Neurotech Pharmaceuticals, Inc.

Quality Control Sample Management Analyst

CUMBERLAND, RIPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Neurotech Pharmaceuticals, Inc.

  • Job overview

    The Quality Control Sample Management Analyst role at Neurotech Pharmaceuticals involves managing sample operations to support Quality Control in a biopharmaceutical setting, ensuring compliance and contributing to drug development for retinal diseases.

  • Responsibilities and impact

    The analyst will handle sample receipt, labeling, submission for testing, visual inspections, reagent management, contract lab coordination, inventory management, SOP revisions, and maintain lab organization while collaborating with multiple teams.

  • Compensation and benefits

    The position offers competitive compensation, health benefits through Blue Cross BlueShield and HealthEquity including FSA, HSA & HRA, a 401(k) with company match, generous vacation and holidays, and coverage of 75% of the annual medical plan deductible.

  • Experience and skills

    Candidates should have a bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences or related field preferred, with 1+ years lab experience, preferably in Quality Control within a cGMP pharmaceutical environment, plus strong communication and attention to detail.

  • Career development

    The role encourages learning and development, supporting growth within a dynamic biopharmaceutical company focused on innovative therapies.

  • Work environment and culture

    Neurotech fosters a collaborative, fast-paced environment valuing teamwork, initiative, and adaptability, with a commitment to equal opportunity and diversity.

  • Company information

    Neurotech Pharmaceuticals is a 20+ year innovative biopharmaceutical company specializing in Encapsulated Cell Technology to treat chronic retinal diseases, with locations in Cumberland, RI and Needham, MA.

  • Team overview

    The analyst will work closely with Quality Control, Supply Chain, and Manufacturing teams, supporting cross-functional collaboration in a laboratory setting.

  • Job location and travel

    This is an on-site position located in Cumberland, RI with no remote or hybrid options.

  • Application process

    Applications are accepted through the Neurotech Career Center; unsolicited resumes are not accepted and no placement fees are paid for such submissions.

  • Unique job features

    The job features working with cutting-edge drug delivery technology for rare retinal diseases and offers significant medical benefit coverage and a strong company culture focused on innovation and employee support.

Company overview

Neurotech Pharmaceuticals, Inc. specializes in developing innovative therapies for chronic eye diseases using its proprietary Encapsulated Cell Therapy (ECT) platform. The company generates revenue through the research, development, and commercialization of its unique biopharmaceutical products. Founded in 2000, Neurotech has made significant strides in ophthalmology, particularly in treating macular telangiectasia and other retinal disorders. Their groundbreaking work has positioned them as a leader in the biotech industry, with a strong focus on improving patient outcomes through cutting-edge technology.

How to land this job

  • Position your resume to highlight your experience with laboratory sample management, especially within Quality Control environments, emphasizing your adherence to Good Documentation Practices (GDP).

  • Focus on showcasing your communication skills and ability to collaborate effectively with Manufacturing, Engineering, and Quality Control teams, as these are key to the role at Neurotech Pharmaceuticals.

  • Apply through multiple channels including the Neurotech Pharmaceuticals corporate career site and LinkedIn to maximize your application’s reach and visibility.

  • Connect with current employees in the Quality Control or Laboratory divisions at Neurotech Pharmaceuticals on LinkedIn, using ice breakers such as commenting on the company’s innovative Encapsulated Cell Technology or asking about their experience working in a fast-paced biotech environment.

  • Optimize your resume for ATS by incorporating keywords from the job description like 'sample management,' 'Good Documentation Practices,' 'laboratory reagent management,' 'contract laboratory coordination,' and 'cGMP pharmaceutical environment' to ensure it passes automated screenings.

  • Utilize Jennie Johnson's Power Apply feature to automate applying through multiple platforms, tailor your resume with relevant keywords, and identify LinkedIn contacts to network with, enabling you to focus your energy on interview preparation and skill development.

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