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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 CSV Particle Counters Engineer / Senior Validation Engineer Responsibilities:
Looking for a strong resource with a diverse skillset focused around Particle Couter Implementation accompanied by a thorough understanding of CSV principles.
- Knowledge and demonstrated experience of Computerized System Validation and Implementation of Particle Counters.
- Running test scripts and documenting results
- Experience working with IT and troubleshooting
- Experience with requirements gathering and root cause analysis activities
- Adherence with project schedule for all assigned activities
- Maintaining clear, detailed and compliant qualification and validation records
- Understanding of system design and/or configuration activities
- General understanding of capital equipment implementation and process knowledge.
- Understanding with demonstrated experience drafting and executing validation documents, such as, Val Plans, URS, IQ/OQ/PQ protocols, RTM, VSR, Deviation Management, Change Management and Project Management
- Understanding of system integrations, including but not limited to understanding of how integrations are designed / constructed, data flow from source systems to target systems, typical testing approach for system integrations
- Designing and executing engineering studies for critical process parameter definition and verification prior to validation
- Conducting and documenting impact and risk assessments with a full understanding of equipment/system/ software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes.
Requirements
- Bachelor’s Degree or equivalent required
- 4 to 6 year of relevant role specific experience
- Proficiency using PC and Microsoft Office tools
- Ability to work as part of a team
- Strong problem-solving and critical thinking skills
- Excellent organizational and time management skills
- Strong attention to detail
- Obvious business maturity and interpersonal skills to be able to effectively communicate and collaborate
- Experience and capability of effectively communicating requirements (written and orally) with rationale to different levels of the client’s organization
- Experience in pharmaceutical cGxP setting with the ability to generate CSV/CQV deliverables
- Knowledge of 21CFR Part 11 Regulation
- Ability to work as part of a team
- Direct experience and understanding of complex automated lab and manufacturing systems
This is an on-site role in Summit, NJ
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
$70,491—$113,521 USD
Benefits
Why Choose Verista?
- 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
Seniority level
Seniority level
Mid-Senior level
Employment type
Job function
Job function
Quality AssuranceIndustries
Pharmaceutical Manufacturing
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