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Biopharmaceutical Manufacturing Associate Jobs in Ohio

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Biopharmaceutical Manufacturing Associate information

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$25

$38

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Ohio is $25.78, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $30.14 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 Ohio are:

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Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, 1% Temporary, and 4% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $53,630 per year, or $25.8 per hour.

Manufacturing Associate I-OSD 1st Shift

Alkermes

Wilmington, OH • On-site

Full-time

Re-posted 20 days ago

Job description


This position reports to a Supervisor, Manufacturing. The hours of this position are Monday to Friday 7:30a to 4:00p.
Position Summary:
This entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches.
Responsibilities
Essential Functions:
The essential functions of this position include:
  • Production, bulk packaging, and inspection of pharmaceutical drug formulations
  • Assisting with facility cleaning and operational maintenance
  • Cleaning all manufacturing equipment and areas
  • Assisting with facility and process validations as required
  • Assisting with environmental and water system monitoring as required
  • Assisting with RCRA and safety inspections as required
  • Documenting all work as required by cGMPs and GDPs on a timely basis
  • Reading and following all Company SOPs and guidelines
  • Abiding by all safety requirements as defined by the company
  • Completing other tasks as assigned by supervision

Qualifications
Preferred Qualifications:
  • Basic knowledge of the Scientific Method
  • Basic math skills including addition, subtraction, multiplication, division, and percentages
  • Basic knowledge of and adherence to current GMPs and GDPs
  • Basic knowledge of chemistry and biology
  • Basic knowledge of HAZCOM, RCRA, and other Safety requirements
  • Basic level of mechanical aptitude
  • Good documentation skills
  • Ability to learn how to operate all types of production equipment (i.e. Blenders, HMIs, Tablet presses, Coaters, Wash off lines, Comils, etc.)
  • Ability to read, understand, and accurately follow company SOPs and guidelines
  • Basic knowledge of computer systems (Microsoft Suite, SAP, Veeva Vault, LMS)
  • Understanding and comprehension of Master Batch Records
  • Detail-oriented
  • Willingness to learn new tasks and skills
  • Ability to work well in a team environment
  • Ability to respond quickly and execute assignments
  • Willingness to readily adapt to changing job duties
  • Positive attitude
  • Understanding of and promotion of company and customer objectives
  • Ability to follow all procedures to ensure a high-quality product

Education and Experience:
Manufacturing Associate I
Basic Qualifications:
  • High School diploma or equivalent

Preferred Qualifications:
  • 0-1 years of experience in a pharmaceutical manufacturing operation, preferably in OSD
  • A bachelor's degree is preferred; other relevant work experience, education, and training will be considered.

Manufacturing Associate II
Basic Qualifications
  • High School diploma or equivalent
  • 1-3 years of experience in a pharmaceutical manufacturing operation.

Preferred Qualifications
  • 1+ year experience in OSD Manufacturing
  • Associate degree or higher in a science/technical discipline
  • Other relative work experience, education, and training will be considered

Manufacturing Associate III
Basic Qualifications
  • High School diploma or equivalent
  • 4-5 years of experience in a pharmaceutical manufacturing operation.

Preferred Qualifications
  • 2-3 year experience in OSD Manufacturing
  • Associate degree or higher in a science/technical discipline
  • Other relative work experience, education, and training will be considered

Working Conditions:
Available for any shift with the possibility for overtime (as necessary)
Physical Requirements:
  • Ability to push and/or pull equipment or product using a pallet jack
  • Ability to lift/move 40 lbs. overhead.
  • Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time
  • Must be able to be medically cleared for respirator use (PAPR)
  • Ability to operate different types of production equipment.
  • Ability to gown correctly for clean room manufacturing operations.
  • Ability to stand or sit for extended periods (up to 4 hours at a time).
  • Must be able to work in an office and a manufacturing environment.

About Us
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.

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