Job Summary
Responsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Lead the authoring and executing of protocols to demonstrate that manufacturing and cleaning processes are executed with consistent quality and results. In addition, this role will coach and assist Pharma Validation Engineers through the validation process.
Job Description
Responsibilities:
- Responsible for revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and method validations of applicable products in an FDA controlled environment. Plan, communicate and lead scientifically sound qualification/validation strategies for large scale projects. Perform engineering studies to determine if projects are feasible.
- Suggest OEE Improvements and suggestions as a member of the continuous improvement team.
- Communicate with appropriate functional groups (i.e. Manufacturing, Engineering, and QC Labs, etc.) in regard to the needs and status of assigned study execution activities.
- Manage vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
- Provide coaching and mentoring to Pharma Validation team.
- Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.
- Develop and execute cleaning validations.
- Responsible for IQ/OQ and PQ phases.
- Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
- Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
- Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.
- Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.
- Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.
Qualifications:
- Bachelor of Science Degree in Biology, Chemistry or Engineering.
- At least 4 years of validation experience in a cGMP Device or Drug environment. Experience with validations of USP water, controlled environments or equipment validations in a regulated environment.
- Experience with validation documentation and related change control.
- Ability to control and coordinate concurrent projects, competing priorities and critical deadlines.
- Experience assessing and initiating actions independently.
- Experience taking charge of a situation, team or project.
- Ability to build and maintain relationships within and between teams.
- Strong oral and writing skills.
Preferred Qualifications:
- Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, or other related field.
- Six Sigma certification.
- Validation experience in a pharmaceutical or Medical Device manufacturing environment.
- Experience with NDA (New Drug Application) and ANDA (Abbreviated New Drug Application) products.
- Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$101,000.00 - $152,000.00 Annual
The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
