Chemist Jobs in Charlotte, NC

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules - both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries. POSITION SUMMARY: This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP's and responsible that personnel are appropriately trained. OVERALL JOB RESPONSIBILITIES: Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project. Provide feedback to management with laboratory standard hours for financial prudence in resource planning, allocation and manpower to ensure within approved budgets while building best in class quality processes and systems at site. Execute and maintain quality system controls to ensure no critical and major market complaints. Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable). Ensuring compliance to systems and procedures throughout product lifecycle. Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS. Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits. Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products. Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab. Apply CAPA for Lab failures in OOS. Prepare in timely fashion updating and revision of SOP, specification, STP and any other documents Assist in timely completion of Tech Transfer of Finished products. Ensure training of QC staff Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc. Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control. Education : B.Sc. in Chemistry with concentration in Biochemistry Experience: • 1-3 years in the field of Pharmaceutical (manufacturing facility). • Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in R&D. Extensive knowledge in general laboratory equipment including but not limited to: HPLC, UV-Vis and FTIR. Knowledge and Skills : Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system. Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices. Technical writing skills to generate SOPs and serve as the Subject Matter Expert. Began training under Six Sigma and Project Management. Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer. Other requirements (licenses, certifications, specialized training) Will be an added advantage if the individual has dealt with multiple audits personally.

Rockwell, NC Responsibilities Perform the receipt and logging of incoming pharmaceutical ingredients Perform the sampling of incoming pharmaceutical ingredients for internal laboratory testing and shipment to external contract laboratories for testing Perform internal laboratory testing (e.g., organoleptic tests, identification (FTIR), pH, viscosity, specific gravity, chemical assays (HPLC), etc.) on incoming pharmaceutical ingredients, in-process samples, finished products and stability samples Calculate adjustments for in-process bulk product Prepare and review internal laboratory testing and external contract testing laboratory reports for raw materials, in-process samples, finished products and stability samples Prepare and review Certificates of Analysis Notify manager immediately of non-conforming data or unexpected occurrences Conducts laboratory investigations under the supervision of the laboratory supervisor Prepare and/or review test procedures, SOPs and protocols as assigned. Prepare and review IQ/OQ/PQ Protocols for production and laboratory equipment Perform IQ/OQ/PQ testing on production and laboratory equipment Complies with all regulatory/in-house requirements which may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP documentation Requirements Combination of advanced degree (such as Bachelors in Chemistry or related science) and 3+ years of experience in high volume manufacturing preferred; extensive years of experience in lieu of advanced degree is acceptable Previous experience within a cGMP compliant facility, Quality Control and USP Standards preferred Ability to perform physical sampling/testing and instrumental chemical analysis in the chemical laboratory (e.g., chromatography, infra-red spectroscopy, titrations, etc.) Excellent analytical and problem-solving skills Excellent time management and organizational skills Ability to work effectively in a fast-paced, rapidly changing environment Excellent people skills, with demonstrated ability to communicate effectively across functional groups Proficiency with Microsoft (MS) Office

Proficient at performing standard laboratory and applications testing. Ability to make detailed observations of lab tests and to accurately record the data and observations in a laboratory notebook and in spreadsheets. Ability to manage laboratory workflow for multiple, concurrent development and applications projects. Communicate results, observations, and work progress to supervisor. Interact with customers by effectively communicating project updates and presenting project results. Build experience to give technical presentations, visit customer sites, and attend trade shows. Work with supervisor, commercial leaders, and sales to understand market needs and develop new products as required. Work with low to moderately hazardous chemicals using appropriate safety procedures and practices. REQUIREMENTS / QUALIFICATIONS: Minimum bachelor's degree in chemistry or related field and 5+ years relevant experience working as a chemist in an R&D environment or related applications area. Experience working in food science is desirable but not required. Strong data observation and interpretation skills. Computer skills and math aptitude. Ability to work independently with minimal supervision and collaboratively in a team environment. Good analytical and problem-solving skills. Attention to detail and accuracy, with ability to compare data, detect inconsistencies, and determine actions for resolution. Strong verbal, written, and interpersonal communication skills with the ability to interact effectively and positively with supervisor, peers, and across functions. Excellent organizational and time management skills with ability to prioritize multiple work deadlines. PHYSICAL DEMANDS: Ability to work an eight (8) hour shift in a lab environment. Must have the ability to stand for long periods of time at a bench performing tasks. Must be able to lift objects that are less than or equal to 30 lbs. Will be required to use computer daily to effectively complete job functions for entire shift. Work Environment: Lab environment FLSA Status: Salary/Exempt Travel Potential: 0-5%

