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<h3>Job Description</h3>
Job Description
Scientific Marketing Manager / Director - in vivo Pharmacology
Location: Remote, USA
Salary: $120,000 - $160,000
 
Combine your passion for science with creativity in scientific marketing.
Join our dynamic marketing team at Pharmaron as a Scientific Marketing Manager. We are seeking an individual who is passionate about drug discovery and preclinical development with experience in drug efficacy testing in disease models. Become part of our team to help us elevate our brand and drive sales.
 
Your Key Responsibilities:
<ul>
<li>Craft compelling narratives: Translate complex scientific concepts into engaging stories that resonate with our audience.</li>
<li>Create new content: Partner with our scientists to create engaging content that showcases our expertise such as brochures, white papers, flyers, webpage content, etc.</li>
<li>Lead marketing campaigns: Develop and execute multi-channel campaigns that increase brand awareness and generate leads.</li>
<li>Analyze and optimize: Track marketing performance, identify trends, and refine our strategies for maximum impact.</li>
<li>Represent our brand: Manage our presence at industry conferences and events.</li>
</ul>
 Your Profile:
<ul>
<li>Location: Remote, the applicant must be located in Europe or North America.</li>
<li>Scientific background: A degree in biology, pharmacology, veterinary medicine or a related field is essential.</li>
<li>Experience: Minimum of 5 years of industry experience related to animal disease models in drug discovery or drug development.</li>
<li>Exceptional communication skills: A passion for writing and the ability to convey complex scientific ideas to diverse audiences.</li>
<li>Passion for learning: A desire to stay updated on industry trends and best practices.</li>
<li>Collaborative spirit: Enjoy working with cross-functional teams and external partners with a willingness to travel as needed.</li>
</ul>
 
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental &amp; Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare &amp; Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&amp;D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
 
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
 
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
 
#LI-EH1

Scientific Marketing Manager / Director - in vivo Pharmacology / Toxicology

<h3>Job Description</h3>
Job Description
Job Title: Quality Control (QC) Chemist (Method Validation) Work Location: Fall River, MA&amp; Work Hours: 8:30AM – 5:00PM (may vary based on business needs)&amp; 
Reports To: Quality Control manager
The Quality Control Chemist is an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory.
Duties and Responsibilities • Preparation of protocols and execution of analytical method validation / verification / method transfer. • Working knowledge on cleaning validation (residue analysis). • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
Education and Experience: • Bachelor's degree (BS or BA), physical sciences, Chemistry preferred • Proficiently speak English as a first or second language Proficiently communicate and understand (read and write) scientific work in English • Must be authorized to work permanently in the United States without company sponsorship • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets. • Working knowledge of Microsoft Office programs and other scientific based software. • Experience in Inhalation products (MDI) is a plus

