Top 63 Sr. director, quality assurance for quality control Jobs in North, Sc

Sr. Director, Quality Assurance for Quality Control
Vaxcyte —North, SC
- $229,000 - $268,000 a year
- Remote
- 11+ years
- Bachelor's degree
- Senior level
REPOST - ICF-IID Program Director: OIDD-Central Office
State of South Carolina —Lexington County, SC
- $92,300 - $133,800 a year
- Full-time
- Current TB test
- RN License
- Physical & Rehabilitation Medicine
- Paid parental leave
- Paid holidays
Manager, FSQA
Aspire Bakeries —West Columbia, SC
- $100,000 - $110,000 a year
- Management
- 5 years
- Ability to lift 50 pounds
- Paid parental leave
- Health savings account
Director of Quality
Harsco Rail —West Columbia, SC
- Full-time
- Analysis skills
- Bachelor's degree
- Mentoring
Quick Apply
1d
Cyber Security Sr Analyst / Specialist - Power Generation Industrial Control Systems and OT (CAYCE, SC, US, 29033)
Dominion Energy —Cayce, SC
- Computer Science
- Up to 50% travel
- 5 years
- Paid holidays
- Health insurance
Mgr Quality Value Stream
Zeus Industrial Products —Orangeburg, SC
- Full-time
- 5 years
- Writing skills
- Engineering
MPPS Policy Deviations Senior Manager
CVS Health —Columbia, SC
- $67,900 - $182,549 a year
- Full-time
- Nursing
- 5 years
- Bachelor's degree
- Health insurance
- Dental insurance
9h
Manager, Production
Lennox International —Orangeburg, SC
- Full-time
- 5 years
- Engineering
- Residential
Quick Apply
Retention Coordinator
CLAFLIN UNIVERSITY —Orangeburg, SC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
Quality Assurance Associate II
AVANTech, LLC —Columbia, SC
- $22 - $27 an hour
- Overtime
- Microsoft Outlook
- Pass drug screening
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Quality Assurance Associate I
AVANTech Incorporated —Columbia, SC
- $18 - $23 an hour
- Overtime
- Microsoft Outlook
- Pass drug screening
- Mid-level
- Paid holidays
- Disability insurance
Warehouse Manager I
Interstate Batteries —Columbia, SC
- Full-time
- Computer literacy
- Mid-level
- Forklift
Quality Assurance Associate II
AVANTech Incorporated —Columbia, SC
- $22 - $27 an hour
- Overtime
- Microsoft Outlook
- Pass drug screening
- Mid-level
- Paid holidays
- Disability insurance
Operations Technician (175228)
Colgate-Palmolive —Orangeburg, SC
- $22.10 - $26.00 an hour
- Night shift
- Background check
- 18 years or older
- Inventory management
- Profit sharing
- Paid parental leave
3d
Supervisor, Field Service
Spectrum —West Columbia, SC
- Overtime
- Writing skills
- Office
- Residential
- Opportunities for advancement
6d
Quality Assurance Associate I
AVANTech, LLC —Columbia, SC
- $18 - $23 an hour
- Overtime
- Microsoft Outlook
- Pass drug screening
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Quality Engineer (Manufacturing)
Prysmian —Lexington, SC
- Full-time
- Engineering
- Mid-level
- 3 years
Quick Apply
Pre-Fabrication Department Lead
AVANTech Incorporated —Columbia, SC
- Full-time
- Background check
- Ability to walk for extended periods
- Pass drug screening
- Opportunities for advancement
Pre-Fabrication Department Lead
AVANTech, LLC —Columbia, SC
- Full-time
- Background check
- Ability to walk for extended periods
- Pass drug screening
- Opportunities for advancement
Quick Apply
Operations Visual Inspector Tier I
NEPHRON SC, LLC —West Columbia, SC
- Mid-level
- High school diploma or GED
- Associate's degree

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sr. director, quality assurance for quality control jobs near north, sc

Sr. Director, Quality Assurance for Quality Control

Vaxcyte -
North, SC

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Job Details

$229,000 - $268,000 a year

Qualifications

Drug regulation
GMP
Global team management
Team development
ICH guidelines
Quality risk management
Pharmaceutical analysis
Quality assurance experience within pharmaceutical industry
Vendor relationship management
Collaboration with manufacturing teams
Managing projects
Verification of laboratory test methods
Quality control experience within pharmaceutical industry
Managing product quality assurance teams
Test validation method
Cross-functional team management
Cross-functional communication

Full Job Description

Join our Mission to Protect Humankind!

Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.

WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values:

RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.

AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.

LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.

MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Summary:

This role is pivotal in ensuring compliance with global regulatory guidelines and supporting our pipeline of high-fidelity vaccines. Vaxcyte is looking for an energetic and talented individual to join our Quality Assurance team as a Senior Director. This role carries dual accountability: providing direct QA support to the analytical operations based in Switzerland, while also managing the San Carlos-based QA team responsible for oversight of smaller-scale analytical activities. The Senior Director will be expected to operate effectively across both sites, navigating the distinct regulatory environments and operational cadences of each. The primary responsibility will be the QA oversight of QC activities associated with Vaxcyte's PCV Polysaccharides and Drug Substances. The Senior Director will work closely with internal teams (Process Development, MSAT, Quality Control, Regulatory, and Stability) and external partners (CDMOs and CTLs) to maintain the compliance of the analytical program.

Essential Functions:

Lead quality oversight activities related to method validation, release and in-process testing for Drug Substance and Polysaccharide
Serve as the primary liaison within Vaxcyte QA and with outside collaborators, building partnerships that support analytical needs for relevant programs.
Represent QA at internal and external cross functional team meetings.
Lead review and approval of internal and external GMP documentation for compliance, including specifications, Certificates of Analysis, validation reports, deviations, change controls, risk assessments, and CAPAs as they relate to polysaccharides and drug substance; apply technical and compliance expertise to critically evaluate reference standards, test methods, protocols, and raw data packages from CMOs and contract testing laboratories.
Partner with QC, vendor management, and contract labs to set key performance indicators for monitoring vendor effectiveness.
Drive resolution of quality performance issues with contract manufacturers and testing organizations
Review Quality Agreements and regulatory documentation as required.
Lead quality investigations of testing deviations and OOS.
Contribute to regulatory filings, respond to questions from health authorities, and ensure quality of documentation used in support of regulatory submissions.
Take part in audit preparations and help ensure ongoing readiness.
Develop, review, and update GMP-related internal policies and procedures as necessary.
Champion a culture of quality excellence and continuous improvement by proactively identifying systemic gaps, driving implementation of sustainable solutions, and establishing performance standards that elevate GMP compliance across internal teams and external partners.

Requirements:

Bachelor's degree in Biochemistry, Chemistry, or a related field with 15+ years of relevant industry experience. Other combinations of education and/or experience may be considered.

Thorough knowledge of applicable FDA, EU, and ICH regulatory guidelines and pharmacopeia for method qualification and validation in biologics and vaccines, along with proven expertise in applying these regulations to develop practical solutions and phase-appropriate analytical strategies.
Experience working with biochemistry, immunoassay, or microbiological assay techniques in a Quality Control environment.
Excellent organizational and project management skills, with the ability to handle multiple projects under tight timelines.
Excellent written and verbal communication skills, including the ability to work effectively in cross-functional teams.
Previous experience in validation and transfer of analytical assays.
Demonstrated ability to build and develop high-performing QA teams and influencing cross-functional and executive stakeholders in a fast-paced commercial-stage biotech company.
Knowledge and experience in Risk Management principles.
Knowledge in both clinical and commercial product desired.
Ability to integrate and interpret interdisciplinary project information; with at least a high-level understanding of the drug/vaccine development process.
Ability to work globally with CMOs in different countries and continents.
Experience managing geographically distributed QA teams across multiple sites or countries, with the ability to build cohesive quality culture and consistent GMP standards across locations.
Experience in BLA submission and commercial launch is highly desirable

Reports to: Executive Director, Quality Assurance

Location: Raleigh, NC

Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy): Remote

Compensation: The compensation package will be competitive and includes comprehensive benefits and an equity component.

Salary Range: $229,000 – $268,000 (North Carolina)

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Apply Now

Refine Your Search

sr. director, quality assurance for quality control jobs in north, sc

Sr. Director, Quality Assurance for Quality Control

REPOST - ICF-IID Program Director: OIDD-Central Office

Manager, FSQA

Director of Quality

Cyber Security Sr Analyst / Specialist - Power Generation Industrial Control Systems and OT (CAYCE, SC, US, 29033)

Mgr Quality Value Stream

MPPS Policy Deviations Senior Manager

Manager, Production

Retention Coordinator

Quality Assurance Associate II

Quality Assurance Associate I

Warehouse Manager I

Quality Assurance Associate II

Operations Technician (175228)

Supervisor, Field Service

Quality Assurance Associate I

Quality Engineer (Manufacturing)

Pre-Fabrication Department Lead

Pre-Fabrication Department Lead

Operations Visual Inspector Tier I

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