Chemist jobs in Lancaster, PA - 40 jobs

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Chemist II Location: LANCASTER, PA Duration: 12+ Months (Possibility of extension ) Shift: 8Am -5Pm JOB DECRIPTION · Provides testing and technical support in the Analytical QC Laboratory . · Processing and testing samples of raw materials, packaging components, bulk and finished products, stability samples, process validation, and cleaning validations for Pharmaceutical Consumer, Inc. and other affiliates to guarantee that they conform to specifications and standard operating procedures (SOPs). · Prepares diluents, solutions, reagents, etc. in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia to expedite laboratory testing. · May review and/or assist in writing SOP's and laboratory investigations. · Provide technical guidance for other less experienced Chemists and Technicians. · Provide technical support and trouble-shooting for analytical issues and investigations. · Complies with cGMP's and safety regulations. · Maintains an environment of respect and teamwork with all coworkers RESPONSIBILITIES: (Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position: Quality & Compliance: · Ensure quality and compliance by the following actions: · Attend GMP training on the schedule designated for this role and as appropriate for this role. · Adhere to strict compliance with procedures applicable to my role. · Exercise the highest level of integrity in the tasks that I perform. · In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace. · Embrace a behavior of employee involvement and commitment to doing the job right the first time. Laboratory Operations : · Supports the laboratory operations by the following actions: · Performs testing on raw materials, in-process, finished product, packaging, and stability samples utilizing instrumentation such as HPLC, GC, FTIR, Dissolution and ICP in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia. · Reviews and approves laboratory data generated by other Analysts for completeness and accuracy. · Assist with support of laboratory investigations as needed. · Reviews and/or assists in providing input and/or writing SOP's. · Perform instrument calibrations and assist in qualifications as trained. · Identifies and implements opportunities to improve laboratory efficiencies. · Assist with the training of other Analysts on specific instruments or techniques. · Participates in meetings outside of the department as determined by a Supervisor. · Performs other related duties as required. EDUCATION: · BS or BA in a Science (Chemistry preferred) or Technical field. EXPERIENCE: · Minimum 3 years GMP QC Laboratory Experience. · Knowledge, Skills and Abilities: · Must be professional and ethical in all activities and relations. · Must demonstrate through example and maintain a positive attitude. · Must exhibit the initiative to take on individual projects, eliminate roadblocks and see them through to completion. · Capable of working both independently and as a team member. · Ability to work and communicate well with personnel in different departments and at various levels of responsibility. Additional Information Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 | LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Carpenter Technology Corporation is a leading producer and distributor of premium specialty alloys, including titanium alloys, nickel and cobalt based superalloys, stainless steels, alloy steels and tool steels. Carpenter Technology's high-performance materials and advanced process solutions are an integral part of critical applications used within the aerospace, transportation, medical and energy markets, among other markets. Building on its history of innovation, Carpenter Technology's wrought and powder technology capabilities support a range of next-generation products and manufacturing techniques, including novel magnetic materials and additive manufacturing. TECHNICIAN III - R&D PRIMARY RESPONSIBILITIES FOR THE TECHNICIAN III - R&D: Perform approved projects related to assigned area with minimal supervision, carry out various analyses, collect and evaluate the data and communicate results. Set up, operate and maintain various pieces of equipment and make repairs as needed. Perform assigned tasks in a timely, accurate and cost-effective manner. Suggest and implement possible modifications of procedures to improve the productivity of preparation and analysis methods or techniques. Maintain complete and accurate records, data books and other required documentation. Prepare test reports and other written reports and required documentation with minimal oversight. Work within the framework of outlined methods in the most efficient manner so that accurate and precise results will be consistently obtained. Assists and may lead the training of designated individuals in the skills needed to operate equipment and perform various tasks. Follow and promote the use of safe working practices. May lead small sub-teams within area. Coaches, mentors and answers technical questions from less experienced Technicians. Prioritize and direct own work with minimal oversight. May oversee the work of less experienced Technicians. Perform all other duties and special projects as assigned. REQUIRED FOR THE TECHNICIAN III - R&D: High school diploma or GED required. Two-year associate degree in a technology related field preferred. Five or more years of related experience required. Manages own time to meet objectives and is proactive in offering help to others. Contributes to achievement of team goals within own area or department; promotes teamwork through understanding of broader team goals. Ability to organize and prioritize tasks and make appropriate decisions. Ability to develop the basic skills needed to set up and operate various pieces of equipment on routine jobs. Ability to work with minimal supervision. Ability to work in a production-oriented environment. Basic problem-solving skills. Interpersonal skills. Basic laboratory skills. Ability to coach and mentor less experienced Technicians. Anticipates and understands customer needs and identifies solutions to nonstandard requests. Verbal and written communication skills. Solves moderately complex problems; makes recommendations to improve standard procedures and/or processes. Excellent written and verbal communication skills, well organized and the ability to prioritize tasks and make appropriate decisions. Willing to work in a fast-paced, ever-changing work environment. Carpenter Technology Company offers a competitive salary and a comprehensive benefits package including life, medical, dental, vision, flexible spending accounts, disability coverage, 401k with company contributions as well as many other options to employees. Carpenter Technology Corporation's policy is to fully and effectively maintain a program of equal employment opportunity and nondiscrimination for all employees, to employ affirmative action for all protected classes, and to recruit and develop the best qualified persons available regardless of age, race, color, religion, sex, gender identity, sexual orientation, marital status, national origin, political affiliation or any other characteristic protected by law. The Company also will recruit, develop and provide opportunities for qualified persons with disabilities and protected veterans.