, INC Idexcel is a global staffing and IT services organization, with a mission to bring great people and great organizations together. Our diverse client base represents a wide range of industries, including technology, telecom, insurance, healthcare, manufacturing, banking & financial services, food & commodities trading and federal organizations. Our teams of experienced recruiters directly work with client companies seeking exceptional people to help with their business initiatives. Idexcel, Inc. is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, disability, military status, national origin or any other characteristic protected under federal, state, or applicable local law. Job Description Job Title: Senior Digital Analytics Duration: 1+ Year contract Location : Charlotte, NC Looking for an experienced Analytics Implementation Analyst with hands on implementation experience is Ensighten Tag Management System. The candidate should be not only be a strong front-end programmer with excellent JavaScript knowledge, he/she should be able to engage with clients internal and external at the technical, business and strategic levels to generate quantifiable value for internal stakeholder initiatives. Responsibilities: •Consult with stakeholders on projects requiring web analytics implementation of Adobe Marketing Cloud tags among others, implementation, platform and process remediation, and reporting and dashboard development. •Support the above analytics needs of stakeholders including but not limited to assistance with the implementation of A/B and multivariate testing tools deployed with the help of Ensighten TMS. •Evaluate business goals and objectives from multiple business teams and develop tracking/tagging strategies to allow individuals and teams to measure success •Assist with implementation of third party pixels for marketing campaigns •Conduct platform training and knowledge sharing in web analytics for stakeholders and the project team •Leverage various platform API's to develop custom dashboards and other applications that provide increased value and ROI Minimum Requirements: •Bachelors degree •Minimum 5 years' experience with web development •Minimum 2 years professional experience implementing web analytics tools such as Adobe Analytics •Strong understanding of HTML and web protocols •Advanced JavaScript skills •Minimum two years' experience with Ensighten Tag Management Solution •Comfortable presenting findings and providing training on analytics tool usage •Strong English communication skills (written and verbal) Preferred: •Experience with iOS and Android app development •Experience using Google or Adobe API's to insert and extract data •Experience with SQL-based queries (PHP, MySQL or other), flat-file handling through programmatic code, and ETL tools •Team leadership / management experience Qualifications Bachelors degree Additional Information All your information will be kept confidential according to EEO guidelines.

The Analytical Chemist is responsible for working in a laboratory environment and performing routine and nonroutine analysis on specialized analytical equipment to identify and solve root cause product concerns as well as qualify raw materials. Through research and analysis using chromatography, spectroscopy, microscopy, rheology, and other analytical techniques, the Analytical Chemist will investigate and troubleshoot issues to support manufacturing. This role will also provide support to EHS SAP data entry and Regulatory requests. Essential Job Functions & Responsibilities: - Support and promote a culture of safety first by personal demonstration of appropriate safety behaviors and actively caring about others. - Support investigation of customer complaints and manufacturing nonconformities, raw materials qualifications, research projects, and unknown sample identification by performing instrumental analyses - Set-up laboratory procedures, equipment, and instrumentation required for tests, research, or process control. - Use statistical tools to evaluate both the test methods as well as the validity of results. - Ensure equipment calibration and maintenance. - Prepares chemical solutions for use in analysis (e.g. solvent extraction) - Analyze, document, and report results. - Provide assistance to laboratory personnel as required. - Provide support to EHS SAP data entry. - Provide support to Regulatory requests. Skills Analytical chemistry, Chemistry, Laboratory, Method validation, Chemical, Gas chromatography Top Skills Details Analytical chemistry Additional Skills & Qualifications Bachelor's degree required, preferably in a chemistry related field. - Master's degree in chemistry, organic chemistry or analytics desirable. - Experience with chromatography, spectroscopy, microscopy, rheology, and other analytical techniques. - Excellent oral, written, and presentation communication skills including the ability to read and properly interpret information, follow safety procedures, and present to large and small groups. - Ability to work with mathematical concepts such as probability and statistical inference. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. - Ability to solve practical 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. - Above-average proficiency in Microsoft Excel - SAP experience preferred. - Demonstrated ability to be very detail oriented and accurate in both written and verbal communications. Pay and Benefits The pay range for this position is $28.00 - $34.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Charlotte,NC. Application Deadline This position is anticipated to close on Apr 7, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

ProSidian is a Management and Operations Consulting Firm focusing on providing value to clients through tailored solutions based on industry-leading practices. We help forward-thinking clients solve problems and improve operations. With a reputation for its strong CONUS/OCONUS practice spanning six solution areas, ProSidian services focus on the broad spectrum of Risk Management, Compliance, Business Process, IT Effectiveness, Energy & Sustainability, and Human Capital. Launched by former Big 4 Management Consultants; our multidisciplinary teams bring together the talents of nearly 190 professionals globally to complete a wide variety of engagements for Private Companies, Fortune 1,000 Enterprises, and Government Agencies of all sizes. Our Services are deployed across the enterprise, target drivers of economic profit (growth, margin, and efficiency), and are aligned at the intersections of assets, processes, policies, and people delivering value. ProSidian clients represent a broad spectrum of industries to include but are not limited to