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Biotechnology Manufacturing Assistant Jobs (NOW HIRING)

Stark Pharma Solutions Inc

MD · On-site

Support commissioning, FAT/SAT , equipment startup, and qualification activities. * Assist with ... Hands-on experience in GMP pharmaceutical or biotechnology manufacturing . * Strong knowledge of IQ ...

Merck & Co.

Operations Manager

Millsboro, DE · On-site

Coordination with venders to determine equipment options * Assist in the procurement and ... GMP, biotechnology manufacturing setting with demonstrated leadership skills * OR Associate ...

MSD

Operations Manager

Millsboro, DE · On-site

Coordination with venders to determine equipment options * Assist in the procurement and ... GMP, biotechnology manufacturing setting with demonstrated leadership skills * OR Associate ...

MSD Malaysia

Operations Manager

Millsboro, DE · On-site

Coordination with venders to determine equipment options * Assist in the procurement and ... in a direct GMP, biotechnology manufacturing setting with demonstrated leadership skills

Merck & Co., Inc.

Operations Manager

Millsboro, DE · On-site

Coordination with venders to determine equipment options * Assist in the procurement and ... GMP, biotechnology manufacturing setting with demonstrated leadership skills * OR Associate ...

Pinnaql, Inc.

... biotechnology manufacturing environment. The role ensures that packaging lines are installed ... * Assist with risk assessments, test planning, and validation strategies in accordance with ...

New

System One

Manufacturing Associate

Novato, CA · On-site

$28/hr

Sunday -Tuesday/ with alternating Saturdays 6pm-7am Overview Leading biotechnology company looking ... * Assist in the development, review, and implementation of operational procedures and process ...

System One

Manufacturing Associate

Novato, CA · On-site

$28/hr

Overview Leading biotechnology company looking for a Manufacturing Associate. Ideal candidates ... substances. * Assist in process optimization initiatives and identify processing issues for ...

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Biotechnology Manufacturing Assistant information

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$12

$20

$39

How much do biotechnology manufacturing assistant jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotechnology manufacturing assistant in the United States is $20.54, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $21.15 per hour, depending on experience, location, and employer.

What is the difference between Biotechnology Manufacturing Assistant vs Laboratory Technician?

AspectBiotechnology Manufacturing AssistantLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require technical certificationsAssociate's degree or relevant technical certification
Work EnvironmentManufacturing floors, production facilities, cleanroomsResearch labs, testing facilities, research environments
Employer & Industry UsageBiotech manufacturing companies, pharmaceutical firmsResearch institutions, biotech labs, pharmaceutical companies

While both roles support biotech operations, the Biotechnology Manufacturing Assistant focuses on production and manufacturing processes in a controlled environment, whereas the Laboratory Technician is primarily involved in research, testing, and experimental procedures. The roles often overlap in skills but differ in daily tasks and work settings.

What cities are hiring for Biotechnology Manufacturing Assistant jobs?

Cities with the most Biotechnology Manufacturing Assistant job openings:

What states have the most Biotechnology Manufacturing Assistant jobs?

States with the most job openings for Biotechnology Manufacturing Assistant jobs include:

What are popular job titles related to Biotechnology Manufacturing Assistant jobs?

For Biotechnology Manufacturing Assistant jobs, the most frequently searched job titles are:

Infographic showing various Biotechnology Manufacturing Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 1% Temporary, and 3% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $42,717 per year, or $20.5 per hour.

Validation Engineer / Validation Specialist

MD • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 18 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Validation Engineer right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Validation Engineer / Validation Specialist

Location: Maryland
Duration: Long-Term Contract

Job Overview

We are seeking an experienced Validation Engineer/Validation Specialist to support equipment, utilities, and facility qualification activities in a GMP-regulated pharmaceutical/biotechnology manufacturing environment. The ideal candidate will have hands-on experience executing validation protocols and supporting commissioning, qualification, and compliance initiatives.

Key Responsibilities

  • Develop, execute, and document IQ, OQ, PQ, and Requalification (RQ) protocols for manufacturing equipment and utilities.
  • Prepare validation reports, SOPs, risk assessments, gap analyses, and technical documentation following GDP and cGMP requirements.
  • Perform thermal mapping studies using Kaye AVS or Veriteq data loggers.
  • Analyze validation data and investigate deviations to ensure compliance with acceptance criteria.
  • Support commissioning, FAT/SAT, equipment startup, and qualification activities.
  • Assist with audits and provide technical support for manufacturing and validation investigations.
  • Review validation documentation and collaborate with Engineering, Manufacturing, Quality, and Maintenance teams.

Required Qualifications

  • Bachelor's degree in Engineering or a related scientific discipline with 4+ years of validation experience, or 8+ years of relevant validation experience without a degree.
  • Hands-on experience in GMP pharmaceutical or biotechnology manufacturing.
  • Strong knowledge of IQ/OQ/PQ, cGMP, GDP, and validation lifecycle.
  • Experience with aseptic processing, cleanrooms, sterilization equipment, and critical utilities (HVAC, WFI, RO, compressed air, etc.).
  • Familiarity with Kaye AVS, Veriteq, EDMS, LIMS, Microsoft Office, and related validation systems.
  • Excellent troubleshooting, documentation, and communication skills.
  • Ability to manage multiple projects independently and in a team environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com