Join an industry leader and make a positive change in the sustainable use of the world's natural resources. Together, we will transform the business and drive the industry toward a greener future. At Metso, you will be supported by our inclusive culture and a network of colleagues from around the world. With us, you will embark on a personal growth journey and are encouraged to realize your potential. This is your invitation to rise above the possible. We are seeking an Analytical Chemist to join our Metso Test Center team. You will be responsible for developing analytical methods and procedures, conducting mineral processing test work, and supporting R&D projects, which involves working with advanced analytical equipment such as ICP, XRF, and XRD. Your role plays a crucial part in establishing and expanding our analytical laboratory capabilities, which will contribute to innovative mineral processing solutions and a more sustainable industry. In this position, you will report to the Test Center Manager. This position is mainly located in Manchester, PA, and includes an initial 6-10 week training period in Pori, Finland. Up to 10% travel may be required at other times. Team you belong to You will join a team of mineral processing and analytical experts dedicated to advancing testing capabilities and delivering high-quality analytical results for customer projects and R&D initiatives. We are currently developing a new analytical laboratory and working on mineral processing test programs and research projects. We work closely with internal stakeholders such as Metso chemists and mineralogists in other labs, and external partners including local academia and industry. Our team culture is all about collaboration, innovation, and continuous improvement. The members of our team are located in Manchester, PA, and Pori, Finland. What you'll do * Develop methods and standards for the new analytical lab at the Metso Test Center. * Prepare samples and conduct analytical testing using ICP, XRD, XRF, and other common equipment. * Calibrate and maintain analytical instruments in good working order. * Participate in planning and execution of customer test work and R&D projects. * Analyze data and prepare detailed reports. * Build and maintain relationships with Metso chemists and mineralogists globally. * Liaise with local academia and industry to advance the lab's capabilities. * Communicate effectively with team members to manage workflow and prioritize activities. Who you are * BS in Chemistry (MSc or PhD is a plus). * Experience in inorganic analytical chemistry. * Hands-on experience with ICP, XRF, and XRD equipment. * Strong analytical mindset and problem-solving skills. * Excellent written and verbal communication skills. * Ability to work collaboratively in a team environment. * Nice to have: Previous experience in mineral processing or related R&D projects. What's in it for you * An inspiring purpose - Be part of transforming the industry and enabling sustainable modern life. * Wellbeing and safety - Occupational healthcare, generous benefits plan, and mental well-being services. * Compensation and rewards - Competitive salary and global incentive program tied to performance. * Hybrid working possibilities - Flexible work arrangements where possible. * A thriving culture - Inclusive, courageous, and caring environment that supports your growth. * Extensive learning opportunities - Global training, mentoring programs, and ambitious projects. * Worldwide support - Collaborate with peers across the globe. Get in touch Want to rise above the possible with us? Click 'Apply now' to leave your application. For additional information, please contact Francesca Palermo, Senior Talent Acquisition Specialist, *************************** How to join - Working at Metso - About Metso - Diversity and Inclusion - Meet our people Metso is an equal opportunity employer committed to fostering an inclusive and diverse workforce culture. All qualified applicants will receive consideration for employment without regard to race, religion, color, nationality, gender, gender identity, sexual orientation, age, status as a protected veteran or status as a qualified individual with a disability. Metso is a frontrunner in sustainable technologies, end-to-end solutions and services for the aggregates, minerals processing and metals refining industries globally. We improve our customers' energy and water efficiency, increase their productivity, and reduce environmental risks with our product and service expertise. We are the partner for positive change. Metso is headquartered in Espoo, Finland. At the end of 2024 Metso had close to 17,000 employees in around 50 countries, and sales in 2024 were about EUR 4.9 billion. Metso is listed on the Nasdaq Helsinki. metso.com

Full-time Description At SPL, we turn science into impact. We're seeking a skilled and detail-oriented Chemist I to join our Metals laboratory team in Reading, PA. In this role, you'll perform analytical testing, method development, and data validation that ensure the accuracy and quality our clients depend on for regulatory compliance and decision-making. Working alongside experienced professionals, you'll gain exposure to advanced laboratory instrumentation, contribute to continuous improvement initiatives, and help deliver precise, defensible results that make a measurable impact. If you're reliable, organized, and eager to learn in a fast-paced laboratory setting, we'd love to hear from you! Why You'll Love This Role Play a hands-on role in transforming data into decisions that make a real-world impact; Work with state-of-the-art laboratory instrumentation and analytical techniques across diverse projects; Build your expertise in method development, data validation, and quality control in a collaborative, learning-focused environment; Contribute to work that supports client success, regulatory compliance, and SPL's mission of turning science into impact. What You'll Do Prepare, analyze, and document client and quality control samples using approved methods and Standard Operating Procedures (SOPs); Operate, calibrate, and maintain analytical instruments to ensure accuracy and reliability of results; Record, validate, and manage analytical data within the Laboratory Information Management System (LIMS) while ensuring traceability and compliance with quality standards; Participate in method development, validation, and troubleshooting activities to enhance analytical performance and efficiency; Support quality assurance initiatives, including audits, corrective actions, and continuous improvement projects; Collaborate with peers and supervisors to meet deadlines, maintain safety protocols, and uphold SPL's commitment to data integrity; Contribute to team training, mentorship, and the continuous improvement of laboratory practices; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's degree in Chemistry, Science, or a related field required; Minimum of two (2) years of analytical laboratory experience required; Experience with ion chromatography (IC), flow injection analysis (FIA), segmented flow analysis (SFA), spectrophotometry, biochemical oxygen demand (BOD), gravimetric analyses, mercury analysis, turbidity, or hardness testing strongly preferred; Experience with ICP, ICP-MS, and EPA methods 200.7, 200.8, 6010, and 6020 strongly preferred; Ability to manage and process high volumes of samples efficiently; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 10 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a Monday through Friday schedule from 9 AM to 5:30 PM; Ability to work outside of scheduled hours, including evenings or weekends, as required to meet operational or workload needs. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

Come check out Turkey Hill! - We're a growing, nationwide company, born and raised in Southcentral Pennsylvania, that has been creating delicious ice cream and beverages since 1931. We offer competitive pay, great benefits, and leadership development opportunities with career-growth potential - join our team today! Hours for this position are 10:25pm to 6:30am. The Fluid Flex I makes an impact by - * Perform and record all sanitation duties as required within the fluid packaging team including Master Sanitation Sheet (MSS) tasks, supporting the environmental program and manual cleaning of all equipment associated with the fluid packaging team areas. * Perform and record all quality assurance (QA) tests and checks pertaining to the fluid packaging team areas. * Proficient in all communication systems and processes, computer programs, and the Key Performance Indicator (KPI) board. * Perform and record all required tasks within the packaging team areas including the spot-pak room, box erector room and drop packer area. * Perform basic maintenance duties for all equipment as required. * Perform all duties within established safety guidelines. This includes but not limited to adhering to Safety in Motion guidelines, LOTO procedures, wearing appropriate PPE, Clarity, BAPP observations and using the correct tools for the task at hand. * Perform all duties within the established Good Manufacturing Practices (GMP) regulations. * Obtain and maintain all required certification for regulatory compliance. * Follow established programs, policies and practices to produce safe quality foods that meet regulatory and company requirements. * Support the development, implementation, maintenance, and ongoing improvement of the SQF 2000 Systems. * Accountable to the Turkey Hill Manufacturing Food Safety and Quality Principles. * Must be able to perform the essential functions of this position with or without reasonable accommodation. You could be a great fit if you have these things - * Must be at least 18 years of age * Must work well in a team environment * Maintain adherence to work hours