Energy, Manufacturing, Chemical, Retail, Healthcare, Telecommunications, Hospitality, Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government Agencies. Learn More About ProSidian Consulting at ****************** Job Description ProSidian Seeks a Quality Control Analyst (Contract Contingent) in Charlotte, NC / Remote to support an engagement for agency of the United States government responsible for consumer protection in the financial sector. The ProSidian Engagement Team Members work to develop and implement a strategy and initiatives to educate, empower, and equip consumers to make better informed financial decisions. Quality Control Analyst Candidates shall work to support requirements for PR0001 Program Support and will review and analyze the curriculum and substance of in-person, Webinar, and small group financial literacy training sessions in order to ensure the best financial education for each participant. The Quality Control Analyst will also analyze the Government's furnished tools, toolkits, and materials in order to determine what needs to be kept, modified, or changed to be most effective to participants. The Quality Control Analyst will ensure that all channels of communication are working, the training sessions run as smoothly and efficiently as possible, and necessary information for the purposes of monthly written reports is gathered, documented, and stored appropriately. Additionally, the Quality Control Analyst will assist and monitor the Curriculum Developer in collecting data via surveys and focus groups to assess the effectiveness of training sessions and implementation methods and provide a detailed monthly report about the data collected. The Quality Control Analyst is responsible for ensuring the curriculum and substantive material be the most effective and accessible tools possible for all training participants. The Quality Control Analyst will be responsible for reviewing and monitoring the curriculum, tools, materials, and handouts to ensure the best source of information and training available to participants during each training session is provided. The Quality Control Analyst will also be responsible for reviewing all tools and materials to ensure all are complaint with Section 504 and Section 508 accomodations, when necessary. Additionally, the Quality Control Analyst will be responsible for administering surveys and focus groups of participants to evaluate the effectiveness of the training sessions and implemented tools used during each session, and subsequently compile the findings into written monthly reports and analyses. Qualifications The Quality Control Analyst shall have consecutive employment in a position with comparable responsibilities within the past three (3) years, Must be able to use a computer to communicate via email; and proficient in Microsoft Office Products (Word/Excel/Power point) and related tools and technology required for the position. Work products shall be thorough, accurate, appropriately documented, and comply with established criteria. The candidate shall ensure that duties are performed in a competent and professional manner that meets milestones/delivery schedules as outlined. To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required: GS-8 Equivalent: Bachelor's degree or equivalent from an accredited college or university in a relevant field with at least 3 years of experience with demonstrated understanding of program management, facilitation, industrial development, data collection and analysis, and organization of large conferences or training sessions. Bachelor's degree required; Masters degree preferred in a relevant field or related subject. At least 3 years of experience providing communication, quality control, and knowledge management expertise. Experience in management of custom survey projects. Experience in data collection, analysis, and written reports summarizing data collected. Ability to coordinate multiple projects simultaneously, work well under pressure and meet deadlines. Ability to work effectively both individually and as a member of a team. Candidate must have strong attention to detail and organizational skills. Demonstrated ability to propose possible resolutions to complex managerial or operational problems. Demonstrated expertise in knowledge management. Demonstrated proactivity, attention to detail, working within deadlines, and ability to juggle multiple priorities in a fast-paced environment. Excellent interpersonal skills, English verbal, written, editing, research, and verbal communication skills. Excellent project management and organizational skills. Familiarity with Section 504 and 508 disability requirements and accommodations. Proficiency in MS Office Applications (Word, PowerPoint, Outlook, Excel) Work products shall be thorough, accurate, appropriately documented, and comply with established criteria. The candidate shall ensure that duties are performed in a competent and professional manner that meets milestones/delivery schedules as outlined. TRAVEL: Travel as coordinated with the technical point of contact and approved in writing by the Contracting Officer in advance, is allowed, in accordance with Federal Travel Regulations. LOCATION: Work shall be conducted at the Charlotte, NC / Remote U.S. Citizenship Required Excellent oral and written communication skills Bilingual candidates preferred Proficient with Microsoft Office Products (Microsoft Word, Excel, PowerPoint, Publisher, & Adobe) Advanced Data Analytics (Time series regressions, knowledge of how to apply appropriate statistical models to each job task) Additional Information As a condition of employment, all employees are required to fulfill all requirements of the roles for which they are employed; establish, manage, pursue, and fulfill annual goals and objectives with at least three (3) Goals for each of the firms Eight Prosidian Global Competencies [1 - Personal Effectiveness | 2 - Continuous Learning | 3 - Leadership | 4 - Client Service | 5 - Business Management | 6 - Business Development | 7 - Technical Expertise | 8 - Innovation & Knowledge Sharing (Thought Leadership)]; and to support all business development and other efforts on behalf of ProSidian Consulting. CORE COMPETENCIES Teamwork - ability to foster teamwork collaboratively as a participant, and effectively as a team leader Leadership - ability to guide and lead colleagues on projects and initiatives Business Acumen - understanding and insight into how organizations perform, including business processes, data, systems, and people