Research assistant jobs in Somersworth, NH

Position:Full-Time Total Rewards: Benefits/Incentive Information LensCrafters is a place for visionaries. We've got a vision for pairing state-of-the-art technology with a truly personal approach to eye care. At LensCrafters, we want every person who enters our doors to feel our passion for care. And that's why we're committed to taking care of you, so you can bring the best quality experience to our patients and customers. LensCrafters is part of EssilorLuxottica, a global leader in the design, manufacture and distribution of world-class vision care products, including iconic eyewear, advanced lens technology and cutting-edge digital solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn! An Independent Doctor of Optometry affiliated with LensCrafters (Luxottica) seeks an Associate Optometrist. You will work within the practice of a LensCrafters Subleasing Optometrist as an employee or contracted doctor. As a private Independent practice, Luxottica operates the optical dispensary while the Affiliated Doctor operates the Doctors office and provides high quality optometric care and service to patients. Working as an Associate Doctor of Optometry within the practice, the terms of agreement, practice model, pay and hours are all negotiated directly between you and the Subleasing doctor. As an Associate of a Subleasing Doctor, Practice Benefits Include: Professional autonomy to care for patients Full scope of practice predicated only on your professional discretion and agreement with the Subleasing Doctor (no company imposed restrictions or quotas to meet) Flexible scheduling available including part-time commitments or the option to add work to an existing practice schedule Work in a fully furnished office with a full suite of OD equipment; many utilize the latest advancement in digital eye examination technology called Clarifye Most offices offer use of the Daytona Optomap Digital Retinal Imaging System and have full tech and pre-testing support Automated on-line appointment book and patient recall system Affiliation Advantages: Luxottica is a leader in the design, manufacture, and distribution of fashion, luxury and sports eyewear. The group's wholesale distribution network covers more than 150 countries across 5 continents and is complemented by an extensive network of approximately 7,400 store locations. Since being founded in 1961, Luxottica has had over 50 years of innovation, growth and financial stability. Your opportunity to work with a full scope Independent LensCrafters practice is waiting. Contact us to get started!Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. Upon request and consistent with applicable laws, EssilorLuxottica will provide reasonable accommodations to individuals with disabilities who need assistance in the application and hiring process. To request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Job Segment: Optometry, Social Media, Healthcare, Marketing

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: • Possess a sound knowledge of the chemical principles and concepts of preparing buffers and tissue culture media and aseptic techniques . • Use established procedures (SOP's) and based on experience, training, and education, interpret complex methodologies (Protocols) provided by scientists. • Utilize good laboratory practices while applying technical expertise to formulate buffers and tissue culture solutions. • Independently perform work in a controlled laboratory environment. May assist others in completing their work. • Document all work utilizing Media Prep Worksheet • Maintain appropriate records pertaining to solution preparation in a fashion that allows for easy data retrieval. • Assist the team with the documentation such as records, reports and worksheets. • Assist with the shipping logistics of the buffer and media solutions. • Perform other applicable duties as deemed appropriate by lab supervisor / manager. Qualifications Additional Skills: 2+ years experience with laboratory operations in a hospital or pharmaceutical setting. Additional Information For more information, please contact Sneha Shrivastava ************

