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<h3>Job Description</h3>
Job DescriptionSalary: $1,615 - $1,793/week based on experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Boylston, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

Project Geotechnical Engineer - Boylston

<h3>Job Description</h3>
Job DescriptionSalary: $1,634 to $1,814/week commensurate with experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Easton, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

Project Geotechnical Engineer - Easton

<h3>Job Description</h3>
Job Description
We are looking for&nbsp;Molecular Biologist&nbsp;for our client in&nbsp;Boston, MA
Job Title:&nbsp;Molecular Biologist
Job Location:&nbsp;Boston, MA
Job Type:&nbsp;Contract Job Description:
Pay Range: $55hr - $60hr
Responsibilities:
<ul>
<li>Conduct experiments to identify and validate drug targets.</li>
<li>Support assay design, optimization, validation, and data analyses.</li>
<li>Design and execute molecular and cell biology experiments.</li>
<li>Troubleshoot and analyze complex data in support of drug discovery projects.</li>
<li>Presentation of results and conclusions both orally and written.</li>
</ul>
Qualifications:
<ul>
<li>Experience with flow cytometry.</li>
<li>Cell culture techniques.</li>
<li>Basic laboratory skills including preparing solutions, pipet use, and GLP.</li>
</ul>
Company Descriptionvisit our career site to see all open positions @ <a href="http://jobs.cynetsystems.com" target="_blank">http://jobs.cynetsystems.com</a> 
<h3>Company Description</h3>
visit our career site to see all open positions @ <a href="http://jobs.cynetsystems.com" target="_blank">http://jobs.cynetsystems.com</a>

Molecular Biologist

<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 
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 
This role is for an advanced personnel who has in-depth knowledge of cell based and potency assays and are comfortable with troubleshooting. The Group Leader’s main technical responsibility will be to serve as SME for mRNA and gRNA potency assays to support several client programs.&nbsp;
Technical Responsibilities:
<ul>
<li>Optimize, technical transfer, qualification, and validation of potency assays used for lot release and characterization of cell and gene therapy products and critical materials.</li>
<li>Acting as an SME resource for potency assays.</li>
<li>Execution of complex GMP release and stability assays such as cell-based functional assays, flow cytometry methods, ddPCR, ELISA, and NGS assays.</li>
<li>Author and review SOPs and technical reports.</li>
<li>Work with cross-functional groups within the client environment to participate in various aspects of method development, transfer, process, and product characterization, comparability, and investigations.</li>
<li>Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance.</li>
</ul>
Leadership Responsibilities
<ul>
<li>Supports and monitors the performance of the team of employees</li>
<li>May participate in new hire interviews</li>
<li>Supports the on-boarding process of new employees</li>
<li>Disseminate administrative communications</li>
<li>Demonstrate and promote the company's vision</li>
<li>Ensure adherence to highest quality and efficiency standards in laboratory operations&nbsp;</li>
<li>Ensure coverage and performance for all shifts, and work duties&nbsp;</li>
<li>Performs administrative tasks for team member growth and development</li>
<li>Adeptly balance technical lab work with leadership responsibilities</li>
<li>Foster morale and teamwork&nbsp;</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor’s degree with 3-8 years of experience</li>
<li>Master’s degree with 2-5 years of experience</li>
<li>Must have experience with potency assay execution</li>
<li>Must have previous experience working in a GMP laboratory</li>
<li>Understanding of industry practices and standards is required</li>
<li>Laboratory supervisory experience&nbsp;is preferred</li>
<li>Team player with excellent oral and written communication skills</li>
<li>Independently motivated, detail-oriented, and excellent problem-solving abilities.</li>
</ul>
Differentiating qualifications:
<ul>
<li>Strong background in cell culture and experience working with cell lines and primary human cells.</li>
<li>Experience with functional, or potency assay transfer and execution in a GMP laboratory.</li>
<li>Broad experience with molecular biology, cellular, and immunoassay techniques including transfections/transductions, ddPCR/qPCR, flow cytometry, ELISA, and NGS.</li>
<li>Experience using data analysis software including JMP</li>
<li>Knowledge of ICH/USP guidelines.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute In Person Meeting&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>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 holidays</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 clients’ 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.

Potency Assay Scientist Group Leader

<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:
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Scientist I, Process Development

