QA Analyst

PSC Biotech; Nebraska; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical premiums paid

Dental premiums paid

Vision premiums paid

401(k) matching

PTO and holidays

Education assistance

Pet Insurance

Fitness perks

Discounts

Job summary

PSC Biotech is seeking a QA Analyst to support QA in a GMP-regulated sterile manufacturing environment, focusing on documentation compliance and quality oversight. You will review records, support deviations and CAPAs, and help ensure manufacturing activities meet quality requirements.

You will collaborate with Manufacturing, QC, Engineering, Validation, and other teams to maintain inspection readiness and promote product quality across the facility.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 2+ years in GMP-regulated pharma/biotech manufacturing.
• Knowledge of GMP documentation and deviations/CAPAs.
• Experience with sterile manufacturing operations.

Responsibilities

• Review batch records, logbooks, and GMP documentation for accuracy, completeness, and compliance.
• Provide routine QA oversight of sterile manufacturing and supporting operations.
• Initiate and support deviations, investigations, CAPAs, and change controls.
• Support root cause analyses, impact assessments, and quality risk assessments.
• Review and approve GMP documentation within assigned level of authority.
• Provide QA support for aseptic processing and contamination-control activities.
• Support environmental monitoring, APS/media fills, and sterilization activities.
• Support qualification and validation activities to ensure compliance with applicable quality requirements.
• Identify, document, and escalation potential GMP, product quality, and compliance concerns.
• Support internal audits, customer audits, and regulatory inspection readiness activities.
• Collaborate cross-functionally with Manufacturing, QC, Engineering, Validation, Warehouse, and other departments to address quality and compliance needs.

Skills

GMP knowledge

Quality systems

Attention to detail

Education

Bachelor's degree in Life Sciences

Job description

York, United States | Posted on 10/12/2026

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services. From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team’s expertise to create a process design for our clients’ products that best suits their needs.

The Experience

With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered a compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At BioTechnique, it’s about more than just a job—it’s about your career and your future.

Your Role

The QA Analyst supports Quality Assurance activities within a GMP-regulated manufacturing environment, with a focus on sterile manufacturing operations and documentation compliance. This role provides routine QA oversight, reviews and approves GMP documentation, supports quality investigations and risk assessments, and helps ensure manufacturing activities meet established quality and compliance requirements. The QA Analyst works cross-functionally with Manufacturing, Quality Control, Engineering, Validation, Warehouse, and other teams to maintain inspection readiness and promote product quality.

• Review batch records, logbooks, and other GMP documentation for accuracy, completeness, and compliance.
• Provide routine Quality Assurance oversight of sterile manufacturing and supporting operations.
• Initiate and support deviations, investigations, Corrective and Preventive Actions (CAPAs), and change controls.
• Support root cause analyses, impact assessments, and quality risk assessments.
• Review and approve GMP documentation within assigned level of authority.
• Provide QA support for aseptic processing and contamination-control activities.
• Support environmental monitoring, aseptic process simulations (APS)/media fills, and sterilization activities.
• Support qualification and validation activities to ensure compliance with applicable quality requirements.
• Identify, document, and escalation potential GMP, product quality, and compliance concerns.
• Support internal audits, customer audits, and regulatory inspection readiness activities.
• Collaborate cross-functionally with Manufacturing, QC, Engineering, Validation, Warehouse, and other departments to address quality and compliance needs.

Requirements

• Bachelor’s degree in Life Sciences, Biology, Chemistry, Engineering, Quality, or a related technical discipline.
• 2+ years Experience working in a GMP-regulated pharmaceutical, biopharmaceutical, biotechnology, or related manufacturing environment.
• Knowledge of GMP requirements and quality systems within a regulated manufacturing setting.
• Familiarity with deviations, investigations, CAPAs, change controls, and quality risk management.
• Understanding of batch record and GMP documentation review practices.
• Familiarity with sterile or aseptic manufacturing operations, environmental monitoring, APS/media fills, sterilization, and contamination control.
• Ability to identify and appropriately escalation quality and compliance concerns.
• Strong attention to detail, organizational skills, and written and verbal communication skills.
• Ability to collaborate effectively across Quality, Manufacturing, Engineering, Validation, QC, Warehouse, and other functional groups.

Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.

• Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
• Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more
• 401(k) and 401(k) matching
• PTO, Sick Time, and Paid Holidays
• Education Assistance
• Pet Insurance
• Fitness Perks and Discounted Rates
• Financial Perks and Discounts

Equal Opportunity Employment Statement

BioTechnique is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.