Chemist jobs in New Hampshire

Job DescriptionSalary: The Chemist 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 using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. PRIMARY DUTIES AND RESPONSIBILITIES Prepares and analyzes products to determine chemical and physical properties. Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed. Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports. Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks. Performs data generation, analysis and more complicated problem solving with a minimal rework. Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting. Works under partial supervision to ensure all work performed is performed 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. Documents work in a clear and organized manner. Follows all safety rules and regulations and conducts periodic safety audits. Follows all cGMP rules and regulations. REQUIREMENTS & QUALIFICATIONS Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required. 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.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management Essential Duties and Responsibilities: * Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples. * Assist in deviation investigation, out-of-specification or aberrant results and process changes * Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data * Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support * Logging and tracking of samples and chemicals. Order chemicals and laboratory supplies as needed * Documents/peer reviews laboratory work using laboratory notebooks/worksheets. Documentation must be detailed, timely and in compliance with cGMP/GDP requirements * May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation * Performs routine data generation and problem solving * Other duties, as assigned Special Demands: * Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear * Ability to sit or stand for prolong periods of time * Must be able to walk and drive between locations * Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves * Must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly * Must be able to occasionally lift and/or move up to 50 pounds * Comfortable with working/handling of hazardous materials Work Environment: Works closely with quality assurance and quality control staff in performing varied work procedures and activities. Interacts with Operations staff. Qualifications: * 0-3 years relevant Analytical Chemistry experience, preferably in Quality Control * Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study * General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred * Excellent organizational skills and ability to document technical data * Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization * Ability to multi-task in a dynamic environment with changing priorities * Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment. #LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. **Summary of Objective:** This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management **Essential Duties and Responsibilities:** + Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples. + Assist in deviation investigation, out-of-specification or aberrant results and process changes + Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data + Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support + Logging and tracking of samples and chemicals. Order chemicals and laboratory supplies as needed + Documents/peer reviews laboratory work using laboratory notebooks/worksheets. Documentation must be detailed, timely and in compliance with cGMP/GDP requirements + May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation + Performs routine data generation and problem solving + Other duties, as assigned **Special Demands:** + Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear + Ability to sit or stand for prolong periods of time + Must be able to walk and drive between locations + Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves + Must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly + Must be able to occasionally lift and/or move up to 50 pounds + Comfortable with working/handling of hazardous materials **Work Environment:** Works closely with quality assurance and quality control staff in performing varied work procedures and activities. Interacts with Operations staff. **Qualifications:** + 0-3 years relevant Analytical Chemistry experience, preferably in Quality Control + Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study + General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred + Excellent organizational skills and ability to document technical data + Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization + Ability to multi-task in a dynamic environment with changing priorities + Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment. \#LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future (***************** **Equal Employment Opportunity (EEO) Statement:** _PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._ _At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Keene State College invites applications for a Chemistry Laboratory Technician to help with laboratory preparation for classes and labs predominately in chemistry, but also in physics, environmental studies, or other areas of need as assigned by the supervisor. This is a 81%-time benefited position, 37.5 hours/week, with appointment dates that run August to May. Responsibilities include: laboratory preparation, set-up, and clean up with appropriate regard for safe operation and safe disposal of chemical waste and oversees inventories including purchasing of chemicals and supplies. Other Minimum Qualifications Associate's degree in Chemistry or related area One to three years related experience and/or training Demonstrated communication skills. Proven organizational skills and attention to detail The ability to establish and maintain effective working relationships with students, faculty, and staff. Additional Preferred Qualifications Bachelor's degree, or an equivalent combination of education and/or experiences from which comparable knowledge, skills and abilities have been achieved. Additionally, the College has identified desirable qualifications that support our commitment to creating and maintaining a diverse campus community including theability to speak a second language or to bring a multicultural perspective to the campus. Additional Job Information Applicants should be prepared to upload the following documents when applying online: Letter of application Resume Contact information for references Application Deadline: Review of applications to begin immediately and will continue until the position is filled or otherwise closed at the College's discretion.

