Job Description
Work Location: Jaffrey, New Hampshire
Shift: No
Department: LS-SC-PEJFCA Membrane Analytical Lab
Hiring Manager: Halle O'Brien
This information is for internals only. Please do not share outside of the organization.
Your Role
Intermediate-level Quality Control Technician in a membrane analytical lab, supporting biopharmaceutical testing operations with a focus on safety, quality, and productivity. Skilled in basic troubleshooting and familiar with Laboratory Information Management Systems (LIMS). Duties Include:
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- Test membranes safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards.
- Safely set up and operate quality lab test equipment and monitor required inputs and outputs.
- Support quality lab operations and projects under the supervision of senior technicians.
- Accurately complete documentation per GMP standards.
- Initiate and participate in Out of Specification (OOS) investigations.
- Assist with execution of protocols, qualifications, and validations.
- Develop skills to independently perform membrane analytical testing.
- Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the working environment and the site.
- Perform basic troubleshooting and equipment set-ups, review and verify test data for accuracy, ensure proper entry into the Laboratory Information Management System (LIMS), support sustainability initiatives, and carry out tasks under close supervision.
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Physical requirements
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- Exposure to machinery and equipment, chemical reagents, biological materials at Biosafety Levels 1 and 2, in a laboratory environment.
- 100% Standing and/or sitting for duration of shift, up to 12 hours.
- Frequent lifting of 20 - 30 lbs. necessary/Max lifting - 40 to 50 lbs.
- Bend and twist as needed.
- Grasp, manipulate and handle objects consistently and regularly, Fine motor skills are required.
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B Shift M-F 2PM -10PM
Who You Are
Minimum Qualifications
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- 1+ years of laboratory or cGMP manufacturing experience.
- High school diploma or GED.
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Preferred Qualifications
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- Associate's degree in Life Science discipline.
- 2+ years of laboratory or cGMP manufacturing experience.
- Aseptic laboratory experience.
- Basic knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements.
- Basic computer skills, familiarity with Microsoft Office applications.
- Reliable and self-motivated.
- Read, follow and understand test methods, operating procedures and related documentation.
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The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.