Deviation Investigator / Validation Engineer
An exciting opportunity is available for an entry-level Commissioning, Qualification, and Validation (CQV) Engineer to join a growing team in the pharmaceutical sector. This role is ideal for recent graduates or early-career professionals looking to build a foundation in regulated environments and gain hands-on experience in deviation investigation and remediation.
About the Role
This position offers training and mentorship in deviation investigation processes and supports various validation activities within pharmaceutical manufacturing. The successful candidate will work closely with experienced professionals and contribute to quality and compliance efforts across multiple systems.
Key Responsibilities
- Assist in deviation investigations and support remediation efforts under guidance.
- Learn and apply industry standards and best practices in CQV activities.
- Collaborate with cross-functional teams to support validation documentation and execution.
- Participate in team meetings and contribute to problem-solving discussions.
- Maintain accurate records and documentation in accordance with regulatory requirements.
Candidate Profile
- Education: Bachelor's degree in Engineering or a STEM-related field (e.g., mechanical, chemical, biomedical).
- Experience: 0-3 years of relevant experience; internship or co-op experience in pharmaceutical or regulated environments is a plus.
- Skills:
- Strong communication and interpersonal skills.
- Proficiency in Microsoft Office and general PC use.
- Ability to work effectively in a team setting.
- Detail-oriented with strong organizational and time management abilities.
- Critical thinking and problem-solving capabilities.
- Comfortable working in dynamic, fast-paced environments.
Work Authorization: Applicants must have the legal right to work in the United States without the need for current or future sponsorship.
Why Join This Team?
- Supportive and collaborative work culture focused on professional growth.
- Opportunities for training and development in pharmaceutical CQV practices.
- Inclusive environment that values integrity, learning, and teamwork.
- Recognition programs and team-building activities
FAQs
Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your CV and details on file so when we see similar roles or see skillsets that drive growth in organisations, we will always reach out to discuss opportunities.
Yes. Even if this role isnāt a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.
We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business.Ā
That's why we recommend registering your CV so you can be considered for roles that have yet to be created.Ā
Yes, we help with CV and interview preparation. From customised support on how to optimise your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.