QC Analyst

About Atrium

About Atrium:
What you do matters. As a people-centric organization, we foster an environment of collaboration, high performance, and innovation where your talents are valued and your achievements are celebrated. Join us and become part of an inclusive team.

Our client is an established organization in the pharmaceutical/biotech industry focused on maintaining high standards of quality and compliance from development through commercialization. They are now looking for a QC Analyst
.

$40/hr - $50/hr

The QC Analyst supports quality and compliance throughout product development and commercialization. Responsibilities include performing analytical testing, data trending, investigations, and supporting lab operations. The QC Analyst role also involves method transfers, validation, and ensuring project milestones are met to improve QC efficiency.

• Conduct routine and complex analytical tests for raw materials, in-process samples, product release, and stability studies per SOPs.
• Maintain training records, adhere to schedules, and complete assignments on time to support QC goals.
• Assist with lab equipment upkeep, reagent/sample preparation, and inventory management.
• Submit and review data promptly to ensure availability for decision-making.
• Perform operational tasks such as sampling, environmental monitoring, and product testing.
• Update controlled documents to support compliance and continuous improvement.
• Follow internal policies and regulatory standards (e.g., GMP, GLP, ICH).
• Collaborate with QC and cross-functional teams to support quality objectives.
• Engage in ongoing training to enhance QC and regulatory knowledge.
• Support data verification for regulatory submissions and inspection readiness.
• Participate in audits and continuous improvement initiatives.
• Coordinate with Manufacturing, Materials Management, and Quality Assurance teams to meet quality standards.

• 2+ years in a regulated pharmaceutical/biotech lab, Quality Control, or other relevant regulated lab setting.
• Strong attention to detail and ability to manage shifting priorities.
• Effective communication and teamwork skills.

• Experience with data analysis to support QC and regulatory activities.
• Familiarity with LIMS and Microsoft Office tools (especially Excel) is a plus.

• Bachelor's degree in Biology, Chemistry, Biochemistry, or other related field preferred.
• Associate's degree or equivalent certifications in the sciences is also accepted.

• Medical, dental, and vision insurance.
• 401(K) plan.
• Paid holidays and sick time.
• Additional benefits available.

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As a woman-owned firm, we value diversity. We are an equal opportunity and affirmative action employer and will consider all applications without regard to race, sex (including gender, pregnancy, sexual orientation and gender identity), age, color, religion or creed, national origin or ancestry, veteran status, disability (physical or mental), genetic information, citizenship or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Candidates who apply for roles through the Atrium website will be added to our candidate pool and may be considered for additional roles of a similar title. Please contact us to request an accommodation.

EOE/M/F/D/V/SO

Position