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Veeva Configuration Specialist

This job is no longer open

About Forge 


Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality.We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bringexpertisein gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside.Our goal is simple but vital to patients living with disease, and we take it seriously.

With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most. Forgeis based in Columbus, Ohio, in a 200,000 square foot facility knownaffectionately by team membersas,the Hearth.The Hearth,is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services. 

About The Team


The Information Technology (IT) department plays a critical role in ensuring the smooth and efficient operation of all technology-related systems within the company. They are responsible for managing and maintaining the company's digital infrastructure, including servers, data centers, and cloud computing platforms. They are responsible for providing technical assistance, troubleshooting issues, and resolving problems related to hardware, software, and network connectivity. The department also ensures data security and privacy by implementing robust cybersecurity measures and protocols.

About The Role


The Veeva IT Systems Analyst is responsible for the maintenance, continuous improvements, and troubleshooting of Forge’s Quality Management System, Veeva Vault. The Veeva Vault Quality system includes QualityDocs, Training, QMS, QRM, LIMS, and other modules that may be implemented in the future. This position will support configuration of Veeva Vault Quality and Platform, as well as supporting any future module implementations. This position must work in cross‑functional groups including Veeva business administrators, business owners, and technical managers.

The position will support change control and validation of Veeva Vault Quality.

What You'll Do


  • Responsible for the management and continuous improvement of the Veeva Vault Platform and all modules within the Veeva Vault Quality Suite.
  • Responsible for designing and implementing configurations within Veeva Vault for new business requirements, proposed changes, and identify and implement necessary configurations changes to address workflow issues.
  • Responsible for working with Computer Systems Validation SME to validate changes per GAMP 5 guideline and current Good Manufacturing (cGMP) regulations to maintain validation state and compliance.
  • Support Veeva Releases and other changes through Change Controls as the system expert.
  • Must be a strong communicator and highly organized to work with multiple cross-functional teams to support the continuous improvement of Veeva Vault across multiple modules at one time. 
  • Train, support and advise Veeva end users on EDMS and QMS system requirements and workflows. Develop training modules for EDMS and QMS.
  • Responsible for writing SOPs and Work Instructions, assists other departments with the generation, review and approval and maintenance of such documents.
  • Provide support during regulatory inspections and internal audits.

What You'll Bring


  • BS Degree in Computer Science, Information Management Systems, Engineering, Science or in a related field required or equivalent work experience.
  • Veeva Vault Platform White Belt Certification is preferred, however other accredited Veeva certification, or equivalent experience may be accepted. 
  • A minimum of 3 years of experience with Veeva Vault Platform configuration is required, familiarity with Veeva Vault Quality is preferred. 
  • Experience with the implementation, validation, and maintenance of a Computer System in an regulated industry (FDA or equivalent) is preferred.

Work Environment and Physical Demands


This position works in a typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. This islargely asedentary role; persons holding office positions aregenerally subjectto inside environmental conditions having the lighting, temperature, and noise of an open floor-plan office environment. Regularlyoperatea computer and other office equipment. Regularly communicate with others in person, over the phone, and electronically. Must be able to move and/or carry objects weighing up to 10 lbs.This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee.

Duties, responsibilities and activities may change or new ones may be assigned.Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics,provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal,stateor local laws.

Life at Forge 


We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases.Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry.Forge’s core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. 

H


ARDWORKING -We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key.

O


PEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback.

P


URPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies.

E


NGAGED -We are fully absorbed by and enthusiastic about our work and take positive action to further Forge’s vision,missionand goals.

We’ve Got You Covered


We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly Un

FORGE


ttable.

  • Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents
  • Flexible PTO (plus 14 paid company holidays)
  • Annual bonus for all full-time employees
  • 401(K) company match
  • Fully-stocked kitchen with free food/drinks
  • 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care
  • Employee Assistance Program 
  • Wellness benefits (financial planning services, mental health counseling, employer paid disability)
  • Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches

This job is no longer open

Life at Forge Biologics

Forge is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping champion teams that are navigating the long road from the lab bench to the bedside. With a patients-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them most.
Thrive Here & What We Value• HARDWORKING• OPEN• PURPOSE DRIVEN• ENGAGED• Patient-First Approach• Forging New Models for Working Together to Better Accelerate Transformative Medicines to Reach Those Who Need Them the Most• Commitment to Following SOPs, Safety Protocols, and Regulatory Guidelines to Ensure Compliance and Product Quality• Flexibility to Work in Shifts, Including Weekends and Holidays, as Required by Manufacturing Schedules• Professional & Personal Development Resources - LinkedIn Learning, a Dedicated Training Staff In-House, Mentoring Opportunities & Access to Leadership Development Coaches</s>
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