BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
This position is based in Hopewell, NJ. Supports QA manufacturing activities with strong focus in QC Microbiology. Support for Biochemistry and the analytical chemistry department may also be required. Candidate will ensure the successful day-to-day management of reviewing and approving GMP paperwork including logbooks, analytical raw data, Environmental Monitoring reports, and other ancillary documentation that support GMP Manufacturing. Candidate will also provide QA oversight of OOS and deviations pertaining to samples from Production, Environmental Monitoring and WFI systems. Will be responsible for leading GEMBA walks on a routine basis to ensure day-to-day compliance and to ensure the laboratory and facility are always inspection ready.
Works to support QA objectives whilst adhering to regulatory compliance and achieving business success. Creates and/or reviews SOPs needed to support the business. Conducts internal GMP inspections and will support Health Authority audits.
Essential Functions of the Job:
Implementing and monitoring all Quality Assurance activities in QC Microbiological laboratories and facility/utility space to ensure compliance with FDA/EU regulations, covering cGMP for commercial medicinal products and clinical material for human use.
Ensuring the QA Compliance of departmental SOPs (writing & revising), ensuring regulatory compliance in conjunction with being ‘fit for purpose’ operationally and commercially.
Knowledgeable in cGMPs: 21 CFR Parts 11, 210, 211, and 600, EU Annex 1.
Demonstrated expertise with ERP systems and lab data acquisition systems such as: Empower, Maximo, Veeva, LIMS, MODA, and SAP.
Ensuring all activities are performed in accordance with GMPs, SOPs and Health and Safety policies.
Awareness of USP/EP, ICH Guidelines, Annex 1, and QC methodology updates to ensure compliance with current testing and specifications.
Ensuring appropriate escalation and follow up for non-conformities within Laboratories and Utility areas and issuing deviations when appropriate.
Ensuring that the Quality department meets or improves key performance indicators (KPIs).
Undertaking any other duties for any department within the business, which may be requested by QA Management, for which training and/or an explanation has been provided and understood.
Perform other duties as assigned
Supervisory Responsibilities:
None
Computer Skills:
Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint, MS Project).
Required Education/Experience:
A bachelor’s degree in: Biology, Chemistry, Biochemistry, or engineering, or other life science degree is required. Advance degree is preferred but not required.
4+ years of QA experience is required. Strong preference for significant prior QC experience.
Experience with writing/reviewing deviations, Environmental Monitoring data/trends, aseptic technique, technical writing, clean room gowning
Must have worked previously in the Biotechnology area of pharmaceuticals.
Travel: 10% Travel may be required.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.