QC Chemist

<h3>Job Description</h3>
Job Description
Responsibilities: Under general supervision, perform all aspects required for the completion of all electric Geographic Information Systems (GIS) work closure and mapping activities. Perform administrative support activities of various degrees of complexity, and to perform as required such duties as:
<ul>
<li>Perform and complete "As Built" design changes for construction and confirming work requests and post updates to Smallworld GIS</li>
<li>Check construction and retirement orders together with their completion reports in the field against the actual installations and retirements of equipment</li>
<li>Perform and complete all types of Data Model changes and map/drawing changes</li>
<li>Assist with the design of Underground systems such as Conventional Manhole, Duct and URD systems utilizing computer systems and perform "As Built" design changes</li>
<li>Provide support to the Regional Control Centers and other clients to ensure accuracy of systems</li>
<li>Assist in recording on appropriate prints or drawings additions and retirements of facilities as shown on construction and retirement orders and associated completion reports</li>
<li>Analyze completion reports and reconcile with information added to or removed from the prints or drawings relating to any asset classes</li>
<li>Work proficiently in MS Office, GIS and EAM Applications</li>
<li>Make contacts with other districts and departments in connection with job duties</li>
<li>Assemble, maintain and/or transcribe information from various sources, prepare and maintain reports, correspondence and records, forms and orders.</li>
<li>Make arithmetical computations; maintain statistical information.</li>
<li>Check data for accuracy and otherwise assist in completing various types of orders, reports, invoices.</li>
<li>Communicate with customers or their representatives, outside agencies, and other departments.</li>
<li>Update company records including but not limited to maps and various reports.</li>
<li>Perform administrative support activities associated with the tasks and responsibilities of the department.</li>
</ul>
Requirements
AAS Degree in applicable Engineering Technology as posted, i.e. GIS, Computer Science, Electrical, Mechanical, or Civil/Structural. For GIS postings, candidates must have an AAS degree in GIS/Computer Science or two (2) years of design work experience in GIS
<ul>
<li>Must pass validated aptitude test</li>
<li>Ability to read maps and construction drawings and knowledge of equipment and materials used in electric plant</li>
<li>Thorough familiarity with applicable accounting procedures.</li>
<li>Thorough familiarity with applicable computer and software systems and procedures.</li>
<li>Ability to direct the work of others engaged in all administrative support activities as required.</li>
<li>Ability to handle contacts with customers, contractors and other departments.</li>
<li>Ability to handle duties which require independent judgment.</li>
<li>Satisfactory completion of validated skills testing (keyboarding), as determined by the Company</li>
<li>Ability to satisfactorily interact with customers, outside agencies and other departments.</li>
<li>Ability to handle duties that require independent judgment.</li>
<li>Ability to make arithmetical computations.</li>
<li>Familiarity with computer applications normally required in a business environment.</li>
<li>Satisfactory completion of validated skills testing (keyboarding), as determined by the Company.</li>
</ul>
Benefits
MWResource offers medical, dental and vision coverage through Capital Blue Cross, short- and long-term disability coverage, employer paid life insurance, and participation in the MWResource 401K plan for US based consultants.
MWResource does not discriminate based on race, gender, color, religion, national origin, age, disability, veteran status, or anything else that makes you part of any group.
Candidates must be authorized to work in the United States.
Candidates will be required to pass a background check and drug screening.
Please note we are not open to outsourcing our recruitment needs.

GIS Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.
Responsibilities Include:&nbsp;
<ul>
<li>Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment</li>
<li>90% Method development,&nbsp;qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
<ul>
<li>May include technology transfer activities, regulatory support, and possible project team participation</li>
</ul>
</li>
<li>10% Analytical testing
<ul>
<li>Liquid Chromatography&nbsp;and Plate-Based&nbsp;</li>
</ul>
</li>
<li>Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.&nbsp;</li>
<li>Experience working in a GMP/GLP environment&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives</li>
<li>Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>BS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>2 years of demonstrated work experience with cell-based assays</li>
</ul>
</li>
<li>Or MS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>6 months of Demonstrated experience with cell-based assays&nbsp;</li>
</ul>
</li>
<li>Experience with&nbsp;experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioassay Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
Seeking a scientist to perform analytical testing for biologic product release and characterization in a cGMP/GLP environment. Responsibilities include routine testing, documentation, troubleshooting HPLC/UPLC/CE methods, and ensuring compliance.
Responsibilities Include:&nbsp;
<ul>
<li>Contributes as part of a team of AD scientists towards execution&nbsp;of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.</li>
<li>Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE, iCE, cIEF, CE-SDS, Titer, Peptide, and Glycan mapping - using established Test Methods, including associated protocol/report documentation and presentations.</li>
<li>Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements.</li>
<li>Responsible for working on other non-lab-based tasks from time to time if assigned.</li>
<li>Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis,&nbsp;and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.</li>
<li>Demonstrate HPLC, UPLC, and/or CE troubleshooting capabilities.</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience with ELISA techniques</li>
<li>Ability to quickly learn new techniques</li>
<li>Strong multitasking and organizational skills</li>
<li>Attention to detail with accurate record-keeping</li>
<li>Ability to follow instructions and adhere to company policies</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>Bachelor’s or Master’s in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other science-related degree concentration</li>
<li>Equivalent directly related work/internship experience with HPLC/UPLC required.</li>
<li>Knowledge of principles of HPLC/UPLC/CE and theories of relevant techniques and a&nbsp;basic understanding of industry practices and standards required</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

