Equipment Commissioning Systems Administrator

Overview

On Site
$market rate
Accepts corp to corp applications
Contract - W2
Contract - Independent
Contract - long term

Skills

Budget
Communication
Attention To Detail
Onboarding
Regulatory Compliance
Good Manufacturing Practice
GMP
Organized
Writing
Standard Operating Procedure
Collaboration
Science
Data Integrity
Pharmaceutical Industry
Management
Documentation
Negotiations

Job Details

Job Title: Equipment Commissioning Systems Administrator

Please see attached.


No candidates with Visas will be accepted for this role. W2 referrals or 1099 candidates that are USor Citizens are accepted.


Thank you

Overview: Our Client's equipment is being moved into a GMP sense so there are new requirements and need to get them up to compliance

Location: New York Fully onsite.

Bill Rate/Budget: 80-$90/hr max

Start Date: Early June start date

Duration: 12 months with 2 potential extensions

Fully onsite

Candidate Type

W2 or 1099

Must Have:

  • Troubleshooting equipment
  • Understanding GMP standards
  • Experience with data integrity
  • Excellent communication skills

Job Description

Our client is seeking a dedicated and detail-oriented Systems Administrator to join our team. This role involves a variety of responsibilities including system administrative work, commissioning equipment, basic troubleshooting, and onboarding equipment to align with our client's standards. The ideal candidate will be hands-on, proactive, and comfortable working in a dynamic environment.

Key Responsibilities:

  • Perform system administrative tasks, including commissioning and basic troubleshooting of equipment.
  • Onboard new equipment to ensure compliance with our client's standards and protocols.
  • Move between various buildings throughout the day to support equipment and systems.
  • Gown into controlled areas as required, adhering to GMP (Good Manufacturing Practice) standards.
  • Collaborate with process sciences, which is transitioning into the GMP space, to ensure equipment is properly controlled and documented.
  • Manage and execute a lighter version of commissioning for equipment categorized as support impact.
  • Work on 320 ECNs (Engineering Change Notices) and 70 systems, including multiple units of the same configuration, organized in a phased approach over the next 18 months.
  • Engage in hands-on work with equipment, including writing SOPs (Standard Operating Procedures), configuration specifications, and templating information.
  • Handle systems that are up to 8 years old and may lack documentation, ensuring data is securely sent to designated locations.
  • Utilize strong interpersonal skills to negotiate and collaborate with process sciences teams.
  • Ensure thorough verification processes are followed, especially during periods of change.

Qualifications:

  • Experience with Biovia U Lab is a plus.
  • Background in data integrity and the pharmaceutical industry.
  • Hands-on experience with commissioning equipment, including direct interaction with equipment to understand its functionality.
  • Strong documentation skills without relying solely on SMEs (Subject Matter Experts) for information.
  • Willingness to gown into controlled areas as needed.
  • Excellent interpersonal and negotiation skills.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.