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Job DescriptionPosition Summary – The QC Chemist II position performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedures. The position will be operating within a GMP environment for an Analytical QC team in a CDMO. Essential Functions • Well versed with various laboratory techniques, including, but not limited to HPLC, GC, titrations, and various wet chemistry techniques., • Carry out routine laboratory work as directed by management and/or senior laboratory personnel with minimal supervision, • Performs complex analyses with moderate supervision., • Conduct routine analytical experiments using established analytical methods and procedures., • Data entry into reports, as directed by senior laboratory personnel., • Verify simple transcription processes, such as checking accuracy of calculations and reviewing daily equipment verifications for compliance., • Support testing for investigations for OOS, OOT, and aberrant results and troubleshooting., • Review and maintain laboratory notebooks., • Ensure data collected is processed and submitted for review in a timely manner., • Aid in investigations for OOS, OOT, and aberrant results and troubleshooting by assisting in root cause determination and report writing., • Maintains laboratory inventory of chemicals, standards, and consumables and orders materials as necessary., • Revises existing methods, SOPs, and Work Instructions as needed. Supervisory responsibilities: • Direct Reports: None, • Indirect Reports: None Key Relationships: • Manufacturing Operations, • Analytical R&D, • Quality Assurance Travel requirements: • N/A Education and Experience • B.S with 4-6 years' experience, or M.S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline, • 2-5 years´ experience in a GMP laboratory setting in the pharmaceutical industry, • Must have experience with general laboratory instruments, such as FTIR, Particle Size, Titration Equipment, and UV-Vis, • Must have experience in HPLC testing and troubleshooting, • Must have prior experience with raw materials or finished products testing in a GMP pharmaceutical environment., • Must be well versed with Good Documentation Practices and ALCOA++ principles., • Technical report writing proficiency preferred Knowledge, Skills, and Abilities • Proficiency in Empower, MS Excel, and MS Word, • Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience, • Thorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical and has a right first-time mentality Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires constant standing, walking, seeing, gripping, & hearing, • Requires frequent sitting, bending, pushing, & reaching, • Requires occasional carrying under 20 LBS., • Requires frequent lifting & pulling under 20 LBS, occasionally 20 – 60 LBS., • Requires occasional twisting Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and Disclaimer The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Powered by JazzHR aS9ej4lZQI

Job Description Position Summary – The Quality Control Raw Materials Chemist I performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedures The ideal candidate will additionally possess superior communication skills. The position will be operating within a GMP environment for a Quality Control CDMO. Essential Functions • Perform testing of raw materials, packaging components, and other samples., • Well versed with various laboratory techniques, including, but not limited to HPLC, GC, titrations, and various raw materials testing techniques., • Conduct routine analytical experiments using established analytical methods and procedures., • Data entry into reports, as directed by senior laboratory personnel., • Verify simple transcription processes, such as checking accuracy of calculations and reviewing daily equipment verifications for compliance., • Support testing for investigations for OOS, OOT, and aberrant results and troubleshooting., • Review and maintain laboratory notebooks., • Ensure data collected is processed and submitted for review in a timely manner., • Maintains laboratory inventory of chemicals, standards, and consumables and orders materials as necessary., • Aid in investigations for OOS, OOT, and aberrant results and troubleshooting by assisting in root cause determination., • Generate and/or review shipping paperwork for third party testing and prepare samples for shipment., • Create purchase requisitions for lab supplies and third-party testing, • Perform weekly laboratory audit inspections, • Perform sampling of raw materials as needed, • Other duties as assigned Supervisory responsibilities: • Direct Reports: None, • Indirect Reports: None Key Relationships: • Manufacturing Operations, • Quality Assurance, • Analytical R&D, • Program Management Travel requirements: • None Education and Experience • Minimum BA or BS in a scientific discipline required, • Minimum 2 – 4 years in a Quality Control setting for Raw Materials Knowledge, Skills, and Abilities • Knowledge of cGMPs, • Good communication, organization and computer skills are required., • Knowledge of Empower and Microsoft Office (Excel, Word) is required; LIMS knowledge is desired., • Ability and willingness to work additional hours as required by business needs, • Experience with testing per USP, EP, BP, and JP monographs., • Ability to interpret various compendial guidelines to ensure specifications meet regulatory requirements., • Experience with laboratory equipment such as HPLC (UV, Ion detectors, RI detectors), GC (Headspace, FID, TCD), FTIR, Auto Titrators, Karl Fischer Titrators, Coulometric Karl Fischer Titrators, Melting Point Apparatus, Muffle Furnace, UV-Vis, Refractometers, and Particle size., • Excellent interpersonal skills and ability to establish and maintain effective working relationships with both internal and external stakeholders, • Ability to work with modest supervision, • Able to multi-task productively, applying time management processes and procedures effectively., • Self-directed Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires constant standing, walking, seeing, gripping, & hearing, • Requires frequent sitting, bending, pushing, & reaching, • Requires constant carrying under 20 LBS, occasionally 20 – 60 LBS., • Requires frequent lifting & pulling under 20 LBS, occasionally 20 – 60 LBS., • Requires occasional twisting Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Powered by JazzHR V5qtfE57G1