scheduled specifically starting, ending, lunch and break schedules * Perform all duties within established Good Manufacturing Practice (GMP) regulations and safety guidelines * Be accountable to the Turkey Hill Food Safety and Quality Principles * Follow established programs, policies and practices to produce safe quality foods that meet regulatory and company requirements * Support the development, implementation, maintenance, and ongoing improvement of Safe Quality Foods (SQF) Food Safety and Quality * Perform all other duties as assigned Our associates enjoy these awesome benefits - * Medical, dental, vision & prescription * Life insurance, short-term & long-term disability * 401(k) with company match - immediately vested * Employee Assistance Program (EAP) * Earn vacation and PTO * Educational assistance reimbursement * Company bonus plan * Free ice cream and beverages! Physical Demands - The physical demands described here are representative of those that must be met to successfully perform the essential functions of the job. * The employee is required to talk and/or hear in a manufacturing setting where noise levels are high (PPE required). * The employee is required to wear mandated PPE based on assigned job area. * The employee is frequently required to stand and walk in an manufacturing environment for 8+ hours. * The employee must be able to ascend and descend stairs, and where applicable and when necessary, to perform various job-related tasks. * Must be able to position self to move, reach with arms/hands, stoop, kneel, crouch, or crawl as needed to perform various job-related tasks. * The employee must be able to inspect all job-related equipment (office or floor) to ensure it is in good working condition prior to use. Must be able to use hands/fingers to handle (or feel) to operate various types of office equipment. * Must be able to operate all job-related equipment (powered, hand or office) as required. * Vision requirements: close vision, distance vision, peripheral vision, and depth perception and adjust focus. * Ability to lift 50 pounds and/or push/pull 50 pounds on a regular basis. * Must have ability to work rotating or non-traditional shifts as needed, including overtime as required by business needs. * Must be able to work in an environment that contain allergens such as Milk, Soy, Wheat, Peanut, Treenuts, Egg, Shellfish, and Fish. * Must be able to work in the environment for the position, which may range from extreme heat to extreme cold or from wet/humid to dry/arid. This job description is not all encompassing, however, is intended to be a general description of the essential functions of this position. It is not intended as an employment contract. This role is considered Safety Critical at Turkey Hill. In order to ensure safety for all of our associates, this role will have a zero tolerance policy when returning a positive drug screen, regardless of Medical Marijuana card holding status. Notice to Staffing Agencies, Placement Services, and Professional Recruiters Turkey Hill, LLC has an internal Staffing Department. Recruiters are hereby specifically directed NOT to contact Turkey Hill employees directly in an attempt to present candidates. Turkey Hill will not accept unsolicited resumes from any source other than directly from a candidate. Any unsolicited resumes sent to Turkey Hill, including unsolicited resumes sent to a Turkey Hill mailing address, fax machine or email address, directly to Turkey Hill employees, or to Turkey Hill's resume database will be considered Turkey Hill property. Turkey Hill will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Turkey Hill will consider any candidate for whom a Recruiter has submitted an unsolicited resume to have been referred by the Recruiter free of any charges or fees. Turkey Hill will not pay a fee to any Recruiter that does not have a signed Turkey Hill contract in place specific to the position for which the resume was submitted. Recruiting vendor agreements will only be valid if in writing and signed by Turkey Hill's Human Resources Manager or his or her designee. No other Turkey Hill employee is authorized to bind Turkey Hill to any agreement regarding the placement of candidates by Recruiters. By submitting a candidate to Turkey Hill, recruiters agree to be bound and comply with this policy.

Universal Ingredients, Inc. is a premier manufacturer of vanilla extracts, other extracts, natural and artificial flavors, food colors, syrups, and sauces. Shank's quality products are widely distributed to industrial, private-label, and grocery customers worldwide. We have an immediate opening for an R&D Laboratory Technician Available Immediately Upon Hire: Medical, Dental, Vision, FSA, HSA, EAP, ID Theft, 401K, and PTO. Disclaimer: Shank's Extracts manufactures various products that identify as major food allergens (milk, eggs, tree nuts, wheat, and soybeans) as well as several other food ingredients. We cannot guarantee you will not be exposed to skin and/or odor contact with these various ingredients. Your health and safety are our number one priority, and we will do our best to accommodate within reason. ESSENTIAL FUNCTION: Prepares bench top and pilot lab flavor/food/beverage prototypes to showcase Universal Ingredients' portfolio & technologies under supervision as required. DUTIES AND RESPONSIBILITIES: Compounds flavor formulas for active project work as instructed by the flavorist. Prepares application samples for ongoing development projects, including scaling, heat treatment, and packaging. Utilizes basic mathematical procedures to calculate flavor adjustment percentages and create chemical solutions. Adjust flavor formulas as instructed by the flavorist and records changes in Excel formulas. Doses finished flavors at tasting strength and prepares flavor and application tastings for flavorist and team. Completes chemical analyses of flavor and application products for commercialization. Maintains raw material inventory through warehouse sampling and proper labeling. Contacts raw material suppliers for samples of ingredients not maintained in warehouse inventory. Fulfills open sample requests in a timely manner by preparing samples, providing copies of necessary documentation, and coordinating shipping. Maintains laboratory equipment and space in a clean, orderly, and safe manner daily. Follows appropriate safety, laboratory, and GMP procedures. Performs other duties as assigned. ESSENTIAL/SKILLS NEEDED: Must have a positive attitude, be self-motivated, detail-oriented and organized. Must work well in a team environment. Ability to work in a fast-paced environment and adapt to constant change in a positive manner. Ability to understand instructions and execute in an efficient and effective manner. Capable of handling multiple projects in a limited time frame. Familiar with food industry practices and procedures, and basic knowledge of GMP's and HACCP. Ability to read and interpret various formula sheets. Ability to use basic lab equipment such as scales, pipettes, pH meters, blenders, mixers, and hot plates/stirrers. Proficient in Microsoft Office and able to learn new software systems quickly. Excellent hand-eye coordination. English comprehension including speaking, reading, and writing is required for our business's necessity to ensure a safe and effective work environment. EDUCATION AND EXPERIENCE High school diploma required. Associate degree in the Sciences preferred. 1-2 years of experience working in a laboratory setting preferred. ERP Experience preferred. Experience in a food manufacturing company preferred. PHYSICAL REQUIREMENTS: Requires standing for an entire shift. Requires frequent lifting and/or carrying objects weighing up to ten (10) pounds. Requires pushing, pulling, bending, twisting, squatting, and lifting close to the body. Require frequent repetitive motion. Ability to work in a consistent area for an entire shift. Must be able to work in various indoor temperatures including elevated heat and humidity. Exposure to elevated noise levels which occur below OSHA thresholds. Infrequent exposure to machine sanitation solutions and detergents. Requires frequent visual quality control observations which may include turning and bending of the neck and head area. Exposure to various odors throughout a work shift. Required to wear Personal Protective Equipment [PPE] Required to follow Good Manufacturing Practices [GMPs] Exposure to food allergens such as, but not limited to, milk, eggs, tree nuts, wheat, and soybeans will occur. Conduct, Quality, Integrity, and Culture Conduct: We will conduct every aspect of our business with honesty, integrity, and openness, respecting human rights and the interests of our employees, customers, and third parties . Quality: Shank's is committed to food safety and product quality. We employ extensive food safety programs and controls at all levels. Our quality standards and food safety procedures are thoroughly being evaluated internally and externally. We continuously strive to improve our performance. Integrity: Shank's and its employees will not offer, give, seek or receive, either directly or indirectly, improper inducements for business or financial gain. Where information is confidential, that confidentiality must be protected. Culture: Shank's respects the cultural values of our employees, contractors, and customers. We also promote a balanced work-life environment. We recognize and celebrate our employees for their hard work and the contributions they make to our company. Shanks Core Values: ASPIRATION: Share a vision for achievement ACCOUNTABILITY: Support company reputation ADAPTABILITY: Evolve to meet business needs ***Competitive compensation and benefits package*** Shank's Extracts, LLC d/b/a Universal Ingredients - Shank's is an Equal Employment Opportunity/Affirmative Action (EEO/AA) Employer.

