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<h3>Job Description</h3>
Job Description RedTown Technical Services, LLC Description:
This PART-TIME position is responsible for all operational weather forecasting aspects of the MQ-4C Triton Mission and its customers. This includes pre-mission planning/setup briefings; DD-175-1 Flight Weather Briefings; takeoff, flight following, on-station execution, and recovery forecasts and briefings; Air Vehicle Operator turnover briefings, and real-time updates to forecasts as conditions and criteria warrant. Services will be provided at Naval Air Station Jacksonville, Florida. 
 
Hourly pay begins at $34.61 Forecaster II rate plus an additional $4.93 per hour for up to 40 hours per week Health &amp; Welfare. Night differential is compounded to base pay.
 
Role and Responsibilities
<ul>
<li>Provide properly formatted pre-mission planning briefs in support of VUP MQ-4C Triton orbits. AORs may be in the EUCOM, INDOPACOM, and/or CENTCOM</li>
<li>Provide properly formatted aviation DD175-1 Flight Weather Briefing's to VUP pilots face-to-face or electronically</li>
<li>Provide properly formatted Air Vehicle Operator turn-over briefings to VUP as scheduled</li>
<li>Provide real-time updates to the forecast when conditions affecting the airborne aircraft or recovery airfield change substantially from forecasted conditions, or as required by VUP pilots</li>
<li>Perform various administrative taskings such as training, quality control, outage reporting, aircraft mishap notifications, attend meetings, and so forth</li>
</ul>
Qualifications/Education Requirements
<ul>
<li>Must be a U.S. Citizen</li>
<li>Must have “at least” two years of aviation forecasting experience with the DOD or other Government agency. </li>
<li>Shall have visual acuity correctable to 20/20 with glasses or contacts throughout the life of the contract</li>
<li>Shall be able to demonstrate sufficient ability to operate all meteorological and communications equipment required for certification</li>
<li>Must be able to obtain and maintain a SECRET level clearance</li>
<li>Shall be able to speak, read, and understand English, and communicate well</li>
</ul>
Preferred Qualifications
<ul>
<li>4+ years of aviation forecasting experience</li>
<li>Familiarity with the Navy's Flight Weather Briefer program</li>
<li>Persons currently holding an active Navy CAC and having an active security clearance within the past 2-years</li>
<li>Experience with EUCOM and/or CENTCOM weather patterns and synoptic scale influences and impacts to operations. Resumes should reflect experience in these COMs when appropriate</li>
<li>Persons who have previously supported the military weather community</li>
<li>Persons having hands-on experience supporting Unmanned Air Vehicles or other Unmanned Aerial Systems</li>
</ul>
Additional Notes
The selected candidate will work in an office-type atmosphere. Meals are taken in conjunction with the shift and candidates will have access to a refrigerator and microwave. The workload will vary and may be stressful at times when adverse weather is present. The candidate can expect irregular work hours to consist of days, evenings, weekends, and holidays. 
Duties may include occasional overtime. The schedule will fluctuate and be determined by the Senior Forecaster. 
RedTown Technical Services, LLC is an Equal Opportunity Employer and does not discriminate against employees or applicants on the basis of race, religion, color, sex, gender identity, national origin, age, United States military veteran's status, ancestry, sexual orientation, marital status, family structure, or mental or physical disability provided the essential functions of the job can be performed with or without reasonable accommodation.
RedTown Technical Services, LLC is an Equal Opportunity Employer and does not discriminate against employees or applicants on the basis of race, religion, color, sex, gender identity, national origin, age, United States military veteran's status, ancestry, sexual orientation, marital status, family structure, or mental or physical disability provided the essential functions of the job can be performed with or without reasonable accommodation.
Reasonable Accommodations
The ADA defines “reasonable accommodation” as a change or adjustment to a job or work environment that allows a qualified individual with a disability to satisfactorily perform the essential functions of a particular job and does not cause undue hardship for the employer. Examples of reasonable accommodations may include: Additional modifying equipment or devices; Modified work schedules; Providing an interpreter; or Making the work environment readily accessible to individuals with disabilities.
<ol>
<li>This Organization Participates in E-Verify- <a href="https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf" target="_blank">https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyPar…</a></li>
<li>“Right to Work” - <a href="https://www.e-verify.gov/sites/default/files/everify/posters/IER_RighttoWorkPoster.pdf" target="_blank">https://www.e-verify.gov/sites/default/files/everify/posters/IER_Rightt…</a></li>
</ol>
**HUBZONE**
Qualified candidates living in a Hubzone will receive preferential consideration in hiring.
 