Full-time Description Job Title: Climate-Ocean and Coastal Law & Policy Research Specialist Supervisor: Dr. Janet Duffy-Anderson Starting Salary Range: $90,000 - $100,000 The Gulf of Maine Research Institute (GMRI) develops and delivers collaborative solutions to global ocean challenges. We are dedicated to the resilience of the Gulf of Maine ecosystem and the communities that depend on it. This position directly supports the Institute's four strategic initiatives: Adapting Fisheries and Seafood, Building Climate Ready Communities, Supporting the Blue Economy and Working Waterfronts, and Supporting Energy Solutions, through the integration of ocean and climate science into legal and policy frameworks. To learn more, visit gmri.org. Position Description: GMRI is seeking a Climate-Ocean and Coastal Law & Policy Research Specialist to investigate and analyze how climate, ocean, and environmental science can inform and interact with legal, regulatory, and broader governance frameworks (e.g., fisheries law, coastal zone management, working waterfront protection, managed retreat, and/or marine CO2 removal). This individual will work in close collaboration with GMRI scientists, program managers, and external partners to examine how scientific knowledge is incorporated into laws, policies, and regulatory decision-making, effectively bridging science and law. The individual will evaluate barriers and opportunities for translating science into governance tools and will help design strategies that strengthen ocean-climate resilience through law and governance. The successful candidate will bring a foundation in environmental or ocean and coastal law (J.D. or PhD preferred; commensurate experience considered), a demonstrated ability to work across legal and scientific domains, and a passion for place-based, community-engaged climate solutions in the Gulf of Maine. The role includes regular engagement with ocean users, public and private coastal property owners and managers (especially working waterfronts), policy researchers, and policymakers across jurisdictional scales. This position enjoys 18 months of fully encumbered institutional salary support thanks to a generous philanthropic gift, enabling a secure runway as the incumbent gets established. Thereafter, the incumbent will have primary responsibility for working collaboratively to sustain the position through competitively awarded grants or other fundraising efforts. This is a full-time (100% FTE) position located in Portland, ME, USA. This position is classified as a Pay Grade 8 role. The salary range for this grade is $68,100-$122,700, and we have budgeted compensation at $90,000- $100,000 commensurate with experience. Responsibilities/ Tasks: Conduct legal and policy research to assess how climate, ocean, and environmental science can inform laws, regulations, and governance related to Gulf of Maine's fisheries, working waterfronts, and/or coastal infrastructure. Develop legal and policy frameworks that support climate adaptation and resilience. Identify barriers and opportunities for integrating scientific knowledge into legal and regulatory frameworks. Collaborate with GMRI scientists and external partners to ensure science-based grounding in all policy outputs. Translate ocean and climate research into accessible policy briefs, legal guidance, and practical recommendations for stakeholders. Engage in field-based work with coastal stakeholders, tribal governments, and communities to inform policy from the ground up. Monitor relevant legal and regulatory developments. Participate in state and regional working groups on marine spatial planning, marine renewable energy, infrastructure siting, and/or ecosystem resilience. Pursue competitive grant funding and/or philanthropic partnerships in collaboration with GMRI's Development team. Participate in policy coalitions, legal forums, and public meetings throughout the Gulf of Maine region. Engage with the media and public through various forms of communication. Requirements Required Qualifications: Juris Doctor (J.D.) or Ph.D. or a minimum of 5 years work experience in marine affairs, ocean, coastal or environmental law, climate policy, fisheries, coastal governance, or closely related field. Demonstrated ability to work across disciplines and integrate science into law or policy guidance. Strong background in fisheries regulations, shoreline access law, working waterfront issues, coastal planning, marine spatial planning, and similar topics. Experience engaging directly with communities, resource users, or tribal entities. Strong written and oral communication skills with a track record of producing reports, and/or scholarly publications, as well as public talks, media appearances, conference presentations. Ability to manage multiple tasks, timelines, and partnerships effectively. Fluent in English. Eligible to work in the United States. Preferred Qualifications: Experience working in or with scientific organizations or interdisciplinary research teams. Familiarity with legal frameworks in the Gulf of Maine or broader Northwest Atlantic. Demonstrated commitment to inclusion in environmental or policy contexts. Established network of interdisciplinary experts to serve as project collaborators Understanding of offshore energy resources and planning, ecosystem-based. management, and/or transboundary or international marine governance issues. Proven success with programmatic fundraising, including federal/state grant writing. Diversity and Inclusion: The Gulf of Maine Research Institute (GMRI) has a long-standing policy and commitment to providing equal access and equal employment opportunities in all terms, conditions, processes, and benefits of employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, family status, veteran status, or any other classification protected by law. GMRI's employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, family status, veteran status, or any other classification protected by law. Applicants and employees are encouraged to voluntarily provide certain status data to assist GMRI in fulfilling various reporting requirements of the federal government. This self-identification is completely voluntary, will be kept confidential and separate from your application data, and used only to meet certain state or federal reporting requirements. Providing or declining to provide this information will not result in adverse action of any kind. Salary and Benefits: GMRI offers a competitive salary and benefits package. Application Instructions: All applications must be accompanied by a cover letter, CV/résumé, and a list of three professional references with their contact information. Review of applications will begin immediately and will continue on a rolling basis until the successful candidate has been selected. The deadline to submit applications is December 20, 2025.

