QC Raw Materials Sampling Group Leader

Laboratory Responsibilities

• Performs all duties relevant to the Quality Control Raw Materials Sampling Analyst position as required.
• Collecting solid and/or liquid samples from raw materials used in the manufacturing process
• Handles, documents, and manages samples according to procedures and GMP requirements
• Perform quality analysis on containers
• Calibrates or verifies calibration of instruments/devices before use.
• Uses sterile technique to gown into a clean room environment
• Maintains laboratory supplies and performs laboratory housekeeping as assigned
• Participates in required training activities
• Documenting all training
• Training new employees on some GMP related responsibility relevant to the supervised functional areas, where appropriate
• Complies with all pertinent regulatory agency requirements
• Communicating findings and recommendations at group meetings
• Participating in and/or leading cross-functional teams to support optimal client services
• Independently investigating team quality deviations and preventing reoccurrences in support of QC operations
• Maintains laboratory supplies, media, and reagents inventory
• Uses Laboratory Information Management System (LIMS) for samples.
• Schedules the tasks above on a weekly, monthly, and quarterly basis
• A strong work ethic and ability to meet physical demands, including but not limited to, routinely lifting objects of 25 lbs. or more, walking and standing for extended periods of time, pushing or pulling carts and drums, and bending down, squatting, or reaching for supplies.

Leadership Responsibilities

• Supports and monitors the performance of the team of employees
• May participate in new hire interviews
• Supports the onboarding process of new employees
• Participates in the training of other employees.
• Performs peer review of data.
• Assists in coordinating equipment maintenance and calibration.
• Disseminate administrative communications
• Demonstrate and promote the company vision
• Meet all quality and productivity metrics, and demonstrate strong teamwork and collaboration
• Coordinate scheduling and allocation of responsibilities, and the new hire onboarding process
• Coordinates training program

Important Role Information: 

Position requires significant time spent in biopharmaceutical manufacturing ISO 8+ level cleanrooms with the following restrictions:

• No cosmetic products (such as makeup, false lashes, spray tans, etc) are permitted and must be removed prior to entry
• Nails must be kept short, trimmed, and unadorned (no nail polish, adornments, etc)
• No jewelry may be worn, (exceptions are medical alert related and one smooth ring band)
• Hair must be able to be neatly tied back and contained in a hairnet and all facial hair must be neatly trimmed and able to be secured in a beard cover.
• Strict hygiene  standards and adherence to hygeine policies

The Ideal Candidate would possess:

• Laboratory experience
• 1+ years of cGMP experience
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a client-facing environment
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Excellent communication (oral and written) and attention to detail
• Proactively plan and multitask to maximize productivity
• Experience with LIMS preferred

Minimum Qualifications:

• Bachelor’s degree in Life Sciences, or other science related degree concentration, or equivalent directly related experience
• 1+ years previous leadership experience
• Authorization to work in the United States indefinitely without restriction or sponsorship

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.