Not sure you live in a Hubzone? Go here and enter your address:
<a href="https://maps.certify.sba.gov/hubzone/map#center" target="_blank">https://maps.certify.sba.gov/hubzone/map#center</a>
Requirements:
 
 
PIa3aa4562d5da-25405-37636107

Weather Forecaster-Jacksonville, FL

<h3>Job Description</h3>
Job DescriptionCompany Description 
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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing.
&nbsp;In 2021, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Become your most extraordinary self!&nbsp; Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. &nbsp;Join Eurofins Panlabs, Inc.&nbsp;part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. &nbsp;Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide!
We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. &nbsp;
The Study Director of Translational Biology Services serves as a scientific and thought leader in the area, using in vitro biology platforms and technologies to model human biology. This role is responsible for managing study conduct from concept and design to execution, data analysis, and reporting, according to client program needs and project specifications. This position will play a key role in supporting commercial operations to identify new markets, customer support, and operations teams in project management, and align the Discovery portfolio with services to meet those demands. This role requires a high level of technical expertise and experience in client communication within a contract research organization. This role will lead strategic initiatives, innovation efforts, and client programs in Drug Discovery Services.
Essential Duties and Responsibilities:
The Study Director is a scientific leadership position, responsible for providing guidance and alignment between our customer base, the industry at large, commercial teams, and service operations. This role will be collaborative and influential in a broad network of business functions in support of delivering high quality services to our valued customers, and driving business growth, brand recognition, and alignment with Eurofins’ core competencies.
<ul>
<li>Develops client and stakeholder relationships through technical leadership and collaboration</li>
</ul>
<ul>
<li>Manages client projects in all phases of study life cycle from study design to reporting and data discussion</li>
<li>Ensures regulatory compliance and quality assurance of client studies</li>
<li>Delivers scientific leadership to executive management in developing portfolio strategy, new growth areas, and new technology planning</li>
<li>Influences scientific community through external marketing, scientific presentations, industry reputation, and brand awareness</li>
<li>Provides leadership in establishing and monitoring unit research and development objectives and commercial lifecycle management</li>
<li>Provides technical leadership to lab operations, business development, and marketing teams</li>
<li>Supports client services team in generating proposals, RFPs, study plans, and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis.</li>
<li>Supports laboratory team, and may be required to conduct experiments at the bench, in a lab setting to support client projects, R&amp;D, training, and troubleshooting</li>
<li>Completes required training and supports 100% of Employee Health and Safety requirements</li>
<li>Conducts responsible use of confidential IT and business systems, as required</li>
<li>Adheres to department SOP and documentation requirements</li>
<li>Ensures accurate data management and reporting, with the highest integrity, and manages quality control on project data and reports</li>
<li>Accountable for delivering to unit and site key performance metrics (quality, delivery on time)</li>
<li>Supports site goals and demonstrates Eurofins’ competencies, as defined in the job plan</li>
<li>Provides training to colleagues and external end users, when required</li>
<li>Performs other duties, as assigned</li>
</ul>
Qualifications 
Basic Minimum Qualifications (BMQ)
<ul>
<li>Demonstrated experience in project management, support of technical correspondence, drafting and presenting of scientific proposals to clients.</li>
<li>Scientific expertise in the areas of: cellular biology, in vitro assays, biomarker discovery, immunology, stem cell biology, or related methods and applications.</li>
<li>Experience and/or knowledge in supporting a functional area within a drug discovery program, from development to IND submission life cycle.</li>
<li>Demonstrated scientific contributions to the industry at large, through publications, and presentations.</li>
<li>Ability to collaborate with cross-functional teams to deliver high quality results in a time-driven manner.</li>
<li>High-level expertise in experimental design, scientific interpretation, reporting, and presentation.</li>
<li>Proven experience with program management and research / development in an industry setting.</li>
<li>Demonstrated experience in designing and presenting custom study proposals and workstream, complete with timeline and deliverable schedules.</li>
<li>Experience in supporting scientific services within a quality management / regulatory framework.</li>
</ul>
Education/Experience (BMQ)
<ul>
<li>M.A. or M.S. with 8 years relevant experience</li>
<li>Ph.D. with 5 years relevant experience</li>
<li>Combination of Education and Relevant Experience</li>
</ul>
Ability / Skills (BMQ):
<ul>
<li>Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health.</li>
<li>Excellent interpersonal, verbal, and written skills, including ability to prepare detailed scientific reports and group presentations.</li>
<li>Ability to lead the project management, plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources.</li>
<li>Exhibits scientific leadership ability, capacity to troubleshoot complex experimental design, and manage risk in study management.</li>
<li>Demonstrated interest in staying current in scientific field of expertise, including staying abreast of industry trends, recent scientific publications, and regulatory requirements.</li>
<li>Demonstrated experience in working effectively with cross-functional teams.</li>
<li>Excellent attention to detail and maintain a high-quality standard of work under defined timelines.</li>
<li>Knowledge of quality management principles, and applications for ensuring scientific services meet industry best practices and regulatory guidelines.</li>
</ul>
 Additional Information 
The position is full-time, Monday-Friday, 8 a.m.- 5 p.m., with overtime as needed.&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 holidays</li>
</ul>
Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Study Director - Translational Biology Services

