Job Description
Job Description
Work Location: Jaffrey, New Hampshire
Shift: Yes
Department: LS-SC-PEJFCF US Jaffrey Wet Lab
Hiring Manager: Ashley Emerald
This information is for internals only. Please do not share outside of the organization. Your Role The intermediate level Physical Test Lab Quality Control Technician will be supporting the full operation of the testing of biopharmaceutical filtration devices with a focus on maximizing safety, quality, and productivity. This role supports intermediate level testing operations through basic troubleshooting on set-ups of testing processes. You will need a basic level of knowledge of the Laboratory Information Management Systems. This is a A shift position 6:00AM - 2:00PM. Duties include:
\n - Test products safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards.
\n - Safely set up and operate quality lab test equipment and monitor required inputs and outputs on equipment such as pressurized vessels, steam equipment, and various test stands.
\n - Support quality lab operations and projects under the supervision of senior technicians.
\n - Accurately complete documentation per GMP standards. Consistently demonstrate understanding of testing and paper and electronic documentation of quality sample processing.
\n - Initiate and participate in Out of Specification (OOS) investigations.
\n - Assist with execution of protocols, qualifications, and validations.
\n - Develop skills to independently perform physical testing.
\n - Ensure a clean and orderly workspace.
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Physical requirements:
\n - Exposure to machinery and equipment, chemical reagents, biological materials at Biosafety Levels 1 and 2, in a laboratory environment.
\n - 100% Standing and/or sitting for duration of shift, up to 12 hours.
\n - Frequent lifting of 20 - 30 lbs. necessary/Max lifting - 40 to 50 lbs.
\n - Bend and twist as needed.
\n - Grasp, manipulate and handle objects consistently and regularly.
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Who You Are Minimum Qualifications: \n - 1+ years of laboratory or cGMP manufacturing experience.
\n - High School Diploma or GED.
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Preferred Qualifications: \n - 2+ years of laboratory or cGMP manufacturing experience.
\n - Associates degree in Life Science discipline.
\n - Knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements.
\n - Computer skills, familiarity with Microsoft Office applications.
\n - Reliable and self-motivated.
\n - Read, follow and understand operating procedures and documentation.
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RSREMD
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.
Job Tags
Work at office, Local area, Immediate start, Shift work,