Makro Scientific: Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Job ID : 43012 Location : Andover, MA Duration : 12 Months Job Title : Investigator Initiated Research (IIR) Associate The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Skills: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Qualifications Experience required: 3-5 Years Education: BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required.

Job Title: Quality Assurance Analyst / Pharma Manufacturing Duration: 12 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Job Description: The Andover Site Operations Management group is looking for an individual to fill a Lead Investigator position within the Andover Site Investigations group. The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The individual will be expected to develop collaborative relationships with the operational leadership and staff in each suite and the appropriate Quality and Functional Area representatives in order to facilitate investigations using continuous improvement techniques. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Additional responsibilities and expectations include: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Be able to use that knowledge to investigate process deviations and atypical results and identify root cause Work with the appropriate people from both the quality and operational organizations develop a corrective action Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Exercise judgment in developing practices, techniques and evaluation criteria for obtaining results A BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. Additional Information Anuj Mehta ************

The Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute that is addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. Our research strategy uses molecular and genomic technologies to address questions related to Oceans and Human Health in two divisions (1) Marine Biomedical Discovery and (2) Healthy Oceans and Fisheries. GMGI is looking for a highly motivated Research Associate who will play an important role in contributing to our eDNA Service Lab within the Healthy Oceans and Fisheries Division. The ideal candidate will have strong experience in molecular biology/ecology applied to fisheries and knowledge of common molecular laboratory techniques and data analysis. The candidate must be capable of working independently to design experiments, generate high quality data, and analyze results for a variety of projects directed by GMGI research staff. Experience with eDNA is highly desirable. This position is an extraordinary opportunity for an ambitious and entrepreneurial person who is interested in helping to contribute to a world-class research institute. Responsibilities · Design and execute experiments using molecular biology/genomics techniques · Perform DNA/RNA isolations and quantification, PCR, qPCR, RT-qPCR, dd PCR · Prepare libraries and run Illumina next-generation sequencing · Conduct eDNA metabarcoding and species presence/absence assays · Apply knowledge of experimental design, bioinformatics, and statistics to analyze results · Participate in field collections for eDNA samples, including tissue dissection and processing · Organize, process, and archive field and lab samples following established protocols · Prepare client-facing reports and scientific communications (presentations, manuscripts, etc) · Communication with clients via email and meetings to provide updates, answer questions, and ensure project success. Qualifications · Bachelor's or Master's degree in biology, molecular biology, marine biology, or related discipline · Hands-on experience with molecular biology techniques including qPCR, RT-qPCR, and Next-Generation Sequencing · Experience working with genomics instruments and laboratory automation tools · Demonstrated ability to plan and carry out experiments independently · Familiarity with the command line interface, Linux, and R; hands-on experience in analyzing metabarcoding data · Strong scientific writing and documentation skills · Excellent verbal communication skills and comfort working in a team setting and with clients · Commitment to scientific integrity and rigorous data quality standards; willingness to troubleshoot · Adaptability and initiative in a fast-paced, start-up and research-driven environment · Enthusiasm and commitment to GMGI's mission for science and education · Self-starting, independent, creative thinker with strong problem-solving skills This position will report to the eDNA Service Platform Manager. Salary commensurate with experience. It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes: • Health and Dental Insurance • Medical and Dependent Flex Spending Accounts • Long Term Disability • Life Insurance • Paid Time Off • 403(b) Retirement Plan • 12 Paid Holidays Applicants must be authorized to work in the US. About GMGI Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to “address critical challenges facing our oceans, human health and the environment through innovative scientific research and education” GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics. GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need. In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization, and in building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: ************