FLSA Status: Exempt Grade Level: S-8 Department: Innovation Group Reports To: Innovation Group Leader or Director of Innovation Direct Reports: Product Development Chemist, Innovation Group Technician Job Summary: Works with customers and AR teams to identify unmet needs, collect design input and develop new product design strategies. Technical and laboratory lead in developing new polymers, robust products, and basic production processes that can be successfully commercialized. Essential Functions: Conducts required laboratory work; including polymerization, formulation, coating and testing Develops new products that lead to sustainable commercial revenue Functions as a technical lead on product development teams Develops design strategies based on robust design input Meets technical commitments in order to complete project progression dates and milestones Contributes to product scale up and development through reproducibility and validation testing support Detailed knowledge of required chemical and physical test methods May supervise and teach other laboratory staff Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums Interfaces with customers on new product applications Interfaces with associates from other departments as needed (e.g. cross-functional teams) Documents lab work in electronic notebook and project reports Performs all duties consistent with established AR guidelines, ISO-9001, and elements of GMP deemed necessary to support the business (as outlined in the Quality Manual) Actively complies with and endorses Department and Company objectives Additional Responsibilities: Performs other duties and responsibilities as assigned. Job Specifications: BS, MS, or PhD in chemistry, polymer science or materials science; adhesive polymerization, formulation, and coating experience preferred Ability to perform duties with minimal or no supervision Ability to manage multiple priorities Requires an demonstrated ability to use sensitive test equipment Ability to employ statistical analysis techniques Ability to manage and supervise laboratory staff Ability to maintain confidentiality of AR information Must communicate fluently in English Excellent oral & written communication skills Excellent interpersonal skills Knowledge of computers & related word processing, spreadsheet & e-mail software-Microsoft preferred

**Quality Control Analyst** Every day, Kelly Science & Clinical connects professionals with opportunities to advance their careers. We currently have exciting temporary opportunity as a **Quality Control Analyst** with a global leader in the production of consumer products and pharmaceuticals in **Lititz, PA** **Location:** Lititz, PA **Contract:** 9mo, possible extension **Schedule:** M-F, 2nd Shift (3P-11:30P) **Compensation** : $26-34/hr **Summary** : The Quality Control Analyst I is an entry level analyst responsible for performing a variety of analytical testing of raw materials and non-testing activities with moderate supervision to support the analytical laboratory. This position is responsible but not limited to the following : capable of basic bench wet and physical chemistry testing, analytical assay testing through chromatography analysis (such as but not limited to UPLC, LC, GC, IC, and UV), peer review (review of standard and reagents), assisting in the upkeep and revisions of laboratory documents (test notes, SOPs, Work Instructions, and Job Aids), and additional tasks as needed. **Responsibilities** + Follow all required procedures (SOP, Kenvue Test Methods, Product Specifications, Raw Material Specifications, Test Notes, and Pharmacopoeia Test Methods) + Perform basic wet bench testing and physical testing + Perform Chromatography Analyses + Participate as needed with laboratory and non-conformance Investigations + Peer Review of Standard and Reagents + Capable of learning new testing techniques + Able to troubleshoot instrument and testing issues. + Document upkeep support (updating as needed SOPs, Test Notes, Job Aids, and Work Instructions) + Participate in the labs 5S program + Proved assistance/lead non-testing projects that is designed to benefit the QC laboratory in process improvements and efficiency gains + Good documentation skills - following GLP practices and laboratory procedures + Remain compliant by completing on-time required trainings + GC, Wet Chem, Analytical Chemistry, Raw Materials **Qualifications** + BS in the Scientific field + Knowledge of GMPs and good documentation practices + Good Communication Skills + Knowledge of Basic Chemistry, able to work in a team environment, work under GMP requirements. + P#1 **Important information:** This position is recruited for by a remote Kelly office, not your local Kelly branch. Must be legally permitted to work in the United States. Send resumes to: ************************************ As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job Posting Title: QUALITY CONTROL ANALYST II (On-Site Landisville, PA) Business Unit: CONNECTED LIVING SOLUTIONS (10020198) Building: TYCO ELECTRONICS KAUFFMAN ROAD (108) Band/Level: 5 Hiring Manager: MITCHELL K MEDFORD Recruiter: Pete Roosendaal Relocation: No Travel: Less than 10% Employee Referral Amount: $1,000.00 Education Experience: Bachelors Degree (High School +4 years) Employment Experience: 1-3 years **At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** Job Description: **Job Overview** TE Connectivity's Quality Assurance Teams are responsible for all or part of an organization's Quality Management System, including conformance and continuous improvement initiatives. They conduct systematic evaluations of products, services, facilities, manufacturing processes, or business processes to ensure quality standards are met. Develop and implement quality plans, programs, and procedures using quality control statistics, lean manufacturing concepts, and six-sigma tools and analyses. They review, analyze, and report on quality discrepancies; investigate problems; execute quality audits; and develop disposition and corrective actions for recurring discrepancies. The team works closely with manufacturing, engineering, customers, suppliers, and subcontractors to ensure requirements are met. **The facility in Landisville, PA, is an ITAR site.