Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted 21 days ago

Senior QC Validation Engineer - Analytical Methods \& GMP Compliance

HP HALDEN PHARMA AS

Where
Norge
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowSenior QC Validation Engineer - Analytical Methods \& GMP ComplianceHP HALDEN PHARMA AS · Norge

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on HP HALDEN PHARMA AS's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

11.4% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.0%1 day
  2. 4.2%3 days
  3. 11.4%7 days
  4. 17.5%14 days
  5. 34.2%30 days
  6. 43.5%60 days
This job: posted 21 days ago

The posting

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

Om bedriften 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.

Posting text belongs to the employer. Removal requests: contact us.

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against HP HALDEN PHARMA AS's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on HP HALDEN PHARMA AS's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    HP HALDEN PHARMA AS's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.