NEW JOB ALERT! I have a Clinical Laboratory Scientist IV - Chemistry position available north of Plainfield, New Hampshire! Details - Full-time - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc) - Sign-on/retention bonus! Requirements - Bachelor's degree - ASCP certification required - Prior lab experience and knowledge Click apply or email your resume to leah@ka-recruiting.com/ call or text 617-746-2751! REF#LM929

Working under the close supervision of an experienced investigator, the associate level Scientist provides support to scientific research efforts. Responsibilities * May independently design and implement protocols and experiments within own area(s) of expertise. * Assists with grant writing and/or makes significant contributions to, and receives authorial recognition for publications in national scientific journals. * Participates in the collection and analysis of data for research projects. May design data collection protocols. * Assists with defining scope and selection of research area(s) for investigation through conceptually related studies or a series of projects of lesser scope. * Participates in the preparation of the design and development of study protocols, statistical analysis and study reports in a highly targeted manner within own area of expertise. Produces scientific content for clinical and regulatory documentation. * Presents at conferences, symposia and provides guidance to collaborators and trainees. * Supervises students and trainees (e.g., residents, research assistants). * Performs other duties as required or assigned. Qualifications * Master's degree in an applicable field of study Required Licensure/Certifications - None * Area of Interest:Research/Science * Pay Range:$56,430.40/Yr. - $87,464.00/Yr. (Based on 40 hours per week, otherwise pro rata) * FTE/Hours per pay period:1.00 - 1.00 - 40 hrs/week * Shift:Day * Job ID:35704 Dartmouth Health offers a total compensation package that includes a comprehensive selection of benefits. Our Core Benefits include medical, dental, vision and life insurance, short and long term disability, paid time off, and retirement plans. Click here for information on these benefits and more:Benefits | DHMC and Clinics Careers Dartmouth Health is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dartmouth Hitchcock Medical Center and Dartmouth Hitchcock Clinics comply with applicable Federal civil rights laws and do not discriminate on the basis of race, color, national origin, age, disability, or sex. We do not exclude or treat people differently because of race, color, national origin, age, disability, or sex.

Working under the close supervision of an experienced investigator, the associate level Scientist provides support to scientific research efforts. Responsibilities May independently design and implement protocols and experiments within own area(s) of expertise. Assists with grant writing and/or makes significant contributions to, and receives authorial recognition for publications in national scientific journals. Participates in the collection and analysis of data for research projects. May design data collection protocols. Assists with defining scope and selection of research area(s) for investigation through conceptually related studies or a series of projects of lesser scope. Participates in the preparation of the design and development of study protocols, statistical analysis and study reports in a highly targeted manner within own area of expertise. Produces scientific content for clinical and regulatory documentation. Presents at conferences, symposia and provides guidance to collaborators and trainees. Supervises students and trainees (e.g., residents, research assistants). Performs other duties as required or assigned. Qualifications Master's degree in an applicable field of study Required Licensure/Certifications None We can recommend jobs specifically for you! Click here to get started.

Are you looking for an opportunity with plenty of growth potential? Do you enjoy working in an exciting, fast-paced, collaborative environment? Are you interested in working with the world's most innovative companies to create a more connected world? Connecting Continents. Impacting Communities. The backbone of the Internet is a series of high-tech subsea fiber optic cables deployed throughout the globe - SubCom has deployed over 50% of them. Our employees ensure data communications networks are engineered, manufactured, deployed to the highest standards, enabling faster and more reliable connectivity to communities worldwide. Every member of the SubCom team plays a role in an end-to-end process that is critical to enterprises, governments, big cities, and rural towns. We encourage, expect, and value creativity, thoughtful risk taking, openness to change, and diverse perspectives. Whether you're a seasoned applicant seeking a new and exciting challenge, or you're new to the workforce and looking for a flexible, rewarding, and fast-paced position with an innovative and stable organization (since 1953), SubCom has opportunities to advance your career. Position Overview The Product Line Management is responsible for the strategic direction, lifecycle management, and profitability of SubCom's undersea, terminal equipment and software portfolio of products. This role leads cross-functional teams to define product vision, drive innovation, and ensure alignment with market needs and business objectives. The ideal candidate combines deep subsea market insight, technical understanding, and business acumen to deliver technical solutions. Responsibilities * Define and execute the product line strategy in alignment with corporate goals. * Identify market trends, customer needs, and competitive dynamics to guide product development and positioning. * Develop long-term roadmaps and investment plans for the product line. * Own the full lifecycle of products-from concept to end-of-life. * Monitor product performance and adjust strategies based on data-driven insights. * Lead cross-functional teams including engineering, marketing, sales, and operations. * Serve as the voice of the customer and market within the organization. * Partner with R&D to prioritize features and innovations that drive value. * Drive cost reduction initiatives and value engineering efforts. * Foster a culture of innovation, accountability, and continuous improvement. Qualifications Qualifications * Bachelor's degree in Engineering, Business, or related field; MBA preferred. * 10+ years of experience in product management, marketing, or strategy roles. * Proven success in managing complex product portfolios and launching new products. * Strong analytical, strategic thinking, and leadership skills. * Excellent communication and stakeholder management abilities. * Experience in Subsea industry NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization. Candidates for positions with SubCom must be legally authorized to work in the United States. Employment eligibility verification will be required at the time of hire. Visa sponsorship is not available for this position. Our selection procedure is based on local, state and federal law. Please be sure to attach a resume to your application. We are not able to consider applications without a resume. BENEFITS SubCom offers a comprehensive benefits package, including but not limited to: competitive salaries, medical, dental, vision, life and disability insurance coverages, FSA, HSA, generous vacation, paid sick leave, paid parental leave, paid holidays, tuition reimbursement, adoption assistance, and a 401(k) plan with generous company match. Additionally, some positions may be eligible for shift differential. AFFIRMATIVE ACTION/EQUAL EMPLOYER OPPORTUNITY SubCom is committed to providing a work environment that prohibits discrimination based on age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation. SubCom engineers, manufactures, and installs subsea fiber optic data cables - the unsung heroes of global communication. With an unrelenting focus on quality, reliability, and value, SubCom offers flexible end-to-end building blocks for the high-tech networks that are the backbone of the world's digital infrastructure. While the company's origins date back to the mid-19th century, SubCom has deployed enough cable to circle the equator more than 25 times since its entry into the communications industry in 1955. SUBCOM'S CORE VALUES Quality - Accountability - Teamwork - Innovation