<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 
Senior Scientist I, Biologics Drug Product Development
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&amp;D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy).
AbbVie is seeking a highly motivated candidate for the position of Senior Scientist I, Biologics Drug Product Development, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics formulation and process development, and characterization. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, science and technology, pilot plants and third-party manufacturers.
Key Responsibilities:
<ul>
<li>Lead the design and execution of biologics drug product formulation and process development, characterization and robustness studies.</li>
<li>Support scale-up and technology transfer activities to internal and external manufacturing sites.</li>
<li>Keep abreast of the latest advances in biologics formulation and process technologies.</li>
<li>Initiate and/or support scientific initiatives to drive innovation, continuously enhance capabilities and improve business processes.</li>
<li>May represent the Bio DPD function in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC team.</li>
<li>Effectively and timely communicates study plans, risks and mitigation plans to stakeholder and line management.</li>
</ul>
Qualifications 
Required Qualifications:
<ul>
<li>Bachelors, Masters, or PhD in pharmaceutics, pharmaceutical sciences, chemistry, chemical engineering, or related disciplines with 8+ (Bachelors), 6+ (Masters), or 0+ (PhD) years of relevant industry experience.</li>
<li>Proven ability to solve critical scientific problems.</li>
<li>Hands-on experience with biologics formulation development and lyophilization.</li>
<li>Hands-on experience with analytical and biophysical characterization of proteins (e.g. HPLC/UPLC, UV-Vis spectroscopy, CE-SDS, icIEF, HIAC, MFI, DLS, DSC, etc), and solid-state characterization methods.</li>
<li>Solid understanding of biologics degradation mechanisms and stabilization strategies.</li>
<li>Hands-on experience with Design of Experiments (DoE), multivariate statistical analyses and data visualization tools</li>
</ul>
Preferred Qualifications:
<ul>
<li>Understanding of relevant cGMP and regulatory guidance.</li>
<li>Experience with sterile manufacturing unit operations (freeze-thaw, mixing, filtration, filling, and freeze-drying) development, characterization, scale-up and technology transfer.</li>
<li>Experience in managing third party manufacturers.</li>
<li>Experience with quality risk management and drug product control strategies.</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>

Senior Scientist I, Biologics Drug Product Development

<h3>Job Description</h3>
Job Description
Earth Systems is not your average environmental consulting firm. We’re hands-on, collaborative, and committed to solving real-world geotechnical and environmental challenges with technical excellence and regulatory know-how. If you want your work to matter—and have the autonomy to lead it—we want you on our Florida-based team.
 
