We have other current jobs related to this field that you can find below
-
Supplier Quality Engineers
1 month ago
Columbus, United States Cummins Quality Full timeSupplier Quality Engineers – Technical Specialist #IN1097 Columbus, Indiana Our culture believes in Powering Your Potential. We provide global opportunities to develop your career, make your community a better place and work with today’s most innovative thinkers to solve the world’s toughest problems. We believe in flexibility for you to explore your...
-
Technical Document Control Coordinator
3 weeks ago
Columbus, United States FedEx Full timeTechnical Document Control CoordinatorPay: $19.91/hour Plus $0.50 Shift DifferentialShift: 2nd Shift Monday-Friday, 2:30pm-11pmLocaction: Logistics Court, Columbus, OH 43217About FedEx Supply ChainFedEx Supply Chain, a subsidiary of FedEx Corp. (NYSE: FDX), is a leader in the third-party logistics industry offering a diverse service portfolio that enables...
-
Packaging Quality Control Specialist
4 days ago
Columbus, Ohio, United States Amerisource Health Services LLC Full timeJoin Our Team at Amerisource Health Services LLCAt Amerisource Health Services LLC, our team members are integral to our mission of fostering healthier futures. Every individual plays a crucial role in our commitment to enhancing the well-being of both people and animals.Your Role:As a Packaging Quality Control Specialist, you will be working the 2nd Shift,...
-
Scientist I, Quality Control
4 weeks ago
Columbus, Ohio, United States Forge Biologics Full timeAbout Forge Our mission at Forge Biologics, is to enable access to life changing gene therapies and help bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table,...
-
Quality Control Scientist I
4 days ago
Columbus, Ohio, United States Forge Biologics Full timePosition OverviewAbout Forge BiologicsForge Biologics is at the forefront of making transformative gene therapies accessible to patients in need. We work closely with pioneers in the gene therapy sector to expedite the development and production of innovative medical solutions. Our commitment to patients drives us to establish new collaborations and...
-
Quality Inspector I
2 weeks ago
Columbus, United States MW Industries Full timeJob Summary:The Quality Control Tech I provides general administrative support to the Quality Control Department.Essential Duties and Responsibilities:• Perform general clerical functions including filing, scanning, data entry, and digital document storage.• Prepare, organize, and file Quality, Production, Inspection and Shipping Records.• Provide...
-
Scientist I, Quality Control
2 months ago
Columbus, United States Forge Biologics Full timeAbout Forge Our mission at Forge Biologics, is to enable access to life changing gene therapies and help bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table,...
-
Scientist I, Quality Control
2 months ago
Columbus, United States Forge Biologics Full timeJob DescriptionJob DescriptionAbout Forge Our mission at Forge Biologics, is to enable access to life changing gene therapies and help bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and...
-
Document Imaging Specialist
7 days ago
Columbus, United States MARYHAVEN,INC Full time $16Job DescriptionJob DescriptionDocument Imaging Specialist Job DescriptionUnique opportunity to join Maryhaven, Central Ohio’s largest and most comprehensive behavioral services provider specializing in addiction recovery. We are looking for skilled, talented, and compassionate people to join our team! Maryhaven was founded on the principles of Diversity,...
-
Document Imaging Specialist
6 days ago
Columbus, United States MARYHAVEN,INC Full timeDocument Imaging Specialist Job DescriptionUnique opportunity to join Maryhaven, Central Ohios largest and most comprehensive behavioral services provider specializing in addiction recovery. We are looking for skilled, talented, and compassionate people to join our team! Maryhaven was founded on the principles of Diversity, Equity, and Inclusion in 1953,...
-
Scientist I, Quality Assurance and Control
4 days ago
Columbus, Ohio, United States Forge Biologics Full timeJob OverviewAbout Forge BiologicsForge Biologics is committed to enhancing access to transformative gene therapies, transitioning innovative concepts into reality. We partner with pioneers in the gene therapy sector to expedite the development and production of groundbreaking medicines. Our focus on patient needs drives us to establish new collaborations and...
-
Quality Inspector I
4 days ago
Columbus, United States MW Industries Full timeJob Summary: The Quality Control Tech I provides general administrative support to the Quality Control Department. Essential Duties and Responsibilities: • Perform general clerical functions including filing, scanning, data entry, and digital document storage. • Prepare, organize, and file Quality, Production, Inspection and Shipping Records. • Provide...
-
Technical Support Specialist
4 days ago
Columbus, Ohio, United States Merit Controls Full timeEmployment Type: Full Time, Exempt, Travel up to 10%Position Overview:The Technical Support Specialist plays a vital role within the Merit Controls team, serving as the primary contact for clients to assist in resolving technical challenges. This position is essential for diagnosing, analyzing, troubleshooting, and swiftly addressing intricate issues while...
