6038 - QA Consultant / Quality Specialist

Verista

Morrisville (NC)

On-site

USD 59,951 - 99,899

Full time

14 days+

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Benefits offered by this job

Competitive pay
Medical, Dental & Vision insurances
401(k) Retirement Plan with employer matching
Paid Time Off and Holidays
Tuition Reimbursement

Job summary

A leading life sciences consulting firm is looking for a QA Consultant in Morrisville, NC. The successful candidate will provide quality oversight of GMP systems, manage investigations and ensure compliance with regulations. Candidates should possess a bachelor's degree in a scientific field and 3–7 years of experience in Quality Assurance. This role requires solid skills in documentation, GMP compliance, and quality systems expertise. Competitive compensation is available for this onsite position.

Qualifications

  • 3–7+ years in Quality Assurance / Quality Systems in a GMP‑regulated environment.
  • Experience supporting QC investigations, CAPAs, and change controls.
  • Strong documentation skills.

Responsibilities

  • Oversee QC exceptions and investigations.
  • Review and approve CAPAs and change controls.
  • Facilitate regulatory inspections.

Skills

Quality Systems expertise
Excellent communication skills
Root cause analysis
GMP compliance
Continuous improvement

Education

Bachelor's degree in a scientific field

Tools

TrackWise
Veeva Vault

Job description

6038 - QA Consultant / Quality Specialist

Join to apply for the 6038 - QA Consultant / Quality Specialist role at Verista.

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.

QA Consultant Responsibilities
  • 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

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.

National (US) Range: $59,951 USD - $99,899 USD

Verista is an equal opportunity employer.

Benefits
  • 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.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • 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.

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