CMC Quality Control Analyst

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          "text": "<p>We are seeking a motivated Scientist to join our CMC Quality Control team supporting daily analytical testing. This role will focus on preparing buffers and media, maintaining cell cultures, managing lab inventory, logging and shipping samples, and performing analytical testing. The position collaborates closely with Technical Operations, Quality Assurance, and internal/external QC teams to support advancement of preclinical gene editing programs.</p><ul><li>Prepare buffers and media to support testing.</li><li>Maintain cells, perform cell culture, and manage cell testing.</li><li>Identify key consumables and supplies within the QC Lab and maintain stock as needed.</li><li>Log incoming samples.</li><li>Ship samples, controls, and reference standards to third-party organizations.</li><li>Perform analytical testing of release and stability samples.&#xa0;</li><li>Maintain lab housekeeping program.</li></ul>",
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          "text": "<p><strong>Minimum Required Qualifications:</strong></p><ul><li>B.S. in Chemistry, Biology, or a related field with 3–4 years of relevant experience.</li><li>Proficiency in mammalian cell culture and cell-based functional assays (ELISA and dPCR required; NGS experience a plus).</li><li>Experience with Good Documentation Practices and electronic lab notebooks (ELN).</li><li>Ability to execute routine testing, follow SOPs, maintain accurate records, and adhere to company policies.</li><li>Strong attention to detail with the ability to critically analyze data and reports.</li><li>Knowledge of GxP principles (hands-on GxP experience preferred).</li><li>Proactive mindset with strong ownership and follow-through.</li><li>Excellent time management and multitasking skills.</li><li>Ability to work independently and collaboratively in a cross-functional environment.</li><li>Effective written and verbal communication skills.</li></ul><p><strong>Preferred Qualifications:</strong></p><ul><li>Experience with LIMS and data management systems.</li><li>Experience authoring, reviewing, and approving documents in electronic document management systems.</li><li>Working knowledge of ICH guidelines, FDA/EMA regulations, and cGMP documentation practices.</li><li>Authorization to work in the United States without restriction or sponsorship.</li></ul>",
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          "text": "<p>The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.</p><p>Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.</p><p><strong>Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!</strong></p>",
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          "text": "<p><u><strong>What to Expect in the Hiring Process:&#xa0;</strong></u></p><ul><li>10-15 Minute Phone Interview with Region Recruiter</li><li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li><li>30 Minute In-Person Onsite Meeting with the Team</li></ul><p><u><strong>Additional Details:&#xa0;</strong></u></p><p>The position is&#xa0;<strong>Full Time, Monday-Friday, 8am-5pm.&#xa0;</strong>Candidates currently living within a commutable distance of&#xa0;<strong>Boston, MA&#xa0;</strong>are encouraged to apply.</p><p><u><strong>Excellent full-time benefits include:</strong></u></p><ul><li>Comprehensive medical coverage, dental, and vision options</li><li>Life and disability insurance</li><li>401(k) with company match</li><li>Paid vacation and holidays</li><li>Annual rate is between $36.00-$40.00, depending on education and experience&#xa0;</li></ul><div sr-tagline=\"\"></div><p><strong>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p>",
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