The Engineering Failure Analysis intern will work in the Analytical Services Lab (ASL) performing characterizations on analytical tools to optimize or improve performance of analytical tools within the lab. The ASL intern will work alongside analysts to gain experience in the failure analysis and materials analysis process. ESSENTIAL JOB FUNCTIONS* Understand and use physical, chemical, and electrical concepts surrounding semiconductor function and manufacturing. Carry out analytical processes such as electrical verifications, chemical and physical de-processing, performing cross-sections, etc. Conduct optical and scanning electron microscopy (SEM) on samples Execute instructions and perform Design of Experiments for improving FA performance Provide verbal and written reports of results to lab personnel and internal customers Work safely with hazardous chemicals and practice good laboratory hygiene Summarize learnings and project into a final report and present to management

Job Title: Research Associate Duration: 06+ months • Possess a sound knowledge of the chemical principles and concepts of preparing buffers and tissue culture media and aseptic techniques. • Use established procedures (SOP's) and based on experience, training, and education, interpret complex methodologies (Protocols) provided by scientists. • Utilize good laboratory practices while applying technical expertise to formulate buffers and tissue culture solutions. • Independently perform work in a controlled laboratory environment. May assist others in completing their work. • Document all work utilizing Media Prep Worksheet • Maintain appropriate records pertaining to solution preparation in a fashion that allows for easy data retrieval. • Assist the team with the documentation such as records, reports and worksheets. • Assist with the shipping logistics of the buffer and media solutions. • Perform other applicable duties as deemed appropriate by lab supervisor / manager. Qualifications • 2+ years' experience with laboratory operations in a hospital or pharmaceutical setting. • Strong analytical and algebra skills. • Must be competent in and understand aseptic techniques and Good Laboratory Practices Additional Information All your information will be kept confidential according to EEO guidelines.

Job DescriptionSalary: The EM Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. PRIMARY DUTIES AND RESPONSIBILITIES Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner on the data sheets- follows GDP. Revises procedures and ELNs under close supervision. Follows all safety rules and regulations and conducts periodic safety audits. Follows all cGMP rules and regulations. Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports. Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts. Performs routine data generation and problem solving with a minimal rework. Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration. Ensures all work performed strictly adheres to Company, client, ISO and Pharmacopeial methodologies. Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. SHIFT Wednesday - Saturday 1st Shift REQUIREMENTS & QUALIFICATIONS Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred. MINIMUM SKILLS REQUIREMENTS Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. Must have excellent organizational, verbal communication and technical documentation skills. Solid computer skills. Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples. Must be a team player with integrity and concern for the quality of Company products, services and staff members.

Requisition ID: 903868 Store #: 000668 LensCrafters Position:Part-TimeTotal Rewards: Benefits/Incentive Information LensCrafters is a place for visionaries. We've got a vision for pairing state-of-the-art technology with a truly personal approach to eye care.At LensCrafters, we want every person who enters our doors to feel our passion for care. And that's why we're committed to taking care of you, so you can bring the best quality experience to our patients and customers. LensCrafters is part of EssilorLuxottica, a global leader in the design, manufacture and distribution of world-class vision care products, including iconic eyewear, advanced lens technology and cutting-edge digital solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn!An Independent Doctor of Optometry affiliated with LensCrafters (Luxottica) seeks an Associate Optometrist. You will work within the practice of a LensCrafters Subleasing Optometrist as an employee or contracted doctor. As a private Independent practice, Luxottica operates the optical dispensary while the Affiliated Doctor operates the Doctors office and provides high quality optometric care and service to patients. Working as an Associate Doctor of Optometry within the practice, the terms of agreement, practice model, pay and hours are all negotiated directly between you and the Subleasing doctor. As an Associate of a Subleasing Doctor, Practice Benefits Include: Professional autonomy to care for patients Full scope of practice predicated only on your professional discretion and agreement with the Subleasing Doctor (no company imposed restrictions or quotas to meet) Flexible scheduling available including part-time commitments or the option to add work to an existing practice schedule Work in a fully furnished office with a full suite of OD equipment; many utilize the latest advancement in digital eye examination technology called Clarifye Most offices offer use of the Daytona Optomap Digital Retinal Imaging System and have full tech and pre-testing support Automated on-line appointment book and patient recall system Affiliation Advantages: Luxottica is a leader in the design, manufacture, and distribution of fashion, luxury and sports eyewear. The group's wholesale distribution network covers more than 150 countries across 5 continents and is complemented by an extensive network of approximately 7,400 store locations. Since being founded in 1961, Luxottica has had over 50 years of innovation, growth and financial stability. Your opportunity to work with a full scope Independent LensCrafters practice is waiting. Contact us to get started! Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. EssilorLuxottica complies with all applicable laws related to the application and hiring process. If you would like to provide feedback regarding an active job posting, or if you are an individual with a disability who would like to request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name, job id number, and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Job Segment: Optometry, Social Media, Healthcare, Marketing