Job Description Position Summary – The Chemist III/Sr. Chemist Raw Materials ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The position will be operating within a GMP environment for a Quality Control CDMO. The ideal candidate will additionally possess superior communication skills, presenting to internal and external clients Essential Functions • Schedule the QC laboratory Raw Materials workload appropriately to meet manufacturing release testing schedules, stability pull dates and timelines., • Monitor weekly laboratory and data review activities for accuracy and track hours needed for completion of tasks., • Oversight for review of QC and Raw Material data for compliance with specifications and regulatory requirements, • Interact with third party laboratories for microbial and analytical testing of raw materials, • Generate and/or review shipping paperwork for third part testing and prepare samples for shipment., • Create purchase requisitions for lab supplies and third-party testing, • Perform weekly laboratory audit inspections, • Perform sampling of raw materials as needed, • Review third party laboratory investigations and protocols., • Execute intermediate to advanced chemical and instrumental testing of raw materials using HPLC, GC, FTIR, UV-Vis, Karl Fischer titration, and wet chemistry., • Ensure all testing meets compendial standards (USP/EP/JP) and regulatory expectations. Conduct peer reviews of data, Certificates of Analysis (COAs), and laboratory logbooks., • Author and review GMP documentation including Standard Operating Procedures (SOPs), protocols, deviations, Corrective and Preventive Actions (CAPAs), and change controls., • Provide technical guidance to junior analysts. Lead method verification, validation, and method transfer activities for incoming raw materials., • Oversee the calibration, maintenance, and troubleshooting of laboratory equipment., • Other duties as assigned Supervisory responsibilities • Direct Reports: No, • Indirect Reports: None Key Relationships • Manufacturing Operations, • Quality Assurance, • Analytical R&D, • Program Management Travel requirements: • None Education and Experience • Minimum BA or BS in a scientific discipline required, • Minimum 5-8 years of Analytical chemistry experience with a cGMP/GLP environment, preferably at a CDMO or pharmaceutical company. Knowledge, Skills, and Abilities • Knowledge of cGMPs, • Good communication, organization and computer skills are required., • Knowledge of Empower required; LIMS and Microsoft Office programs knowledge is desired., • Ability and willingness to work additional hours as required by business need, • At least 5 years’ experience in a CRO environment, • Experience with USP, EP and JP monographs., • Experience with laboratory equipment such as HPLC (UV, Ion detectors, RI detectors), GC (Headspace, FID, TCD), FTIR, Auto Titrators, Karl Fischer Titrators (Volumetric and Coulometric), and Particle size., • Excellent interpersonal skills and ability to establish and maintain effective working relationships with both internal and external stakeholders, • Excellent verbal and written communication skills, • Ability to work with minimal supervision, • Experience in Data Review of Analytical data per GDP guidelines., • Proven ability to review and evaluate the compliance and completeness of analytical data., • Able to multi-task productively, applying time management processes and procedures effectively., • Works toward common goals by supporting, encouraging, and sharing information with colleagues., • Strong analytical skills and ability to understand business and financial implications of contracts, • Self-directed Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires frequent sitting and walking, • Requires carrying under 20 LBS, occasionally 20 – 60 LBS, • Requires pushing, & pulling under 20 LBS, occasionally 20-60 LBS, • Requires occasional bending, twisting, reaching, & gripping, • Requires constant seeing & hearing Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and Disclaimer The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Powered by JazzHR 9s721DUGQ2

MedPharm in Durham, NC seeks a Quality Control Raw Materials Chemist I to perform testing in a GMP environment.

Job Overview QC Chemist C will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Education & Experience BS or MS in Chemistry or Pharmaceutical Sciences, or related field.