** **Job Responsibilities** + Assist the Quality Manager in establishing, implementing, and maintaining the Quality Management System (QMS). + Support continual improvement activities to enhance the QMS. + Support the implementation of configuration management for Engineering Change Orders (ECO) + Support the maintenance of Engineering documentation files and logs. + Support the part number integration process. + Perform Measurement, Test & Inspection of product at Receiving Inspection, In-Process, and Final test. + Conduct QMS, process, and product audits in accordance with the QMS internal audit requirements. + Support product & process failure root cause analysis + Provide support to the manufacturing departmental Quality Control Inspectors as needed to ensure products and processes comply with the relevant quality management system requirements. + Support return product analysis, and customer complaint systems for root cause analysis and corrective actions + Prepare QA reports as directed by the QA Manager. + Support the control of non-conforming material process. + Assist in developing quality plans and implementing established methods for inspection and test procedures for new and existing products. + Work with cross-functional teams to improve processes and to drive product quality. + Other appropriate duties as assigned. **Job Requirements** + Participating in process analysis, advanced product quality planning, validating new products and processes, and design reviews. + Validating products and processes through measurement system analysis and capability studies and participating in verification and production line error-proofing requirements. + Monitoring the quality testing procedures to ensure that all the procedures are performed according to the established specifications, test methods, and protocols. + Supporting the project team in preparing process flow diagrams, design failure mode and effect analysis (DFMEA), preventive actions, and troubleshooting processes. **What your background should look like** **Qualifications** + Knowledgeable in electronics and electronic assembly/inspection. + Working knowledge of methodologies for inspecting parts for tolerance specifications. + Must be able to read and follow all written and implied directions, policies, and procedures. + Ability to analyze and resolve problems using various failure analysis techniques to isolate failures down to the root cause. + Good organization, verbal, writing, and listening skills. + High level of attention to detail and accuracy + Work independently in a team environment. + Must be proficient with Microsoft Office applications (Word, Excel, PPT, etc.) + Demonstrates broad knowledge of theory and principles within a professional discipline. + Requires the ability to apply skills and knowledge to understand specific needs or requirements. + Analyzes information and generates ideas. + Develops solutions to a variety of problems of moderate scope and complexity. + Identifies and corrects issues that are not immediately evident in existing systems or processes. + Generally requires a Bachelor's Degree in an appropriate field or local equivalent with a minimum of 3 years of progressively responsible professional-level experience. + Experience with configuration management is a plus. + Working knowledge of ISO 9001 is a plus. + Working knowledge of AS9100 is a plus. **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **COMPENSATION** - Competitive base salary commensurate with experience: $72,900 - $108,600 (subject to change dependent on physical location) - Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. - Total Compensation = Base Salary + Incentive(s) + Benefits **BENEFITS** - A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits. **EOE, Including Disability/Vets** **IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD** TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests payment or fees** from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come **only from actual email addresses ending ************ . If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities. **Job Locations:** Posting City: LANDISVILLE Job Country: United States Travel Required: Less than 10% Requisition ID: 145231 Workplace Type: External Careers Page: Quality TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of 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.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Job Description Title: Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used in the manufacture of pharmaceutical and nutritional products. This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation. Position Summary: In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed. The incumbent will perform analysis on raw materials following prescribed procedures to provide the information base leading to material disposition, as well as assist in troubleshooting and problem solving as directed. Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Position Duties & Responsibilities : Perform standard qualitative and quantitative analysis: • Utilize standard analytical chemistry techniques: wet analytical methods, HPLC, UV, GC, AA, polarimeter, FT-IR, NIR, RAMAN, etc.) to test raw materials in accordance with approved testing procedures, including those from company, the National Formulary (NF), the United States Pharmacopoeia (USP), the European Pharmacopoeia (EP), and the FDA. • Properly document and maintain records of all analysis information of assigned materials on data sheets and laboratory notebooks for permanent file. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Communicate to supervision in a timely manner all non-compliance situations, and assist in investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor, for example, revise existing analytical testing monographs to comply with compendia changes or other specific needs. • Accurate, complete and timely fulfillment of the job responsibilities will, in part, ensure GMP compliance as outlined in various Bayer and U.S. government rules and regulations. Documentation Review: • Review testing documentation performed by other analysts for compliance with BAYER, FDA, National Formulary (NF), United States Pharmacopoeia (USP), and European Pharmacopoeia (EP) procedures. Safety: • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations. Qualifications Requirements/Preferences: • Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Chemistry degree is preferred. • At least 1-3 years of experience in a GMP laboratory environment. Master's degree in a related field with 1 year of experience may be considered. • Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position. • Basic experience with Personal Computer (PC). • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Good working knowledge of advanced laboratory instrumentation and computers are required; This is defined as strong troubleshooting skills for assigned area such as HPLC, GC, AA, UV, TOC, NIR and/or dissolution and low error rates with microbiology or chemistry techniques for defined area • A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is required • Demonstrated ability to clearly communicate technical information in writing required. • Demonstrated ability to manage key projects and display area of expertise; i.e. clear/consistent notebook skills and function as an independent worker. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Demonstrated ability to take initiative and display a willingness to learn required. • A thorough understanding of National Formulary (NF); United States Pharmacopeia (USP); and European Pharmacopeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures is required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Enter here Travel Requirements: None Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) Additional Information All your information will be kept confidential according to EEO guidelines.

