Quality Assurance Associate II/III

Serán BioScience 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 task 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 BioScience 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. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon. Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Benefits Summary: Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance. The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701 Duties and Responsibilities Participates in internal and third-party audits. Supports client audits and regulatory inspections Supports company’s supplier quality program Assists in the oversight and implementation of continuous improvement of the company’s Quality systems Supports the risk management program and conducts risk assessments Document authorship, review, and approval of SOPs, reports, and quality records. Other related duties as assigned Required Skills and Abilities Knowledge of GMP and FDA regulations for drug manufacturing (21CFR 210-211) Excellent verbal and written communication skills Excellent time management skills with a proven ability to meet deadlines Excellent organizational skills and attention to detail Demonstrated ability to collaborate and work in cross-functional teams Scientific curiosity and willingness to learn Strong analytical and problem-solving skills Ability to prioritize tasks and to delegate them when appropriate Education and Experience Minimum of a Bachelor's Degree, preferably in a scientific discipline 3+ years previous manufacturing, quality control, or quality assurance experience Working knowledge of Veeva preferred Physical Requirements 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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      "text": "Duties and Responsibilities ",
      "content": "\n<li>Participates in internal and third-party audits.</li>\n<li>Supports client audits and regulatory inspections</li>\n<li>Supports company’s supplier quality program</li>\n<li>Assists in the oversight and implementation of continuous improvement of the company’s Quality systems&nbsp;</li>\n<li>Supports the risk management program and conducts risk assessments</li>\n<li>Document authorship, review, and approval of SOPs, reports, and quality records.</li>\n<li>Other related duties as assigned&nbsp;</li>\n"
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