemistries to discover key insights related to material properties and chemical design</li>
<li>Invent and document relevant intellectual property and present findings to broad audiences</li>
<li>Champion best practices in data quality and experiment lineage across the organization</li>
<li>Act as the glue between collaborators working at the interface of soft-matter science and machine learning</li>
</ul>
Ideal Qualifications:
<ul>
<li>Minimum of a Ph.D. (or exceptional M.S. plus 4 years' experience) in Materials Science, Chemistry, Chemical Engineering, Physics, Applied Math, or similar major. Outstanding candidates of any educational background will be considered</li>
<li>Background in physical chemistry, electrochemistry or colloids</li>
<li>Experience with soft-matter, colloidal, electrochemistry and / or polymer systems</li>
<li>Experience with modern materials discovery workflows</li>
<li>Proficiency in Python or other scientific programming tools</li>
<li>Strong problem-solving skills and the ability to work collaboratively in a multidisciplinary team</li>
<li>Ability and openness to learn new tools and techniques and share examples</li>
<li>Excellent communication skills and a collaborative mindset</li>
</ul>
Benefits:
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

AI / Materials Research Scientist 1900S-2

<h3>Job Description</h3>
Job DescriptionJob Title: Sr ScientistJob Description
Join our team as a Sr Scientist, where you will support the Analytical Method Development Team as a Subject Matter Expert. You will be instrumental in test method transfer, analytical test method validation, and driving continuous improvement initiatives. Your expertise will also contribute to test method validation, process validation, and QC testing and development on lipid nanoparticles (LNPs). Additionally, you will support deviations and investigations for Out of Specification (OOS) results, Corrective and Preventive Actions (CAPA), and root cause analysis.
Responsibilities
<ul>
<li>Serve as a Subject Matter Expert for test method transfer and analytical test method validation.</li>
<li>Assist with test method validation and process validation.</li>
<li>Support QC testing and development on lipid nanoparticles (LNPs).</li>
<li>Investigate deviations and support OOS, CAPA, and root cause analysis.</li>
<li>Drive continuous improvements in processes and methodologies.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in method development, analytical chemistry, and quality control.</li>
<li>Experience with HPLC, validation, LNP, and protein assays.</li>
<li>Strong knowledge of analytical method development, protein chemistry, ELISA, capillary electrophoresis, FDA regulations, and PCR.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree with 10+ years of experience, Master's degree with 7+ years of experience, or PhD with 5+ years of experience.</li>
<li>Understanding of HPLC, capillary electrophoresis, and PCR.</li>
<li>Experience mentoring and supporting the development of junior scientists.</li>
</ul>
Work Environment
This role is 100% onsite, operating Monday to Friday from 9:00 am to 5:00 pm. The position requires travel to Fargo, North Dakota. You will be an individual contributor with responsibilities to mentor other scientists, working within a team of nine and reporting directly to the Sr Manager of Method Validation. High degrees of collaboration and communication skills are essential in this dynamic and growth-oriented environment.
Pay and Benefits
The pay range for this position is $100000.00 - $110000.00/yr.
They will receive health, dental, vision, 401k. They will get holidays and vacation time as well and a yearly bonus of 10%.
Workplace Type
This is a fully onsite position in Waltham,MA.
Application Deadline
This position is anticipated to close on Jul 28, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Senior Scientist