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: • Responsible for the execution and analysis of experiments and analytical procedures. • Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision. • Plans and prioritizes concurrent experimental procedures. • Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results. • May provide oral presentations on results to other department members. • Works under active supervision. • Follows established procedures. • Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. • Contributes to the completion of milestones associated with specific projects. • Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources. • Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. Experience: • 0 to 3 years. Skills: • The Commercial Cell Culture Development (CCCD) department is responsible for the development, characterization, scale-up, and transfer of cell culture processes for late stage clinical and commercial manufacturing of therapeutic proteins and antibodies. • In addition, the department provides technical expertise and support for improving the performance of commercial manufacturing processes. • Department is seeking to employ a motivated individual for a 12-month temporary position. • This individual will work with a team of scientists and engineers to develop/optimize mammalian cell culture processes. • Responsibilities include conducting cell culture experiments using small scale (i.e. shake flasks, spin tubes, well plates) platforms and bench top bioreactors, running biochemical assays, and performing routine lab duties. • The individual will also be responsible for designing experiments, monitoring cell culture parameters and documenting all studies. • Experience in a basic biology lab setting, including aseptic techniques is a plus. • Excellent oral and written communication skills are required. • Must be able to work well independently and contribute as a member of a team. Qualifications Education: • The candidate should have a B.S. degree in Biology, Bioengineering, or related field and a minimum of 1 year of molecular biology and/or mammalian cell culture laboratory experience. • Candidate must have excellent organizational skills and be able to work as part of a team. Additional Information For more information, Please contact Rakshak singhal ************

Makro Scientific: Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description Job ID : 43012 Location : Andover, MA Duration : 12 Months Job Title : Investigator Initiated Research (IIR) Associate The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Skills: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Qualifications Experience required: 3-5 Years Education: BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required.

Job Title: Quality Assurance Analyst / Pharma Manufacturing Duration: 12 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Job Description: The Andover Site Operations Management group is looking for an individual to fill a Lead Investigator position within the Andover Site Investigations group. The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. This position will report to the Manager of Investigations within the Site Operations Management Function. The candidate will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. The individual will be expected to develop collaborative relationships with the operational leadership and staff in each suite and the appropriate Quality and Functional Area representatives in order to facilitate investigations using continuous improvement techniques. The incumbent will be expected to have experience in the area of quality and compliance and a working knowledge of the appropriate regulations. Experience with and in depth understanding of cell culture and chromatography is highly desirable. They will be expected to assist in continually defining and improving the philosophy and justifications involved in investigations and to continually evolve to meet changing business needs. Additional responsibilities and expectations include: Have a fundamental understanding of the investigation process as it applies to manufacturing issues Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical. Be able to use that knowledge to investigate process deviations and atypical results and identify root cause Work with the appropriate people from both the quality and operational organizations develop a corrective action Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards Exercise judgment in developing practices, techniques and evaluation criteria for obtaining results A BS or MS, preferably in a scientific or engineering discipline preferable. A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required. Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred. The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills. Additional Information Anuj Mehta ************

