Manager, Computer System Quality

Use Your Power for Purpose

This is a permanent individual contributor role within PGS QSEO Transformation providing Quality Authority oversight for Core GMP PGS/ERP computer systems and Artificial Intelligence (AI). This includes PGS/ERP Quality oversight responsibilities for Core computer system validation and life cycle deliverables change control investigations and periodic reviews etc.

This role also provides PGS Quality review and approval for related GMP SOPs and Subject Matter Expert validation guidance to internal customers (e.g. Digital PGS sites) on GMP computer system and ERES compliance including risks standardization CSA approaches and strategies.

What You Will Achieve

PGS Quality Authority review/approval for specific Pfizer GMP Core Digital solution documentation including validation documents change management records GMP investigations and periodic reviews.

Quality guidance and support to the GMP Core computer systems teams on aspects of the systems life cycle as defined by the Pfizer GMP policies and procedures e.g. Risk assessments Validation Plans Strategies Protocols GMP requirements verification testing and Validation summaries including deviations system change controls and periodic reviews.

PGS/ERP Quality review/approval for GMP related Computer System Standard Operating Procedures

Quality expertise and counsel for computer systems validation and use/maintenance of Electronic Records and Electronic Signatures (ERES).

Support regulatory or internal audits related to GMP core computer system compliance as required.

Assist sites as requested to support regulatory inspections or internal audits related to CSV/ERES. This may include review of draft regulatory observation responses and support during the inspection/audit to respond to queries and remediation.

Support the CSSV IMEx program by delivering on defined metrics and KPIs

Partner with Digital stakeholders business SMEs and business Quality as necessary for effective delivery and management of core solutions. (i.e. CSQ Partner)

Participate in the development of PGS Pfizer Quality Standards and Guidelines for computer validation and ERES activities to support PGS needs.

Facilitate cross-site/function discussion forums (e.g. CSV CIG) to share Digital developments best practices and industry trends and to enable site SME input into Pfizer guides and PQSs.

Support Revolution activities related to CSA L2 process

Duties can be adjusted based on the groups requirements and needs.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelors degree with at least 4 years of experience; OR a masters degree with at least 2 years of experience; OR a PhD with 0 years of experience; OR as associates degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience

• Experience of enterprise system validation/compliance/ deployment and intimate knowledge of PGS Revolution CSA process and Pfizer Digital life cycle methodologies (S/ADLC)

• Demonstrated experience with computer system validation lifecycle processes and regulations

• Knowledge of Computer System Quality regulations (e.g. 21 CFR part 11 EU Annex 11 Data Integrity guidance CSA) and GAMP5

• Basic understanding of data analytics statistics and Artificial Intelligence.

• Excellent communication skills with the ability to build relationships influence outcomes and to deliver effective viewpoints or presentations to a variety of audiences.

• Command of the English language

• Be self-motivated and flexible with the ability to work effectively in a dynamic problem-solving environment.

• Ability to work within tight timeframes and respond to changing requirements.

• Ability to interact comfortably with all levels of management and colleagues.

• Ability to work independently and manage multiple projects simultaneously

• Competency in MS Office and other tools (e.g. MS Project)

Bonus Points If You Have (Preferred Requirements)

• Involvement in industry discussion forums on CSV-related topics

• Experience of interacting with auditors and inspectors

• Good understanding of Quality Management System regulations and Pfizer Quality Standards

• Experience of Data science/engineering
  
  
  PHYSICAL/MENTAL REQUIREMENTS
  Normal office work environment. Potential extended periods of sitting.
  
  NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
  Minimal travel (less than 10%)
  
  Work Location Assignment:Hybrid

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.

To learn more about acceptable and prohibited uses of AI during the recruitment process please review our candidate AI-use guidelines available onPfizer Careers.