Job DescriptionJob Description
Description
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
Senior CQV Engineer Responsibilities :
Draft protocol templates, media fill summaries, and standardized reportsPopulate bracketing documentation tables and support protocolMaintain central trackers for protocol reviews, approvals, and interventionsCoordinate feedback cycles across site / global stakeholders and update documents accordinglyProvide day-to-day execution support to ensure delivery remains on scheduleSupport documentation drafting and onsite coordination cross-functionally with Validation and QA leadsRequirements :
Bachelors Degree in an industry-related fieldMinimum 5+ years industry experience, including direct experience with Media Fill ValidationDemonstrated experience in Commissioning & Validation activitiesDemonstrated experience authoring and executing protocols, drafting media fill summaries and standardized reportsExperience in a pharmaceutical / FDA-regulated manufacturing environmentWorking knowledge of cGMP and facility / equipment validation requirementsAbility to write clearly, concisely, and persuasively in a professional environmentDemonstrated ability to interact effectively with all levels of the organizationAbility to work as part of a cross-functional teamStrong problem-solving, critical thinking skills, and attention to detailAbility to work on-site, full-time , in Greenville, NCFor US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
Verista is an equal opportunity employer.(US) Range$70,491—$104,439 USD
Benefits
Why 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 Insurance.Medical, Dental & Vision insurancesFSA, DCARE, Commuter BenefitsSupplemental Life, Hospital, Critical Illness and Legal InsuranceHealth Savings Account401(k) Retirement Plan (Employer Matching benefit)Paid 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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