HPLC 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 
Technical expert that will drive late-stage process development activities of novel antibody-drug conjugates (ADCs).&nbsp; Independently identify, develop, and execute laboratory experiments to address critical project needs.&nbsp; Continuously seek to improve existing laboratory methods and processes.&nbsp; Read and adapt literature to accomplish assignments.&nbsp; Demonstrate mastery of a broad range of experimental techniques and methods of data analysis.&nbsp; Collaborate effectively with cross-functional groups ensure robust process scale-up and tech transfer to manufacturing sites.
Responsibilities:
<ul>
<li>
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
•Independently design and conduct critical experiments that further project goals.
•Implement and may innovate new experimental protocols/techniques.
•Understand the goal and maintain a high proficiency in his/her projects as well as the overall
program.
•Interpret results and draw conclusions from own multistage experiments, note significant
deviations, then suggest, design, and pursue relevant experiments.
•Understand relevant scientific literature and apply theoretical framework to solving problems within
scientific discipline in a timely manner.
•Perform routine and complex tasks competently and independently and generate reliable and
consistent results.
•Impact projects mostly through lab and/or pilot plant based activities.
•Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
•Understand and adhere to corporate standards regarding code of conduct, safety, appropriate
handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care
where applicable.
</li>
</ul>
Qualifications 
<ul>
<li>
•Bachelor’s Degree or equivalent education with typically 5 years of experience, or Master’s Degree
or equivalent education with typically two years of experience.
•Theoretical and practical knowledge to carry out the job functions.
</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​
​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive 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 determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with 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>

Scientist I, Process Development

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Manufacturing Sciences and Technology (MSAT) Upstream Group is looking for a highly motivated and versatile candidate to join our multidisciplinary team of scientists and engineers in Andover, MA.
</li>
<li>
MSAT supports portfolio of late-stage development of commercial biopharmaceuticals and vaccines, and is responsible for process troubleshooting, process improvements and second- generation process development.
</li>
<li>
We are looking for someone who is eager to contribute independent thinking and technical excellence to the upstream fermentation team.
</li>
<li>
The Scientist will be a part of a diverse and motivated team of scientists, engineers, and technical professionals that are focused on fermentation processes to produce biotherapeutics.
</li>
<li>
The role is well-integrated into the rest of the MSAT Microbial Team.
</li>
<li>
This role will collaborate with other MSAT scientists to setup bioreactors and execute well-designed experiments, including but not limited to basic analytics, data acquisition and documentation of work.
</li>
<li>
The candidate would also be responsible for user-level maintenance of the relevant equipment and associated documentation.
</li>
<li>
Plan and execute upstream process experiments at benchtop scales
</li>
<li>
Participates and significantly contributes to discussions in lab and project team meetings on design of experiments (bioreactor and shake flask) and interpretation of experimental data.
</li>
<li>
Acts as a technical resource within the upstream group. Provides formal/informal mentoring to junior colleagues within work group/project team.
</li>
<li>
Works under limited supervision with periodic review of achievement of results and experimental approaches employed.
</li>
<li>
Manages own time to meet agreed targets. Develops plans for short-term work activities on own projects.
</li>
<li>
Ensures effective, high-quality, timely and appropriate documentation in electronic laboratory notebooks and internal technical reports; presents data/ strategy to scientists and management in appropriate internal and external venues (technical meetings, project team meetings, conferences) as appropriate.
</li>
<li>
Contributes to safe, efficient, effective and harmonious lab environment, ensures appropriate cleanliness and status/ operability of shared or assigned lab space or equipment; strong lab citizen and collaborative team player; approaches the job with energy and commitment; frequently demonstrates initiative.
</li>
<li>
Participate in multi-disciplinary teams to resolve complex issues
</li>
<li>
Assist in manufacturing investigations and process troubleshooting
</li>
<li>
Assist on process improvement projects
</li>
</ul>
Qualifications
<ul>
<li>
Ph. D. with 0-4 years of experience in biotechnology ;OR
</li>
<li>
Master's degree in a relevant discipline with at 3-5 years of applicable bioprocess experience ;OR
</li>
<li>
Bachelor's degree with at least 7 years of experience
</li>
<li>
Proficient in aseptic technique (required)
</li>
<li>
Proficient in benchtop bioreactor operation and associated analytical tools (required)
</li>
<li>
Experience with bench scale cell culture and/or bacterial fermentation (required)
</li>
<li>
An in-depth knowledge of bioreactor operations fed-batch, perfusion, and continuous modes of cell culture
</li>
<li>
Strong trouble-shooting skills and extreme attention to detail required
</li>
<li>
Ability to troubleshoot technical issues, plan and carry out experiments independently, and work with complex instrumentation and software.
</li>
<li>
Excellent oral and written communication skills.
</li>
<li>
Strong analytical and computer skills.
</li>
<li>
Involves typical bioprocessing lab activities
</li>
<li>
Ability to routinely lift 50 lbs.
</li>
<li>
Standing for prolonged periods of time, walking, bending, and using tools.
</li>
<li>
Ability to perform mathematical calculations and ability to perform complex data analysis.
</li>
</ul>
Preferred:
<ul>
<li>
Prior experience developing and maintaining scale down models of commercial biopharmaceutical processes
</li>
<li>
Prior experience in developing commercially relevant cell culture processes to produce pharmacologically active proteins
</li>
<li>
Experience with control and data acquisition systems
</li>
<li>
Demonstrated experience developing or introducing new technology into commercial processes
</li>
<li>
Knowledge of all aspects of cell culture/fermentation, including batch, fed-batch, perfusion and harvest/clarification operations
</li>
<li>
Familiarity with DoE and other statistical tools
</li>
<li>
Experience with processing and interpreting large data sets
</li>
<li>
Familiarity with regulatory filings, cGMP requirements and operational constraints
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Bench Scientist

