Project Admin Engineer / Project Coordinator - Pharma Manufacturing
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
Project Admin Engineer Responsibilities :
Maintain project tracking systems and update batch readiness toolsSupport administrative reporting and weekly metric submissionsCollaborate with cross-functional teams to ensure documentation accuracy and alignmentAnticipate and problem solve logistics and warehousing coordinationTrack material shipments and documentation for warehouse Goods ReceiptLog manufacturing information in SAPAssist with deviation tracking and documentation closure follow-upRoute GMP and manufacturing documents for approval using internal systems (e.g., Veeva Vault)Manage the lifecycle of controlled documents, ensuring up-to-date status and complianceTrack document effectiveness and maintain metadata in appropriate systemsSupport the creation of reports, charts, and visual aids for communicationRequirements :
Minimum Education : Bachelor's degree. Preferred Education : BS in Professional Writing, Science, Engineering, Pharmacy, Pharmaceutical Sciences, Business or related fieldExceptional attention to detail and organizational skillsClear and professional communication skillsExperience with document management and tracking systemsCapable of multitasking and prioritizing independentlyComfortable in fast-paced environments with frequent changesFoundational project coordination or administrative experienceOnsite requirement in Indianapolis, INPreferred Qualifications :
Experience with GMP documentation processesFamiliarity with Veeva Vault and document lifecycle systemsExposure to SAP, TrackWise, and Ariba platformsWorking knowledge of Microsoft Teams and other collaborative toolsUnderstanding of database structures and document control workflowsNational (US) Range : $56,980 - $93,541 USD
Benefits
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.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 Bereavement