<h3>Job Description</h3>
Job Description
Engineer Science into Impact
At EmergingDx Inc, we are reimagining diagnostics at the edge of science, engineering, and innovation. As an institution for integrated innovation, we fuse biology, technology, and systems design to build transformative diagnostic tools that improve human health and empower clinicians, patients, and communities.
We’re looking for an In Vitro Diagnostics (IVD) Scientist/Engineer to join our mission-driven team. You’ll help architect, prototype, and validate next-generation diagnostic platforms—from rapid point-of-care assays to integrated microfluidic systems for disease monitoring and early detection.
This role is ideal for someone who thrives at the intersection of biological insight and engineering ingenuity, and who wants to shape the future of healthcare from the bench to the field.
Responsibilities (What You’ll Do)
<ul>
<li>Design, develop, and optimize IVD assays (immunoassays, molecular diagnostics, or clinical chemistry) for lab-on-chip and point-of-care platforms</li>
<li>Collaborate with cross-functional teams to integrate biological assays with microfluidic, optical, and electronic systems</li>
<li>Lead analytical validation studies including sensitivity, specificity, reproducibility, and regulatory performance metrics</li>
<li>Prototype, test, and troubleshoot diagnostic systems across wet lab and hardware environments</li>
<li>Contribute to product development processes including documentation, risk analysis, quality systems (ISO 13485), and FDA regulatory pathways</li>
<li>Apply systems thinking to challenges in sample preparation, biomarker detection, signal amplification, and data analysis</li>
<li>Effectively communicate results and technical insights to clients and stakeholders through both written reports and oral presentations</li>
<li>Develop and manage fast-paced project timelines while proactively identifying and mitigating risks</li>
<li>Stay current on scientific literature, emerging technologies, and clinical needs in diagnostics</li>
<li>Craft and deliver clear, compelling narratives—both written and oral—conveying technical project progress and proposed initiatives</li>
</ul>
Qualifications (What You Bring)
<ul>
<li>PhD in Bioengineering, Molecular Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or related field</li>
<li>5+ years of experience in vitro diagnostics, medical devices, or translational research</li>
<li>Strong knowledge of assay formats: ELISA, lateral flow, qPCR, CRISPR-based diagnostics, isothermal amplification, or electrochemical detection</li>
<li>Experience with fluidic handling systems (manual and automated), sample matrices (blood, saliva, urine), and surface functionalization</li>
<li>Familiarity with data acquisition and analysis, including use of MATLAB, Python, or other statistical tools</li>
<li>Comfortable working across disciplines with engineers, designers, and clinicians</li>
<li>Adaptability in fast-paced environments</li>
<li>Detail-oriented, systems-focused, and passionate about delivering health impact through innovation</li>
<li>Proven track record of leading R&amp;D programs to deliver innovative, high-quality outcomes on schedule, aligned with stakeholder expectations and technical goals</li>
<li>Excellent verbal and written communication skills</li>
<li>Bonus: Experience in microfabrication, biosensor integration, point-of-care regulatory submissions, or multiplexed assay development</li>
</ul>
Why EmergingDx
<ul>
<li>You’ll work on products, platforms, and ventures — not just features</li>
<li>You’ll gain ownership, mentorship, and momentum</li>
<li>You’ll be part of something bigger: a community shaping what’s next</li>
<li>We offer a competitive salary with full benefits package.</li>
</ul>
Ready to redefine diagnostics? Send your resume to <a href="mailto:careers@emergingdx.com" target="_blank">careers@emergingdx.com</a>
Subject: In Vitro Diagnostics Scientist/Engineer – [Your Name]
Due to the nature of our business and information associated with this position, interested candidates must be US Citizens or Permanent Resident.
At EmergingDx Inc, we are proud to be an Equal Opportunity Employer committed to building and sustaining a talented, inclusive, and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, marital status, national origin, age, veteran status, disability, or any other legally protected status.
Note to recruiters: We are not seeking assistance for this position. Please do not contact us via phone or email regarding this opening.
As a U.S. Government contractor, we are required to collect certain applicant information for federal reporting purposes.

