Sr Associate I, Quality Assurance Operations

Biogen, Inc.; North Carolina; On-site; USD 81,000 - 105,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life insurance

Wellness programs

Vacation time

Paid holidays

Retirement plan

Tuition reimbursement

Employee stock purchase plan

Job summary

Biogen RTP seeks a Sr. Associate I to oversee strategic, tactical, and operational QA activities within the Quality Assurance organization at the RTP facility.

You will coach peers, guide regulatory compliance, support audits, and contribute to Global Quality Systems, ensuring safety, efficacy and product quality across manufacturing, QC, engineering and validation teams.

Qualifications

• Bachelor’s Degree required in life science or related field.
• Minimum 4 years of quality experience in GMP pharmaceutical/biotech manufacturing.
• Experience reviewing and approving batch records.
• Experience conducting investigations reported to quality management/regulatory bodies.
• Advanced understanding of global quality systems, GxP, and regulatory requirements.

Responsibilities

• Batch Record Review impacting product disposition for GMP production activities.
• Assess exceptions/investigations and support root-cause analysis.
• Review GMP controlled documents and ensure regulatory compliance.
• Assist QA management in day-to-day Quality Management Systems activities.

Skills

Bachelor degree required

4+ years QA in GMP pharma/biotech

Batch records review

Investigations & CAPA

Global quality systems

GxP regulations

Cross-functional collaboration

Quality management systems

Communication skills

Education

Bachelor’s Degree in Life Science

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.

• 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
• Employee Resource Groups participation

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.

As Biogen recently acquired Apellis, you can find additional open jobs on our Apellis website here.