Aurolife is seeking a Chemist B to ensure products and materials meet quality standards and regulatory requirements.

Job Overview Chemist B is responsible for ensuring that products and materials meet established quality standards and regulatory requirements by conducting laboratory tests, analyzing results, and maintaining accurate documentation. Knowledge in USP/ICH/FDA Ability to learn quickly and decision mak

MedPharm Ltd in Durham, NC seeks a Quality Control Raw Materials Chemist I to perform testing using HPLC, GC, and titration techniques in a GMP environment.

Aurolife is seeking a QC Chemist C to perform a range of analytical tests to assess strength, identity and purity of samples within the stability team.

Job Overview QC Chemist C will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist C will be responsible for review of analytical documents, investigations, maintaining GLP status in lab. Education & Experience BS or MS in Chemis

A pharmaceutical company in North Carolina seeks a QC Chemist III to ensure compliance in the testing and documentation of raw materials.

Qualifications Bachelor’s degree in Chemistry, Biochemistry, or related field.

Electrical Project Manager & Estimator – Lead Multi-State Commercial Projects and Licensing Compliance.Company: Palmetto Electric Solutions, Inc.Salary/Pay Rate: $125,000 to $150,000 per year (based on experience).Job/Employment Type: Full Time.You will serve as a vital leadership asset, managing

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of between $25/hr.There is no payment required in order to apply or to work as an In-Home Usage Tester.You do

Provide engineering and instrumentation support for a broad range of GMP laboratory equipment and systems across QC operations, including PCR, Biochemistry, Microbiology, and Bioassay laboratories.

SGX, part of the Propelis Group, brings together more than 150 years of combined experience from SGS&Co and SGK, forming a powerhouse in packaging graphics, prepress, and print production.We offer a full suite of solutions, including artwork and file preparation, plate and cylinder production, and m

The company’s signature solutions, GuaranteedPOWER® and PerpetualPOWER® are industry firsts, improving reliability, sustainability and safety to solve the power problem for facility leaders.Concentric helps data centers, distributors, manufacturers, utilities, communications infrastructure and m

Dykema Gossett, PLLC, a leading national law firm celebrating its 100.This position serves as a consultative partner to Dykema case teams and clients, supporting eDiscovery needs across the full lifecycle of a matter.Responsibilities include workflow design, data triage and preparation, processing,

Caravel BPM Technology Solutions – where caring and community is in our company DNA, we are always striving to be our best selves and we’re compelled to ask the questions that lead to innovation.As the Project Manager you will be responsible for the coordination and completion of projects on-tim

Senior Project Manager – Medicaid & Health and Human Services.Known for “Delighting the Client” through performance, innovation, and an employee-centric culture, S2Tech is a fast-growing IT consulting company serving clients in over a quarter of the United States.We are widely recognized as a

Project Manager, Developer Marketing.The ideal candidate will bring strong project management discipline, experience managing multiple concurrent workstreams, and a track record of keeping complex marketing projects on schedule, aligned, and delivered to a high standard.Location: Bay Area, CA(Remote

Woodard & Curran is a national engineering, science, and operations firm with a simple vision for clean water, a safe environment, healthy communities, and happy people.As an employee-owned company, we strive to cultivate diverse teams and encourage collaboration in an equitable and inclusive cultur

WELLTOWER – REIMAGINE REAL ESTATE WITH US.At Welltower, we’re transforming how the world thinks about senior living and wellness-focused real estate.As a global leader in residential wellness and healthcare infrastructure, we create vibrant, purpose-driven communities where housing, healthcare,

State Of CT (Department of Burea of Information and Technology Services).State client Exp Must and Active PMP Certification.The Project Manager will lead a cross-functional project team, driving meaningful change, and ensuring the delivery of high-impact digital services to the State of Connecticut.