Job Title: Research Associate Duration: 06+ months • Possess a sound knowledge of the chemical principles and concepts of preparing buffers and tissue culture media and aseptic techniques. • Use established procedures (SOP's) and based on experience, training, and education, interpret complex methodologies (Protocols) provided by scientists. • Utilize good laboratory practices while applying technical expertise to formulate buffers and tissue culture solutions. • Independently perform work in a controlled laboratory environment. May assist others in completing their work. • Document all work utilizing Media Prep Worksheet • Maintain appropriate records pertaining to solution preparation in a fashion that allows for easy data retrieval. • Assist the team with the documentation such as records, reports and worksheets. • Assist with the shipping logistics of the buffer and media solutions. • Perform other applicable duties as deemed appropriate by lab supervisor / manager. Qualifications • 2+ years' experience with laboratory operations in a hospital or pharmaceutical setting. • Strong analytical and algebra skills. • Must be competent in and understand aseptic techniques and Good Laboratory Practices Additional Information All your information will be kept confidential according to EEO guidelines.

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

Job DescriptionSalary: $50K - $55K The Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute that is addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. Our research strategy uses molecular and genomic technologies to address questions related to Oceans and Human Health in two divisions (1) Marine Biomedical Discovery and (2) Healthy Oceans and Fisheries. GMGI is looking for a highly motivated Research Associate who will play an important role in contributing to our eDNA Service Lab within the Healthy Oceans and Fisheries Division. The ideal candidate will have strong experience in molecular biology/ecology applied to fisheries and knowledge of common molecular laboratory techniques and data analysis. The candidate must be capable of working independently to design experiments, generate high quality data, and analyze results for a variety of projects directed by GMGI research staff. Experience with eDNA is highly desirable. This position is an extraordinary opportunity for an ambitious and entrepreneurial person who is interested in helping to contribute to a world-class research institute. Responsibilities Design and execute experiments using molecular biology/genomics techniques Perform DNA/RNA isolations and quantification, PCR, qPCR, RT-qPCR, dd PCR Prepare libraries and run Illumina next-generation sequencing Conduct eDNA metabarcoding and species presence/absence assays Apply knowledge of experimental design, bioinformatics, and statistics to analyze results Participate in field collections for eDNA samples, including tissue dissection and processing Organize, process, and archive field and lab samples following established protocols Prepare client-facing reports and scientific communications (presentations, manuscripts, etc) Communication with clients via email and meetings to provide updates, answer questions, and ensure project success. Qualifications Bachelors or Masters degree in biology, molecular biology, marine biology, or related discipline Hands-on experience with molecular biology techniques including qPCR, RT-qPCR, and Next-Generation Sequencing Experience working with genomics instruments and laboratory automation tools Demonstrated ability to plan and carry out experiments independently Familiarity with the command line interface, Linux, and R; hands-on experience in analyzing metabarcoding data Strong scientific writing and documentation skills Excellent verbal communication skills and comfort working in a team setting and with clients Commitment to scientific integrity and rigorous data quality standards; willingness to troubleshoot Adaptability and initiative in a fast-paced, start-up and research-driven environment Enthusiasm and commitment to GMGIs mission for science and education Self-starting, independent, creative thinker with strong problem-solving skills This position will report to the eDNA Service Platform Manager. Salary commensurate with experience. It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes: Health and Dental Insurance Medical and Dependent Flex Spending Accounts Long Term Disability Life Insurance Paid Time Off 403(b) Retirement Plan 12 Paid Holidays Applicants must be authorized to work in the US. About GMGI Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics. GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need. In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization, and in building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: ************

