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Grand River Aseptic Manufacturing

Biopharmaceutical Inspector 2nd Shift Entry Level

Entry-Level JobVerifiedNo experience needed

Career Insights for Quality Technician (General)

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What they do

A Quality Technician inspects products to assure compliance with given standards including durability , functionality, quality, and safety.

$43,635 / year median in Michigan

+2% projected growth

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Job Description

Description Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day! Overview of this
Position:
As a Biopharmaceutical Inspector you'll play a crucial role in ensuring the quality and compliance of our products. You'll be responsible for visual inspections of our sterile liquid medication, along with some labeling, and packaging of products according to established procedures and cGMP regulations under the oversight of the FDA. With guidance from experienced technicians and supervisors, you'll help uphold our high standards and contribute to the success of our Finishing department.
Non-Negotiable Requirements:
High School Diploma/GED Proficiency in Microsoft Word, Excel, and Outlook Ability to pass a vision screening and Visual Inspection Qualification testing (can wear glasses/contacts)
Preferred Requirements:
Associate degree or equivalent Familiarity with QA principles and procedures in a pharma, biopharma, or biotech manufacturing environment Knowledgeable about GMP standards Experience in an FDA-regulated environment Previous experience in pharmaceutical inspection OR packaging with a solid understanding of cGMP and FDA guidelines. Responsibilities Include (but are not limited to): Inspection along with some, labeling and package finished products (sterile liquid medicine) Operate Finishing equipment Adhere to finishing procedures and PDA guidelines Accurately document data and complete any corresponding paperwork Contribute to maintaining an FDA-compliant facility Full job description available during formal interview process. What Sets GRAM Apart from
Other Employers:
BENEFITS
starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums! Paid
VOLUNTEERISM
starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO:
Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF
Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS
We offer 10 paid holidays per calendar year with immediate eligibility!
PAY:
Depends on Experience and is discussed during the interview process. If you meet the required criteria listed above, GRAM welcomes you to apply today! GRAM supports Equal Opportunity Employment