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Full Time Biopharmaceutical Manufacturing Jobs (NOW HIRING)

Kinetic Personnel Group

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Quality Assurance Biopharma

Tustin, CA · On-site

$25 - $37.50/hr

Quality Assurance Specialist - Biopharmaceutical Manufacturing Location: Tustin, CA Employment Type: Full-Time Schedule: Multiple shifts available Position Summary We are seeking a Quality Assurance ...

New

BioTalent

Manufacturing Associate

Tustin, CA · On-site

$40K - $60K/yr

Tustin & Costa Mesa, CA Full-time | On-site If you're looking for an opportunity to build your career in biopharmaceutical manufacturing and contribute to therapies that improve patients' lives, I'd ...

ABEC Inc

Applications Engineer

Bethlehem, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full time onsite role at our Bethlehem, PA facility. Applications Engineer ... Develop technical and commercial proposals for biopharma manufacturing solutions. * Interpret ...

ABEC Inc

Applications Engineer

Bethlehem, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full time onsite role at our Bethlehem, PA facility. Applications Engineer ... Develop technical and commercial proposals for biopharma manufacturing solutions. * Interpret ...

ABEC Inc

Automation Technician

Springfield, MO · On-site

$35K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Type Full-time Description Help Power the Future of Biopharmaceutical Manufacturing We're looking for a hands-on Automation Technician to support the design, programming, testing, and ...

ABEC Inc

Applications Engineer

Bethlehem, PA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Description This is a full time onsite role at our Bethlehem, PA facility. Applications Engineer ... Develop technical and commercial proposals for biopharma manufacturing solutions. * Interpret ...

ABEC Inc

Automation Engineer

Springfield, MO · On-site

Job Type Full-time Description Help Power the Future of Biopharma At ABEC , you'll design and deliver the automation systems behind the equipment used to manufacture life-saving medicines, vaccines ...

ABEC Inc

Automation Engineer

Bethlehem, PA · On-site

This is a full-time onsite role at our Bethlehem facility. Help Power the Future of Biopharma At ABEC , you'll design and deliver the automation systems behind the equipment used to manufacture life ...

ABEC Inc

Automation Engineer

Bethlehem, PA · On-site

This is a full-time onsite role at our Bethlehem facility. Help Power the Future of Biopharma At ABEC , you'll design and deliver the automation systems behind the equipment used to manufacture life ...

ABEC Inc

Automation Engineer

Bethlehem, PA

... full-time onsite role at our Bethlehem facility. Help Power the Future of Biopharma At ABEC , you'll design and deliver the automation systems behind the equipment used to manufacture life-saving ...

Kinetic Personnel Group

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Upstream, Downstream and Formulation Openings

Tustin, CA · On-site

$20 - $21/hr

  • Medical

  • Dental

  • Vision

Biopharmaceutical Manufacturing Schedule: Multiple Shifts Available Employment Type: Full-Time Position Summary A leading biopharmaceutical manufacturing company in Tustin, CA is seeking motivated ...

ABEC Inc

Project Engineer

Springfield, MO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Springfield, MO (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As ...

ABEC Inc

Project Engineer

Springfield, MO

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Springfield, MO (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As ...

ABEC Inc

Project Engineer

Bethlehem, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Bethlehem, PA (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As a ...

ABEC Inc

Project Engineer

Springfield, MO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Springfield, MO (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As ...

ABEC Inc

Project Engineer

Bethlehem, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Bethlehem, PA (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As a ...

ABEC Inc

Project Engineer

Bethlehem, PA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Biopharmaceutical Innovation Bethlehem, PA (Full-time/Onsite) Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As a ...

ABEC Inc

Project Engineer

Wilson, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Type Full-time Description Ready to make an impact? Join ABEC and play a key role in designing systems that power life-saving biopharmaceutical manufacturing. As a Project Engineer , you won't ...

ABEC Inc

Vessel Designer

Springfield, MO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full-time onsite position located at ABEC's Springfield, MO facility Company Background: For over 50 years, ABEC has been a leading supplier to the biopharmaceutical manufacturing industry.

