About the Company
Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop, and deliver innovative medicines that help patients prevail over serious diseases. With a strong commitment to scientific excellence and patient focus, we strive to transform patients’ lives through science and responsible practices.
Job Description
We are seeking a highly motivated and detail-oriented Laboratory Compliance Officer with a strong focus on Quality Assurance and Quality Control to join our team. This is a 100% remote position, allowing you to work from anywhere within the specified region while collaborating with our global teams. The successful candidate will be responsible for ensuring that all laboratory operations, processes, and documentation adhere to internal policies, industry regulations (e.g., GLP, GCP, GMP), and relevant national and international standards. You will play a critical role in maintaining the integrity and quality of our laboratory data and systems, contributing directly to our mission of delivering life-changing medicines.
Key Responsibilities
- Develop, implement, and maintain robust QA/QC programs and compliance strategies for laboratory operations.
- Conduct regular audits and inspections of laboratory facilities, equipment, and processes to identify non-compliance and recommend corrective actions.
- Ensure all laboratory documentation, including SOPs, protocols, and reports, are accurate, complete, and compliant with regulatory requirements.
- Investigate and document deviations, out-of-specifications (OOS) results, and quality incidents, coordinating root cause analyses and CAPA implementation.
- Provide expert guidance and training to laboratory staff on compliance policies, procedures, and best practices.
- Stay updated on evolving regulatory requirements and industry standards, recommending necessary adjustments to internal systems.
- Prepare and submit compliance reports to management and regulatory bodies as required.
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure integrated compliance.
Required Skills
- Bachelor's degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy, Biotechnology).
- Minimum of 3 years of experience in laboratory QA/QC or compliance roles within the pharmaceutical or biotechnology industry.
- In-depth knowledge of GLP, GCP, and GMP regulations and guidelines.
- Proven ability to conduct internal audits and manage CAPA processes.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong written and verbal communication skills.
- Proficiency with laboratory information management systems (LIMS) and quality management systems (QMS).
Preferred Qualifications
- Master's degree or Ph.D. in a relevant scientific field.
- Certification in Quality Assurance (e.g., ASQ Certified Quality Auditor).
- Experience with regulatory submissions and interacting with regulatory agencies.
- Experience in a remote work environment.
Perks & Benefits
- Comprehensive health, dental, and vision insurance.
- 401(k) retirement plan with company match.
- Generous paid time off, including holidays and sick leave.
- Flexible remote work options with home office stipend.
- Professional development and continuing education opportunities.
- Employee assistance programs and wellness initiatives.
- Performance-based bonuses and recognition programs.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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