Pharmaceutical Jobs

Submit your resume for Pharmaceutical Jobs

 
Finding a recruitment partner who truly understands pharmaceutical manufacturing and regulated environments is not easy. Too many generalist agencies blur the lines between GMP-critical roles and generic engineering or quality positions, sending unsuitable resumes for non-regulated industries when you need professionals experienced in validated pharma processes.

In pharmaceutical hiring, nuance matters. You need a partner who understands the difference between CSV and CQV, between QA oversight and operational quality, and between process engineering and automation validation - without requiring constant explanation. The right recruitment partner speaks the language of compliance, patient safety, and regulatory scrutiny as fluently as you do.

Key Takeaways:

  • Pharmaceutical jobs require specialist GMP expertise, where validation, documentation, and compliance are critical.
  • Delta V engineer jobs, Automation engineer jobs, Validation engineer jobs, and CQV engineer jobs are essential to compliant drug and biologics manufacturing.
  • QA Engineer jobs pharma, QAV engineer jobs, CSV jobs, and Quality jobs pharma directly protect patient safety and regulatory approval.
  • Drug safety jobs and Pharmacovigilance jobs ensure post-market monitoring and global regulatory reporting.

Pharmaceutical Jobs in Life Sciences

What are life sciences pharmaceutical jobs?
Pharmaceutical jobs in life sciences support the development, manufacture, and delivery of medicines, vaccines, and biologics within highly regulated GMP environments. These roles span engineering, quality, validation, and process disciplines, all working together to ensure products are manufactured safely, consistently, and in full regulatory compliance.

We support hiring for CQV engineer jobs, Qualification engineer jobs, and Process Engineer jobs pharma, ensuring manufacturing systems, equipment, and processes meet GMP and regulatory standards. For post‑market and patient‑focused functions, we recruit experienced professionals into Pharmacovigilance jobs and Drug safety jobs, helping organisations maintain global compliance and product safety.

Role Contract Rate (UK/EU) Permanent Salary (UK) Permanent Salary (US)
QA Engineer (Pharma) £45-£60 p/h £45,000 - £60,000 $80,000 - $110,000
Validation/ CSV Engineer  £50 - £75 p/h £50,000 - £75,000 $95,000 - $130,000
CQV Engineer £55 - £85 p/h £60,000 - £85,000 $105,000 - $145,000
Process Engineer (Pharma) £50 - £80 p/h £55,000 - £80,000 $100,000 - $140,000

Experience in pharma and life sciences typically involves working in GMP‑regulated environments where quality, documentation, and compliance are essential. Whether in quality, validation, CQV, process engineering, automation, or drug safety, employers want people who understand regulated manufacturing, can produce clear technical documentation, and appreciate how their work affects product quality and patient safety. Strong communication, attention to detail, and teamwork are just as important as technical expertise.

How to secure a Pharmaceutical Job

  • Highlight any experience working in GMP‑regulated environments, including documentation, compliance, or manufacturing support.
  • Make sure your resume demonstrates involvement in quality, validation, engineering, process, or safety‑related activities.
  • Consider completing industry‑recognised training or certifications to strengthen your credibility in regulated life sciences environments.
  • Focus your job search on pharmaceutical and biotech hubs where demand for skilled professionals is highest and opportunities are more diverse.

Frequently Asked Questions

Do I need specific qualifications to work in pharmaceuticals?

Most roles require relevant life sciences training and basic GMP knowledge. Additional certifications can help you stand out.

What experience is essential for pharmaceutical jobs?

Hands‑on work in a GMP‑regulated environment and familiarity with compliance and documentation processes are key.

Are pharmaceutical jobs remote?

Some roles—like regulatory or pharmacovigilance—can be remote or hybrid. Most engineering and manufacturing roles require on‑site work.

What technical skills are most useful?

GMP understanding, documentation skills, validation basics, and experience with regulated systems or equipment.

 

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