In-Demand Lab technician Jobs

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QC Analytical Methods & Tech Transfer Lead

Opella Healthcare Group -
Virginia QLD

Apply Now

Job Details

Full-time
4 days ago

Qualifications

Laboratory experience
Laboratory information management systems
Master's degree
Bachelor's degree
Communication skills

Full Job Description

Role Title: QC Analytical Methods & Tech Transfer Lead

Report to: Orwa Shueibi - QC Lead

Location: Virginia, Brisbane

Working Pattern: 4 office based/1 remote

You’ve built experience, now use it where bold ideas meet real impact. At Opella, we’re challenging how self-care works for millions of people and need leaders and experts ready to shape what’s next. As an QC Analytical Methods & Tech Transfer Lead you’ll bring your skill, your curiosity and your drive to make health simpler, smarter and more human.

Role Summary

A process leadership and specialist role within Quality Control focused on analytical methods, validation, and technical transfer within a GMP-regulated laboratory environment.

This role is accountable for ensuring analytical methods received from Development Centre (DC) or external sources are effectively transferred, validated/verified, and fit-for-purpose for routine QC use.

The position acts as the single point of contact (SPOC) for PPM on QC analytical topics, ensuring alignment across stakeholders while driving method readiness, compliance, and implementation across a diverse product portfolio.

The role combines technical expertise, cross-functional coordination, and operational oversight, ensuring data integrity (ALCOA+), audit readiness, and sustainable QC operations

Main Responsibilities

Method Transfer & Implementation:

Lead and coordinate transfer of analytical methods into QC, ensuring suitability for routine testing.
Method Validation & Verification: Define, author, and oversee validation/verification strategies (aligned with ICH Q2(R2)), ensuring compliance and robustness.
SPOC for PPM (QC Topics): Act as primary interface for analytical methods, results, OOS events, risks, and timelines.

Method Readiness & Gap Assessment:

Assess incoming methods for readiness; identify gaps and drive resolution with stakeholders.
Documentation Authoring & Governance: Prepare and/or remediate Validation/verification plans, Protocols and reports, Method summaries and traceability matrices, Supporting data packages
Data Integrity & Compliance: Ensure adherence to ALCOA+, GMP, and audit expectations across all activities.

Operational:

Stakeholder Collaboration: Partner with QC, QA, DC, and external laboratories to ensure aligned and compliant delivery.
Issue Resolution: Support and contribute to OOS, deviations, and method-related investigations.
Operational Suitability: Ensure methods are practical, efficient, and sustainable for routine QC operations.

About You

We believe that professionals with the following experience and skillsets are well-suited for this position:

Bachelor’s or master’s degree in chemistry or relevant scientific discipline
Strong experience in analytical method validation, verification, and tech transfer within GMP QC
Demonstrated experience authoring and defending validation protocols and reports
Experience with compendial and non-compendial methods
Strong understanding of: ICH Q2(R2), ICH Q14, GMP / PIC/S requirements, Data integrity (ALCOA+)
Proven troubleshooting capability across methods, instrumentation, and sample matrices
Experience working with complex raw material or finished product matrices
Strong stakeholder management and communication skills Essential Skills & Experience

Desirable

Experience in pharmaceutical, consumer health, or nutraceutical environments
Familiarity with:
- External laboratory management
- Tech transfer governance
- QC systems (e.g., LIMS)
- OOS, deviations, CAPA, and change control processes
Experience interfacing with PPM or project portfolio structures

Deliverables / Outcomes

Successful and compliant transfer of analytical methods into QC
Methods demonstrated to be fit-for-purpose and operationally sustainable
Clear visibility of QC readiness, risks, and timelines
Strong stakeholder alignment and effective issue resolution
Audit-ready validation documentation and data integrity compliance

This is more than the next step in your career, it’s a chance to lead change and help reinvent self-care for the world. If you’re ready to challenge, inspire and deliver impact that matters, we’re ready for you. We are challengers. We are Opella.

About Us:

Opella is the self-care challenger with the purest and third-largest portfolio in the Over The Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally.

Our mission is to bring health in people’s hands by making self-care as simple as it should be. For half a billion consumers worldwide – and counting.

At the core of this mission is our 100 loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world’s most loved brands, including Allegra, Buscopan , Doliprane ,Dulcolax, Enterogermina , Essentiale and

Mucosolvan .

As a globally certified B Corp company, we are active players in the journey towards healthier people and planet . Find out more about our mission at www.opella.com .

Apply Now

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