In Vitro Diagnostics Scientist/Engineer - Redefine Diagnostics

<h3>Job Description</h3>
Jog Title: Chromatography Principal Scientist
<ul>
<li>Location: Cambridge, MA</li>
</ul>
About the Job
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Sanofi is seeking a highly motivated individual to join our analytical group as a Chromatography Principal Scientist. The group is part of the synthetic platform within Global CMC Development that is striving to become an industry leader in the development of transformative medicines. &nbsp;&nbsp;
The primary responsibility of this position is to provide analytical support to the chemistry teams and to develop analytical methods using equipment including HPLC, UHPLC, GC, and potentiometry.
Key Responsibilities 
<ul>
<li>
Develop specific and robust analytical methods using equipment including HPLC, UHPLC, GC, TLC, and potentiometry and be responsible for validating the methods when necessary
</li>
<li>
Analyze synthetic molecules mainly by HPLC/UHPLC, GC, potentiometry, and TLC.
</li>
<li>
Perform quantification of impurities
</li>
<li>
Perform mass balance studies
</li>
<li>
Design and implement analytical strategies for synthesis intermediates and raw materials
</li>
<li>
Develop effective collaborations with others within project teams and between analytical groups
</li>
<li>
Generate technical reports independently
</li>
<li>
Share knowledge and experience of analytical method development for synthetic molecules
</li>
<li>
Introduce innovative analytical approaches to facilitate optimal decision-making.
</li>
<li>
May serve as a project lead
</li>
</ul>
About you
Basic Qualifications 
<ul>
<li>
A Masters degree or equivalent in Analytical Chemistry or related field with a minimum of 4 years of experience in the pharmaceutical/biotech industry. A PhD in Analytical Chemistry is preferred.
</li>
<li>
Expertise in the operation of LC and GC
</li>
<li>
Familiarity with the operation of potentiometry titrator, and TLC from multiple manufacturers
</li>
<li>
Extensive experiences in method development using HPLC/UPLC and GC
</li>
<li>
Experiences in analytical method validation
</li>
<li>
Record of adhering to and promoting lab safety practices
</li>
<li>
Good communications skills
</li>
</ul>
Preferred Qualifications
<ul>
<li>
In-depth understanding of the separation principles of LC and GC
</li>
<li>
Deep expertise in chromatography method development and trouble shoots
</li>
<li>
Knowledge of QbD concepts, specification setting, and cGMP, with experience in contributing to regulatory submission
</li>
<li>
Communicates effectively in individual and group settings and collaborate effectively in a multi-disciplinary team setting
</li>
<li>
Demonstrated project management skills
</li>
<li>
Consistent record of collaboration with scientists and other stakeholders at external enterprises
</li>
<li>
Advanced scientific network in the industry and academia
</li>
<li>
Record of patents and publications
</li>
</ul>
Why Choose Us? 
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA #LI-SA​ #LI-Onsite
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Chromatography Principal Scientist

<h3>Job Description</h3>
Nightingale Nurses is seeking a travel Clinical Lab Scientist (CLS) for a travel job in Boston, Massachusetts.
Job Description &amp; Requirements
<ul>
<li>Specialty: Clinical Lab Scientist (CLS)</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 08/04/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days</li>
<li>Employment Type: Travel</li>
</ul>
About Nightingale Nurses
the first name in travel nursing
\n
You may not realize it, but as an RN with real world hospital experience, you are legendary. To the lives you’ve helped save, the patients you’ve cared for, and to the hospitals where you’ve done it. And you’re just getting started.
\n
Legendary is where Nightingale begins. We’re the first name in travel nursing, representing only the very best RNs. That’s why hospitals prefer us, allowing us to offer exceptional travel nursing assignments all over the US, as well as the highest pay rates and most extensive benefits in the industry.
\n
Nightingale facilitates every aspect of your travel nursing assignment, so you can focus on doing what you do best. We want you to grow, explore, and enjoy unrivaled liberty, the freedom to nurse.

Travel Microbiology Lab Manager

<h3>Job Description</h3>
Working at Freudenberg: We will wow your world! Responsibilities: 
<ul>\n
<li>Perform precise measurements using metrology tools and equipment.</li>
\n
<li>Conduct measurements on products and contamination.</li>
\n
<li>Calibrate, maintain, and repair metrology equipment and tools.</li>
\n
<li>Document and report all measurement, calibration, and test results.</li>
\n
<li>Identify and solve any problems that may affect the accuracy of measurements.</li>
\n
<li>Collaborate with engineering teams to identify measurement requirements.</li>
\n
<li>Develop, implement, and maintain calibration processes and procedures.</li>
\n
<li>Ensure compliance with quality control standards and procedures.</li>
\n
<li>Work as part of a team of Metrology Technicians to provide accurate results to the engineering team.</li>
\n
<li>Contribute to continuous improvement efforts in the measurement process.</li>
\n</ul>
\n Qualifications: 
<ul>\n
<li>Proven experience as a Metrology Technician or similar role.</li>
\n
<li>Associate degree in Metrology, Engineering, or a relevant field; certification in metrology is a plus.</li>
\n
<li>Knowledge of GD&amp;T (Geometric Dimensioning and Tolerancing).</li>
\n
<li>Understanding of technical prints.</li>
\n
<li>Prior experience with CMM (Coordinate Measuring Machine).</li>
\n
<li>Knowledge of metrology principles and measurement tools.</li>
\n
<li>Experience with calibration procedures.</li>
\n
<li>Excellent problem-solving skills.</li>
\n
<li>Strong attention to detail and manual dexterity.</li>
\n
<li>Ability to read and interpret technical manuals and diagrams.</li>
\n
<li>Strong communication skills to collaborate with engineering teams.</li>
\n
<li>Knowledge of industry standards and regulatory compliance requirements.</li>
\n</ul>
\n Communication &amp; Collaboration: Communicates clearly and concisely, while engaging proactively with colleagues at all levels of the organization. Value for Customers: Anticipates, understands and meets internal/external customers' needs and expectations. Develops solutions based on a customer centric approach. Innovation: Drives and supports innovative ideas, while taking informed risks to seek and develop new or improved solutions. Drive &amp; Execution: Proactively identifies what needs to be done and takes action. Explores new ways and pursues new opportunities. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg-NOK General Partnership

