Validation Specialist I — GMP Qualification & Validation
Grifols, S.A
Grifols, S.A. is looking for a Validation Specialist I / II in Clayton, NC, responsible for managing validation activities for various projects within the manufacturing environment. The role thrives on collaboration with cross-functional teams and requires a solid background in STEM fields. The ideal candidates will have documented experience in the pharmaceutical industry, along with technical proficiency in validation processes. This position offers the chance to impact healthcare positively while working within an innovative company. #J-18808-Ljbffr Grifols, S.A
- ...Location: Clayton NC Overview: Validation Specialist I / Validation Specialist II position... ...position is responsible for assigned qualification and validation related activities related... ..., flow diagrams) for compliance to GMP/Validation principles and provides feedback...SuggestedWork at office
- ...Validation Area Specialist - Finished Production Facility: Engineering & Technical Location: Clayton... ...with hearing protections. Qualifications Bachelor's Degree in Engineering, Computer... ...manufacturing preferred. Knowledgeable in GMP concepts preferred Knowledge of...SuggestedFor contractorsWork experience placementLocal areaShift work
- ...required Minimum of two (2) years of instrument, laboratory validation, or engineering experience in the pharmaceutical industry or... ...IL) spaces at the expansion facility as well as QC equipment qualification. QC Equipment in Scope Kardex Remstar Verticle Carousel...Suggested
- ...facility. The role requires a Bachelor's degree in Engineering or a relevant field and a minimum of four years of experience, preferably in a GMP environment. We offer competitive pay, generous paid time off, and a collaborative work environment. #J-18808-Ljbffr Merck & Co.Suggested
$90k - $120k
...highly skilled and detail‑oriented QC Equipment Validation Engineer to support laboratory validation and equipment qualification activities for a QC expansion project in... ...completed protocols for accuracy, completeness, and GMP compliance Maintain the validated state of QC...Suggested- ...Bachelor’s degree in Engineering or Science and at least four years of relevant experience in a GMP-regulated environment. The successful candidate will drive equipment qualification, coach team members, and ensure operational reliability. Excellent benefits include leading...
- • Provide validation & technical support through the preparation, execution, data analysis, & report writing for IV, OV & PV protocols • Ownership of Change Requests (CR's) related to project validation responsibilities • Perform compliance & technical reviews/approvals...Work experience placementLocal area
- ...critical decision making, and strategy Drive equipment qualification, optimization, and validation within the area, and maintain quality of equipment and... ...degree with six (6) years of relevant experience in a GMP‑regulated environment. May consider a High School diploma...Local areaShift work
$90k - $120k
Piper Companies is looking for a skilled QC Equipment Validation Engineer to support laboratory validation and equipment qualification activities in Clayton, NC. This critical hands-on role involves ensuring compliance and managing validation efforts across production...- ...Responsibilities include driving process improvement, equipment qualification, and mentoring team members. Applicants should have a Bachelor'... ...at least four years of engineering experience, preferably in a GMP regulated environment. Opportunities for career development and...
- ...Information Management System (LIMS) in the Quality Control (QC) department. Responsibilities include designing the system, overseeing validations, and troubleshooting electronic lab systems. The ideal candidate should hold a BA/BS in a STEM curriculum with relevant...
- Grifols, S.A in Clayton, NC is seeking a QC Supervisor III to oversee Quality Computer System Validation processes. This role requires a STEM degree with extensive experience in software validation and proven leadership in managing teams. The successful candidate will...
- Initial Therapeutics, Inc. in Clayton, NC seeks a Validation Lead for IT & Automation projects. This role involves validation services, compliance checks, and technical support for pharmaceutical production. Candidates must have at least 7 years of experience in a pharmaceutical...
- Merck & Co. is seeking a Validation Lead to oversee validation services for IT and automation projects within the pharmaceutical sector. The ideal candidate will have a Bachelor's Degree in Engineering or related field and at least seven years of relevant experience. Strong...
