Senior QA Compliance & Validation Specialist - Life Sciences
Initial Therapeutics, Inc.
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, leading improvement activities, and providing quality oversight. The ideal candidate will possess a Bachelor's degree in Life Sciences, Quality Risk Management experience, and proficiency in regulatory requirements. We offer competitive pay and benefits. #J-18808-Ljbffr
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Senior QA Compliance & Validation Specialist - Life Sciences in Clayton, NC vacancy
- ...a Quality Assurance role in Clayton, NC, focused on ensuring compliance with quality and regulatory standards. Candidates should have... ...School Diploma or equivalent and preferably a Bachelor’s in Life Sciences. The position requires at least seven years of relevant experience...Senior
- ...Merck & Co. is seeking a Quality Assurance professional in Clayton, North Carolina, responsible for ensuring compliance with quality systems and regulations. This role includes leading improvement activities, reviewing quality-related documentation, and providing support...Senior
Merck & Co. Inc
Clayton, NC4 days ago - ...looking for a Quality Assurance professional based in Clayton, North Carolina. The role involves ensuring plant systems batch release compliance and managing quality oversight. The ideal candidate will have a strong background in quality risk management and regulatory...Senior
Initial Therapeutics, Inc.
Clayton, NC10 hours ago - ...Novo Nordisk is seeking a QA compliance professional for the Finished Production unit in Clayton, NC. The role involves ensuring compliance with QA regulations, overseeing batch release activities, and leading local improvement initiatives. Candidates should have a minimum...SeniorLocal area
Novo Nordisk
Clayton, NC23 hours ago - ...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...Suggested
Novo Nordisk A/S
Clayton, NC1 day ago - ...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-18...Senior
Novo Nordisk A/S
Clayton, NC4 days ago - ...Grifols, S.A in Clayton, NC, is seeking a Sr. Supervisor or Supervisor III for Quality Assurance (QA). The role involves overseeing QA systems, ensuring compliance, and providing technical expertise in quality matters. Applicants should have a strong STEM background, with...Senior
Grifols, S.A
Clayton, NC1 day ago - ...BioSpace in North Carolina seeks a Quality Assurance professional to ensure compliance with regulations within aseptic production and quality processes. This role involves decision-making regarding quality issues, coaching for audits, and reviewing complex documentation...Senior
BioSpace, Inc.
Clayton, NC10 hours ago - ...Finished Production area. This role ensures compliance with regulations and provides quality oversight on validation activities for injectable treatments.... ...will have a Bachelor’s degree in Life Sciences alongside seven years of QA experience. Join us to help maintain high...Senior
Merck & Co. Inc
Clayton, NC3 days ago - ...A/S is seeking a Quality Assurance Area Specialist III for their facility in Clayton, NC. This role involves performing QA compliance activities for the Finished Production unit... ...will have a Bachelor's degree in Life Sciences, seven years of QA experience, and expertise...Senior
Novo Nordisk A/S
Clayton, NC23 hours ago - ...Validation Specialist I / Validation Specialist II Location: Clayton, NC, US Contract Type: Regular... ...acceptability of the data and compliance with the protocol. Conducts discrepancy... ...Specialist I Requires a BS/BA degree in STEM (Science, Technology, Engineering, and...Full timeContract workWork at office
Grifols, S.A
Clayton, NC10 hours ago - ...seeking a Quality Assurance professional responsible for ensuring compliance with quality processes and regulations. The role involves... ...quality improvements. The ideal candidate has at least seven years of QA experience in a pharmaceutical environment and holds a Bachelor’...Senior
Initial Therapeutics, Inc.
Clayton, NC4 days ago - ...Quality Assurance professional to ensure compliance with quality regulations at their... ...This role requires extensive experience in QA and strong expertise in regulatory requirements... ...will possess a Bachelor’s degree in Life Sciences, seven years of related experience, and...Senior
BioSpace, Inc.
Clayton, NC10 hours ago - ...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...Senior
Grifols, S.A
Clayton, NC10 hours ago - ...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...
Grifols, S.A
Clayton, NC10 hours ago - ...products Tuition Assistance Life & Disability Insurance... ...is to provide/lead validation services required for... ...Reports to Senior Project Manager, Site... ...responsibilities Perform compliance & technical reviews/approvals... ...Engineering, Computer Science, or applicable technical...For contractorsWork experience placementLocal areaShift work
Merck & Co. Inc
Clayton, NC4 days ago - ...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...Senior
Grifols, S.A
Clayton, NC4 days ago - 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 attractive...Senior
- Grifols, S.A in Clayton, NC is seeking candidates for Sr. Quality Associate II and Principle Quality Associate roles. These positions involve supporting quality processes, analyzing data, and leading projects in a dynamic environment. The ideal candidates will have strong...Senior
Grifols, S.A
Clayton, NC1 day ago - ...S.A in Clayton, North Carolina seeks a Sr. Manager, Quality Audits. In this role, you’ll perform routine GMP audits and provide compliance guidance across the Quality organization. The ideal candidate should possess extensive pharmaceutical experience, ideally in manufacturing...Senior
Grifols, S.A
Clayton, NC1 day ago - .../ Principle Quality Associate to join their international team. The role involves supporting the Alpha-1 product line, ensuring compliance with quality standards, and interfacing with various groups such as Manufacturing and Regulatory. Candidates should possess a BS/...Senior
$90k - $120k
...detail‑oriented QC Equipment Validation Engineer to support... ...accuracy, completeness, and GMP compliance Maintain the validated state... ...Engineer: Bachelor’s degree in Life Sciences, Chemistry, Engineering, or... ...preferred Compensation for the Senior Validation & Quality...Piper Companies
Clayton, NC4 days ago- ...department processes and ensures reliability in 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,...
Novo Nordisk
Clayton, NC4 days ago - 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...Senior
- Merck & Co. is seeking a qualified Engineering professional in Clayton, NC to support department processes and ensure equipment reliability in our pharmaceutical manufacturing facility. The role requires a Bachelor's degree in Engineering or a relevant field and a minimum...
- Merck & Co. in Clayton, NC is seeking a qualified engineer to ensure compliance of processes with standards and improve reliability of process control systems. You will collaborate with local and global teams, assisting in managing budgets and developing automation standards...SeniorLocal area
- ...NC to 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...
$125k - $155k
A leading life sciences firm is looking for an Automation Engineer in Clayton, NC, for a 12-month onsite contract. The role involves providing automation support for production and packaging operations within a regulated environment. Candidates should possess hands-on experience...Contract work$125k - $155k
...Companies is seeking an Automation Engineer to support a large-scale pharmaceutical manufacturing expansion for a leader in the life sciences industry for a 12-month onsite contract opportunity based out of Clayton, NC . This Automation Engineer will provide hands‑on automation...Full timeContract work- Merck & Co. is seeking a Project Manager in Clayton, North Carolina, to lead multi-disciplined project teams ensuring timely and budget-friendly project completion. Candidates should possess a Bachelor's degree in Engineering and a minimum of 8 years of project management...Senior
Merck & Co. Inc
Clayton, NC4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior QA Compliance & Validation Specialist - Life Sciences. Be the first to apply!
Related searches
- quality assurance associate Clayton, NC
- quality assurance specialist Clayton, NC
- qa associate Clayton, NC
- qa specialist Clayton, NC
- validation specialist Clayton, NC
- verification & validation engineer Clayton, NC
- verification engineer Clayton, NC
- validation consultant Clayton, NC
- validation engineer Clayton, NC
- senior manager quality engineering Clayton, NC