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Associate CSV Engineer Analyst - 2924BC

Verista
United Statesfull_timeVerifiedPosted 10 Jan 2023

About the role

Verista’s 700 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. Whether it’s 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

Verista is currently seeking Validation Engineers with experience in facilities, equipment and process validation within a pharmaceutical or biotechnology manufacturing environment to support CQV (Commissioning, Qualification & Validation) activities.

Typical Responsibilities Include:

1-2 years Pharmaceutical Validation or Recent College Grad with a Science Degree and CO-OP experience in Pharmaceutical Industry

Recent College Grad Science Degree with CO-OP experience in Pharmaceutical Industry

Designing and executing validation including support of computer system validation protocols to ensure consistency of data production and compliance with client’s quality standards (including internal ISPE referenced guidelines, client procedures, and 21 Code of Federal Regulations Part 2XX and 8XX level standards which apply to the equipment and product being validated). • Ensuring product and process development activities have all necessary validation and supporting justification.

• Developing technical documents utilizing a simple non-technical general description. This requires understanding of highly technical automated equipment. • Running test scripts and making recommendations for design or process modification based on test results.

• Owning validation process (or portion thereof) not only from an engineering standpoint but also from a client and team relationship standpoint.

• Developing and writing technical change controls from a general non-technical description of the change to a product, process, equipment, protocol, packaging, outcome, or location of equipment.

• Documenting the planning and design required to support the changes, approvals, and testing.

• Managing the overall documentation development and approval process including explanation and justification of document testing, content, and strategy from a quality and regulatory standpoint to facilitate acceptance and approval of the document by required signatories.QA

Requirements

  • Life Sciences industry experience including prior experience implementing systems within a GxP environment.
  • Strong experience working with SDLCs.
  • Strong written and oral communication skills.
  • Strong interpersonal skills.
  • Experience at working both independently and in a team-oriented, collaborative environment is essential.
  • · Flexible during times of change.
  • Can conform and swiftly adjusts to shifting priorities, demands and timelines through analytical and problem-solving capabilities.
  • Manages complex issues and risks and troubleshoots them as they arise. This role will regularly interface with all levels of the organization and with external vendor

#LI-RC1


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 for Employee option.
  • 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

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Company

Verista

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