Verista
From Verista's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
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.
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
Support timely completion of product complaint investigations, in compliance with global and local procedures.
Assess incoming complaints and determine next steps needed to adequately address the complaint issue(s) in a timely manner.
Determine the appropriate level of return sample analysis needed.
Perform visual and/or functional analysis as needed.
Verify and close relevant complaints with minimal supervision.
Support inventory management of complaint samples.
Support QA personnel in writing GMP documents, and completing complaint process metrics, including second person verification (SPV) of complaints data.
Conduct PM activities in the Life Science Industry ensuring the project meets the demands of the client.
Understand Lifecycle management for Quality Applications.
Must be willing to work onsite in Indianapolis, IN.
Associate's degree in Engineering, Life Sciences, or a related field.
Strong computer literacy in all Microsoft Office applications.
Strong attention to detail.
High degrees of self-management and problem solving.
Ability to work under tight deadlines
Strong interpersonal skills and extremely resourceful
Knowledge of regulatory requirements (e. g. cGMP, 21 CFR 820, ISO 13485, Canadian MDR)
Knowledge of complaint handling and quality systems; device/combination product complaint experience preferred
Veeva QualityDocs experience
For 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.
National (US) Range
$65,296—$95,358 USD
High growth potential and fast-paced organization with a people-focused culture
Competitive pay plus performance-based incentive programs
Company-paid Life, Short-Term, and Long-Term Disability Insurance.
Medical, Dental & Vision insurances
FSA, DCARE, Commuter Benefits
Supplemental Life, Hospital, Critical Illness and Legal Insurance
Health Savings Account
401(k) Retirement Plan (Employer Matching benefit)
Paid Time Off (Rollover Option) and Holidays
As Needed Sick Time
Tuition Reimbursement
Team Social Activities (We have fun!)
Employee Recognition
Employee Referral Program
Paid Parental Leave and Bereavement
Verista 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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