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Validation - Commissioning/Qualification Specialist / Specific Commissioning and Validation support
Net2Source Warren, NJ
$113k-131k (estimate)
Full Time | Business Services 3 Months Ago
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Net2Source is Hiring a Validation - Commissioning/Qualification Specialist / Specific Commissioning and Validation support Near Warren, NJ

This job offer is not available in your country.

NetSource Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of % in the last years with over employees globally, with over locations in the US and global operations in countries.

We believe in providing staffing solutions to address the current talent gap Right Talent Right Time Right Place Right Price and acting as a Career Coach to our consultants.

Job Description : Validation Qualification Specialist

This role is % Onsite

Work Schedule : Mon - Fri, Business Hours

PURPOSE AND SCOPE OF POSITION :

The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers.

The incumbent in this role, contributes to the completion of milestones associated with facility, utility, and equipment qualification.

With minimum supervision and given general instructions, this individual independently carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope.

As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.

REQUIRED COMPETENCIES :

Knowledge, Skills & Abilities :

Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment with the site validation program;

highly attentive to spelling, grammar, punctuation, and overall document quality.

  • Process oriented with solid critical thinking skills; adaptive and able to develop new / improved strategies, approaches, and procedures
  • Strong understanding of cGXP requirements and good documentation practices relating to systems, equipment and instrumentation within the pharmaceutical industry.
  • Familiarity with CFR Part compliance.
  • Knowledge of pharmaceutical laboratory and manufacturing systems, utilities, and facilities. Preferred protocol execution experience with controlled temperature units (Kaye validators, Ellab), biological safety cabinets (cleanroom foggers), cryogenic storage systems, etc.
  • Experience writing and executing commissioning / qualification / validation documents including VMP, URS, FAT, SAT, IOPQ, RTM, and summary reports
  • Experience writing protocol deviations, investigating out of specification results, and performing corrective and preventive actions.
  • Ability to interact effectively with cross-functional groups.
  • Strong ability to organize assigned tasks in a high paced environment and concurrently monitor tasks / assignments with others that may impact timely completion.

Ability to effectively manage multiple tasks and activities simultaneously

Strong written and verbal communication skills, including solid presentation skills. Proficient at writing well-formulated emails and reports.

Ability to follow oral and written instructions, read and interpret engineering manuals / drawings relevant to the assigned task.

Ability to effectively communicate with employees, contractors and vendors.

Strong computer skills in Microsoft Office Suite Word, Excel and Outlook, and the ability to learn new software as required for equipment qualification.

Competencies :

  • Professional Knowledge
  • Problem Solving
  • Team Player / Building Relationships
  • Multi-tasking
  • Customer Focus
  • Action and detail oriented
  • Active Listening
  • Decisive
  • DUTIES AND RESPONSIBILITIES

Maintains all qualified equipment / systems in compliance with policies, guidelines, and procedures :

a. Develops qualification protocols, and associated reports while adhering to a change management process.

b. Supports the execution of equipment / systems qualifications and validation protocols.

c. Supervises vendors for qualification functions.

d. Develops written procedures for calibration and preventive maintenance of equipment and systems.

e. Supports calibration, equipment qualification and system validation activities.

f. Develops validation / qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls.

Manages projects of limited scope and complexity within their functional area :

a. Supports laboratory equipment / systems implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.

b. Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment / systems to meet business needs in accordance with required schedules or dates.

c. Completes all calibration, qualification and validation documentation with accuracy, completeness, and compliance to Client standards.

Provides excellent customer service and support :

a. Regularly reviews, prioritizes, and promptly responds to customer equipment qualification / system validation and support requests.

b. Provides technical support and guidance on calibration and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.

c. Maintains a positive relationship with all team members and site customers while promoting a positive team environment.

EDUCATION AND EXPERIENCE

a. degree in Engineering or equivalent required

b. Minimum years of experience in FDA regulated industry, with years of experience in facility / utility / equipment qualification required.

Additional Job Requirements :

Lab w / o blood & animal

Why work with us - At NetSource, we believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value.

We want you to fit in with an inclusive culture, focus on work-life fit and well-being, and a supportive, connected environment;

but we also want you to stand out with opportunities to have a strategic impact, innovate, and take necessary steps to make your mark.

We help clients with new skilling, talent strategy, leadership development, employee experience, transformational change management and beyond.

Less than 1 hour ago

Job Summary

JOB TYPE

Full Time

INDUSTRY

Business Services

SALARY

$113k-131k (estimate)

POST DATE

03/08/2023

EXPIRATION DATE

08/10/2024

WEBSITE

net2source.com

HEADQUARTERS

SOMERSET, NJ

SIZE

200 - 500

FOUNDED

2007

TYPE

Private

CEO

ASHISH GARG

REVENUE

$50M - $200M

INDUSTRY

Business Services

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About Net2Source

Net2Source provides application development, workforce management and project consulting services for healthcare and finance industries.

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