<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>
Responsible for generating and processing single-cell, spatial, and functional genomics data, as well as supporting standard immunoprofiling activities such as cell culture and flow cytometry.
</li>
<li>
Follow existing lab standard operating procedures to: Participate in sample collection of murine and human tissues, including the preparation of tubes, interfacing with in vivo scientists to retrieve samples, isolation of primary immune cells, and standard mammalian cell culture
</li>
<li>
Participate in sample preparation of murine and human tissues, including tissue fixation, dissociation, sectioning, and antibody staining
</li>
<li>
Generate spatial and single-cell data via a number of commercial workflows, including 10x Genomics and Parse Technologies
</li>
<li>
Interpret quality control metrics for spatial, single-cell and cytometry experiments
</li>
<li>
Typical bench work, including sitting, pipetting, lifting &lt;10lb items
</li>
<li>
Reports to a scientific director of the Systems Immunology Lab
</li>
<li>
Collaborates with and supports several multi-disciplinary experimental teams on a per-project basis
</li>
</ul>
REQUIREMENTS
<ul>
<li>
Masters + 3 years of experience in Biology, Immunology, or a related field; OR
</li>
<li>
PhD +0 yrs experience in Biology, Immunology, or a related field
</li>
<li>
3+ years of hands-on experience with standard immunoprofiling technologies, including:
<ul>
<li>
Flow Cytometry
</li>
<li>
Single-cell library preparation (ideally 10x Genomics or Parse Technology)
</li>
<li>
Preparation and loading of Illumina sequencing libraries
</li>
<li>
Bonus: generation of spatial transcriptomics data (any technology)
</li>
</ul>
</li>
<li>
3+ years of experience with primary immune cells, including:
<ul>
<li>
Primary immune cell isolation
</li>
<li>
Maintenace of immune cell lines
</li>
<li>
Cell culture and in vitro stimulation of primary immune cells
</li>
<li>
Bonus: experience with CRISPR mediated functional genomics, including electroporation of primary immune cells
</li>
</ul>
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist Cellular Genomics

<h3>Job Description</h3>
Job DescriptionSalary: 
Job Title: Professional Engineer - Geotechnical Engineering
Location: NY Metro Area (Job Sites) Employment Type: Full-Time
 
Why Should You Join AEIS?
If you're considering AEIS LLC for your next career move, this is the most important question to ask.
At AEIS, we believe in building real relationships, not just contracts. The work you do here isnt just about inspections its about craftsmanship, collaboration, and commitment to quality. And like any meaningful relationship, there needs to be a true fit between you and us in values, purpose, and expectations.
This is where youll spend most of your working life. We want it to be worth it for you and for us. When the fit is right, our employees grow into trainers, QA leads, and technical experts. If you're serious about quality and looking for more than just a job, we invite you to explore this opportunity.
About AEIS
AEIS is a leading inspection services and materials testing company in the NY Metro area and proud to be an AWS Accredited Test Facility. With a 20,000 sq. ft. state-of-the-art metallurgy lab in South Plainfield, NJ, our team works at the intersection of construction, failure analysis, welding engineering, and NDT.
We began our welding inspection journey at the World Trade Center Transportation Hub project, and since then, AEIS has contributed to nearly every major bridge, rail hub, and airport project in the NY Metro region. We are highly respected by major public agencies, including:
<ul>
<li>The Port Authority of NY &amp; NJ (PANYNJ)</li>
<li>Metropolitan Transportation Authority (MTA)</li>
<li>New York State Department of Transportation (NYSDOT)</li>
<li>NYC Department of Environmental Protection (NYCDEP)</li>
<li>New York Power Authority (NYPA)</li>
<li>NJ Transit Authority </li>
</ul>
 
Job Summary:
Join our team as a Professional Engineer - Geotechnical Engineering and play a key role in delivering innovative solutions for complex geotechnical projects in the NYC Metro Area. We're seeking an experienced expert with a strong background in soil mechanics, foundation design, and geotechnical analysis.
 