Unfortunately, the Project Manager role is not able to provide sponsorship now or anytime in the future.This role requires you to be located in the Indianapolis area because this is a hybrid role and requires one a day a week in the office.The Project Manager (PM) works in conjunction with internal

We are looking for a Project Manager to lead large-scale commercial electrical construction projects within a self-perform electrical contractor environment, with direct ownership over healthcare, institutional, and complex commercial builds.This role is responsible for driving projects from precons

Remote can be anywhere in the US, but Houston (TX), Atlanta (GA), Dallas (TX), and other Texas metro areas, Chicago (IL), Denver (CO), Salt Lake City (UT), Phoenix (AZ), Nevada, and Boise (ID) are preferred.Lead the execution of complex electrical distribution and critical infrastructure projects wh

Senior Clinical Research Associate - Cardiovascular Medical Device.Senior Clinical Operations Manager.Class III catheter-based systems.We operate with a purpose-driven, agile, and collaborative culture, where each team member plays a meaningful role in advancing solutions that improve patient outcom

VERSYS (Verified Systems) is growing our team of experienced .Mission Critical Project Managers.If you’ve led power, controls, or cooling scopes in environments where uptime, documentation, coordination, and precision are non-negotiable, we want to hear from you.You’ll lead Data Center a

Frontier Research AI Scientist.Ent is the intent-aware workspace security platform for securing human and AI-driven work.Built to protect productivity, the new attack surface, Ent understands not just what users and agents do but why, and intervenes at the moment of risk before incidents occur.Where

Under general supervision of the Manager of Clinical Systems or higher, the Clinical Systems Associate Project Manager T will assist with designing, documenting, and standardizing processes to support the implementation of Monday.This role will collaborate with project teams and work with end users

Technical Project Manager with deep Splunk expertise.Splunk and observability initiatives.This role requires a strong blend of.Splunk deployments, enhancements, and migrations.The ideal candidate understands the.Define project scope, timelines, milestones, and deliverables.Manage project plans, trac

They made it easier for me to live, breathe, eat, and stay clean.Without them, I’d be waiting somewhere, waiting for someone to give me a chance to live.What You Will Do to Change Lives .The Senior IT Project Manager, Planning & Implementation is responsible for leading the planning, coordi

Power Generation Project Manager.Orbital Engineering is seeking a.Power Generation Project Manager.This remote position will be based in the.The ideal candidate will bring a strong combination of project management capability, technical understanding, client relationship skills, and experience suppo

Candidates must reside and work in one of the following states due to tax and compliance requirements: AR, AZ, CA, CO, FL, GA, ID, IL, LA, MD, MO, NC, NJ, NV, NY, OH, TX, VA, WA, WI, or WY.This position has geographic-based pay ranges.Final compensation and geographic tier placement are determined b

We are currently seeking qualified candidates for consideration to fill an open Project Manager position in our Environmental Division.This position will be working remotely for our client’s office in Rochester, NY area.The candidate will work with, and report to, their Director, Fleet Planning &

Jeppesen ForeFlight is seeking a customer-facing.Senior Manager of Implementation: US remote opportunity.As the selected candidate, you will successfully manage multiple customer software implementation projects and programs across the Americas through effective planning, scheduling and controlling,

Overview: As a One Inc Project Manager in our Delivery organization, you will be client facing and the driving force behind project success, taking ownership of every aspect from initiation to completion of client implementations.You will be responsible for translating objectives into actionable pla

POSITION: Project Manager – Environmental Due Diligence.LOCATION: Flexible/Remote in Ohio.The Project Manager within AEI’s Due Diligence division will perform various environmental due diligence projects focused on commercial real estate.The ideal candidate will have previous experience performi

Generative Studio X (GSX), the agentic orchestration platform for enterprises providing the infrastructure to govern, coordinate, and scale AI agents across their organization.Building AI agents is no longer the challenge.Connecting them into a coordinated, governed system is.A strategic control pla

Project Manager (Construction).House Buyers of America is looking for a Field Manager who will be responsible for the project management of our home renovations.This person will oversee all aspects of 5-10 projects per month including bidding out jobs, permitting work and ensuring everything is comp

Senior eDiscovery Project Manager.CGS is seeking a Senior eDiscovery Project Manager to join our team supporting the legal organization within a large Federal agency.CGS brings motivated, highly skilled, and creative people together to solve the government’s most dynamic problems with cutting-edg

Rwazi is a global consumer-intelligence company.We turn real-world data — collected by contributors on the ground in markets around the world — into intelligence that the world's leading brands use to make decisions.Behind every dataset is a network of real people doing real work in the field, a

Brookwood Group has been protecting owner interests in construction since 1989.Our lineage traces back to George T.Heery: one of the original developers of the Construction Project Management profession and creator of the Bridging delivery method.We've managed over $10 billion in construction progra

Employment Type: Full-Time, Experienced .Department: eDiscovery Management.CGS is seeking an eDiscovery Project Manager to join our team supporting the legal organization within a large Federal agency.CGS brings motivated, highly skilled, and creative people together to solve the government’s mo