Job Description
Work Location: Jaffrey, New Hampshire
Shift: Yes
Department: LS-SC-PEJFCG Jaffrey QC Micorlab
Recruiter: Katherine Hall
Hiring Manager: Zachary Rice
This information is for internals only. Please do not share outside of the organization.
Your Role:
Intermediate level Microbiology Lab Quality Control Technician responsible for making medias, sterilizing equipment, preparing test devices of biopharmaceutical filtration membranes with a focus on maximizing safety, quality, and productivity. Supports intermediate level testing operations through basic troubleshooting on set-ups and retention testing processes.
Basic level of knowledge of the Laboratory Information Management System.
Responsibilities include but are not limited to:
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- Making medias, sterilizing equipment, preparing test devices 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.
- 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 Media Prep. tasks.
- Ensure a clean and orderly workspace.
- Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the work center and the site.
- Review and verify process data. Ensure accurate entry of data into the Laboratory Information Management System.
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Physical Attributes:
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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.
- Grasp, manipulate and handle objects consistently and regularly.
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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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- Associates Degree.
- 2+ years of laboratory or cGMP manufacturing experience.
- Aseptic laboratory experience.
- Experience with EHS, ISO, cGMP, and other manufacturing regulatory requirements.
- Microsoft Office experience.
- Ability to read, follow and understand test methods, operating procedures, and 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.