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Biopharmaceutical Manufacturing Associate Jobs in Georgia

SRG Government Services

Warehouse Associate

Atlanta, GA · On-site

$22/hr

Warehouse Associate Location: Marietta, GA Industry: Pharmaceutical Hours: 6am-2:30pm with ... Client is a fully integrated biopharmaceutical company focused on developing, manufacturing and ...

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Pfizer

Whether you are involved in manufacturing, testing, or compliance, your contribution will ... Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking toptalentwho are ...

All JobsBiopharmaceutical Manufacturing Associate JobsBiopharmaceutical Manufacturing Associate Jobs in Georgia

Biopharmaceutical Manufacturing Associate information

See Georgia salary details

$15

$22

$33

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Georgia is $22.90, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $26.78 per hour, depending on experience, location, and employer.

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

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

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

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.
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The most popular types of Biopharmaceutical Manufacturing jobs in Georgia are:

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For Biopharmaceutical Manufacturing Associate jobs in Georgia, the most frequently searched job titles are:

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Cities in Georgia with the most Biopharmaceutical Manufacturing Associate job openings:

Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 27% Part Time, 2% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $47,633 per year, or $22.9 per hour.

Warehouse Associate

SRG Government Services

Atlanta, GA • On-site

$22/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Warehouse Associate
Location: Marietta, GA
Industry: Pharmaceutical
Hours: 6am-2:30pm with mandatory OT and possible weekends (one could be required to come in later, stay later, etc. so need to be flexible with schedule).
Salary: Up to $22/hr.
Employment Type: Contract with the possibility to go perm (depends on client needs, performance, attendance, etc.)
Environment:
Client is a fully integrated biopharmaceutical company focused on developing, manufacturing and commercializing specialty products. Our diversified product portfolio in the specialty neurology and women's health space, together with our non-promoted complex formulations of generic drugs, form the foundation of our unwavering commitment to improve patients' lives.
Description
Coordinates the flow of raw materials and finished product through the warehouse and manufacturing areas.
Essential Responsibilities:
  • Receives incoming inventory items, verifies accuracy against PO, generates and applies batch labels, stocks inventory in the proper location and maintains the item receiving paperwork.
  • Move materials physically and within ERP Computer System to storage areas and ERP Computer System areas.
  • Create Journals (Movement, Transfer, Adjustment) as required and maintain appropriate paperwork.
  • Manage and process production and DEA waste area
  • Responsible for outbound shipping, included packing, labeling and shipping.
  • Maintain all assigned training compliance.
  • Submit/Maintain all documentation in accordance with good manufacturing practices and all applicable SOPs.
  • Performs cycle counts and inventory as required
  • Interact in a professional manner with internal and external customers
  • Monitor production schedule and anticipate production support requirements.
  • Any other activities to support the Marietta site
Core Competencies
  • Demonstrates characteristics of a good team member
  • Initiative to help without direct supervisor or lead direction.
  • Contributes fair share of the work.
  • Maintains good performance standards.
  • Works assigned shifts and stays to complete as needed to support production demands
  • Prepares materials for next batch or process
  • Maintains good attendance standards.
  • Maintain GMP Compliance.
  • Complies will all Safety Policies and consistently performs duties safety.
Minimum Qualifications
  • High School Diploma (or equivalent) or technical school certificate
  • 1 -2 years Warehouse experience.
  • Familiarity with Microsoft Office applications required.
  • Experience with SAP is highly desirable.
  • Previous experience working in a regulated environment (GMP or FDA; preferred)
  • Steel toed boots required.
Physical Requirements
  • Must be able to bend repeatedly and lift up to 50 lbs.
  • Must be able to be on feet extended periods of time
EOE/ADA
IND123
SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model-partnering closely with clients to understand not only the role, but the company's culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

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