Sr. Pharma Cleaning Validation Engineer

Woodstock Sterile Solutions•Woodstock, IL

1d•Onsite

About The Position

The position will focus on the validation of product cleaning processes in a pharmaceutical environment. This position is also a member of a team responsible for the design, schedule, execution, and evaluation of scientifically and statistically sound qualification experiments which define and demonstrate that critical Cleaning, Controls, Equipment, Facilities, Processes and Utilities function in a consistent and repeatable manner, and are in compliance with regulatory requirements, product license restrictions, and policies affecting final product integrity. The position schedules activities involving manufacturing equipment to maximize equipment utilization, prepares detailed, concise documentation dossiers on completed studies that summarize the experimental results, specifications, and conformance to defined acceptance criteria, provides technical support to Business Development, Engineering, Manufacturing, Quality Assurance, Quality Control, and Regulatory Affairs as needed. Assists the Validation department in developing policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements. Assists the departmental Manager in the development and training of Validation Engineer/Technician(s).

Requirements

Bachelor of Science in Engineering or Science discipline preferred.
A minimum of three years experience in validation within a pharmaceutical manufacturing operation or five years experience in pharmaceutical operations.
Enhanced knowledge of cGMPs, pharmaceutical manufacturing methods and validation principles.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Ability to work independently on multiple projects in parallel.
Be knowledgeable. Bring experience to the organization. Learn new skills; collect new information. Demonstrate a willingness to share skills and information with others.
Demonstrate initiative. Develop ideas and collect them from others. Continuously seek opportunity. Be detail oriented. Clarify issues, investigate.
Excellent documentation skills.
Excellent problem solving and analytical skills.
Full complement of business computer literacy skills (e.g., word processing, spreadsheets, database software etc.) is preferred.
High level of attention to detail.
Make sound judgments. Blend knowledge and analysis with logic, active listening, and a continuing interest in simplification. Act ethically.
Meet deadlines and work under pressure with limited supervision.
Must be able to interact effectively with a variety of individuals and personalities within and between departments.
Possess and demonstrate excellent verbal, written and interpersonal communications skills.
Should be familiar with cGMP and safe work practices.
Strong Mechanical aptitude.
Strong problem solving and analytical skills.
Strong communication and organizational skills.
Works well in a team environment.
Works well under pressure and able to prioritize workloads.
Demonstrated ability to read, write, and speak clear English.

Responsibilities

Validation empowered representative on cross-functional project teams.
Validation Project Manager for cross-functional project teams.
Assists the departmental Manager in the development and training of Validation Engineer/Technician(s).
Limited oversight of Validation Engineer/ Technician(s).
Researches governmental regulatory requirements on each assigned project to ensure that each study subject is challenged to meet required specifications.
Prepares scientifically sound Validation Study Protocols that incorporate the defined specifications into acceptance criteria and assessment procedures.
Schedules the execution of Validation studies with the appropriate department(s).
Prepares detailed, concise documentation dossiers on completed studies that summarize the studies experimental results and specifications and their conformance to defined acceptance criteria.
Authors, executes, and closes studies in support of Equipment Change Controls.
Maintains close contact with Business development, Engineering, Continuous Improvement and Manufacturing groups to assure effective communication on challenges and opportunities related to validation.
Provides technical support to Business Development, Engineering, Continuous Improvement, Manufacturing, Quality Assurance, Quality Control, and Regulatory Affairs as needed.
Proven technical understanding and validation experience within a pharmaceutical environment.
Assists the Validation department in developing policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements.
Supports the facility in internal and external inspections. Subject Matter Expert (SME), reviewer, or approver of controlled documents within area(s) of expertise.
Works directly with management, contract customers, and/or contract engineers.
Maintain effectiveness of the Quality System components relevant to this position.
Other duties as assigned.