- ...time (% can change on a case-by-case basis based on the role). Qualifications Bachelor’s degree (engineering, technology or related field... ...environment Excellent written communication skills required GMP knowledge required Basic investigation and systematic problem...Work at officeLocal area
- Merck & Co. in Clayton, North Carolina is seeking a specialist in Computer Systems Validation to ensure compliance with regulations across IT solutions. The role requires collaboration with project teams and a focus on quality and patient safety. The ideal candidate has...
- ...new product programs for prototypes and validations, including processes, equipment, and... ...analysis on previously performed validation/qualifications and if required, design and implement... ...of good manufacturing practices (GMP’s) encompassing plastics extrusion lines...Daily paidTemporary workLocal areaFlexible hoursShift work
- ...Manager. Essential Functions Support validation & verification within area Ensure quality... ...a motorized vehicle based on the role. Qualifications Bachelor's Degree in Engineering,... ...technical experience required, preferably in a GMP regulated environment May consider High...Local areaShift work
- ...and quality risk management. Candidates should have a Bachelor's degree in Engineering, Science, or a relevant field. Experience in a GMP regulated environment is preferred. The position offers competitive pay and generous benefits. #J-18808-Ljbffr Initial Therapeutics,...
- ...Manager. Essential Functions Support validation & verification within area Ensure quality... ...a motorized vehicle based on the role. Qualifications Bachelor’s Degree in Engineering,... ...technical experience required, preferably in a GMP regulated environment May consider High...Local areaWorldwideShift work
- Initial Therapeutics, Inc. is looking for an expert in IT compliance for their Clayton, NC location. The role involves managing compliance, process improvements, and ensuring IT solutions meet regulatory standards. The ideal candidate should have significant experience ...
- ...practical CAM skills in Fusion 360, learn regulatory and GMP requirements for product‑contact parts, and contribute... ...exam for powered industrial trucks. Does not require a valid drivers license. Qualifications Bachelor's Degree in Engineering (preferably in maintenance...Local areaShift work
- Initial Therapeutics, Inc. in Clayton, North Carolina invites applications for an IT Systems Manager role. Your primary responsibility will be managing systems throughout their lifecycle, ensuring project deliverables are met, and maintaining compliance with Novo Nordisk...
$74.97k - $128.52k
...product introduction and expansion Design, procure, and validate fixtures, tools, and shop aides including (lifting equipment,... ...operations managers. You'll win us over by having the following qualifications: Basic Qualifications: ~ Bachelor's Degree or higher in...Permanent employmentFor contractorsLocal areaImmediate startRelocation package- ...Collaborative, cross-functional team environment Growth opportunities in a technical manufacturing setting Requirements: QUALIFICATIONS ~ Bachelors degree in engineering (Industrial, Manufacturing, Mechanical, or related) ~3+ years of manufacturing/...Full timeTemporary work
- Tekni-Plex is seeking a Process Engineer I at their Clayton, NC site. In this role, you will manage and execute key projects focused on new product programs, ensuring compliance with manufacturing standards. You will provide essential support for quality assurance and process...
- Merck & Co. in Clayton, NC is seeking a qualified individual to provide routine support & troubleshooting for its manufacturing facility. This role involves the development of specifications, ensuring quality processes, and participation in project collaborations. The ideal...
- Tekni-Plex, Inc. is looking for a Process Engineer I in Clayton, NC. This role involves managing Level 1 and 2 technology projects, supporting manufacturing operations, and driving process improvements. The ideal candidate will have a bachelor's degree in a related engineering...
- ...vehicle license & operate a motorized vehicle based on the role. Qualifications Bachelor's Degree in Engineering, Science, or relevant... ...engineering or technical experience required, preferably in a GMP regulated environment May consider High School Diploma or equivalent...Local areaWorldwideShift work
- ...with Engineering and Operations teams. Participate in process validations, risk management activities, and quality planning as... ...Regulatory, and Supply Chain to resolve quality-related issues. Qualifications Bachelor’s degree in engineering (Mechanical, Industrial, Biomedical...Daily paidTemporary workWork at officeLocal areaFlexible hours
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