Requisition ID: 903874 Store #: 001083 LensCrafters Position:Full-TimeTotal Rewards: Benefits/Incentive Information LensCrafters is a place for visionaries. We've got a vision for pairing state-of-the-art technology with a truly personal approach to eye care.At LensCrafters, we want every person who enters our doors to feel our passion for care. And that's why we're committed to taking care of you, so you can bring the best quality experience to our patients and customers. LensCrafters is part of EssilorLuxottica, a global leader in the design, manufacture and distribution of world-class vision care products, including iconic eyewear, advanced lens technology and cutting-edge digital solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn!An Independent Doctor of Optometry affiliated with LensCrafters (Luxottica) seeks an Associate Optometrist. You will work within the practice of a LensCrafters Subleasing Optometrist as an employee or contracted doctor. As a private Independent practice, Luxottica operates the optical dispensary while the Affiliated Doctor operates the Doctors office and provides high quality optometric care and service to patients. Working as an Associate Doctor of Optometry within the practice, the terms of agreement, practice model, pay and hours are all negotiated directly between you and the Subleasing doctor. As an Associate of a Subleasing Doctor, Practice Benefits Include: Professional autonomy to care for patients Full scope of practice predicated only on your professional discretion and agreement with the Subleasing Doctor (no company imposed restrictions or quotas to meet) Flexible scheduling available including part-time commitments or the option to add work to an existing practice schedule Work in a fully furnished office with a full suite of OD equipment; many utilize the latest advancement in digital eye examination technology called Clarifye Most offices offer use of the Daytona Optomap Digital Retinal Imaging System and have full tech and pre-testing support Automated on-line appointment book and patient recall system Affiliation Advantages: Luxottica is a leader in the design, manufacture, and distribution of fashion, luxury and sports eyewear. The group's wholesale distribution network covers more than 150 countries across 5 continents and is complemented by an extensive network of approximately 7,400 store locations. Since being founded in 1961, Luxottica has had over 50 years of innovation, growth and financial stability. Your opportunity to work with a full scope Independent LensCrafters practice is waiting. Contact us to get started! Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. EssilorLuxottica complies with all applicable laws related to the application and hiring process. If you would like to provide feedback regarding an active job posting, or if you are an individual with a disability who would like to request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name, job id number, and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Job Segment: Optometry, Social Media, Healthcare, Marketing

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: • Responsible for the execution and analysis of experiments and analytical procedures. • Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision. • Plans and prioritizes concurrent experimental procedures. • Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results. • May provide oral presentations on results to other department members. • Works under active supervision. • Follows established procedures. • Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. • Contributes to the completion of milestones associated with specific projects. • Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources. • Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. Experience: • 0 to 3 years. Skills: • The Commercial Cell Culture Development (CCCD) department is responsible for the development, characterization, scale-up, and transfer of cell culture processes for late stage clinical and commercial manufacturing of therapeutic proteins and antibodies. • In addition, the department provides technical expertise and support for improving the performance of commercial manufacturing processes. • Department is seeking to employ a motivated individual for a 12-month temporary position. • This individual will work with a team of scientists and engineers to develop/optimize mammalian cell culture processes. • Responsibilities include conducting cell culture experiments using small scale (i.e. shake flasks, spin tubes, well plates) platforms and bench top bioreactors, running biochemical assays, and performing routine lab duties. • The individual will also be responsible for designing experiments, monitoring cell culture parameters and documenting all studies. • Experience in a basic biology lab setting, including aseptic techniques is a plus. • Excellent oral and written communication skills are required. • Must be able to work well independently and contribute as a member of a team. Qualifications Education: • The candidate should have a B.S. degree in Biology, Bioengineering, or related field and a minimum of 1 year of molecular biology and/or mammalian cell culture laboratory experience. • Candidate must have excellent organizational skills and be able to work as part of a team. Additional Information For more information, Please contact Rakshak singhal ************

The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. PRIMARY DUTIES AND RESPONSIBILITIES Performs validation testing to analyze samples to determine an accurate microbiological procedure for the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs Disinfectant Efficacy testing for client's facilities utilizing specific disinfectants, surfaces, and organisms determined by the clients. Perform feasibility work with guidance from USP and BA SOP's. Being able to work independently with little to no guidance to figure out and apply test methods to different products and materials. Documents work in a clear and organized manner. Revises procedures and ELNs under close supervision. Writes validation reports and client protocols for QC Micro to follow for routine testing. Follows all safety rules and regulations and conducts periodic safety audits. Follows all cGMP rules and regulations. Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports. Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts. Performs data generation and problem solving with a minimal rework. Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration. Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies. Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. REQUIREMENTS & QUALIFICATIONS Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidance's is preferred. MINIMUM SKILLS REQUIREMENTS Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. Must have excellent organizational, verbal communication and technical documentation skills. Solid computer skills. Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples. Must be a team player with integrity and concern for the quality of Company products, services and staff members.