Key Responsibilities:
Technical
<ul>
<li>Conduct geotechnical site investigations, including soil sampling and testing.</li>
<li>Conduct and supervise detailed building inspections to ensure conformance to NYC &amp; NYS codes, focusing on underpinning, geotechnical drilling (Rock Coring/Test Pits/Cone Penetration Tests/Standard Penetration Tests), deep foundations installation (Driven Piles/Micropiles/Helical Piles/Caissons), civil, and structural aspects.</li>
<li>Prepare comprehensive inspection reports, ensuring all records reflect progress, violations, and compliance with regulatory standards. Ensure the confidentiality of client information and proprietary data.</li>
<li>Review and analyze the design of foundations, retaining walls, and other geotechnical structures.</li>
<li>Develop and implement geotechnical engineering plans and specifications.</li>
<li>Conduct stability analyses for slopes and excavations.</li>
<li>Evaluate soil-structure interaction and settlement analyses.</li>
</ul>
Project Management
<ul>
<li>Manage geotechnical projects from conception to completion.</li>
<li>Coordinate with multidisciplinary teams, including architects, engineers, and contractors.</li>
<li>Prepare and manage project schedules, budgets, and resources.</li>
<li>Ensure compliance with regulatory requirements, industry standards and project objectives are met by closely monitoring progress.</li>
</ul>
Documentation and Reporting
<ul>
<li>Prepare comprehensive technical reports and records.</li>
<li>Maintain accurate records, calculations, and drawings.</li>
<li>Develop and implement quality control procedures.</li>
</ul>
Requirements:
Education
<ul>
<li>Bachelor's or Master's degree in Civil Engineering, Geotechnical Engineering, or related field.</li>
</ul>
Professional License
<ul>
<li>Valid Professional Engineer (P.E.) license in NY &amp; NJ.</li>
</ul>
Experience
<ul>
<li>5+ years of experience in geotechnical engineering, preferably in a consulting/ quality assurance environment.</li>
</ul>
Skills
<ul>
<li>Strong knowledge of geotechnical engineering principles, soil mechanics, and foundation design.</li>
<li>Excellent communication, problem-solving, and project management skills.</li>
<li>Familiarity with local building codes and regulations.</li>
<li>Required to travel to project sites in the New York City Metro Area and work at project offices on site.</li>
</ul>
Benefits
<ul>
<li>401(k)</li>
<li>Health, Dental, Vision Insurance</li>
<li>Paid Time Off (PTO)</li>
<li>Professional Development Support</li>
<li>Employee Referral Program</li>
<li>Internal mentorship and cross-training opportunities</li>
</ul>

Professional Engineer (PE) - Geotechnical

<h3>Job Description</h3>
Job Title: Biotechnologist Associate 
Location: Portsmouth, NH, 03801 
Duration: 12 Months
Job Type: Contract 
Work Type: Onsite 
Shift: 12 Hour Shift - Night Shift from 07:00 PM to 07:00 AM - Rotating Shift
Job Description:
<ul>
<li>The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. </li>
<li>They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. </li>
<li>Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. </li>
<li>Attain qualification for all assigned tasks and maintain individual training plan. </li>
<li>Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. </li>
<li>Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. </li>
<li>Must be willing to gown and work in a "clean room" environment. </li>
<li>Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects. </li>
<li>Perform other duties as assigned. </li>
<li>High School Diploma or equivalent experience minimum with an AS/BS preferred </li>
<li>Preferred area of study: Science related field, degrees in Genetics are relevant. </li>
<li>Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred. </li>
<li>Prior experience with Aseptic Techniques and gowning procedures is preferred. </li>
<li>Working experience in manufacturing; cGMP setting preferred. The ideal candidate will have experience within the Cell and Gene Therapy field. </li>
<li>Able to follow documentation procedures for day-to-day tasks in a regulated industry </li>
<li>Proven logic and decision-making abilities, critical thinking skills. </li>
<li>Strong written and verbal communication skills.</li>
</ul>

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