Top 21 Quality assurance associate Jobs in Pittsboro, Nc

Sr Associate I, Quality Assurance Operations
Biogen —Research Triangle Park, NC
- $81,000 - $105,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Mentoring
- Paid parental leave
- Employee stock purchase plan
QA Operations Head (Associate Director)
Novartis —Durham, NC
- $138,600 - $257,400 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Health insurance
- 401(k) matching
Quality Assurance Associate
InfoQuest Consulting Group Inc. —Holly Springs, NC
- Email
- 5 years
- Bachelor's degree
- Continuous improvement
Senior Quality Assurance Associate
WEP Clinical —Morrisville, NC
- Full-time
- Hybrid work
- Microsoft Excel
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Health savings account
PT Quality Assurance Associate
Food Lion —Siler City, NC
- Part-time
- High school diploma or GED
- Communication skills
- Entry level
Sr Associate II, Technical Quality
Biogen —Research Triangle Park, NC
- $93,000 - $121,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Senior level
- Paid parental leave
- Employee stock purchase plan
Associate Director, Quality Assurance (Clinical Research Preferred)
IQVIA —Durham, NC
- $88,600 - $246,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Mentoring
- Work from home
Quality - Microbiology Lab Associate (3rd Shift)
The Clorox Company —Morrisville, NC
- $25.39 an hour
- Full-time
- Microsoft Outlook
- Ability to walk for extended periods
- Mid-level
- Health insurance
- 401(k)
1d
Sr. Associate II, Compliance
Biogen —Research Triangle Park, NC
- $93,000 - $121,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Senior level
- Paid parental leave
- Employee stock purchase plan
Sr Associate I, Quality Control Microbiology
Biogen —Research Triangle Park, NC
- $81,000 - $105,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Mid-level
- Paid parental leave
- Employee stock purchase plan
Sr. Associate III, Compliance
Biogen —Research Triangle Park, NC
- $111,000 - $149,000 a year
- Full-time
- 6 years
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Employee stock purchase plan
Associate Director, Laboratory Quality Operations
Alcami Corporation —Morrisville, NC
- Full-time
- 7 years
- Computer literacy
- Master's degree
Sr. Associate III, Compliance - QRM Lead
Biogen —Research Triangle Park, NC
- $111,000 - $149,000 a year
- Full-time
- 6 years
- Bachelor's degree
- Training & development
- Paid parental leave
- Employee stock purchase plan
Associate Director, Quality Assurance - Regenerative Organ Manufacturing (RMOMAL)
United Therapeutics —Research Triangle Park, NC
- Full-time
- Microsoft Outlook
- Master's degree
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
Associate Director, QC Biological (Microbiology Focused)
FUJIFILM —Holly Springs, NC
- Call employer
- Bachelor's degree
- Doctor of Philosophy
- Conflict management
Associate Director, Program Quality Management
FUJIFILM —Holly Springs, NC
- Call employer
- 7 years
- Doctoral degree
- Product management
2d

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QA Operations Head (Associate Director)
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Sr Associate I, Quality Assurance Operations

Biogen -
Research Triangle Park, NC

Apply Now

Job Details

Full-time
$81,000 - $105,000 a year

Benefits

Paid parental leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
Tuition reimbursement
Parental leave
Vision insurance
401(k) matching
Gym membership
Life insurance

Qualifications

Manufacturing facility experience
Bachelor's degree
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Regulatory/legal compliance standards in production
Production batch record review
Quality control communication
Content review
Quality control records management
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

This is a full time on-site position with M-F business hours

About This Role

The Sr. Associate I is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. This individual has advanced understanding of the Quality Management Systems and applies that knowledge by coaching peers and ensuring continuous improvement cross-functionally. The Sr. Associate I provides guidance regarding regulatory compliance, technical expertise, independent assessment and expert consultation to Manufacturing, Quality Control, Engineering, Validation, and other supporting departments in a manner consistent with site and Corporate policies, cGMP, safety, environmental and human resources policies and procedures. This individual will assist with regulatory and third party audits, aid in the development and implementation of Global Quality Systems, and manage Quality projects and other initiatives.

What You’ll Do

Batch Record Review impacting Product Disposition: Review all Quality related documents (e.g., production records, procedures, work instructions, raw data, in process testing, raw material disposition, etc.) for compliance and determine acceptability for use in GMP production activities and/or release of product for further processing and/or distribution.
Exceptions and CAPA: Assess criticality of exceptions/investigations for product impact. Conduct investigations and perform thorough reviews of the investigations and provide feedback to the department owner. Support investigations with the ability to analyze the defect and determine potential areas within the process that may have attributed to the defect.
Controlled Document Workflows: Review of GMP controlled documents to ensure changes and reasons are accurately reflected in the workflow, content is compliant with all applicable regulations and company directives, changes will not have an adverse impact to product quality and setting appropriate release dates.
Complete area walkthroughs and work observations to identify compliance gaps. Collaborate with Manufacturing and Area Subject Matter Experts to identify appropriate corrective actions.
Support resolution of both technical and compliance issues/gaps of moderate complexity. Help in implementation of Quality Systems/System Improvements and technical problem solving.
Assist Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by Biogen.
Support and/or assist in GxP quality systems-related training. Provide some mentorship and training within and across functions.
Support area release, changeovers and equipment release, visual inspection of equipment, shutdown activities, equipment tracking workflows, work order reviews and approvals.
Other duties as assigned.

Who You Are

You are task oriented and focused on continuous improvement. You are curious and eager to learn. You ask copious questions and excel at root cause analysis. Additionally, you have excellent communication/collaboration skills, logical thinking, and can work across all levels of the organization.

Required Skills

Bachelor’s Degree required, preferred in life science
Minimum 4 years of relevant Quality experience within a GMP pharmaceutical or biotech manufacturing environment
Experience reviewing and approving batch records
Experience conducting and explaining investigations to quality management and regulatory bodies
Advanced understanding of global quality systems applications, principles, concepts, practices and standards and GxP regulations
Must be able to work effectively, both independently and within a team framework across all business areas and levels within the organization locally and globally
Excellent written, verbal, and interpersonal communication skills required in order to condense complex subjects into key bullet points, articulate recommendations and decisions to Quality Management and regulatory bodies, develop strong networks cross-functionally to drive collaboration, processes and decisions

Preferred Skills

Experience in drug substance manufacturing, biologics, and/or Contract Manufacturing Organizations (small molecule)
Experience supporting product disposition
Experience conducting and explaining investigations to quality management and regulatory bodies is strongly preferred

Job Level: Professional

Additional Information

The base compensation range for this role is: $81,000.00-$105,000.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to:

Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Apply Now

Refine Your Search

quality assurance associate jobs in pittsboro, nc

Sr Associate I, Quality Assurance Operations

QA Operations Head (Associate Director)

Quality Assurance Associate

Senior Quality Assurance Associate

PT Quality Assurance Associate

Sr Associate II, Technical Quality

Associate Director, Quality Assurance (Clinical Research Preferred)

Quality - Microbiology Lab Associate (3rd Shift)

Sr. Associate II, Compliance

Sr Associate I, Quality Control Microbiology

Sr. Associate III, Compliance

Associate Director, Laboratory Quality Operations

Sr. Associate III, Compliance - QRM Lead

Associate Director, Quality Assurance - Regenerative Organ Manufacturing (RMOMAL)

Associate Director, QC Biological (Microbiology Focused)

Associate Director, Program Quality Management

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