Skill Source is a leading placement service specializing in manufacturing operations both on the production floor and front office. We work hard finding the right complimentary fit for both client and qualified candidates. We facilitate this by asking not just the right questions technically but the right questions to fit you personally. We have a substantial client base to work with so there is a very good chance we can find you the next step in a more satisfying career. Submit your hard earned resume today and let us see what we can do for you! Job Description My growing client is looking for a skilled Metal Anodizing/Plating Technician. Full time position with a growing up and coming manufacturing company! Great pay and benefits! First shift position. Growth opportunities available. Qualifications At least 2yrs experience processing metal coatings (anodizing) onto metal parts (medical device or aerospace a plus) MUST have experience disposing hazardous materials in compliance with OSHA and/or HAZMAT guidelines Chemistry Degree - Associates or better strongly preferred. Additional Information These are permanent positions NOT contract! Excellent pay (Pay commensurate with experience) and benefits packages! Some of our clients pay FULL medical! Please feel free to review our other opportunities at ***************************

Responsibilities: Must have 2+ years experience working in a quality control position for apparel manufacturing, cut & sew knits experience preferred Ensure garments are being sewn to specifications and adhering to quality guidelines of factory, as per approved technical packages Measure garments on active QC area to ensure they are accurate to specifications Trimming, pressing, packaging final product Collaborates in all areas of this department Logging any defects, such as holes, stains, shading Identify repetitive issues with quality of production, and escalate issues to the Factory Operations Supervisor for corrective action Regularly report QC findings and concerns to Factory Operations Supervisor and Factory leadership team ● Be accountable to maintain quality standards of the factory and the company, ensuring garments are accurate to specifications before passing to the next phase of production Voluntary overtime as needed Work in a safety sensitive environment Job Knowledge, Skills and Abilities: Adaptability: Ability to adapt to changes in the work environment, manage competing demands. Must be able to perform job functions with limited supervision. Organization skills: 5s standards; 1) Sort 2) Set In Order 3) Shine 4) Standardize 5) Sustain Dependability: Ability to follow instructions, respond to management direction. Ability to maintain confidentiality. Language: Ability to read and interpret documents such as safety rules, operating and maintenance instruction, and procedures manuals in English or Spanish. Demonstrated ability to communicate orally and in written form effectively with other employees. Mathematical: Ability to do simple math, such as add, subtract, multiply, and divide. Planning and Organizing: Ability to prioritize and plan work activities and use time efficiently. Problem Solving: Ability to solve practical problems and interpret and resolve problem issues using a variety of instructions or guides furnished in written, oral, diagram, or schedule form. Technical: Must have computer skills (google, gmail, google sheets) Physical Demands: Working by standing multiple hours of the work day, reaching, bending. occasional lifting (max. 50lbs) and walking Founded in 2013 by Sasha Koehn and Erik Allen Ford, Buck Mason makes simplified clothing for the modern man. At the heart of everything we do is the unclouded California ethos of quality, restraint, and integrity. We take iconic pieces and reconstruct them in hard-wearing fabrics, with timeless details, and the perfect fit. Our goal is to offer fashion that is less complicated, building pared-down essentials that live beyond a single season. With its corporate offices headquartered in Los Angeles, Buck Mason's retail footprint extends from sea to sea, through e-commerce and brick-and-mortar locations in Los Angeles, San Francisco, New York, Brooklyn, and more. Join us at Buck Mason, where style meets substance, and every team member plays a vital role in our success. Ready to make your mark? Apply now!

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization 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 Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Employee Responsibilities: Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels) Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus Preparing samples for analysis and running some instrumentation with minimum supervision Set up and validate new analytical or related processes used by the department Prepare standards and samples for analysis Execute method transfer protocols Document work as required for GMP compliance Perform monthly maintenance of laboratory equipment Qualifications EDUCATION and/or EXPERIENCE: Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience Authorization to work in the United States indefinitely without restriction or sponsorship Must be able to speak well to technical lab skills Additional Information Position is full time, Monday to Friday, 3PM - 11PM. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Chemist II Location: LANCASTER, PA Duration: 12+ Months (Possibility of extension) Shift: 8Am -5Pm JOB DECRIPTION · Provides testing and technical support in the Analytical QC Laboratory. · Processing and testing samples of raw materials, packaging components, bulk and finished products, stability samples, process validation, and cleaning validations for Pharmaceutical Consumer, Inc. and other affiliates to guarantee that they conform to specifications and standard operating procedures (SOPs). · Prepares diluents, solutions, reagents, etc. in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia to expedite laboratory testing. · May review and/or assist in writing SOP's and laboratory investigations. · Provide technical guidance for other less experienced Chemists and Technicians. · Provide technical support and trouble-shooting for analytical issues and investigations. · Complies with cGMP's and safety regulations. · Maintains an environment of respect and teamwork with all coworkers RESPONSIBILITIES: (Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position: Quality & Compliance: · Ensure quality and compliance by the following actions: · Attend GMP training on the schedule designated for this role and as appropriate for this role. · Adhere to strict compliance with procedures applicable to my role. · Exercise the highest level of integrity in the tasks that I perform. · In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace. · Embrace a behavior of employee involvement and commitment to doing the job right the first time. Laboratory Operations: · Supports the laboratory operations by the following actions: · Performs testing on raw materials, in-process, finished product, packaging, and stability samples utilizing instrumentation such as HPLC, GC, FTIR, Dissolution and ICP in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia. · Reviews and approves laboratory data generated by other Analysts for completeness and accuracy. · Assist with support of laboratory investigations as needed. · Reviews and/or assists in providing input and/or writing SOP's. · Perform instrument calibrations and assist in qualifications as trained. · Identifies and implements opportunities to improve laboratory efficiencies. · Assist with the training of other Analysts on specific instruments or techniques. · Participates in meetings outside of the department as determined by a Supervisor. · Performs other related duties as required. EDUCATION: · BS or BA in a Science (Chemistry preferred) or Technical field. EXPERIENCE: · Minimum 3 years GMP QC Laboratory Experience. · Knowledge, Skills and Abilities: · Must be professional and ethical in all activities and relations. · Must demonstrate through example and maintain a positive attitude. · Must exhibit the initiative to take on individual projects, eliminate roadblocks and see them through to completion. · Capable of working both independently and as a team member. · Ability to work and communicate well with personnel in different departments and at various levels of responsibility. Additional Information Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724| LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Carpenter Technology Corporation is a leading producer and distributor of premium specialty alloys, including titanium alloys, nickel and cobalt based superalloys, stainless steels, alloy steels and tool steels. Carpenter Technology's high-performance materials and advanced process solutions are an integral part of critical applications used within the aerospace, transportation, medical and energy markets, among other markets. Building on its history of innovation, Carpenter Technology's wrought and powder technology capabilities support a range of next-generation products and manufacturing techniques, including novel magnetic materials and additive manufacturing. Technician III - R&D Primary Responsibilities for the Technician III - R&D: Perform approved projects related to assigned area with supervision, carry out various analyses, collect and evaluate the data and communicate results. Set up, operate conventional machinery including: Manual lathes, Bridgeport, milling machine and grinders and drill presses CNC Operation both milling and turning, including CNC programming Cylindrical grinder operation and surface grinder operation EDM operation / willing to learn the operation Operation of radial cutoff saws Operation of all HEM saws Set up and maintain various pieces of equipment and make minor repairs as needed. Work to set machine shop and equipment priorities based on data for machine setup, changeover time, and project priorities. Assist other technicians and engineers in developing drawings, test specimens, and cutting plans. Proactive about safety and involvement with department safety initiatives. Assist in the training of designated individuals in the skills needed to operate equipment and perform various tasks. Prepare test reports and other written reports and required documentation with oversight. Maintain complete accurate records and documentation. Suggest possible modifications of procedures to improve the productivity of preparation and analysis methods or techniques. Perform all other duties and special projects as assigned. Required for the Technician III - R&D: High school diploma or GED with a two-year technical degree in a technology related field. Five or more years of related experience required. Knowledge of CNC programming. Specialized knowledge of machine shop theory and procedures. Specialized knowledge of shop mathematics, machinability of materials, and layout techniques. Preferred for the Technician III - R&D Working knowledge of reference calibration standards and electrodes. Working toward Machinist papers. Ability to make changes in CNC programs in both the flat and round cells. Ability to write CNC programs in both the flat and round cells. Ability to machine special fixtures and adapters. Ability to cross-train in at least one other cell/area. Ability to work with minimal supervision. Ability to work with a continuous improvement mindset, i.e., make recommendations to improve processes, use team approach to problem solving. Excellent written and verbal communication skills, well organized and the ability to prioritize tasks and make appropriate decisions. Willing to work in a fast paced, ever-changing work environment. Carpenter Technology Company offers a competitive salary and a comprehensive benefits package including life, medical, dental, vision, flexible spending accounts, disability coverage, 401k with company contributions as well as many other options to employees. Carpenter Technology Corporation's policy is to fully and effectively maintain a program of equal employment opportunity and nondiscrimination for all employees, to employ affirmative action for all protected classes, and to recruit and develop the best qualified persons available regardless of age, race, color, religion, sex, gender identity, sexual orientation, marital status, national origin, political affiliation or any other characteristic protected by law. The Company also will recruit, develop and provide opportunities for qualified persons with disabilities and protected veterans.