<h3>Job Description</h3>
Job Description
Description:
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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.
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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.
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We are looking for someone who is eager to contribute independent thinking and technical excellence to the upstream fermentation team.
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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.
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The role is well-integrated into the rest of the MSAT Microbial Team.
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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.
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The candidate would also be responsible for user-level maintenance of the relevant equipment and associated documentation.
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Plan and execute upstream process experiments at benchtop scales
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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.
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Acts as a technical resource within the upstream group. Provides formal/informal mentoring to junior colleagues within work group/project team.
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Works under limited supervision with periodic review of achievement of results and experimental approaches employed.
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Manages own time to meet agreed targets. Develops plans for short-term work activities on own projects.
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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.
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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.
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Participate in multi-disciplinary teams to resolve complex issues
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Assist in manufacturing investigations and process troubleshooting
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Assist on process improvement projects
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Qualifications
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Ph. D. with 0-4 years of experience in biotechnology ;OR
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Master's degree in a relevant discipline with at 3-5 years of applicable bioprocess experience ;OR
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Bachelor's degree with at least 7 years of experience
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Proficient in aseptic technique (required)
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Proficient in benchtop bioreactor operation and associated analytical tools (required)
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Experience with bench scale cell culture and/or bacterial fermentation (required)
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An in-depth knowledge of bioreactor operations fed-batch, perfusion, and continuous modes of cell culture
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Strong trouble-shooting skills and extreme attention to detail required
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Ability to troubleshoot technical issues, plan and carry out experiments independently, and work with complex instrumentation and software.
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Excellent oral and written communication skills.
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Strong analytical and computer skills.
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Involves typical bioprocessing lab activities
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Ability to routinely lift 50 lbs.
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Standing for prolonged periods of time, walking, bending, and using tools.
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Ability to perform mathematical calculations and ability to perform complex data analysis.
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Preferred:
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Prior experience developing and maintaining scale down models of commercial biopharmaceutical processes
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Prior experience in developing commercially relevant cell culture processes to produce pharmacologically active proteins
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Experience with control and data acquisition systems
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Demonstrated experience developing or introducing new technology into commercial processes
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Knowledge of all aspects of cell culture/fermentation, including batch, fed-batch, perfusion and harvest/clarification operations
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Familiarity with DoE and other statistical tools
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Experience with processing and interpreting large data sets
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Familiarity with regulatory filings, cGMP requirements and operational constraints
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</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.

Senior Scientist, Upstream Process Development (MSAT)

Bench Scientist

<h3>Job Description</h3>
Job DescriptionSalary: 
AEIS is a premier inspection services and materials testing company in the New York Metropolitan area. Our dedicated team takes an interdisciplinary approach to solving complex problems. We are currently looking for a Civil and Geotechnical Subject Matter Expert.The successful candidate for this position will have a New York (and preferably NJ) Professional Engineer license. The person will :
<ul>
<li>ensure conformance to codes by preparing and conduction building inspections; identifying violations; recommending compliance procedures; documenting observations.</li>
<li>ensure quality by supervising/conducting materials and structural component tests and evaluations for material characterization and failure analysis; maintaining standards; analyzing findings; preparing reports.</li>
<li>complete engineering projects by organizing and controlling project elements.</li>
</ul>
 
Responsibilities:
<ul>
<li>Prepare inspection schedule by studying permits, plans and specifications; estimating travel and inspection times; coordinating site visits; developing schedules.</li>
<li>Determine compliance to codes by inspecting work in progress and accomplished, including Geotechnical, Civil and Structural.</li>
<li>Attain compliance to codes by issuing notices for corrections; interpreting codes; recommending compliance procedures.</li>
<li>Record compliance by documenting progress and violations.</li>
<li>Maintain safe and healthy work environment by following organization standards and legal regulations.</li>
<li>Update job knowledge by tracking and understanding new standards; participating in educational opportunities, trade shows and conferences; reading technical/professional publications.</li>
<li>Enhance department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments by complying with federal and state regulations.</li>
<li>Implement corrective action when non-conforming work or departures from policies and procedures are uncovered.</li>
<li>Sign or otherwise approve inspection reports and inspection certificates.</li>
<li>Determine materials durability by conducting failure tests; analyze findings.</li>
<li>Improve materials, products and processes by recommending changes based on analytical findings; investigate and resolve concerns; develop new tests.</li>
<li>Improve quality results by following ISO 17020 and 17025 standards; study, evaluate, and re-design processes; implement changes.</li>
<li>Help customers by answering technical questions; respond to requests.</li>
<li>Contribute to team effort by accomplishing related results as needed.</li>
<li>Determine project responsibilities by identifying project phases and elements; assigning personnel to phases and elements; reviewing bids from contractors.</li>
<li>Determine project specifications by studying project design, customer requirements, and performance standards; completing technical studies; preparing cost estimates.</li>
<li>Determine project schedule by studying project plan and specifications; calculating time requirements; sequencing project elements.</li>
<li>Maintain project schedule by monitoring project progress; coordinating activities; resolving problems.</li>
<li>Control project plan by reviewing design, specifications, and plan and schedule changes; recommending actions.</li>
<li>Control project costs by approving expenditures; administering contractor contracts.</li>
<li>Develop project objectives by reviewing project proposals and plans; conferring with management.</li>
<li>Prepare project status reports by collecting, analyzing, and summarizing information and trends; recommending actions.</li>
<li>Maintain project database by writing computer programs; entering and backing up data.</li>
<li>Ensure confidentiality of information obtained in the course of its inspection activities. Proprietary rights of the company and clients shall be protected.</li>
<li>Ensure that purchase orders are reviewed and approved for technical content prior to release.</li>
<li>Ensure that sampling plan and procedures are documented/reviewed to avoid deterioration or damage to inspection items while under your responsibility.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor of Science Degree in Civil, Structural or Geotechnical Engineering</li>
<li>Professional Engineering License with registration in New York</li>
<li>Knowledge of NYC Building Codes</li>
<li>Must have pile driving experience</li>
</ul>
Salary is commensurate with experience in a similar role and includes a comprehensive benefits package. This role is an exempt, full-time salaried position.

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