Validation Engineer

Leiters Inc•Buena Vista, NJ

2d•$97,308 - $121,608

About The Position

The Validation Engineer reports directly to the Manager of Validation. The role is responsible for acting as a Subject Matter Expert (SME) for the Commissioning, Qualification, and Validation (CQV) processes for the site. This includes commissioning and qualification of the equipment, process validation, facilities qualification, utilities qualification, electronic system validation, shipping validation, and program maintenance. This role ensures all systems operate within regulations to ensure the production of quality products. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further – Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company – we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today

Requirements

Bachelor's degree in a STEM field required; i.e. engineering, chemistry, or relevant industry experience.
4+ years of validation experience, preferably in a highly regulated environment.
Demonstrated ability to conduct statistical analysis using software (JMP, MiniTab, Saas, etc.)
Strong curiosity and willingness to learn, along with the tenacity and drive to see projects through.
Willingness to support tasks outside normal job description, as needed. Can-do attitude!
Ability to create technical and professional documents.
Strong attention to detail and accuracy.
Ability to multi-task, with strong organization and time-management.
Ability to work under pressure and independently with the ability to make decisions according to established guidelines and accomplish tasks accurately and on a timely basis.
Proficient written, verbal and oral English communication skills are required.
Proficiency with Microsoft 365 tools including Outlook, Microsoft, and Excel.

Nice To Haves

Experience in project management preferred
Understanding of 503B regulatory requirements, cGMP standards, and USP guidelines is a plus!

Responsibilities

Works on projects/matters in a supporting capacity. Communication may be directed towards the project team and direct management, or the audience may be a wider cross-functional group.
Work alongside commissioning agents to complete initial facility qualification and bring systems and processes online.
Utilizes Project Management skills to plan and coordinate efforts with a cross-functional team.
Completes tasks in a timely fashion and communicate task status to management and/or project team.
Adheres to GDP/GMP guidelines to author, review, or support technical documents including but not limited to change controls, and CAPAs.
Coordination of Validation activities with stakeholders.
Support in writing and executing protocols for Validation work.
Identifies and resolves non-conformances/discrepancies encountered during IQ/OQ/PQ execution and work with cross function team to implement mitigation solutions.
Generate reports and summarize results, including confirming the document is suitable to be shared with regulatory agencies.
Supports creation or revision of Validation templates for protocols and reports.
Supports creation and review of Engineering Documentation (URS, FS, SAT, FAT).
Act as a subject matter expert for all site qualification and validation activities.
Supports project work as a specialist on complex technical matters.
Mentoring of less experienced team members.
Other duties as assigned.

Benefits

Smart healthcare coverage options that rewards wellness (and puts money back in your pocket!)
Flexible Spending & Health Savings Accounts (FSA & HSA) available
Dental & Vision insurance
Employer Paid Life Insurance & Employee Assistance Program
Short Term & Long-Term Disability Insurance
Up to 4% 401K Matching (100% vested on day one!)
Generous Paid Time Off Options – vacation, sick, paid leave and holidays!
$5,250 Annual Tuition Reimbursement after 6 months
$1,000 Referral Bonus Program with no limit
Eligible for annual bonus program