About TRI-K Since 1974, TRI-K Industries, Inc. has been a leading manufacturer of specialty ingredients, bringing innovative concepts and products to life for the cosmetics industry. TRI-K strives to keep ahead of the curve with a specialization in cosmetic proteins and multi-functional peptides, natural actives, preservatives, and mild surfactants. TRI-K is a member of the Galaxy Group, with sales offices, manufacturing facilities and partners around the world. At TRI-K, we combine an awareness of consumer trends with innovative technologies to maintain our superior offering in the industry. Our in-house development team is constantly pioneering the discovery of new materials, resulting in enhanced consumer benefits. TRI-K Industries is a wonderful place to start your career with opportunities to learn and grow. Role Purpose: Assists QC Manager and performs quality control procedures designed to ensure continuous production and shipment of cosmetic ingredients consistent with established standards. Serves as key member of Proteins Division Quality Unit (PDQU) with authority to test, approve or release FG or RM, following ISO and GMP Protocols. Position Reports to: Quality Control Manager Positions Reporting to this Position: none Position is located in Derry, NH. Requirements Role Objectives: Essential Duties and Responsibilities include the following. Other duties may be assigned. Secondary responsibility for Quality Control Department (verification, review, approval & release) including Quality testing. Performs Quality functions related to shipping, as needed Key member of Proteins Division Quality Unit (PDQU) Accurately analyzes and performs chemical testing of FG, in-process batches, raw materials, according to established standards Accurately maintains and updates Quality control data base on a daily basis As part of PDQU, tracks, investigates and reports deviations from established Quality Control Standards Participates in cross-functional teams to increase efficiency, solve problems and improve quality systems Secondary responsibility for approval and release of incoming raw materials, maintenance of RM data base and related specifications Assists with aseptic sampling of products, labeling and proper storage of retains Become fully trained on PD products, including Specifications, methods and equipment Member of team who evaluate and respond to quality issues presented by customers Ability to use and maintain analytical equipment necessary for quality testing Follow safe laboratory guidelines and plant safety protocols As part of PDQU, maintains equipment, calibrations, and documentation according to SOP & Work Instructions, following ISO and GMP protocols Maintains Quality Control objectives, complementary to corporate policies and goals Competencies: To perform the job successfully, an individual should demonstrate the following competencies: Language Ability- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. Math Ability- Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. Reasoning Ability- Ability to solve problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Computer Skills- Knowledge of Word Processing software; Spreadsheet software and Internet software. Work Environment- While performing the duties of this job, the employee is frequently exposed to work near moving mechanical parts; fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Demands- While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and taste or smell. The employee is occasionally required to sit; climb or balance and stoop, kneel, crouch, or crawl. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Qualifications: Bachelor's degree from four-year college or university, preferably in Chemistry, Biology or a related field. One to two years related experience and/or training; or equivalent combination of education and experience is a plus. We offer a competitive compensation package including: • Medical • Dental • 401 (K) • Vision • Paid Time Off • Life Insurance • In addition to other programs and plans TRI-K Industries is an equal opportunity employer, and we celebrate and value diversity in our workforce. Hiring decisions are based on qualifications, merit, and business needs. Monday-Friday, 1:00 PM to 9:30 PM