Communication - ability to effectively communicate to stakeholders of all levels orally and in writing Motivation - persistent in pursuit of quality and optimal client and company solutions Agility - ability to quickly understand and transition between different projects, concepts, initiatives, or work streams Judgment - exercises prudence and insight in decision-making process while mindful of other stakeholders and long-term ramifications Organization - ability to manage projects and activity, and prioritize tasks ------------ ------------ ------------ OTHER REQUIREMENTS Business Tools - understanding and proficiency with business tools and technology, including Microsoft Office. The ideal candidate is advanced with Excel, Access, Outlook, PowerPoint and Word, and proficient with Adobe Acrobat, data analytic tools, and Visio with the ability to quickly learn other tools as necessary. Business Tools - understanding and proficiency with business tools and technology, including Microsoft Office. The ideal candidate is advanced with Excel, Access, Outlook, PowerPoint and Word, and proficient with Adobe Acrobat, data analytic tools, and Visio with the ability to quickly learn other tools as necessary. Commitment - to work with smart, interesting people with diverse backgrounds to solve the biggest challenges across private, public and social sectors Curiosity - the ideal candidate exhibits an inquisitive nature and the ability to question the status quo among a community of people they enjoy and teams that work well together Humility - exhibits grace in success and failure while doing meaningful work where skills have impact and make a difference Willingness - to constantly learn, share, and grow and to view the world as their classroom ------------ ------------ ------------ BENEFITS AND HIGHLIGHTS ProSidian Employee Benefits and Highlights: Your good health and well-being are important to ProSidian Consulting. At ProSidian, we invest in our employees to help them stay healthy and achieve work-life balance. That's why we are also pleased to offer the Employee Benefits Program, designed to promote your health and personal welfare. Our growing list of benefits currently include the following for Full Time Employees: Competitive Compensation: Pay range begins in the competitive ranges with Group Health Benefits, Pre-tax Employee Benefits, and Performance Incentives. For medical and dental benefits, the Company contributes a fixed dollar amount each month towards the plan you elect. Contributions are deducted on a Pre-tax basis. Group Medical Health Insurance Benefits: ProSidian partners with BC/BS, to offer a range of medical plans, including high-deductible health plans or PPOs. ||| Group Dental Health Insurance Benefits: ProSidian dental carriers - Delta, Aetna, Guardian, and MetLife. Group Vision Health Insurance Benefits: ProSidian offers high/low vision plans through 2 carriers: Aetna and VSP. 401(k) Retirement Savings Plan: 401(k) Retirement Savings Plans help you save for your retirement for eligible employees. A range of investment options are available with a personal financial planner to assist you. The Plan is a pre-tax Safe Harbor 401(k) Retirement Savings Plan with a company match. Vacation and Paid Time-Off (PTO) Benefits: Eligible employees use PTO for vacation, a doctor's appointment, or any number of events in your life. Currently these benefits include Vacation/Sick days - 2 weeks/3 days | Holidays - 10 ProSidian and Government Days are given. Pre-Tax Payment Programs: Pre-Tax Payment Programs currently exist in the form of a Premium Only Plan (POP). These Plans offer a full Flexible Spending Account (FSA) Plan and a tax benefit for eligible employees. Purchasing Discounts & Savings Plans: We want you to achieve financial success. We offer a Purchasing Discounts & Savings Plan through The Corporate Perks Benefit Program. This provides special discounts for eligible employees on products and services you buy on a daily basis. Security Clearance: Due to the nature of our consulting engagements there are Security Clearance requirements for Engagement Teams handling sensitive Engagements in the Federal Marketplace. A Security Clearance is a valued asset in your professional portfolio and adds to your credentials. ProSidian Employee & Contractor Referral Bonus Program: ProSidian Consulting will pay up to 5k for all referrals employed for 90 days for candidates submitted through our Referral Program. Performance Incentives: Due to the nature of our consulting engagements there are performance incentives associated with each new client that each employee works to pursue and support. Flexible Spending Account: FSAs help you pay for eligible out-of-pocket health care and dependent day care expenses on a pre-tax basis. You determine your projected expenses for the Plan Year and then elect to set aside a portion of each paycheck into your FSA. Supplemental Life/Accidental Death and Dismemberment Insurance: If you want extra protection for yourself and your eligible dependents, you have the option to elect supplemental life insurance. D&D covers death or dismemberment from an accident only. Short- and Long-Term Disability Insurance: Disability insurance plans are designed to provide income protection while you recover from a disability. ----------- ------------ ------------ ADDITIONAL INFORMATION - See Below Instructions On The Best Way To Apply ProSidian Consulting is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, or Vietnam era, or other eligible veteran status, or any other protected factor. All your information will be kept confidential according to EEO guidelines. ProSidian Consulting has made a pledge to the Hiring Our Heroes Program of the U.S. Chamber of Commerce Foundation and the “I Hire Military” Initiative of The North Carolina Military Business Center (NCMBC) for the State of North Carolina. All applicants are encouraged to apply regardless of Veteran Status. Furthermore, we believe in "HONOR ABOVE ALL" - be successful while doing things the right way. The pride comes out of the challenge; the reward is excellence in the work. FOR EASY APPLICATION USE OUR CAREER SITE LOCATED ON ************************* OR SEND YOUR RESUME'S, BIOS, AND SALARY EXPECTATION / RATES TO ***********************. ONLY CANDIDATES WITH REQUIRED CRITERIA ARE CONSIDERED. Be sure to place the job reference code in the subject line of your email. Be sure to include your name, address, telephone number, total compensation package, employment history, and educational credentials.

