Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values :
- We empower and support our colleagues
- We commit to client success at every turn
- We have the courage to do the right thing
- We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
- We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Job Responsibilities :
Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment / systems / software, and processes as part of a team as directed by the project leaderRunning test scripts and documenting resultsAdherence with project schedule for all assigned activitiesMaintaining clear, detailed records qualification and validationDocumenting impact and risk assessments as part of a teamCompleting user interface testing, software verification, and complete alarm testing on automated systemsDeveloping, reviewing, and executing testing documentationMaking recommendations for design or process modification based on test results when executing test scriptsGeneral understanding of capital equipment implementation and process knowledgeRequirements :
Must be willing to work onsite in Portland, ME.Bachelor's or equivalent STEM degree required (Biomedical Engineer, Chemical Engineer, etc.)Demonstrated experience in leading CQV activities specific to Process Equipment (internship experience preferred)Proficiency using PC and Microsoft Office toolsOutgoing personality with strong ability to communicate effectively with peers in clear, concise termsAbility to work as part of a teamStrong problem-solving and critical thinking skillsExcellent organizational and time management skillsStrong attention to detailGMP and Good Documentation PracticeIntermediate skills with WORD (authoring / editing large technical documents with styles, tables, TOCs, track changes)Basic skills with EXCEL and PowerPointStrong interpersonal skills and clear communication capabilitiesExperience with and tolerance for high levels of challenge and changeExperience in GMP regulated environmentProven attention to detail and organization in project workCapable of working on assigned tasks without mentorshipWhy Choose Verista?
High growth potential and fast-paced organization with a people-focused cultureCompetitive pay plus performance-based incentive programsCompany-paid Life, Short-Term, and Long-Term Disability Insurance.Supplemental Life, Hospital, Critical Illness and Legal InsuranceHealth Savings AccountPaid Time Off (Rollover Option) and HolidaysAs Needed Sick TimeTuition ReimbursementTeam Social Activities (We have fun!)Employee RecognitionEmployee Referral ProgramPaid Parental Leave and BereavementVerista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com
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