We are seeking a Geotechnical Engineer with a background in Geology, Environmental Science, or Environmental Engineering who thrives in a multidisciplinary environment. Candidates must reside in Florida and have direct experience with Florida regulations and field conditions. This is a field-forward position with a focus on practical problem-solving and project leadership in the Southeastern region.
 
Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations including site reconnaissance, subsurface explorations, soil/rock classification, and in-situ testing</li>
<li>Analyze data for foundation design, slope stability, settlement analysis, and pavement recommendations</li>
<li>Prepare detailed geotechnical reports with practical engineering solutions</li>
<li>Develop project scopes, proposals, and budgets; assist with project management and client communications</li>
<li>Oversee field exploration programs, coordinate lab testing, and ensure QA/QC on deliverables</li>
<li>Work closely with regulatory agencies to ensure compliance with FDEP, FDOT, and other Florida-specific environmental/geotechnical regulations</li>
<li>Mentor junior staff and support business development through local networking and technical presentations</li>
</ul>
 
Required Qualifications:
<ul>
<li>Bachelor's degree in Geotechnical Engineering, Geology, Environmental Engineering, or related field (Master’s preferred)</li>
<li>5+ years of experience in geotechnical engineering or applied environmental consulting</li>
<li>PE or the ability to obtain PE in Florida within 12 months</li>
<li>Proficiency in AutoCAD, gINT, GeoStudio, or similar software</li>
<li>Strong writing skills and experience preparing detailed technical reports</li>
<li>Current driver’s license and willingness to travel to project sites across Central Texas</li>
</ul>
 
What We Offer:
<ul>
<li>Competitive salary </li>
<li>Medical, dental, vision, and life insurance</li>
<li>401(k) with company match</li>
<li>PTO, holidays, and flexible field scheduling</li>
<li>Mileage reimbursement</li>
<li>Paid training, certifications, and continuing education</li>
<li>Growth-focused culture with a seat at the table</li>
</ul>
 
Must be authorized to work in the United States. Sponsorship is not available for this position.
 
Ready to take your career to the next level in a place where your skills are valued and your impact is real? Apply now to join Earth Systems.

Geotechnical Engineer

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>Free uniforms</li>
<li>Paid time off</li>
<li>Training &amp; development</li>
</ul>
 This is an entry-level position! No experience is necessary! Window Cleaning Technician Benefits and Perks: 
<ul>
<li>Money -- and opportunity to make more. Starting between $15-20 per hour with potential for commissions and bonuses. You decide how much you can make!</li>
<li>Paid vacation days and paid holidays.</li>
<li>Work comfortably and casually. Shine t-shirts, sweatshirts and polo shirts are all provided to you for free. And we provide all the equipment youll need too!</li>
<li>Paid training learn a valuable trade, advancing your skills, and get paid while doing so. Even if you dont have experience, it doesnt matter well train you!</li>
<li>Vehicles are provided for you, so no using your own gas.</li>
<li>An incredible, team-focused Shine culture that models the five core values we hold true.</li>
<li>Shine uses the latest technology and equipment to ensure youre well equipped on the job.</li>
</ul>
 Window Cleaning Technician Job Summary: 
<ul>
<li>Each day, youll meet with the rest of the team to understand the days game plan.</li>
<li>Youll drive in our Shine vehicle to customers homes or businesses (typically with another team member) throughout the day and perform our services specific to that customers needs.</li>
<li>You may meet customers to ensure were meeting their expectations on the job that day.</li>
<li>Youll end your day back at the Shine office to recap the day.</li>
</ul>
 Window Cleaning Technician Qualifications: 
<ul>
<li>Must like to work with people</li>
<li>Must have reliable transportation</li>
<li>Must be able to lift and carry a ladder up to 30 pounds.</li>
<li>Must not be afraid of heights</li>
<li>Must be able to work outside</li>
</ul>
 THE SHINE STORY: What started as one guy with a desire to create opportunities for others is now a nationwide family of businesses - working to spread light, caring, excellence, and team success. In 1998, Chris Fisher graduated college and set out on a journey to build a company. From one guy with a squeegee, Shine is now a growing national franchise company employing great people who make exceptional teams. With more than 45 locations across 15 states, Shine has grown into one of the leading home services businesses in the country. We Need People Like YOU! Whether you have no experience at all or are already a window cleaning expert, we are looking for those who display strong character, work ethic, and are driven to be the best! Shine provides all the training, technology, support, and know-how to help you get it done. You bring a smile and a heart for learning and the Shine business will work very well for you. Our hope and intention is that our communities will see something different in us - something inspiring - something attracting. Let your light shine! Apply today!