Monroe NC Contract - 1st Shift, 5/40 Pay Rate: $27.50/Hr. Benefits: medical, dental, vision, 401k Requirements: Metallurgical Lab Analyst U.S. Person Requires an AA/AS degree and minimum 2 years of prior relevant experience or a University Degree in a related field or in absence of a degree, 4 years of relevant experience 2+ years of experience in quality or inspection work with a focus on metallurgical laboratory environment 2+ years of experience with Microsoft Office applications Ability to lift up to 30 pounds and stand for extended periods of time. Must be able to operate precision equipment – manual dexterity is required for machine setup and adjustment of samples Job Summary: Metallurgical Lab Analyst Our client is seeking an onsite Metallurgical Lab Analyst for its Monroe, NC Additive Manufacturing facility. The role involves conducting comprehensive material testing, with a focus on metallurgical analysis of Additively Manufactured components, powder sample evaluation, and both destructive and non-destructive testing methods. The analyst will manage the day-to-day operations of lab tests, maintenance of equipment, ensure adherence to quality standards and reporting protocols, and validate material properties to meet engineering specifications. Duties: Metallurgical Lab Analyst Prepare metallurgical specimens with cutting, mounting, polishing, and etching equipment Perform microscopy and metallurgical analysis on samples to assess thickness, density, microstructure, and surface roughness Destructively test specimens to determine mechanical properties such as hardness, tensile strength, and fatigue strength Prepare and test metal powder samples for chemical composition and physical size, shape, and size distribution Collaborate within a cross-functional team between material science, quality, engineering, and planning to support and execute needed tests and documentation Operate and maintain all metallurgical lab equipment and support equipment through development of preventative maintenance program Coordinate with equipment manufacturers for troubleshooting, maintenance, and calibration of metallurgical lab equipment Track and maintain the procurement, receipt, and inventory levels of all consumables required to operate equipment and perform tests Track and maintain all waste streams generated by metallurgical lab processes to remain compliant with company, regulatory, and government waste handling requirements Follow and maintain all equipment work instructions, test procedures, and standard work within the site's Quality Management System (QMS) with guidance from material science, quality, and engineering functions Crosstrain in other operations and quality functions within facility to support other roles and departments as needed such as dimensional inspection, powder handling, equipment operation, etc. Support and promote compliance to all quality requirements within the QMS and industry regulations, such as AS9100, as pertaining to the role Coordinate with engineering, quality, and digital technology teams to establish automated and connected data management systems for collecting, analyzing, and reporting test data Interface with and execute instructions within PLM, ERP, & MES systems (Teamcenter, SAP, and Solumina) for production execution, inventory tracking, and scheduling Must be willing and able to attend occasional Zoom meeting before or after hours to facilitate global collaboration Preferred Skills: Metallurgical Lab Analyst Metal Additive Manufacturing process understanding; hands-on AM experience Experience with image and/or data documentation and reporting Metal powder handling and testing experience Ability to understand and write standard work, policies, and procedures pertaining to laboratory test methods and techniques 74165 EEO Statement Apollo Professional Solutions, Inc. is an equal opportunity employer. We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, marital status, age, national origin, ancestry, disability status, medical condition, pregnancy, genetic information, protected veteran status, gender, sexual orientation, gender identity or expression, or any other status or characteristic protected under federal, state, or local law.

