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🟢 Actively Hiring · Posted 24d ago ⏳ Closes in 67 days UK Corridor 🛡️ UK Work Eligibility 🏢 Company - Private

HRJOB8543 Quality Assurance Lead

Salary Range
£27,963 - £30,200
£2,330 - £2,517 / mo

Career Integrity & Compliance Audit Report

OP-VERIF-A9291F0A ✓ Passed Inspection

This vacancy has been independently reviewed by the OppaJob Transatlantic Career Intelligence Desk to confirm authentic direct employer recruiting, verify compensation transparency, and eliminate applicant processing fees.

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Corporate Registration Verified UK Companies House registration standing active
✓
Prevailing Wage Benchmark UK National Minimum Wage & Equality Act 2010 aligned
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Zero-Intermediary Direct Pipeline Direct candidate ATS submission. 100% free with zero recruitment charges.
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Corridor Right-to-Work Match UK Work Eligibility

Transatlantic Cost of Living & Purchasing Power Benchmark

Verified Analytics
Location Base
Loughborough, England
Tier-1 UK Economic Zone
Est. Take-Home Pay
68% - 74% (After PAYE & NI)
Single tax filer baseline
Transatlantic Parity
1.0 GBP ≈ $1.28 USD Living Standard
Direct corporate benchmark
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Position Overview & Specifications

Hours: 37.5 hours per week

Salary: Competitive

Ref No: HRJOB8543

Business Unit: Pharma Services

Location: Loughborough, Leicestershire

Open To: Internal and external candidates

Please note this is a re-advertisement, if you have applied for this position within the past 6 months, we will be unable to accept your application at this time

About The Role

Working as part of the Quality Assurance team based in our Charnwood site in Loughborough, you will be responsible for supporting the Quality Management System (QMS) and verifying the adherence of manufactured products for human use, in line with current Good Manufacturing Practice (cGMP).

As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.

About You

To be successful in this role, we’re looking for you to have:

  • Bachelor’s degree (or above) in a scientific (Chemistry, Biology or Pharmacy) or technical (Engineering) discipline (or equivalent)
  • Significant experience in a Quality role within a Pharmaceutical Quality System.
  • Effective communication skills (both written and oral)
  • Proficiency in use of IT applications (Word, Excel, Outlook, Project, PowerPoint etc)
  • Excellent attention to detail
  • Proven ability to work effectively on own initiative as well as effectively contributing to the team environment

The following criteria would also be beneficial to your application, but is not essential:

  • Masters or PhD (or equivalent)
  • Previous experience in writing and producing detailed reports
  • Direct experience in the manufacture of solid oral dosage products
  • Quality Risk Management
  • Root Cause Analysis
  • Lean six sigma trained

Reward

For the successful candidate, we offer an attractive benefits package which includes a competitive salary, a flexible hybrid working model with a degree of home working, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more.

To Apply: Apply online by submitting a CV that details how you meet the essential and desirable criteria

Closing Date: 6 January 2023 at 1700 hours

We reserve the right to close this vacancy early, if we receive sufficient applications for the role. Therefore, if you are interested, please submit your aplication as early as possible.

#LI-CT1

Candidate Selection & Onboarding Process

1

Application & Resume Screening

Submit your tailored CV/Resume directly to the talent acquisition portal.

2

Technical & Competency Interviews

Virtual interviews with the hiring manager and multidisciplinary team.

3

Formal Offer & Benefits Negotiation

Written agreement outlining compensation, equity, retirement vesting, and relocation allowances.

4

Onboarding & Corporate Integration

Equipment provisioning, team orientation, and commencement of duties.

United Kingdom Right to Work & Skilled Worker Visa Guide

Corridor Intelligence

Employment in the United Kingdom requires legal Right to Work verified under the Home Office Points-Based Immigration System:

🇬🇧 Skilled Worker Visa (Tier 2)

Sponsoring employers must hold an active Home Office A-rated Sponsor License and assign a valid Certificate of Sponsorship (CoS). Role must meet the general minimum salary threshold (£38,700) or occupation going rate.

🏛️ Settlement (ILR) Pathway

Continuous employment under Skilled Worker status establishes eligibility for Indefinite Leave to Remain (ILR) after 5 continuous years, leading to British Citizenship.

⚖️ Official regulatory reference: UK Visas and Immigration (UKVI) & Home Office Sponsor Register.

Candidate Preparation Blueprint: Biotech & Pharmaceuticals

Recruitment Insights

Based on transatlantic hiring benchmarks for HRJOB8543 Quality Assurance Lead roles across Almac Group's corporate sector, successful applicants typically excel across three core dimensions:

1. Domain Competency

Demonstrated portfolio evidence, architecture/system design case studies, or validated professional certifications directly applicable to Biotech & Pharmaceuticals.

2. Behavioral & Leadership

STAR method competency responses highlighting cross-functional leadership, conflict resolution, and delivering measurable enterprise ROI under tight timelines.

3. Compensation Alignment

Total compensation expectation aligned within the benchmarked £27,963 - £30,200 bracket, including retirement vesting and health parity.

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Hiring Organization
Almac Group

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Location: Loughborough, England
Eligibility: UK Work Eligibility
Schedule: Company - Private
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