Quality Control Validation

Net2Source (N2S); Vacaville (CA); On-site; USD 62,000 - 69,000; Full time

Job summary

Net2Source Inc. is hiring a Validation Engineer for an onsite, 12+ month engagement in California. The role runs Monday–Friday, 8:00 AM–4:00 PM, onsite five days a week.

You will support QC equipment qualification activities in a cGMP-compliant environment and help drive continuous improvement initiatives. The candidate will qualify laboratory equipment, coordinate with lab staff and vendors, and sign qualification documentation under Genentech policies.

Qualifications

• BS/BA degree in a relevant scientific discipline.
• Experience in pharma/biopharmaceutical industry or equivalent.
• Knowledge of cGMP or equivalent regulations.

Responsibilities

• Qualify laboratory equipment per EQ policies, plans and procedures.
• Coordinate with lab personnel to define qualification requirements.
• Author, review and execute equipment qualification protocols.
• Coordinate equipment qualification with vendors and support groups.
• Identify business, quality, and compliance gaps.
• Sign documents for activities per Genentech policies and job descriptions.
• Support QC laboratory operations as requested by Senior Management.

Skills

cGMP knowledge

Verbal and written communication

Prioritization

Strategic thinking

Decision making

Relationship building

Education

BS/BA degree (scientific)

Job description

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 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.

Company: One of Our Clients

Job Title: Validation Engineer

Duration: 12+ Months (Extendable)

Pay Range: $45-$50/hr on w2

Job Overview

Schedule: Monday – Friday, 8:00 AM – 4:00 PM (includes a 30-minute unpaid lunch)

Location: 100% Onsite (5x/week)

Job Summary

With direct supervision, the candidate is responsible for the support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and corporate principles, quality policies, standards, and core values. Maintains the company’s right to operate, supply to patients, and cost-effectiveness by actively participating in continuous improvement projects.

Duties

Technical Responsibilities

• Perform qualification of laboratory equipment in accordance with EQ policies, plans, and procedures.
• Coordinate with laboratory personnel to define qualification requirements.
• Author, review, and execute equipment qualification protocols.
• Coordinate equipment qualification activities with vendors and other support groups.
• Identify business, quality, and compliance gaps.
• Sign documents for activities as authorized and described by Genentech policies, procedures, and job descriptions.
• Perform any other tasks as requested by Senior Management to support QC laboratory operations.

Job Requirements

Education

• BS/BA degree (preferably in a relevant scientific discipline).
• Experience (may vary depending on site size/scope)
• Experience in the pharmaceutical/biopharmaceutical industry, or an equivalent combination of education and experience.
• Knowledge of cGMP or equivalent regulations.
• Minimum of two years’ experience in Validation or equipment qualification is desired.
• Ability to make sound decisions about scheduling and managing priorities.
• Flexibility in problem-solving, providing direction, and work hours to meet business objectives.
• Possesses strong verbal and written communication skills and the ability to influence at all levels.
• Capable of building trustful and effective relationships.
• Able to think strategically and translate strategies into actionable plans.
• Takes responsibility, drives results, and achieves expected outcomes.
• Work Environment / Physical Demands / Safety Considerations
• Standard office environment

Regards,

Prateek Pampattiwar

Recruitment Specialist

Net2Source Inc.

Global HQ Address –270 Davidson Ave, Suite 704, Somerset, NJ 08873, USA

Office: [phone] x 324 | Cell: [phone]| Fax: [phone]| Email: [e-mail]