{"id":3887604,"date":"2026-10-02T11:06:28","date_gmt":"2026-10-02T08:06:28","guid":{"rendered":"https:\/\/laura.fi\/vacancies\/company\/senior-qc-validation-engineer-analytical-methods-gmp-compliance\/senior-qc-validation-engineer-analytical-methods-gmp-compliance\/"},"modified":"2026-10-02T17:36:25","modified_gmt":"2026-10-02T14:36:25","slug":"3887604","status":"publish","type":"job_listing","link":"https:\/\/laura.fi\/en\/vacancies\/company\/senior-qc-validation-engineer-analytical-methods-gmp-compliance\/3887604\/","title":{"rendered":"Senior QC Validation Engineer – Analytical Methods & GMP Compliance"},"content":{"rendered":"

Are you an experienced validation professional looking to work in a highly regulated and advanced pharmaceutical environment?<\/p>\n

At Halden Pharma, we are strengthening our QC Validation and Compliance team and are now looking for a Senior Validation Engineer \/ Specialist to play a key role in ensuring quality, compliance, and robustness of our analytical methods.<\/p>\n

This is a unique opportunity to join a specialized pharmaceutical manufacturing company where you will work closely with experts across QC, QA and production – and contribute directly to delivering medicines to patients.<\/p>\n

**About the role:**<\/p>\n

In this position, you will support the team within analytical method validation and play a central role in method transfers, implementation, and lifecycle management.<\/p>\n

You will work in a dynamic environment with a high level of cross-functional collaboration and exposure to both internal stakeholders and external partners.<\/p>\n

**Key responsibilities:**<\/p>\n

– Lead method transfer, validation, verification and implementation within the QC Chemistry Laboratory<\/p>\n

– Author, review and approve analytical methods and related documentation<\/p>\n

– Collaborate with external laboratories, including contract setup and approval of transfer protocols and reports<\/p>\n

– Prepare and approve key quality documentation (SOPs, protocols, reports, risk assessments, specifications)<\/p>\n

– Ensure timely implementation of pharmacopeia updates and verification of compendial methods<\/p>\n

– Support organization within analytical validation field providing scientific and regulatory expertise<\/p>\n

– Execute change control, handle deviations and drive CAPA processes in line with the Quality Management System<\/p>\n

– Represent the department in audits and interactions with customers and regulatory authorities<\/p>\n

**Who we are looking for:**<\/p>\n

We are looking for someone who combines strong technical expertise with a pragmatic and collaborative mindset.<\/p>\n

**Qualifications:**<\/p>\n

– Bachelors or masters degree (or equivalent) in Chemistry, Pharmacy, Biotechnology, Microbiology or another related field<\/p>\n

– Several years of relevant professional experience in analytical method development, optimization, and validation within biotechnology, life sciences, diagnostics, pharmaceuticals, or a related field.<\/p>\n

– Experience with multiple analytical techniques<\/p>\n

– Knowledge of USP and Ph. Eur. is an advantage<\/p>\n

– Familiarity with regulatory guidelines such as ICH Q2 (R2), ICH Q14 and EU GMP Annex 1 are beneficial<\/p>\n

**Personal qualities:**<\/p>\n

– Structured and quality-focused, with the ability to manage complex tasks<\/p>\n

– Proactive and solution-oriented, with a drive to deliver results<\/p>\n

– Strong collaboration skills and ability to work across functions and cultures<\/p>\n

– Clear and confident communicator in English (written and verbal)<\/p>\n

– Takes ownership and demonstrates sound judgment within area of expertise<\/p>\n

**Why join Halden Pharma?**<\/p>\n

– Work in a highly competent and collaborative environment<\/p>\n

– Being part of a company with advanced manufacturing technologies and strong growth ambitions<\/p>\n

– Opportunity to influence and shape validation practices in a regulated setting<\/p>\n

– International work environment with exposure to global customers and partners<\/p>\n

**Om bedriften**<\/p>\n

Halden Pharma is a specialized pharmaceutical manufacturing company with advanced manufacturing technologies and strong growth ambitions. The company operates in a highly regulated and advanced pharmaceutical environment, emphasizing quality, compliance, and robustness in its processes. Halden Pharma fosters a highly competent and collaborative international work environment with exposure to global customers and partners.
\n<\/p>\n

\n
Employment relationship:<\/span>Employment <\/span><\/div>\n
Wage:<\/span>Other <\/span><\/div>\n
Number of positions:<\/span>1<\/span><\/div>\n
Notes for applying:<\/span>Apply here: https:\/\/arbeidsplassen.nav.no\/stillinger\/stilling\/df5fc425-f5a6-4abe-a791-40506b23eab7<\/span><\/div>\n
Source: Job Market Finland\/Ty\u00f6markkinatori<\/div>\n<\/div>\n","protected":false},"author":0,"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false,"_promoted":"","_company_tagline":"","_company_website":"","_company_twitter":"","_company_video":"","_filled":0,"_featured":0,"_remote_position":0,"_job_salary":"","_job_salary_currency":"","_job_salary_unit":""},"job_listing_region":[],"job-categories":[1522],"job-types":[555],"job_listing_tag":[1139],"class_list":["post-3887604","job_listing","type-job_listing","status-publish","hentry","job_listing_type-keikkatyo","job_listing_tag-teollisuus-tuotanto","job_source-tyomarkkinatori","worktime-kokopaivainen","job-type-keikkatyo"],"acf":[],"yoast_head":"\nSenior QC Validation Engineer - Analytical Methods & GMP Compliance - Laura.fi<\/title>\n<meta name=\"description\" content=\"Are you an experienced validation professional looking to work in a highly regulated and advanced pharmaceutical environment? 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