About AniLocus
Founded in June 2021, AniLocus has rapidly emerged as a growing biotech startup that specializes in utilizing innovative technology to support the research and development of better, safer therapeutics for the most important people in the world: patients.
Our Guiding Principles
- Exemplary Research Services: We deliver top-tier research services that surpass industry standards, ensuring impactful and dependable results.
- Integrity in Research: Our foundation is built on integrity; we maintain transparency and rigorous standards in all our endeavors.
- Employee-Centric Philosophy: We prioritize the well-being, professional growth, and job satisfaction of our employees, fostering a collaborative and inclusive work environment.
- Sustained Growth: We continually seek innovative growth opportunities, propelling our company and team members towards new frontiers.
Your Career at AniLocus
- Innovative Culture: We embrace creative and critical thinking, fostering an environment that thrives on tackling complex challenges.
- Pioneering Research: Your work will directly impact the future of biotechnology, contributing to transformative therapeutic developments.
- Professional Advancement: We are committed to your continuous learning and career progression, offering extensive opportunities for skill enhancement.
Job Overview
As the Quality Control (QC) Manager at AniLocus, you will play a critical role in ensuring the highest standards of quality and compliance across all stages of our preclinical research operations. You will be responsible for developing, implementing, and managing quality control processes and procedures to ensure the integrity and reliability of our data and services. Your expertise will help us maintain regulatory compliance, enhance operational efficiency, and drive continuous improvement in our research and development activities.
Responsibilities
- Develop, implement, and maintain quality control protocols and procedures to ensure compliance with GLP (Good Laboratory Practice) and other regulatory standards.
- Conduct regular audits and inspections of laboratory processes, equipment, and documentation to ensure adherence to quality standards.
- Review and approve study protocols, data, and reports to ensure accuracy, consistency, and compliance with regulatory requirements.
- Train and mentor laboratory staff on quality control procedures, regulatory compliance, and best practices.
- Investigate and resolve any quality-related issues or deviations, implementing corrective and preventive actions as necessary.
- Collaborate with the R&D, Operations, and Regulatory teams to ensure seamless integration of quality control processes into all aspects of our research activities.
- Prepare and present quality control reports to senior management, clients, and regulatory agencies as required.
- Stay up-to-date with industry trends, regulatory changes, and advancements in quality control methodologies.
Skills & Qualifications
- Associate’s Degree, Bachelor’s Degree, Master’s, or PhD in a Biology, Biotechnology, Biomedical Engineering, or relevant field or Certification in Quality Control (e.g., ASQ Certified Quality Technician (CQT)).
- Proven experience in a quality control or quality assurance role within a biotech, pharmaceutical, or similar industry.
- Strong understanding of regulatory requirements and quality standards.
- Excellent analytical and problem-solving skills.
- Detail-oriented with a commitment to maintaining high-quality standards.
- Strong communication and interpersonal skills.
Preferred Qualifications:
- Experience with GLP (Good Laboratory Practice) and GMP (Good Manufacturing Practice) environments.
- Familiarity with quality control software and tools.
Working Conditions:
- This position can be performed remotely, with occasional on-site requirements based on business needs.
- Flexible working hours may be required to accommodate different time zones and executive schedules.
Salary and Benefits
- Salary: $28-56 per hour. Negotiable and based on experience, qualifications, and market rates for Germantown, Maryland.
- Work Schedule: Part-time, 20-30 hours/week.
- Work Environment: Remote
- Commuter Benefits: We provide commuter benefits (up to $200 per month).
- Professional Development: Opportunities for professional growth and advancement in a cutting-edge research environment.
How to Apply
If you are passionate about advancing pharmaceutical research and meet the qualifications outlined above, please submit your resume and cover letter through our online application portal. Please note, positions will remain open until they are filled.
AniLocus is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
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