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Biopharmaceutical Manufacturing Associate Jobs (NOW HIRING)

System One Holdings, LLC

Manufacturing Associate

Novato, CA · On-site

$28 - $32.20/hr

Operate and support biopharmaceutical manufacturing processes including mammalian cell culture ... Associate's degree in a science-related field or biotech certificate with 2+ years of experience in ...

Adecco

Senior Manufacturing Associate

Plainville, MA · On-site

$31/hr

If Senior Manufacturing Associate sounds like something you would be interested in, and you meet ... Strong understanding of GMP regulations and biopharmaceutical manufacturing processes * Proven ...

GSK Internships & Co-ops powered by Atrium

PA · Hybrid

GSK is a global biopharma company with a special purpose - to unite science, technology and talent ... The Production organization is comprised of manufacturing associates, supervisors, managers, and ...

GSK Internships & Co-ops powered by Atrium

PA · Hybrid

GSK is a global biopharma company with a special purpose - to unite science, technology and talent ... The Production organization is comprised of manufacturing associates, supervisors, managers, and ...

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Biopharmaceutical Manufacturing Associate information

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$18

$27

$40

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for biopharmaceutical manufacturing associate in the United States is $27.12, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.73 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, and why are they important?

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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Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $56,412 per year, or $27.1 per hour.
Biopharmaceutical Manufacturing Associate

Biopharmaceutical Manufacturing Associate

Lancesoft INC

Rockville, MD • On-site

$23 - $25/hr

Contractor

Posted 17 days ago

Job description

Job Title: Biopharmaceutical Associate I

Location: Rockville MD 20850

Duration: Minium 12 months with possibility of extension up to 18 months (Opportunity to convert to an FTE)

 

Shifts:

Training Shifts

  • First 6 Weeks
  • Monday – Friday (8:00 – 5:00 PM)

After Training Shifts (24/7/365 Operations)

  • Day Shift: 6:00 AM EST – 6:30 PM EST
  • Night Shift: 6:00 PM EST – 6:30 AM EST
  • Weekend: Rotating Biweekly Schedule
  • One Week – 2 Days On, 2 Days Off, 3 Days On
  • Other Week – 2 Days Off, 2 Days On, 3 Days Off

 

Job Purpose:

  • The Rockville Biopharm site exists to produce and deliver biopharmaceutical drug substance of the highest quality in a safe, compliant, reliable, and cost-effective manner for their patients. The vison is to be wholly entrusted to make innovative, high-quality medicines by leveraging the best talent & technology, on a platform of continuous improvement to supply every patient, every time.

 

Key Responsibilities:

  1. Preparation, cleaning, sterilization, batching, pasteurization, or filtration & delivery of media and solutions for cell culture & purification operations.
  2. Perform the set-up, operation, cleaning, and break down of process equipment.
  3. Perform sampling procedures on various analytical instruments to analyze cell culture, solution, and/or product concentration characteristics.
  4. Operate Filter integrity equipment to confirm the integrity of filters pre & post use.
  5. Perform process operations, equipment, and instrument monitoring & trending to enable proactive identification of issues to escalate and correct with applicable departments.
  6. Set-up fixed & mobile process equipment and parts with CIP (Clean In Place) skids to carry out validated cleaning & sterilization processes.
  7. Follow appropriate standard operating procedures (SOP’s), protocols, and batch records/logbooks to safely perform operations & document compliantly with good documentation and data integrity practices.
  8. Follow all related safety policies and procedures and put safety first by playing an active role in identifying and correcting unsafe behaviors and conditions.

Education, Knowledge, Experience Required:

Education

  • Minimum Level of Education Required- High School Diploma or Equivalency
  • Preferred Level of Education- Bachelor of Science/Art/associate’s degree in Biological Sciences, Chemical Sciences, Engineering, or equivalent technical discipline.

 

Job Related Experience

  • Minimum Level of Experience - 0-1 years of directly related Manufacturing experience in the pharmaceutical or biotechnology industry.

 

Compliance & Documentation

  • Ability to follow detailed instructions and document accurately
  • Practices good documentation and data integrity standards
  • Adheres to safety procedures and promotes a strong safety culture

 

Communication & Teamwork

  • Proficient in speaking, reading, writing, and understanding English.
  • Strong verbal & written communication skills
  • Demonstrated ability to work effectively in a team
  • Willing & able to work 24/7 rotating shifts

 

Technology Tools

  • General proficiency with Microsoft Office (Excel, Word, Outlook)
  • Basic knowledge of ERP Systems (M-ERP) per global/local procedures
  • Familiar with automation systems & emerging digital platforms.

 

Physical Requirements

  • Able to lift & carry materials up to 50 lbs.

Company Description

LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.
LanceSoft logo

About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

Social media

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