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Quality Assurance Engineer
- Bend, Oregon, United States
- Bend, Oregon, United States
Über
Successful candidates will understand that effective communication is essential for alignment on strategies and approaches, and correcting deficiencies while maintaining good working relationships. Qualified candidates will have a thorough understanding of current regulations and guidelines such as but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5 is required.
Duties and Responsibilities
Generates and/or supports the generation of risk assessments, user requirements specifications (URS), C&Q plans, change controls, SOPs, CAPAs, and other relevant documents
Supports validation lifecycle activities such as, but not limited to, change management, periodic reviews, and re‑qualification to ensure that qualified systems remain in their validated state
Makes compliance decisions to support commercial operations
Mentors colleagues on the reasons or justifications of the requirements and practices
Drives process improvement initiativesn
Provides support during clients and regulatory audits
Performs other related duties as assigned
Responsibilities may increase in scope to align with company initiatives
Required Skills and Abilities
Understanding of current regulations and guidelines (e.g., 21 CFR Parts 11, 210, and 211, EudraLex Volume 4 - Annex 15, GAMP 5, etc.) and how to apply them to support the validation effort
Technical writing skills to effectively develop procedures, discrepancies, change controls, CAPAs and associated documents needed to support the validation effort
Hands‑on experience with the qualification of facilities, utilities, equipment and/or computerized systems, cleaning or process validation (Experience in at least two of these areas is required)
Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross‑functional team
Strong time‑management skills and the ability to organize and coordinate multiple projects at a time
Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
Ability to prioritize tasks and to keep leadership apprised of performance to timelines
Accepts feedback from a variety of sources and constructively manages conflict
Experience in Oral Solid Dose operations and spray drying is preferable
Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with aptitude to learn new software and systems
Education and Experience
Bachelor’s degree in a science, engineering, or related field
Minimum of 4 years required within pharmaceutical industry, with preference given to those with 5-10 years of experience
Minimum of 4 years of experience performing qualifications and/or validations is required
Physical Requirements
Prolonged periods sitting at a desk and working on a computer
Prolonged periods of mobility between offices and campus buildings
Adheres to consistent and predictable in‑person attendance
Benefits 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.
Level and compensation will be based on experience.
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.
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Sprachkenntnisse
- English
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