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
- ...Validation Specialist I / Validation Specialist II Location: Clayton, NC, US Contract Type: Regular... ...position is responsible for assigned qualification and validation related activities related... ..., flow diagrams) for compliance to GMP/Validation principles and provides feedback...SuggestedFull timeContract workWork at office
- ...Primary responsibility is to provide/lead validation services required for the successful... ...environments with hearing protections. Qualifications Bachelor's Degree in Engineering, Computer... ...manufacturing preferred. Knowledgeable in GMP concepts preferred Knowledge of standard...SuggestedFor contractorsWork experience placementLocal areaShift work
$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- ...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
- ...support the continuous improvement of manufacturing processes. The role involves providing technical support and ensuring compliance with GMP regulations. Ideal candidates have a Bachelor's degree in a related field, minimum four years of relevant experience, and CLEAN 1Star...Suggested
- ...Novo Nordisk A/S is seeking a QA Area Specialist III in Clayton, NC, focused on validation activities within Finished Production. This role involves quality oversight, decision-making on compliance issues, and ensuring adherence to regulations. The ideal candidate will...
- ...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...- ...manufacturing operations. The position requires a Bachelor's degree in Engineering or Science and a minimum of four years of experience in a GMP regulated environment. Key responsibilities include coaching team members, driving equipment optimization, and maintaining organized...
- ...years of engineering experience. The role includes responsibilities such as coaching team members, driving process optimization, and validating equipment processes. Benefits include competitive pay, generous paid time off, and health insurance effective from day one. #J-1...
- Initial Therapeutics, Inc. is seeking a Quality Assurance professional in Clayton, North Carolina, with at least 7 years of experience in quality assurance and compliance in the pharmaceutical industry. The role involves ensuring plant systems batch release compliance,...
- ...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...
- ...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...
- ...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...
- ...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...
- ...The Position Validation Lead (Project Quality) for IFP expansion projects. Provides comprehensive validation subject matter expertise... ...contributors (local & abroad) Other accountabilities, as assigned Qualifications Bachelor’s degree in pharmaceutical, engineering, or other...Local area
- Scorpion Therapeutics is seeking a Validation Lead (Project Quality) for IFP expansion projects. In this role, you will provide comprehensive validation expertise, guiding project execution and compliance with Novo Nordisk validation procedures. The position offers an...
- ...documentation review 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...
- ...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
- ...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...Local areaShift work
- ...impact project focused on commissioning, integration, and validation within a regulated GMP environment . Overview of Opportunities We are... ...on, field-based positions supporting commissioning and qualification activities . Key Responsibilities (Across Roles)...
- TekniPlex is looking for a Process Engineer I for our facility in Clayton, NC. In this role, you will manage Level 1 & 2 technology projects related to new product programs and provide technical assistance for continuous improvement initiatives while ensuring compliance...
- ...highly technical expertise in Engineering, Validation, Automation, Compliance, and Safety (EHS... ...control documentation. Required Qualifications Automation & Control Systems Minimum... ...environments. Knowledge of GxP, GMP, and computerized system compliance requirements...Full timeImmediate start
- 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
...new 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 Industrial...Permanent employmentFor contractorsLocal areaRelocation package$155k - $175k
...across finished product areas. Assist in commissioning and sustaining automated equipment by validating data exchange, system reliability, and operational readiness. Qualifications 3-7 years of experience working within industrial automation, OT, or manufacturing IT...Contract 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
- ...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
- Initial Therapeutics, Inc. seeks a qualified engineer to ensure compliance of new processes and equipment within aseptic production in Clayton, North Carolina. The role involves developing improvement plans for process control systems and participating in global project...
- ...requires a Bachelor's Degree in Engineering and at least 2 years of experience in the biotech or chemical industry, preferably with GMP experience. Responsibilities include troubleshooting mechanical systems, ensuring production compliance, and managing cross-functional...
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