Window Cleaning Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing analytical testing and characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques as well as supporting laboratory operations and maintenance. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, report authoring, and department documentation support.
 RESPONSIBILITIES: The responsibilities of this position include, but are not limited to:
<ul>
<li>Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, mRNA and vaccines.</li>
<li>Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques.</li>
<li>Provide general laboratory support, including ordering/replacement of reagents and consumables, general maintenance of equipment, continuous improvement activities, and participating in periodic lab inspections.</li>
<li>The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression.</li>
<li>This position will be responsible for preparing data summary presentations, providing data verification support, compiling data, and using lab-based systems for data collection such as Empower and electronic laboratory notebooks.</li>
<li>Effective communication skills are required for interactions with laboratory scientists, project managers and colleagues from numerous functions.</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>At least a BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent&nbsp;</li>
<li>1+ years of industry experience utilizing some sort of chromatography (preferrably HPLC)</li>
<li>Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, mRNA, or antibody drug conjugates and how to characterize them with analytical techniques</li>
<li>Must be eligible to work in the United States indefinietly without restriction or sponsorship (OPT, H1B, etc.)</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques</li>
<li>Strong computer skills and experience with lab-based computer systems</li>
<li>Ability to collect and analyze data sets</li>
</ul>
 Additional Information 
Positions are full-time, working&nbsp;Monday-Friday 8am-5pm,&nbsp;overtime as needed.&nbsp; Candidates currently&nbsp;living within commutable distance to Andover, MA&nbsp;are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
<ul>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Compensation: $22.00-$32.00 per hour</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Characterization Scientist

<h3>Job Description</h3>
Job Description
Our client is a well established leader in the Geotechnical Engineering field serving the Pittsburgh Area. This is a great chance to join an experienced and growing engineering firm. They offer exceptional geotechnical and civil engineering services, as well as construction inspection and field and laboratory testing of soil, rock, concrete, and asphalt.
They offer a competitive salary with bonus opportunities, along with an excellent benefits package. This is a perfect opportunity to join an experienced and growing engineering firm. If you have at least 10 years of experience, Bachelor or Master of Science in Civil Engineering or Environmental Engineering with Geotechnical specialty and registration as Professional Engineer (PE) in Pennsylvania please send your resume today.
Equal Opportunity Employer.
Company DescriptionPatrice &amp; Associates is a National Executive Search firm and has been in business for more than 35 years. Over these years, we have honed our methods that make us stand apart from our competition. 
<h3>Company Description</h3>
Patrice &amp; Associates is a National Executive Search firm and has been in business for more than 35 years. Over these years, we have honed our methods that make us stand apart from our competition.

