Novartis Posted July 20, 2026

Process Specialist

İstanbul Kurtköy, Turkey Temporary (Fixed Term)
Manufacturing & CMC

Novartis is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description SummaryYou will have the opportunity to apply your expertise at the frontline of delivering high-quality pharmaceutical products to patients.As a Process Specialist, you will play a central role in Novartis manufacturing operations by:•           Supporting daily production activities•           Solving process-related issues•           Driving continuous improvement initiativesThis position requires close collaboration across multiple functions to:•           Strengthen quality standards, productivity, and compliance•           Contribute to a safe and high-performing operational culture

Major accountabilities: Process Specialist is responsible for the daily management of the production team in shifts and ensures that manufacturing activities are executed safely, efficiently and according to plan, in full compliance with HSE and GMP requirements.This role combines:People managementOperational coordinationQuality oversightContinuous improvementwithin a regulated manufacturing environmentProvide frontline technical support for process-related issues in daily manufacturing operationsSupport the manufacturing team during:New product introductionProcess changesDrive continuous improvement initiatives to enhance quality and productivityEnsure strict adherence to safe and compliant execution of production activities in line with:Production plansGood Manufacturing Practice (GMP)Standard Operating Procedures (SOPs)HSE guidelinesInternal guidelinesCollaborate closely with cross-functional teams to:Manage quality deviationsImplement corrective actionsSupport regulatory inspections and audits, ensuring consistency between manufacturing practices and documentationLead, coach, and motivate the production team during the shift; act as the first point of contact on the shop floorEstablish and monitor clear task allocation, including:Staffing levelsBreak planningAbsence managementShift organizationOversee production quality and documentation, including:Batch record reviewLogbooksAdministrative follow-upSupport management of:DeviationsComplaintsOOS (Out-of-Specification)OOE (Out-of-Expectation)CAPA actionsand collaborate with relevant stakeholders during investigationsEscalate and support resolution of operational or technical issues to ensure production continuityContribute to talent development, including:TrainingCoachingPerformance managementSuccession planningActively contribute to:Continuous improvementEfficiency gainsAudit readinessCross-team collaborationManage Tier-1 meetings with shift operators prepare and distribute shift reports.Provide front line expert support for all process-specific issues to productionKey user responsibilities for all Manufacturing Systems (WERUM PAS-X MES, SAP S4HANA, Serialization (OPTEL) & Aggregation (AGE)Coordinate and ensure the completion of all production operations on time, in accordance with the documentation and in compliance with GMP, SSE and 5S rules Operation Schedule.Key performance indicators: Achieve plant KPIs , (PSP, Volume, BOMA, ROA, On time Compliance Activities, TPT, On Batch Record Review and Deviation Management , POV )Adherence to the production plan, achieving line OAEs and yield targetsAdherence to the GMP and HSE rulesEssential RequirementsMinimum 2 years of relevant experience in a manufacturing environmentTechnical education or equivalent industrial manufacturing experience;Pharmaceutical /Chemical manufacturing processesEquipment used in production5S & Lean Production and Kaizen KnowledgeStrong knowledge of:GMPQuality systemsCompliance requirementsStrong analytical and problem-solving skillsStrong Communication SkillsAbility to work in shifts effectively with diverse teamsGood command of English (for communication and documentation)Ability and willingness to work with English documentationProven experience in:Team coordinationPeople managementPerformance monitoringStrong focus on:QualitySafetyCollaborationSkills: Data AnalyticsDigital skillsGeneral HSE Knowledge  GMP KnowledgeProcess excellenceResilienceLanguages:EnglishTurkish (Local Language)

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
İstanbul Kurtköy, Turkey
Employment type
Temporary (Fixed Term)

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 1527 comparable Manufacturing & CMC roles across 125 biopharma companies.

1527Comparable roles tracked
1434Currently active
125Companies hiring similar roles
44Countries represented

Salary context

456 of 1527 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $540,400 (median $140,000)

Where these roles are based

Top locations among the 1527 comparable roles

United States782
India104
Germany74
Singapore67
France64
Ireland54

+ 38 more countries

Seniority mix

705 of 1527 peers have a known seniority level

Senior251
Manager165
Principal79
Associate68
Director64
Associate Director44
Senior Director21
Intern/Fellow/Postdoc8
Executive/VP5

Therapeutic area mix

7 of 1527 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease6
Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Novartis İstanbul Kurtköy, Turkey
Same function Same country
40%similar
Novartis İstanbul Kurtköy, Turkey
Same function Same country
40%similar
Novartis İstanbul Kurtköy, Turkey
Same function Same country
40%similar
Novartis İstanbul Kurtköy, Turkey
Same function Same country
40%similar
Novartis İstanbul Kurtköy, Turkey
Same function Same country
40%similar
Novartis İstanbul Kurtköy, Turkey Manager
Same function Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Process Documentation Specialist
Novartis · İstanbul Kurtköy, Turkey · Seniority not listed
Function Therapeutic area Seniority Country
40%
Kaplama Operatörü (Geçici)
Novartis · İstanbul Kurtköy, Turkey · Seniority not listed
Function Therapeutic area Seniority Country
40%
Warehouse Management Partner
Roche · Istanbul, İstanbul, Türkiye · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Integrated Bioanalysis Oncology Development
AstraZeneca · Cambridge, Massachusetts, United States of America · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.