LinkedIn and 3rd parties use essential and non-essential cookies to provide, secure, analyze and improve our Services, and to show you relevant ads (including professional and job ads) on and off LinkedIn. Learn more in our Cookie Policy.
Select Accept to consent or Reject to decline non-essential cookies for this use. You can update your choices at any time in your settings.
COMPI is a full service engineering contracting and consulting services company with a life sciences division specializing in pharma, biotech, API, Medical Device and laboratory facilities. We are seeking an experienced Senior Validation Engineer to join our growing team. COMPI differentiates itself through an integrated approach to engineering, construction commissioning and validation.
Responsibilities
Support Client commissioning / validation for facility, utility, equipment, cleaning and process validation projects
Prepare and execute commissioning / validation lifecycle documents
Participate in any stage of clinical or commercial production including green field construction, facility renovation, new product development, product launch, or product/process upgrade
Write summary reports for validation and qualification protocols
Support project milestones, priorities and deadlines
Write operating procedures for technical equipment and practices and procedures
Perform system and process risk assessments and analyses
Schedule and coordinate protocol execution with other departments including manufacturing, facilities and project management
Develop project specific validation plans and strategy
Able to manage and execute multiple projects to meet client’s priorities
Provide a practical approach to problem solving
Individuals must represent COMPI at client sites and interact confidently with clients, contractors, management and peers
Requirements
Bachelor’s degree in a related life sciences or requisite industry training and experience
5 – 10 years GMP experience
Aseptic process experience preferred
Critical utility experience preferred
Ability to converse about scientific matters
Ability to work independently or in collaboration with others
In depth understanding and application of validation principles, concepts, practices and standards
Proficient in current Good Manufacturing Practices and other applicable regulations
Experienced with all pertinent industry best practices (e.g., ISPE) including development and execution of all applicable system life cycle deliverables (e.g., URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report
Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., EMEA, GCP, GLP, GMP, QSR) and internal requirements employing regulatory guidance and industry standards
Excellent written communication skills with emphasis in technical writing
Proficient in Microsoft Word, Excel, Power Point and Projects
Salary range is 85-175K, depending on experience level
On the job training will be provided by the validation team and manager, and through industry training and certification courses, both online and in person.
All candidates must be legally eligible to work in the United States.
Just be willing to travel regionally and / or nationally throughout the U.S.
We are an equal opportunity employer M/F/D/V
COMPI does not accept unsolicited resumes from recruiters / third parties.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Strategy/Planning and Information Technology
Industries
Design Services
Referrals increase your chances of interviewing at GBA by 2x