QC Utilities & Raw Materials Team Lead

Eurofins

Not Interested
Bookmark
Report This Job

profile Job Location:

Rensselaer, NY - USA

profile Monthly Salary: Not Disclosed
Posted on: 4 days ago
Vacancies: 1 Vacancy

Job Summary

The QC Utilities & Raw Materials Team Lead is a hands-on leadership role supporting Quality Control operations within a regulated biopharmaceutical manufacturing environment. This position combines routine QC testing responsibilities with day-to-day team leadership training coordination and operational oversight for utilities and raw materials testing.

The ideal candidate brings prior GMP laboratory experience a strong testing background and proven ability to support and guide junior staff while maintaining compliance productivity and data integrity.

Key Responsibilities

Laboratory & Technical Responsibilities

  • Perform QC Utilities and Raw Materials testing including:
    • pH
    • Conductivity
    • Nitrate identification
    • Total Organic Carbon (TOC)
    • Appearance testing
  • Receive handle log and dispose of samples in accordance with GMP requirements
  • Calibrate and verify calibration of laboratory instruments and equipment prior to use
  • Accurately document test results and investigate or escalate quality anomalies as needed
  • Utilize LIMS for sample management data entry and documentation
  • Maintain laboratory supplies reagents and inventory; perform general laboratory housekeeping
  • Comply with all applicable regulatory safety and data integrity standards
  • Participate in required training and continuous improvement initiatives
  • Communicate testing results trends and recommendations during group meetings
  • Independently investigate quality deviations and implement corrective actions to prevent recurrence
  • Schedule testing activities on a weekly monthly and quarterly basis

Team Lead & Leadership Responsibilities

  • Support monitor and coordinate the daily activities of the Utilities and Raw Materials QC team
  • Assist with onboarding and training of new hires including GMP-related responsibilities
  • Coordinate and maintain training plans and competency documentation
  • Perform peer review of analytical data and documentation
  • Assist with scheduling task allocation and resource planning
  • Support equipment maintenance and calibration coordination
  • Participate in interviews and hiring activities as needed
  • Disseminate administrative and quality-related communications
  • Promote teamwork accountability and adherence to company values
  • Meet or exceed quality productivity and compliance metrics

Work Environment & Physical Requirements

This role requires extensive time in ISO 8 or higher biopharmaceutical cleanroom environments with strict adherence to hygiene and gowning requirements including:

  • No cosmetics or cosmetic products
  • Short clean unadorned nails
  • No jewelry (exceptions for medical alert items and one smooth ring)
  • Hair and facial hair must be secured with appropriate coverings

Physical requirements include:

  • Lifting 25 lbs. or more
  • Standing and walking for extended periods
  • Pushing or pulling carts and drums
  • Bending reaching and handling laboratory materials

Qualifications :

Required

  • Bachelors degree in Life Sciences or a related scientific discipline (or equivalent experience)
  • 1 years of cGMP laboratory experience
  • 1 years of leadership or team lead experience
  • Strong attention to detail and documentation practices
  • Excellent written and verbal communication skills
  • Ability to multi-task plan proactively and work independently or collaboratively
  • Authorization to work in the U.S. without sponsorship

Preferred

  • Experience with utilities or raw materials testing
  • Experience using LIMS
  • Prior work in a regulated biopharmaceutical manufacturing environment

Additional Information :

What to Expect in the Hiring Process: 

  • 10-15 Minute Phone Interview with Region Recruiter
  • 45-60 Minute Virtual Interview with Manager and/or Group Leader
  • 30 Minute Virtual Interview with Site Director 

Additional Details: 

This is a full-time onsite position based on a first-shift schedule (Sunday through Wednesday 7am-5:30pm) with overtime required as needed. Candidates located within a commutable distance to Rensselaer New York are strongly encouraged to apply. 

Excellent full-time benefits include:

  • Comprehensive medical coverage dental and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Hourly rate is between $28-$33 depending on education and experience 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.


Remote Work :

No


Employment Type :

Full-time

The QC Utilities & Raw Materials Team Lead is a hands-on leadership role supporting Quality Control operations within a regulated biopharmaceutical manufacturing environment. This position combines routine QC testing responsibilities with day-to-day team leadership training coordination and operatio...
View more view more

About Company

Company Logo

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eur ... View more

View Profile View Profile