Senior QC Validation Engineer - Analytical Methods & GMP Compliance

Publiceringsdatum: 2026-10-01

Har du övervägt att arbeta inom yrken med teknisk inriktning-branschen? En möjlighet har öppnat upp för dig att börja arbeta som civilingenjör, kemi hos HP HALDEN PHARMA AS. HP HALDEN PHARMA AS behöver någon som vill arbeta heltid. Om du är tillgänglig för tills vidare, ta en titt på denna jobbannons.

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Jobbannons

Are you an experienced validation professional looking to work in a highly regulated and advanced pharmaceutical environment?

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.

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.

About the role:

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

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

Key responsibilities:

Lead method transfer, validation, verification and implementation within the QC Chemistry Laboratory

Author, review and approve analytical methods and related documentation

Collaborate with external laboratories, including contract setup and approval of transfer protocols and reports

Prepare and approve key quality documentation (SOPs, protocols, reports, risk assessments, specifications)

Ensure timely implementation of pharmacopeia updates and verification of compendial methods

Support organization within analytical validation field providing scientific and regulatory expertise

Execute change control, handle deviations and drive CAPA processes in line with the Quality Management System

Represent the department in audits and interactions with customers and regulatory authorities

Who we are looking for:

We are looking for someone who combines strong technical expertise with a pragmatic and collaborative mindset.

Qualifications

Bachelor's or master's degree (or equivalent) in Chemistry, Pharmacy, Biotechnology, Microbiology or another related field

Several years of relevant professional experience in analytical method development, optimization, and validation within biotechnology, life sciences, diagnostics, pharmaceuticals, or a related field.

Experience with multiple analytical techniques

Knowledge of USP and Ph. Eur. is an advantage

Familiarity with regulatory guidelines such as ICH Q2 (R2), ICH Q14 and EU GMP Annex 1 are beneficial

Personal qualities:

Structured and quality-focused, with the ability to manage complex tasks

Proactive and solution-oriented, with a drive to deliver results

Strong collaboration skills and ability to work across functions and cultures

Clear and confident communicator in English (written and verbal)

Takes ownership and demonstrates sound judgment within area of expertise

Why join Halden Pharma?

Work in a highly competent and collaborative environment

Being part of a company with advanced manufacturing technologies and strong growth ambitions

Opportunity to influence and shape validation practices in a regulated setting

International work environment with exposure to global customers and partners

About the company

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.