Universal Ingredients, Inc. is a premier manufacturer of vanilla extracts, other extracts, natural and artificial flavors, food colors, syrups, and sauces. Shank's quality products are widely distributed to industrial, private-label, and grocery customers worldwide. We have an immediate opening for an R&D Laboratory Technician Available Immediately Upon Hire: Medical, Dental, Vision, FSA, HSA, EAP, ID Theft, 401K, and PTO. Disclaimer: Shank's Extracts manufactures various products that identify as major food allergens (milk, eggs, tree nuts, wheat, and soybeans) as well as several other food ingredients. We cannot guarantee you will not be exposed to skin and/or odor contact with these various ingredients. Your health and safety are our number one priority, and we will do our best to accommodate within reason. ESSENTIAL FUNCTION: Prepares bench top and pilot lab flavor/food/beverage prototypes to showcase Universal Ingredients' portfolio & technologies under supervision as required. DUTIES AND RESPONSIBILITIES: Compounds flavor formulas for active project work as instructed by the flavorist. Prepares application samples for ongoing development projects, including scaling, heat treatment, and packaging. Utilizes basic mathematical procedures to calculate flavor adjustment percentages and create chemical solutions. Adjust flavor formulas as instructed by the flavorist and records changes in Excel formulas. Doses finished flavors at tasting strength and prepares flavor and application tastings for flavorist and team. Completes chemical analyses of flavor and application products for commercialization. Maintains raw material inventory through warehouse sampling and proper labeling. Contacts raw material suppliers for samples of ingredients not maintained in warehouse inventory. Fulfills open sample requests in a timely manner by preparing samples, providing copies of necessary documentation, and coordinating shipping. Maintains laboratory equipment and space in a clean, orderly, and safe manner daily. Follows appropriate safety, laboratory, and GMP procedures. Performs other duties as assigned. ESSENTIAL/SKILLS NEEDED: Must have a positive attitude, be self-motivated, detail-oriented and organized. Must work well in a team environment. Ability to work in a fast-paced environment and adapt to constant change in a positive manner. Ability to understand instructions and execute in an efficient and effective manner. Capable of handling multiple projects in a limited time frame. Familiar with food industry practices and procedures, and basic knowledge of GMP's and HACCP. Ability to read and interpret various formula sheets. Ability to use basic lab equipment such as scales, pipettes, pH meters, blenders, mixers, and hot plates/stirrers. Proficient in Microsoft Office and able to learn new software systems quickly. Excellent hand-eye coordination. English comprehension including speaking, reading, and writing is required for our business's necessity to ensure a safe and effective work environment. EDUCATION AND EXPERIENCE High school diploma required. Associate degree in the Sciences preferred. 1-2 years of experience working in a laboratory setting preferred. ERP Experience preferred. Experience in a food manufacturing company preferred. PHYSICAL REQUIREMENTS: Requires standing for an entire shift. Requires frequent lifting and/or carrying objects weighing up to ten (10) pounds. Requires pushing, pulling, bending, twisting, squatting, and lifting close to the body. Require frequent repetitive motion. Ability to work in a consistent area for an entire shift. Must be able to work in various indoor temperatures including elevated heat and humidity. Exposure to elevated noise levels which occur below OSHA thresholds. Infrequent exposure to machine sanitation solutions and detergents. Requires frequent visual quality control observations which may include turning and bending of the neck and head area. Exposure to various odors throughout a work shift. Required to wear Personal Protective Equipment [PPE] Required to follow Good Manufacturing Practices [GMPs] Exposure to food allergens such as, but not limited to, milk, eggs, tree nuts, wheat, and soybeans will occur. Conduct, Quality, Integrity, and Culture Conduct: We will conduct every aspect of our business with honesty, integrity, and openness, respecting human rights and the interests of our employees, customers, and third parties. Quality: Shank's is committed to food safety and product quality. We employ extensive food safety programs and controls at all levels. Our quality standards and food safety procedures are thoroughly being evaluated internally and externally. We continuously strive to improve our performance. Integrity: Shank's and its employees will not offer, give, seek or receive, either directly or indirectly, improper inducements for business or financial gain. Where information is confidential, that confidentiality must be protected. Culture: Shank's respects the cultural values of our employees, contractors, and customers. We also promote a balanced work-life environment. We recognize and celebrate our employees for their hard work and the contributions they make to our company. Shanks Core Values: ASPIRATION: Share a vision for achievement ACCOUNTABILITY: Support company reputation ADAPTABILITY: Evolve to meet business needs ***Competitive compensation and benefits package*** Shank's Extracts, LLC d/b/a Universal Ingredients - Shank's is an Equal Employment Opportunity/Affirmative Action (EEO/AA) Employer.