<h3>Job Description</h3>
Job DescriptionDescription:
1st shift- 6:30 am- 3 pm
 
SCA Pharmaceuticals is a dynamic rapidly growing company consisting of passionate individuals who believe in our mission of 
providing high quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety and integrity, our commitment to accountability and ownership, teamwork and creating better solutions by simplifying the complex.
Summary:
The Prep Technician will be responsible for sanitizing products prior to them entering the cleanroom. The position will also ensure that the detail, scheduling, and methods of cleaning are sufficient according to the standard operating procedures to protect the raw materials, products, clean room (material transfer, formulation, bag fabrication and fill rooms) and non-clean room (cart loading, sterilization, and pack-out areas) environments from the introduction of microbial contamination or infestation.
Essential functions:
<ul>
<li>Choose appropriate sanitization materials and perform material cleaning in accordance with the Standard Operating Procedures</li>
<li>Wipe all material surfaces as directed following appropriate procedures to ensure complete sanitization</li>
<li>Transfer materials during sanitization processes, one tote at a time, to a clean, sanitized tote</li>
<li>Verify materials and documentation throughout processes including appropriate counts, materials, and documentation</li>
<li>Document contact time using proper forms and other information as required</li>
</ul>
 
Requirements:
Required Qualifications &amp; Experience:
<ul>
<li>High School Diploma or equivalent.</li>
</ul>
Desired Knowledge, Skills, and Abilities:
<ul>
<li>Must have strong discipline and following of Standard Operating Procedures repeatedly.</li>
<li>Ability to obtain sterile gowning qualification.</li>
<li>Strong attention to detail.</li>
<li>Must be able to learn gowning procedures and wear sterile Personal Protective Equipment to include a respirator each day </li>
<li>Physically capable of being on feet for up to five hours doing physical labor of sanitizing the work area</li>
<li>Gain and maintain gowning certification</li>
<li>Must be able to lift, push, pull and carry up to 40+ pounds.</li>
</ul>
SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law

Clean Room Prep Technician

<h3>Job Description</h3>
Job Description
BIOPHARMASPEC Inc. is a highly experienced Contract Research Organization (CRO) to the Pharmaceutical and Biotechnology industries, specializing in the structural and physicochemical characterization of biopharmaceuticals in early research, development and pre-clinical stages.&nbsp; Our scientists include pioneers in the fields of protein and carbohydrate sequence analysis and disulfide bridge determination.&nbsp;
BioPharmaSpec Inc. is currently recruiting Scientists at all levels (BS, MS, PhD) with experience to assist with and further develop our advanced biopharmaceutical analysis protocols, principally by Mass Spectrometry, HPLC and associated classical microchemical and biophysical techniques including CD and FT-IR.&nbsp;
Duties will include:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Working with our expert scientists in preparing, improving and carrying out analytical experiments and data acquisition on numerous different products produced by BioPharmaSpec’s clients
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Complex interpretations and the preparation of analytical reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assisting in the development and application of novel Bioinformatics protocols for data analysis
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Preparation and review of Standard Operating Procedures
Qualifications and Skills:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; BA/BS plus research/analytical experience or PhD in Biochemistry, Chemistry, or Biology
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; An interest in the molecular structure of complex biomolecules
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; An aptitude for logic, attention to detail and the precise handling of scientific data
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Knowledge of Bioinformatics and/or Python programming would be advantageous&nbsp;
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Good practical laboratory and benchwork skills
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; A background in analytical chemistry or biochemistry with experience in any of the following areas: mass spectrometry (LC-MS(MS) and/or GC-MS), liquid chromatography (HPLC/UPLC), Amino Acid Analysis, protein and/or carbohydrate sequencing, Higher Order Structure characterization and experience of microchemical manipulation on a nano- or pico-scale.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Good basic computer skills with an understanding of Microsoft Office, with particular emphasis in Excel and complex spreadsheets
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong writing and verbal communication skills
BioPharmaSpec has excellent benefits and is a growing international CRO with labs in the US, UK and Europe. Opportunities exist for cross-lab collaborations as part of our dynamic team of scientists. &nbsp;Applicants are invited to submit a full resume and relevant experience to <a href="mailto:group.usa@biopharmaspec.com" target="_blank">group.usa@biopharmaspec.com</a>.&nbsp;

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