Job Details Legal Address - Littleton, NHDescription PURPOSE AND SCOPE The Quality Control Laboratory Analyst I is primarily responsible for daily performance of the testing of all raw materials, batches, and finished goods. ESSENTIAL JOB FUNCTIONS Test and release applicable raw materials. Test and release bulk batches. Complete finished goods testing. Complete stability testing. Ability to preform analytical and microbial testing. Preparing as needed and shipping samples for outside microbiological and analytical testing. Prepare and execute in-house microbiological testing for environmental and production samples. Prepare and execute analytical methods based on Approved Laboratory Methods. Assist in ordering and maintaining stock of all laboratory equipment and chemical standards. Assist QC Manger and QA/RA Manager in developing and maintaining laboratory GLP's. Monitor work activities to ensure adherence to Standard Operating Procedures, QA Manuals and programs. Assist with developing new testing validations and methods on Analytical Equipment Provide QC assistance and support to managers, supervisors, and manufacturing personnel. Undergo training on SOP's as listed on the accompanying Training Matrix. Participate and interact in internal and external training programs. Other duties as assigned ABOUT OUR COMPANY: At Adventure Ready Brands we pride ourselves on exhibiting quality in all we do. We are built upon core values that cultivate a culture of growth focused on results, customer satisfaction, leadership, innovation and initiative, as well as communication and teamwork. We offer Medical, Dental, and Vision insurance, FSA, HSA, Supplemental Life Insurance, Long Term Disability, 401k with matching program, paid maternity and parental leave, as well as company paid Short Term Disability, a company paid Life Insurance policy. At ARB, we provide weekends off, Paid Time Off after 90 days, paid holidays after 30 days, and a work environment with a hardworking, dedicated, and friendly staff! Qualifications 0-3 years laboratory experience or the equivalent combination of education (associates degree, or relevant life science courses and experience). Understanding or Previous experience in a GMP and GLP environment. Proficiency with Microsoft Office (Excel and Word) Understanding and knowledge of pharmaceutical cGMP, FDA guidelines and industry standards. Must be well organized.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com) Job Summary The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza's manufacturing demands. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. 8 Hour Day Shifts: Monday through Friday Key Responsibilities Running test samples for in-process, lot release and stability studies. Reviewing assays. Writing quality records (Deviations, CAPA, Change Control) and test methods. Performs other duties as assigned. Key Requirements Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline. Use of Microsoft Suites (Word, Excel, PowerPoint). Use of Laboratory computer systems. Experience using GMP Quality Systems such as: TrackWise, LIMS preferred. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

The Quality Control Technical Transfer Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing, and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Responsibilities: Applies job skills and company's policies and procedures to complete a variety of tasks. Running test samples for In-Process, Lot Release and Stability studies. Running test samples for (but not limited to) investigations, transfers and validations. Reviewing assays Training others Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods Projects - such as method transfers, new instruments, method qualifications Use of Microsoft Suites (Word, Excel, PowerPoint) Use of Laboratory computer systems Potential previous use of GMP Quality Systems such as: TrackWise, LIMS Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Apply Data Integrity principles in all aspects of work, in compliance with our DI policies, guidelines and procedures. Perform other duties as assigned. Requirements/Qualifications: Associate's Degree Microbiology, Biochemistry or Related Science Fields Strong ability to speak publicly. Strong ability to interpret data both alone and with guidance. Perform assigned, complex and/or varied tasks. Prioritization and problem solving. Comprehend and follow instructions. Direct, control and plan tasks/projects. Brainstorming Strong ability to communicate in both written and verbal format . Exercises judgment within defined procedures and practices to determine appropriate action. Self-motivated team player Completes assignments on-time and accurately Displays commitment to quality and performs job functions to the best of his/her ability Relate to others in a team setting. Maintain positive attitude in a team environment. Timeliness in completing assigned tasks. Works entire assigned shift, including arriving on time

