Production Technician 3, Processing
Millipore Corporation

Work Location: Indianapolis, Indiana
Shift: No
Department: LS-SC-POEMC3 Indianapolis Clinical Operations B1
Recruiter: Katherine Hall

This information is for internals only. Please do not share outside of the organization.

Your Role

The Production Technician, Processing will utilize experience and training to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through several job functions and be required to demonstrate increasing skill levels.

Responsibilities include but are not limited to:

• Comply with all Company and GMP compliance policies/procedures.
• Perform area sanitization procedures in a GMP Manufacturing facility.
• Perform filter integrity testing.
• Clean miscellaneous pieces of manufacturing equipment and vessels.
• Perform raw material weighing (dispensing) and bulk formulation.
• Assist PT3 operators as instructed.
• Perform system maintenance PM's / procedures.
• Perform sterile filtrations, unload the autoclave, and complete Steam-in-Place operations, as deemed necessary by area management.
• Assist in training/directing PT1 operators.
• Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in that training by passing test(s) administered by the company or consultant providing such training.
• Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist.

Physical Attributes:

• Regular use of hands and arms.
• Frequent standing, walking, and sitting.
• Occasionally required to stoop, kneel, bend, crouch, or crawl, talk or hear.
• Regularly lift and /or move up to 10 pounds, frequently lift and/or move up to 25 pounds.
• Specific vision abilities required by this job include close vision, distance vision, color vision and peripheral vision.

Who You Are:

Minimum Qualifications:

• High School Diploma or GED.
• 3+ years' work experience Good Manufacturing Practices (GMP) in a regulated manufacturing facility.

Preferred Qualifications:

• Bachelor's Degree in Chemistry, Biology, Biochemistry, or other Life Science discipline.
• Ability to read, comprehend, and discuss detailed GMP documentation.
• Knowledge of and experience in bulk formulation along with equipment cleaning, preparation, and assembly.

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.

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