Quality Control Sampling Group Leader

The Quality Control Sampling Group Leader is a hands-on leadership role responsible for overseeing raw material and container sampling activities within a GMP-regulated biopharmaceutical manufacturing environment. This role combines routine laboratory sampling responsibilities with oversight of daily team operations training scheduling and compliance.

Laboratory Responsibilities

• Perform all duties associated with Quality Control sampling activities in support of manufacturing operations
• Collect solid and/or liquid samples from raw materials and manufacturing components
• Handle document and manage samples in compliance with GMP and site SOPs
• Perform quality inspections and analysis of containers and materials
• Calibrate or verify calibration of instruments and devices prior to use
• Gown and work within ISO 8 cleanroom environments using proper sterile technique
• Maintain laboratory areas supplies reagents media and sampling equipment
• Use the Laboratory Information Management System (LIMS) for sample tracking and documentation
• Schedule sampling and lab activities on a weekly monthly and quarterly basis
• Participate in investigations of quality deviations and implement corrective actions to prevent recurrence
• Communicate findings deviations and recommendations during group meetings
• Participate in and/or lead cross-functional initiatives to support optimal client services
• Maintain compliance with regulatory agency and company requirements
• Participate in required training activities and maintain complete training records
• Support physical demands of the role including lifting 25 lbs or more standing/walking for extended periods and handling carts drums and materials

Leadership Responsibilities

• Support and monitor the performance of a team of Quality Control Sampling employees
• Coordinate daily work assignments scheduling and workload allocation
• Train and onboard new employees and support ongoing technical and GMP training
• Conduct peer review of analytical and sampling documentation
• Assist with equipment maintenance coordination and calibration activities
• Support interviews and hiring activities as needed
• Disseminate administrative and operational communications
• Promote company values quality culture and teamwork
• Ensure team meets quality productivity and compliance metrics
• Coordinate and maintain the group training program

Important Role Information

This position requires significant time working in ISO 8 biopharmaceutical cleanroom environments with strict hygiene and gowning requirements including:

• No cosmetic products permitted in cleanroom areas
• Nails must be short clean and unadorned
• No jewelry permitted except medical alerts and one smooth ring band
• Hair must be secured in a hairnet; facial hair must be contained in a beard cover
• Strict adherence to site hygiene policies is required

Qualifications :

Ideal Candidate:

• Laboratory experience in a regulated environment
• 1 year of cGMP experience
• Strong organizational scientific and computer skills
• Excellent written and verbal communication skills
• High attention to detail and documentation accuracy
• Ability to work independently and collaboratively in a client-facing environment
• Ability to multitask prioritize work and adapt to evolving priorities
• Experience with LIMS preferred

Minimum Qualifications:

• Bachelors degree in Life Sciences or a related scientific field (or equivalent relevant experience)
• 1 year of prior leadership or lead-level experience
• Authorization to work in the United States without sponsorship

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 (Monday through Friday 8am to 4pm) 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