AbbVie Pharmacyclics Senior IT Compliance Manager in Sunnyvale, California
Senior IT Compliance Manager
Location: Sunnyvale, CA
# of Openings: 1
Pharmacyclics is committed to the development and commercialization of novel therapies intended to improve the quality and duration of life and to resolve serious unmet medical needs for cancer patients. Pharmacyclics is a wholly-owned subsidiary of AbbVie (NYSE:ABBV), a global, research-based biopharmaceutical company. Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products and a pipeline containing multiple promising new molecules that are being studied in more than 200 clinical trials for over 20 different types of cancer.
More than 1,200 Pharmacyclics and AbbVie research scientists, clinicians, marketing, operations and corporate professionals work in the San Francisco Bay Area. They combine their expertise in immuno-oncology, stem cells, and cell-signaling with their knowledge of bispecific antibodies, antibody-drug conjugates (ADCs), and covalent-inhibitor technologies to discover and develop novel cancer treatments. Together, we are striving to outsmart cancer.
General Position Summary/Purpose:
The Senior IT Compliance Manager will be responsible for driving ongoing Compliance of Quality and IT Systems, Audit Remediation, and supporting various IT client organization including but not limited to Manufacturing, Regulatory, Quality Control, and R&D business units. Collaborate with the leadership of the Pharmacyclics IT compliance programs to ensure proper fulfillment with company-wide IT compliance obligations, including 21 CFR Part 11, HIPAA, PCI, SSAE18, GDPR or other federal or state and international regulations as identified. The individual will provide support to ensure IT Change management, CAPA, Deviations, training and SOP and IT systems reviews are conducted in accordance with established policies and procedures. In addition, the individual will have hands on experience in driving Internal and External audit exercise.
Key Accountabilities / Core Job Responsibilities:
Provide oversight and collaboration in policy development, management and enforcement of approved policies, procedures, and governance of IT Compliance (GXP, SOX and Security) programs.
Provide guidance and oversight in the development and maintenance of policies, procedures, and other guidance documents that provide compliance to internal and external IT controls.
Work as part of IT compliance groupto support operational change control process and provide oversight and compliance approvals of project deliverables; IT change requests and IT issue reports.
Track and ensure completion of Audit and Inspection related findings are completed on time
Provide guidance in development and maintenance of assessment programs for IT process, people, and procedures.
Collaborate with other stakeholders to conduct IT vendor/supplier audits and adherence to company policies and procedures
Provide management oversight for managed services vendor staff working on IT Compliance and operational activities.
Qualifications and Requirements:
BS/MS Degree in Computer Science, Information Technology, or related discipline with 8 years post-graduation work experience.
10+ years of pharmaceutical regulatory, audit and IT compliance experience.
Excellent communication and documentation skills with strong attention to detail and well organized.
Strong knowledge of information security governance, risk, and IT Controls compliance program,
Deep understanding of regulatory requirements in technologically progressive Biotechnology, Pharmaceutical FDA and or SOX regulated IT environments.
Experience with conducting risk assessment and knowledge of current industry good practice for risk assessment methodologies and tools, e.g., GAMP, NIST, ICH Q9)
Proven people management experience, including managing of virtual and managed service partners and teams.
Demonstrated leadership skills with ability to work and communicate effectively with Senior ITLT and executive levels
Demonstrated strong knowledge of FDA, SOX audit procedures and IT Quality system validation best practices.
Certification in one or more of the following areas is a plus: CQA, CMQ/QE, CISA, CISM, CRISC etc.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled