Demo

Technical Laboratory Supervisor - 2nd Shift

Werfen
Orangeburg, NY Full Time
POSTED ON 1/24/2025
AVAILABLE BEFORE 11/17/2025

Overview

Position Summary:

Responsible for the technical analysis of raw materials, in-process and finished products, product failures and complaints; support and/or technical support of validations; verification of product claims and dating: and/or provides technical support for formulation and QC testing. Supervises staff as needed.

Responsibilities

Key Accountabilities:

  • Coordinates studies which are appropriate for validation, process improvement, product failure or complaint.
  • Performs automated and manual processes/assays per organization Standard Operating Procedures (SOP), Standard Production Method (SPM) or Quality Control Monographs (QCM)
  • Develops and recommends revisions and improvements to production and quality system documentation.
  • Participates in project teams as directed.
  • Responsible for coordinating and performing preventive maintenance, troubleshooting, cleanliness and calibration of laboratory equipment. Ensures that appropriate records are maintained
  • Assures as necessary that Statistical Process Control records are maintained
  • Prepares Change Orders, Condition for Release, and Incident Reports, etc. as required
  • Sets a personal example of behavior and commitment to company values and plant objectives to encourage a high level of morale and teamwork for all employees
  • Identify department training needs and implement appropriate training measures; mentor and train staff to enhance both individual and department performance.
  • Performs all work within organization according to organizational policies, GMP, and ISO Standards
  • Performs other duties and responsibilities as assigned

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions

 

 

Networking/Key Relationships:

  • To be determined based on department needs

 

Skills & Capabilities:

  • Functional/technical skills
  • Understanding of Good Manufacturing Practice (GMP), Good Laboratory Practices (GLP)
  • Demonstrated ability to organize work assignments
  • Knowledge of laboratory equipment/QC instruments
  • Proficiency in common laboratory techniques
  • Oral and written communication skills
  • Business acumen, timely decision making

Qualifications

Minimum Knowledge & Experience Required for the Position:

  • Requires BS in a Science or Medical Technology or equivalent, plus minimum four years of experience of clinical laboratory or formulation.
  • Supervisory experience preferred.
Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement The annual salary range Werfen reasonably expects to pay for the position is $70,000 to $85,000.  Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business. 

Travel Requirements: 

  • <5% of time

 

Salary : $70,000 - $85,000

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