Metrology Technician - 1st Shift

<h3>Job Description</h3>
We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
Benefits:
<ul>
<li>This is a full-time or part-time REMOTE position</li>
<li>You’ll be able to choose which projects you want to work on</li>
<li>You can work on your own schedule</li>
<li>Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work</li>
</ul>
Responsibilities:
<ul>
<li>Give AI chatbots diverse and complex chemistry problems and evaluate their outputs</li>
<li>Evaluate the quality produced by AI models for correctness and performance</li>
</ul>
Qualifications:
<ul>
<li>A current, in progress, or completed Masters and/or PhD is preferred but not required</li>
<li>Fluency in English (native or bilingual level)</li>
<li>Detail-oriented</li>
<li>Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning</li>
</ul>
Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

Chemical Technician

Senior Chemist

<h3>Job Description</h3>
Job DescriptionBiologist I/II – Immunology &amp; Cell Biology (Contract)
Location:&nbsp;Worcester, MA (100% Onsite)
Type:&nbsp;6-Month Contract | Full-Time
Bioresearch Center&nbsp;is seeking a motivated and detail-oriented&nbsp;Biologist I or II&nbsp;to join our&nbsp;Immunology Discovery Dermatology&nbsp;team. This is an exciting opportunity to contribute to cutting-edge research focused on evaluating novel biotherapeutics and small molecules using in vitro and ex vivo models.
You’ll play a key role in designing and executing experiments with mammalian cell lines and primary human immune cells, supporting drug discovery efforts in a collaborative and fast-paced environment.
 Key Responsibilities
<ul>
<li>Design and execute in vitro and ex vivo pharmacology studies using mammalian cell lines and primary immune cells.</li>
<li>Perform aseptic cell culture, including immune cell isolation and maintenance of stable cell lines.</li>
<li>Conduct downstream analyses such as flow cytometry, ELISA, and MSD.</li>
<li>Analyze, interpret, and present experimental data to cross-functional teams.</li>
<li>Maintain accurate and detailed laboratory records and ensure reproducibility through quality control measures.</li>
</ul>
Qualifications
<ul>
<li>BS or MS in Biology, Molecular Biology, Immunology, or a related field.</li>
<li>3–5 years of relevant hands-on experience in academia or industry.</li>
<li>Proficiency in aseptic tissue culture, immune cell handling, and mammalian cell line maintenance.</li>
<li>Experience with flow cytometry and protein detection assays (ELISA, MSD).</li>
<li>Strong data analysis skills using Microsoft Excel and GraphPad Prism.</li>
<li>Excellent organizational, communication, and collaboration skills.</li>
</ul>
PhD holders are welcome to apply, though this role is ideally suited for candidates with BS/MS-level training.
 Top Skills We’re Looking For
<ul>
<li>In vitro pharmacology</li>
<li>Primary immune cell culture</li>
<li>Flow cytometry and ELISA/MSD</li>
<li>Data analysis and documentation</li>
<li>Team collaboration and scientific communication</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $35.00 - $38.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Worcester,MA.
Application Deadline
This position is anticipated to close on Jul 25, 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.

Biologist II

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, Sterility, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).</li>
<li>Documents work in a clear and organized manner.</li>
<li>Revises procedures and ELNs under close supervision.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs routine data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.
 
SHIFT
Sunday-Wednesday, 1st shift.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

257 Science Jobs