Pfizer

pharmaceutical

OperationsSpecialist(Contractor)

Turkey FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Operations Specialist (Contractor) at Pfizer. Skills: managing quality events, process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. managing quality events across Pfizer’s commercial operations. ensuring timely, compliant, and high-quality execution in line with global quality standards”

What You'll Achieve.

ensuring timely, compliant, and high-quality execution in line with global quality standards; ensure its accurate application and compliance; ensure deliveries are completed on time, even in challenging situations

Industry & Context.

pharmaceutical
Problems you'll solve

root cause analysis (RCA)

What They're Looking For.

Must Have

Excellent written and spoken English, including technical writing, is mandatory, Ability to work effectively, under strict timelines and SLA commitments, Proven follow-up discipline and resilience when working with internal and external stakeholders, Ability to challenge, influence, and drive compliance in a professional and fact-based manner, organizational skills and ability to manage multiple quality events in parallel, Comfortable working in a global, multicultural environment, Self-motivated, Good communication and interpersonal skills

Nice to Have

1 year + experience in audit, compliance, or quality operations, in a regulated environment, Background in pharmaceutical or other life sciences preferable though not essential, A service-oriented and compliance-focused mindset, High level of attention to detail and documentation accuracy

What You'll Do.

managing quality events across Pfizer’s commercial operations

and high-quality execution in line with global quality standards

manage end-to-end cases

root cause analysis (RCA)

development of remedial measures

stakeholder alignment and follow- up through completion

Review and manage cases within defined scope

compliant documentation

impact assessments and CAPA descriptions and follow up records

Follow up with internal stakeholders and vendors

Actively track timelines

and ensure adherence to SLAs

Support remediation efforts for audit findings

Maintain high-quality documentation aligned with predefined standards

Proactively identify recurring issues and improvement opportunities

Support continuous improvement of processes in scope

How You'll Work.

Team & Collaboration

cross-functional coordination; stakeholder alignment; working closely with internal stakeholders, and vendor partners across regions; Follow up with internal stakeholders and vendors

Communication Scope

written and verbal English; Good communication and interpersonal skills; technical writing

Process & Methodology

resource planning, manage multiple quality events in parallel

Full Job Description

We believe that our people are our most valued resource and the foundation of our success. Why don’t you start your career in a multinational and challenging work environment in the pharmaceutical sector? We invite you to Pfizer for our new organizational structure in Global Operations Services Center (GOSC) which delivers services to Europe, AfME, LATAM, NA and APAC from Pfizer Türkiye. We are hiring Operations Specialists who will be accountable to managing quality events across Pfizer’s commercial operations, ensuring timely, compliant, and high-quality execution in line with global quality standards. **Role Purpose** The Operations Specialist will manage end-to-end cases, including review, documentation, root cause analysis (RCA), development of remedial measures, stakeholder alignment and follow- up through completion. The role requires strong written and verbal English, high attention to detail, persistence in stakeholder follow up, and the ability to drive compliance within strict timelines. This is a high-visibility role working closely with internal stakeholders, and vendor partners across regions. **We are looking for:** * Preferably 1 year + experience in audit, compliance, or quality operations, in a regulated environment * Background in pharmaceutical or other life sciences preferable though not essential * A service-oriented and compliance-focused mindset * High level of attention to detail and documentation accuracy * Ability to work effectively, under strict timelines and SLA commitments * Proven follow-up discipline and resilience when working with internal and external stakeholders * Ability to challenge, influence, and drive compliance in a professional and fact-based manner * Strong organizational skills and ability to manage multiple quality events in parallel * Comfortable working in a global, multicultural environment * Self-motivated * Good communication and interpersonal skills * Excellent written and spoken English, including technical writ

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