Pay Range: $22-27.50 Our client's Additive Design and Manufacturing (ADaM) team is seeking an onsite Metallurgical Lab Analyst for its Monroe, NC Additive Manufacturing facility. The role involves conducting comprehensive material testing, with a focus on metallurgical analysis of Additively Manufactured components, powder sample evaluation, and both destructive and non-destructive testing methods. The analyst will manage the day-to-day operations of lab tests, maintenance of equipment, ensure adherence to quality standards and reporting protocols, and validate material properties to meet engineering specifications. What You Will Do: * Prepare metallurgical specimens with cutting, mounting, polishing, and etching equipment * Perform microscopy and metallurgical analysis on samples to assess thickness, density, microstructure, and surface roughness * Destructively test specimens to determine mechanical properties such as hardness, tensile strength, and fatigue strength * Prepare and test metal powder samples for chemical composition and physical size, shape, and size distribution * Collaborate within a cross-functional team between material science, quality, engineering, and planning to support and execute needed tests and documentation * Operate and maintain all metallurgical lab equipment and support equipment through development of preventative maintenance program * Coordinate with equipment manufacturers for troubleshooting, maintenance, and calibration of metallurgical lab equipment * Track and maintain the procurement, receipt, and inventory levels of all consumables required to operate equipment and perform tests * Track and maintain all waste streams generated by metallurgical lab processes to remain compliant with company, regulatory, and government waste handling requirements * Follow and maintain all equipment work instructions, test procedures, and standard work within the site's Quality Management System (QMS) with guidance from material science, quality, and engineering functions * Cross-train in other operations and quality functions within facility to support other roles and departments as needed such as dimensional inspection, powder handling, equipment operation, etc. * Support and promote compliance to all quality requirements within the QMS and industry regulations, such as AS9100, as pertaining to the role * Coordinate with engineering, quality, and digital technology teams to establish automated and connected data management systems for collecting, analyzing, and reporting test data * Interface with and execute instructions within PLM, ERP, & MES systems (Teamcenter, SAP, and Solumina) for production execution, inventory tracking, and scheduling * Must be willing and able to attend occasional Zoom meeting before or after hours to facilitate global collaboration Qualifications You Must Have: * Typically requires an AA/AS degree and minimum 2 years of prior relevant experience or a University Degree in a related field or in absence of a degree, 4 years of relevant experience * U.S. Person (U.S. citizen, permanent resident, refugee or asylee) or eligible to obtain necessary export authorizations required * 2+ years experience in quality or inspection work with a focus on metallurgical laboratory environment * 2+ years experience with Microsoft Office applications * Ability to lift up to 30 pounds and stand for extended periods of time. * Must be able to operate precision equipment - manual dexterity is required for machine setup and adjustment of samples Qualifications We Prefer: * Metal Additive Manufacturing process understanding; hands-on AM experience * Experience with image and/or data documentation and reporting * Metal powder handling and testing experience * Ability to understand and write standard work, policies, and procedures pertaining to laboratory test methods and techniques Benefits provided: 401K, medical, dental, and vision, sick time as applicable to state law Butler America Aerospace, LLC. is proud to provide an equal opportunity workplace and be an affirmative action employer. Consider Butler because we are committed to hiring and retaining a diverse workforce. We recognize that we thrive on diversity and inclusion for the benefit of our employees, our customers, and the communities where we are located. Employment decisions are made without regard to race, color, religion, gender, national origin, ethnicity, veteran status, disability status, age, sexual orientation, gender identity, gender expression, marital status, mental or physical disability or any other legally protected status.

**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** TE Connectivity's Quality Test Lab Supervisor will manage the quality technician team (on site), driving product and production systems to comply with TE specified requirements per customer and contractual agreements. Focusing on production testing for qualified product supporting conformance to customer and regulatory requirements. The Quality Lab Supervisor will be required to manage ADP Workforce Manager for timecards, SAP input, test scheduling, retention test requirements, and will be required to be a certified IPC-J-STD trainer for the plant. **Job Responsibilities** The responsibility of the Quality Lab Supervisor will be to provide leadership for our Quality Technician team and guide the implementation of continuous improvement to meet required quality objectives. + Create, update, and provide training to quality technician team for all test related functions. + Coordinating lab activities among technicians ensuring standard and efficient processes are followed. + Supervisory responsibilities include interviewing; hiring; training; scheduling; monitoring work; providing communication, feedback and ongoing support; performance reviews; career development; discipline; addressing complaints and resolving issues in accordance with applicable laws and/or company policy; timekeeping; and monitors and ensures a positive work environment for employees. + Directs lab activities in accordance with production schedules and established priorities, ensuring maximum utilization of assigned resources, machines, personnel, and materials. + Oversees lab operations for an assigned shift using documented planning methods which allow for reaction to unforeseen changes in demand or capacity. + Follows engineering specifications for process and test parameters + Assists lab technicians in the interpretation of procedures, methods and correct use of test equipment to ensure procedures are followed. + Maintains a working knowledge of lab equipment and the associated customer or regulatory test requirements. + Manage and direct quality technician's process and schedule. + Support Overtime requirements as specified, be open to flexibility in completing assigned tasks. + Manage and implement cross functional training to the quality technician team. + Manage quality technicians' timecards through ADP Workforce Manager + Participates in team driven activities to facilitate test lab improvements or new program development projects. + Understands and supports quality policies and implements guidelines to assure adherence to quality documents and standards. + Promote and Drive "Zero Defect" mentality within the quality Organization with proactive tools such as Lean, Six-Sigma, Poka-Yoke (Error Proofing), Measurement System Analysis, Advance Product and Quality Planning (APQP) Statistical Process control (SPC) and Process Failure Mode and Effects Analysis (PFMEA) + Become a certified IPC-J-STD trainer for the facility + Understands, supports, and implements company policies. + Works with cross-functional teams to ensure safe and quality testing. + Support and complete other requests per Manager **This is a 1st shift position.