Verista, Inc.
6038 - QA Consultant / Quality Specialist
Verista, Inc., Morrisville, North Carolina, United States, 27560
6038 - QA Consultant / Quality Specialist
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise We are seeking a
QA Consultant
to join the Quality Systems organization at our RTP facility. This role provides quality oversight of GMP systems, supports QC investigations, manages CAPAs and change controls, and ensures the site maintains compliance with regulatory and corporate standards. Ideal for someone with strong Quality Systems expertise and the ability to collaborate cross-functionally in a fast-paced environment. Oversight of
QC exceptions
(Investigations, LEs, OOS, ARs, PEs) for DS/DP Review and approval of
CAPAs ,
change controls , and GMP documentation Issuance of
GMP records
such as BPRs, SLRs, labels, and logbooks Author key quality reports (Site Management Review Report, Trending Report, Site Master File) Facilitate SMR/QMR meetings and site governance boards (Deviation & CAPA Review Boards) Develop and deliver
GxP/Quality Systems training Support regulatory inspections and collaborate with global Quality System teams Generate and analyze Quality System metrics and identify improvement opportunities Requirements: Bachelor’s degree in a scientific field (Biology, Chemistry, Engineering, etc.) 3–7+ years in
Quality Assurance / Quality Systems
in a GMP-regulated environment Experience supporting
QC investigations , CAPAs, and change controls Strong documentation, root cause analysis, and GMP compliance skills Experience with systems such as TrackWise, Veeva Vault, or other QMS tools (preferred) Onsite requirement in Morrisville, NC five days/week What We're Looking For
Strong Quality Systems expertise Excellent communication and documentation skills Ability to drive continuous improvement Comfortable making timely, risk-based QA decisions Salary & Benefits For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. *Verista is an equal opportunity employer. National (US) Range $59,951 - $99,899 USD Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture Competitive pay plus performance-based incentive programs Company-paid Life, Short-Term, and Long-Term Disability Insurance. Supplemental Life, Hospital, Critical Illness and Legal Insurance Health Savings Account Paid Time Off (Rollover Option) and Holidays As Needed Sick Time Tuition Reimbursement Team Social Activities (We have fun!) Employee Recognition Employee Referral Program Paid Parental Leave and Bereavement Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. For more information about our company, please visit us at Verista.com Equal Employment Opportunity statement: Verista is an equal opportunity employer.
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Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise We are seeking a
QA Consultant
to join the Quality Systems organization at our RTP facility. This role provides quality oversight of GMP systems, supports QC investigations, manages CAPAs and change controls, and ensures the site maintains compliance with regulatory and corporate standards. Ideal for someone with strong Quality Systems expertise and the ability to collaborate cross-functionally in a fast-paced environment. Oversight of
QC exceptions
(Investigations, LEs, OOS, ARs, PEs) for DS/DP Review and approval of
CAPAs ,
change controls , and GMP documentation Issuance of
GMP records
such as BPRs, SLRs, labels, and logbooks Author key quality reports (Site Management Review Report, Trending Report, Site Master File) Facilitate SMR/QMR meetings and site governance boards (Deviation & CAPA Review Boards) Develop and deliver
GxP/Quality Systems training Support regulatory inspections and collaborate with global Quality System teams Generate and analyze Quality System metrics and identify improvement opportunities Requirements: Bachelor’s degree in a scientific field (Biology, Chemistry, Engineering, etc.) 3–7+ years in
Quality Assurance / Quality Systems
in a GMP-regulated environment Experience supporting
QC investigations , CAPAs, and change controls Strong documentation, root cause analysis, and GMP compliance skills Experience with systems such as TrackWise, Veeva Vault, or other QMS tools (preferred) Onsite requirement in Morrisville, NC five days/week What We're Looking For
Strong Quality Systems expertise Excellent communication and documentation skills Ability to drive continuous improvement Comfortable making timely, risk-based QA decisions Salary & Benefits For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. *Verista is an equal opportunity employer. National (US) Range $59,951 - $99,899 USD Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture Competitive pay plus performance-based incentive programs Company-paid Life, Short-Term, and Long-Term Disability Insurance. Supplemental Life, Hospital, Critical Illness and Legal Insurance Health Savings Account Paid Time Off (Rollover Option) and Holidays As Needed Sick Time Tuition Reimbursement Team Social Activities (We have fun!) Employee Recognition Employee Referral Program Paid Parental Leave and Bereavement Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. For more information about our company, please visit us at Verista.com Equal Employment Opportunity statement: Verista is an equal opportunity employer.
#J-18808-Ljbffr