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com) Job Summary The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza's manufacturing demands. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. 10 Hour Day Shifts Either: Key Responsibilities Running test samples for in-process, lot release and stability studies. Reviewing assays. Writing quality records (Deviations, CAPA, Change Control) and test methods. Performs other duties as assigned. Key Requirements Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline. Use of Microsoft Suites (Word, Excel, PowerPoint). Use of Laboratory computer systems. Experience using GMP Quality Systems such as: TrackWise, LIMS preferred. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com) Job Summary The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza's manufacturing demands. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. 8 Hour Day Shifts: Monday through Friday Key Responsibilities * Running test samples for in-process, lot release and stability studies. * Reviewing assays. * Writing quality records (Deviations, CAPA, Change Control) and test methods. * Performs other duties as assigned. Key Requirements * Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline. * Use of Microsoft Suites (Word, Excel, PowerPoint). * Use of Laboratory computer systems. * Experience using GMP Quality Systems such as: TrackWise, LIMS preferred. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Apply today for a rewarding career with opportunities for growth!! Must live a commutable distance to Derry, New Hampshire. We are looking for to fill full-time year round position. Mon-Fri 8:00am-4:30pm Compensation is $20-22/hour (DOE) plus benefits The Analyst I Organic Extractions prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP's. Analyst I Organic Extractions responsibilities include, but are not limited to, the following: Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include: Preparation of samples using standard techniques Performing chemical analysis using standard techniques Calculating data Recording and reporting data and any unusual test occurrences to the supervisor Performing routine instrument maintenance Responsible for performing job functions in compliance with Eurofins EHS and QA standards Responsible for general housekeeping in his/her work area Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems. Works under close supervision using routine and standard methods Aliquots and weighs samples Washes glassware Conducts all activities in a safe and efficient manner Performs other duties as assigned The ideal candidate would possess: Ability to use calculator/mathematical formulas and concepts Ability to complete work within time and quality constraints Can work independently following written or verbal instructions Cooperate and coordinate both orally and in writing Able to follow and learn appropriate protocols in one or more of the following disciplines: Organic preparation Metals preparation and analysis Gas Chromatography Gas Chromatography/Mass Spectrometry Wet Chemistry Qualifications Basic Minimum Qualifications: A minimum of an Associate of Science degree in Chemistry or equivalent experience Experience in an environmental lab is a plus At least 1-2 year's preparation, analytical experience, or combination, at company or equivalent experience elsewhere preferred Some previous PFAS experience preferred Experience with LC/MS-MS operation and general maintenance preferred Demonstrated effective communication skills and relate well to people in direct communication Consciousness of and a positive attitude toward quality, service and safety procedures Sound reasoning, good judgment and decision making Strong organization and problem solving skills Detail oriented, ability to handle multiple tasks simultaneously and able to coordinate multiple priorities Versatility, flexibility in dealing with people Ability to synthesize and retain information Computer skills, experience with LIMs software a plus Ability to perform basic math skills including multiplication, division and algebra Work independently Work within time constraints Must be able to lift up to 25 lbs frequently, and up to 50 lbs occasionally Willingness to put in overtime hours, as necessary to meet work needs Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Final candidate will be given pre-employment background check and drug screen Perform other duties as assigned Additional Information Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company 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 discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. We do not offer Visa Sponsorship for this role. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary of Objective: This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management Essential Duties and Responsibilities: Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples. Assist in deviation investigation, out-of-specification or aberrant results and process changes Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support Logging and tracking of samples and chemicals. Order chemicals and laboratory supplies as needed Documents/peer reviews laboratory work using laboratory notebooks/worksheets. Documentation must be detailed, timely and in compliance with cGMP/GDP requirements May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation Performs routine data generation and problem solving Other duties, as assigned Special Demands: Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear Ability to sit or stand for prolong periods of time Must be able to walk and drive between locations Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves Must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly Must be able to occasionally lift and/or move up to 50 pounds Comfortable with working/handling of hazardous materials Work Environment: Works closely with quality assurance and quality control staff in performing varied work procedures and activities. Interacts with Operations staff. Qualifications: 0-3 years relevant Analytical Chemistry experience, preferably in Quality Control Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred Excellent organizational skills and ability to document technical data Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization Ability to multi-task in a dynamic environment with changing priorities Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment. #LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. **Essential Duties and Responsibilities:** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. + Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed + Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss + Initiate the production of batch documentation used for engineering and cGMP production. + Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes + Complete executed Batch Records accurately and completely prior to submission to supervision for review + Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements + Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions + Cross train to increase technical skills across the department + Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. + As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. + Work with enabling groups to improve/implement processes. + Other duties as assigned. + Strong interpersonal skills + Strong working knowledge of MS Office suite is preferable + Attention to detail and positive attitude are key attributes + Able to follow rules and regulations perfectly + Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. **Qualifications:** The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. **Required:** + High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred + Experience and knowledge of formulation/compounding tools and equipment + Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations + Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. \#LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future (***************** **Equal Employment Opportunity (EEO) Statement:** _PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._ _At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com) Job Summary The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza's manufacturing demands. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. 10 Hour Night Shifts 7pm to 530am Key Responsibilities * Running test samples for in-process, lot release and stability studies. * Reviewing assays. * Writing quality records (Deviations, CAPA, Change Control) and test methods. * Performs other duties as assigned. Key Requirements * Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline. * Use of Microsoft Suites (Word, Excel, PowerPoint). * Use of Laboratory computer systems. * Experience using GMP Quality Systems such as: TrackWise, LIMS preferred. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.