** **What your background should look like:** + Bachelor's degree in a related field is preferred + 7+ years of experience in Quality; with three or more years in a supervision role + Competent with Microsoft Office applications + General understanding of Statistical Process Control + Ability to read and interpret prints and customer requirements + Proficient with standard dimensional gages-caliper, micrometer, drop Indicator, comparator + Proficient with vision Systems, Digital Optical Comparator, and other advanced measurement test equipment + Highly Proficient with QPL test equipment and processes (vibration table, mechanical life, solderability, etc.) + Familiar with problem solving tools-RCA, 8D report, fishbone diagram, 5 whys, etc. + Proven an effective member of a problem-solving team + Proven in leadership of a team + Self-Starter, driven to implement change and improvements for the vision of the company + Excellent written and verbal communication skills **Competencies** Managing and Measuring Work Motivating Others Building Effective Teams Values: Integrity, Accountability, Inclusion, Innovation, Teamwork SET : Strategy, Execution, Talent (for managers) **ABOUT TE CONNECTIVITY** TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, renewable energy, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 8,000 engineers, working alongside customers in approximately 140 countries. TE ensures that EVERY CONNECTION COUNTS. Learn more at ********** and on LinkedIn (************************************************** ,Facebook (***************************************** ,WeChat, (http://**********.cn/chn-zh/policies-agreements/wechat.html) Instagram andX (formerly Twitter). (*********************************** **COMPENSATION** - Competitive base salary commensurate with experience: $90,600 - $136,000 (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** Location: FAIRVIEW, NC, US, 28730 City: FAIRVIEW State: NC Country/Region: US Travel: Less than 10% Requisition ID: 132544 Alternative Locations: Function: 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.

Job Details Rock Hill, SC Plant - Rock Hill, SC Full Time 3rd ShiftDescription We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities Follow project instructions from manager or supervisor Follow all health and safety regulations when operating machinery Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn Complete all assigned tasks in a timely and efficient manner Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools Clean and clear debris and hazardous materials Ensure equipment and tools are cleaned and stored properly Verify lumber dimensions and counts Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications Must be 18 years of age Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds Ability to work outside in all weather Positive attitude and work ethic Basic Mechanical Functions Able to work independently or as an active member of a team Excellent interpersonal skills and communication with all levels of management Confined Space Entry training is a plus but not required Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities * Follow project instructions from manager or supervisor * Follow all health and safety regulations when operating machinery * Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn * Complete all assigned tasks in a timely and efficient manner * Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools * Clean and clear debris and hazardous materials * Ensure equipment and tools are cleaned and stored properly * Verify lumber dimensions and counts * Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications * Must be 18 years of age * Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds * Ability to work outside in all weather * Positive attitude and work ethic * Basic Mechanical Functions * Able to work independently or as an active member of a team * Excellent interpersonal skills and communication with all levels of management * Confined Space Entry training is a plus but not required * Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules - both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. POSITION SUMMARY: This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP's and responsible that personnel are appropriately trained. As a member of Site Investigation Team (SIT) needs to investigate quality events and perform Root Cause Analysis (RCA). OVERALL JOB RESPONSIBILITIES: Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project. Execute and maintain quality system controls to ensure no critical and major market complaints. Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable). Ensuring compliance to systems and procedures throughout product lifecycle. Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS. Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits. Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products. Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab. Apply CAPA for Lab failures in OOS. Complete and maintain certified investigator training requirements to ensure SIT representation for identified area(s). Performing the investigation of quality events assigned using root cause analysis tools defined by company procedures, maintain timelines for closure of investigations assigned and to identify and initiate CAPA's. Participate in continuous improvement initiatives for investigations and associated investigation certification process. Work with CIT team as needed for Major and Critical Investigations to align with corporate guidelines. Comply with applicable FDA and international regulatory laws/standards and the Code of Conduct. Maintain knowledge of current regulatory requirements and standards as they pertain to the Stability and Quality Control departments. Represent Glenmark as appropriate in FDA, notified body, internal and other regulatory audits. Work in close collaboration and support with other members of the CMC team responsible for drug product development and support to management, as necessary Domestic and international travel up to 5% may be required to accompany technical staff in the factory acceptance and inspection of laboratory equipment. Ensure training of QC Analyst (Entry level Positions) Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc. Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control. Education : A minimum of a Bachelor's degree in Chemistry / Pharmaceutical Sciences or Equivalent. Experience: • 4+ years in the field of Pharmaceutical (manufacturing facility). • Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in Analytical R&D. Extensive knowledge in general laboratory equipment including but not limited to: GC, HPLC, Polarography, Particulate Matter, UV-Vis and FTIR Knowledge and Skill: Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system. Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices. Technical writing skills to generate SOPs and serve as the Subject Matter Expert. Completed training on Six Sigma, certified Green belt professional. Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer. Will be an added advantage if the individual has dealt with multiple audits personally.

