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Process Engineer I SS
Location:
US-OH-West Chester
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Veristas 700 experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. Whether its compliance, quality management, verification, validation, automation, IT infrastructure, data analysis, manufacturing, or packaging, we deliver solutions that are right the first time.

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.

This role must be on-site in West Chester Ohio.

Typical Project Accountabilities Include:

  • Authoring and executing Process Validation and Process Performance Qualification (PPQ) Protocols as part of team as directed by the project leader.
  • Authoring and executing laboratory studies for various process development, scale-up and validation activities as well as for deviation investigation and manufacturing process improvements.
  • Authoring associated validation summary reports.
  • Adherence with project schedule for all assigned activities.
  • Maintaining clear, detailed records of qualification and validation.
  • Provide routine progress updates and elevate identified issues to project team.
  • Under direction of / in collaboration with senior engineers, provide the following:
    Develop / revise User Requirement Specifications (URS) for manufacturing or test equipment
    Develop and execute engineering studies and author / close out documentation, including summary reports
    Review validation / qualification documentation, resolve discrepancies, and close out documentation
    Provide technical support during ramp up of manufacturing processes
    Coordinate the activities of third party personnel, as applicable

Requirements

  • Bachelors Degree in chemical, biomedical/biochemical engineering, biological/chemical sciences or equivalent required.
  • Proficiency using PC and Microsoft Office tools.
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms.
  • Ability to work as part of a team.
  • Ability to think critically and demonstrate troubleshooting and problem-solving skills.
  • Excellent organizational and time management skills.
  • Strong attention to detail.
  • Possess excellent interpersonal, verbal, and written communication skills.
  • GxP and Good Documentation Practice training (may be completed at onboarding).
  • Process training (may be completed at onboarding).
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes).
  • Basic skills with EXCEL and PowerPoint.
  • Strong interpersonal skills and clear communication capabilities.
  • Experience with and tolerance for high levels of challenge and change

Benefits

Why Verista?

  • High growth potential and fast paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company paid medical premiums.
  • Company paid Life, Short-Term, and Long-Term Disability insurances
  • Dental & Vision insurances
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • Leadership development training, career planning, and tuition reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Maternity, Parental Leave and Bereavement

Verista is a leading business, technology and compliance company that enables clients to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing, and distribution. This experience brings together decades of knowledge, the most advanced engagement platforms, as well as transformative technologies. This allows clients to benefit from the ease, efficiency, and trust that results from working with one partner who excels across specialties.

For more information about our company, please visit us at (link removed) or follow us on LinkedIn(link removed)>

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.

$70,000 - $118,000

*Verista is an equal-opportunity employer.

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Verista

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