Quality Assurance Associate II​/III

Serán Bio Science is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential tasks include reviewing and approving production records, analytical data, and internal QA documentation.

Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience.

Serán Bio Science develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting.

Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.

• Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
• Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas
• Initiates and oversees investigations
• Manages corrective and preventive actions (CAPA)
• Supports internal audits, client audits and regulatory inspections, with the potential to host
• Manages controlled document issuance and archival
• Performs quality reviews with minimal oversight
• Communicates quality-related information to internal teams with minimal guidance
• Responsibilities may increase in scope to align with company initiatives
• Performs all other related duties as assigned

• Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required
• Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices
• Excellent organizational skills and attention to detail
• Excellent time management skills with a proven ability to meet deadlines
• Strong analytical and problem-solving skills
• Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
• Demonstrates the ability to collaborate and work in cross-functional teams
• Accepts feedback from a variety of sources and constructively manages conflict
• Ability to prioritize tasks and to delegate them when appropriate
• Excellent verbal and written communication skills
• Ability to function well in a high‑paced and at times stressful environment
• Proficient with Microsoft Office Suite or related software
• Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions

• Bachelor’s degree, preferably in a scientific discipline
• 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II
• 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III
• Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred

• Prolonged periods of sitting or standing at a desk and working on a computer
• Must be able to lift up to 15 pounds at times
• Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
• Adheres to consistent and predictable in‑person attendance

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