The Analytical Chemist is responsible for working in a laboratory environment and performing routine and nonroutine analysis on specialized analytical equipment to identify and solve root cause product concerns as well as qualify raw materials. Through research and analysis using chromatography, spectroscopy, microscopy, rheology, and other analytical techniques, the Analytical Chemist will investigate and troubleshoot issues to support manufacturing. This role will also provide support to EHS SAP data entry and Regulatory requests. Essential Job Functions & Responsibilities: * Support and promote a culture of safety first by personal demonstration of appropriate safety behaviors and actively caring about others. * Support investigation of customer complaints and manufacturing nonconformities, raw materials qualifications, research projects, and unknown sample identification by performing instrumental analyses * Set-up laboratory procedures, equipment, and instrumentation required for tests, research, or process control. * Use statistical tools to evaluate both the test methods as well as the validity of results. * Ensure equipment calibration and maintenance. * Prepares chemical solutions for use in analysis (e.g. solvent extraction) * Analyze, document, and report results. * Provide assistance to laboratory personnel as required. * Provide support to EHS SAP data entry. * Provide support to Regulatory requests. Skills Analytical chemistry, Chemistry, Laboratory, Method validation, Chemical, Gas chromatography Top Skills Details Analytical chemistry Additional Skills & Qualifications Bachelor's degree required, preferably in a chemistry related field. * Master's degree in chemistry, organic chemistry or analytics desirable. * Experience with chromatography, spectroscopy, microscopy, rheology, and other analytical techniques. * Excellent oral, written, and presentation communication skills including the ability to read and properly interpret information, follow safety procedures, and present to large and small groups. * Ability to work with mathematical concepts such as probability and statistical inference. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. * Ability to solve practical 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. * Above-average proficiency in Microsoft Excel * SAP experience preferred. * Demonstrated ability to be very detail oriented and accurate in both written and verbal communications. Pay and Benefits The pay range for this position is $28.00 - $34.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Charlotte,NC. Application Deadline This position is anticipated to close on Apr 7, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities * Follow project instructions from manager or supervisor * Follow all health and safety regulations when operating machinery * Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn * Complete all assigned tasks in a timely and efficient manner * Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools * Clean and clear debris and hazardous materials * Ensure equipment and tools are cleaned and stored properly * Verify lumber dimensions and counts * Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications * Must be 18 years of age * Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds * Ability to work outside in all weather * Positive attitude and work ethic * Basic Mechanical Functions * Able to work independently or as an active member of a team * Excellent interpersonal skills and communication with all levels of management * Confined Space Entry training is a plus but not required * Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

Job Details Rock Hill, SC Plant - Rock Hill, SC Full Time 2nd ShiftDescription We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities Follow project instructions from manager or supervisor Follow all health and safety regulations when operating machinery Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn Complete all assigned tasks in a timely and efficient manner Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools Clean and clear debris and hazardous materials Ensure equipment and tools are cleaned and stored properly Verify lumber dimensions and counts Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications Must be 18 years of age Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds Ability to work outside in all weather Positive attitude and work ethic Basic Mechanical Functions Able to work independently or as an active member of a team Excellent interpersonal skills and communication with all levels of management Confined Space Entry training is a plus but not required Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. POSITION SUMMARY: This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP s and responsible that personnel are appropriately trained. As a member of Site Investigation Team (SIT) needs to investigate quality events and perform Root Cause Analysis (RCA). OVERALL JOB RESPONSIBILITIES: Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project. Execute and maintain quality system controls to ensure no critical and major market complaints. Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable). Ensuring compliance to systems and procedures throughout product lifecycle. Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS. Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits. Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products. Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab. Apply CAPA for Lab failures in OOS. Complete and maintain certified investigator training requirements to ensure SIT representation for identified area(s). Performing the investigation of quality events assigned using root cause analysis tools defined by company procedures, maintain timelines for closure of investigations assigned and to identify and initiate CAPA s. Participate in continuous improvement initiatives for investigations and associated investigation certification process. Work with CIT team as needed for Major and Critical Investigations to align with corporate guidelines. Comply with applicable FDA and international regulatory laws/standards and the Code of Conduct. Maintain knowledge of current regulatory requirements and standards as they pertain to the Stability and Quality Control departments. Represent Glenmark as appropriate in FDA, notified body, internal and other regulatory audits. Work in close collaboration and support with other members of the CMC team responsible for drug product development and support to management, as necessary Domestic and international travel up to 5% may be required to accompany technical staff in the factory acceptance and inspection of laboratory equipment. Ensure training of QC Analyst (Entry level Positions) Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc. Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control. Education : A minimum of a Bachelor s degree in Chemistry / Pharmaceutical Sciences or Equivalent. Experience: 4+ years in the field of Pharmaceutical (manufacturing facility). Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in Analytical R&D. Extensive knowledge in general laboratory equipment including but not limited to: GC, HPLC, Polarography, Particulate Matter, UV-Vis and FTIR Knowledge and Skill: Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system. Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices. Technical writing skills to generate SOPs and serve as the Subject Matter Expert. Completed training on Six Sigma, certified Green belt professional. Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer. Will be an added advantage if the individual has dealt with multiple audits personally.

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures