We are seeking a Validation Engineer to join our team working in the pharmaceutical packaging industry and play a key role in ensuring that manufacturing processes, equipment, systems, and packaging operations consistently meet applicable quality, safety, and regulatory requirements for our clients.
The ideal candidate is a highly detail-oriented professional who understands the importance of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) and takes pride in maintaining the highest standards of quality and data integrity.
This role is well suited for someone who thrives in a high-integrity, highly collaborative team environment and is committed to doing the right thing when it comes to product quality, patient safety, regulatory compliance, and operational excellence.
Key Responsibilities
- Develop, execute, and maintain validation and qualification protocols and reports for pharmaceutical packaging equipment, processes, and systems.
- Develop and execute packaging validation activities, equipment specifications, protocols, reports, deviations, and change controls with completeness, accuracy, and compliance with GMP principles and company expectations.
- Support equipment qualification activities, including IQ, OQ, and PQ, as applicable.
- Partner closely with Quality Assurance, Manufacturing, Engineering, Maintenance, and other cross-functional teams to resolve issues and support successful validation activities.
- Identify potential quality and safety risks and proactively communicate concerns.
- Contribute to the development and improvement of validation strategies, procedures, and processes.
Required Qualifications
- Experience in validation, qualification, engineering, or a related role within the pharmaceutical, medical device, biotechnology, or regulated manufacturing industry.
- Working knowledge of GMP and GDP principles.
- Understanding of validation and qualification methodologies, including IQ/OQ/PQ.
- Strong technical writing, documentation, and communication skills.
- Exceptional attention to detail and commitment to data integrity.
- Ability to work effectively in a cross-functional, team-oriented environment.
- Strong problem-solving and organizational skills.
- Demonstrated commitment to quality, safety, compliance, and ethical conduct.
Preferred Qualifications
- Experience with pharmaceutical packaging equipment and processes. Primary packaging (solid-dose filling, capping), secondary packaging (labeling, printing, cartoning, walleting, wrapping, etc), and tertiary packaging (casepacking, palletizing).
- Experience supporting packaging line qualification or validation.
- Experience with Pharma serialization regulations, concepts, and solutions.
- Familiarity with risk-based validation approaches and regulatory expectations.
- Knowledge of computerized systems validation or automation
What We Value
We are looking for a person who:
- Demonstrates high integrity, attention to detail, and takes ownership of their work.
- Understands that accurate and compliant documentation is essential in a regulated environment.
- Follows GMP and GDP requirements consistently, even when no one is watching.
- Collaborates openly and respectfully with colleagues across functions and stays calm in a dynamic environment.
- Asks questions, raises concerns, and speaks up when something does not meet expectations.
- Approaches problems with curiosity, accountability, and a continuous-improvement mindset.
- Takes pride in producing thorough, accurate, and inspection-ready work.
If you are a validation professional who is detail-oriented, collaborative, technically capable, and committed to doing things the right way, we encourage you to apply.
Our Team-
You will join a high-integrity, highly collaborative team where engineering, quality, manufacturing, and operations work together toward a common goal: delivering safe, compliant, and high-quality pharmaceutical packaging solutions.
We believe strong teams are built on trust, accountability, transparency, respect, and a shared commitment to quality and safety.
Why Join Us?
LMN Services is a small, focused engineering firm specializing in Pharmaceutical automation services, trusted by some of the biggest players in the Pharmaceutical industry. Our employees value making a meaningful contribution in a regulated environment while working alongside top-notch professionals who take quality, compliance, and teamwork seriously.