FLSA Status: Exempt Grade Level: S-8 Department: Innovation Group Reports To: Innovation Group Leader or Director of Innovation Direct Reports: Product Development Chemist, Innovation Group Technician Job Summary: Works with customers and AR teams to identify unmet needs, collect design input and develop new product design strategies. Technical and laboratory lead in developing new polymers, robust products, and basic production processes that can be successfully commercialized. Essential Functions: Conducts required laboratory work; including polymerization, formulation, coating and testing Develops new products that lead to sustainable commercial revenue Functions as a technical lead on product development teams Develops design strategies based on robust design input Meets technical commitments in order to complete project progression dates and milestones Contributes to product scale up and development through reproducibility and validation testing support Detailed knowledge of required chemical and physical test methods May supervise and teach other laboratory staff Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums Interfaces with customers on new product applications Interfaces with associates from other departments as needed (e.g. cross-functional teams) Documents lab work in electronic notebook and project reports Performs all duties consistent with established AR guidelines, ISO-9001, and elements of GMP deemed necessary to support the business (as outlined in the Quality Manual) Actively complies with and endorses Department and Company objectives Additional Responsibilities: Performs other duties and responsibilities as assigned. Job Specifications: BS, MS, or PhD in chemistry, polymer science or materials science; adhesive polymerization, formulation, and coating experience preferred Ability to perform duties with minimal or no supervision Ability to manage multiple priorities Requires an demonstrated ability to use sensitive test equipment Ability to employ statistical analysis techniques Ability to manage and supervise laboratory staff Ability to maintain confidentiality of AR information Must communicate fluently in English Excellent oral & written communication skills Excellent interpersonal skills Knowledge of computers & related word processing, spreadsheet & e-mail software-Microsoft preferred

Full-time Description Are you ready to catapult your lab career into supporting environmental sustainability? We are seeking an experienced Laboratory Analyst II to join our Inorganics team in Reading, PA. In this role, you'll perform analytical testing and sample processing that deliver the accurate, defensible data our clients depend on for environmental compliance and decision-making. You'll operate advanced instrumentation, interpret results, and ensure quality standards are met while expanding your technical expertise across diverse analytical methods. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! **Please note - This position follows a Monday - Friday schedule of 6 AM to 2:30 PM, with rotating weekend and holiday coverage required.** Why You'll Love This Role Perform advanced sample preparation and analysis across specialized areas; Work with state-of-the-art instrumentation, technology, and Laboratory Information Management Systems (LIMS); Lead by example in quality, accuracy, and turnaround times that drive client trust and environmental compliance; Contribute to audits, SOP development, and process improvements that strengthen laboratory operations. What You'll Do Perform sample preparation, analysis, and quality control testing in accordance with Standard Operating Procedures (SOPs), approved methods, and regulatory standards; Accurately document all work and enter results into the Laboratory Information Management System (LIMS); Review and interpret data for accuracy, consistency, and reasonableness; escalate discrepancies or unusual findings; Perform analytical calculations and prepare reports as required; Maintain and troubleshoot laboratory instrumentation and equipment; perform routine calibrations and preventative maintenance; Support quality assurance and continuous improvement initiatives, including audits, corrective actions, and SOP revisions; Provide cross-training support and collaborate effectively with team members and management to meet deadlines and workload demands; Provide client-facing support, including phones and assist walk-in clients with sample intake as required depending on work location; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's Degree in Chemistry, Biology, Environmental Science; 2-3 years of professional hands-on laboratory experience, preferably within environmental testing; Experience with analytical techniques including ion chromatography (IC), flow injection analysis (FIA), segmented flow analysis (SFA), spectrophotometry (Spec), biochemical oxygen demand (BOD), and gravimetric (grav) methods strongly preferred; Demonstrated proficiency with laboratory instrumentation, standardized testing methods, and interpretation of analytical data across multiple techniques; Experience with LIMS and/or other laboratory management software strongly preferred; Proficiency in Microsoft Office (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 10 paid holidays plus a generous time off plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a Monday through Friday schedule of 6 AM to 2:30 PM, with rotating weekend and holiday coverage; Flexibility to work outside of normal hours to support business needs and deadlines. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

Job DescriptionResponsibilities: Ensure garments are being sewn to specifications and adhering to quality guidelines of factory, as per approved technical packages Measure garments on active sewing floor to ensure they are accurate to specifications Ensure correct sewing operations, machine set ups, thread color, label placement and trims are being implemented according to specifications Ensure sewing floor is cleanly so as not to contaminate garments Regularly check stitching and needle quality Identify machines that are in poor working order and initiate repair with in-house mechanic Initiate repairs of incorrectly sewn garments on sewing floor Evaluate bundles for complete and accurate sewing before passing Identify repetitive issues with quality of production, and escalate issues to the Factory Operations Supervisor for corrective action Regularly report Inline QC findings and concerns to Factory Operations Supervisor and Factory leadership team Be accountable to maintain quality standards of the factory and the company, ensuring garments are accurate to specifications before passing to the next phase of production Voluntary overtime as needed Work in a safety sensitive environment Must have 5+ years experience working in a quality control position for apparel manufacturing, cut & sew knits experience preferred Reports to: Factory Operations Supervisor Job Knowledge, Skills and Abilities: Adaptability: Ability to adapt to changes in the work environment, manage competing demands. Must be able to perform job functions with limited supervision. Organization skills: 5s standards; 1) Sort 2) Set In Order 3) Shine 4) Standardize 5) Sustain Dependability: Ability to follow instructions, respond to management direction. Ability to maintain confidentiality. Language: Ability to read and interpret documents such as safety rules, operating and maintenance instruction, and procedures manuals in English or Spanish. Demonstrated ability to communicate orally and in written form effectively with other employees. Mathematical: Ability to do simple math, such as add, subtract, multiply, and divide. Planning and Organizing: Ability to prioritize and plan work activities and use time efficiently. Problem Solving: Ability to solve practical problems and interpret and resolve problem issues using a variety of instructions or guides furnished in written, oral, diagram, or schedule form. Physical Demands: Working by standing, reaching, bending. occasional lifting (max. 50lbs) and walking Founded in 2013 by Sasha Koehn and Erik Allen Ford, Buck Mason makes simplified clothing for the modern man. At the heart of everything we do is the unclouded California ethos of quality, restraint, and integrity. We take iconic pieces and reconstruct them in hard-wearing fabrics, with timeless details, and the perfect fit. Our goal is to offer fashion that is less complicated, building pared-down essentials that live beyond a single season. With its corporate offices headquartered in Los Angeles, Buck Mason's retail footprint extends from sea to sea, through e-commerce and brick-and-mortar locations in Los Angeles, San Francisco, New York, Brooklyn, and more. Join us at Buck Mason, where style meets substance, and every team member plays a vital role in our success. Ready to make your mark? Apply now! We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.