-
Documentation Specialist II
1 week ago
Columbus, United States Blue Star Partners LLC Full timeJob Title: Documentation Specialist II Location: Columbus, OH – 100% Onsite – Local candidates only Period: 10/07/2024 to 10/07/2025, possibility of extension Hours/Week: 40 hours (Hours over 40 will be paid at Time and a Half) Rate: $20 - $24/hour Contract Type: W-2 only Scope of Services: The Documentation Specialist prepares, edits, files, and...
-
Documentation Specialist II
1 week ago
Columbus, United States Blue Star Partners LLC Full time $20 - $24Job DescriptionJob DescriptionJob Title: Documentation Specialist IILocation: Columbus, OH – 100% Onsite – Local candidates onlyPeriod: 10/07/2024 to 10/07/2025, possibility of extensionHours/Week: 40 hours (Hours over 40 will be paid at Time and a Half)Rate: $20 - $24/hour Contract Type: W-2 onlyScope of Services:The Documentation Specialist prepares,...
-
Quality Systems Specialist
2 months ago
Columbus, United States Forge Biologics Full timeJob DescriptionJob DescriptionAbout ForgeForge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient...
-
Analyst I, Quality Control
5 days ago
Columbus, United States Forge Biologics Full timeJob DescriptionJob DescriptionAbout Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient...
-
Analyst I, Quality Control
1 month ago
Columbus, Ohio, United States Forge Biologics Full timeAbout Forge Our mission at Forge Biologics, is to enable access to life changing gene therapies and help bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table,...
-
Quality Assurance Senior Specialist
4 days ago
Columbus, Ohio, United States Cardinal Health Full timeOverview of Quality Assurance at Cardinal HealthQuality Assurance plays a crucial role in developing and enforcing quality protocols, procedures, and systems to ensure that products and services adhere to regulatory standards and specifications.Role of the Quality Assurance SpecialistThe Quality Assurance Specialist (QAS) is responsible for conducting...
-
Quality Assurance Specialist
1 month ago
Columbus, United States Forge Biologics Full timeAbout Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in...
Quality Control Technical Document Specialist I
3 months ago
Nature and Scope The Quality Control Technical Document Specialist I will author, edit, review, evaluate, and maintain GMP documentation (RM documents, FP documents, Analysis SOPs, Validation Protocols, Technical reports, etc. and all required revisions). The individual will co-ordinate with Document Control and Change Control reviewers from the document's initiation to the approval stage. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Ensure all work is performed and documented in accordance with existing company policies, procedures, Current Good Manufacturing Practices, health, and safety requirements. Plan daily workload to meet requirements. Draft Raw Material, In-Process, and Finished Product documents. Draft Instrument SOPs, Analysis SOPs, Method Validation/Transfer Protocols/Reports, Component Specifications, Risk Assessments, and Memos. Perform Bacterial Endotoxin Calculations, Finished Product Residual Solvent Calculations, Stability Sample Quantity Determinations, and Raw Material Code Requests. Stay current with various industry standards and expectations (USP monograph, ICH guidelines, FDA guidelines, EU guidelines, etc.). Coordinate with QA to perform Gap Assessments on current ARI documents against USP resources (general chapters/monographs). Review the USP monograph/manufacture Certificate of Analysis changes and implement on Quality Control Documentation system. Manage the Change Control Process for technical documents generated or revised within Quality Control by facilitating interdepartmental communication/coordination. Manage and track the status of technical documentation being drafted or undergoing revision within Quality Control. Procure and distribute templates from Document Control for the generation of new documents. Provide support as a technical documentation subject matter expert and communicate effectively with cross-functional departments to ensure timely delivery of documents. Maintain and analyze data/results in database and conduct trend analysis to perform annual product review report. Participate in projects identified. Ability to work overtime as needed. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Bachelor's degree in microbiology, Chemistry, Pharmaceutical Science, or related field required. 1 year of pharmaceutical experience in Microbiology, Biology, chemical testing, laboratory setting with a working knowledge of chemistry and instrumental analysis techniques, method development and validations preferred. Expertise in authoring scientific documents in a pharmaceutical environment. Ability to digest complicated technical subject matter and work with incomplete information in a fast-paced, continually changing environment. Ability to effectively communicate between various departments (QA, QC, DC, R&D, etc.). Ability to perform multiple activities at the same time and produce outstanding results to meet required deadlines. Excellent writing and editing skills, and a keen attention to detail. Excellent organizational, interpersonal and communication skills (oral and written). Proficient in Microsoft Office applications. Takes initiative with minimal supervision. Ability to identify, manage, negotiate, and resolve issues independently. Physical Environment and Requirements Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential fo