ABEC Inc

Project Controls Technician

Springfield, MO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Type Full-time Description Help Drive the Success of Complex Global Engineered Projects Are you ... ABEC, a global leader in biopharmaceutical manufacturing solutions, is seeking a Project Controls ...

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Full Time Biopharmaceutical Manufacturing information

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How much do full time biopharmaceutical manufacturing jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for full time biopharmaceutical manufacturing 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 are the most commonly searched types of Biopharmaceutical Manufacturing jobs?

The most popular types of Biopharmaceutical Manufacturing jobs are:

Full Time Biopharmaceutical Manufacturing jobs near you

Quality Assurance Biopharma

Kinetic Personnel Group

Tustin, CA • On-site

$25 - $37.50/hr

Full-time

Posted 2 days ago

New

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Job description

Quality Assurance Specialist – Biopharmaceutical Manufacturing

Location: Tustin, CA
Employment Type: Full-Time
Schedule: Multiple shifts available

Position Summary

We are seeking a Quality Assurance Specialist to support quality operations within a fast-paced biopharmaceutical manufacturing environment. This position will help ensure manufacturing activities comply with cGMP, FDA regulations, company procedures, and established quality standards.

The QA Specialist will work closely with Manufacturing, Quality Control, Supply Chain, and other departments to review documentation, support investigations, identify quality issues, and maintain compliance throughout the manufacturing process.

Key Responsibilities

  • Review and approve manufacturing and quality documentation, including batch records, logbooks, SOPs, forms, and controlled documents.
  • Perform in-process and floor QA oversight of biopharmaceutical manufacturing activities.
  • Ensure manufacturing operations are performed in accordance with cGMP requirements and approved procedures.
  • Review batch records and production documentation for completeness, accuracy, and compliance.
  • Support investigations related to deviations, nonconformances, and quality events.
  • Assist with CAPA development, implementation, and effectiveness monitoring.
  • Participate in change control activities and assess potential quality impacts.
  • Support internal audits, customer audits, and regulatory inspections as needed.
  • Identify potential compliance issues and communicate findings to appropriate management.
  • Assist with SOP development, revision, and implementation.
  • Review and maintain quality records and documentation in accordance with company procedures.
  • Partner with Manufacturing and QC personnel to resolve documentation and quality issues.
  • Provide guidance and training to employees regarding cGMP and quality requirements.
  • Maintain accurate and timely quality documentation.
  • Perform other quality-related duties as assigned.

Qualifications

  • Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemistry, Pharmaceutical Sciences, or a related Life Sciences field preferred.
  • 1–3 years of experience in Quality Assurance, Quality Control, or biopharmaceutical manufacturing preferred.
  • Working knowledge of cGMP and FDA regulations.
  • Experience reviewing batch records, SOPs, manufacturing documentation, or other controlled documents.
  • Familiarity with deviations, CAPA, change controls, and investigations.
  • Strong attention to detail and documentation skills.
  • Ability to identify compliance issues and effectively communicate concerns.
  • Strong written and verbal communication skills.
  • Ability to work effectively with cross-functional teams in a regulated manufacturing environment.
  • Proficiency with Microsoft Office.

Preferred Experience

  • Experience working in a biopharmaceutical, pharmaceutical, biotechnology, or CDMO environment.
  • Experience with electronic Quality Management Systems (eQMS).
  • Experience supporting FDA or customer audits.
  • Knowledge of 21 CFR Part 11 and data integrity principles.
  • Experience with aseptic processing, formulation, upstream, or downstream manufacturing is a plus.

Work Environment

This position operates in a regulated biopharmaceutical manufacturing environment and may require gowning and working in controlled manufacturing areas. The employee must be comfortable working around manufacturing equipment and following strict safety, quality, and documentation procedures.

Ideal Candidate: A detail-oriented QA professional who understands cGMP requirements, is comfortable working directly with manufacturing teams, and can identify and address quality issues before they impact product quality or compliance.