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Perform QA oversight and documentation review in a GMP biopharmaceutical manufacturing environment including batch records, raw materials, deviations, and audits. | Requires BS in scientific field with 7+ years industry experience including 4-6+ years in GMP biopharmaceutical operations and quality, plus familiarity with electronic quality management systems and clinical manufacturing. | Job Title: Senior Associate, Quality Assurance Location: Bothell, WA (Onsite) Schedule: 4-day, 10-hour shifts (Wed–Sat or Sun–Wed) Summary: The Senior Associate, Quality Assurance is responsible for performing routine QA activities that support ongoing manufacturing operations at a clinical and commercial manufacturing facility. This onsite role provides direct QA oversight, batch record review, raw material disposition, and support for investigations, change controls, and continuous improvement efforts. Key Responsibilities • Review and approve executed electronic batch records, comments, and discrepancies. • Review test results and perform LIMS review steps to issue Certificates of Analysis (as applicable). • Provide QA support on the manufacturing floor, including cleanroom operations. • Act as a QA point of contact for escalations, troubleshooting, and process support. • Perform hands-on QA activities such as patient apheresis intake and drug product pack-out. • Compile, review, and approve lot disposition documentation. • Conduct raw material disposition and approve raw material specifications. • Review and approve Deviations, CAPAs, Change Controls, Excursions, and Nonconformance records. • Support process/method qualifications and validation activities through QA review of protocols, data, and reports. • Participate in internal audits and operational excellence initiatives. • Promote a strong culture of safety, compliance, and continuous improvement. Qualifications • BS degree in a relevant scientific field (biochemistry, bioengineering, chemical engineering, etc.) with 7+ years of industry experience. • 4–6+ years in GMP biopharmaceutical operations, including 2+ years in GMP Quality. • Experience with electronic quality management systems (deviations, CAPAs, change controls). • Experience in clinical and cGMP manufacturing environments. • Familiarity with cellular therapy and/or lentiviral vector manufacturing preferred. • Strong analytical, communication, and cross-functional collaboration skills. • Ability to prioritize, meet deadlines, and adapt in a fast-paced, start-up environment. • Proficiency with digital GMP platforms.

Lead client account management, media strategy, team supervision, content development, budget oversight, and new business growth in healthcare PR. | Bachelor’s degree in communications or related field, 4-5 years of healthcare PR experience, strong writing and editing skills, project and budget management, and proficiency with Microsoft Office and social media. | My client is a boutique healthcare and life sciences PR agency on a mission to make a meaningful impact. Their work helps amplify vital disease awareness, communicate cutting-edge research, and support life-changing healthcare solutions. You'll join a smart, mission-driven team that values collaboration, accountability, and the power of great storytelling to inspire change. As Account Supervisor, you’ll play a lead role in managing client accounts for some of the world’s most recognized healthcare brands. You’ll guide junior staff, act as the primary client contact, and deliver strategic counsel that drives results. Responsibilities: Client & Account Management • Serve as day-to-day client contact, ensuring strategic alignment and timely execution • Develop and execute media strategies and communications plans • Maintain deep knowledge of client products, industry landscape, and competitive environment • Oversee reporting systems and ensure high-quality service delivery Media Strategy & Execution • Lead media outreach efforts, including creative pitch development and targeting • Cultivate relationships with key media contacts • Strategize use of traditional and digital media tools for maximum visibility • Ensure campaign results are effectively showcased Team Leadership • Supervise junior staff, offering feedback, mentorship, and project oversight • Assign responsibilities thoughtfully and model strong work ethic • Address performance issues with clarity and collaboration Writing & Content Development • Produce polished, strategic written materials: press releases, pitches, backgrounders, etc. • Incorporate feedback and maintain high editorial standards Budget & Fiscal Oversight • Develop estimates and monitor budgets for accuracy and efficiency • Manage invoicing processes and support client financial planning New Business & Agency Growth • Identify potential leads and support proposal development • Conduct research to shape new business strategy and presentation content Qualifications • Bachelor’s degree in communications, public relations, journalism, or related field • 4–5 years of relevant PR/communications experience, ideally with a healthcare focus • Strong writing and editing skills with keen attention to detail • Experience managing projects, junior staff, and budgets • Proficiency in Microsoft Office and knowledge of social/digital platforms Apply below or get in touch directly to learn more!