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Pharmaceutical Manufacturing Associate Jobs (NOW HIRING)

TekWissen LLC

Manufacturing Associate

Indianapolis, IN · On-site

$15 - $19/hr

Assemble and label pharmaceutical clinical trial treatments and supplies accurately. * Follow all regulatory manufacturing standards, procedures, and compliance requirements. * Support the safe and ...

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Pharmaceutical Manufacturing Associate information

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How much do pharmaceutical manufacturing associate jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for pharmaceutical manufacturing associate in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

What does a pharmaceutical manufacturing associate do?

A Pharmaceutical Manufacturing Associate is responsible for producing medications and related products in a controlled, regulated environment. They operate and monitor manufacturing equipment, follow strict safety and quality protocols, document production processes, and ensure compliance with Good Manufacturing Practices (GMP). Their work helps guarantee that pharmaceutical products are safe, effective, and consistently meet quality standards. They may also assist in cleaning and maintaining equipment, preparing raw materials, and supporting process improvements.

What are the key skills and qualifications needed to thrive as a pharmaceutical manufacturing associate?

Pharmaceutical Manufacturing Associates require knowledge of GMP regulations, attention to detail, and at least a high school diploma—though an associate's or bachelor's degree in a science field is often preferred. Familiarity with manufacturing equipment, batch record documentation systems, and safety compliance tools such as LIMS (Laboratory Information Management Systems) is typical. Strong teamwork, communication, and problem-solving skills help individuals excel in this role. These abilities ensure product quality, regulatory compliance, and efficient production in a highly regulated environment.

What are some common challenges faced by pharmaceutical manufacturing associates during production runs?

Pharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and ensuring consistent batch quality. Working in a regulated environment means that associates must be detail-oriented and ready to document every step to comply with regulatory standards. Additionally, they may need to adapt quickly to schedule changes or production demands, while collaborating closely with quality assurance and engineering teams to resolve any issues that arise.

What is the difference between Pharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectPharmaceutical Manufacturing AssociateQuality Control Technician
CredentialsHigh school diploma or equivalent; GMP trainingHigh school diploma or equivalent; GMP and lab safety training
Work EnvironmentManufacturing floors, production linesLaboratories, testing facilities
Job FocusAssembling, packaging, and operating manufacturing equipmentTesting raw materials, in-process samples, and finished products
Industry UsageUsed across pharmaceutical manufacturing plantsCommon in quality assurance labs within pharma companies

The Pharmaceutical Manufacturing Associate primarily works on production lines, ensuring the manufacturing process runs smoothly, while the Quality Control Technician focuses on testing and verifying product quality. Both roles require GMP knowledge and are essential in pharmaceutical production, but they differ in daily tasks and work environments.

How do you get into a pharmaceutical manufacturing associate career?

To become a pharmaceutical manufacturing associate, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education or technical training in fields like biology or chemistry. Relevant skills include attention to detail, knowledge of Good Manufacturing Practices (GMP), and familiarity with manufacturing equipment. Gaining experience through internships or entry-level positions can also improve job prospects.

Is a pharmaceutical manufacturing associate a good job?

A pharmaceutical manufacturing associate is a vital role in the production of medications, involving tasks such as operating equipment, following safety protocols, and maintaining quality standards. It often offers stable employment, opportunities for skill development, and may require certifications like GMP training; the job environment is typically clean and regulated. Whether it is a good job depends on individual career goals and interest in the pharmaceutical industry.

What cities are hiring for Pharmaceutical Manufacturing Associate jobs?

Cities with the most Pharmaceutical Manufacturing Associate job openings:

What are the most commonly searched types of Pharmaceutical Manufacturing jobs?

The most popular types of Pharmaceutical Manufacturing jobs are:

What states have the most Pharmaceutical Manufacturing Associate jobs?

States with the most job openings for Pharmaceutical Manufacturing Associate jobs include:

What are popular job titles related to Pharmaceutical Manufacturing Associate jobs?

For Pharmaceutical Manufacturing Associate jobs, the most frequently searched job titles are:

Aseptic Manufacturing Associate (Weekdays)

Grand Rapids, MI • On-site

Grand River Aseptic Manufacturing, Inc.
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Grand River Aseptic Manufacturing, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Job description

Description

Aseptic Manufacturing Associate (Weekdays)


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:

The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management.


Shift Details: The primary location for this role is the Butterworth Facility, on shift A (Monday - Wednesday, and every other Thursday, from 6:00 am to 6:00 pm).


Non-Negotiable Requirements:

  • A bachelor's degree OR a high school diploma and 2+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level I role.
  • A bachelor's degree OR a high school diploma and 3+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level II role. Must also have experience working in a sterile manufacturing environment.
  • A bachelor's degree OR a high school diploma and 4+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level III role. Must also have experience working in a sterile manufacturing environment.
  • Qualification for use of a full-face respirator is required when working with hazardous chemicals. PAPR is required for working with hazardous chemicals during chemical dispense and addition activities.

Preferred Requirements:

  • Previous experience in pharmaceutical manufacturing or a laboratory environment is preferred.

Responsibilities Include (but are not limited to):

  • Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed.
  • Accurately document data and complete batch records as needed.
  • Perform cleaning and sanitization duties as instructed by the applicable procedure.
  • Successfully complete facility's aseptic gowning and manufacturing qualification program.
  • Perform duties in Grade 5, ISO 6, ISO 7, and ISO 8 cleanrooms.
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!

PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness 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!

Apply